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Lisa V: Diffuse Scleroderma and Raynaud's

When I first got sick, I thought I was dying.

Chrysanthemums for Lisa by Sherrill Knaggs, ISN Artist I am thirty-nine years old. I have had scleroderma for seven years. When I first got sick, I thought I was dying. My fingers started hurting really bad. I did not know what in the world was wrong with me. My local doctor sent me to the emergency room, where an internal medicine specialist diagnosed me with Raynaud's. I had been his patient for a year. He finally told me that if I did not get to a rheumatologist soon, that I could die.

I started out at the Medical Mall in Jackson, Mississippi, until I got on disability. Once I got my disability I found my own doctor. I have a great doctor. She has been able to get my disease under control. Her name is Dr. Valee Harisdangkul, and she is wonderful. When I started seeing her, the scleroderma had already moved to my face. Since then it has moved back down to my elbows. My hands and arms are crippled.

In the last eight months I have felt better than I have since I have been sick. I am a survivor. I have a nineteen-year-old daughter, and a four-year-old grandson. That's worth fighting for!

For the first year I did not lay down, I did not sleep. If I even looked at a bed I would scream. I was taking a strong dose of pain relievers but I am back down to a lower dose now. I am on various medications for circulation, damaged nerve endings, blood thinning, finger and elbow ulcers, and for stress.

If you wonder how I type, I use one finger on my left hand. On my right hand, all my fingers are bent under, and my arms are contracted at the elbow.

My mother has been to every doctor appointment with me since I have been sick. We traveled to Oxford, Tupelo, Tennessee, and back to Jackson, Mississippi, for treatment. She has stuck with me from me screaming in pain, day after day, and not being able to ride but for a short distance at a time without pulling over for a break.

I love my mother. There is nothing better than having her at my side. She has probably heard and responded to my every cry. May God bless her! Thanks, Mom.

All my meanness as a teenager is paying off. I have strong will power, and a lot of faith. Please feel free to email me if you like. Thank you so much for letting me share my feelings. I hope this will help somebody who is going through the same thing I am.

To Contact the Author
Lisa
New Email: sunnylogan63@yahoo.com
Story posted 8-14-02
Story paragraph added 8-20-02
Email updated 7-13-03
Story edited 7-13-03 SLE
New email address needed 9-2-03 SLE
New email posted 8-14-04 SLE
ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Contractions
Diffuse Scleroderma
Finger Ulcers
Raynaud's
Scleroderma
Sclerodactyly (contracted hands)
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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Go to Lisa W: Diffuse Scleroderma, CREST and Multiple Sclerosis
 
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