In this New Pace video, here’s the “Dear Scleroderma” full first episode by Jessica Massengale.
“That’s one major thing that I learnt, to never judge a book by its cover.”
Jessica also created the Scleroderma Strong project, which started as a small page for her to share the alterations happening to her body caused by the disease, but has grown to a community of scleroderma survivors.
Eight years ago, Jessica Massengale was diagnosed with scleroderma, an autoimmune disease that causes scaring in her skin and some internal organs.
Since then, she has been raising awareness of this disease and helping others going through the same battle as her.
Scleroderma News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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