Visit Sclero Forums, Chats and Blogs!
 
Search sclero.org:
 
The most important thing in the world to know about
scleroderma is sclero.org with 5,000+ pages in 23 languages!
 
Donate in MemoryIn loving memory of Tom Regensburger, and Vera Kortan . (Donate)
Home   Medical   News   *Sclero Forums*   Support   Languages/Countries
Earn $150 on July 30th in Boston Marketing Research Study if you have scleroderma or CTD and have been screened for pulmonary hypertension!
Frog jumping for joy by Shelley EnszPDF Flyer: Boston Marketing Research Study. Schlesinger Associates-Boston, a national marketing research company, is currently looking for patients who have been diagnosed with Scleroderma or other Connective Tissue Disease, who either have pulmonary hypertension or who are regularly screened for it, to participate in a July 30th paid marketing research study in Boston. Read PDF Flyer: Boston Marketing Research Study or call Katherine at 617-542-5500 x310. Schlesinger Associates-Boston. Posted 07/26/10.
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
Stories in Other Languages: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish
Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010

Joanna: Morphea

My ex-husband said I looked like Lizard Lady of the Circus and I never forgave him.

One Day Lily by Sherrill Knaggs, ISN Artist I noticed an oval spot on my hip two weeks after I'd had a surgery that was particularly scary for me at age twenty-six. My doctor thought it was ringworm and treated it.

I had to see a dermatologist when the spot stayed and I started getting more spots on my ribcage and hips. The diagnosis was morphea. The first dermatologist said I had more spots than he could find on any one person in his medical books and treated me with a steroid tape that I had to cut into the shape of each spot on a daily basis. It was depressing, time consuming and gave me chemical burns, so I stopped using it. My ex-husband said I looked like Lizard Lady of the Circus and I never forgave him.

Later, I saw another dermatologist because I was tired of dealing with the thick, dry skin and I was still getting more spots. She was concerned about my developing lupus and she ran tests. The tests showed no lupus but I was told there was no cure for the morphea and it should run its course in about ten years.

I was already embarrassed to wear a bathing suit; I had brown patches on my back that looked like big bruises.

When I was pregnant with my daughter, my husband was practically accused of beating me. I had huge spots in various stages all over my belly, my ribs, and my back.

Some spots are oval. Some have no shape. The spots on the inside of my elbow-bend have faded but I still get new spots on my body. They get bright pink when I am upset and I get new spots if clothes rub my skin tightly. To this day I haven't found a lotion or moisturizer that calms them.

I have had people ask me if I've been cut, burned, and beaten. After my divorce, I considered putting body makeup on when I started to date. Lately, I've noticed my hands feel tight inside their skin and I don't know if it is related to the morphea or if it is just arthritis, so off I'll go back to the doctor. But I won't go back to the one who said it would burn out after ten years because it's already been twenty-four years since the first spot appeared.

I noticed shiny patches on my maternal grandmother's knees a couple of years before she died at eighty-six. She had it too. I pray my daughter doesn't develop it.

It frightens me because I have so much of it and it won't go away. I wonder if my lungs will be affected because sometimes I wake up and my chest feels constricted. Antidepressants only help so much and I really hate my body.

To Contact the Author
Joanna
Email: baycliffpwds@hotmail.com
Story edited 01-21-08 JTD
Story posted 01-23-08 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
LINKS
Morphea
Morphea Stories
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Sclero Forums
Symptoms of Systemic Scleroderma
Types of Scleroderma
What is Scleroderma?
ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill KnaggsSherrill 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 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
Mars: Scleroderma with Full Gastrointestinal Involvement I finally started total parenteral nutrition (TPN, or tubal feeding) in May 2010 and it was an absolute success...
Sonya D: Surviving Daughter of Systemic Scleroderma Patient (Portugal) She had difficulty eating, drinking and digesting her food, but yet doctors had no clue...
Hazel: Morphea Scleroderma In 1962 when I was just twelve years old, my mother took me to our family doctor with what looked like a blister under my right eye...
Angela R: Linear Morphea Scleroderma I am twenty-five now and only have the two spots that I deal with pretty easily. I just hope it doesn't get worse...
Heather A: Scleroderma (South Africa) My fingers started to curl up and I could not wear any rings on my fingers anymore as they were so swollen...
More New Stories: May-July 2010
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 Joanne: Diffuse Scleroderma
 
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

This website is certified by Health On the Net Foundation. Click to verify.
This site complies with the HONcode standard for trustworthy health information: verify here.

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.
Privacy Policy, Financial Disclosure, and Disclaimer.
© Copyright 1998-2010 International Scleroderma Network
All Rights Reserved
 
Home   Donate   Medical   News   *Sclero Forums*   Support   Translations   Search