When I was first told about the strong possibility of having endometriosis I felt alone. The words made life feel like it had come to a standstill. The anger attached because of how much I'd been dismissed and my symptoms seen as something "psychological" and not being validated. I knew nobody who had this condition which I'd never heard of. The hours after that appointment researching what endometriosis was. I saw C that same day and when she said to me " I've got that too" it had become the most comforting words I'd heard that day. To meet someone who could share the same struggle with me and not pretend to know what I was dealing with. To have someone who I could share this uncertain journey with and who'd be able to advise because they'd been where I was when first receiving a diagnosis. I found the processing of what I was dealing with hard. There were so many things that came into question fertility being the biggest one. When you're young you have dreams of what you want in life when you become an adult things like having your own children and bringing them up to be the best that they can possibly be. I'm going to be honest here but it was so overwhelming. The amount of misinformation I was given by professionals who clearly misunderstood the condition. The best thing I ever done was join online support groups and meeting other women who suffer from this horrendous condition.
Those women who are also known as my endo sisters. They became my hope on the dark days and understand what I was thinking and feeling. To read posts from other women with the same fears as me. To finally not feeling ashamed of saying what I was thinking and hearing/seeing the words "me too." The girls who have become like family and who just get how much suffering we have to deal with and the things endometriosis does. My endo sisters are my biggest supporters and have been the light when I've been in the darkness💛🎗
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