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.

Shop to Support Cure JM

We have compiled a list of Cure JM items you can purchase, as well as other products, that might help you and your child in their JM journey.

Skin Disease, Victoria Werth

Skin Disease for Clinicians

Dr. Victoria Werth, M.D., discusses the identification and treatment of skin manifestations associated with dermatomyositis. Her talk covers diagnostic criteria, various skin manifestations, the latest treatment approaches, and the complexities of managing this condition, all aimed at improving patient outcomes and quality of life.

Town Hall June 2024, Thorington, Turnier, Emotional Distress

Helping Parents & Kids When They Express High Emotional Distress

This expert-led presentation is for parents about how to help their kids and themselves when their kids express high levels of emotional distress. Our presenters will talk about ways parents can calm themselves, share tips for talking to kids with age-appropriate information, and know when to find help from a professional. There will be a Q&A session immediately following the presentation.

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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