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Scleroderma Support

You are not alone! How can we help you?
Overview
Awareness
Blogs
Books
Brochures
Caregiving
Disability
Doctors
Donations
Forums
Hotline/Phone
Humor
Photos
Stories
Support Groups
Videos

Overview

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.

Awareness

Scleroderma Awareness BraceletDid 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)

Blogs

Enjoy our Scleroderma Patient and Caregiver Blogs!

Books

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.

Brochures

Scleroderma BrochureWhat 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)

Caregiving

Overview
Blogs
Forums
Grief/Bereavement
Poetry
Respite Care
Stories

Disability Resources

Disability Overview
Assistive Devices
Disability Discussions
U.K. Disability
U.S. Disability
Free/Low Cost Meds
Hospice
International Relief
Medic Alert Programs
Palliative Care
Patient Rights
Patient Programs
Scholarships
Wish Granting

Doctors

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

Donations

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

Forums

Scleroderma Forums Video
Video: Why I Love Sclero Forums

Presented by Amanda Thorpe
*More Scleroderma Videos*

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

Hotline/Phone

CoffeeOur 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!

Email

We are here to help you! Email [email protected] with your questions, concerns or comments.

Photos

Browse our Sclero Forums Photo Gallery for images of members and scleroderma symptoms, or view our ISN Photo Repository for scleroderma symptom images and slideshows.

Humor

Join us in the World's First Virtual Pity Party!

Welcome
Diagnosis Roulette Wheel
Judy T's Pity Party Story
Medical Misadventures
Meditation for Depression
Pity Party Mugs
Pity Party Music
Pity Party Slogans
Pity Party Supplies
Undiagnosable Blues
Virtual Dartboard

Personal Stories

View Our Story Listings:

By Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms

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

Support Groups

Sclero Forums. Our worldwide online scleroderma support group is in session around the clock!

Worldwide Support Group Listings.

Videos

What is Scleroderma Video
Video: What is Scleroderma?

Presented by Isabella Ensz
*More Sclero Videos*

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.

Go to Caregivers/Caregiver Stories
 
 

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, Volunteer, or Donate.

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 or update any page content or links.

Toll Free US/Canada Scleroderma Hotline: 800-564-7099

 
The most important thing in the world to know about scleroderma is sclero.org!
Copyright 1998-2015, International Scleroderma Network. AKA Scleroderma from A to Z and SCLERO.ORG. All Rights Reserved.
Copyright 1998-2015, International Scleroderma Network. AKA Scleroderma from A to Z and SCLERO.ORG. All Rights Reserved.