2021 Impact Report and 2022 Goals

Watch this special recording of our 2021 Cure JM Impact Report and Goals for 2022, featuring three speakers and three members of our Board of Directors. This informative presentation includes a brief overview of the organization and the Clinical Care Network, and a comprehensive overview of what Cure JM accomplished in 2021.

Featuring:

  • Jim Minow, Executive Director, Cure JM Foundation
  • Andrew Heaton, PhD, Chief Science Officer, Cure JM Foundation
  • Shannon Malloy, Director of Development and Family Engagement, Cure JM Foundation

Traveling with JM

Planning a trip or vacation can be challenging, especially when you have a child with juvenile myositis. With spring break and summer break just around the corner, the pressure might be even greater. However, at Cure JM, we want to help ensure that you and your child can enjoy all the delights of a vacation with minimal stress.

A Grandparent Spotlight – Anita

Cure JM recently had the pleasure of interviewing a remarkable individual who hails from Canton, Ohio, and brings a wealth of experience and love to her family. With a vibrant history spanning over five decades of marriage, three daughters, and a rich tapestry of grandchildren and great-grandchildren, Anita Mottice’s journey is as inspiring as it is heartwarming. As a retired nurse and devoted wife, Anita shares her profound connection with her family, particularly her grandchild Sydney, who has been diagnosed with Juvenile Myositis (JM).

GCOM 2024 Round Up

Recently, Cure JM’s Jim Minow was able to attend the Global Conference for Myositis. This conference was not only informational, but was a most impressive day for Cure JM. The conference brings together leading myositis researchers from around the world to share results and collaborate on future projects leading to better care and improved treatments for our JM kids.

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

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