The Scleroderma Foundation Gets Into the Podcast Business


The Scleroderma Foundation is a non-profit organization dedicated to helping support patients as well as educate and raise awareness and money for vital research into the condition.

MORE: Twelve things to care for when you have scleroderma.

This is the first podcast episode produced by the Scleroderma Foundation. It features the organization’s CEO Robert Rigg, Board Vice Chair Dr. Carol Feghali-Bostwick, and the Greater Chicago Chapter’s Executive Director Stephanie Somers-Gresh.

The trio talks about various topics related to scleroderma, including the various chapters within the Scleroderma Foundation, the organization’s annual conference, federal funding for research, research programs, how scleroderma patients can contribute towards research, and raising awareness of the disease.

MORE: How serious is scleroderma?

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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