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Join a Stepping Out to Cure Scleroderma Walk

Click here to see events happening throughout New England!

Join a Support Group

Click here to find a support group near you. We're here to help.

Watch a Video

Choose from a variety of scleroderma information videos offered by the Scleroderma Foundation, or news on Scleroderma Foundation New England.

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Andrew Botieri speaking at 2016 National ConferenceNational Conference Videos are in!

A selection of videos covering various speakers at the 2016 National Conference in New Orleans, LA have been posted. Go to our video gallery page to link to videos on scleroderma lung disease, skin care and wound management, collagen, yogic breathing and more.

Chapter Support Group Meetings

Find a support group in your area or connect with others by phone. Support groups are a great way to share information and provide encouragement to one another. Looking to start a new support group? Contact us!

Click here for more information >>

advo-interior-new.jpgYour Voice Can Make a Difference

Help researchers share information to advance research for fibrotic illnesses, using scleroderma as a prototypical condition! Support H.R. 3666 The Scleroderma and Fibrosis Research Enhancement Act. Click here to download a letter to fill out and send to Robert Riggs at the Scleroderma Foundation, 300 Rosewood Drive, Suite 105, Danvers, MA 01923, or e-mail the completed letter to Robert at The foundation will make sure that the signed letters get to the correct congressional office. 


Amazon SmileGive Back through Amazon Smile

When you shop at, Amazon will donate a portion of the purchase price from eligible purchases to the nonprofit of your choice. The same Amazon you know, just now with a donation back to the New England Chapter. Simply select Scleroderma Foundation New England, and a portion of your purchase price will help us fund education, support, research and awareness for those living with scleroderma! Giving though Amazon Smile is easy. Find Amazon Smile here log into your existing account, type in Scleroderma Foundation, New England Chapter and search, select us to start giving. To keep giving make sure to log in though Amazon Smile each time you shop.

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About Us

Board of Directors
Don Legere, President
Katherine Bedard, Vice President
Peter L. Hart, Treasurer

Board Members
Elysia Cappellucci
Tony Cappellucci
Marie Coyle
Tim Hagan
Jane Ladas
Don Legere
Andrea Mahoney
Selena Valeriani

Board Advisors
Tom Curran
Walter Zagrobski

Medical/Scientific Advisory Board
Vincent Falanga, M.D.
Harrison Farber, M.D.
Carol Feghali Bostwick, Ph.D.
Humphrey Gardner, M.D.
David M. Leader, DMD
Thomas Medsger, Jr., M.D.
John Mulliken, M.D.
Nicole Orzechowski, D.O.
Andrew Plaut, M.D.
Robert Simms, M.D.
Michael Whitfield, Ph.D.
Michael York, M.D.

Contact Information

Executive Director: Jack Armitage,
Office Manager: Rebecca Dube

Office Mailing Address
Scleroderma Foundation, New England Chapter
462 Boston Street, Suite 1-1
Topsfield, MA 01983

Phone: 978-887-0658
Fax: 978-887-0659
General Information:

Our Mission

The MISSION of the Chapter is to help constituents make contact with each other through support groups, newsletters, and meetings;

To EDUCATE and INFORM the public about scleroderma, what it is, and its consequences through a central base;

To PROMOTE and raise funds for medical research seeking the cause of and cure for scleroderma.


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Photo Gallery

Look through photo galleries from previous events held by our chapter.



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Watch videos on scleroderma, news events, and a few fun extras. 


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