Montpelier Tomorrow

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Pub Date Aug 21 2014 | Archive Date Jan 15 2015

Description

Mid-life mom, Colleen Gallagher would do anything to protect her children from harm. When her daughter's husband falls ill with ALS, Colleen rolls up her sleeves and moves in, juggling the multiple roles of grandma, cook, and caregiver, only to discover that even her superhuman efforts can't fix what's wrong.

Mid-life mom, Colleen Gallagher would do anything to protect her children from harm. When her daughter's husband falls ill with ALS, Colleen rolls up her sleeves and moves in, juggling the multiple...


Advance Praise

An affecting, deeply honest novel; at the same time, a lacerating indictment of our modern health care system.

"Characters are vivid, relatable, and all too imperfectly human." --Jewell Parker Rhodes

"Each time I have reread this novel, I have felt rewarded by the connection it offers to the central character, Colleen. I can think of no single page in which her voice is not an irreplaceable gift to the reader." --Kevin McIlvoy

"An engrossing account of the impossible choices faced by caregivers..." --Kathryn Shonk

KIRKUS REVIEW

After a woman’s son-in-law contracts amyotrophic lateral sclerosis, she tries to help the family, but the burdens of caregiving take her relationships to the breaking point.

Kindergarten teacher Colleen Gallagher, 53, is glad to help out when her daughter Sandy’s husband, Tony, gets a fatal diagnosis: ALS, aka Lou Gehrig’s disease. With a newborn, a toddler, a high-pressure job and Tony’s medical procedures to manage, Sandy needs all the help she can get. Colleen is all too familiar with being a young widow left to raise small children on her own; her husband died in a car accident when Sandy was 5. Though Tony’s family and friends start out with optimism and good intentions, tempers are soon frayed and patience worn out by the constant demands of caretaking. Sandy is often angry and resentful; Colleen feels like a slave. In the end, the survivors will have to go on with their lives. MacDonald (co-author of The Quiet Indoor Revolution, 1992) gives an unflinching portrait of dealing with a debilitating chronic illness: the expense, the logistics, the red tape, and especially the brutal, exhausting, undignified truths of nursing: “None of the caregivers’ manuals mentioned the orange shit that oozed out Tony’s rectum only half-way so that I had to dig out the rest as I wiped his butt.” The characters have a maddening way of making things more difficult for themselves; despite Tony’s wealthy parents, all the household DIY chores—scraping plaster, sewing drapes, cleaning gutters—for some reason fall to Colleen. But it’s really health care that doesn’t make sense. Tony’s doctor recommends a life-prolonging feeding tube. Why? “Because doctors love technology. Also, she doesn’t have to live here,” a nurse explains. Commenting on Tony’s feeding chair, she continues, “When I started in this profession, you never would have seen equipment like that in a home. It doesn’t belong here.” MacDonald saves her debut novel from being too didactic by her well-rounded characters and Colleen’s complex, thoughtful responses to the untenable situation.

Literary Fiction Book Review: http://literaryfictionreview.com/montpelier.php

Verdict: A heartrending story of love, loss and the endurance of the human spirit.

An affecting, deeply honest novel; at the same time, a lacerating indictment of our modern health care system.

"Characters are vivid, relatable, and all too imperfectly human." --Jewell Parker Rhodes

...


Available Editions

EDITION Paperback
ISBN 9780990715818
PRICE $18.99 (USD)

Average rating from 5 members


Featured Reviews

Painful to read, but ultimately true to our human frailties and strengths. Colleen, a woman with a life of her own, steps up to become the main support for her family when son-in-law Tony contracts a fast-moving form of ALS,. Colleen becomes care-giver for all involved, despite a rocky relationship with her daughter. I highly recommend this book.

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