Living with Endometriosis and Pelvic Congestion Syndrome

I have endo! I don't have pcs but I know people that do and I know it is UNBEARABLE. Both are very sucky to have, my cat helps with my endo he pushes on my stomach.

I've never been officially diagnosed through a lap with endo (I have with PCS through a CTV scan) they assume I have it because it runs in my family and I have all the main symptoms (tmi but my grandma had blood clots the size of baseballs that would clog the toilet)

Does it hurt for you to push on your uterus area? I think it's an endo symptom but not sure, the spot that hurts to touch has been hurting without touching it lately

I used too, I bled from January-June straight before they finally switched my bc again and now since I switched I've only spotted/bled after sex

Do u bleed heavily too

Yep I am in my 30s I only have one ovary I was diagnosed a year ago and b4 they did my d And surgery they told me I had pcos too

I can't always tell if my general pain is from endo or PCS but some specific PCS symptoms I have are my left foot getting hot red/purple, pain with standing too long/pain with sitting too long, veins popped out in my stomach/vulva/legs/feet (mostly always the left side), numb legs/tingly legs, persistent genital arousal disorder (PGAD) - one of the worst symptoms tbh, vulvar itching, feeling full and very bloated when I go from laying down to standing and several others that are also endo symptoms. I am only 20 years old and want children so I am trying to stay away from vein sclerotherapthy and coil embolizatio...they just keep switching my bc and hoping it does something but I'm exhausted/depressed and just want relief. I sure you can both understand that feeling

Yes what are your symptoms I’m so sorry

I’m sorry

I pcos and endometriosis

Do u pcos and endometriosis