Welcome to my blog!

Hi there!

This blog is related to my autobiography DMD Life art and me plus there will be non related posts. I have the disease Duchenne Muscular Dystrophy and that has left me in a near paralyzed state, I wrote this book in 10 months using one finger clicking one mouse button on one on screen keyboard! Be a follower by clicking in the box on the right and you'll get every new post I make. Feel free to join in with your comments and enjoy!

Ian,

Author and Digital Artist
Showing posts with label enjoyed. Show all posts
Showing posts with label enjoyed. Show all posts

Monday, 18 June 2012

You've got to laugh

Available in EBOOK and PAPERBACK versions

My mum has a saying, "You've got to laugh or you'll end up crying". How true that is these days! There's a lot with DMD that can certainly make you upset and sometimes you can't avoid that. Although when happy moments come they are often remembered and thoroughly enjoyed.

We still laugh at the time that I was flung off a horse (I landed in soft snow), the horse ran off and my dad was running after it!

Extract;
...I was out riding; my father and cousin .... were walking beside me. After a gentle ride past some snow banks the horse suddenly got startled and threw me off! I landed in some soft snow in a daze. My cousin was standing there laughing as my father chased after the bolting horse, I can remember his hat falling off and flapping behind him in a comical manner....

There's always something good to smile about in life, finding those moments is the hard part!

Read through my happy memories in my book DMD LIFE ART & ME!

EBOOK available here; https://www.smashwords.com/books/view/69702

Available on Amazon USA here; http://www.amazon.com/DMD-Life-Art-Ian-Griffiths/dp/1907652337/ref=sr_1_1?ie=UTF8&s=books&qid=1288120811&sr=8-1

Available on Amazon UK here; http://www.amazon.co.uk/DMD-LIFE-ART-AND-ME/dp/1907652337/ref=sr_1_1?ie=UTF8&s=books&qid=1288105302&sr=8-1


Foreword

I’m Ian Griffiths from South Wales. This book is a story of my life so far up to the age of twenty five years. I live with and suffer from the ill effects of DMD which stands for Duchenne Muscular Dystrophy. It is a severe muscle wasting disease and a life limiting terminal illness. It won’t kill you in six months in the traditional sense of ‘terminal’, but it’s far crueller than that, it steals every muscle in your body first and then kills you, anywhere up to the age of thirty. There have been cases of men living past that into their forties and fifties but only with drastic interventions such as ventilators and tracheotomies, more on this can be found by reading on.
I hope to cover a few things in this book, from a history of my childhood years to a more detailed history from sixteen years onwards and finally onto my current problems and triumphs. At times things I write may make you smile or may make you pause and think about the seriousness of life with this devastating disease. I really hope there will be a cure but currently for us supposedly ‘older’ guys with DMD (over twenty one), there seems very little hope. If I don’t see a cure in my lifetime, I hope my campaigning helps in some way bring it about for future generations, so another child won’t have to see their body wither and die before their time.

Monday, 7 May 2012

School days.

FREE ebook offer still on!!!!!! 19 days left!!!!!

Everyone needs an education, especially so for those with DMD. The majority of those living with DMD have perfectly capable minds. Such a mind needs teaching and molding!

I think for most children getting up in morning on a school day is a major chore! It is usually a bit more of a hassle for those with DMD! Just getting dressed might take some thought, then waiting for accessible transport, even just trying to find a safe place to unload can be fraught and then getting around school requires resourcefulness. After all that I still quite enjoyed school and learning, I was not to fond of homework though ha ha!

Extract;
...My usual school day routine was to be up at quarter past seven in the morning, eat breakfast usually golden brown toast with jam or [chocolate spread] and then I’d be whisked upstairs so my mother could dress me...

That was only a taster, read more about my high school starts in my book DMD LIFE ART & ME!  


Please visit here to buy my paperback version; http://duchennemen.net16.net/Buy-my-book-s/
Don't forget my FREE e-book offer!!!!! For one month only until the 26th of May my e-book version of DMD LIFE ART & ME is FREE, you can get your FREE version here; https://www.smashwords.com/books/view/69702

Only 19 days left!!!!!

Thursday, 3 May 2012

Vacation memories

FREE e-book offer!!!! Just 23 days to go!!!!

Vacation memories.

I don't mention every vacation I've been on in my book or it would be about 1000 pages long! I do mention a few of the places I've been too. Around the same time as we got drenched in Lancaster, my family and I went to Lake Ambleside in the Lake District in NorthWest England.

After some huge persuading I reluctantly rolled my wheelchair on to a boat. I really don't like being on anything that floats at the best of times! However I really enjoyed it once we were underway looking at the beautiful scenery that reminded me of home.

Extract;
...I took my chair (reluctantly) on a canal barge and on a boat cruising up Lake Ambleside in Lancashire...

Read about more my vacation adventures in my book DMD LIFE ART & ME! (For you e-book readers turn to page 32)



Please visit here to buy my paperback version; http://duchennemen.net16.net/Buy-my-book-s/





Don't forget my FREE e-book offer!!!!! For one month only until the 26th of May my e-book version of DMD LIFE ART & ME is FREE, you can get your FREE version here; https://www.smashwords.com/books/view/69702

Only 23 days left!!!!!



Foreword

I’m Ian Griffiths from South Wales. This book is a story of my life so far up to the age of twenty five years. I live with and suffer from the ill effects of DMD which stands for Duchenne Muscular Dystrophy. It is a severe muscle wasting disease and a life limiting terminal illness. It won’t kill you in six months in the traditional sense of ‘terminal’, but it’s far crueller than that, it steals every muscle in your body first and then kills you, anywhere up to the age of thirty. There have been cases of men living past that into their forties and fifties but only with drastic interventions such as ventilators and tracheotomies, more on this can be found by reading on.
I hope to cover a few things in this book, from a history of my childhood years to a more detailed history from sixteen years onwards and finally onto my current problems and triumphs. At times things I write may make you smile or may make you pause and think about the seriousness of life with this devastating disease. I really hope there will be a cure but currently for us supposedly ‘older’ guys with DMD (over twenty one), there seems very little hope. If I don’t see a cure in my lifetime, I hope my campaigning helps in some way bring it about for future generations, so another child won’t have to see their body wither and die before their time.