Hi all, I’m 35 with suspected endo and been on arm implant (nexplanon) + desogestrel (progesterone only pill) for a year and a half.
The implant on its own stopped the worse of cramps and heavy bleeding, but I was getting light bleeds almost daily for a couple of months, so was prescribed first a combined mini-pill (still bleeding), then the progesterone pill instead, keeping the implant in.
About 4 months ago I started getting very bad nausea almost daily, and IBS symptoms I couldn’t shift (mild diarrhoea, can’t fully empty bowels, bloating and burping, loss of appetite because of the nausea), with a month relief when I started antidepressants (citalopram).
Figured out my arm implant is in end-stage (6 months left to 3 year official expiry), so this could all be my progesterone levels getting low.
My question is if the idea is keeping a high dose of progesterone, do I get a replacement implant, or double up on the progesterone pill? Does anyone have experience of hormonally controlling suspected endo, and any interactions with IBS? I’ve got my first gynaecology review appointment in June 2024 (haha), but have to make a little-informed decision before then as the nausea and ibs are too much for me.
Additionally, while the antidepressant is working wonders, depression is a side-effect of hormonal contraception. I’ve had depression on and off since I started my periods, and have almost always been on hormonal contraceptives for pregnancy-protection, bar when I got my two children. I’ve also started getting anxiety when I got Covid a year and half ago (correlates with hormonal experimentations). Any comment/your experience of this welcome!
Thanks