Share Your Story : Andy

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Andy was diagnosed with Endometriosis when she was 23.  Now 29, Andy hasn’t let her diagnosis slow her down:  She’s earned her Ph.D., is always active and continues to increase her physical activity.  She also loves to bake and spend time with her family and fur-babies on the coast of Australia.  Her positive attitude is an inspiration!

Andy’s Journey: I was diagnosed with endometriosis in 2008, during the first year of my PhD at the age of 23, after five years of severe pain and being bounced around from one doctor to another. Some doctors told me I was overacting and that it was “just period pain”, whilst one doctor told me it was PCOS. From the age of 18 I was taking Yasmin for the control of a few cysts a scan had found on my ovaries at that age. However Yasmin did nothing to control my pain and in fact after five years I developed more cysts and horrible headaches.

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Suicide & Endometriosis

Two yellow ribbons coming together for Endometriosis and Suicide Awareness

I find it interesting that both the Endometriosis Awareness ribbon and the Suicide Awareness ribbon are yellow ribbons…

Today while perusing Facebook, I ran across a post where a Virginia Endometriosis Awareness group had posted that there’s been 8 women who committed suicide this year due to their Endometriosis.  Where they got their stats, or if it’s just in VA, or…national…or global…I don’t know.  (For clarification on these statistics, see the Comments Section below). But, I do know that that’s 8 too many…and I was struck dumb, literally frozen in my chair struggling not to cry.

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