For the 300,000 Americans living with the immune disease scleroderma, better treatments can't come soon enough. The rare and ...

For the 300,000 Americans living with the immune disease scleroderma, better treatments can't come soon enough. The rare and ...

Using skin and blood samples from scleroderma patients, the team grew lab-based skin: pinkish, pancake-like, little disks of ...

New 3D tissue model offers a breakthrough tool for understanding and treating scleroderma and other fibrotic diseases.

In a recent press release, Boehringer Ingelheim reveals a collection of unique and personal stories revolving around people living with scleroderma. Ingelheim, Germany, 29 June 2018 – Boehringer ...

"Every day is a new day. And every day you wake up and you thank God for breath, but you never know what's going to happen ...

Scleroderma is a chronic autoimmune disease of women. Over time, people living with scleroderma develop progressive and irreversible scarring. Scarring, called fibrosis, affects the lungs, heart ...

Briskey, 41, is a wife and mother of two young boys. She grew up in the Phoenix area before moving to Salem. She had been ...

Thu, 24 Oct 2024 03:32:51 GMT (1729740771496) Story, non-I.S. - News3 v1.0.0 (common) 905cd67f34238b4df12d38a3faad3f239d074ab2 ...

Barb Heenan loaded 43 oxygen tanks into her team's RV at the start of RAGBRAI so she can complete the ride while battling a rare disease.

On Thursday, KCCI introduced you to Barb Heenan, who was diagnosed with a rare autoimmune disease called scleroderma. She is set to finish the last two days of the ride.

Heenan was first diagnosed with limited systemic scleroderma at 22 years old, ... "You have to continue living no matter how hard it is and whatever struggles you have to go through to make it work.