BS of my MS Making Sense of a Disease that Doesn't Make Sense
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Sprache:Englisch
Fr. 21.90
inkl. gesetzl. MwSt.Beschreibung
Produktdetails
Format
ePUB
Kopierschutz
Ja
Family Sharing
Ja
Text-to-Speech
Ja
Erscheinungsdatum
01.04.2013
Verlag
LinkUp PublishingSeitenzahl
112 (Printausgabe)
Dateigröße
966 KB
Sprache
Englisch
EAN
9780988578012
Lauri Wolf's lifestyle had been independent and productive before MS toppled it over. "Expect the best but prepare for the worst" became her survival philosophy for coping with shattered dreams and a forced transition into a new reality.
Responding to a new diagnosis of MS is no different from responding to any other unexpected, earth-shattering change. "Everyone has her own cross to bear" implies that some sort of suffering plagues each of us. There is no rehearsal opportunity; you can never be "ready" for a disease you will battle for a lifetime. This visitor derailed and over- turned Wolf's world like an uninvited houseguest who shows up without warning and unpacks a mountain of luggage.
To provide an understanding of her particular journey, The BS of my MS begins by describing an assortment of physical ailments that occurred over the four years prior to Laura Wolf's diagnosis but whose source was unclear; the methods specifically used to make a diagnosis of her neurological case; and how the final classification of MS was determined.
The book also explores the following:
. The importance of examining the validity of alleged MS causes and cures and critically evaluating claims for potential "remedies"
. "Going the distance" to manage bladder, muscle, and a variety of other health problems caused by MS
. Addressing health issues that are not related to MS
. Facing parenting challenges and raising resourceful kids
. Living with the emotional lows
. Prevailing with an optimistic mindset
Wolf desperately sought information on how to manage her life with MS but was unable to find a single manual written by an individual, rather than an organization, about how to deal with specific physiological, psychological, or parenting challenges for people with this mystifying disease. There simply was no such book; so, she decided to write one.
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