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The boy in the moon : = a father's j...

Brown, Ian.

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The boy in the moon : = a father's journey to understand his extraordinary son /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	The boy in the moon :/ Ian Brown.
Reminder of title:	a father's journey to understand his extraordinary son /
Author:	Brown, Ian.
Published:	New York :St. Martin's Griffin : 2012.,
Description:	293, [3] p. ;21 cm.
Notes:	Includes a Reading Group Guide.
Subject:	Genetic disorders in children - Patients - Canada. -
ISBN:	9780312675417 (pbk.) :

The boy in the moon : = a father's journey to understand his extraordinary son /
Brown, Ian.

The boy in the moon :a father's journey to understand his extraordinary son /Ian Brown. - 1st St. Martin's Griffin ed. - New York :St. Martin's Griffin2012. - 293, [3] p. ;21 cm.

Includes a Reading Group Guide.

This "is Ian Brown's powerful, honest, and emotionally complicated memoir of raising his son, Walker -- one of only a few hundred people worldwide who live with an extremely rare genetic mutation. Born with CFC (cardiofaciocutaneous) syndrome, Walker Brown is a mystery, as remote to his family as the moon. Unable to speak or swallow, compelled to hit himself, requiring surgeries, and round-the-clock care, he becomes the focus of his father's keen intelligence. " --P. [4] of cover.

ISBN: 9780312675417 (pbk.) :US14.99Subjects--Topical Terms:

2021548
Genetic disorders in children
--Patients--Canada.

LC Class. No.: RB155.5 / .B76 2012

Dewey Class. No.: 618.920042

The boy in the moon : = a father's journey to understand his extraordinary son /
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020 $a 9780312675417 (pbk.) : $c US14.99
020 $a 0312675410 (pbk.)
035 $a LIB-BW-103-A-004
040 $a BTCTA $b eng $c BTCTA $d BDX $d YDXCP $d CWJ $d CNTCS $d WLM $d UAT
050 # 4 $a RB155.5 $b .B76 2012
082 0 4 $a 618.920042 $2 23
100 1 $a Brown, Ian. $3 2021547
245 1 4 $a The boy in the moon : $b a father's journey to understand his extraordinary son / $c Ian Brown.
250 $a 1st St. Martin's Griffin ed.
260 # $a New York : $b St. Martin's Griffin $c 2012.
300 $a 293, [3] p. ; $c 21 cm.
500 $a Includes a Reading Group Guide.
500 $a "Originally published in hardcover in Canada by Randon House Canada, a division of Random House of Canada Limited" --T.p. verso.
520 # $a This "is Ian Brown's powerful, honest, and emotionally complicated memoir of raising his son, Walker -- one of only a few hundred people worldwide who live with an extremely rare genetic mutation. Born with CFC (cardiofaciocutaneous) syndrome, Walker Brown is a mystery, as remote to his family as the moon. Unable to speak or swallow, compelled to hit himself, requiring surgeries, and round-the-clock care, he becomes the focus of his father's keen intelligence. " --P. [4] of cover.
650 # 0 $a Genetic disorders in children $x Patients $x Family relationships $z Canada. $3 2021548
650 # 0 $a Genetic disorders in children $x Patients $z Canada $v Biography. $3 2021549
650 # 0 $a Parents of children with disabilities $z Canada $v Biography. $3 2021550
650 # 0 $a Children with disabilities $z Canada $v Biography. $3 2021551
650 # 0 $a Genetic disorders. $3 750480
650 # 0 $a Fathers and sons. $3 572084