SCLERO.ORG
Search
SCLERO.ORG is retiring 4-24-2021. Thank you for the memories! You'll still find us in the Wayback Machine, and we'll carry your stories in our hearts forever.
Patient & Caregiver Stories Main Menu

(English) by First Name: A B C D E F G H I J K L M N O P Q R S T U V-Z

By Language: French   German   Greek   Italian   Polish   Romanian   Russian   Spanish   Turkish

By Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms

Cris: Morphea Scleroderma

Spanish

Painted Turtle Photo by Shelley EnszHello everyone, my name is Cris, I am twenty-two years old and I have suffered from this illness for three years, since I got pregnant. It all started with a white spot in my abdomen. My baby girl was born and the doctors said it was a normal spot since it did not hurt or anything.

Some time passed and the spot began changing in appearance. I went to another doctor and after a lot of tests he determined I had scleroderma. I began a very strong and very expensive treatment with periodic filtration, but due to the high cost I was unable to keep with it.

About three months ago I went to the dermatologist and now I am taking methotrexate, colchicine, vitamin E and folic acid. However I feel like it only takes away the pain and the swelling, but the appearance of my skin is the same, fibrous and with a brown tint. This sometimes makes me depressed because I am young and I would like to wear a two piece swimsuit or a short shirt.

In spite of this, I am still standing, and ready to fight, so we've got to move forward. Please contact me on msn, I would like to talk to someone who also has this illness, since it is not very common.

To Contact the Author

Cris
Email: [email protected]
Story edited 03-23-2010 JTD
Story posted 04-20-2010 SLE

Story Artist: Shelley Ensz
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
Español/Spanish:
Cris: Esclerodermia Morphea
Acerca de la Esclerodermia

English:
Morphea Scleroderma
Morphea Stories
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Sclero Forums *Online Support Group!*
Symptoms of Systemic Scleroderma
Types of Scleroderma
What is Scleroderma?

ISN Translator and Editor: Alba León

Alba LeonAlba León is the ISN Translator for this page. She is studying international relations in Mexico City.

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 Crissie: Surviving Sister of Scleroderma Patient
 
 

SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses. We are a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team. Donations may also be mailed to:

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA
Email [email protected]. Disclaimer. Privacy Policy.