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	<title>Dementia Stories Archives - BRACE Alzheimer&#039;s Research</title>
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		<title>Gideon Luke</title>
		<link>https://www.alzheimers-brace.org/gideon-luke/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 16 Feb 2021 12:45:52 +0000</pubDate>
				<category><![CDATA[Dementia Stories]]></category>
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					<description><![CDATA[<p>Not so long ago, my father passed away after eight long hard years suffering dementia.</p>
<p>The post <a href="https://www.alzheimers-brace.org/gideon-luke/">Gideon Luke</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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		<span class="fl-heading-text">Gideon Luke</span>
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	<p>Gideon Luke of The-Marketing-Department, Weston-Super-Mare, tells the very personal story behind his decision to make an appeal video as a gift for BRACE.</p>
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	<p>Not so long ago, my father passed away after eight long hard years suffering dementia. For six of those years, my aged mother was there supporting him day and night as dementia took more and more of him away from us and more of us away from him.</p>
<p>He had been a Captain in the Merchant Navy and travelled all of the seven seas, transporting chemicals and materials in a super-tanker. He’d visited some of the most interesting places on earth and survived tsunamis as well as all sorts of other natural dangers at sea, while ensuring that his crew were safe and that the complex cargo was in no danger. They respected his judgement, followed his orders and he was highly regarded amongst his peers for his expertise and experience.</p>
<p>When he came home he’d bring things he thought would delight me and he’d tell me tales of where he’d been and things he had seen – the world sounded so big and amazing to me as a youngster and deeply interesting as I grew up hearing more about it. Occasionally he’d phone from wherever he was, and I remember one particular instance, hearing steel drums in the background while he was visiting Bermuda – lucky for some I thought! The downside, of course, was that his job took him away from us for long periods and sometimes when we needed him most. How ironic that at the end of his life, when he was always home, dementia had taken him away from us forever.</p>
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	<p>Having read many books on the subject to try and understand his condition better, the point which had the most impact on me was, that despite a familiar glint in his eye, he was quickly forgetting the life he had lead travelling the world, the amazing places he had been and loving family he had.</p>
<p>....Just like someone had deleted it.</p>
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	<p>I can’t really conceive of how that must have felt for him, but I know what it is to have a parent affected by such a dreadful disease and sincerely hope, with the scientists and technologies that now exist, that we’re moving increasingly closer to a cure – and that’s why I think BRACE is important. Their scientists’ brains are working on a cure for our loved ones’ brains, our parents' brains and our brothers' and sisters' brains, so one day it can be beaten. Time's up dementia.</p>
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</div><p>The post <a href="https://www.alzheimers-brace.org/gideon-luke/">Gideon Luke</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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		<title>Hannah Fielding</title>
		<link>https://www.alzheimers-brace.org/hannah-fielding/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 04 Feb 2021 12:52:00 +0000</pubDate>
				<category><![CDATA[Dementia Stories]]></category>
		<guid isPermaLink="false">https://www.alzheimers-brace.org/?p=787</guid>

					<description><![CDATA[<p>My journey with BRACE started in 2016 when I decided to run the London Marathon and fundraise for this amazing cause.</p>
<p>The post <a href="https://www.alzheimers-brace.org/hannah-fielding/">Hannah Fielding</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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	<p>My journey with BRACE started in 2016 when I decided to run the London Marathon and fundraise for this amazing cause.</p>
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	<p>Alzheimer’s and dementia sit closely within my heart - in 2010 my world changed forever when my grandma, my best friend, my confidant, my counsellor, my life coach, sadly got diagnosed with a strand of dementia and Alzheimer’s disease. This not only affected her but everyone around her who loved and cared for her so much. With watching this disease unfold first hand I decided that I wanted to give something back by fundraising – this led me to the fantastic team at BRACE. With their help and support, and with sheer determination, I managed to complete the London Marathon.</p>
<p>Completing the marathon and fundraising at the same time was one of the best experiences of my life. After training for months, raising money through countless cake sales, non-uniform days, charity events and even appearing in the local newspaper, crossing the finish line was the most rewarding and satisfying experience I’ve ever had. I would definitely recommend it to anyone!</p>
<p>Unfortunately the deterioration in my grandma’s health got worse and shortly after the marathon she passed away. But this didn’t stop me, I had hope. Hope of a better future for the next generation and hope that no family would face what my family once faced. The team at BRACE stayed in contact with me through this time and for this I will be forever grateful.</p>
<p>After two years, I decided it was time for a new adventure and this time I found myself fundraising for BRACE by taking part in a skydive! A once in a life time opportunity! Fundraising through raffles, sweepstakes and with the support of family and friends I soon found myself ready to jump out of a plane at 15,000 ft. A liberating and indescribable feeling.</p>
<p>My advice to anyone would be to just go and do it! Life is for living, so make it count! Drop an email, write a letter, make a phone call. You can do anything you want to in life. I just want to say a special thanks to BRACE for their support and guidance as I know I definitely wouldn’t have run a marathon or jumped out of a plane without them. Together we can beat dementia, together we have hope.</p>
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</div><p>The post <a href="https://www.alzheimers-brace.org/hannah-fielding/">Hannah Fielding</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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		<title>Wendy Mitchell</title>
		<link>https://www.alzheimers-brace.org/wendy-mitchell/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Mon, 01 Feb 2021 12:53:00 +0000</pubDate>
				<category><![CDATA[Dementia Stories]]></category>
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					<description><![CDATA[<p>Former NHS Manager who was diagnosed with Young Onset of dementia aged 58</p>
<p>The post <a href="https://www.alzheimers-brace.org/wendy-mitchell/">Wendy Mitchell</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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	<p>So often when people hear the word ‘dementia’ they think of the end stages and when diagnosed with Young Onset so many people fall into a state of despair, believing it to be the end. But often that’s due to societies attitude, due to the stigma associated with dementia. Imagine if that was you being given a diagnosis? What would you think?</p>
<p>That’s what I though back in July 2014 because no one told me any different. I was given a handshake, a sad look and discharged by the consultant who diagnosed me. No words of encouragement, no support in how to adapt. For a while I thought it was the end.</p>
<p>But once me and my daughters got our heads around the diagnosis, I wasn’t prepared to accept it was the end. There’s always a way to overcome the problems we face.</p>
<p>People forget there’s a beginning, there’s a middle with so many adventures still to be had. I was determined to continue having adventures no matter what others thought.</p>
<p>I realised a diagnosis was simply the start of a different life, a life of adapting and continually adapting as dementia throws more challenges your way. I think of it as playing a game where I’m trying to stay one step ahead of dementia, trying to outwit it at every turn. What’s the alternative? To sit and allow dementia to win?</p>
<p>I found a passion for research – clinical, social and technological. After all, how can we change the future if those of us living with dementia now, don’t test new drugs and new theories on how best to live?</p>
<p>I also found the best support in the community was Peer support. Support from those who are living through the same experience. No one judges you, no one corrects you. We share stories, we share ideas and we support one another.</p>
<p>So what would my advice be to someone newly diagnosed?</p>
<p>Yes, it’s a bummer of a diagnosis but don’t dwell on the losses. Don’t dwell on the future as you have no control over either. Instead concentrate on what you CAN do and enjoy today and if today is a bad day, maybe tomorrow will be better.</p>
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</div><p>The post <a href="https://www.alzheimers-brace.org/wendy-mitchell/">Wendy Mitchell</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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		<title>Susan Marshfield MBE</title>
		<link>https://www.alzheimers-brace.org/susan-marshfield-mbe/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Sat, 16 Jan 2021 12:55:00 +0000</pubDate>
				<category><![CDATA[Dementia Stories]]></category>
		<guid isPermaLink="false">https://www.alzheimers-brace.org/?p=793</guid>

					<description><![CDATA[<p>BRACE volunteer and former Honorary President</p>
<p>The post <a href="https://www.alzheimers-brace.org/susan-marshfield-mbe/">Susan Marshfield MBE</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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		<span class="fl-heading-text">Susan Marshfield MBE</span>
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	<p><strong>How long have you been involved with BRACE?</strong></p>
<p>Almost 30 years! BRACE had just formed when my late husband went to the old clinic at Blackberry Hill Hospital. Professor Wilcock and Mary Sansbury, who were co-founders of BRACE, were among the doctors there. I was introduced to Mary by Professor Wilcock, because she was looking for people to support the new charity.</p>
<p><strong>When did your late husband’s battle with dementia start?</strong></p>
<p>Jack’s battle with dementia started quite abruptly. The directors of the company he worked for sold up, so he made the decision to leave. It was during this time things started to get quite difficult, so we went to the GP. We were sent to the memory disorder clinic at Blackberry Hill. In those days there was very little support.</p>
<p>At the time I was a Councillor, but I had to leave to find paid work as Jack couldn’t work. At this point he started to do odd things; I would come home to find he had put ten teabags in the kettle, as he’d added a tea bag each time he wanted a cup of tea.</p>
<p><strong>When did things get worse?</strong></p>
<p>One day, I got home and discovered that he wasn’t there, at which point I had to change how I cared for him. He was spotted by a lorry driver near a motorway junction. Thankfully, the driver called the police and he was picked up. From then on though, he was not left alone.</p>
<p><strong>How did Jack’s dementia affect you and your family, and were your children supportive?</strong></p>
<p>I have two sons, both supportive in their own way. One who lives nearby could cope with Jack’s dementia; if I ever badly needed help, such as getting Jack into the bath, I could call him and he would come to help. My younger son found the last 18 months of Jack’s life very difficult. He found seeing his father incredibly upsetting. He wanted to remember Jack as he had been, not this person who didn’t know him.</p>
<p>For the last two or three years Jack thought I was his mother. He said he kept seeing this other man in the house; I assured him that there wasn’t anyone else in the house. But one day he pointed at his reflection in the mirror, saying “that’s him”. When I said it was his own reflection, he said “well if I ever looked like that, I’d kill myself”. He thought he was a young man, adding “he looks as old as you, and you’re my mother!”. That was quite hard to come to terms with, and even though it happened a long time ago, I still think about it sometimes.</p>
<p>Eventually Jack developed pneumonia and spent his last two weeks in Professor Wilcock’s ward at Blackberry Hill Hospital. I would go in to feed him, but he became unable to swallow or talk, even walking was extremely difficult. He died aged 67.</p>
<p>He was 59 when diagnosed. I wouldn’t wish him the last two years of his life. It’s almost cruel in a way, for someone who has always been active to have to live this way and for the family to have to watch and know how little they can do.</p>
<p><strong>What was Jack like? </strong></p>
<p>Jack was very much a family person and did lots of things with our boys. For two years he ran a local junior football team so that our son and his friends could play. He was also a good footballer in his youth and played for Brentford juniors. These boys often became ball boys on Saturday for the big clubs and he did his stints at Arsenal, a team he supported for the rest of his life.</p>
<p>In our household we all supported different teams! Jack; Arsenal, Me; Sunderland, older son; West Ham, younger son; Tottenham. We were quite competitive about it!</p>
<p>Jack also had two West Highland White Terriers to keep him company, and he enjoyed being with them. Sadly, one of them died after Jack was diagnosed, but the other kept going until a few months after Jack’s death.</p>
<p><strong>Why Should people support BRACE?</strong></p>
<p>People should support BRACE because it’s a more personal charity. Alzheimer’s Research UK and the Alzheimer’s Society raise lots of money and do lots of research, but for people like me who have experienced the disease, I feel BRACE is more personal. It’s local to the South West and you can see where your money is going, especially if you attend the events BRACE puts on.</p>
<p>When I met Prince William when I collected my MBE, I told him about my involvement with BRACE. He told me “You stay with that. In the next 20 years we have to break through because there’ll be thousands more in need”. He was right. We are all living longer and we need to take note of that. It’s very important that charities like BRACE are supported so that research can continue.</p>
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</div><p>The post <a href="https://www.alzheimers-brace.org/susan-marshfield-mbe/">Susan Marshfield MBE</a> appeared first on <a href="https://www.alzheimers-brace.org">BRACE Alzheimer&#039;s Research</a>.</p>
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