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
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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
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
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
Cure JM held its first post-COVID Family Conference earlier this summer. The conference was an extraordinary experience for families and leaders on so many levels,
Since it is Rare Disease Month, we would like to take a moment and shine the spotlight on some of our amazing JM warriors.
First, a few terms to know when talking about Myositis Specific AutoAntibodies. So why do we talk about Myositis Specific Autoantibodies? We know that JDM
Here are some ideas shared with us by JM grandparents on how how to best support their grandchild, siblings, and family.
One common issue that we hear about from our families is that after diagnosis their child has trouble falling asleep or staying asleep. This can
Despite battling juvenile dermatomyositis (JDM) as a child, Alex Hackney never envisioned becoming a marathon runner, let alone completing prestigious races like the Chicago and
Each January, I share with our community a few personal New Year’s resolutions for the year ahead. I believe these resolutions help us keep a
Juvenile myositis, including juvenile dermatomyositis and juvenile polymyositis, is a group of rare and life-threatening autoimmune diseases, in which the body’s immune system attacks its
Two special guest speakers, Michelle Vogel, MPA, IV Solutions RX, and Laurel Cherwin, BSN, RN, IgCN, Octapharma, shared information on navigating affordable treatments and care
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