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Community Partners

We're proud to work collaboratively with the following organizations in the scleroderma, rare disease, and disability communities.

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The Scleroderma Foundation of Greater Chicago (SFGC) has been serving the scleroderma community for more than 40 years. They provide education programs that connect you with experts in the field to help you understand scleroderma, explore treatment options, manage symptoms and improve quality of life. Their support groups provide a forum to share experiences and ask questions among a group of people who understand what you're going through, regardless of where you live. They work to stimulate and support research that will advance treatment and ultimately find the cause and cure for scleroderma.

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Project Scleroderma's two part mission is to raise the global level of scleroderma awareness through informative videos and documentaries as well as to support the patient community as they work to cope with the challenges presented by scleroderma.

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Rare Disease Diversity Coalition (RDDC) brings together rare disease experts, health and diversity advocates, and industry leaders to identify and advocate for evidence-based solutions to alleviate the disproportionate burden of rare diseases on communities of color.

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The Waiting Room Entertainment is a resource and services hub for the disabled community at large. By providing interactive opportunities to followers that may not be able to access them for various reasons. The company consists of several programs that include Jacob’s Hugs Registry, Social Club, Speak Out, and Resource Corner.

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