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Laura H.: Mother of Son with Linear Morphea
Spanish

Apricot Watsonia by Sherrill Knaggs, ISN Artist I am the mother of a twelve year old boy. About a year ago he got a spot in his face, and at first I thought he had hit himself with something, since he is a bit clumsy. But when I saw that the bruise would not go away, I took him to the doctor and he sent me to a dermatologist, who, after a biopsy diagnosed linear morphea.

At first I did not think too much of it, because time went on and his condition remained the same, but now, after a year, everything has changed. What started as a bruise in his forehead, has come down to his nose, and his forehead has sunk a bit.

The dermatologist says it is not too important, and I get really worried when she says it will keep growing. She says that his face will keep on looking sunken because he is left without fat in that area.

To be honest I think it is very important. The medicine she has sent me is Lexxema to be applied whenever I see a red spot.

Please, if somebody could give me any tips of something I can do to really help my son, I would greatly appreciate it.

To Contact the Author
Laura H.
Email: sejolajo@hotmail.com
Story edited 07-23-07 JTD
Story posted 08-17-07 SLE

ISN Senior Artist: Sherrill Knaggs
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
(Español/Spanish) Laura H.: Morfea Lineal
ENGLISH:
Juvenile Scleroderma
Linear Scleroderma, En Coup de Sabre
Morphea
Morphea Stories
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Sclero Forums
Symptoms of Scleroderma
Types of Scleroderma
What is Scleroderma?
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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