Ebook Breathing Should Never Be Hard Work: One Man's Journey With Idiopathic Pulmonary Fibrosis

Ebook Breathing Should Never Be Hard Work: One Man's Journey With Idiopathic Pulmonary Fibrosis

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Breathing Should Never Be Hard Work: One Man's Journey With Idiopathic Pulmonary Fibrosis

Ebook Breathing Should Never Be Hard Work: One Man's Journey With Idiopathic Pulmonary Fibrosis

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About the Author

Robert Davidson was born in London, England in May 1947 and moved to Canada with his wife Heather in 1973. Robert is a Chartered Accountant and Trust and Estate Practitioner and a fellow of The Institute of Chartered Accountants in England & Wales. He worked with various CA firms in London before joining Price Waterhouse in Toronto. After a 9 year spell as the CFO of a large private company he opened his own tax practice in Markham Ontario, running that until January 2010 when Idiopathic Pulmonary Fibrosis made it impossible to service his clients.Robert founded the Canadian Pulmonary Fibrosis Foundation in late October 2009, just 3 months before his life-saving double lung transplant on January 30, 2010.Robert and his wife live in Markham Ontario. He has two sons. Mark, who also lives in Markham with his wife, Alyshia and new baby daughter Alexis. His other son, Matthew, lives in Neurenberg, Germany where he works with Adidas and is marrying Gemma there in June 2013....

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Product details

Paperback: 120 pages

Publisher: FriesenPress (February 14, 2018)

Language: English

ISBN-10: 1460209796

ISBN-13: 978-1460209790

Product Dimensions:

5.5 x 0.3 x 8.5 inches

Shipping Weight: 5.6 ounces (View shipping rates and policies)

Average Customer Review:

3.9 out of 5 stars

8 customer reviews

Amazon Best Sellers Rank:

#1,236,578 in Books (See Top 100 in Books)

I read this book as my brother, too, was suffering from this horrible disease, (Pulmonary Fibrosis, Familial type) and I had just read the first three chapters, and thought, oh, he needs to read this, too. (as he had been talking about seeking a transplant in the future) So I purchased it, and had it shipped to him. It gave him a lot of hope, and sent him on his way to be tested for a transplant, but alas, it wasn't meant to be, I suppose. He passed away, the same day that he was listed, at UCLA. Thank you Robert for the spark of hope you gave my brother. If only he had been listed much earlier. This disease is the worst possible of all diseases (I think, except for possibly ALS), and has taken away four of our family members. May they all Rest in Peace. Thank you for telling your story, Robert, and I hope your gift of life continues to give you life, for many years to come.

Thank you for writing your story! It helped me to remember, after watching my husband fight this disease for 3 years that's there is still another chapter to be written! One of survival! Life after Idiopathic Pulmonary Fibrosis! I will read this often while we battle on. My husband is a fighter! We find so often doctors almost seem reluctant to give you any hope, they don't seem able to face you either at the same time! It's like not talking about the elephant in the room. We've been told the worst, but no one has really ever talked with us on positive out comes of transplant. Hope even a little, for even a little while is so good to feel! The end stage stuff was very hard to read! We've not walked that journey yet! I pray that maybe a cure or treatment will by the grace of God be available before then. We are hanging on to the hope that we are one of the lucky ones, that this disease will be slow in its progress. I will pray for your good health. Also for the family that gave you the gift of life. May god bless and reward you! He already has!

The book is very informative for old patients, especially those who are preparing for a transplant and those who have had a transplant. A little too much on some personnel issues.

Was helpful in understanding the disease and inspiring to keep living through this disease.while the travel was interesting, I was a little lost in these parts.

As a lung transplant recipient I would have liked to see more detailed info about his journey through the transplant than his his detailed account of his trips. Got confused and thought it was a travel guide.

I would recommend this to other IPF patients. Reading this was scary but gave me something to think about in the future.

got this book for my father who is suffering from the same lung disease.. he liked it but did mention how the main guy talks a lot about his trips to out of country (china.) i asked him and he said he would rate the book 3 stars.

With so little written on IPF, I appreciate learning of the authors journey. A little too much on the vacation details but all in all a good quick read that gives some hope.

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