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Yally: Dermatitis with Linear/Morphea
Spanish

Apricot Watsonia by Sherrill Knaggs, ISN Artist I am Yally, mother to a lovely girl called MC, who is seven years old. A year ago she was diagnosed with linear morphea. She has a spot on her left leg, that almost covers it completely.

Now she takes colchimedio 0.5 one pill a day and Daivonex cream every night, as well as Methotrexate two pills every eight days on Sundays.

Physically she is a healthy girl. My concern has always been taking the drugs for an unlimited amount of time, what side effects it can have. She gets checked periodically, and up to now everything is okay, thank God.

Thank you for this web site and I would like to be in touch with you, and to know more about eating habits, exercise and in general the normal life my little girl can lead.

To Contact the Author
Yally
Email: mcacosta558@hotmail.com
Story edited 10-09-06 JTD
Story posted 11-15-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
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Juvenile Scleroderma
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ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill Knaggs Sherrill Knaggs, ISN Artist, created the digital photo to illustrate the story on this page. Sherrill lived in New Zealand. Her story was featured in ISN's book, Voices of Scleroderma Volume 2.
ISN Translator and Editor: Alba León
Alba Leon, ISN TranslatorAlba León is the ISN Translator for this page. She is studying international relations in Mexico City.
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith Thompson Devlin is the ISN Story Editor for this story. She is also lead editor of the ISN's wonderful Voices of Scleroderma book series!
New Personal Stories
Maria T: Daughter of Deceased Scleroderma Patient (Italy) He, upon looking at my mom's face and hands diagnosed her with sclerodermia, in fact he took care of her until the end...
(Italiano) Maria T: Figlia di una Paziente Defunta di Sclerodemia (Italia) Lui, come vide a mia madre disse "tu hai la sclerodermia", guardandole le mani e la faccia...
(Update) Dee B: Limited Scleroderma/CREST Syndrome (South Africa) There is so much I want to add to my original letter after reading more of other peoples stories. I am certainly not getting better but wish I was...
Tessa: Morphea The nurse just told me that I have morphea and knew nothing about it and she told me to look online for information...
More New Stories: August-November 2009
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