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Vali: Mother of Linear Scleroderma Patient
Italian

Yellow Orchid for Vali by Ione Bridgman, ISN ArtistMy name is Valentina, and I have a ten year old daughter. This summer I realized that my little girl had lines in her forearms, arms and in a leg and knee joint that were dark on the outside, but lighter in co lour inside, as if she had a bad tan. In the thigh she had a scar that began in her buttocks and ended in her leg, but this shrank a bit.

A dermatologist diagnosed her with Linear Scleroderma, but another one said it was Linear Lichen Planus. My daughter's feet, when she walks, turn inside, and she is often warm, but doesn't have a fever.

Does this correspond to any of the diagnosis? I am a concerned mother looking for other opinions. Do you have any?

Thanks in advance. I trust you! I am in terrible shape.

To Contact the Author
Vali
Email: valentyna82@live.it
Story edited 12-15-08 JTD
Story posted 01-20-09 SLE

Story Artist: Ione Bridgman
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
Italian:
Vali: Sclerodermia Lineare
Cos'è la Sclerodermia

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ISN Artist: Ione Bridgman
Ione Bridgman ISN Artist Ione Bridgman created original artwork to illustrate this page. She is 90 years old, and lives in New Zealand. Her lovely paintings illustrate many of our pages and the covers of our  Voices of Scleroderma Book Series .
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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Go to Vanessa: Linear Scleroderma
 
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