Ebook , by Tim Wotton
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, by Tim Wotton
Ebook , by Tim Wotton
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Product details
File Size: 1427 KB
Print Length: 271 pages
Publisher: Austin Macauley Publishers (April 28, 2014)
Publication Date: April 28, 2014
Sold by: Amazon Digital Services LLC
Language: English
ASIN: B00K0SG2T0
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Amazon Best Sellers Rank:
#1,770,240 Paid in Kindle Store (See Top 100 Paid in Kindle Store)
This is a must read once you pick it up you wont be able to put it down. So encouraging, informative, and can make you smile against a no one else can see from your outside. Im a grandmother of a 6 year old cfer. We were told at 3 weeks our lilliana, had cystic fibrosis. Im ashamed to admit i had no clue what c f was. Or understand how to help my daughter son in law, and our precious lilly learn to live with c f. Our lilly is now 6 Tims book has covered already so many situations my daughter has came up against.This book will help us all as her family and friends. This opens our minds to such a more postive look and how to keep lilly more postive to live her life to the fullest. From the day your told your world becomes consumed how long will we have them. Then you read this and you understand you dont focus on how long you will have them. Its how strong you can help your loved one be to challenge cystic fibrosis. I would ask anyone facing something any heath challenge to read this postive, informative, humorous book. You will be ready to take on this secret world. And i say secret because so few people understand or even know what cystic fibrosis is. This book helps you understand you can still be in charge of your life. And a postive to anyone you know dealing with c f . You will learn how not to let this disease Define you. I will finish up by saying thank you Tim for writing this book. I hope anyone that reads shares their experience in reading this. I promise will put down with a new fire in living life to the fullest.
As the mother of a CF child who almost made it to her ninth birthday, Tim’s story was overwhelming and emotional. On one hand, I had to read his story in stages because my throat was too clogged to think and my eyes too blurry. On the other hand, I almost felt guilty as I thought about all the angst, pain, suffering and mental struggles that my Chrissy did not have to live through like the sad times in between the pages of Tim’s life. I am thrilled with the idea that God has pushed Tim further along in his blessed life with Katie and little Felix. The struggle is real and Tim’s strong character is fabulous. I am so glad that Julie on We Love Memoirs suggested that I read this book. It was educational and illuminating and I applaud Tim’s courage and candor.
This book is a very insightful and honest introspective account of Tim's life as a cystic fibrosis (CF) patient. It start from his youth and then focuses quite a lot on his daily events as he nears his tremendous milestone of turning 40 years old. Tim does not hold back in his challenges and descriptions of his mechanisms of coping with CF. From the rigorous medical treatments, dealing with relationships, coping with a full-time job, his dedication to physical activity, and to dealing with the challenges of his CF comrades are some of the topics covered. If you don't know much about CF, it will enlighten you of the challenges faced by CF patients, even though they often appear fine on the outside. If you are aware of CF, this will give you hope and courage to keep pushing forward daily, and to have the appreciation of the subtle beauties in life that are often overlooked by most us. This is a terrific account and pushes the awareness of CF to another level. It should also give others that have CF in their lives at some level the hope to keep fighting on.
Tim Wotton grips you into a delightfully raw, unscripted look into his life with Cystic Fibrosis. He articulates the thoughts of every CF adult regarding healthy people and their nonsensical complaints about life. Wotton shows everyone that despite having a genetic, uncureable disease you can live a normal life with Cystic Fibrosis. A wonderful read and an inspirational book for all. This book will is a must for family members of a cf person because it truly conveys what a CF patient goes through on a daily basis. This book will take you into an unforgettable story of perseverance and triumph over the dreaded 40 year mark. If you read nothing else this year read this. It will humble you.Anna C.
I really enjoyed this book on Kindle. Tim Wotton writes with wit and intelligence and provides an insight into CF which I'd previously known little about. Despite living with this terrible disease his entire life Tim proves that no matter how awful things may seem it's possible to live the most productive and fulfilling of lives. A fantastic book with lessons and wisdom that will have meaning for most.
Tim is my mate. Being able to say that is a privilege. Reading this book is an emotional roller coaster. It doesn't matter if you know Tim or not, you should read this book to get an insight into living with CF and hear the story of a wonderful person.
Tim Wotton in the run up to his fortieth birthday gives an honest and at times humorous account of what life is like living with Cystic Fibrosis. Tim is one of the oldest survivors of the disease and is an inspiration to all. We can all take something from this book that will educate and inspire us... whatever we do... Life is what we make it and Tim has certainly made it. Tim was told he would not make it to his seventeenth birthday, so with his fortieth birthday in sight he decides to write down his thoughts and the book takes us in diary form through his thirty-ninth year, through to the milestone birthday.I learnt so much from this book, not only about Cystic Fibrosis, but about courage and determination and that a positive outlook to life can make a huge difference. The book is great for raising Cystic Fibrosis awareness. All who have or know someone with the condition will get some helpful insights and useful information from reading this book. The book will also be helpful to anyone facing challenges in their own life. It is always much easier I find to talk and learn from people who are going through the experience than get bogged down by all the medical jargon. I thank Tim Wotton for opening my eyes and making me more aware to a medical condition, I knew very little about.
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