Here’s my top ten list of lessons learnt in the last few months since the publication of my book about surviving the chronic illness cystic fibrosis (CF)*…
1. Proof is in the pudding. The feedback so far has been extremely promising and affirming for me as the author. Word of mouth and some marketing have helped it become viral and popular. It has been ticking the boxes in readers that I hoped it would – it’s been providing people with more knowledge about the illness (know), it’s been emotive through tears and laughter (feel) and is offering them perspective on their own lives and where appropriate some tactics to manage CF or other health conditions (do). Below are some sample reviews I’ve received…
“This brilliantly written book is a compulsive read. I struggled to put it down from the very first page. Tim’s honesty and openness drew me deep into his personal journey. At the same time his passion and gratitude for life in the face of painful, unrelenting challenges inspired a great deal of self-reflection. The text is profoundly moving yet filled with humour and light.” Work colleague
“Loved this book very true to life for me as I also have cfrd. An invisible illness that very few understand unless you have a loved one with it or have it yourself. Very well written, a great read!!!” CF adult
2. Cherry picking. It always intrigues me which story, joke, poignant moment, insight or chapter of the book appeals to each reader and why it resonated with them. Some have expressed their surprise at exactly how candid my writing has been, but in my defense and to borrow a line from the Mastermind TV programme – ‘I’ve started, so I’ll finish!’
3. Who knew? Book reviews received on Amazon are not syndicated onto both the UK site (co.uk) and world-wide (.com). websites so if someone has reviewed me for one site, it won’t appear on the other! Also, Amazon reviews are extremely important to where an author is placed in the chart of top writers for both the co.uk and .com. After a spate of kind reviews, I recently was placed 433 out of 6 million world-wide authors. Thanks to those who have already written reviews and given me 5 stars. Feel free to add more please!
4. Great pretender. Signing my book in public situations (my mum’s house and at Wimbledon Waterstones) and ‘pretending’ to be an author feels humbling and invigorating. It’s a special moment of celebration for the community of people who’ve followed by life-story all these years. It’s been great to have the company of close family (including Katie, Felix, Jez and Julie) and friends at these events which have doubled up as vital fundraisers for CF.
5. Marathon man. The promotion and marketing of one’s book is a marathon not a sprint – day by day, week by week, month by month you reach new audiences. There’s rarely a ‘big bang’ moment in the early days.
6. Counter-intuitive. There’s no real science behind who does or doesn’t buy or onwards promote the book. Some people whom I expected to have bought or marketed the book have not done so yet; while there have been complete strangers around the world who have purchased it straight away.
7. The write way. People are really appreciating my written style, the insight and the engaging prose contained in the short, thought-provoking chapters of the memoir. I am often hearing that they read it very easily and ‘can’t put it down’. It’s certainly an encouraging sign that there’s an appetite for my reflections.
8. By popular demand. I am receiving a lot of requests from readers to write a follow-up which is a good sign that there’s a growing appetite for my story and how it comes across. The good news is that my second memoir is already being written… I’ll keep you posted of progress.
9. Tongue-tied. It was surreal being recently interviewed for a UK national newspaper (Express Online) by a long-term friend from my Southampton school.
10. CF waits for no one. During the first few months of the book’s release I suffered with the backdrop of quite a serious lung infection and a marked increase in my habitual coughing both during the day and frustratingly during the night. CF is not at all sentimental and can be the worst party-pooper. It certainly appears not to be climbing on my band wagon of celebration for the book. There is also the not unsubtle irony of the title of my book ‘How have I cheated death?’ when I’m feeling so unwell and coughing so heinously.
So, it appears that I’m on the ‘write path’ with this memoir. Its popularity and positive feedback received justified the vision I had a few years ago, plus all the effort to write it in my spare time and secure a publisher.
My book arrived at a good time for me as an author and for those who’ve read it so far. Perhaps it was ‘write on time’…
Tim Wotton – the best-selling author (in his own house)
Winner of a copy of my book – In my last blog post, I asked for suggestions for another CF-related book or film title… The winning title was ‘Harry Potter and the Half Lung Function’ by Jess. Well done! She will receive a copy of the book in the post.
How to order a copy
Go to the relevant sites below or in the UK go to a WH SMITH, Waterstones or Foyles bookstore and give them my name, book title and this ISBN number (9781849637190). It’s also available via GARDNER’S, BERTRAM’S, AUSTINMACAULEY.COM, BLACKWELL’S, PLAY.COM, AMAZON.CO.UK AND AMAZON.COM
I will keep you posted on my life affirming moments, trials and tribulations as and when they happen. Please keep reading and sharing my blog and sign-up (on the right hand side tab) if you have not already done so.
Yours cup half full.
* Cystic Fibrosis is one of the UK’s most common life threatening inherited diseases, affecting over 10,000 people. The condition affects the internal organs, especially the lungs and digestive system, by clogging them with thick sticky mucus. This makes it hard to breathe and digest food. Each week, five babies are born with the condition, however, each week, three young lives are also lost to it. There is currently no cure for CF. However, existing gene therapy trials in the UK are bringing people with the illness closer to a form of cure but CF is not that well known and would benefit from more public donations. For more information and to find out more view the CF Trust Website.