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| Help us get one step closer to finding a cure! We invite you to join us and thousands of others who are supporting the National Scleroderma Foundation's cause at one of our Stepping Out to Cure Scleroderma awareness walks. Let's take one step closer to finding a cure together. |
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| Double or triple your impact! Did you know your gift could be doubled, tripled, or matched?
When your workplace has a matching gift or workplace giving program, you can multiply your impact to the National Scleroderma Foundation. Use our matching gift tool to find out if your company matches your donations. |
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| Miss something at Conference? Access the recordings for a limited time Don’t forget: All 2023 National Scleroderma Conference participants have 30 days to access sessions and slides after the conference via the Airmeet platform. Please email info@scleroderma.org if you are unable to find your unique login link. |
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| Did you know that federal lawmakers are back in their home states and districts until September 4th? That means it's time for our scleroderma community to mobilize and get some face time with members of Congress. |
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| Join the Action Alert Network Whether it’s through a letter, fax, email, phone call, or in-person, connecting with your U.S. Representative and Senators is an important step in educating government officials about scleroderma and the impact it has on individuals and families. Action Alerts are time-sensitive announcements sent via email when it’s time to take action and contact your legislators about a vote or sponsorship of a bill that impacts people affected by scleroderma. |
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| 2024 Grant applications deadline is quickly approaching The National Scleroderma Foundation is the leading nonprofit supporter of peer-reviewed, scleroderma research to discover the cause, understand the mechanism, and overcome scleroderma forever. Since its inception, the Foundation has committed over $30.8 million for scleroderma research, which continues as a priority of our mission. Funding opportunities are available for early career and established investigators, and applications are due by September 15, 2023. |
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Localized Support Group for Adults and Parents ZOOM: Wednesday, August 15, 7 p.m. ET
The Localized Support Group for Adults and Parents is hosting guest speaker Tom Seaman on Tuesday, August 15th at 7 pm ET.
Tom is a life coach, author, podcaster, and inspirational speaker. Tom covers a variety of topics related to health issues and adapting to adversity in life.
This presentation will be open to everyone in the scleroderma community. Please email localizedsg@scleroderma.org for the zoom link. |
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