Magic Moments

Recently being filmed for a BBC documentary about ‘Bucket Lists’ got me thinking how my life-limiting cystic fibrosis (CF)* motivates me to live every day like it’s my last day on earth…

‘Bucket Lists’ (what some people choose to do if they have a reduced or terminal health prognosis, before they “kick the bucket”) tend to be outlandish and quite expensive ideas, such as holidays of a lifetime, seeing wonders of the world or enjoy life events in exotic locations.

The BBC liked my variation of a Bucket List and wanted to give the programme some balanced opinions. My ‘list’, though never formally written down, is one that anyone can choose to follow, often costs nothing and can be achieved every day.

Man in the moment
As a direct result of having been told I wouldn’t live past 17 because of my chronic CF, now at 43, I feel empowered to live every day like it could be my last.

Every hour of every day is important for me as I never know when I will run out of time. Having CF and type 1 diabetes drives my thirst for life. The way I see it, each day surviving my conditions is physically and mentally debilitating; but at the same time, every day is poignant and needs to feel special to counteract the harshness. Thus it has to be punctuated by magic moments which must be savoured to the maximum. These moments form my unofficial bucket list.

My wife, Katie, and seven-year-old son, Felix, provide the necessary motivation to keep on top of my survival battle and offer me a ready supply of life-affirming memories.

I’m around for them as much as possible, and give Felix quality time, coaching him to play hockey, taking my turn to get up early with him at the weekend, going on family days out and taking Katie out for dinner.

I dress each day like it’s my last day on Earth, and never leave my favourite clothes in the wardrobe waiting for that special moment. I don’t see the need to gripe about the small things I hear around the office, instead I take time each day to appreciate something natural like a sunset or landscape.

I also take full advantage of the windows in each day to fit in socialising, my business consultant job, and not forgetting my vital exercise in the form of hockey on some Saturdays and evening gym sessions.

But it’s more than this. Put yourself in my shoes to really understand my plight.

If tomorrow wasn’t a given, what would you do differently today? What would you spend time thinking about? How would you live and leave your lasting legacy?

Living and leaving my legacy
I passionately feel that it’s crucial to cherish the life you have right now, not the life you hope to have in 10 years-time. Every extra day that I can wrench from my conditions gives me more time to create my lasting memory as well as leave a positive trace with people I know or meet.
magic moments

Think of my scenario as a form of Groundhog Day, where I wake each morning to the wide-range of opportunities and moments available to secure my own legacy. The trick is to have your eyes and mind open and be ready to seize and appreciate them. As a sample, during the course of most days, I do the following:

Wear those meaningful items of clothing
Say something kind to a loved one
Do that thoughtful act for a friend in need
Make a stranger feel happy and special
Message someone I’ve not been in contact with for a while
Smile at someone who never usually smiles
Give my son an extra-long hug
Make my wife laugh
Stop still in awe to witness a beautiful landscape, sunset, cloud formation or the wonders of nature
Close my eyes and feel content about an aspect of my life

… as tomorrow may never come and I would have missed the chance!

As much as I despise my daily health battle (consisting of 2-3 hours of meds), it has given me a perspective on life that many people may never attain or will only encounter later in life. People with a life-threatening condition have a pronounced ability to not only identify, but fully appreciate magic moments, as they contrast so strikingly with the usual daily hardship. As I said, I find it liberating to look at each day as potentially my last day on Earth.

Why don’t you give it a try? Start your unwritten bucket list and see how it makes you feel?

Elton John: “I guess that’s why they call it the blues
Don’t wish it away
Don’t look at it like its forever

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.

Tim Wotton (CF author)

In other news
My CF memoir is a finalist for the UK People’s Book Prize! Please help me to win by adding a comment via this link. I find out if I’m the eventual winner early in 2015!

My lovely CF friend, Lucy Watson, shares helpful eating tips via her CF and Healthy blog. This post is about the benefits of Turmeric. It’s a must read…

* 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.


About Tim Wotton

I live with my lovely wife (Katie) and spirited ten-year old son (Felix) in Morden, Surrey; working full-time as an internal communications specialist in the Oil & Gas sector. I have played sport, particularly hockey, tennis all my life and now regularly go to the gym. Cystic fibrosis has been a huge factor in my life, but not one that overshadows it. I have always had great support from my loving family - parents Margaret and Douglas (RIP), elder brother Chris and my twin brother Jez. I have many rich life insights based on knowing I have a reduced life expectancy and battling against the odds for over 44 years. My eyes and heart have been opened by my health struggle. I feel empowered to share my life lessons to help anyone with health and life issues to overcome. My passions include Paul Smith clothes, dress shirts (believing that it's enlightening to dress like it's your last day on earth), Alfa Romeo cars, spicey food, Harlequins and England rugby, Southampton FC, Wimbledon village and common, Dorset, seascapes, sunsets and military history. I am available for public speaking on this subject matter and can be contacted via timwottonAThotmailDOTcom. I have written a book 'How have I cheated death?' based on my euphoric countdown year to 40 which was published in 2014 and won the 2015 'Best Achievement' Award at the UK People's Book Prize. It is available via e-book, audiobook and paperback at Amazon and to order from UK bookstores. 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
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8 Responses to Magic Moments

  1. Isobel Warner says:

    Brilliant writing Tim, truly inspirational. looking forward to seeing you all in April Love Isobel x

  2. Jayne says:

    Very inspiring Tim, thank you. I know we all forget how beautiful life is and can be if we focus on who and what we have in life and be grateful. Despite your health struggles, I’m sure your life is far more fulfilled than a lot of people’s and you’ve learnt not to sweat the small stuff. Thanks again. Yours, cup half full sister from around the world.

  3. Penny says:

    Just finished your inspiring book. Heard you on radio 4 earlier this year. Our one year old grandson has cf so wanted to learn more and be positive. Your book has helped us. Best wishes to you , Katie and Felix.

    • Tim Wotton says:

      Dear Penny,
      Thanks so very much for your kind sentiment re my book and how’s it’d helped you. Do give your grandson a hug from me and shower him in positivity.
      Best wishes

  4. Vicky says:

    Hi Tim, I’ve just finished your book which is very inspiring. I’m a Paediatric Physio for our local CF group – I know it’s a love hate relationship with us ‘terrorists’!! Thank you for being brave & speaking out – there’s too much silence about CF. As a fellow Christian I too pray for increased awareness, understanding & ultimately a cure. But on a personal note I have battled daily with clinical depression for 30 years, another silent/misunderstood condition. So your ‘fight’ also spoke to me & has challenged me to find hope in the hours, days & even months to come. Thank you ……

    • Tim Wotton says:

      Dear Vicky, It’s great to hear from you and for being open about your daily battle. I’m deeply touched that my book connected with you on many levels and has got you thinking about how to replicate my coping mechanisms in your life.
      God bless and take care

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