AVAILABLE in EBOOK and PAPERBACK versions
I have what I call Duchenne's induced paralysis (a term I invented), I can move my hands and legs only a few centimeters but basically nothing else moves although crucially I still have the ability to feel. That can be a blessing and a hardship. One of the hardest things usually happens at 5AM, that being my legs get terribly itchy. I could wake my mother but I desperately don't want to do that because she needs to sleep. All I can do is tough it out waited for the itch to go. It's a small problem in the grand scheme of things but it sure is annoying! The best part about feeling is the control it gives me when painting using my computer mouse. I need very fine motor skills to follow any sketched lines I drew.
Extract...
.... I indeed do still feel although it’s a royal pain when something is aching or needing to be scratched! When I get extreme back ache whilst sitting in my chair, I need to call my mother and she repositions me using my hoist. What takes five seconds for the non disabled, takes me ten minutes of re-jigging!
Read more about Duchenne's induced paralysis 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
My new Ebook Poetic Diversions available to buy here; https://www.smashwords.com/books/view/206857
All links available in my website here; http://duchennemen.net16.net/Buy-my-books/
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.
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
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 itchy. Show all posts
Showing posts with label itchy. Show all posts
Monday, 3 September 2012
Monday, 16 July 2012
Small Victories
Available in EBOOK and PAPERBACK versions
As I was waiting to go to bed my sling strap was resting on my arm in a really irritating and itchy place. So I decided I would try to move it myself. What an arduous task indeed! I moved my hand the few millimeters that it can move and moved my leg the few centimeters it can move. After a battle for two minutes or more I finally won! I got it to move, what a victory it felt like, it even made me giggle!
Extract;
.....[One summer a few years ago] I was trying to hit a red cricket ball that my father was gently throwing towards me. With a swift action I just about managed to take a small swing at the ball; I could only move my hand an inch or two [because my arm was propped up]. The ball would just hit the wooden stick and drop like a stone onto my clear plastic wheelchair table....
It is always a struggle moving the tiny amounts that I can but it's so liberating to do something for myself! That's why it is so important to focus on what you can do whether you have a disability or not! Read more about my small victories 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
All links available in my website here; http://duchennemen.net16.net/Buy-my-book-s/
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.
As I was waiting to go to bed my sling strap was resting on my arm in a really irritating and itchy place. So I decided I would try to move it myself. What an arduous task indeed! I moved my hand the few millimeters that it can move and moved my leg the few centimeters it can move. After a battle for two minutes or more I finally won! I got it to move, what a victory it felt like, it even made me giggle!
Extract;
.....[One summer a few years ago] I was trying to hit a red cricket ball that my father was gently throwing towards me. With a swift action I just about managed to take a small swing at the ball; I could only move my hand an inch or two [because my arm was propped up]. The ball would just hit the wooden stick and drop like a stone onto my clear plastic wheelchair table....
It is always a struggle moving the tiny amounts that I can but it's so liberating to do something for myself! That's why it is so important to focus on what you can do whether you have a disability or not! Read more about my small victories 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
All links available in my website here; http://duchennemen.net16.net/Buy-my-book-s/
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.
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