Endometriosis Support Group
Endometriosis is a common medical condition where the tissue lining the uterus is found outside of the uterus, typically affecting other organs in the pelvis. The condition can lead to serious health problems, primarily pain and infertility. A major symptom of endometriosis is pain, mostly in the lower abdomen, lower back, and pelvic area.
http://www.feinberg.northwestern.edu/obgyn/divisions/biology/bulun/aromatase%20inhibitors.html
i had a hyst in 2000, and I had many hormonal problems, they tried everything, I thought i was going nuts(anxiety, depression)finally they tried "bioidentical" hormones, better now!
have you ever tried just progest? it helped me for about 6 mths.
I do believe that endo affects our hormones, probably a great deal. Also having ovarian cysts can affect your mood as well. I just had a cyst rupture last week, and I noticed that my mood had changed very much to depression. I think most doctors don't know what they are talking about when it comes to endo. I am lucky to have finally found one that seems to know what he is doing, but it has taken me a very long time.
That;s another thing that has me vexed, I have been experiencing alot of pain on my left side for over a year. I was able to get an ultra sound done last March and it showed a 2.4cm cyst. I was told that this is why I'm in so much pain on that side. NOW this gyno says that it is in no way causing that pain because of the type of cyst it is, or WAS. It was a follicular cyst, the type us women get every month along with our period. It appears when you ovulate and dissipates once your period is done. SO I'm back to square one on my left sided pain. I ask this gyno about getting a scan and she doesn't agree that I should have one. She totally feels that once my periods stop, so will the pain and I can't seem to tell her any different.
I'm about ready to cry at this point!!!! It's not like I've given up, I'm trying to get the right kind of help. All these doctors want to do is mess with my hormones by giving them to me or taking them away!!! Most of them don't even recognize this as a disease, they just see it as an annoying women's disorder! We really need to raise awareness, especially with these "doctors"!!!!
Thank you everyone for your input!
I'm seriously thinking about sending her some literature about different views on endo. Perhaps it will "plant a seed", but I'm sure that's just wishful thinking. It couldn't hurt though. :)
Thanks!
and sswarning~ i totally agree with this having something to do with our hormones being screwed up. you would think that perhaps instead of all this trial and error crap that they could check out levels and possibly personalize our treatments accordingly...at least as far as trying to balance our levels out.
I'm not on any birth control...and I do not have extra bleeding, only during period.