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 ;2009
Stories by Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms
Stories by Language: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish

AJ: Linear Scleroderma

I grew up being poked and prodded and
paraded in front of one specialist after another.

Straw Hat with Flowers, photography by Shelley EnszI have had linear scleroderma since 1968, when I was seven years old. I always felt like I WAS scleroderma, as I have never met anyone else with the same diagnosis.

I grew up being poked and prodded and paraded in front of one specialist after another. Sometimes whole classes of medical students were brought to look at me.

Scleroderma affected the left side of my body, wrecking havoc in a very short amount of time. My left leg is two and a half inches shorter than my right and much smaller.

Due in a very large part to my mother's persistence and nightly therapy, I have good use of my leg and arm. Also, I believe Dr. Claybaugh, who treated me at Wesley Hospital in Wichita Kansas, saved my life in more ways than one. Mainly by finally fixing on a diagnosis and listening to my mother and her thoughts and feelings regarding my illness.

I did not realize how much I had to say, I have never discussed scleroderma with anyone. Most doctors I have seen since my last visits with Dr. Claybaugh (1974?) do not even know how to spell scleroderma, let alone treat any problems I might have that are associated with this disorder.

I am so fortunate that my scleroderma stopped advancing with only small advances on my right side. But I can say that scleroderma affected my life and still affects me in ways incomprehensible to "normal" people. I remember wishing as a child that I had polio instead. People could spell it and while they did not understand it's dimensions, it was accepted in ways scleroderma never was. Weird, huh?

I am sorry for the little girl I was with scleroderma. I enjoyed no personal space, was so sick for so long. The agony of my limbs slowly drawing up is something I cannot describe accurately, and besides, it is a private matter. But I am also happy for the little girl who had the extreme luck of meeting a fine physician such as Dr. Claybaugh and the many physical therapists who were endlessly patient with a mad little girl who tried to hate them all.

Well, that is such a small part of my story, but I hope it finds it's way to a mother with a sick little girl. If it does, do not despair. I have a good life. I have a good job, own my own home, my own car. But the best thing of all, something the doctors warned my mother I would never have—two beautiful, healthy children!

To Contact the Author
AJ Miller
(AJ we need your new email address.)
Posted 3-1-99
LINKS
Linear Scleroderma
Types of Scleroderma
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
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.
 
Go to Alana: Scleroderma (Peru)
 
SCLERO.ORG is brought to you by the nonprofit International Scleroderma Network (ISN). The ISN is a full-service nonprofit scleroderma charitable foundation providing stellar research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension.
  1. Post a message in Sclero Forums!
  2. Email: isn@sclero.org
  3. English Email Form
  4. Español Email Form
  5. Italiano Email Form
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
United States
Toll Free Hotline in U.S.
Hours: 9am-3pm CST only.
Please leave a complete message, in English.
1-800-564-7099
Direct Line
1-952-583-5735
We are also known as the Scleroderma from A to Z web site.
© Copyright 1998-2010 International Scleroderma Network
All Rights Reserved