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Kichy: Localized Morphea Scleroderma

(Spanish) Kichy: Esclerodermia Localizada, Morfea

Flowers for Kichy by Sherrill Knaggs, ISN Artist I am a thirty-four-year-old professor at the Autonomus University of Chihuahua.

A month ago, I was diagnosed with localized morphea. Due to this diagnosis, I am having second thoughts about having another child, which I want so much. At present, I have a one-year-old baby girl. I am weighing the pros and cons on this topic because of the disease I have been diagnosed with.

The dermatologist that I have been seeing, came up with this diagnosis after doing a skin biopsy which resulted positive to scleroderma. All I can recall about the conversation with my doctor was that I had scleroderma morphea.

It all started when I began noticing red blemishes on my forearms, which sometime later turned hard and changed in color, somewhat lighter than the natural color of my skin. Although I have not felt any additional effects because of this illness, I have noticed new blemishes on my waistline and on my calves. These have remained red up until now.

My doctor has made me go through many lab tests, but up until now, everything has turned out negative. Seeing this, I have not taken my doctor's diagnosis too seriously.

At present, my doctor has me on a cream by the name of Visderm-H at 1%, Colchicina, and a antibiotic, because she believes that I have a bacteria hidden in my body known as 'Borrelia', but the lab tests have always shown that I am okay.

Although my family is worried about my condition, I have faith that everything will turn out well, and I believe that if I have this disease it is because God has a mission for me. All I ask God for is to give me the strength I need to face this illness. If anyone out there has any suggestions or recommendations, please contact me; I will be eternally appreciative.

To Contact the Author

Email: [email protected]
Story posted 9-26-03

ISN Senior Artist: Sherrill Knaggs
Story Translator: Edwin Lamoli-Torres
Story Editor: Judith Devlin
Localized Morphea
La Esclerodermia desde la A hasta la Z (Spanish)
Historia Kichy (Spanish)

ISN Artist: Sherrill Knaggs (In Loving Memory)

Sherrill KnaggsSherrill 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 Translator: Edwin Lamoli-Torres

Edwin Lamoli-Torres is the ISN Spanish Translator for this story. He is a retired professor from the University of Puerto Rico at Mayaguez, where he taught English as a second language.

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 Kim K: Mother of Morphea Patient

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)