Actress Esme Creed-Miles HD Photos and Wallpapers February 2025

This morning I completed my second laparoscopic surgery to remove endometriosis from my pelvis. Whilst I love any and all sympathy (ahahaha) – what I really want to do is say this: For years pre my diagnosis I was in agony and multiple doctors and expert gynecologists told me nothing was wrong with me. I have spent allot of time in the emergency room this year due to chronic pain and when I’m not in pain, dealing with the fatigue and discomfort that comes along with the disease. I am SO insanely lucky to have been operated on today. One in ten women suffer from this disease and it’s widely misunderstood and under-diagnosed, if you have this condition (or if you think you do and no one will tell you so🤬): I see you and I’m sending you so much love. I have the recourses to afford excellent healthcare and it’s still hard for me, so I’m sending support to all those who are still on waiting lists – still being gaslit by their doctors – still waiting in emergency rooms because the triage system makes no accommodations for endometriosis related agony. This is not just “period pain”: you are a warrior. Thank you endlessly to the friends who have been there for me this year and today, to my family who drop everything to rescue me when I’m in pain, to the casting directors and directors who gave me opportunities that have afforded me this care and the ability to take care of my body with healthy food and supplements – this SHOULD be available to ALL women, and I intend to make it a mission of my humble existence to inform others on this condition and help those who need it most. If you are a fellow endo warrior, comment here I’d love to meet you ❤️ P.s : Golden hour in the hospital room ?!

This morning I completed my second laparoscopic surgery to remove endometriosis from my pelvis. Whilst I love any and all sympathy (ahahaha) – what I really want to do is say this: For years pre my diagnosis I was in agony and multiple doctors and expert gynecologists told me nothing was wrong with me. I have spent allot of time in the emergency room this year due to chronic pain and when I’m not in pain, dealing with the fatigue and discomfort that comes along with the disease. I am SO insanely lucky to have been operated on today. One in ten women suffer from this disease and it’s widely misunderstood and under-diagnosed, if you have this condition (or if you think you do and no one will tell you so🤬): I see you and I’m sending you so much love. I have the recourses to afford excellent healthcare and it’s still hard for me, so I’m sending support to all those who are still on waiting lists – still being gaslit by their doctors – still waiting in emergency rooms because the triage system makes no accommodations for endometriosis related agony. This is not just “period pain”: you are a warrior. Thank you endlessly to the friends who have been there for me this year and today, to my family who drop everything to rescue me when I’m in pain, to the casting directors and directors who gave me opportunities that have afforded me this care and the ability to take care of my body with healthy food and supplements – this SHOULD be available to ALL women, and I intend to make it a mission of my humble existence to inform others on this condition and help those who need it most. If you are a fellow endo warrior, comment here I’d love to meet you ❤️ P.s : Golden hour in the hospital room ?!

This morning I completed my second laparoscopic surgery to remove endometriosis from my pelvis. Whilst I love any and all sympathy (ahahaha) – what I really want to do is say this: For years pre my diagnosis I was in agony and multiple doctors and expert gynecologists told me nothing was wrong with me. I have spent allot of time in the emergency room this year due to chronic pain and when I’m not in pain, dealing with the fatigue and discomfort that comes along with the disease. I am SO insanely lucky to have been operated on today. One in ten women suffer from this disease and it’s widely misunderstood and under-diagnosed, if you have this condition (or if you think you do and no one will tell you so🤬): I see you and I’m sending you so much love. I have the recourses to afford excellent healthcare and it’s still hard for me, so I’m sending support to all those who are still on waiting lists – still being gaslit by their doctors – still waiting in emergency rooms because the triage system makes no accommodations for endometriosis related agony. This is not just “period pain”: you are a warrior. Thank you endlessly to the friends who have been there for me this year and today, to my family who drop everything to rescue me when I’m in pain, to the casting directors and directors who gave me opportunities that have afforded me this care and the ability to take care of my body with healthy food and supplements – this SHOULD be available to ALL women, and I intend to make it a mission of my humble existence to inform others on this condition and help those who need it most. If you are a fellow endo warrior, comment here I’d love to meet you ❤️ P.s : Golden hour in the hospital room ?!