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Linda W: Surviving Daughter of Scleroderma Patient
In memory of Barbara "Bobbi" Bast 1947-2003
She requested this about two weeks before she died.

Clematis All she wanted was for others to learn of this disease and know her story. She requested this about two weeks before she died on October 24, 2003.

Barbara or "Bobbi" as she liked to be called, was diagnosed with CREST in 1990. She had major joint pain on a regular basis along with other symptoms, bowel problems and a lot of pain. After doing some reading about CREST syndrome she (and eventually her doctor) realized she had scleroderma. The worse seemed to have started with having a knee replacement, then a new knee cap, as they put the wrong size in the first time. Healing was very slow for her. As time went on she developed a sore on her elbow that did not heal, so they removed part of her elbow. Her fingers started getting sores that would not heal, so five of her fingers were amputated, at different times.

Then she had a second knee replacement, the other one this time. Another sore started and would not heal, so again the doctors decided to remove the parts of her that did not heal. She was on so many medications! She was placed in a nursing home after that knee surgery. She started to get involuntary shakes in her arms and legs and was embarrassed by this. Her kidneys and liver were starting to fail also. She developed a bad infection on the knee so they decided to remove the artificial knee and put spacers in so that maybe the infection would go away.

Mom then had a colonoscopy and when she came out of recovery the next day her small intestine started to bleed and they could not stop it. She was put in intensive care, and given five units of blood. The doctors told my family that we should decide if she would want to keep fighting or not.

After so many years of constant pain, she had been saying all along that she did not want to live like this. So we stopped everything; the pills, the blood, everything, and let her body decide when to go. She was kept comfortable on pain medication until the end. The infection finally got to her lungs. She died with her husband, her two daughters and her son at her side.

My mom was the strongest person I have ever known, and mom, I hope this helps in some small way of what you wanted me to do for you. There are so many details only you could really explain. I love you and miss you so much.

To Contact the Author
Linda W.
Email: lindalouwho1@sbcglobal.net
Story posted 11-06-03
Email address posted 07-06-05 SLE

Story Artist: Ione Bridgman
Story Editor: Judith Devlin
LINKS
Gangrene and Amputations
Bowel Involvement
CREST
Kidney Involvement
Liver Involvement
Scleroderma
Survivor's Stories
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
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