Fans of Bob Saget are mourning his death this week. Joining the list of celebs and fans pouring out tributes to the "Full House" TV star and comedian is the Scleroderma Research Foundation (SRF).

Kheesa J was diagnosed with scleroderma, a rare autoimmune disease. Her daughter was an infant, and doctors told her she had five years to live. Seventeen years later, she's stable and has another ...

After years battling scleroderma, Andrew Botieri completed a novel just before undergoing a rare double lung and kidney ...

As Bob Saget is remembered by his friends and co-stars, one memory that stands out is his commitment to finding a cure for scleroderma, a rare disease for which Saget was the most high-profile ...

Two years before his death, Bob Saget quietly offered his support to a family whose 9-year-old daughter is suffering from Scleroderma, the same disease that took the life of his sister in 1994. Saget ...

PHILADELPHIA (WPVI) -- When a rare disease strikes, getting a diagnosis can take years, enabling the disease to progress. A young woman from the Mayfair section of Philadelphia details her battle to ...

As people learned about the death of comedian Bob Saget, many close to him suggested that a donation to research into a medical condition his sister suffered with and died from would be a fitting ...

AND STILL MAKING HISTORY. REALLY GREAT STUFF AND PEOPLE FROM ALL OVER THE WORLD COME TO IOWA FOR THIS RIDE, EACH EMBARKING ON THE JOURNEY FOR DIFFERENT REASONS. KCCI ALYSSA GOMEZ SHARES HOW ONE RIDER ...

First Bari Martz’s fingers turned blue. Then she started gasping for breath, and her joints stiffened so that she couldn’t even open her hands. Subscribe to read this story ad-free Get unlimited ...

Scleroderma is a health condition that involves thickening of the skin and may also affect internal organs. This condition can be difficult to diagnose due to the fact that several other health ...

Individuals with scleroderma -- a rare autoimmune disorder of unknown origin -- are living significantly longer today, compared with 30 years ago, and the physicians who treat this rare disease of ...