Welcome to the Scleroderma Foundation of California
Laura Fuhrman,
President of Scleroderma Foundation of California
Understanding Scleroderma
What is Scleroderma
Scleroderma or systemic sclerosis, is a chronic autoimmune disease (- Read more about Understanding Scleroderma
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Bark for a Cure - Pet Photo Contest
All funds raised support the mission of the Scleroderma Foundation of California.
THE HELEN GREENBURG MEMORIAL FUND
Was established in 2021 to honor the memory of our beloved friend, Helen Greenburg.
All gifts will support our patient services programs to further her commitment and devotion to supporting the Foundation and making a difference in the lives of those affected by scleroderma.
We hope you will consider a gift in her memory.
Helpful Links/Organizations:
NeedyMeds: Is a National non-profit that connects people to countless healthcare programs, discounts, websites, sliding scales and educational forums they offer for people living with chronic illness and their families, free and anonymously - that will help them afford or save on their healthcare expenses.
Videos
Also view our 
YOUTUBE CHANNEL
Jim's 2022 Journey
My name is Jim Hines. I am a retired engineer and instructor. I am a supporter of my wife Roberta of 45 years who is living with Scleroderma.
She has endured the trials and tribulations of the disease throughout her life starting with Raynaud’s, to gastric, pulmonary, and other issues.
FIND MORE WAYS TO HELP!
We are part of an inspiring community.
Together, we can accomplish so much more.
Join us and support our mission.
Contact us to find out more about volunteer opportunities, fundraising events,
and ways that you can help us get our message to your friends and family.
Sign up to to receive our Foundation updates for news, patient education, and events.
Email: info@myscleroderma.org