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

Susan L: Diffuse Scleroderma

I was so relieved to finally have a diagnosis.

Yellow Flowers by Sherrill Knaggs, ISN Artist I first noticed the swelling in my hands and feet shortly after my daughter was born in 2005, and thought that it was post-pregnancy fluid. But the edema did not get better by two months, so I went to the family physician. He referred me to a rheumatologist and also wanted me to get chest x-rays. It turned out that I had walking pneumonia.

The rheumatologist's nurse practitioner did not know what I had and kept trying different medicines. The only medicine that seemed to help was prednisone because when I tried to stop taking it, the swelling came right back. By May 2006, she was almost ready to diagnose me with sero-negative rheumatoid arthritis. I decided to see another rheumatologist and on my first visit, I heard the diagnosis: scleroderma. At that time I was taking prednisone (see Prednisone Warnings for Scleroderma) , plaquenil, and a pain medication.

I was so relieved to finally have a diagnosis. I thought that meant I would get the proper treatment, but there is no treatment or cure. My skin tightening progressed to my trunk and thighs. The edema was gone but my skin was tightening so that I did not have wrinkles on my forehead. My sclerodactyly prevented me from making fists and completely straightening my fingers.

I went to see a scleroderma expert who thought I had a rapidly progressing case and suggested that I take my blood pressure every day. She prescribed some medication and said I would have to get my blood tested regularly. It was getting harder to fasten my bra across my back and change diapers. Raynaud's was pretty bad that winter and I started to fear going outside. I started to worry that I would not live to see my children graduate. But I was not going to give up.

It has been nine months and I am doing better. I also used acupuncture and massage therapy, and herbal supplements on and off during this time. I can pick up the skin on the back of my hand. I see five wrinkles on my forehead. My knees are not as stiff so it is easier to squat. My skin tightening on my trunk and thighs is gone. I do have these nodules on my chest and back that are not painful (since January 2006). I also have some neuralgia symptoms occasionally. My lungs are fine and I do not have problems with reflux or swallowing so I am hoping that I won't get any internal organ involvement. I am delighted to feel better!

My lab work continues to show I am ANA negative, RH negative, and I only test high for gamma globulin. My SED rate has gone down from 64 to 23. I am no longer worried about living to see my children graduate. I am hoping that I will be healthy enough to dance at their weddings!

Iʼd be interested in hearing from anyone who has developed diffuse scleroderma after childbirth or who have young children."

To Contact the Author
Susan
Email: susanotrl@yahoo.com
Story edited 10-09-07 JTD
Story posted 10-18-07 SLE
Story edited 10-22-07 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
LINKS
Alternative Therapies
Antibodies
Diffuse Scleroderma
Diffuse Scleroderma Stories
Plaquenil
Prednisone (Warnings for Scleroderma)
Raynaud's
Raynaud's Stories
Sclerodactyly
Sclerodactyly Stories
Skin Fibrosis
Skin Fibrosis 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 Susan M: CREST, Raynaud's and Hashimoto's
 
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