Nichole’s Myositis Blog

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Nicole's Myositis Blog

Nicole Smith shares her Myositis blog for Myositis Awareness Month and MSU’s #MyositisLIFE project. 

Diagnosed with Dermatomyositis in 2012, I was looking for an easy (and interesting) way to share my story with friends, family and the world. So I attempted the whole blogging thing. Any way to get info out about Myositis is a good thing!

Check out Nicole’s blog here: https://nikilee766.wordpress.com/2012/05/

 

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Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

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