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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!
Frog jumping for joy by Shelley EnszPDF 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.
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Monica O: Daughter of Mother with CREST

Argentina

Miniature Red Rose by Sherrill Knaggs, ISN Artist I am Argentinean. My mother, who is now seventy-six years old, was diagnosed with advanced CREST scleroderma, after thirty years of going through several doctors and suffering without knowing why.

She is now under treatment, but suffers with pulmonary hypertension, calcifications in her trachea, bronchi, and part of a lung. The fingers and toes of her right side present necrosis, and she is in terrible pain due to her legs being affected with calcinosis under the upper part of her foot.

I would like to know if there is something that can help ease the pain and, however slightly, improve her quality of life.

It is awful to see how she gets worse day by day. I feel powerless, because I do not know what to do. She asks God every day for patience.

Thank you for reading this.

To Contact the Author
Monica
New email address needed 10-10-06 SLE
Old Email Prefix: piscis.mg
Story edited 08-16-06 JTD
Story posted 09-26-06 SLE

ISN Senior Artist: Sherrill Knaggs
Story Translator: Alba León
Story Editor: Judith Thompson Devlin
LINKS
Caregiver Stories
CREST Scleroderma
Pulmonary Hypertension
Pulmonary Hypertension Stories
(Español/Spanish) Monica O: Hija de Paciente con Esclerodermia CREST
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 and Editor: Alba León
Alba Leon, ISN TranslatorAlba León is the ISN Translator for this page. She is studying international relations in Mexico City.
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith 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
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Go to Monika K: Morphea Scleroderma
 
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