Available in EBOOK and PAPERBACK versions!
When I was around twelve to fourteen I started researching DMD on the internet. I looked at terms like heart complications and breathing problems. I went through the list thinking I've got that and that but not this, this and this. I presumed in my naivéty that 'Oh I'd never get those symptoms'. I just couldn't equate that to me!
Extract;
...To me I thought I would go on and on staying the same; not equating what I had learnt about my DMD to me possibly getting worse...
As I got older the reality quickly set in and all the list had said I developed. Follow me on my travels through Duchenne's in my book DMD LIFE ART & ME!
Available as a PAPERBACK 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
Get you very reasonably priced EBOOK 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.
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 couldn't. Show all posts
Showing posts with label couldn't. Show all posts
Tuesday, 5 June 2012
Tuesday, 8 May 2012
The DMD balancing act
FREE ebook offer still on!!!!!! 18 days left!!!!!
Last night I had tremendous difficulties trying to move my wheelchair. I have a very light control which is very easy to move but I simply couldn't operate it at all. My arm was tired because I'd been typing with my mouse. Only when my arm was moved could I just barely move and get to bed.
Those moments are very worrying as you feel out of control. Thankfully because I have voice recognition I can do my work on these tired days. Perhaps I should have used it but sometimes quietly typing helps me express myself better. The DMD balancing act goes on!
I remember in school how I used to be able to eat a snack at break time but then it took too long. DMD certainly is relentless
Extract;
...A short recess was always taken at quarter past ten that lasted 15 minutes; I used to eat a small snack that was until it took me longer than a quarter of hour to eat it!...
Read more about the constant DMD balancing act 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 18 days left!!!!!
Last night I had tremendous difficulties trying to move my wheelchair. I have a very light control which is very easy to move but I simply couldn't operate it at all. My arm was tired because I'd been typing with my mouse. Only when my arm was moved could I just barely move and get to bed.
Those moments are very worrying as you feel out of control. Thankfully because I have voice recognition I can do my work on these tired days. Perhaps I should have used it but sometimes quietly typing helps me express myself better. The DMD balancing act goes on!
I remember in school how I used to be able to eat a snack at break time but then it took too long. DMD certainly is relentless
Extract;
...A short recess was always taken at quarter past ten that lasted 15 minutes; I used to eat a small snack that was until it took me longer than a quarter of hour to eat it!...
Read more about the constant DMD balancing act 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 18 days left!!!!!
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