Our nonprofit International Scleroderma Network offers a full range of support services for people who care about scleroderma and related illnesses. We provide the world's largest portal of quality medical information for scleroderma…plus blogs, books, brochures, photos, resource listings, stories, and videos.
For personal support, we operate a Scleroderma Hotline, answer email inquiries, and the marvelous Sclero Forums, with stellar, well-moderated support and top quality medical information.
Did you know you can help raise scleroderma awareness? The nonprofit International Scleroderma Network offers scleroderma awareness bracelets! Bracelets for just $2.50 each with free shipping and handling! They say "scleroderma" on one side and "sclero.org" on the other. (Also see Get Scleroderma Awareness Bracelets)
Enjoy our Scleroderma Patient and Caregiver Blogs!
The Voices of Scleroderma book series is based on this sclero.org website, and features articles by world scleroderma experts plus inspiring personal stories. It is great for patients and caregivers alike.
What in the world is Scleroderma? (.DOC/Word format) You may print this brochure (as many as you want) and give them to your family, friends, doctors, classmates, and clinics. It includes a handy systemic scleroderma symptom checklist! (Also see: What is Scleroderma?, Systemic Scleroderma Symptoms, and Scleroderma Symptom Checklist)
Free/Low Cost Meds
Medic Alert Programs
ISN Guide to Scleroderma Experts. Many scleroderma patients seek a consultation with doctors who specialize in scleroderma. This is a great way to get information on the latest therapies available. ISN
Scleroderma Donations. We are a full-service scleroderma nonprofit charitable foundation, established in 2002. Your support helps us tackle scleroderma research, support, education and awareness. We send Sympathy acknowledgement cards for donations in memory. We also accept vehicle donations, providing free tow away for cars, trucks, motorcycles, snowmobiles, boats (basically any motorized transport) in the U.S. and Canada! ISN
Sclero Forums offers stellar and well-moderated online support groups for scleroderma and related symptoms or illnesses.
Remember to sign up for daily curated medical news updates by subscribing to our News subforum.
Patients, caregivers, friends, family, and survivors are all welcome, all throughout the world! ISN
Our scleroderma hotline is toll-free in the United States and Canada. It is 1-800-564-7099. Our hotline specialists are not medical professionals, so we cannot provide specific medical advice, but we can often steer you in the right direction. For specific health concerns, you will probably want to consult a listed scleroderma expert.
Our direct number (at your expense) for people outside the U.S. is 952-831-3091. Call today and ask for our free Welcoming Email!
We are here to help you! Email [email protected] with your questions, concerns or comments.
Join us in the World's First Virtual Pity Party!
Diagnosis Roulette Wheel
Judy T's Pity Party Story
Meditation for Depression
Pity Party Mugs
|Pity Party Music
Pity Party Slogans
Pity Party Supplies
Scleroderma Patient, Caregiver and Survivor Story Collection. Be inspired and learn about scleroderma from the world's largest collection of stories for scleroderma and related illnesses! ISN
Sclero Forums. Our worldwide online scleroderma support group is in session around the clock!
Scleroderma Video Series. We have produced a wide range of videos about scleroderma, including all the various types of scleroderma, and its symptoms. They are a great way to learn about scleroderma, and to enlighten others! ISN.
Reading Voices of Scleroderma Books: Diana Kramer.
Sharing Scleroderma Awareness Bracelets: Deb Martin, Brenda Miller, Vickie Risner.
Thanks to UNITED WAY donors of Central New Mexico and Snohomish County!
Patricia Ann Black: Marilyn Currier, Shelley Ensz, Richard Howitt, Gerald and Pat Ivanejko, Juno Beach Condo Association, Keith and Rosalyn Miller, and Elaine Wible.
Gayle Hedlin: Daniel and Joann Pepper and Nancy Smithberg.
Janet Paulmenn: Anonymous, Mary Jo Austin, Shelley Blaser, Susan Book, Dennis and Pat Clayton, Grace Cunha, Cindy Dorio, Michael and Patricia Donahue, Shelley Ensz, Nancy Falkenhagen, Jo Frowde, Alice Gigl, Margaret Hollywood, Karen Khalaf and Family, Susan Kvarantan, Bradley Lawrence, Jillyan Little, Donna Madge, Michele Maxson, Barry and Judith McCabe, John Moffett, My Tribute Foundation, Joan-Marie Permison, John Roberts, Margaret Roof, Maryellen Ryan, Mayalin and Kiralee Murphy, Nancy Settle-Murphy, and Bruce and Elizabeth Winter.
SCLERO.ORG is the world leader for trustworthy research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. We are a service of the nonprofit International Scleroderma Network (ISN), which is a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team, or Volunteer. Donations may also be mailed to:
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA
Email [email protected] to request our Welcome email, or to report bad links or to update this page content.