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| eLetter #946 | December 3, 2021 |
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Thank you!
The Scleroderma Foundation is deeply grateful to all who celebrated GivingTuesday on November 30 by making a generous donation to advance our mission of support, education, and research.
If you missed the date, don’t worry! You can still make a gift at scleroderma.org/givingtuesday.
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Learn How: Healthy Meal Prep, Chef Katie Simmons
VIDEO: Recorded July 2021
Watch this presentation about healthy meal preparation from the 2021 virtual National Scleroderma Conference with Chef Katie Simmons. Chef Katie shares recipes for breakfast, lunch, dinner, and even dessert! Learn chefs' tricks and supermarket shortcuts for creating delicious and nutritious meals that are easy on the scleroderma gut.
WATCH
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COVID-19, Vaccines & Pediatric Scleroderma
VIDEO: Recorded October 2021
Watch this presentation from the 2021 virtual Kids Get Scleroderma, Too! Conference with Kathryn Torok, MD, as she discusses COVID-19, vaccines, and pediatric scleroderma.
WATCH
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How to Dance in the Rain
VIRTUAL: February 26, 2022; 1 PM Eastern
Life isn't about waiting for the storm to pass, it's about learning to dance in the rain. Offered by the Michigan chapter, the conference, How to Dance in the Rain, is a time for individuals with scleroderma, their loved ones and caregivers to find hope and to connect with one another. The event starts with opening remarks from Michigan Chapter Executive Director Laura Dyas and includes educational seminars from medical professionals, Q&A segments, exercises, and more. Click the link below on February 26 to attend.
ATTEND
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Connect
Connecting with others affected by scleroderma is central to moving forward. Connecting recharges your batteries and broadens your perspective on living with scleroderma. And sometimes, it's just a chance to talk to someone else without explaining your disease. Many scleroderma support groups are meeting virtually to stay connected during the pandemic. A few virtual groups focus on specific topics.
Visit the Foundation website to find a group for you.
SUPPORT
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Disclaimer: The 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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