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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 Scleroderma
Types of Scleroderma
What is Scleroderma?
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
Mila: Morphea Now I am twenty-five years old, and that spot has grown throughout my right leg and on one side of my belly button...
(Español/Spanish) Mila: Morfea Hoy en día tengo 25 años y esa mancha está en toda mi pierna derecha y al lado de mi ombligo...
(Español/Spanish) (Update) Jeins: Esclerodermia Sistemica Difusa y Dermatopolimiositis Ya había escrito mi historia hace 3 años cuando recién estaba pasando por la enfermedad. Para quienes no lo saben tengo esclerodermia y dermatomiositis desde los 19 años.
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
More New Stories: November 2008
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