Scleroderma Foundation Video

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I have been so lucky to meet people who suffer with Scleroderma, Raynaud's, and other various Auto-immune diseases through Instagram. Totally random, right? But it's been really cool. One of the gals that I've 'met' is a very talented artist. She created some superhero and princess prints that she is selling to help pay for her medical bills. Her etsy shop can be found here: https://www.etsy.com/shop/kcmcreations and her facebook page here: https://www.facebook.com/kcmcreations?ref=profile

Yesterday she shared a link to a YouTube video that I wanted to share here. Its so hard to know what the future holds for me with this disease, and it's kind of hard for people to really understand what this disease does to people, so this video was awesome to kind of explain what Scleroderma is, and how it has impacted the lives of a few people. I totally cried because of the familiarity, so be prepared. It's a fantastic video. I'm just going to post a link to the video instead of inbed the video here on my blog. It makes the blog hard to load. :)

Scleroderma Foundation | Michigan Chapter
http://youtu.be/mAUoltkn5xM

Kind of neat right?

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