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Davie's Mom: Mother of Linear Scleroderma Patient

I looked at her arm and there was a white line from the fingers to the shoulder.

Flower for Davie by Shelley Ensz My beautiful, talented daughter was diagnosed with linear scleroderma at the age of fourteen. She had just won a ballet scholarship to Las Vegas University for two weeks in the summer. Davie had performed in the Nutcracker Ballet in December when she came down with a high fever and what the doctor called a sun fungus on her right arm.

The doctor gave Davie antibiotics and cream for her arm, and also said she had strep throat. Nothing was mentioned of her arm again until March 2001. She ran out of her cream and said it hurt if she did not use it. I looked at her arm and there was a white line from the fingers to the shoulder.

After approximately thirty doctors, she was diagnosed with scleroderma. She is now sixteen and can only straighten her arm to a ninety-degree angle. Thankfully, it did not spread to any other areas. She is on medication, when I can get her to take it. She tried the UVA1 therapy at the University of Michigan, but to no avail. Dr. Maureen Mayes has said Davie could be a candidate for skin grafts. We have to wait and see. If anyone has tried this, I would love some input.

Davie continues her love for dance. She is also on the varsity pom-pom team at school.

To Contact the Author

Davie's Mom
Email:[email protected]
Story posted 11-18-01
Story edited VH1: JTD 9-4-03

Story Artist: Shelley Ensz
Story Editor V1: Judith Devlin
Juvenile Scleroderma
Linear Scleroderma
Voices of Scleroderma Volume 1

This Story is Featured in Voices of Scleroderma Volume 1

Voices of Scleroderma Volume 1 The story on this page is featured in the top-notch Voices of Scleroderma Volume 1 which features articles by top scleroderma experts, including Dr. Joseph Korn, as well as 100 true patient and caregiver stories from this website! The book delivers excellent information and support for scleroderma patients and caregivers. It's a great way to inform family and friends about scleroderma, too!

ISN Story Editor: Judith Thompson Devlin

Photo of JudithJudith 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!

Go to Dawn: Confirmed Early Scleroderma

SCLERO.ORG was the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses from 1998 to 2021. It was a grassroots movement from the original Scleroderma from A to Z web site, which was founded by Shelley Ensz. We were a 501(c)(3) U.S.-based public charitable foundation. We closed this web site and our nonprofit agency in April 2021.

International Scleroderma Network (ISN)