Hi everyone :) For those who aren't close to me, I was formally diagnosed with endo and polycystic ovaries about 3 and a half years ago, but I have been suffering the symptoms since early high school.

I used to think the pain was normal. I'm sure many of my friends remember when I fainted in the middle of by boarding school's dining hall just because of my period cramps. I was told time and time again by doctors that it's normal, or to go on birth control, one even told me I should get pregnant to stop the growth for 9 months. I have spent thousand's of dollars on different doctors and tests.

I'm sure many women have similar stories to this one. It's not a great feeling being constantly burdened with excruciating pain that comes out of nowhere. It affects my relationship, my social life and my physical and mental wellbeing. I'm an active person, so it's a kick in the gut when I feel I can't even reach my full potential when this silly little disease gets the best of me. Current tests indicate that I have a more serious stage of endo, explaining all the pain I get.

I have finally found an amazing doctor though! Unfortunately, there are not many specialists in this field that 'close the gap' in medical fees. With my full time studies, and only part time work, it's been difficult to save so much for a surgery so soon, in addition to paying bills and groceries. It almost feels shameful to ask, but I would truly appreciate if my friends, loved ones, or anyone feeling a little generous would be kind enough to help out. A little goes a long way!

(Of course I won't take offence if you don't donate, every one has their own financial struggles).