I have had the symptoms of IC and Endometriosis for as long
as I can remember but thought that I was normal. One thing that did not seem
normal to me was that I was not getting pregnant, and I had no idea why. Friends,
family, and acquaintances all around me were starting families and some were
experiencing unplanned pregnancies, but my husband and I were not able to do
conceive
In the summer of 2012, shortly after our relocation to
Phoenix, my Endo, PFD and IC symptoms hit a peak. I was having a difficult time
urinating, and it really hurt to empty my bladder. I was diagnosed with PFD and
IC before my laparoscopy in November. During the laparoscopy, I was officially
diagnosed with Endometriosis, even though the medical term was brought up to my
attention long before the laparoscopy.
Now everything was starting to make sense. For four years I
had been trying to conceive, while constantly wondering why I was unable to
conceive with my husband. Now I knew that the issue was most likely
Endometriosis, a medical term that I despise. Despite my disgust for the term, my
goal is to raise Endo awareness while documenting my fertility journey.
I am nervous and scared to share this part of my life with
you. However, I feel that I owe it to every woman who has or will continue to
suffer from Endometriosis.
This is for all of the women who have been down such a long,
dark path of learning to cope and become at peace with fertility issues. I want
to be your voice. This is my journey, no filter.
xo Heather
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