Is Anyone On Disability For Endometriosis? | MyEndometriosisTeam

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Is Anyone On Disability For Endometriosis?
A MyEndometriosisTeam Member asked a question 💭

I have several painful conditions, endometriosis being one of them, my pain is so severe and now been hospitalized twice due to small bowel obstruction. Also they found I have an autoimmune type of esophagitis. My insides are constantly inflamed and my cysts are very painful especially before and during my period and it’s getting worse every month, last two periods I ended up in the ER. I can barley eat due to all the stomach issues and the fatigue is real. Any advice for getting disability??

posted August 23, 2023
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A MyEndometriosisTeam Member

I am on disability for endometriosis. I can work part time when I’m m in a good space physically. It took me two tries. My advice is get a good lawyer.
I also have major bowel and digestion problems.
Find a way to keep positive and I will keep you and all our endometriosis sisters in my prayers.
Diane

posted August 24, 2023
A MyEndometriosisTeam Member

See an artheitis/auto immune doc. If you have not

posted August 24, 2023
A MyEndometriosisTeam Member

Have you seen an arthritis, autoimmune doc. Had blood work ran? That is your first step to getting answers, what about a neurologist as well? Those 2 will be the most important, besides your endometriosis and women's specialty dr/surgeon.

posted September 27, 2023
A MyEndometriosisTeam Member

In the process, will let you know how it goes...🤞🏾

posted September 27, 2023
A MyEndometriosisTeam Member

If you have not see a gastrointologist doc. Have them look as far down as possible with and upper scope. Take care honey, I'm so sorry this is happening to you.

posted August 25, 2023

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