Tips and links for dealing with insurance claims, denials and appeals, making phone calls, changes in health care law, help with medical bills, and more.
Do you know the warning signs of depression and anxiety? Has your child had a mental/emotional health assessment? Here are some resources for you, your child, and other family members.
Cure JM Foundation is a 501(c)(3) nonprofit, volunteer-managed organization dedicated to finding a cure for juvenile myositis (JM).
At age 4 Parker was diagnosed with juvenile dermatomyositis. Only 2 in a million children are affected. We started Cure JM to find a cure and help kids like Parker.
Here are some ideas shared with us by JM grandparents on how how to best support their grandchild, siblings, and family.
Progress and Prognosis in Juvenile Dermatomyositis, Juvenile Dermatomyositis: A 20-year Retrospective Analysis of Treatment and Clinical Outcomes, Juvenile Dermatomyositis: A Case Study, and others.
There are a number of published studies about juvenile myositis. Browse this list of over 100 published research studies and abstracts.
Featuring Jim Minow, Executive Director of Cure JM, Dr. Andrew Heaton, Ph.D, Chief Scientific Officer, and Shannon Malloy, Director of Development and Family Engagement.