My Chronic Illness Story: Juvenile Dermatomyositis
Hey there, I'm Juli :) I'm here to talk to you about my rare autoimmune disease, juvenile dermatomyositis. With only three out of every million children getting diagnosed each year, there aren't many resources out there for this illness. I'm hoping that by sharing my story I can both help someone else out there feel less alone and also raise awareness about this rare and debilitating illness. Please share this video if you feel like it will help someone. For more information you can visit the Myositis Association https://www.myositis.org/

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STAGE 4 Cancer After MONTHS of Itching! - Amanda | Stage 4 Hodgkin Lymphoma | The Patient Story

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Tessa's Juvenile Dermatomyositis (JDM) Story

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The Myositis Association, Patient stories, Dermatomyositis

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JUVENILE DERMATOMYOSITIS (JDM) | ABP Board Review

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Why EDS is more than "just loose joints" | (MIS)Treated

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What Happened to Samantha?

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