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“After school with Juvenile Dermatomyositis… My body is tired, my muscles hurt, but I keep pushing. Some battles are invisible, but I’m still fighting. 💜” “School is done… but the pain and fatigue are still here. Living with JDM is a daily fight.” #JuvenileDermatomyositis #JDMWarrior #AutoimmuneAwareness #RareDiseaseWarrior #afterschool
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"Living with Juvenile Dermatomyositis is not easy, but we will never g...
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Jaylon is bravely fighting a rare autoimmune disease called Juvenile Dermatomyositis. This illness has taken away his ability to walk, run, and enjoy life like other children his age. Every day is a battle with pain, weakness, and exhaustion, but Jaylon continues to fight with incredible courage. Doctors believe that specialized treatment at Duke University Hospital could give Jaylon the chance at better care, therapy, and hope for recovery. Unfortunately, the cost of travel, hospital care, and
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Entertainment on Instagram: "This movie was so beautiful 🎬: Love, Kennedy Although Kennedy Hansen is a funny, loving child, she inexplicably begins to fall ill. It takes years for the diagnosis: Juvenile Batten Disease - an extremely rare, terrible and terminal prognosis. There is no cure for Batten Disease, and after living only 16 years, Kennedy leaves behind a great legacy of love and friendship. But her story doesn’t end at her de*th. That’s when the miracles really begin. 📺: Tubi, PLEX, A
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