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
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
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
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
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
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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