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Life Happens Next
Get Free Ebook Life Happens Next
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Audible Audiobook
Listening Length: 2 hours and 54 minutes
Program Type: Audiobook
Version: Unabridged
Publisher: HarperAudio
Audible.com Release Date: August 21, 2012
Whispersync for Voice: Ready
Language: English, English
ASIN: B0090CJ44W
Amazon Best Sellers Rank:
WOW. This look into the inner workings of Shawn McDaniel, a profoundly disabled 15 year old, blew me away. Terry Trueman advocates for those with disabilities simply by making them as human as everyone else. Seems like a harsh thing to acknowledge-- that able-minded/bodied people fail to see the other-abled among them as not-quite-human, doesn't it? But it's necessary to admit that we do this. LIFE HAPPENS NEXT has the message that even if others look or process thoughts differently, they deserve recognition of having the same dreams, feelings, and longing for to be touched. The message is loud and clear without being the slightest bit preachy or sad. Knowing that Terry has a profoundly disabled son makes Shawn's story all the more poignant to me. I will never look upon a person such as Shawn in the same way again--which has been quickly averting my eyes and acting as if they are invisible so as not to "stare". LIFE HAPPENS NEXT is a story that screams in a voice that cannot speak, "I am here. I am loved. I matter."
I was a jr. high librarian until recently. Terry Trueman has never disappointed a reluctant reader at our school. This book is a stand alone and delivers a powerful lesson about why we have purpose in life - no matter what the circumstances. Love this author for this age group and older.
"Life Happens Next" is a courageous story because it addresses conditions like CP and Downs...yet the story flows so nicely that these serious disabilities seem secondary to the interesting personalites of the main characters. It takes a creative person to write a story like that. Congrats to Terry Trueman for this heartfelt story.
This book really provided an inside look into mental disabilities and physical disabilities. We read it for a college "Individuals with Exceptionalities" class, and learned a lot from it. I would recommend this for anyone who desires to become sensitized to the issues of Exceptionalities. It's a must read for all educators!
meh
A lot of sequels aren't very good, but this sequel is really good. Trueman's usual humor comes through and so does his love of these characters. He makes me want to keep reading and the writing really touches my heart. Bravo Terry!
I bought this because my granddaughter was to read it for school. I ended up reading it. Very insightful about disabilities.
An interesting yet entirely speculative and grossly unrealistic story written from the perspective of an adolescent male with severe cerebral palsy. The protagonist has absolutely no ability/capacity to communicate with others or to control his body in any manner, yet is able to perfectly relate his lived experience to the reader (the first of dozens of major incongruities). The only times he feels freed from his burdensome body are when he has grand mal seizure dreams (a fanciful notion displaying the author's profound ignorance regarding the lived experience of those who undergo grand mal seizures which are, actually, quite terrifying and unpleasant, in reality) and when he is dreaming at night. He engages in various fantasy activities both during his dream periods and when daydreaming during alert periods. Though he attends school, no mention is made of exactly what he spends his time doing there every day, apart from having his diapers changed.This primary character repeatedly identifies himself as being a "gifted" individual. The particular "gift" he perceives himself as having comes in the form of an eidetic auditory memory (a purely fantasy-related notion that is not based on science and has never been demonstrated by any human being, nor was any evidence of this ability ever tested or displayed in the storyline - see "echoic memory" articles for more data on this). Thus, the author, via the protagonist insists on "telling" rather than "showing" the reader the "gifts" and several other characteristics about this and other characters. The "sainthood" of his sister and mother are two other "tell but don't show" phenomena.This author creates caricatures, rather than characters. This severely disabled teen has near-magically managed to have a family that is always kind and generous to him, never perceives him as a burden or gets frustrated with him for any reason, with the exception of his father who doesn't live with the family anymore, yet makes his son a hero by writing poems about him. None of them are ashamed, angered, or embarrassed by his presence in their lives, no matter when or where his grand mal seizures or tic-like screaming vocalizations may occur.His caregivers at home and school are always gentle, protective, and kind to him and any time any potential threat may appear in his life, he always has a "rescuer" readily at hand. Having been an RN for more than a quarter century and now being disabled myself, I can assure you that there are no severely disabled individuals who are so consistently and predictably protected from harmful others or environments, unless they are literally living in a medical "bubble". Thus, this isn't any form of a realistic book about living with disabilities. It's fantasized and twisted into a cartoonish vision of what the author would like the life of a severely disabled person to be like, rather than what it ever has been or ever will be.The author displays a profound disrespect for those actually living with severe disabilities by refusing to engage in extensive research regarding the realities of life with severe CP and/or severe developmental delays/Down's Syndrome. She projects her own fantasies onto their lives and the lives of those who are actually providing hands-on care for them, around the clock, for years/decades at a time. The author does manage to accurately reflect the layers of isolation that often separate the severely disabled from others, along with throwing in her religious wishes as to how such individuals might be able to connect with the souls of others via dreams and visions.I profoundly reject her loose and excessive use of the term "retard' to describe either one of the two disabled individuals in this story. It's profoundly undignified/disrespectful and is grossly inconsistent with the generally positive self-concept of the protagonist. I have never found those within the black community who use the "N" word to describe themselves to EVER be individuals with any degree of genuinely high self-esteem. Those are both terms of bigotry, anger, and shame - not celebratory terms, in any form.In general, this book displays the profound naivete of the author both as to how to write quality literature and how to relate what the inner lived experiences of others are in a meaningful and realistic way. She would have been better off titling the book, "My Fantasy Of The Lives Of Those With Profound Disabilities". That would have been a more truthful and mature reflection of the book's contents. (less)
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