Living rare: finding my voice with diffuse systemic scleroderma

https://rarerevolutionmagazine.com/living-rare-finding-my-voice-with-diffuse-systemic-scleroderma/ Kristina Hamilton is a patient advocate living with diffuse systemic scleroderma. Diagnosed in 2022, she shares her lived experience to raise awareness of rare and often misunderstood autoimmune diseases. Through storytelling and advocacy, Kristina is committed to helping others feel seen, less alone and empowered to use their voices within the rare disease community