Permanent #CeasefireNow !!! We must keep protesting, shutting shit down, donating, calling & writing elected officials, posting and uplifting the voices on the ground!!!
Netanyahu must listen to the families of the hostages who have been screaming and protesting for months and take the deal to free them!!!
Permanent #CeasefireNow !!! We must keep protesting, shutting shit down, donating, calling & writing elected officials, posting and uplifting the voices on the ground!!!
Netanyahu must listen to the families of the hostages who have been screaming and protesting for months and take the deal to free them!!!
Permanent #CeasefireNow !!! We must keep protesting, shutting shit down, donating, calling & writing elected officials, posting and uplifting the voices on the ground!!!
Netanyahu must listen to the families of the hostages who have been screaming and protesting for months and take the deal to free them!!!
This is infuriating and unacceptable and why N95 masks need to be mandated in healthcare. High risk people should not have to risk death and having permanent, new health issues in trying to get the care they need. @ucsfhealth
#Repost @disability_visibility
・・・
“Help me urge @ucsfhealth to require all staff, patients, and visitors to wear N95 masks
#N95s4UCSF #KeepMasksInHealthcare
Link in bio
My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became a terrifying reality when I had a medical emergency that required a visit to the ER and brief hospitalization in the ICU.
Disabled, immunocompromised, and chronically ill people know fully well that the world is not designed for us and how we are often dehumanized and considered burdens by the medical industrial complex. It is an exhausting struggle to be seen and heard while fighting to survive in the face of systemic oppression.
While I was in the hospital I tweeted some of my experiences because I needed to document what was happening and do something while filled with fear.
Writing and organizing is a way to channel my rage and process my medical trauma.
I call upon you all to help me push for a N95 mask mandate at UCSF Health.
No one should have to delay care or risk infection from COVID when receiving necessary medical care.
Image description: A picture of me, an Asian American disabled woman. There is a tracheostomy at my throat connected to a ventilator tube. A white gauze dressing is tucked around the tracheostomy. I am wearing a camouflage jacket. My eyes are swollen after crying uncontrollably for hours and barely able to open. I look miserable.”
This is infuriating and unacceptable and why N95 masks need to be mandated in healthcare. High risk people should not have to risk death and having permanent, new health issues in trying to get the care they need. @ucsfhealth
#Repost @disability_visibility
・・・
“Help me urge @ucsfhealth to require all staff, patients, and visitors to wear N95 masks
#N95s4UCSF #KeepMasksInHealthcare
Link in bio
My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became a terrifying reality when I had a medical emergency that required a visit to the ER and brief hospitalization in the ICU.
Disabled, immunocompromised, and chronically ill people know fully well that the world is not designed for us and how we are often dehumanized and considered burdens by the medical industrial complex. It is an exhausting struggle to be seen and heard while fighting to survive in the face of systemic oppression.
While I was in the hospital I tweeted some of my experiences because I needed to document what was happening and do something while filled with fear.
Writing and organizing is a way to channel my rage and process my medical trauma.
I call upon you all to help me push for a N95 mask mandate at UCSF Health.
No one should have to delay care or risk infection from COVID when receiving necessary medical care.
Image description: A picture of me, an Asian American disabled woman. There is a tracheostomy at my throat connected to a ventilator tube. A white gauze dressing is tucked around the tracheostomy. I am wearing a camouflage jacket. My eyes are swollen after crying uncontrollably for hours and barely able to open. I look miserable.”
This is infuriating and unacceptable and why N95 masks need to be mandated in healthcare. High risk people should not have to risk death and having permanent, new health issues in trying to get the care they need. @ucsfhealth
#Repost @disability_visibility
・・・
“Help me urge @ucsfhealth to require all staff, patients, and visitors to wear N95 masks
#N95s4UCSF #KeepMasksInHealthcare
Link in bio
My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became a terrifying reality when I had a medical emergency that required a visit to the ER and brief hospitalization in the ICU.
Disabled, immunocompromised, and chronically ill people know fully well that the world is not designed for us and how we are often dehumanized and considered burdens by the medical industrial complex. It is an exhausting struggle to be seen and heard while fighting to survive in the face of systemic oppression.
While I was in the hospital I tweeted some of my experiences because I needed to document what was happening and do something while filled with fear.
Writing and organizing is a way to channel my rage and process my medical trauma.
I call upon you all to help me push for a N95 mask mandate at UCSF Health.
No one should have to delay care or risk infection from COVID when receiving necessary medical care.
Image description: A picture of me, an Asian American disabled woman. There is a tracheostomy at my throat connected to a ventilator tube. A white gauze dressing is tucked around the tracheostomy. I am wearing a camouflage jacket. My eyes are swollen after crying uncontrollably for hours and barely able to open. I look miserable.”
This is infuriating and unacceptable and why N95 masks need to be mandated in healthcare. High risk people should not have to risk death and having permanent, new health issues in trying to get the care they need. @ucsfhealth
#Repost @disability_visibility
・・・
“Help me urge @ucsfhealth to require all staff, patients, and visitors to wear N95 masks
#N95s4UCSF #KeepMasksInHealthcare
Link in bio
My recent column in Teen Vogue about the surge and its impact on me as a high risk disabled person became a terrifying reality when I had a medical emergency that required a visit to the ER and brief hospitalization in the ICU.
Disabled, immunocompromised, and chronically ill people know fully well that the world is not designed for us and how we are often dehumanized and considered burdens by the medical industrial complex. It is an exhausting struggle to be seen and heard while fighting to survive in the face of systemic oppression.
While I was in the hospital I tweeted some of my experiences because I needed to document what was happening and do something while filled with fear.
Writing and organizing is a way to channel my rage and process my medical trauma.
I call upon you all to help me push for a N95 mask mandate at UCSF Health.
No one should have to delay care or risk infection from COVID when receiving necessary medical care.
Image description: A picture of me, an Asian American disabled woman. There is a tracheostomy at my throat connected to a ventilator tube. A white gauze dressing is tucked around the tracheostomy. I am wearing a camouflage jacket. My eyes are swollen after crying uncontrollably for hours and barely able to open. I look miserable.”
Friends friending while keeping each other safe @k8beastman 🥰✨💕😷
Slides from @clean.air.club 💕
(Not pictured: multiple tests leading up to our hang, hot hands hand warmers in pockets and gloves, and a stroll)
Hang on my loves. Let us learn to weave 💜
image by @faratucker
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
I came across Lauren’s (@iamlaurenhannah ) story though this tweet just the other day and it broke my heart. 💔
The system is failing people. Especially in the U.S where the safety nets are so inadequate, the #1 reason people declare bankruptcy, and #MECFS is so underfunded, misunderstood, not believed, and stigmatized. ME/CFS used to be known as Chronic Fatigue Syndrome but the name felt trivial to many comparison to the realities of living with it.
In her last blog post, Lauren wrote (in Dutch),
“I know you guys are tired of it, but I’m going to say it anyway. Please protect yourself against COVID-19. It still ensures that too many people have to live with a severe disability. Long COVID and ME are not very different. Believe me, you don’t want this to happen to you.”
Lauren’s blog:
https://hersenmist.wordpress.com/
(it’s in Dutch but you can use Google translate)
Lauren’s X/Twitter:
@dutchlauren
Lauren did not get ME/CFS from Long COVID, but it is one of the more common chronic illnesses/disabilities that people get due to Long COVID. Long COVID is not a joke, protect yourself and others by wearing a respirator (N95 is best, KN95 next best).
Hearts are especially heavy in the Long COVID & ME/CFS community today. 💜
For those dealing with ME/CFS and Long COVID, I see you and I will continue to fight with you.
🙏🏼❤️🔥🙏🏼
If you are struggling/thinking of suicide in the U.S. you can call or text 988. (Disclaimer that less than 2% of calls resulted in 911 being called). If you google “suicide hotline” you can find others in your respective counties.
#MECFS #RememberLauren #MillionsMissing
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
🐸🥰🐸
Repost @blossoming.resistance (music added by me)
・・・
“[Image 1: Drawing of Frog & Toad sitting by a fireplace sharing drinks, Text reads Frog & Toad Reciprocity & Community Care Rooted in disability justice.
Image 2: Frog’s arms stretched out while talking, Toad sitting looking at Frog, Text reads Frog & Toad show us that reciprocity looks different depending on needs, situation, access, capacity.
Image 3: Frog talks arm around Toad who is in pajamas and eyes closed while they stand on the porch, Text reads As disabled, crip, neurodivergent, edgewalking beings…
Image 4: Toad brings tea to Frog who is in bed, Text reads Sometimes we caregive…
Image 5: Frog leans in the window giving Toad company while Toad is in bed, Text reads And other times we are cared for…
Image 6: Toad brings Frog a big bowl of cookies, Text reads Community care is when those whose needs are most inaccessible are centered and not forgotten.
Image 7: Frog & Toad sit together on the porch, garden in the background, Text reads Disability justice is a guide for community care.
Image 8: Toad reads to Frog, Text reads May we continue to weave reciprocity in wild & beautiful ways.
Image 9: Frog & Toad stand looking in a mirror, Text reads And in these moments may we remember the humble non-binary complexities of Frog & Toad that encompass & embody what care is.
Image 10: Frog & Toad sit on a rock, their backs to us, looking out at the water around them, Text reads In this time of collective grief, may we mend through remembrance. May Frog & Toad guide us on a journey of how disability justice is the key to reciprocity, community care & our collective thriving.] “
#disabilityJustice #frogAndToad #queerCrips #reciprocity #communityCare #collectiveCare
💜💔💜💔
#Repost @sonyareneetaylor
・・・
“Full Version: A Prayer for the Collective
My video got cut off as a Reel. This is the full version. Captions are up on YouTube, linked in my Stories ❤️🩹”
Repost @vicgovdh featuring @sickandtiredaus
・・・
“Jordan got COVID in January 2022, and his life hasn’t been the same since.
He shares with us how his life has been impacted by long COVID and urges Victorians to stay ahead of the virus.
To learn more about the symptoms and diagnosis of long COVID, visit the link in bio.“
This could be us but you human. 🐰
An invitation to lean into a moment of breath and softness.
Repost @naturre