Tell Us What Matters Most to You: A Survey for Patients and Families.

Your voice matters to us. At Cure JM, we’re all about putting patients and families first, and your insights help shape our mission to support the juvenile myositis community.

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* 1. Please tell us a little about yourself:

Parent

Patient

Grandparent

Sibling

Spouse

Other (please specify)

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* 2. How many years has it been since diagnosis?

Less than 1 year

1-5 years

5-10 years

More than 10 years

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* 3. Please rank the following research priorities in order of importance to you, with 1 being the most important and 13 being the least important. Consider what matters most for your child, your family, and the broader juvenile myositis community.

There are no right or wrong answers—your input will help shape future research efforts.

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* 4. What challenges or needs related to living with juvenile myositis would you like Cure JM to address through our programs, research, or support resources?

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* 5. Email address (Optional -- if you would like to receive the survey results):