Volunteer Spotlight- Kristine Alderfer

As a member of the Cure JM community, you have likely heard the name Kristine Alderfer, a devoted parent of a teen with JM who has become a leader, serving as the President of our Board of Directors.

Kristine has been involved in Cure JM through volunteer roles for many years, and her involvement has become a family affair, as her daughter Katherine is a patient advocate for others with the disease. For over a decade, the Alderfer family has volunteered their time and talents to deliver a lasting impact on our mission. The family has hosted countless JM research fundraisers, including Christmas Shop for a Cure, Evening Under The Stars, and Cure JM marathons.

Most recently, Kristine has taken her leadership to new heights, serving as the Volunteer Chair of Cure JM’s National Family Conference.

We would like to thank the Alderfer family for carrying out the work that supports our community. Click below to hear about Kristine and Katherine’s rare disease journey.

Read Kristine’s Story

Love Letter to a grandparent

Love Letter to My Grandparents

Dear NaNa & PaPa, I appreciate all the love you have given me throughout my life. From the very beginning, you have been my biggest supporters, and

Walk Strong 2025 March Town Hall

Cure JM 2025: The Road Ahead

Hear a Critical Update from our Executive Director and learn more about WHY and HOW we Walk Strong Together. Featuring Cure JM Executive Director, Jim Minow, Director of Development and Community Engagement, Shannon Malloy, Board Member and Southern California Walk Chair, Zack Harrison, and Chapter & Walk Manager, Nicole Ryba.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

Cure JM supports families, patients, and the juvenile myositis research community.

Interested in DIY fundraising but need help?

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To have your fundraiser matched, add “DIY Match” in the memo of your online gift or check.