Free Special Events Promotion for Scleroderma Groups
From the International Scleroderma Network
For all languages and all countries. This free offer is for all scleroderma groups, including individuals who want to start a group.

With approval, any scleroderma support group or organization — worldwide — can receive a totally free listing for their special events in ISN's Newsroom. We will post your special events notice until your event is over.

Special events may include fundraisers, conferences (for either patients or medical professionals), kick-off meetings for support groups, and special topics or speakers at meetings.

If you have a web page for your group or special event, we will link to it. If your organization does not have a web site yet, you may request a free web page. If your organization already has a web page, you may also join ISN's free Scleroderma Webmasters Association to further promote your site.

Effective January 2002, we no longer offer free promotion for (U.S.) Scleroderma Foundation groups, because their groups and events are now listed exclusively through their national offices.

We reserve the sole right to determine what groups are eligible for this offer, and to rescind the offer at any time. An example of groups that may not be approved include those designed to promote just one form of treatment for scleroderma, rather than general support for all scleroderma patients and/or caregivers.

Dozens of groups have their home page on this web site. You can check them out through the listings on the Support Group page. You'll notice that there is a standard format for each page, which is modified a bit as needed for each group.

This offer is made by the nonprofit International Scleroderma Network, as part of our mission to network and empower our worldwide scleroderma community. Get your free Special Events Promotion with this easy online form:

Special Events Promotion for Scleroderma or Related Illnesses
Your name (Required):
Your email (Required):
Contact Information
Title of Special Event:
Name of Your Organization:
Event leader:
Event Leader's phone #:
Organization's website:
Special Event web page:
Event Leader's Email:
Special Event Information
Your page will stay most current if for meeting dates you enter simply "second Tuesday of every month" or "Please call for meeting information" rather than listing specific dates.
Description of Special Event :
City, State and Country
of special event:
Language if other than English:
Please tell us about your event (date, time, location, prices):
Affiliation
If this group is part of a larger organization, we would like to mention it. Is your group affiliated with the:
1. (U.S.) Arthritis Foundation? Yes No
2. International Scleroderma Network (ISN) ? Yes No
3. (U.S.) Scleroderma Foundation? Yes: Please stop here and contact the national SF for a listing on their site. No
4. Any other group? If so, enter here:
ISN Artist: Ione Bridgman
Ione Bridgman ISN Artist Ione Bridgman created original artwork to illustrate this page. She is 90 years old, and lives in New Zealand. Her lovely paintings illustrate many of our pages and the covers of our  Voices of Scleroderma Book Series .
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Go to Thank You for Your Submission
Contact ISN. We are a full-service nonprofit scleroderma charitable foundation.

Email Inquiry Form (English)
Email Inquiry Form (Spanish)
Email Inquiry Form (Italian)
Email: isn@sclero.org
Or, post a message in our terrific
Sclero Forums Online Support Group!

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
USA
Toll Free Hotline in U.S.
1-800-564-7099
Direct Line
1-952-831-3091 (U.S.)

Donate in Memory to the nonprofit International Scleroderma Network at sclero.org. We will make a custom donation form and link for you, and send thank you's and acknowledgement cards. We list donors and events in our website and newsletter.

Please help raise awareness of scleroderma and related illnesses by mentioning and linking to the nonprofit International Scleroderma Network at sclero.org in conversations, speeches, web sites, and publications.

(We are also known as the Scleroderma from A to Z web site.)
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