Article about Juvenile Myositis and the Cure JM Foundation

Have you heard of the Cure JM Foundation? I hadn't until this article appeared in my Facebook feed today:

http://www.claiborneprogress.net/view/full_story/23438860/article-Family--friends-raising-awareness-of-rare-disease

They are having a walkathon, "Let's Walk for Casey," in memory of a beautiful young lady Casey Nicole, whose life was shortened by juvenile myositis.

There is an opportunity to leave comments on the article page. Some of you may wish to leave comments about myositis and what it would mean to you if a cure were found.

Here is a link to the Cure JM Foundation: http://www.curejm.org/