 About Cure JMThe Cure JM Foundation was established in October 2003 with the goal of raising awareness of this rare disease and funding research to find a cure for Juvenile Myositis, including Juvenile Dermatomyositis and Juvenile Polymyositis. The founders of the Cure JM Foundation are Harriet Bollar, grandmother of a child with JM, and Shari Hume and Lisa Felix, both mothers of children with JM. They were brought together only by circumstance, but with the same determination to cure their child or grandchild; and to never, ever let another child suffer from Juvenile Myositis. Click here to view the Cure JM Foundation tri-fold brochure
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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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