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Post by hopelasts on Feb 18, 2014 16:38:10 GMT -5
Hello endosisters!
I'm new to this website but i'm always looking for ways to interact with others who are going through this. I was diagnosed in Aug. 2012 through surgery, although I have suffered with symptoms for years. The surgeon found it on my uterus, however i believe it is in other locations as well because my symptoms have never went away. I have a lot of left kidney pain, lower left abdominal pain that I feel mostly after eating or drinking. I have been trying the endo diet and interstitial cystitis diet as well as this is another one of my diagnosis as of Dec 2013. Interstitial cystitis is a bladder syndrome and although it is extremely uncomfortable I feel like its more than that I think I may have endometriosis on my bladder and bowl and it is being misdiagnosed for interstitial cystitis. Anyone else going through this?
I'm having a terrible day of pain, i'm a full time student and I just got a job after being out of work for a year with no help. I'm not too sure how this message board works but I really hope someone sees this and it speaks to them.
Thank you in advance for taking the time to read this. Much love, Imari
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Emily
Full Member
Posts: 148
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Post by Emily on Feb 18, 2014 19:09:55 GMT -5
Hi Imari, welcome to the boards! I was diagnosed a little over a year ago and have been having tons of trouble with bladder and GI pain. I was also diagnosed with IC, but my urologist thinks that endo may be on my bladder. It's really quite a mess to try to figure out what is endo and what is not, so I definitely feel your pain. Oddly enough, most of my issues are on my left side as well! Have you tried pelvic physical therapy? I know a lot of ladies here swear by it.
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