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Online Educational Resources Available

Visit our YouTubeWordPress, and SlideShare websites to access our online resources!

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Make a Difference!

When you shop with AmazonSmile, a portion of your purchase goes to the Scleroderma Foundation Greater Chicago Chapter!

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Madison Support Group

You are not alone - Learn more and how to RSVP here!

 

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Join us and step out to cure scleroderma!

2017 summer walks are just around the corner! Click here to find the walk in your area and thank you for your support!

 

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Scleroderma Foundation: Greater Chicago Chapter

Coming Up:

April 22, 2017 : Patient Education Conference - Oak Brook, IL 
Join us for a day of learning and community! Get more information and register. 

 

May 7, 2017 : Food Fight for Scleroderma - AceBounce Chicago
Competition is heating up at our 9th annual celebrity chef cook-off event! Learn more and join us!

 

About Us

Making life easier for patients. Making strides toward a cure.

The mission of the Scleroderma Foundation is focused on three critical goals:

  1. SUPPORT: To help patients and their families cope with scleroderma through mutual support programs, peer counseling, physician referrals, and educational information.
     
  2. EDUCATION: To promote public awareness and education through patient and health professional seminars, literature, and publicity campaigns.
     
  3. RESEARCH: To stimulate and support research to improve treatment and ultimately find the cause of and cure for scleroderma.

Whether you're a scleroderma patient, have a friend or family member with scleroderma, or just want to learn more about the disease, we have valuable resources, education opportunities and fundraising events for you!

 

Contact Information

Chapter Contact:
Stephanie Somers Gresh, Executive Director
Melissa Spear, Marketing & Fundraising Manager
Scleroderma Foundation, Greater Chicago Chapter
134 N. LaSalle St. Suite 1360
Chicago, IL. 60602
Phone: 312-660-1131
Fax: 312-660-1133
Email: GCchapter@scleroderma.org 
Facebook: facebook.com/gcscleroderma
Twitter: @chiscleroderma
Instagram: @chiscleroderma

Board of Directors 
Tony Cogan, President 
Julie L. Drewniak, Vice President/Secretary 
Jennifer Bryson, Treasurer
Rosemary Arnold
Mary Carns
Cleetus Friedman
Carol Goldman
Peter Goldman
David Helfand
Mike Robbins
Renee Trikolas 
John Varga, M.D.
Jules Cogan 

Medical Advisory Board
Richard Burt, M.D.
Jane Dematte, M.D.
Ikuo Hirano, M.D.
Amy Paller, M.D.
Stuart Rich, M.D.
Dean Schraufnagel, M.D.
Nadera Sweiss, M.D.
John Varga, M.D.

 

 

Patient Education

Our next Patient Education event is in Oak Brook, IL on April 22! Get more information and register here. If you are looking for more educational resources, please visit YouTube and SlideShare for past conference presentations and videos.

Education Summit 

 

Patient Support

Support groups provide a forum to share thoughts, concerns and information. They are a great way to share information and provide encouragement to one another. Find a support group in your area or connect with others by phone.

Looking to start a new support group in your area? Contact us at 312-660-1131.


National Gold Sponsor

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National Bronze Sponsor / Conference Platinum Sponsor

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National Bronze Sponsor

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