Norman McNamara lives with Lewy Body dementia and has written “The Lewy Body Soldier”

Untitled design-13My name is Norrms McNamara. Someone once told me having Lewy Body`s Type Dementia is like having two diseases, you HAVE Dementia, and you KNOW you have Dementia. The same person, a Consultant, also told me that right up to the end of life, the person with Lewy Body’s will still have moments, if not hours/days of clarity. I lost both my Father and incredibly wonderful grandmother to Dementia. (I say that because she brought me up, I am who I am today because of her)

I have read the book, seen the last page, read the last line, I know what happens and know what can happen unless they find a cure for this awful disease. So when I was diagnosed myself nine years ago, aged just 50, I was absolutely petrified, and with good reason.

No cure, no sign of a cure on the horizon and after checking out what help there was available for somebody my age with dementia, which turned out to be practically non-existent, I was at a loss at what to do. I was so lucky in one way because my wife Elaine had been, and still is a carer for 30+ years and it was her who helped me get my diagnosis as she recognised the signs.

So what’s changed in the last nine / Ten years? A huge amount actually, we now have memory cafes all over the world, we have so many groups globally connecting up and beginning to talk about this disease. We have TV adverts, politician’s talking about it in Government’s and generally a better understanding, so why, oh why, is it still in the shadows when it comes to

TELLING THE TRUTH ABOUT THIS DISEASE!!?

It is only because relatives of those with Dementia and those actually living with dementia have started to write books about it are we starting to know the real truth about this disease, and this is exactly what this book is all about. This is a book written by someone who has Lewy Body’s type dementia but is still lucky enough to have the abilities, with a LOT of help, to write it, but let’s make one thing clear

This book is not for the faint-hearted.
This book is not about Clever Medical Terms or graphs.
This book doesn’t wear Rose tinted glasses.

This book is about not only about how hard it is to live with this awful disease, how hard it is to get help etc., but ALSO  a book of helpful hints about HOW to get help, what to do when you go for a diagnosis and what to do after. It’s a book of hope, but most of all it’s a book of truth, and about, as they say,

“Hearing it right from the horse’s mouth.”

I am at peace with my illness, I believe every day is a bonus and every breath I take is a blessing, and no matter what happens, if I can give a little back to all those around me who have helped me along my way, then so be it.

Best wishes, Norrms Mc NamaraFounder of Global Purple Angel dementia awareness Campaign

A A A A A A A b Smiling

Now recognised in 55 Countries around the world with 860 Global Purple Angel dementia ambassador’s.

To find out more please contact

https://www.purpleangel-global.com/

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Facebook
https://www.facebook.com/norm.mac1

Twitter

@Norman Mc Namara

Amazon book also availiable on Amazon USA and Amazon EU

https://www.amazon.co.uk/Lewy-Body-Soldier/dp/1536805874

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Welcome Peggy Bushy, author of Lewy, Mom, and Me

 

Lewy, Mom and Me CoverBy Peggy Bushy

When Lewy Body Dementia entered my home, the world as I knew it began to shift, and I found myself in a constant state of confusion. My sweet mother, who lived in our home, was hallucinating, her stories and behavior were becoming more and more bizarre, and I had no idea why – neither did any of the doctors I consulted. Lost and alone, I could feel myself becoming a little more unglued with every passing day while I watched the family rules fly out the window one by one. “Wait! I depend on those family rules.” They may not be the same as the neighbor’s rules but they’re mine, they’ve been mine forever, and I’m comfortable with them.

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Meet Krysten Lindsay Hager – How Young Adult Fiction Helps Heal and Educate

By Krysten Lindsay Hager

competingwiththestarAfter my dad passed in the summer of 2015, I was sitting on my couch watching TV when I got a message from some readers asking what happened next for my characters Nick and Hadley from my book, Next Door to a Star. I was in my grief bubble, and this email was a welcome bright spot letting me know someone cared enough about the characters to want to know their future. I thought writing about what happened next might be a way to get my mind off grieving. It was when I got to sixty pages that I realized I might have a book. Continue reading