Being as I am a new phenomenon to many of you (!), I figure I should at least introduce myself and what I plan to be writing about for The Fight Like A Girl Club. My name is Annie Martin. I am 23 years old.  I have been mysteriously ill …

Right now, I am less than two weeks away from a partial liver transplant. I am 29 years old. Finding out you have any life-threatening disease is scary (to put it mildly), but finding out you have a disease that carries the stigma of cirrhosis… well, let’s just say it …

I suffer from EDS. I am both Hypermobility type and Vascular type. Can I get a “WOO HOO!” for winning the dysfunctional genetic lottery? LOL! It is a horrible disease; the Hypermobility type caused me a great deal of pain. I suffer from numerous subluxations and dislocations. Every joint is prone to it. I have intense pain, swelling, skin discoloration etc…I am hypersensitive to barometric pressure changes and can predict weather better then any meteorologist I have ever seen on TV!

I can remember having lupus symptoms like joint pain and extreme fatigue as far back as six years ago. For many of us Lupus has always been a silent disease until that day we are struck with a severe flare up. The road has been rough, but I'm glad to finally know my health status after being in the dark about it for so many years!