(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

Silvia: Mother of Son with Morphea

Lima, Peru

I have a thirty-year-old son who got a whitish-pink spot on his thigh. He went to a dermatologist and got a biopsy done. His diagnosis was "Late stage of Morphea."

Well, I am a desperate mother, because they tell me it is a type of cancer. I would like to know whether there is a specialist that can give me information on this result and its treatment, and whether this is a lifetime illness.

Please, I hope you can understand my desperation. I would be really thankful, and I will wait for anybody that can help me.

Webmaster's Note: We have good news for you! Morphea is not cancerous. "End stage morphea" would mean that the morphea spot is no longer active and perhaps beginning to fade, which usually happens in two to five years, even without treatment. Fortunately, people with morphea have a normal life expectancy!

To Contact the Author

ISN Artist: Sherrill Knaggs (In Loving Memory)

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 Translator and Editor: Alba León

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

ISN Story Editor: Judith Thompson Devlin

Judith 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!

TOLL FREE HOTLINE, U.S. and Canada: 1-800-564-7099
Ask for our Free Info Packet by email or postal mail!

SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses.

We are a service of the nonprofit International Scleroderma Network (ISN), which is a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team, or Volunteer. Donations may also be mailed to:

The most important thing in the world to know about scleroderma is sclero.org!