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Noor Taher Top 100 Instagram Photos and Posts

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Most liked photo of Noor Taher with over 239.7K likes is the following photo

Most liked Instagram photo of Noor Taher
We have around 101 most liked photos of Noor Taher with the thumbnails listed below. Click on any of them to view the full image along with its caption, like count, and a button to download the photo.

Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - a praia & the sun…❤️‍🔥
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Noor Taher Instagram - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Noor Taher Instagram - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Noor Taher Instagram - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Noor Taher Instagram - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Noor Taher Instagram - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Noor Taher Instagram - …🎀
Noor Taher Instagram - …🎀
Noor Taher Instagram - في ذكرى كل ليان حول العالم💔 In memory of every Layan around the world💔 الأغنية: حدود ووعود - @hayazaatry ‎#مدرسة_الروابي_للبنات
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - she smiles!
Noor Taher Instagram - 🫧🫧🫧
Noor Taher Instagram - 🫧🫧🫧
Noor Taher Instagram - … & thats just what they’ll do 👢 @revolve
Noor Taher Instagram - … & thats just what they’ll do 👢 @revolve
Noor Taher Instagram - … & thats just what they’ll do 👢 @revolve
Noor Taher Instagram - pt. 2 with a tutuuu
Noor Taher Instagram - pt. 2 with a tutuuu
Noor Taher Instagram - pt. 2 with a tutuuu
Noor Taher Instagram - pt. 2 with a tutuuu
Noor Taher Instagram - lil studio moment w @zaidallozi 🐇
Noor Taher Instagram - lil studio moment w @zaidallozi 🐇
Noor Taher Instagram - lil studio moment w @zaidallozi 🐇
Noor Taher Instagram - @redseafilm 🐇
Noor Taher Instagram - @redseafilm 🐇
Noor Taher Instagram - 💌 @redseafilm
Noor Taher Instagram - 💌 @redseafilm
Noor Taher Instagram - 💌 @redseafilm
Noor Taher Instagram - 💌
Noor Taher Instagram - 💌
Noor Taher Instagram - 💌
Noor Taher Instagram - mirror mirror on the wall.. 🪩
Noor Taher Instagram - mirror mirror on the wall.. 🪩
Noor Taher Instagram - mirror mirror on the wall.. 🪩
Noor Taher Instagram - mirror mirror on the wall.. 🪩
Noor Taher Instagram - mirror mirror on the wall.. 🪩
Noor Taher Instagram - loewe u and leave u🌹 @loewe
Noor Taher Instagram - loewe u and leave u🌹 @loewe
Noor Taher Instagram - loewe u and leave u🌹 @loewe
Noor Taher Instagram - loewe u and leave u🌹 @loewe
Noor Taher Instagram - loewe u and leave u🌹 @loewe
Noor Taher Instagram - #ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers
Noor Taher Instagram - #ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers
Noor Taher Instagram - IT’S LIVE! @ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور 📍FULL link in bio • رابط المقابلة في البايو Production / @bukhashbrothers #ABtalks #NoorTaher #AndriaTayeh #أندريا_طايع #نور_طاهر
Noor Taher Instagram - ?
Noor Taher Instagram - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Noor Taher Instagram - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Noor Taher Instagram - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Noor Taher Instagram - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Noor Taher Instagram - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Noor Taher Instagram - Ramadan haircare routine ✨ @lorealpro @lorealpro_education_middleeast #lorealpro
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher Instagram - celebrating love, family, new family🤍… & dolphins
Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 239.7K Likes - For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜

239.7K Likes – Noor Taher Instagram

Caption : For as long as I can remember, I’d find myself passed out on the floor not remembering what happened with a throbbing pain in my head. I was always confused why bright lights would trigger a migraine which later would result in me having absent seizures that I wasn’t even aware of. Fast forward to March 2022 when I was at a party with flashing lights and abruptly had consecutive tonic and clonic seizures which terrified everyone around me. Tests were done and I thought I was fine, until a while back when I had more consecutive and intense seizures. I was rushed by an ambulance to the ICU where I had to stay for a couple of weeks. The experience was terrifying and depressing to say the least, but I was finally diagnosed and I learned that I have epilepsy. For those who don’t know, epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations and sometimes loss of awareness. Epilepsy is hard to live with, its not just temporary seizures and waking up from them, its having painful bruises on every part of your body and not remembering how you got them, and having to spit out blood because you’ve bitten your tongue and the insides of your mouth during a seizure. To say it’s exhausting is an understatement. I’m thankful to say that I have the most amazing support system around me, my closest friends and family have been patient and reassuring trying to understand epilepsy and help me through it, you know who you are and I love you. Another special thanks to the amazing neurologist and nurses that made my stay in the ICU a somewhat bearable experience. If I were to say that I’m motivated and hopeful about my diagnosis then I’d be lying, I am terrified. However I’m also trying my best and for now, I think thats enough. If you are also diagnosed with epilepsy, or any type of seizure disorder, know that you are not alone, I’m sharing my story because I want to be the person I needed to talk to, and to raise awareness about a condition thats not nearly talked about enough. I have epilepsy. It doesn’t have me. 💜
Likes : 239666Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168.7K Likes - a praia & the sun…❤️‍🔥

168.7K Likes – Noor Taher Instagram

Caption : a praia & the sun…❤️‍🔥
Likes : 168683Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 168K Likes - better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤

168K Likes – Noor Taher Instagram

Caption : better late than never.. some more Tokyoooo🚦🍓🍡🤖 🐰🍨 💤
Likes : 167953Noor Taher - 149.1K Likes - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍

149.1K Likes – Noor Taher Instagram

Caption : To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Likes : 149092Noor Taher - 149.1K Likes - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍

149.1K Likes – Noor Taher Instagram

Caption : To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Likes : 149092Noor Taher - 149.1K Likes - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍

149.1K Likes – Noor Taher Instagram

Caption : To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Likes : 149092Noor Taher - 149.1K Likes - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍

149.1K Likes – Noor Taher Instagram

Caption : To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Likes : 149092Noor Taher - 149.1K Likes - To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍

149.1K Likes – Noor Taher Instagram

Caption : To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
Likes : 149092Noor Taher - 145.3K Likes - …🎀

145.3K Likes – Noor Taher Instagram

Caption : …🎀
Likes : 145251Noor Taher - 145.3K Likes - …🎀

145.3K Likes – Noor Taher Instagram

Caption : …🎀
Likes : 145251Noor Taher - 124K Likes - في ذكرى كل ليان حول العالم💔 In memory of every Layan around the world💔 الأغنية: حدود ووعود - @hayazaatry ‎#مدرسة_الروابي_للبنات

124K Likes – Noor Taher Instagram

Caption : في ذكرى كل ليان حول العالم💔 In memory of every Layan around the world💔 الأغنية: حدود ووعود – @hayazaatry ‎#مدرسة_الروابي_للبنات
Likes : 123987Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 112.3K Likes - she smiles!

112.3K Likes – Noor Taher Instagram

Caption : she smiles!
Likes : 112262Noor Taher - 103.1K Likes - 🫧🫧🫧

103.1K Likes – Noor Taher Instagram

Caption : 🫧🫧🫧
Likes : 103088Noor Taher - 103.1K Likes - 🫧🫧🫧

103.1K Likes – Noor Taher Instagram

Caption : 🫧🫧🫧
Likes : 103088Noor Taher - 101.6K Likes - … & thats just what they’ll do 👢 @revolve

101.6K Likes – Noor Taher Instagram

Caption : … & thats just what they’ll do 👢 @revolve
Likes : 101582Noor Taher - 101.6K Likes - … & thats just what they’ll do 👢 @revolve

101.6K Likes – Noor Taher Instagram

Caption : … & thats just what they’ll do 👢 @revolve
Likes : 101582Noor Taher - 101.6K Likes - … & thats just what they’ll do 👢 @revolve

101.6K Likes – Noor Taher Instagram

Caption : … & thats just what they’ll do 👢 @revolve
Likes : 101582Noor Taher - 101.4K Likes - pt. 2 with a tutuuu

101.4K Likes – Noor Taher Instagram

Caption : pt. 2 with a tutuuu
Likes : 101396Noor Taher - 101.4K Likes - pt. 2 with a tutuuu

101.4K Likes – Noor Taher Instagram

Caption : pt. 2 with a tutuuu
Likes : 101396Noor Taher - 101.4K Likes - pt. 2 with a tutuuu

101.4K Likes – Noor Taher Instagram

Caption : pt. 2 with a tutuuu
Likes : 101396Noor Taher - 101.4K Likes - pt. 2 with a tutuuu

101.4K Likes – Noor Taher Instagram

Caption : pt. 2 with a tutuuu
Likes : 101396Noor Taher - 100.1K Likes - lil studio moment w @zaidallozi 🐇

100.1K Likes – Noor Taher Instagram

Caption : lil studio moment w @zaidallozi 🐇
Likes : 100109Noor Taher - 100.1K Likes - lil studio moment w @zaidallozi 🐇

100.1K Likes – Noor Taher Instagram

Caption : lil studio moment w @zaidallozi 🐇
Likes : 100109Noor Taher - 100.1K Likes - lil studio moment w @zaidallozi 🐇

100.1K Likes – Noor Taher Instagram

Caption : lil studio moment w @zaidallozi 🐇
Likes : 100109Noor Taher - 98.7K Likes - @redseafilm 🐇

98.7K Likes – Noor Taher Instagram

Caption : @redseafilm 🐇
Likes : 98717Noor Taher - 98.7K Likes - @redseafilm 🐇

98.7K Likes – Noor Taher Instagram

Caption : @redseafilm 🐇
Likes : 98717Noor Taher - 96.4K Likes - 💌 @redseafilm

96.4K Likes – Noor Taher Instagram

Caption : 💌 @redseafilm
Likes : 96372Noor Taher - 96.4K Likes - 💌 @redseafilm

96.4K Likes – Noor Taher Instagram

Caption : 💌 @redseafilm
Likes : 96372Noor Taher - 96.4K Likes - 💌 @redseafilm

96.4K Likes – Noor Taher Instagram

Caption : 💌 @redseafilm
Likes : 96372Noor Taher - 83.6K Likes - 💌

83.6K Likes – Noor Taher Instagram

Caption : 💌
Likes : 83577Noor Taher - 83.6K Likes - 💌

83.6K Likes – Noor Taher Instagram

Caption : 💌
Likes : 83577Noor Taher - 83.6K Likes - 💌

83.6K Likes – Noor Taher Instagram

Caption : 💌
Likes : 83577Noor Taher - 83.2K Likes - mirror mirror on the wall.. 🪩

83.2K Likes – Noor Taher Instagram

Caption : mirror mirror on the wall.. 🪩
Likes : 83237Noor Taher - 83.2K Likes - mirror mirror on the wall.. 🪩

83.2K Likes – Noor Taher Instagram

Caption : mirror mirror on the wall.. 🪩
Likes : 83237Noor Taher - 83.2K Likes - mirror mirror on the wall.. 🪩

83.2K Likes – Noor Taher Instagram

Caption : mirror mirror on the wall.. 🪩
Likes : 83237Noor Taher - 83.2K Likes - mirror mirror on the wall.. 🪩

83.2K Likes – Noor Taher Instagram

Caption : mirror mirror on the wall.. 🪩
Likes : 83237Noor Taher - 83.2K Likes - mirror mirror on the wall.. 🪩

83.2K Likes – Noor Taher Instagram

Caption : mirror mirror on the wall.. 🪩
Likes : 83237Noor Taher - 77.4K Likes - loewe u and leave u🌹 @loewe

77.4K Likes – Noor Taher Instagram

Caption : loewe u and leave u🌹 @loewe
Likes : 77387Noor Taher - 77.4K Likes - loewe u and leave u🌹 @loewe

77.4K Likes – Noor Taher Instagram

Caption : loewe u and leave u🌹 @loewe
Likes : 77387Noor Taher - 77.4K Likes - loewe u and leave u🌹 @loewe

77.4K Likes – Noor Taher Instagram

Caption : loewe u and leave u🌹 @loewe
Likes : 77387Noor Taher - 77.4K Likes - loewe u and leave u🌹 @loewe

77.4K Likes – Noor Taher Instagram

Caption : loewe u and leave u🌹 @loewe
Likes : 77387Noor Taher - 77.4K Likes - loewe u and leave u🌹 @loewe

77.4K Likes – Noor Taher Instagram

Caption : loewe u and leave u🌹 @loewe
Likes : 77387Noor Taher - 47.3K Likes - #ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers

47.3K Likes – Noor Taher Instagram

Caption : #ABtalks Together with @andria_tayeh & @noorrtaher – مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers
Likes : 47284Noor Taher - 47.3K Likes - #ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers

47.3K Likes – Noor Taher Instagram

Caption : #ABtalks Together with @andria_tayeh & @noorrtaher – مع أندريا و نور أندريا طايع ونور طاهر ممثلتان صاعدتان في العالم العربي. نعُرفهن بتنافسهن الشهير على الشاشة في المسلسل الدرامي مدرسة الروابي للبنات على نتفليكس. عرفتوهم كأعداء في المسلسل، لكن هل تعرف كيف تبدو صداقتهم في الحياة الواقعية؟ أندريا ونور يكشفان عن لحظات خاصة من علاقتهما في برنامجنا حيث يتحدثان عن الغيرة والمنافسة والحب وتقبل الذات والمزيد. معارف، أفضل الأصدقاء، أعداء أم مجرد زملاء فقط؟ انت صاحب القرار. تابعو معنا. Andria Tayeh and Noor Taher are both upcoming actresses in the Arab world. They are known for their famous on-screen rivalry on the Netflix drama series called AlRawabi School for Girls. You know them as nemeses on the show, but do you know what their friendship is like in real life? Andria and Noor uncover special moments of their relationship on this #ABtalks Together as they talk about jealousy, competition, love, self-acceptance and more. Acquaintances, best friends, enemies or just co-stars? You decide. Stay Tuned. Tuesday 9 pm (GST) on YouTube. الثلاثاء ٩ مساءً بتوقيت الإمارات على اليوتيب. Production / @bukhashbrothers
Likes : 47284Noor Taher - 27.3K Likes - IT’S LIVE! @ABtalks Together with @andria_tayeh & @noorrtaher - مع أندريا و نور 📍FULL link in bio • رابط المقابلة في البايو Production / @bukhashbrothers #ABtalks #NoorTaher #AndriaTayeh #أندريا_طايع #نور_طاهر

27.3K Likes – Noor Taher Instagram

Caption : IT’S LIVE! @ABtalks Together with @andria_tayeh & @noorrtaher – مع أندريا و نور 📍FULL link in bio • رابط المقابلة في البايو Production / @bukhashbrothers #ABtalks #NoorTaher #AndriaTayeh #أندريا_طايع #نور_طاهر
Likes : 27271Noor Taher - 3 Likes - ?

3 Likes – Noor Taher Instagram

Caption : ?
Likes : 3Noor Taher - 3 Likes - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!

3 Likes – Noor Taher Instagram

Caption : 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Likes : 3Noor Taher - 3 Likes - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!

3 Likes – Noor Taher Instagram

Caption : 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Likes : 3Noor Taher - 3 Likes - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!

3 Likes – Noor Taher Instagram

Caption : 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Likes : 3Noor Taher - 3 Likes - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!

3 Likes – Noor Taher Instagram

Caption : 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Likes : 3Noor Taher - 3 Likes - 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!

3 Likes – Noor Taher Instagram

Caption : 6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
Likes : 3Noor Taher - 3 Likes - Ramadan haircare routine ✨ @lorealpro @lorealpro_education_middleeast #lorealpro

3 Likes – Noor Taher Instagram

Caption : Ramadan haircare routine ✨ @lorealpro @lorealpro_education_middleeast #lorealpro
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
Likes : 3Noor Taher - 3 Likes - celebrating love, family, new family🤍… & dolphins

3 Likes – Noor Taher Instagram

Caption : celebrating love, family, new family🤍… & dolphins
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