As Happy as Larry

In the 1890s, before boxing was fully legalised, a man called Larry Foley won the biggest prize in boxing, it was a purse of $150,000, equivalent to $4,000,000 today. A New Zealand newspaper ran the story after the win and the headline “Happy as Larry” has gone on to express how we feel when we simply can’t stop smiling and we’re overwhelmed with happiness, a phrase many of us use daily.

Larry Foley

Don’t get me wrong, I have ups and downs like everyone else, just this month I’ve fallen down the stairs. I’m not too bothered by the initial physical effects of a fall, bruising and pain is something I get used to. It’s the muscle memory change or the fatigue that affects me most, one day you can take a certain step or kerb, no problem. The next day that ability has gone and that’s how quickly my Muscular Dystrophy is affecting me this year.

There is no point in going on about this though, there are far too many good things going on that outweigh the occasional mistimed footing or weak knee. I’ll stick to the positivity, thank you.

I’ve said it many times before in conversation and written on paper; I’m a very lucky man. My diagnosis could have been worse, I have some great family and friends around me, life’s good and I never, ever take that for granted.

Since I started my ‘Move a Mile for Muscles’ event in January it just seems to get bigger and better as we go into a new month and a new challenge. There is not a week goes by that I’m not in touch with The Discovery Channel; they are always asking if I’m okay or need any help at all. I never knew that winning a competition (My World Bigger #MYWB) would be this rewarding, but it is and it’s a fantastic bit of security that comes with a feeling of solidarity and team work. The same can be said of Muscular Dystrophy UK, Jo McGuinness is a Senior Manager, Regional Development in the south and again is constantly in touch to make sure I’m okay, safe and happy as these events draw closer.

Of course I’m supported by my ever-suffering wife and our girls as I come up with what some might say is another ‘far out’ idea. And of course my friends have been fantastic, as always. Just this week my friend Jo Entwistle has been running around Leeds organising our route to the First Direct Arena and sorting prizes out for our raffle taking place at The Duncan pub on Saturday evening. I was again, very lucky this week when another friend; Jon Howe put me in touch with Simon Rix. Simon is a member of the band the Kaiser Chiefs and asked us how he could get involved and help us, his attitude was one of open arms, this is greatly appreciated and I feel extremely humbled by it.

So you see that’s why I’m happy as Larry right now and this nicely leads me on to talk about our mile this weekend.

On Saturday 16th April we will take on Mile 4 of the year and set off from the Queens Hotel in Leeds and make our way to the Josh Warrington fight at the First Direct Arena.

Josh Warrington is the current WBC European Featherweight champion and he is a beacon of inspiration for young people in Leeds and beyond. Not only this, he also unites the community around him and has given tireless support to local and grass roots sport, something I consider to be imperative.

I chose to walk to Josh’s fight because in early January when I first started all of this, Josh was there on social media supporting me, and he vowed to join us on a mile in August which we are very much looking forward to. There was no prompting or asking, it was an offer Josh made and one I won’t forget.

You can count on me to be relentless about this condition and its many different strains. Over the last four weeks I have seen 10-year-old Archie Hill walk with me around the Oval in London whilst tackling his own Duchenne Muscular Dystrophy. I have had my car washed by a young man called Callum, again with Duchenne Muscular Dystrophy, who was raising funds for his own specialist power chair, and all the while not one complaint was made and not one moan was heard.

I would like to thank all my friends and family that are helping me this year, far too many to mention. Also, thank you for the many donations. We have raised £7000.00 so far; the equivalent to 200 hours of research, and we need every single minute of that to find treatments.

Finally, good luck Josh Warrington, you should be very proud of yourself, for all that you do and all that you are. You’re an inspiration that certainly keeps me fighting and I’m sure many others too, I do hope that come the end of Saturday night, you are as happy as Larry too.

Marching On Together.

You can follow me on twitter @HywoodMartin

#MoveAMileForMuscles

#IfICanYouCanToo

You can make a donation here https://www.justgiving.com/Martin-Hywood3

 

Influence & Inspiration

To make my world bigger is something I’ve been working on for a few years now, as things have got harder for me physically I seemed to have opened up more doors and gone further than I ever thought possible. This month we won a competition with the Discovery Channel just by telling people my plans for 2016 (and a lot of asking for votes!).

You may ask where I get my sense of adventure from, my direction, and the desire to push myself and learn along the way. I’d said it was definitely from my dad, a man influenced by The Goons and Monty Python. Add in a passion for travel and educating and in some distorted way that moulded me. The comedy element is an important factor because as children that’s how I, my brothers and sister learnt, obviously not orthodox but fantastic nonetheless, I’ll explain…

Our mum used to work as a waitress at the local Berni Inn and our dad used to drop Mum at work for her night shift, drive round the corner and then ask “Who wants to play the ‘Where are we’ game?” We would all shout back “YES!” and then we would either jump in the boot of our car or the back of Dad’s work van. Eyes closed, we would either be driven a few streets or perhaps miles and we would take turns at guessing where the vehicle had stopped, mostly in high-pitched voices à la Harry Secombe or Peter Sellers. Our parents also took advantage of sunny Sundays, and the ‘spare’ fiver or tenner for fuel would take us miles. Dad’s excursions, inclusive of a history lesson, were like his comedy influences, you never knew where you would be taken and the facts would be a bit leftfield.

An example would be a visit to Warwick Castle, we couldn’t afford admission so we’d go as far as the portcullis, and we wouldn’t be told that what we saw before us was built by William the Conqueror in 1068, no, it would be a petrifying story about the holes in the roof above and that hot oil and wax was poured on potential intruders. Sometimes we’d go to the coast on that thin fuel allowance, stop at Lulworth Cove and Dad would say “If you ever need to know about coastal erosion then look up this place; read a book”. Then, we’d get in the car and drive home again. The seed of curiosity was planted and I went on to get an ‘A’ in GCSE Geography, using Lulworth and coastal erosion as my subject matter.

So this then leads me on to talk about my most recent mile, and my next. I wrote about the facts of Iffley Road in my last blog, yet I had no idea how much of a challenge it was going to be. As soon as I stepped out onto the track I had a huge psychological battle which I managed to overcome and win, I couldn’t believe I did it.

What of the Oval then? I can tell you this; it hosted the very first FA Cup Final between the Wanderers and the Royal Engineers in 1872. Morton Betts scored the only goal of the game on 15 minutes and the Wanderers won! A distinctive feature of this ground is its neighbouring Victorian gasometer; built in the 1800s it now has a listed status. Just like my father, I do not feel it necessary to state the obvious, that it is most definitely one of the most famous cricket grounds in the world; read a book.

Saturday is my third mile of the year and like last month’s mile, when I was joined by the fantastic Tommy Lloyd, I will be once again joined by a young man who has also been pushing himself for others.

Archie Hill was diagnosed with Duchenne Muscular Dystrophy in 2008 at just 3 years old. Duchenne is a severe degenerative muscle-wasting disease, which will unfortunately lead to paralysis and will significantly shorten his life. Selflessly, Archie and his family have asked to ‘Move a Mile For Muscles’ with me to raise much-needed awareness and funds. Archie has put himself up to help others more than once. Alongside other boys with Duchenne, Archie and the group took their fight for Translarna (the first treatment approved for the underlying cause of DMD,) to the very top and knocked on 10 Downing Street asking for answers on access to rare disease drugs.

Archie at No 10

 

Just like Tommy, I consider Archie to be courageous and he should be an inspiration to many at such a young age. So I can most certainly say that I will complete Saturday’s mile whatever it takes, and hopefully won’t get beat up by myself like I did at Iffley Road.

Archie is moving a mile for muscles and if he can, WE can too!


Thanks for the sense of adventure Dad and for making my world bigger.


“Always look on the bright side of life” x

You can sponsor OUR miles here ... https://www.justgiving.com/Martin-Hywood3

You can watch my short film here... 

Follow me on Twitter https://twitter.com/HywoodMartin

#MoveAMileForMuscles

#IfICanYouCanToo

 

The Eleventh Hour

It seems I’ve made a mistake. The chance to vote for #MYWBpledge did not finish at midnight last night, it finishes at midnight TONIGHT!

This is my last chance to encourage you to vote for me…

In the 70s I used my legs to bounce on my space hopper. In the 80s I used my legs to ride my Burner BMX. In the 90s I remember running across a road in West Yorkshire to get to the hospital to be part of the birth of my first born; Lucie. In the 00s I used my legs to walk down the aisle to marry the most beautiful woman I ever did meet.

Now, what does the future hold for my legs? I really don’t know.

I do know this; I intend to fill 2016 with fantastic memories for my girls. The whole point of me entering this competition is for my girls to see what can be achieved regardless of what some might say is difficult and challenging circumstances. Also, I hope that what we are doing now will help somebody with my condition in a few years’ time. I hope that others don’t fall like I do, don’t feel weak like I do and don’t feel constantly exhausted like I do. I hope that many more people will be able to do all of what I’ve mentioned above because we’re raising awareness and funds right now.

I’m not a natural at what I do, every time I have gone onto a radio station I have nearly been sick, every time I’ve stood up in front of all my colleagues or any audience I have panicked so much my heart feels like it will pop out of my chest, it really doesn’t sit well with me to talk about this condition but it has to be done, otherwise nobody would ever know.

Since I started raising awareness I have kept a scrapbook, a portfolio of memories for Lucie, Olivia and Skye to look back on. It contains every blog, every newspaper article, photos, certificates and acknowledgements of our achievements. This is my legacy to them; this is how I’m trying to be the best Daddy I can be.

A saying I’ve heard often and stuck by myself is that if you do not like something in life then change it, if you cannot change it then change your attitude towards it, so that’s what I do. I cannot take any medicine, there is no prescription for me but what I do have is my family, friends and my challenges to keep me on my feet.

I’ve seen other parents score strikes when bowling to rapturous applause and joyous laughter “That was my Daddy’s strike”, I’ve seen other parents win a race at a school sports day “That was my Daddy that won that” as they lean to my youngest daughters ear and this is also something I cannot do, I can, however walk and so that’s what we’ll do. We will walk one mile-a-month to iconic sporting arenas and events in 2016 which is an Olympic year and also 50 years since England won the World Cup. Then my girls can say “That was my Daddy that walked that!”

I’m a very lucky man, everyone I have asked to help me in 2016 has been extremely accommodating with an ‘open arms’ attitude for which I am very grateful. This started in autumn of 2015 when I asked actor, Ralph Ineson to help with my very own short film to promote my intentions for 2016, he replied “It would be an honour to get involved” and this, with the help of friends, Paul Adams and Steve Richmond, is how we made this short film.

So far we have raised 36 hours of research in the first two months of this year and we’ve already made some fantastic memories and you can see them here.

https://flipagram.com/f/kf4hokUCIq

So you see this competition is imperative, it is an opportunity to take my Orange t-shirt on tour for all to see, so people can raise questions about the condition of which I can answer and to raise funds to treat others in the future.

This is not a vanity project; it’s not about me at all really. A very big reason is for this one picture right here, the people in it, our year ahead and the memories we’re going to make

This is a life changing opportunity to make my world bigger with The Discovery Channel UK and you can come with us too!

So, for the very last time of asking…

1. Vote for "Martin from Buckinghamshire"

2. Vote for two other people.

3. Fill out Name, email and phone number.

4. Hit "Submit"

5. When you receive a "Thank You!" you have successfully voted

http://www.discoveryuk.com/pledges/vote-now-2/

Thank you to everyone that has voted, shared, hit RT and encouraged others to vote for me, I’ll probably never be able to thank you all enough but you must know it’s appreciated from the bottom of my heart.

#MoveAMileForMuscles

#IfICanYouCanToo

Standing on the Shoulders of Giants

Mile 2: Iffley Road, Oxford.

It was in 2013 that I started to raise awareness about Muscular Dystrophy; I wanted to ‘Move a Mile for Muscles’ and all I could think of was the most famous mile in history.

On the 6^th of May, 1954 Sir Roger Bannister ran a sub four minute mile at the Iffley Road track in Oxford and I’ve always wanted to get onto that hallowed ground. I never got round to it, it’s something that I’ve always put off “We’ll go there another day, we’re too busy”. So in 2013 I did carry out my mile but in the luxury of a venue nearer to home and more convenient to myself.

Things have changed and an opportunity has presented itself to me and there is no way that I will be turning it down, I will be getting onto one of the most famous tracks in the world. 

I have become so intrigued and interested with sports people that are mostly alone in their event and how they overcome everything that comes with that. Some might say that Roger Bannister was not alone and he was helped by pace makers, similar to that of a boxer with his team in the corner of the ring. The pace makers of the mile were Chris Chataway (co-founder of the Guinness book of records) and Chris Brasher (sports journalist and co-founder of the London Marathon), these three men were a band of brothers and had a lot to prove as Bannisters training techniques were considered controversial and most certainly unorthodox for a runner.

The event nearly never happened at all, there was a very strong wind on the day and Bannister decided he would rather save himself for another day but at 18:00 the wind dropped enough to get the race underway. The gun fired and they were off! The stadium announcer on that day was Norris McWhirter (Guinness book of records presenter) and the BBC commentary came from Harold Abrahams (1924 Olympic 100 metre champion).

Each time the men crossed the line the time was announced and could be heard by the men. The first lap was 58 seconds, on time. On the second lap they heard 1.58, again, good and on time. After the third lap the men heard the announcement of 3 minutes, 1 second and this wasn’t good enough. Bannister kicked and crossed the line at the point of exhaustion.

Chris Brasher setting the pace for Sir Roger Bannister

The final announcement was made… “As a result of Event Four, the one mile, the winner was R.G. Bannister of Exeter and Merton colleges, in a time which, subject to ratification, is a track record, an English native record, a United Kingdom record, a European record, in a time of three minutes...” The complete time was not heard because of the erupting crowd but Bannister had done it!

Away from the track Sir Roger Bannister spent most of his life as a Neurologist in Oxford, which struck a chord with me. It was a neurologist in Oxford that gave me the diagnosis of my condition and the coincidences don’t stop there. It is no secret that I have great difficulty in walking and that I’m grateful for this diagnosis and not anything else. Also, the love and appreciation I have for my family, I write about them in nearly every blog and how I wish to be the best role model I can be.  Imagine my surprise then when I heard a recent interview with Sir Roger…

“I’m having troubles with walking, so I do have difficulties. Ironically it’s a neurological disorder of Parkinson’s. I’m being well looked after and I don’t intend to let it interfere with my other activities. Life has its physical challenges, I’ve not been free of other illnesses but I take every day as it comes and the pleasure I receive, much of it is seeing what my grandchildren are achieving. I once said, as someone was commiserating with me about having this illness I said just consider the alternatives, which is the way I look at it.

There is a gentle irony about it but I’ve seen and looked after patients with so many neurological and other disorders that I’m not surprised that I’ve acquired an illness; it’s in the nature of things. I think it’s important to be a good father and grandfather and of course what we pass on, we pass the gifts of the children and grandchildren whom we have raised. The most important part of my life has been my family, I’m extremely grateful for my wife who has always supported me, putting that alongside my career these have gone hand in hand.

One of my pleasures in life has been walking, apart from of course, running and I founded a walking club in Oxford and we had our 100^th walk a little while ago but of course now the walks were always followed by lunch so now I’m a very happy member of the lunching group that hears about the walk and therefore vicariously enjoys the walk”

 

So it is with humour and a tongue firmly in my cheek that I say there is little difference between myself and Sir Roger Bannister except about 44 years and the fact my mile will take about 44 minutes.

I have been invited to the historic race track at Iffley Road, Oxford to stand on the shoulders of giants and walk one mile in my very own shoes. Three minutes and 59.4 seconds was the world record time and I actually feel lucky that my time will be a lot longer. This will give me the opportunity to appreciate not only where I’ll be, but also the family and friends that will enjoy this experience with me.

You can sponsor me here> https://www.justgiving.com/Martin-Hywood3 

'Like' our Facebook page> https://www.facebook.com/MileForMusclesCountMeIn/ 

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If I Can, You Can Too.

Sometimes it feels good to be different, it might be painful and sometimes uncomfortable but I like to push myself. I’m Martin; I’m 42 years old, living and adjusting to a life with Limb Girdle Muscular Dystrophy. I’m a husband and also a father to three great girls, the youngest of whom I’ve never picked up, never been able to carry and cuddle, I’ve always been too weak. It’s these things that are difficult for me to handle but we carry on and adjust, regardless. And besides, I consider myself lucky enough to be a family man; my girls are the ones that push me on, to keep fighting.

Since I was diagnosed at 23 years old my focus and attitude has always been positive, there is no point in being anything else, if I do become anything else then I know I will suffer physically and I can’t afford to let that happen. As I’ve mentioned, I’m grateful to have what I have and with that said I’m prepared to do all I can to help others.
For the last three years I’ve been part of Muscular Dystrophy UK’s ‘Move A Mile For Muscles’ campaign, each year I have pushed myself more and challenged myself exactly the same as an athlete would, my preparation is similar too because every challenge is relevant to that person’s ability. I train, I diet and I set myself up to finish what I set out to do the best way I can.

This year will be different, very different indeed. 2016 is an Olympic year and as I’m losing the ability to walk at all, I want to lead by example and get as fit as I possibly can and I’m challenging you to do the same. I never expect anyone to do anything that I’m not prepared to do myself; also this challenge comes with a positive twist. Have you ever watched a sporting event or seen a sporting, iconic arena on telly and thought “I’d love to go there one day; I’d love to do that”? Well this year I’ll be fulfilling some dreams for myself and others along the way, very simple ones but good ones nonetheless.

My challenge is to move a mile for muscles once a month this year to iconic sporting events and arenas all over the country, raising much needed funds and awareness along the way.

These are my miles…
Walk one mile around Stoke Mandeville Stadium
Walk a mile round Iffley road track in Oxford (where Roger Bannister broke the record for a four minute mile)
Walk one Mile around the Oval cricket ground, London.
Walk one mile to tower bridge, London, to watch and support the Marathon runners.
Race a mile around Brands Hatch circuit pushing myself to the absolute limit in a BMW M3.
Walk up Wembley Way on FA cup final day
Walk one mile to watch the F1 at Silverstone
Walk One mile to watch tennis at Wimbledon
Walk one mile to Elland Road stadium
Walk one mile around the Olympic stadium, London.

Every mile will be completed with a blog with reasoning and heritage. You can come with me too, that’s my gauntlet being thrown down to you. Do you think you could get yourself fit enough to move a mile for muscles in this Olympic year? Inspire your family, get them off the couch and get them out. Ever wanted to go to a sports event but never got round to it? Get up and go!

I have been with my wife for about 20 years and every year she says that she’d love to go to Wimbledon, this year we will and we’ll do it for a great cause too!
You’re welcome to come along with me or take up your own challenge and move a mile for muscles by yourself. I challenge you to come up with an original idea to get people up and motivated; motivated enough to help others.

All of this will be exhausting, it will absolutely drain me but I’m hoping to have family and friends with me to make this a real team effort. I have an opportunity here and there is no way I’m going to let this go.
As I’ve got older I’ve started to read more and more and last year a friend recommended that I read about a runner called Steve Prefontaine and I did…
“To give anything less than your best, is to sacrifice the gift.”

I can walk, so I will.

Ambulant

Once again, I've been lucky enough to have someone else join me on my blog. Steve Davies is a friend of mine with Becker Muscular Dystrophy and wanted to join me in trying to explain some of the frustration behind being an ambulant disabled person...