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 laugh. Show all posts
Showing posts with label laugh. Show all posts

Tuesday, 26 June 2012

Making the best out of a bad situation

Available in EBOOK and PAPERBACK versions

I always try to look for the positive in every situation. What comes to mind is a trip to a hospital appointment to find out how bad my breathing was etc and afterwards I went to a marina and got some artwork ideas. It was a perfect distraction to the humdrum of DMD. Whenever I get ill one thing I rarely seem to lose is my sense of humour. After all having a laugh can help you feel better!

Extract;
....I’ve always liked sunsets and sunrises and had a really pleasurable time making this [artwork]. It just goes to show how positive reinforcement can lead to even greater things....

The first piece of art I uploaded to an art website received positive feedback even though the DMD I have limits the types of art I can produce. Never let limits hold you down, there's always an alternative.

Find out more 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, 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.

Thursday, 31 May 2012

Waistcoat dilemmas..

I have never seen my mother laugh so much when I was mentioning the idea of trying to get into a waistcoat for an upcoming family wedding. I was saying how it wouldn't be great to end up in A & E, clutching a broken arm on the day of said wedding! I knew that my arms would have tremendous trouble being bent back trying to fit into the waistcoat and I joked that I may break an arm!

Who said contractures don't make you laugh!

Extract;
...DMD can cause “Contractures”. Where ankle, knee, hip and arm joints have shorter muscles connected to them causing bent and deformed limbs; because of the associated Duchenne’s muscle cell death. That makes it impossible to completely straighten your arms or legs without causing huge damage and pain...

Thankfully I don't have to wear a waistcoat, so I will not need to grace the A & E department with a visit! (God willing).

Read about the lighter side of life with Duchenne's in my book DMD LIFE ART & ME!

You can buy your paperback copy of my book on Amazon 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

Also available as an E-book here; https://www.smashwords.com/books/view/69702

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.