Hello, my name is Aubrey. I am 28 and I have endometriosis and PCOS. Around 9 years ago, I started going to the ER for rupturing ovarian cysts. If you’ve ever felt that pain, you know it’s unbearable to the point that you start throwing up. It started to be pretty common for me; every 6 or so months I would experience another ruptured cyst and my mom would take me to the ER. I never really thought anything of it because the dr. would just tell me, “oh every women has cysts and some rupture and some don’t.” So I was like, okay cool, so this is normal I guess. Wrong.
I was on two rounds of Clomid and the second round was awful. One summer day I’m at lagoon with my sister and her kids and I started feeling really uncomfortable, almost gassy but I could not pass gas. We left and I was still hurting and the pain increased, and my right side lower abdomen was bulging. She rushed me to the ER and at this point I had already been consulting with dr. Google to see what it could be, first thing came up was OHSS ovarian hyper-stimulation syndrome. After some ultrasounds and ctscans it was confirmed that Clomid gave me OHSS. I remember the dr. telling me, “your ovaries are supposed to be the size of almonds. Yours are currently the size of an avocado.” The nurse there was super kind and told me that she had tried different fertility pills too and ended up in the same boat as me, but she prayed and said “Okay God, I’ll stop taking these pills if you give me a baby,.” And then she had 7 kids. She was like, “so you know, be careful what you wish for.”
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