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

Tina M.: Keloids

I have always scarred and they never went away.

I have always scarred and they never went away. When I was seven years old I cut my heel on our stove and now at forty-six years old, it still looks the same as fresh it did when I was seven.

After I had my first surgery in August 1999, I learned I had keloids. I have lots of scars after four major surgeries.

My husband calls them my battle scars or unfinished tattoos. What is strange is that I have two tattoos and they never scarred up at all. Everything else did.

Is there a study that is free to those of us with keloids so we can find out our family history or origin?

I would like too know why I have this because my sister and brothers do not have this. I take after my father's side of the family and I think this is where the keloids come from, because no one else has it. I was told that I have a little Native American and African American bloodline so maybe that is where this comes from. All my father's family have passed away. My siblings take after my mother's side. What I have read it is passed from parent to child and so on.

To Contact the Author

Email: [email protected]
Story edited 09-23-06 JTD
Story posted 10-26-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin

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 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 Tommi: Diffuse Scleroderma
Recent Donors
See ISN News for recent donors, including memorials for
Christine Kane, Joleen M. Cascaden.

SCLERO.ORG is the world leader for trustworthy research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. 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:

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA

Email [email protected] to request our Welcome email, or to report bad links or to update this page content.

TOLL FREE HOTLINE 800-564-7099
Free to U.S. and Canadian Callers. Ask for our Free Info Packet by mail or email!
Scleroderma, Pulmonary Arterial Hypertension, and related illnesses.
Privacy Policy.

The most important thing in the world to know about scleroderma is!
Donate Now
Copyright 1998-2017, International Scleroderma Network. AKA Scleroderma from A to Z and SCLERO.ORG. All Rights Reserved.