We invite you to join the UK Scleroderma forum!
This forum, which is brought to you by the nonprofit International Scleroderma Network (ISN) at SCLERO.ORG, is open to anyone in the United Kingdom who has scleroderma or has an interest in it.
As you join our online community, please acquaint yourself with the Forum Guidelines and then feel free to share your challenges and triumphs in the company of people experiencing the same challenges and triumphs as you.
Have a look at the other forums and make yourself at home. Post photos of your family or view pictures of scleroderma symptoms in our Photo Gallery. Join any of our weekly hosted chats. Peruse our blogs with fascinating articles by scleroderma patients and caregivers. Share our full selection of scleroderma videos with your friends and family, so they can begin to understand what living with scleroderma is like.
We're very glad to have you and I look forward to seeing you on the forums! Visit UK Scleroderma forum now!
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.