
Dear Friends,
Hello and Happy Summer Scleroderma Friends!
Hoping you all are enjoying the summer and that you have time to spend with friends and family.
The Scleroderma Foundation of California is enjoying a very busy summer with our A Million Steps for Scleroderma LA/OC in La Mirada, which was well attended and helped us achieve our fundraising goals. Thank you to all of the talented individuals who made this fundraising event possible.
Our next A Million Steps for Scleroderma San Diego event is on August 17, and "Jim’s 2025 Journey," conducted by our intrepid and ambitious board member, Jim Hines, will take him through much of Italy this year. As always, you can follow his journey through his wife Roberta’s blog on our website.
Registration is now open for our San Diego Patient Education Day on September 6, and we have scheduled our Northern California Patient Education Day on December 6th, with further details and registration coming soon.
Plans are well underway for our 24th Key to A Cure Gala on October 18 at the Marina del Rey Marriott Hotel – please be sure to “save the date.” Additionally, our support groups are ongoing, with more groups forming to enhance scleroderma awareness in our community.
As always, we welcome your interest, ideas, and support.
Let us hear from you!
Laura Fuhrman
President, Board of Directors
The Scleroderma Foundation of California
Laura Fuhrman, President
Joel Cherman, VP
Sharon Friedman, VP, Governance
David Parker, Secretary
Daniel Furst, M.D., Past President
Chris Pettit, Acting Treasurer
As a team, we are dedicated to organizing fundraising events aimed at enhancing patient education and promoting scleroderma awareness.
Chris Corman
Stephen Elrod
Nancy Garza
Evan Greenburg
Shervin Ghanoongooi
Johanna Herrmann
Jim Hines
Kristy Kubota
Brittany Stone
These individuals are essential in organizing fundraising events that raise awareness for scleroderma and enhance patient education.
Andrew Emmett, Executive Director, is dedicated to enhancing patient education and raising scleroderma awareness through various initiatives. Tina Burger, Patient Services Director, plays a vital role in supporting patients at our fundraising events. Alejandra Serrano, Patient Support, ensures that those affected by scleroderma receive the necessary resources and information. Emmanuel Munda, our Marketing, Event, and Technology Consultant, is instrumental in organizing impactful fundraising events that promote scleroderma awareness.
The Scleroderma Foundation of California is dedicated to promoting scleroderma awareness and providing patient education. You can visit us at 8929 S. Sepulveda Blvd. Suite #401, Los Angeles, CA 90045-3603. For inquiries about our fundraising events or any other information, please call us at 424-227-6475 or email us at info@myscleroderma.org.
The Scleroderma Foundation of California is a 501 (c)(3) tax-exempt organization dedicated to raising funds through various fundraising events. Our mission includes promoting patient education and enhancing scleroderma awareness in the community. Federal Tax ID: 77-0229244. Foundation Tax 990 Filings.
We are no longer affiliated with the National Scleroderma Foundation or their website. This is the only place to stay informed about our fundraising events, patient education initiatives, and scleroderma awareness activities happening in California!









Scleroderma Foundation of California
8929 S. Sepulveda Blvd. Suite 401