It’s so important to not compare your energy levels to those around you without a #chronicillness Difficult to do but important! I’ve been hit hard with #fatigue today 💤
It can be so awful to get stuck with a disease you never could have imagined happening to you. A big sense of injustice arises. But it does help to know that you arent alone, so heres a reminder! #spoonie#autoimmunedisease#gpa#chronicdisease#chronicillness
You know you’re a veteran of Chronic Illnesses when you are disappointed with a good appointment because now, you have to go run twenty more tests to figure out what obscured problem you have now #ChronicIllness
@nytimes I hope a cure for endometriosis is found in my lifetime. It is a horrible disease that affects every facet of your life. Even on the mini pill, I have symptoms. Wouldn't wish it on my worst enemy. #endowarrior
“Every patient deserves to be treated with dignity and respect. Nobody should be made to feel inferior or afraid, or that they cannot trust their doctor.”
https://t.co/KVafeVT6mf
#endo#endometriosis#endowarrior
The book that every #endometriosis patient needs — it's part practical #selfcare manual, and part support and #advocacy guide for people with endometriosis. https://t.co/47M57Vhf5K @jessicamurnanes @knowyourendo https://t.co/AcpFzNegof
There is a lack of awareness about #endometriosis of the diaphragm among patients as well as healthcare professionals causing delays in diagnosis.
https://t.co/H2smwbTl1u
The more people shine a light on #endometriosis and it’s devastating effects the more chance we have of receiving the funds needed to do the research to make a difference. https://t.co/Ov8YpWfI5W
For the last 7+ years living with #endometriosis /#PCOS, I’ve struggled with anxiety, depression & the constant what if on whether I’ll one day be a #mom. This #NationalInfertilityAwarenessWeek, if you’ve stayed up late wondering the same ... just know that you’re not alone.💕