Endometriosis ~ My Journey

As it is the final day of endometriosis awareness month I wanted to share something more personal in relation to how Endometriosis affects me. I have been debating this month on how much to share as I do not want anyone’s sympathy I just want awareness of this disease to be out there so others recognise signs and are diagnosed earlier.

  1. Every day I suffer with various pains predominantly in my pelvic area and back.  
  2. The pain I experience is as follows: stabbing pains, constant dull ache, nipping, twisting and stretching my insides, constant stich in my sides, feeling as someone is punching at my organs and burning sensations as if my insides are about to explode.
  3. It takes 2hrs every morning to get my pain under control to be able to move and start my day.
  4. I suffer with nausea and vomiting which regularly hits me so bad…

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About our last embryo

I have Endometriosis, Adenomyosis and Hashimoto's Thyroiditis. I've had Lyme, Bell's Palsy and the Shingles before I was 25. I've done IVF twice, with and without immunosuppression and FET. I am married to my best friend and I am Infertile.
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