The good part
Stage 1
One time, my menstrual pain was too much, so my mother decided to take me to the immediate care in the area as it was a weekend. Nothing against them, but they were no help. The male doctor said it was period pain and he couldn't do anything for me. Tylenol to the rescue again?!
Then the day came that changed everything! After my soccer final game, I was in extreme pain, so we took a trip to the emergency room. I was scared but knew there was nobody else. When we got there, we waited forever! But once I was in a room, I explained my situation, and they ran lots of tests on me. The doctors knew something was wrong from the ultrasound. They asked if I had an OBGYN; we said yes; they called her at midnight and talked to her about their findings. We had an appointment in three days.
Before my Surgery
Stage 2
At the OBGYN appointment, they took new ultrasound images. The doctor described a normal uterus as looking like a horseshoe or a pearl. Well, mine looked like a heart. She wanted to confirm with the main surgeon.
So one of the head doctors decided to come and see me. She wanted to check to see if there was a clear path for the blood to leave my body during my period, and you could say I failed that test. There was a piece of tissue blocking the exit point for the blood, and only portions of the blood were leaving during my period, which was not good at all.
They decided I needed surgery, but before that, they wanted to make sure that they knew everything that was going on inside, so they ordered an MRI.
Stage 3
After that, my OBGYN decided to stop my period until we figured out the next steps. This was when the doctors said that the only way they could fix the problem( removing the tissue blocking my exit) was with surgery. They also were going to try to reconstruct my heart-shaped uterus and make it into a normal one so I could have a normal period
Once I got the MRI, they found out I had only 1 kidney. We learned that there is something called Ohvira, which is a complex condition where women with double uteruses will most likely have only 1 kidney. (we did not know how important this was until we visited a kidney specialist in the months that followed)


