The Scleroderma Association of Queensland is a self-help group providing support, information and counselling to people with scleroderma and their families and friends.
The Association realises that sufferers often feel alone and isolated. We have members all over Queensland from Coolangatta to Cook Town and Winton (the town of Waltzing Matilda) to the East Coast.
We are a non-profit organization dedicated to raising money for scleroderma research, all of the work is carried out on a voluntary basis by the members. Scleroderma patients and their family members/caregivers are invited to this support group. Together we all draw strength, hope and inspiration from each other. Please join us!
Meetings are held monthly on the 2nd Tuesday of each month, except January. The meetings take place in the Hamilton Room at Brisbane City Hall. Quarterly meetings are also held on the Gold Coast.
Contact information updated per Robyn Sims on 11-19-10, SLE.
Meeting information last updated per June Meyer on 07-23-07, SLE.
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
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