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| eLetter #998 | December 2, 2022 |
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Thank You!
The National Scleroderma Foundation extends its deepest gratitude to all who supported us on GivingTuesday by making a gift or by sharing our message with others!
If you missed the day, don’t worry! You can still make a gift at scleroderma.org/givingtuesday.
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Mental Health Matters: Chronic Disease and How to Support Your Mental Health
VIRTUAL: 7 p.m., Eastern Time, Tuesday, Dec. 6
Join the Tri-State Chapter and the Hospital for Special Surgery for the Scleroderma, Vasculitis and Myositis Center's Winter 2022 Patient Education Forum.
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Ohio Education Event
The Ohio Chapter is having a virtual caregiver education panel at 10 a.m., Eastern, Saturday, Dec. 3. There will be a panel discussion with Debbie and Darryl Haussler, Keith and Lucille Miller, and Kevin and Mariann Boyanowski. The educational event will feature open discussions exploring emotions around scleroderma and breakout sessions with caregivers and individuals living with scleroderma. All are welcome.
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Parents of Children with Scleroderma Support Group
VIRTUAL: 7 p.m., Eastern Time, Wednesday, Dec. 8
If you care for a child living with scleroderma, do not miss the Parents of Children with Scleroderma Online Support Group! The group will cover various topics to help parents navigate caring for children with scleroderma and finding support. The group meets virtually via Zoom on the first Wednesday of even months (e.g., June, August, etc.) from 7:30 - 9 p.m. and the first Wednesday of odd months (e.g., July, September, etc.) from 3 - 4:30 p.m.
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A Lasting Mark Foundation
Our friends at A Lasting Mark Foundation would like to spread some holiday cheer and comfort to our pediatric scleroderma community! Learn more about the incredible mission of A Lasting Mark Foundation. A Lasting Mark Foundation would like to send a Holiday Swag in a Bag to children and teens up to 18 years old living with scleroderma. To receive your special gift, fill out the form. Please be sure to use the code: Warmwishes. The deadline to order is Dec. 3. Our sincere gratitude goes to A Lasting Mark Foundation for this special gift!
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Disclaimer: The National Scleroderma Foundation in no way endorses any drugs, treatments, clinical trials, or studies reported in the eLetter. Information is provided to keep the readers informed. Because the manifestations and severity of scleroderma vary among individuals, personalized medical management is essential. Therefore, it is strongly recommended that all drugs and treatments be discussed with the reader’s physician(s) for proper evaluation and treatment.
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