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Earn $150 on July 30th in Boston Marketing Research Study if you have scleroderma or CTD and have been screened for pulmonary hypertension!

PDF Flyer: Boston Marketing Research Study. Schlesinger Associates-Boston, a national marketing research company, is currently looking for patients who have been diagnosed with Scleroderma or other Connective Tissue Disease, who either have pulmonary hypertension or who are regularly screened for it, to participate in a July 30th paid marketing research study in Boston. Read PDF Flyer: Boston Marketing Research Study or call Katherine at 617-542-5500 x310. Schlesinger Associates-Boston. Posted 07/26/10.

Patient & Caregiver Stories Main Menu

(English) Stories 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

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

Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010

Missy K: Diffuse Scleroderma

South Africa

I am a twenty-seven-year-old female. I was diagnosed with lung fibrosis five years ago.

In July 2005, I was diagnosed with Diffuse Scleroderma.

I am on chemotherapy and often feel sick. I had never heard of scleroderma before and would like to correspond with other sufferers.

To Contact the Author

Missy K
Email: smiso789@webmail.co.za
Story edited 11-11-05 JTD
Story posted 11-11-05 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin

LINKS
Diffuse Scleroderma
Lung Fibrosis
What is Scleroderma?

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 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!

New Personal Stories

Mars: Scleroderma with Full Gastrointestinal Involvement I finally started total parenteral nutrition (TPN, or tubal feeding) in May 2010 and it was an absolute success...

Sonya D: Surviving Daughter of Systemic Scleroderma Patient (Portugal) She had difficulty eating, drinking and digesting her food, but yet doctors had no clue...

Hazel: Morphea Scleroderma In 1962 when I was just twelve years old, my mother took me to our family doctor with what looked like a blister under my right eye...

Angela R: Linear Morphea Scleroderma I am twenty-five now and only have the two spots that I deal with pretty easily. I just hope it doesn't get worse...

Heather A: Scleroderma (South Africa) My fingers started to curl up and I could not wear any rings on my fingers anymore as they were so swollen...

More New Stories: May-July 2010

We will edit your story, create original artwork to decorate it, prepare it for the web, and post it on this site. Just fill out our simple Story Submission Form for your story, updates, or email address changes.

Go to Missy S: Lupus, Scleroderma, CREST and Depression

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