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Marion: Friend of Systemic Scleroderma Patient
I would just like to say, thank you, Bridget, for being you!

Daffidols by Sherrill Knaggs, ISN Artist My name is Marion, and I am telling this story about my friend, Bridget. Bridget was born with a hip problem and over many years, it finally crumbled away. Bridget was diagnosed about seven years ago with systemic scleroderma with signs of stiffness in parts of her body and taut skin, mainly on her hands, arms and face. All of this didn't seem fair to be happening to someone who had already gone through years of trauma.

Being around Bridget on a regular basis, you never really noticed how quickly this disease was taking affect, until one day, we were looking at photos taken just a couple of years ago. She was nearly double her size but because she always felt so cold she wore layers and layers of clothes, which masked just how much weight she had actually lost.

Doctors have told Bridget that she will have a short life expectancy. She has accepted this but still wanted to hear from, or meet other people in our area who have this disease. She even had her story put in our local paper to try to get some sort of response.

Despite everything Bridget has gone through she had a baby four years ago, a beautiful little girl weighing 2lb 4oz. Bridget has carers to help with tasks that she can't manage to do herself in her everyday life but she is so independent. I have watched her get annoyed with herself because she hasn't been able to do something but even more annoyed when someone else has gone to do it for her.

Taking a deep breath and a few minutes to think she, nine times out of ten, comes up with a way of getting around the problem so that she can manage to do the task in hand herself.

I would like to find someone mainly in our area who has had any experience with this disease to contact us as it will really make her feel that she is not alone. Bridget is one in a million not because of her illness but for the way she will listen about everyone else's little ailments and never turns them away she listens to everyone's problems and is always there to comfort others when they are down.

I would just like to say, thank you, Bridget, for being you!

To Contact the Author
Marion
New email address needed 08-06-09 SLE
Old Email Prefix: garethtopping20
Story edited 01-06-08 JTD
Story posted 01-17-08 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Thompson Devlin
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ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill Knaggs Sherrill 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
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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