For my next adventure………A FIREWALK……..!🙄
Wendy Mitchell is fundraising for Dove House Hospice.
Well everyone needs something to focus on to take their mind off the approaching winter and to stop getting excited about Christmas……so on October 27th I’m heading for Dove House Hospice to take part in a Firewalk!
I saw it first advertised on Twitter ages ago and asked if they thought I’d be able to do it – having a wobble and a stick in tow….They contacted the organisers who said they’d be my stick and support me through the fire🤓 No going back then…….
My dear friend, Alex Preston gave me some valuable advice………..Keep Walking! Don’t stop!🔥 note to self……….😳
We need to use hospices more for people with dementia. A hospice is associated with being a place to die for those with cancer, but they have so much more to offer, especially those living with a life limiting condition, such as dementia. They have the ‘talking’ skills we…
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A Short Post On Mamchester Arena Incident
Saddened. RIP to the young ones who are never going home from what should have been a fun night out.
Same Difference sends thoughts and best wishes to readers in Manchester after last night’s tragic incident. We hope that you and your loved ones are safe and unaffected.
To those killed- RIP. To their families, thoughts and sincere condolences.
To those who will now become disabled- your lives will change beyond recognition, but we hope you will eventually be happy in your new lives.
There will be no further posts today. Posting resumes tomorrow. We share the shock and sadness of many and will be spemding today following related news.
Friday. A bottle of cordial and Gills tin of beans.
What is this country coming to when a bottle of juice is a treat??
This is somewhat different to the usual weekly blog that I write. I don’t often write about events outside the weekly demo, to be honest I wasn’t sure that my readers would want to read it. But I thought I’d tell you anyway. Some might want to listen.
I was awoken quite early by a crank call, made by someone for reasons known only to themselves. They appeared to find it humorous to make fun of what we do, and the help that we give to people. Some people are very strange, and sadly this isn’t unusual its become par of the course. I don’t take it to heart and I did report it.
You see, in the over 3 1/2 years that I’ve been doing this I have encountered many negative things. Name calling, swearing, being told by G4S that they were going to knock myself and a friend…
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Why I believe some clinicians struggle diagnosing dementia…….
This week I’m changing Gp practice. My daughters don’t like my Gp and I don’t like their chemist. I got on well on my own before they ‘tried to help’. I’d go on line, in my own time, re order my perscription, collect the perscription and then collect my tablets. This happened every 2 months – perfect. Then the chemist got involved. First he wanted to put my tablets in blister packs, which for some are very useful, but not when you take trial tablets and they insist on me taking Donezepil in the evening, which has never worked for me.
So then they suggested I let them order my perscription and for me simply to pop in and pick it up – no need for me to do anything but pick it up – sounded perfect so I agreed……..bad move…..
The first time I went in there was a…
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The “why haven’t you killed yourself yet?” scandal : Another angry voice.
Guest poem by Alison Bolus…….
Alison is in her 50’s and was an editor before dementia entered her life so was well versed in the art of words. Sadly now, dementia has meant she finds writing difficult, however, she simply takes as long as it takes and writes the most wonderful poems.
Remember, we all had talents pre dementia, we don’t suddenly lose those talents overnight. We simply have to adapt and learn new ways…….
This is her latest:
Faltering, stumbling, I reach for the letters that I use to employ with delight to define me, explain me, to justify me.
My tools, my craft.
Some light touch here, some emphasis there.
Just might strike a chord.
Letters sliding down the stairs of poesy and hoping for a soft landing.
Tiptoeing around my soul.
But now the words rebel.
They sense my growing decline.
They note the hesitation in my clichés.
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MS sufferer who struggles to walk had mobility allowance axed ‘because she could squeeze person’s thumb’ : Daily Record.
Debenhams soak homeless man on Boxing Day – ruin his clothes, donated food
At this time of year, how cruel do you have to be deep inside to do this?
Posted on Facebook yesterday evening:
What have we become in the UK – a nation of bullies?
So to some of you you know my predicament of being homeless. But yesterday morning I woke up feeling wet socks and clothes thought I might of left a bottle open or something. I then get told by the security of Debenhams I have 10 minutes which was fine. But as he walked away he said enjoy your water bed. So I bite back as it being boxing day. So I then begin to pack up my bedding to then discover that the secunity guard from the inside of debenhams had flooded all my bedding. And ruined clothing food dog bedding public donations brought by the kind members of public. So a few of us went into speak to management didn’t do anything apparently it’s acceptable to bullying the…
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Challenges of Living alone with dementia versus being in a couple…….
A blog post by Wendy Mitchell I can relate to a bit…
I first published this blog back in October last year, but it seems a good one to reblog……
No one gives you a handbook when you’re diagnosed and one of the most difficult things for couples and families to accept is that you will need help and support and ‘training’ on how to support a loved one with such a diagnosis. It must be a difficult concept to come to terms with. After all here is someone you may have lived with for 20-30 years – why on earth would you need training? But why wouldn’t you need training on how to support someone with a complex brain disease?
Training and support for couples and families in the practicalities is something else that’s sadly lacking post diagnosis.
It got me thinking about how lucky I am, in many ways, to live alone. It’s a family joke that my eldest daughter…
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