I am a thirty-four-year-old woman, and I have been suffering from localized morphea scleroderma for about twenty years.
The disease initially started with a very small mark on my right thigh that seemed to be a bruise. Then the lesion changed its appearance and extended along the entire leg. Meanwhile, a small mark also appeared on my face, which was almost certainly another manifestation of the same disease. I went to see various specialists, almost all of whom agreed on the diagnosis and on the impossibility of an ad hoc therapy, explaining to me that the real cause of the disease is unknown, along with its treatment. They suggested I try various treatments that have not been of much benefit apart from softening the skin.
I had a series of immunological tests performed (including antinuclear antibodies) to check if this was a systemic form of scleroderma. Fortunately, these tests were all negative.
Now, having read the information on sclero.org, I am no longer sure that these results completely rule out the more serious form of this disease. For the record, I also suffer from celiac disease.
*Editorial note by Dr. Magdalena Dziadzio and Dr. Mario Gismondi: From the data currently available, there is no evidence that the localized form of scleroderma can turn into the systemic disease.
New email address needed 08-01-06 SLE
Old Email Prefix: alessandrastaiti
Story posted 2-14-01
Editorial Note added 3-15-02
by Dr. M. Dziadzio and Dr. M. Gismondi
Translated from Italian
by Kevin Howell 6-17-02
Story edited VH1: JTD 9-4-03
Story Artist: Shelley Ensz
Story Editor V1: Judith Devlin
(Italianio) Alex: Sclerodermia Localizzata
(Italiano) Sclerodermia dalla A alla Z
Voices of Scleroderma Volume 1
The story on this page is featured in the top-notch Voices of Scleroderma Volume 1 which features articles by top scleroderma experts, including Dr. Joseph Korn, as well as 100 true patient and caregiver stories from this website! The book delivers excellent information and support for scleroderma patients and caregivers. It's a great way to inform family and friends about scleroderma, too!
Kevin Howell is the ISN Translator (Italian to English) for this story. He is a Clinical Scientist for Professor Black at the Royal Free Hospital in London.
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, Shelley Blaser, Susan Book, Dennis and Pat Clayton, Grace Cunha, Cindy Dorio, Shelley Ensz, Nancy Falkenhagen, Jo Frowde, Margaret Hollywood, Karen Khalaf and Family, Susan Kvarantan, Bradley Lawrence, Jillyan Little, Michele Maxson, John Moffett, Joan-Marie Permison, John Roberts, Margaret Roof, and Maryellen Ryan.
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.