Elinor: A Grandparent’s Story of Hope

Elinor, A Grandparent's Story of Hope, with grandson and dog

My grandson, Connor, was diagnosed at a very young age. Since he was two years old, he has struggled with rigorous and invasive treatments. From then on, we knew he needed to have all his family’s love and support, now more than ever.

Life hasn’t been easy for him, and it breaks my heart to see him learn to manage and cope with incredibly stressful situations. Nothing that I would want my grandson to face in his young life. Like many other JM families, I have felt hopeless and powerless to make a difference, as I know I cannot make all the stressful situations disappear. But I know I want to be there for him and be someone he can depend on.

With all the love in the world, I do my best to help fundraise for Cure JM. I am hopeful that the talented and capable researchers will transform the funds raised into something that will improve my grandson’s future and the future of other kids with JM. Even if I cannot dedicate time to bigger and grander events, I try my best to support our JM kids as best I can.

Currently, Connor is doing better and is much stronger. He is now a teen, and even though he receives IVIG every four weeks, he enjoys the little things in life. It warms me inside to hear him talk about his friends, interests, and opinions. One of my favorite moments is seeing him enjoy bike riding. While this doesn’t mean he is completely free of tough moments, I am thankful to be with him on his journey and proud to see him come so far.

Like many older kids, Connor is very private about his diagnosis and thinks seriously about what kind of future lies ahead for him. Since he was diagnosed so young, he can’t remember life without hospital visits and treatments. Whenever I hear that he has some doubts and fears for the future, I do my best to encourage him. I do my best to keep that spark of hope alive.

It’s true that this disease can be mentally and emotionally taxing, but with the power of my words and my love, I cannot help but believe that he can make great things happen in this world.

Through me, I want Conor to find the courage, strength, and support to keep fighting. He is my inspiration, and so, in turn, I will inspire him.

Photo of Mark Zuckerberg and Priscilla

Cure JM Research Consortium Receives Prestigious Chan Zuckerberg Grant

The Chan Zuckerberg Initiative has awarded Cure JM and a consortium of Cure JM-funded researchers a coveted $2 million rare disease research grant to identify new biomarkers in JM and improve precise, personalized care through the identification of cell-to-cell interactions that drive inflammation in juvenile myositis.

Randy and three other grandmothers at conference

Grandparent Alliance

What is the Grandparent Alliance?  We are grandparents of a grandchild living with juvenile myositis.  Our mission as grandparents is to learn about juvenile myositis and support

Why I Walk- Sammie Fish

Why I Walk: Steps Toward a Cure with Sammie Fish

Sammie Fish was 14 when juvenile dermatomyositis (JDM, a rare form of juvenile myositis (JM) changed her life in 2017. A doctor’s warning that she might never reach remission, tied to a lifetime of medication, shook her world. But Sammie, now 21, didn’t back down. Today, she’s a college grad, a new teacher in her dream job, and Co-Chair of Cure JM’s Ohio Chapter alongside her mom. She walks for herself, for kids like her, and for a cure. That’s why hundreds of Cure JM families and friends across the nation join Walk Strong, because every step pushes us toward a JM-free future

Join Cure JM

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

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