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Has anybody had something done to see if Endo was on their bladder, bowel, or other places? If so, can you tell me about how they found it and how it was taken out. Also, if you don't mind, your symptoms with the Endo other than the pelvic area? I'm trying to figure out if my symptoms may be Endo that traveled elsewhere in my body?
My dr found everything via laproscopic. Endo is considered an auto immune disease by some.
The Center for Endo Care reviewed my case and think the endo has moved to my bladder, originally found in 2013 in my intestine. Recently I've been having pressure on my bladder so I can't tell if I have to go potty and sometime when I do actually go potty is hurts like a mother!
Yes. The doctor thinks that it's RA or Lupus, that just isn't showing on the blood test. According to him, some people have it for 10 years before it shows on the test.
Yes it travels and grows into stages at times. Mine is 4+ however i also have pelvic adheisive disease stage 4+ the endo endo is under the adheisive disease basically unless i dont have adheisions by chance in a certain area. There are alot of symptoms ! Hard crazy periods started young usually ...pain pain pain . I personally was underdiagnosed for my two lovelys from age 13 to 46 then it was everywhere just last july 2015 . I had a endometriosis biopsy . In the office hurt like hell. I you honestly believe you have it push push and keep pushing until they either give u a lap or a endo biopsy.
Best of health and bestest of luck hun
KellxXx
If u have chronic joint inflammation, has your dr ever mentioned possible rheumatoid arthitis maybe?
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