PROJECT SCLERODERMA

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Scleroderma is a rare autoimmune disorder. Scleroderma literally means "hard skin", inflammation triggers the body's own immune system to make too much collagen, leading to hardening and tightening of the skin and connective tissues.

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HAVERTOWN

Address: 119 HASTINGS AVE, HAVERTOWNWeb: Sign in to see organisation websiteFacebook: ProjectSclerodermaRevenue: 111726ICO: 320456063

Project Scleroderma, raising awareness with documentaries PROJECT SCLERODERMA RUN GREG RUN IN THE NEWS PROJECT SCLERODERMA Scleroderma is a rare autoimmune disease that causes a hardening of the bodys connective tissue. Scleroderma literally means hard skin. This disease can also affect internal organs resulting in lifethreatening consequences. PROJECT SCLERODERMA Our Mission is to Spread Awareness PROJECT SCLERODERMA Latest Documentary ABOUT RUN GREG RUN Make a Difference in 1 Minute Scleroderma is a rare autoimmune disease that causes a hardening of the bodys connective tissue.

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David

1. What innovative strategies can NGOs use to raise awareness about rare diseases like scleroderma, and how can they engage the community in these efforts?

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Hannah

2. How can storytelling through documentaries impact public perception of autoimmune diseases, and what role does it play in supporting patients and their families?

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PROJECT SCLERODERMA

November is Pulmonary Arterial Hypertension (PAH) Month. To kick things off, we’re featuring Nola, who candidly shares her journey living with both scleroderma and PAH in this video. "Being told you have not one, but two rare diseases is difficult," she says.

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Patrick

Let's spread the word about Scleroderma and support those battling this challenging condition! πŸ’™ Every small effort counts! #ProjectScleroderma

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Christine

Incredible work being done by Project Scleroderma! πŸ‘ Raising awareness is so crucial for better understanding and support for patients. Let's share these stories and make a difference together! #SclerodermaAwareness

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Diseases, Disorders, Medical Disciplines N.E.C. Category

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Scleroderma Australia was formed in 2005 to facilitate a national representative voice in supporting our scleroderma community across Australia.

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