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Cincinnati Children’s Hospital Upcoming Events

JOIN US! Two Upcoming Events for Juvenile Dermatomyositis Families & Patients

Online Town Hall

Friday June 2nd 1:00 p.m. Eastern Sun Protection Tips & Tricks for Summer PRESENTED BY Sheila Angeles-Han MD, MSc Physician, Division of Rheumatology Cincinnati Children’s Hospital Medical Center Kalyani S. Marathe, MD, MPH Division Director of Dermatology Cincinnati Children’s Hospital Medical Center

Register to attend at www.curejm.org/town-halls

In-Person Family Social Event

Vote for the best day for your family to attend at https://www.surveymonkey.com/r/TX8LDSH

Join fellow juvenile dermatomyositis families for an afternoon to connect and learn with each other and physicians and researchers from Cincinnati Children’s Hospital Medical Center. Juvenile Myositis clinicians will discuss the latest advances in JM treatments and research, followed by a Q&A session.

cincinnati-june-event-flyer-PRESSDownload

Walking Strong – Empowered by Unity

Like other teens new to the JM journey, Catie Beth Caldwell and Madi Cook were two individuals who felt alone at the beginning of their journeys. Catie Beth was diagnosed just before the Covid-19 pandemic took hold of the world as we knew it. With this came feelings of isolation and loneliness. These emotions were commonplace for many teens but were only compounded by teens new to a rare disease diagnosis. These first years of the “new normal” were difficult to navigate.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

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

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