All I want for Christmas is my endometriosis surgery.
Hi everyone, my name is Yami. Since I was 15-16 I’ve been experiencing debilitating symptoms that at first seemed to only be gastrointestinal.
Over the years I would receive many diagnosis reports and different treatments but nothing worked for too long. PCOS, Fatty Liver, Gastroparesis, IBS, ovarian cyst ruptures, pelvic floor issues, etc.
Upon individual research over time, I began to explore the idea of having endometriosis, likely linked to my bowels. I found a specialist who agreed with me, but the only way to concrete know for sure is laparoscopic surgery.
With insurance, I’m still looking at around $1000-$1500 for the time off alone. I would have to be off work for a minimum of two weeks, highly likely more time if the Endo turns out to be deeply widespread in my body. The risk of Endo in my bowels is very high.
I have waited and pushed it off for a while but with symptoms getting worst sporadically and not responding to treatments that helped before, I know I need to do this.
So I need your help! Help me raise the funds to get my surgery and make up for the cost of being in recovery ❤️
Any little bit helps and I greatly appreciate your consideration. I hope I can finally get some concrete answers and get on the right path to long term treatment!
There is no cure to Endo. But let’s start fighting this battle.


