Hello.
The blog A Manifesto For Radical Inclusion written by Dr Al Power on ChangingAging has a taste of Richard Taylor in it. The gloves are no longer hanging on the wall of the gym, they are coming off, all around the world.
As Al mentioned last week, Richard once sent him an email saying, “Welcome. I’ve been waiting for you.” I can only borrow these wise words, “Al, welcome. I’ve been waiting for you too.”
In fact, I’ve been waiting for everyone who cares about people with dementia to realise that inclusion is not at all radical, it is our most basic of human rights.
Al wrote in his blog last week, “Richard’s voice will continue to speak in a thousand different ways, in the voices of those whose lives he touched.” This is indeed the truth and legacy of this great and wonderful man many of us had the privilege to know and call a friend, and although many of my private emails to Richard also started with ‘hello’, it will be one of my missives from here on.
Many of the things written in Dr Power’s article I have been advocating for over six years, and others living with dementia have been advocating for them for much longer. Richard was one of the early advocates, along with Christine Bryden and Peter Ashley.
Those of us following in their footsteps have still got a great deal to do, as it seems, as if being inclusive of people with dementia is still seen as radical, it seems no-one has been listening.
Perhaps it is giving up the position of power people without dementia have had over people with dementia for so long is what is going to be the hardest to shake.
The notion that what people with dementia experience, is in fact, often NOT what others have been assuming, and telling the world it is like, is obviously ruffling lots of feathers.
There are a few friends I have made along the road of this wild ride called dementia, and I can see a few whose gloves been placed on firmly and fairly since Richard Taylors death, and together, perhaps after all, we will change the world for people with dementia.
At least, for now, I have a renewed hope and a newly inspired determination to keep going.

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Thanks for sharing this Faith, and for writing your blogs… which we will add to DAI, with your permission? xox
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We will together make sure Richard’s legacy lives on and continues to get stronger through taking off the gloves. Inclusion is now something that boards, committees and the general public should be aware of. We will no longer be told to sit in the corner. ONE AND ALL, WE ARE COMING AND OUR VOICE IS STRONG.
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OUR VOICE IS STRONG… and collectively, GETTING MUCH STRONGER xox
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PS I am being educated daily….by the experts 🙂
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as are we… xx
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Dear Kate, where I get it from… I have an idea from my late Dad, hence, I was connected to him until his last breath. I advocated HIS voice from the beginning. It was never about me. My family relationships have broken down solely because of this. I have no regrets and my journey has become stronger and I will do what ever it takes to contribute to all the changes you and others deserve. Best wishes from me xx
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Thank you so much for your ongoing support, and for what you have done already xox
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Of course we will change the world for PWD dear Kate. It’s a matter of history (change is in the air) though, like you, I sometimes wonder what it will take.
“De-isolation” to start with 😊
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I do still wonder what it is going to take… but love you and Veda for your support! xox
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