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| Quarterly stakeholder updates recording available National Scleroderma Foundation CEO Mary J. Wheatley, IOM, CAE, recently reviewed key mission metrics with Foundation stakeholders. Watch this quarter’s update at the link below on our YouTube channel.
You can sign up now for our 2023 sessions! |
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| Give the Gift of Membership Did you know you could give someone the gift of a Champion membership to the National Scleroderma Foundation?
For only $35 per year ($45 international), your loved one will receive 10 member benefits including:
• A printed subscription to our Scleroderma Voice magazine
• An exclusive opportunity to meet our CEO
• And more!
To give a loved one the gift of membership, call our office at (800) 722-HOPE [4673] or complete the Champion membership form at scleroderma.org/membership. |
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| Join us for the 2023 Stepping Out to Cure Scleroderma walk season! We are excited to share that the 2023 walk season has launched with a new look celebrating 20 years of our community gathering to participate in Stepping Out to Cure Scleroderma awareness walks. We hope you will celebrate with us and join one of our many walks scheduled across the country both in person and virtually.
To find your walk, visit sclerdoerma.org/steppingout. Check back often. Walks continue to be added regularly to this site. |
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| The Pulmonary Fibrosis Foundation Are you looking for information about interstitial lung disease? Check out the Pulmonary Fibrosis Foundation. Visit their website at the link to learn more. |
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| 2023 Pre‑Doctoral Summer Fellowship Awards The National Scleroderma Foundation is now accepting applications for the 2023 Pre‑Doctoral Summer Fellowship Awards. Applications are due 5 p.m. Eastern Time, Friday, April 28. Learn more about the application process at the link. |
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| Parents of Children with Scleroderma ZOOM: 7:30 p.m., Eastern Time, Wednesday, Feb. 1
If you care for a child living with scleroderma, do not miss the Parents of Children with Scleroderma Online Support Group! The group covers 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. Email Pamela Pour for the meeting information. |
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If you no longer wish to receive this weekly message from the National Scleroderma Foundation, you may unsubscribe. |
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