The medicalcommunity said that Simon was "incompatible with life"
but the Crosier family refused to accept that diagnosis. "I Am Not
a Syndrome - MyName is Simon" is the moving and gripping story of a
baby diagnosed withTrisomy 18, a genetic disorder in which a person
has a third copy of materialfrom chromosome 18. Produced
byindependent book publisher All Star Press, "I Am Not a Syndrome -
My Nameis Simon" details the struggle of Sheryl's son Simon from
the early stagesof pregnancy to his life here on earth.
During thisdifficult time, Sheryl confronts a sometimes
difficult andindifferent medical system to advocate on Simon's
behalf. This is a trulyinspirational story with a strong pro-life
message.
"I longed totell Simon s story of hope, faith, love and the
peace which God grantedme," explained Sheryl. "I write this book to
demonstrate thatour children are not a label and are not defects
They have a name andidentity. They are children of God."
Born on September7, 2010, in St. Louis, Missouri, Simon Dominic
Crosier was diagnosed withTrisomy 18 and lived for three memorable
months. Despite his disabilities, Simon had a huge impact on all
who came into contact with him. The book isabout Simon s short and
meaningful life, his family and his wonderfulcaregivers. "I Am Not
a Syndrome - My Name is Simon" documents thefamily s battle to
advocate for their precious son against an oftentimesindifferent
and callous medical community.
"Strugglingwith the fragility of Simon s life was one thing.
However, struggling with thepopular pragmatic culture that measures
human life in terms of dollars ratherthan dignity, is quite
another. Yet, all along the way, again and again, Sheryland Scott
discovered and were made disciples of 'Life.' This story
celebratesboth the pain and the joy of love " stated Rev. Robert J.
Hermann, BishopEmeritus in Residence, St. Louis Archdiocese of St.
Louis.
The Crosierfamily had to overcome challenges put in their way by
medical professionals andeven extended family members who never
valued Simon s fragile existence the waythey did. Author Sheryl
Crosier's hope is that this story will help motivatehealth-care
professionals and anyone else that reads this account. The lives
ofchildren, regardless of their diagnosis, possess inherent dignity
and value, and they deserve the best care our advanced country has
to offer.
"Numeroustimes I would say to medical professionals," explained
Sheryl. That wewant Simon, special needs and all. But then we would
hear callus responses suchas 'incompatible with life' and 'failure
to thrive' and 'not for Simon.'"
"I Am Not aSyndrome - My Name is Simon" is now available from
publisher All StarPress - Books that Change Lives.
A portionof proceeds from every sale of this book will go to
SOFT, Support Organizationfor Trisomy 18, 13 and Related
Disorders.
TESTIMONIALS
"Be preparedfor smiles, laughter and tears. This is a book well
written by an amazingtrisomy Mom "
AlexHauber
Executivedirector Trisomy Advocacy Group
"SherylCrosier s memoir, I m Not A Syndrome - My Name is Simon,
of her journey duringher pregnancy and her infant son Simon s short
but important life, is a storyof the heart and spirit. It is also a
story of the head that explores thecapabilities and constraints of
modern medicine and policy, parental rights andethical decision
making."
Pamela Healey, Ph.D. mother to Conor, Trisomy 18.
"This bookis a love story shared by a family who believes that
every life has purpose andworth."
Ann Barnes, RNand mother of Megan (1985-2004) born with Trisomy
18.
Co-author ofCare of the Infant and Child with Trisomy 18 or 13
(2011)
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