This has truly been an exhausting and trying journey for me. I was diagnosed two years ago and I had no clue on how to deal with such news nor did I have a clue of what my condition was until after my first lap. surgery. For many years I battle with this condition but I always thought it was just my cycle and just to pop a few pain pills here and there I would be just fine. But one summer I started having pains like my cycle every other day and I knew something was not normal about this pain. It would happen at any given time and whatever I was doing at the time had to come to a complete stop. This went on for years I went to Dr after Dr trying to figure out what was going on with me. I was back and forth to the hospital and only sent home with more pain pills. It wasn't until my mom took me to her Gynecologist that I had to under go a pap and ultrasound and he found that I had cysts on my ovaries on the size of a tangerine and he decided to go in and perform exploratory surgery. Since then it has been a none stop roller coaster in my life and my bed and heating pad have become my best friends. I started this blog to share my story and to help no only myself cope with this condition but to give a listening ear and helping hand to other women and young girls like me who have no outlet or no one to turn to. Endometriosis is not a condition to be taken lightly it has been over looked for years but it needs to be brought to the forefront to raise awareness and help us find a cure. So throughout this journey I will blog each day on my health and how I fight through endo and facts and awareness to help my endo sisters all over the world...
#TEAMFIGHTLIKEAGIRL#ENDOMETRIOSIS#TEAMYELLOW4ENDO#
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