When our daughter was diagnosed with juvenile dermatomyositis in 2009 we were at a point in our lives that we didn't know what to believe about this disease. Her doctor and staff gave us the web site to Cure JM Foundation. The Cure JM foundation has been very informative with info and encouraging. The Foundation has helped my daughter see she is not alone in the and through CJMF we have talked with others going through some of the same difficulties. Not to mention the Love and support . We made a page for our daughter to help Cure JM Foundation spreed the word about this disease. These kids deserve a cure!!