Fear of Diagnosis: Seeking Advice

I was diagnosed 3 years ago when I had a chocolate cyst removed and it was diagnosed as endo. Another lump showed up and I had to have a hysterectomy and lump removal, but they got everything out so very little to no pain now!

I was diagnosed and got surgery 2 years ago this August. My periods were so bad back when I was 16 I was almost passing out. My mom put me on birth control and later told me she had endo in her 20s. So my symptoms were mostly my periods. They were heavy, black blood, lower back pain, extreme nausea, dizziness if I hadn't taken pain killers yet, taking 6+ pills a day during period, 7 day long period, bad cramps that made me freeze but I couldn't be sitting down either and if I was then I had to hoist my butt to hover over the chair until it passed. Even though I was 90% sure I had endo at 16 I wasn't mentally ready for surgery and recovery until I was 20. The birth control actually helped quite a bit (less days bleeding) and surgery made my periods 100x better. Now I just take 1 pain killer for the first 2 days and the last 2 just chill. It has cut down on the bleeding, pain, just everything, and now my blood is red instead of black! But I had to fight tooth and nail to be heard by doctors. The local place just kept saying yeah what do you want us to do? And I just wanted anything to help. I found a specialist who heard my symptoms over the phone and asked why I hadn't had an ultrasound yet. You are your biggest advocate. Do not be silenced.

I haven't been diagnosed either but i Definitely know I have it I changed my whole diet and it changed my whole life because certain foods flare up endo