Donation Street, Shop Save and Support Us
Over 2,200+ pages in 22 languages!
Custom Search
Patient & Caregiver Stories Main Menu
(English) Stories by First Name: A B C D E F G H I J K L M N O P Q R S T U V-Z
All Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
Stories by Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms
Stories by Language: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish
Catherine: Mother of Linear Scleroderma Patient
My mouth does not close as the lips cannot cover my protruding top jaw, and there is little saliva flow over these teeth.

Birdhouse at Gallteria by Shelley Ensz My linear scleroderma started on my left cheek at the age of four and by the time I was eight, that side of my face was quite deformed. The growth of my left jawbones were affected; hence, the removal of teeth when I was sixteen in preparation for surgery. My mouth does not close as the lips cannot cover my protruding top jaw, and there is little saliva flow over these teeth.

From what I remember, the proposed surgery was to break my top jaw and make it fit my mouth without touching the skin that had been affected by the scleroderma. This skin is now quite soft. This surgery, I presume, would also improve my bite. At the moment, my jaw does not meet and chewing is difficult.

Now the doctors seem to be reticent to cut into the scleroderma skin to puff out my cheek to make it look normal. My family and I are not critical of this or the five years on the waiting list, but at twenty-three, I would like something done.

I would love to hear from anyone who has linear scleroderma or had reconstructive facial surgery for it, or who is knowledgeable about such procedures.

~ Update 5-24-03 from Emma ~

I have had linear scleroderma since I was four years old on the left hand side of my face which made my face look crooked.

On December 2, 2002, at the age of twenty-six, I had an operation to make my face look similar to everbody else's. My surgery was done at Middlemore Hospital in New Zealand, by an oral surgeon called Lance West. He broke both of my jaws and pulled the top one back and brought the bottom one up to meet the top one, so now my face looks straight and I can close my mouth without my teeth sticking out.

To Contact the Author
Catherine and Emma
Email: emwalkinton@yahoo.co.nz
Story posted 1-1-2000
Update posted 5-24-03
Story edited VH1: JTD 9-4-03

Story Artist: Shelley Ensz
Story Editor V1: Judith Devlin
LINKS
Linear Scleroderma
Voices of Scleroderma Volume 1
This Story is Featured in Voices of Scleroderma Volume 1
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!
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
Mila: Morphea Now I am twenty-five years old, and that spot has grown throughout my right leg and on one side of my belly button...
(Español/Spanish) Mila: Morfea Hoy en día tengo 25 años y esa mancha está en toda mi pierna derecha y al lado de mi ombligo...
(Español/Spanish) (Update) Jeins: Esclerodermia Sistemica Difusa y Dermatopolimiositis Ya había escrito mi historia hace 3 años cuando recién estaba pasando por la enfermedad. Para quienes no lo saben tengo esclerodermia y dermatomiositis desde los 19 años.
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
More New Stories: November 2008
Submit Your Patient, Caregiver or Survivor Story in:
Arabic  | Dutch  | English  | Español  | Deutsche (German)
Italiano  | Polski  | Russian  | Spanish  | Turkish  | Other Languages
We will edit your story, create original artwork to decorate it, prepare it for the web, and post it on this site. Just fill out our simple Story Submission Form for your story, updates, or email address changes.
Keep on Surfing!
Go to Catherine C: Surviving Daughter of Pulmonary Fibrosis Patient
Contact ISN. We are a full-service nonprofit agency.
Email: isn@sclero.org or
Post in Sclero Forums!
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
USA
Toll Free Hotline in U.S.
1-800-564-7099
Direct Line
1-952-831-3091 (U.S.)
(We are also known as the Scleroderma from A to Z web site.)
© Copyright 1998-2008 International Scleroderma Network
All Rights Reserved