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Submitted URL: http://scleroderma.org/
Effective URL: https://scleroderma.org/
Submission: On February 18 via api from US — Scanned from DE
Effective URL: https://scleroderma.org/
Submission: On February 18 via api from US — Scanned from DE
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NATIONAL SCLERODERMA FOUNDATION Search for: Donate Menu Select LanguageChinese (Traditional)EnglishFrenchHindiPortugueseSpanish Powered by Google Übersetzer Stepping Out to Cure Scleroderma News Kids Resources Calendar Contact Login Search * Understanding Scleroderma * Treating Scleroderma * Living Well with Scleroderma * Advancing Research and Treatment * Get Involved * Find your Chapter * Donate Back Understanding Scleroderma * Get the Facts * What is Scleroderma? * Who Gets Scleroderma? * Forms of Scleroderma * Symptoms of Scleroderma * Glossary of Terms * Diagnosis * Diagnosis & Tests * Newly Diagnosed * Pediatrics * Scleroderma and Kids * Diagnosing Pediatric Localized Scleroderma * Prognosis for Pediatric Localized Scleroderma * Diagnosing Pediatric Systemic Sclerosis Find Your Path! Back Treating Scleroderma * Build Your Treatment Team * Find a Treatment Center * Find Your Local Chapter * Treatment & Trials * Treatments & Medications * Find a Clinical Trial * Pediatrics * Treating Pediatric Localized Scleroderma * Treating Pediatric Systemic Sclerosis Read the Latest Research News Back Living Well with Scleroderma * Patient & Caregiver Education * Education * 2024 National Scleroderma Conference * Local Programs * National Programs * Virtual University * Caregivers & Friends * Scleroderma Voice Magazine * Pediatrics * Pediatric Education * 2024 Kids Get Scleroderma, Too! National Conference * Pediatric Resources & Supportive Care * Find Support * Find Support Groups * Virtual Groups * Inspire Discussion Board * Resource Center * Resources * Health and Safety Back Advancing Research and Treatment * Researchers & Grants * Scleroderma Research Grant Program * Grant Opportunities * Grant Application Form & Instructions * Current Grantee Reporting Forms * Our Grant Awardees * Mentor Programs * Pre-Doctoral Fellowship Recipients * Global Webinar * Pharma & Biotech Patient Engagement * Patients as Partners * Continuing Education * Continuing Medical & Nurse Education: The Lung in Scleroderma * Continuing Medical & Nurse Education: Hand Involvement in Scleroderma Back Get Involved * Why It Matters * Impact on People with Scleroderma * Voices of Scleroderma * Major Initiatives * Accelerate Research * Collaborations * Where Your Money Goes * Give * Ways to Give * Leave a Legacy * Scleroderma Hope Society * Fundraise With Us * Join a Walk * Start a Fundraiser * Be a HopeRaiser * Become a Member * Member Benefits * Scleroderma Voice Magazine * Advocacy * Our Priorities * Take Action * Prepare Your Story * Talk to Your Elected Official * Advocate Resources * 2023 Scleroderma Awareness Month * Corporate * Corporate Philanthropy Program * Sponsorship Opportunities * Our Partners Our Mission The National Scleroderma Foundation’s mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. Our vision is to be a relentless force in finding a cure and improving the lives of people affected by scleroderma. Find Your Best Path Where to Start More than 300,000 Americans live with some type of scleroderma. Today, the face of scleroderma includes people of all ages, genders, and backgrounds. Scleroderma can affect young parents, children, grandparents, and teenagers. Thanks to the passion and dedication of countless volunteers, scientists, and supporters, we’re advancing our mission faster than ever. Find What You Need One of the most challenging things about scleroderma is that it presents differently in each person. Find the right resources for you. Find Support Share and learn from others, at different places in their journey, through ‘Living with Scleroderma Groups’ for adults, children, and those who care for them. Learn More Find Resources No matter what type of scleroderma or where you or your child are on your journey, the Scleroderma Foundation can help you find your best path. learn more Find a Scleroderma Center Find the right specialists to make up your team. Locate designated scleroderma centers, specialists, clinical trials, studies, and get help navigating the healthcare system. Learn More Connect Locally The Foundation can connect you with others living with scleroderma through our nationwide network of chapters, in addition to more than 100 support groups. Find Your Chapter Find a Support Group Get Involved Find a Walk Near You Stepping Out to Cure Scleroderma walks give you a way to get involved and help advance the mission. Join a Walk Learn More about Scleroderma Learn about scleroderma, the facts, the latest research, and treatments through our Fact Sheet. Fact Sheets Support the Mission The need is great, and the path forward is challenging. You can help make a difference in the lives of people with scleroderma today by supporting our mission. Donate Now featured news Read the latest news and information from the Foundation. February 1, 2024 Foundation Leader Named Fellow of National Academy of Inventors for Pioneering Contributions to Fibrosis Research Dr. Carol Feghali-Bostwick, a distinguished translational researcher and the SmartState and Kitty Trask Holt Endowed Chair for Scleroderma Research… read more January 29, 2024 The Assistance Fund Opens New Program for Systemic Sclerosis ORLANDO, Fla., January 29, 2024 (Newswire.com) – The Assistance Fund, an independent charitable patient assistance organization that helps patients and… read more January 1, 2024 2024 Membership Drive Now Open The National Scleroderma Foundation’s mission is to advance medical research, promote disease awareness, and provide support and education to people with… read more December 13, 2023 Smart Ways to Give Before 2023 Ends Are you hoping to close this year with a charitable gift that supports the scleroderma community and reduces your… read more Sign Up for a Foundation Event Upcoming Events February 13, 2024; 7 p.m. Eastern Newly Diagnosed Support Group Email for meeting details February 17, 2024; 10 a.m. MT Caregivers Connection Support Group Email for meeting details February 20, 2024; 7 p.m. Eastern Bereavement Support Group Sign up February 20, 2024; 7 p.m. Eastern Localized Scleroderma Support Group Email for meeting details Research Initiatives The Foundation’s peer-reviewed research grant program is a leader in scleroderma research. Learn more about how this program accelerates the search for better treatments, and ultimately, a cure. Research Funded by the Foundation Read my inline content Subscribe and receive a weekly email with important information about scleroderma and the National Scleroderma Foundation Subscribe National Scleroderma Foundation 300 Rosewood Drive, Suite 105 Danvers, MA 01923 info@scleroderma.org (800) 722-4673 * About the Foundation * Mission, Vision & Values * Board of Directors * Medical & Scientific Advisory Board * Patient Advisory Board * Our Team * Our Partners * IRS Form 990 * Audited Financials * Annual Progress Report * Careers * Charity Navigator * Candid (Guidestar) * Privacy Policy * Media & News * State Fundraising Disclosure * Giving Nonprofit Website Design by Elevation ©2023 National Scleroderma Foundation Follow Us: * social * social * social * social * social Please ensure Javascript is enabled for purposes of website accessibility × Register Here Originaltext Diese Übersetzung bewerten Mit deinem Feedback können wir Google Übersetzer weiter verbessern