Juvenile Dermatomyositis and Juvenile Polymyositis are the most common forms of JM (Juvenile Myositis) - a rare autoimmune disease that affects approximately 5,000 children in the United States. JM attacks children of all ages, causing a variety of debilitating symptoms including:

•   Muscle weakness and pain

•   Severe fatigue

•   Rashes

•   Swallowing and digestive difficulties

•   Lung and heart problems

•   Vasculitic ulcers

•   Calcinosis

Some children may experience a remission, while others will battle JM their entire life, and complications from this disease can prove fatal. Medication can help to alleviate the symptoms of JM, but there is no known cure.

As its name implies, the Cure JM Foundation, a 501c(3) non-profit organization, was created specifically to find such a cure, while also providing support and information for families suffering from JM.


Patients Needed!

Twin/Sibling Study
The National Institutes of Health is seeking research subjects from the JM community. Click here to see how you and your family can help.

In Memory of
Mikey Galvin

On May 27th, 2005 Michael Ryan "Mikey" Galvin passed away due to complications from JM. Click here to learn more.


This website is provided for educational and informational purposes only. Cure JM is not engaged in rendering medical advice or professional services and this information should not be used for diagnosing or treating a health problem. The site author and the content providers make no representation or warranties, expressed or implied. Providing links to other websites does not imply that Cure JM endorses the information or services provided on those websites. The organizations operating those websites are solely responsible for the content found on their websites.
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Site designed by Gary Bickal, GBST Media Services.
 

Breaking News and Events

Cure JM Foundation approves $1Million Grant for Juvenile Myositis Research!

Attention Runners and Walkers!

Cure JM is assembling a team for this year's Bank of America Chicago Marathon. Registration for the marathon closes soon, so CLICK HERE NOW for more information. We're also looking for volunteers to help out on race day and sponsors for the Cure JM Team. Click here for more information.

Read all about it!

Parent Power leads to JM research support! An update from Dr. Lauren Pachman! The latest edition of Cure JM News is now available online. Click here to download a copy.

Celebrate Those Special Occasions

Here's the perfect gift for anyone whose life has been touched by a child with JM.

For more information, click here.

Watch Cure JM in action!

Click here for the new Cure JM Foundation video (high-speed Internet connection recommended).