Surgery for Endometriosis

After a long battle with health and misdiagnosed conditions over the past few years, my daughter finally received a true but unfortunate diagnosis last month.

PCOS and highly likely Endometriosis.
For those that do not know, Endometriosis can only be 100% diagnosed & treated through surgery. But with that comes either high cost (specialist & private hospital) or a very lengthy and uncertain wait (general surgeon & 2.5+ years on the public hospital waitlist).
For the past 5 years she has been living with Disabilities from an accident which has made life harder and dire due to her limited abilities. Employment is almost impossible to get and she has not worked in over 3 years due to her Brain Injury.
For the past 10+ years she has been living through incredible pain each day in her Ovaries, Uterus and Cervix not just during menstruation periods, but each day.

Her specialist has run all the tests and scans needed, requested additional appointments with other medial specialist while also booking her for Surgery just 6 weeks after the initial due to symptoms and test results.
My daughter is facing Endometrial Cancer and the likelihood of the pain / condition returning in just 3-5 years which means more surgery.
So with all the statistics, research and recommendations in mind she is facing and strongly pushing for a Hysterectomy (Uterus and Ovaries) during the Laparoscopic Endometriosis Surgery. To remove the extreme daily pain, symptoms, reoccurrence and restore quality of life.
This comes with a high cost for Private Hospital and Specialist. Or face over 2 years waiting for a surgery date in the public sector.

We have no help from others, a 1 income household in a world that has rising cost crippling us all. All of her medication, treatments and appointments for her Brain Injury have been privately paid and without government assistance.
So every bit of money spent goes to bills and appointments without enough left for her much needed surgery.