Welcome to the team Leah!
We are excited to announce that, effective today, Leah Kleine has joined the Scleroderma Warriors Board of Directors as acting Treasurer. We are confident that Leah’s accounting and budgeting expertise…
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Caring for someone with scleroderma can be overwhelming. Empathy, positivity, patience and financial management are just a few of the feelings and responsibilities caregivers face. Always remember the quality of support you can offer depends on your own health and well-being so don’t forget to take care of yourself first.
2021 Scholarship Awarded!
Our 2021 Scleroderma Warriors Scholarship has been awarded! Join us in congratulating Katie. Upon being awarded the scholarship, Katie requested that we share her essay on our website for others…
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Newly Diagnosed: Taking the First Step on Your Journey – From Scleroderma News
Becoming educated is a good place to start on your journey with scleroderma. Whether you are a patient or a caregiver, knowing as much as possible about the disease will…
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Meet a Warrior – Kimberly
Meet Kimberly. She has been on a journey to Duke University for a Stem Cell Transplant. Kim was diagnosed and has been living in chronic pain since 2012, and was…
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“I Feel Like The Tin Man”…Nicola’s Story.
At the age of 24, Nicola Whitehill was given 15 months to live after being diagnosed with Scleroderma, a rare chronic illness affecting every part of the body. Now approaching…
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My Battle With Scleroderma…Cj’s Story
June is Scleroderma Awareness Month. In honor of Scleroderma Month I am being called to share my story, so that my pain has a purpose for ALL the Scleroderma Warriors…
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Guide for New and Future Patients
This 17 page guide put together by The Scleroderma Education Project is an amazing resource for both patients and their loved ones. A huge thanks to the Scleroderma Education Project!…
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Online resources and support
Access information about online resources and a range of helpful products.
