Support and Resources Helping you find your best path by connecting with others and your community.
Support Groups

Nobody in our community needs to go it alone. One of the core parts of the National Scleroderma Foundation’s mission is to provide support and education to people living with scleroderma, and their families and loved ones.

The National Scleroderma Foundation Upper Great Lakes Chapter hosts the following chapter support groups:

  • Autoimmune and Scleroderma (Virtual)
  • Grand Rapids
  • North Metro Support Group (MN) (Virtual)
  • West Metro Support Group (MN) (Virtual)
  • Wisconsin (Virtual)

Below, find links the Foundation’s national support groups and peer-mentor program.

Resources

The National Scleroderma Foundation has gathered a number of resources, from information sheets to video lectures, that can help patients better understand the symptoms related to scleroderma, as well as the research that is happening to search for treatments and a cure.

Chapters are the front line of contact between individuals affected by scleroderma and the National Scleroderma Foundation. They know the individuals in their community. The chapter embodies the strength of the scleroderma community. Each chapter plays an essential role in delivering the organization’s mission.

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Sign Up for a Foundation Event Upcoming Events
  • Denver Support Group

    Denver Support Group
    Hybrid Event

    The Denver Mile High Support Group is a hybrid group that meets on the second Saturday of each month from 10:00am to 12:00pm MT. All meetings will be held virtually November 2026 through April 2027. Register here: https://us02web.zoom.us/meeting/register/Y13HcUtVRuS_hDzfoJhU2w Please contact DenverSG@sclerodermavolunteer.org with any questions or for more details if you would like to attend in […]

  • Pacific Northwest Support Group

    Pacific Northwest Support Group
    Virtual Event

    The Pacific Northwest Support Group meets on the 2nd Saturday of each month from 10:00am to 12:00pm PT. Please register here: https://scleroderma.org/PacificNorthwestSG Questions? Email: PacificNorthwestSG@sclerodermavolunteer.org