These stories can help other women so they do not feel so alone when trying to cope with effects of this disease.
Endometriosis post menopausal
In late 2012, at age 47.5, I was declared post menopausal based on blood work. In early 2013, an intra-uterine polyp had developed (and burst), and I bled profusely for 2 weeks. No doubt, retrograde bleeding resulted in some endometrial cells lodging in my pelvis.
I had a D&C to clear out the polyp, and we've since learned there is a statistically significant correlation between the D&C procedure and endometriosis development.
All through 2013 and most of 2014, the pain got worse. Despite what web sites and others say there is NO blood test, imaging or anything else that can signal to the doc you have endometriosis.
I was disbelieved by my gyn group to a person, and a second opinion doc (internal specialist) said I needed a healer and that I had adhesions.
Abdominal laparoscopy occurred in late 2014 confirmed endometriosis in my abdomen; and the female surgeon was dismissive in post-op stating "you only had 7 lesions". Three weeks after laparoscopy the pain came roaring back and I lived with it.
In fall 2015 I went back to the docs with a bad flare up and we scheduled a hysterectomy and bilateral oophorectomy (this occurred in 2016). I'm one month out from the surgery as of today and am cautiously optimistic.
I plan to demand aromatase inhibitors as the next step if the pain continues after a 3 month waiting period. Needless to say, I'm unhappy with my docs but they are in my health plan. I cannot believe I am the ONLY post menopausal patient of theirs with this condition. I keep suggesting they publish my case if it is so unique.
Also, can anyone out there let this forum know why in the heck doctors push estrogen replacement therapy when endometriosis is an estrogen dependent condition? Makes me want to scream.
Join in and write your own page! It's easy to do. How? Simply click here to return to Your length of time for diagnosis of endometriosis.
As featured in: