I was 16 (now 27) when i started with endo symptoms and didnt get diagnosed till i was 21 did any one else suffer or suffering with it this long and still no where in finding anything that helps with the side affects and pain ?? Ive now been told i could also have andomeosis after have my 8 ovarian cyst removed along with my right ovary and falopian tube.
I have had numerous contraceptive pills, the c injection, m coil and the zoladex injection and nothing so far has helped, im just expected to carry on with tramadol pain killers, iron tablets and which dont help when pains & bleeding are at there worst. I was very lucky to become a mummy 18 months ago (was told i wouldn't be able to conceive natrually at 19, then told my pregnancy wouldn't last term well go over 6 weeks then 12, and i went ten days over 40weeks 😁) and i really hate that i seem to be getting worse and no where with managing the endometriosis and its like my gps have given up but refuse to give me a hysterectomy.
Sorry for the extra long post xx