March is Endometriosis Awareness Month

It is so important to learn all about this invisible Illness. It’s not just during your periods. It’s pain anywhere at anytime. It can mimic IBS and gas. I’ve had pains in all sorts of places. Education is key. And expect to see a lot this month as we wear yellow to show support. The more we know, the better armed we are to speak up to our doctors and find the one who will listen and help. Right now excision is the only true pain relief we have. There is no cure, there’s no miracle pill or shot to alleviate the pain we feel daily. Nothing can fix our infertility issues, it is what it is. A disease that needs a cure just like cancer! I have found my support group in my #endosisters on twitter and my family is always there for me. Lets let all of the other girls know we are here to help and listen!


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.
This entry was posted in endometriosis awareness, excision surgery for endometriosis, hope and love, infertility, invisible illness and tagged , , , , , , , . Bookmark the permalink.

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