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 501(c)(3) nonprofit organization with a mission to improve the day-to-day lives of Myositis patients. MSU is a patient-centered organization, founded by Myositis patients, for Myositis patients, and believes education, support, advocacy, and assistance are key to helping patients and caregivers. As a nonprofit, we rely on donations for funding and volunteers to help manage our fast growing organization.

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PIONEER, Idera clinical trial for dermatomyositis

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