Donation is Tax Deductible and Greatly Appreciated!
Formerly the Scleroderma Foundation of Greater Washington, DC
Now part of the Scleroderma Foundation of Greater Chicago
The DC Foundation has officially become part of the Scleroderma Foundation of Greater Chicago, expanding our ability to serve patients, caregivers, and families throughout Washington, DC, Maryland, Virginia, and on the Eastern Seaboard. Our commitment to the DC community remains strong, and is growing.
We provide education, support, advocacy, and connection for individuals and families affected by scleroderma in: Washington, DC, DMV, Northern Virginia, Maryland, DC Metro, and beyond. Whether you are newly diagnosed or have been living with scleroderma for years, we are here to support you.
Learn More HERE
Our Greater Washington, DC Support Group meets regularly on the 4th Wednesday at 7:00 p.m. ET. and is open to patients, caregivers, and advocates. Connect with us for peer connection with people who get it. Learn while joining us in a safe space for questions and support. We offer this group and many more. Learn More HERE
Ready to make a difference? Advocacy comes in many forms. From sharing your story and raising awareness to educating decision-makers and supporting research efforts. Our Scleroderma Advocacy Team empowers patients, caregivers, families, and supporters to raise awareness, influence change, and amplify the voices of those affected by scleroderma. No experience is required. We provide training, resources, mentorship, and a welcoming community every step of the way.
Learn More HERE
This year, the Walk to Cure Scleroderma movement is happening everywhere. Will you join us for Walk to Cure Scleroderma Hometown Edition?
Walk you favorite neighborhood trail, climb a local landmark, gather friends at a park, or take an iconic challenge like the Appalachian Trail, crossing the Brooklyn Bridge, or a walk along the National Mall. Wherever you walk, your steps help raise critical funds, spread awareness, and move the mission forward. Learn More HERE
