Search sclero.org:
Thanks to Actelion
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

Lynne: Morphea

I have had this skin disorder for almost eighteen years
and I just accept it as being part of my life.

Butterflies and Flowers by Ione Bridgman, ISN Artist Reading the stories on this site really took me back to my own childhood. I am a woman of twenty- five and pregnant with my first child.

I remember the day so well that this discovery began. One day when I was seven years old, my family and I went swimming in the local river. When we returned home my mother bathed and dried me. She noticed a reddish circle on my lower back. She was very worried and called the local doctor. The doctor came to the house, but was unsure about my spot so referred us to the local hospital.

After a few months, I was seen by many different doctors, many of them just wanting to take a look. Because I was very young I do not remember much about the time, but I know my parents were very worried.

There was a special doctor who was from New York, but living in our country at the time, and I remember seeing him. He diagnosed it as Morphea and showed me many pictures of different people with the same skin disorder. My mum is still convinced that the morphea had something to do with the river that I went swimming in.

As the years went by, the skin on my back hardened and turned a pale brownish color. It did grow quite a lot. It started about the size and shape of a fifty-cent coin and now covers most of my spine to the side of my back. Yet I have to say that I do not think it has grown for many years now. It has never caused me any problems at all. Now the affected area is darker than my other skin but it does not look too bad. It isn't too hard anymore either, it just feels a little drier.

The doctors that I saw at the time of diagnosis did not know very much at all, but they did advise my mother to keep my skin protected in the sun and to prevent sunburn, which I really never did do. I loved going to Cyprus with my partner and soaking up the sun, which actually made my Morphea blend in with the rest of my skin, as my pigment darkened. I was also told to only use baby oil on my skin; no perfumes, make-up, or bubble bath. Yet again, because I love fragrance lotions and have always taken bubble baths, I did not follow the doctor's instructions. When the doctor advised these things he said he was not sure, but it may help. But as you can see, I have led a completely normal life, although the worry is normal.

When I first got access to the Internet I could not help but look up Morphea as I never again saw a doctor. I was horrified by some of the stories, yet I have witnessed myself that Morphea definitely does not necessarily deprive you of anything. I hope that other sufferers are as fortunate as me with having so few symptoms. I have had this skin disorder for almost eighteen years and I just accept it as being part of my life.

If anybody would like to email me to ask questions or just to talk I would love to hear from you!

To Contact the Author
Lynne
New email address needed 08-06-09 SLE
Old Email Prefix: Lynnemw
Story posted 1-25-03

Story Artist: Ione Bridgman
Story Editor: Judith R. Thompson
LINKS
Morphea Scleroderma
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 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
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 Lynsey: Daughter of Patient with Scleroderma and Lupus
 
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