Thanks for taking the time to learn about Scleroderma.

Hannah was diagnosed with Linear Scleroderma en Coup de Sabre, a rare form of this autoimmune disease, when she was in kindergarten. It left scarring and a bone depression on her face and scalp. Since then, the disease has come in and out of remission, most recently reactivating when covid hit in 2020. Hannah is very fortunate to not have had any lasting complications from the disease, but for many others, it impacts mobility, breathing, digestion, fine motor function, and generally causes a lot of pain. Scleroderma is a fatal disease for many as it can attack vital organs.

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