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

Robin T: CREST Syndrome

I lost my left index finger to frost bite.

Purple and Yellow Water Lilies by Sherrill Knaggs, ISN ArtistHello, my name is Robin, and I was diagnosed with CREST Syndrome about twenty four years ago. The first symptom I was aware of was a sore on my left index finger. It just would not heal. So I went to the doctor and he ran some test and did a test on a spot on my back. The test came back that I had CREST Syndrome.

Mostly I started with Raynaud's Phenomenon. My hands were always cold and turning white, purple then red then back to normal, and hurting. Then I developed a sore on my finger tip that wouldn't go away. And my doctor sent me to another doctor to look at it and he said he would have to dig the ulcer out of the tip of my finger. Well the all heck broke loose. The stupid doctor didn't know what he was doing. My finger died and got frost bite in June.

That night after the doctor did the surgery I was in so much pain that I was taking aspirins every hour. I even called the doctor at around 1:00 AMand told him that my finger didn't look so good and he told me that he didn't have office hours until one o'clock in the afternoon.

So in the morning after I put two of my children on the bus for school and I went to my family doctor on emergency call. He saw my finger and said he couldn't do anything for me, so he was sending me to a vascular surgeon.

I saw that doctor at 10:00 AM and was in the hospital by 10:30 AM. I lost my left index finger to frost bite. After that I never went back to that doctor who did the surgery.

I learned to take care of my hands myself. I found a rheumatologist who was fantastic, and I loved him to no end. He explained everything to me about the CREST and everything I had to deal with.

Then I moved to Tennessee, where I got divorced, and lived with my children and happily with nine fingers. I found another rheumatologist and he couldn't believe that I had CREST for so many years and I was doing so well.

My hands hurt a lot now. I have a lot of calcium built up on my fingers, but the doctors cannot operate any more. I have had four operations in the past six years and they just can't do anything else for my fingers. So I have bumps on both hands.

Well, I have to stop typing right now. My hands hurting too much. I'll try to get back later to finish.

To Contact the Author

Robin
Email: tngannyx4@yahoo.com
Story edited 01-16-08 JTD
Story posted 01-18-08 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin

LINKS
Calcinosis
Calcinosis Stories
CREST Scleroderma
CREST Stories
Raynaud's
Raynaud's 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 Rodger Mansfield: Widower of a Diffuse Scleroderma Patient
 
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