#Alzheimer&039;s Society
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Alzheimer’s Society facing criticism over 'The Long Goodbye'
A short film by the UK-based Alzheimer’s Society has generated a wide range of strong emotions from those with dementia and their families. In addition to the original video campaign embedded above, there is also an extended cut version and a profile of a couple who faced a heartbreaking FTD diagnosis. The crux of the criticism comes from the film’s fatalistic point of view, framing dementia as…
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DAILY DOSE: Boeing's Starliner crewed launch delayed four days; ApoE4 gene variant linked to distinct Alzheimer's form.
BOEING STARLINER CREWED LAUNCH POSTPONED FOUR DAYS MINIMUM. The first crewed launch of Boeing’s Starliner spacecraft has been postponed for at least four days due to an issue with an oxygen relief valve on the Centaur stage of the Atlas V rocket. Scheduled to launch at 10:34 p.m. EDT on May 6, the mission was halted about two hours prior, as NASA declared the rocket was not in a flight-ready…
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#abortion#aerospace#Africa#Alzheimer&039;s disease#Asia#Australia#climate change#conservation#environment#Europe#evolution#Featured#Genetics#mental health#North America#politics#society#South America#zoology
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Dementia, David Cameron and losing ground
We are trying to recover the system, undo the logjam of unattended outpatient appointments or hip and knee replacements postponed, or hernias and cataracts that have been delayed.
I am no historian. I struggle with details. Dates and times have never been my thing. I am however a reflector. I look at the world around me, absorb its colours and ponder. I was going to say ‘think’ although FEEL is probably more accurate. For once, I will not quote Bruce Lee (Google, ‘almondemotion Bruce Lee’ if you like). What do I feel about the situation in 2021 for those living with…
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#Alzheimer&039;s Society#Covid#David Cameron#Dementia#Dementia Friendly#forget-me-not#Hospitalisation#hospitals#Person Centred Care
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Bill Gates Personally Invests $100 million in Alzheimer’s Research
Bill Gates Personally Invests $50 million in Alzheimer’s Research
Ramin Talaie/Getty Images
Bill Gates, Billionaire Microsoft co-founder will invest $50 million in the Dementia Discovery Fund (DDF). Gates’ investment is personal and unrelated to the Gates Foundation.
In an interview with Reuters, the philanthropist described the emotional and financial tolls of the brain-wasting disease:
It’s a huge problem, a growing problem, and the scale of the tragedy –…
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#Alzheimer’s Disease International#Alzheimer’s Society charity#bill gates#Bill Gates Alzheimer&039;s Research#Bill Gates investments#Dementia Discovery Fund#Jeremy Hughes
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Alzheimer's Society responds to life expectancy figures | Care Industry News
Alzheimer’s Society responds to life expectancy figures | Care Industry News
Source: Alzheimer’s Society responds to life expectancy figures | Care Industry News
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#adult social care services#Alzheimer&039;s Care#Alzheimer’s Society#chronic lack of funding to the social care system#dementia care#inadequate underfunded care#life expectancy
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Dementia support worker and hubby walk coastal path
Dementia support worker and hubby walk coastal path
A Devon dementia support worker who has seen first-hand how badly coronavirus has hit people affected by dementia on her patch, has laced up her trainers and trekked the South West coastal path to help raise funds.
(more…)
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Ruth Langsford Breaks Down In Tears As She Wins £33,000 For Charity On Alan Carr's Epic Gameshow
Ruth Langsford Breaks Down In Tears As She Wins £33,000 For Charity On Alan Carr’s Epic Gameshow
Bless her.
Ruth Langsford has broke down in tears after she won a whopping £33,000 for a charity on Alan Carr’s Epic Gameshow.
The This Morning host was on the new ITV game show alongside her husband Eamonn Holmes when she won the money for the Alzheimer’s Society.
The pre-recorded game show aired for the first time on Saturday night as Alan is bring back old game shows but in a new form.
Ruth’s…
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#Alan Carr#Alan Carr&039;s Epic Gameshow#Alzheimer&039;s Society#charity#Eamonn Holmes#money#Ruth Langsford#tv#tv news
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I’ve wanted to write this tribute for many months. Unashamedly there follows a rather extensive post, one of the longest I’ve ever published. I suspect few people will reach the end of it. However, it’s important for me to share these stories, for our library of memories. Who knows, there may just be a snippet of something you’ll find useful too …
Celebrating the gifts
Five years and two months after Barry and I returned to England, I was heartbroken to become motherless.
Today, Friday 28th September 2018, I begin my 60th year on this planet, and shall be celebrating the gifts of three incredible women who nurtured me as loving mothers do. Each in their own special way. I’ll also acknowledge how incredibly fortunate I’ve been to love, and be loved, by these magnificent matriarchs.
Remembering and celebrating June
Barry’s mum June died in July 2014, aged 90.
I’d known June since February 2005, and we soon formed a strong bond. Like me she didn’t suffer fools gladly, was outspoken and rather intolerant (oh my, that’s not sounding great is it?). She was also intelligent, funny, confident and strong (I’m liking the sound of those shared attributes much more!).
Patricia June Teutenberg, like my birth mum Irene, was a teacher. She specialised in English. She was also for many years a ‘Surf Lifesaver’ in Ohope. It was at a ‘Surf Lifesaving’ competition in Gisborne, that she met Frank, her future husband and Barry’s dad. Similar to Irene, Frank and June had a short courtship, married and settled in Gisborne where they went on to have four children. Three boys and a girl. She often said that when her daughter Jenny was born, it was “The best day of my life.” Though I recall her saying one day, after she’d become poorly (more to come) and I entered the hospital room to visit, “Here’s my favourite girl.” Jenny was in the room! We both laughed, and still find the incident highly amusing.
Her will to live, despite debilitating illnesses since 2010, was astounding. I never once heard her complain or ask “Why me?” It’s rather a long story, but worth mentioning that eating raw fish if you’re a child or senior person, brings with it a risk of the anaerobic organism aeromonas. The marinated fish had been part of a special dinner Barry and I had held a few nights after returning to Gisborne in November 2010.
Unfortunately, by the time the cause of her severe and unrelenting diarrhoea had finally been investigated properly by the hospital and her GP, around four months later, she’d suffered devastating indignities at home and in hospital. It often felt she’d been dismissed by health professionals due to her age. Which angered me intensely. A few people felt my wrath, which in turn led to a more thorough investigation rather than dismissing her needs as a human being.
The consequences are likely to have considerably shortened her life. Her mother had lived until she was almost 104 years young. June was understandably disappointed not to follow in her footsteps. Her family were too. I was devastated that the marinated fish we’d served her was most likely the reason for her ill-health. It didn’t affect our relationship thank goodness, and I fought alongside her children to get her the best care possible whilst we were in New Zealand.
The Teutenberg’s at our Wainui Beach wedding
Dancing with June
January 2010 with her daughter Jenny and my friend Arlene
We used to do all sorts of things together. Like weekly Line Dancing (she hated the routine ‘Oklahoma’ I recall!), steam train rides, local outings, and road trips.
Queenstown, July 2011
She recovered from the 2010 challenges, and in 2011 travelled to Queenstown for her granddaughters’ wedding along with her family. That Christmas she bought a one-way ticket to Sydney, so stay with her youngest son Peter, and then up to Gladstone to stay with Jenny. Sadly, a few months later, her bowel problems returned and she went downhill to the point that she wasn’t able to care for herself at home. Just after she’d bought herself a brand new car bless her!
June and Suki
The last time I saw June at Te Wiremu
I hated leaving her in the Nursing Home Te Wiremu when we left Gisborne in March 2013, though was reassured it was a caring place she’d settled into. She had a nightly Baileys (home made by Barry of course!), inviting her neighbours in for a before-dinner-tot. We’d chat on the phone from UK though, and the Nursing Home even managed to organise a Skype session so we could see each other. The wonders of the 21st century!
The Teutenberg four at June’s plot unveiling, March 2013
I cried uncontrollably when I heard from Ray that she’d died in her sleep. A theme that would be continued four years later …
My dear friend Therése
My other kiwi mum, Therése, died in April this year, aged 81.
We’d met when I first lived and worked in Gisborne, from the end of October 2001 to July 2002. Therése was an Registered Nurse at the Maternity Unit there; she’d also managed a Nursing Home, Leighton House, in Gisborne for a number of years.
I lodged in the downstairs flat of her wonderful Wainui Beach home, from February to July 2002; my parents stayed there with me when they came for their five-week jaunt around the North Island with me. The views from the balcony and proximity to my favourite beach in the world were a treasure I’ll never forget. We frequently walked on the beach, and in the summer she’d swim daily in the ocean. She couldn’t understand why I wouldn’t. It amused her greatly my fear of drowning (the sea there is known for its rip tides, and I’m not a strong swimmer).
Therése soon became one of my dearest friends.
Cornwall in 2004
In August 2004, at the grand age of 67, she took the opportunity to come to England and travel with me before I emigrated to New Zealand. We spent three fantastic weeks touring England and Ireland together, staying with friends and at backpackers. I can’t begin to tell you what fun we had along the way. St Christopher was spoken to frequently, when I got lost. Therése was a devout Catholic, and her prayers to find our way were always answered. She’d seek a church to visit at almost every town we visited. I went in with her once. For me, that was more than enough. The Catholic GP in 1976 who felt it necessary to ‘punish’ me in cruel ways as a pregnant teenager, is indelibly imprinted in my brain. Listening to sermons of ‘sinful girls’ will never be acceptable. For Therése though, the church was a refuge. A support. Her place of comfort. We respected each other’s views, it was of no consequence they differed so vastly.
Like me, she’d brought up her children for many years as a single parent, working tirelessly to do her best to provide what they needed to thrive. All five are amazing, successful people.
Therése had been wanting to find her Irish ancestors. I’ve recently discovered she was actually baptised Sheila Therese McCaughan, but always went by Therése. We only found her maiden name in one area, right up in the north, whereas my name ‘Walsh’ was common all over. She was ecstatic to meet some distant relatives, and we visited and took photos of them. Sadly I don’t have copies here. My Irish photo album is in New Zealand. I have found one photo I must have photographed in New Zealand last year, of us in Cornwall.
In December 2009, Therése was the mother and father of the bride at our wedding. I stayed at her Wainui home with my daughter Kimberley the evening before, and we walked across the road once we got the signal from Barry that all was ready. The ‘aisle’ was the sand-dunes of this spectacular beach, and we headed arm-in-arm to the driftwood and sunflower adorned ‘altar’.
The mother of the bride
Walking me down the aisle/sand dunes
Beautiful woman
Therése sold her Wainui home some years ago, knowing it was too far from the city, and too much to maintain as she aged. She bought a unit at a fabulous ‘Lifestyle Village’ in a place called Beetham, in Gisborne.
Saying haere ra in March 2013
When we left Gisborne in March 2013, Therése was among the crowd of family and friends who farewelled us. It was heartbreaking to leave her, but my priorities had to be with my birth parents. She understood this, but hated me going. She’d call me frequently – generally around 7am due to the time differences!
Around the same time as dad had a stroke, May 2014, I heard that Therése had suffered a similar problem. I was distraught, knowing I couldn’t leave dad to go and see her, and that I may never see her again. I managed to call her while we were at St Richard’s Festival in Droitwich, and speak to her, which was comforting. Like June though, she was packed-full of fortitude, and she rallied and recovered. She never did drive again which upset her immensely, but she did return home.
In early 2016 she moved from there to Beetham Healthcare, the Nursing Home, where thankfully mum and I were able to visit and take her out a few times. She seemed so happy there, surrounded by amazing nurses, carers and friends. I was also able to spend precious time with her in March 2017.
Out to the Verve Cafe February 2016, with mum
A beach outing March 2017
With Therése in March 2017
Rest in peace my darling friend.
Good Night Irene
A mere five weeks later, on 14th May 2018, my birth mum Irene unexpectedly died. It was a dreadful shock for us all, though I’m increasingly realising as time moves on it was quite a perfect passing for her. Far preferable to one I’d imagined.
When Barry and I arrived in UK in May 2009, for our first six months of narrow boating adventures, we’d remarked gratefully how amazing it was that both sets of our parents were still alive and together. Barry’s dad Frank sadly succumbed to a brain tumour and died in November 2009, aged 89. My dear dad experienced a slow decline from his previous full and active life, from our arrival in March 2013 until his death in February 2015 aged 94.
Consequently nine years on from those fateful words, we’re both now orphans.
It feels weird. Much of those intervening years I’ve been instrumental in accessing health and social care for them all, in NZ and then UK. I do increasingly feel a sense of relief that fighting to do all I could to keep them as cared for and safe as possible is over. I wish it was easier to navigate the health and social care system. It’s an absolute minefield in my experience. Thank goodness I do have those qualities previously mentioned, because it’s the only way I got as far as I did!
Aged seven years
Irene Kirton was born in Sunderland on 24th March 1833 (though if you read her order of service it’ll tell you the 23rd – whoops!). She was the only child of Jack and Alfena Kirton. As a child I remember Alfena seemed to revel in tales of a terrible traumatic birth. Having witnessed a few of those personally (and my first experience was sadly quite awful, as the aforementioned GP decided he’d come and ‘do the birth’, nothing like a bit more ‘punishment’ for the sinful teenager), I can imagine in 1933 there would’ve been some indelible life-changing horrors in the birthing world.
Severn Valley Train trip in 2015 with mum – we chatted about her experiences as a wartime evacuee
Not long after the outset of the First World War, mum was sent south to the country in 1939 as an evacuee. Aged just six years old. Her mum and dad would travel down frequently on Jack’s motorbike. Mum told me the other children there used to hit her and call her names. It didn’t take long for Alfena and Jack to decide they missed her too much, and didn’t feel she was any safer in Oxfordshire than Sunderland, and they went and picked her up a few months later. What an unimaginable experience that must have been for her.
Irene flourished in her teenage years, and had a group of friends she went walking in the Yorkshire Dales and Lake District. She had a long-term boyfriend, Ray, for many years and was a very beautiful woman. Her school friend who now lives in Florida, told me recently mum and another girl constantly vied to be top of the class. Being extremely intelligent, she gained a place at University and was one of only four women in a class of over 50, at Birmingham University from the age of 18.
It was obvious from talking to her she adored life in Birmingham, and the freedom of living as a student. However she also studied well, gaining a First Class Honours Degree in Chemistry, and winning the Frankland Prize in July 1954. It’s intriguing that said prize was a book, ‘The New Naturalist:Britain’s Structure and Scenery’. Decades later, with dad, she had little choice but to join him on naturist holidays! What a difference two letters makes …
After leaving University Irene got a job as a Research Chemist with Cortaulds in Coventry. Irene and Don became a couple in November 1954, and married in July 1955. A whirlwind romance! Dad was 13 years older than mum, and he’d travelled widely before marrying. Mum had been offered a prestigious post in Scotland but turned it down to become a wife. I guess that’s what was expected in the 1950’s? I suspect she had moments of regret around this, as not long afterwards my older sister Katherine was born in May 1958. Followed by me 15 months later. A planned home birth the midwife only just managed to be in attendance at. My father, knowing my ‘due date’ was two weeks later, was away on business. Poor mum was at home, alone, with my toddler sister sleeping when she laboured. She had to waddle next door twice to get Peter, the neighbour, to walk to the telephone box to call the midwife, who was initially dismissive – probably wanting to stay in her warm bed! It’s unbelievable nowadays with the connectivity we enjoy, to imagine how challenging it would have been for mum. What an amazing woman.
She went on to have my other two sisters, Linda and Vivien over the next few years. Dad was desperate for a son, but after daughter number four was born he decided he couldn’t afford to take another chance, bought himself a train set, and had ‘the snip’.
For many years mum worked as a Science teacher. She even taught at the John Willmott, the Grammar School I attended from 1971 to 1976. She incredibly balanced an almost full time job with caring for four children, and a husband, and for a few years my elderly and often cantankerous grandma Alice Maud too. Unsurprisingly the overwork and stress caused her to experience symptoms of a stomach ulcer, and her doctor advised she needed to slow down. Dad must’ve been beside himself, as his own father had died suddenly when dad was only 14 – of a burst stomach ulcer!
In 1977, mum became the second mum to my own daughter, Lisa Marie, while I did my Registered General Nurse training at Kidderminster General Hospital. I shall always be grateful to her and dad for supporting me so much during that time, enabling me to have a subsequent 35 year career as a nurse and then a midwife.
I recall mum saying to me, “Thank you for making my life more adventurous.” She and dad had regularly driven to Germany when I lived there from 1981 to 1985, and they’d toured Holland, and Berlin amongst other places on those holidays.
Then in March 2002, mum and dad travelled to New Zealand to spend time with me, and for five weeks we toured the North Island together. Dad celebrated his 82nd birthday there. Amazing. I got to know them both quite intimately, sharing backpacker bedrooms along the way, and we had many giggles and extraordinary experiences. Mum got dad to buy her a carved bone ‘Manaia’, from Wai-o-Tapu for her 69th birthday, and wore it almost every day from then on.
A young and very beautiful Irene
At Durham with mum’s parents Alfena and Jack Kirton
Holiday in the Isle of Wight around 1975
Mum being mum to Lisa, Cromer, 1977
Grandad Kirton’s funeral
Dad and mum in New Zealand, March 2002
This treasured spiritual guardian carving stayed with her until the very end.
After I immigrated to New Zealand in January 2004, mum was a significant support to my younger daughter Kimberley, when she was in need of a mother figure.
Reading the book of family love on her 80th birthday
Before we arrived in March 2013, I collated photos and stories from all her family about what they loved about her. We presented it to her on her 80th birthday in the Lake District. On the day before she died, two of my sisters visited her and took her for lunch with their families. I’m told she’d been reading the book from us all that day. That was such a comfort to me.
I was extremely grateful to be able to take her back to Aotearoa, in January 2016, to commemorate the anniversary of dad’s passing and remember the special times we all shared there.
Mum and dad and their four girls, April 2007, taken by Barry
Summer 2008
Summer 2008
Aboard Northern Pride, 2009
Accompanying me to Northern Pride for our narrowboat wedding, 26th September 2009
Accompanying me to Northern Pride for our narrowboat wedding, 26th September 2009
A smile to light up the world
Mum’s 80th March 2013
Wainui Beach, January 2016
Cruising round Poverty Bay, Gisborne
Rangimarie, Anaura Bay, where Barry and I spent our honeymoon in 2009
I love this image of mum at Mahia, January 2016
Out for her birthday, March 2015
On the beach in Brighton, 2016
At the Chinese restaurant near her home, shortly after my birthday last year
Devastating dementia
In the spring of last year, I noticed mum displaying similar characteristics to those I’d seen in dad when we first returned to UK in 2013. This time, with the benefit of hindsight, I recognised symptoms of early Alzheimers Disease. It took six months of patience and persistence to obtain a definitive diagnosis, and commence Donezpezil Hydrochloride, to try and slow the progress of this debilitating condition. Fortunately it worked. She suffered short-term memory loss, but never deteriorated to the extent dad had.
Visiting us at our Lichfield Calendar Club store, December 2017
Christmas Day 2017
On the steps of the home she loved, the longest ever, 20 years
Her daily walk around the Park Home site where she lived, with Frankie
I knew though it was only a matter of time. She had as much support as possible to remain at home, where she felt safe, and where she talked to dad. She never recovered from his death, and spoke of how much she missed him every day. She’d talk to him frequently, especially as she went to sleep. I’d love to think they’re together somehow.
At my younger sister’s wedding, February 2015, only a week after her soulmate had died
I wasn’t prepared for her sudden death from a massive heart attack whilst in the bath – one of her comforts each day. None of us were. For mum though, it seems it was a blessing.
Alzheimer’s Fundraiser 59 years after she birthed me
In memory of mum, and for all the amazing people who supported her on her final journey, we chose to request donations to Alzheimer’s Society for her funeral in lieu of flowers.
We raised just under £200 for this valuable organisation.
A couple of weeks ago I was impressed to read a post from Facebook, asking if I wanted £5 for the charity of my choice for my upcoming birthday. No strings attached. 100% donation. It also suggested I ask family and friends too, and set up a fundraising page. ALL the money raised I was assured goes directly to the chosen charity.
How could I refuse? With little hesitation I took up their generosity. Which charity do you think I chose?
Of course. It was a no brainer. British Heart Foundation could have been the one, but to be honest we had no idea she had a heart problem until it stopped suddenly! I chose Alzheimer’s Society. My target was £150. So far I’ve raised £159 thanks to generous people.
My birthday is today, 28th September. The page will run until Monday 1st October. If you’d like to donate, please go to this link – https://www.facebook.com/donate/278801879622658/
If you’re reading this after said date, please give anyway, directly, and mention Irene Walsh if you feel it’s appropriate – https://www.alzheimers.org.uk
Thank you for reading my cathartic words 🙂
My first birthday without a mum in the world I've wanted to write this tribute for many months. Unashamedly there follows a rather extensive post, one of the longest I've ever published.
#Aeromonas#Alzheimer&039;s Disease#Alzheimer&039;s Society#Dog and Doublet#family#Gisborne#Manaia#Matriarchs#Mothers#New Zealand#Queenstown#Wainui Beach
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Take action and help improve the lives of people with dementia
Take action and help improve the lives of people with dementia
‘This year, Dementia Awareness Week is changing to Dementia Action Week (21 to 27 May). Raising awareness and offering support will always be important, but it’s time we all act to make change happen for people affected by dementia.
In the UK, one person develops dementia every three minutes, yet too many people feel excluded and face the disease alone.’ Alzheimer’s Society
That’s why, this…
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Chicago's Corr Kendricks Drops "Best of Me"
Chicago's @CORRKendricks Drops "Best of Me"
Corr Kendricks links with producer Pop Traxx for a melodic new street anthem, “Best of Me.” Featuring Jayy Guapo, the two MCs tell stories of fake friends, and overcoming obstacles, while remaining optimistic through the struggle, and Kendricks uses his rugged voice to deliver the catchy chorus. Stream “Best Of Me” below, and be on the lookout for even more new music from Corr Kendricks in the…
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#Allies of World War I#Alzheimer&039;s Society#American Swedish Institute#Andrew House#Asylum seeker#Axis powers#Babysitting#Best of Me#Chicago#Corr Kendricks#Donald Trump#Jayy Guapo#Pop Traxx#United Kingdom#United Nations
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Study: 100,000 Moroccans Live with Alzheimer’s Disease
Study: 100,000 Moroccans Live with Alzheimer’s Disease
Rabat – The study warns that the number of individuals living with dementia will continue to increase in the coming years, which will put pressure on the country’s economy.
Although the country does not provide official statistics on the prevalence of dementia or Alzheimer’s, the study estimated that the rate of Alzheimer’s disease is not as high as other countries.
According to the 2017 World…
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#000 cases of Alzheimer&039;s in Morocco#100#Alzheimer&039;s disease in Morocco#Dementia in Morocco#Morocco#News#Society
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DAILY DOSE: Controversial Alzheimer's drug dropped; Social media CEOs join Congressional circus.
ALZHEIMER’S DRUG BITES THE DUST. Biogen, a biotech company, has ceased all work on Aduhelm, its Alzheimer’s drug, due to its failure in the market following a controversial approval in 2021. The rights to the drug are reverting to Neurimmune. Biogen also discontinued the Phase 4 ENVISION trial, mandated by the FDA, as previous trials didn’t conclusively prove Aduhelm’s effectiveness in slowing…
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#Africa#Alzheimer&039;s disease#artificial intelligence#Asia#Australia#cancer#drug development#Europe#evolution#Featured#North America#pollution#social media#society#South America#technology
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Stunning gene therapy breakthroughs are a riposte to our truth-tarnished times
This article titled “Stunning gene therapy breakthroughs are a riposte to our truth-tarnished times” was written by Robin McKie, for The Observer on Sunday 17th December 2017 05.35 Asia/Kolkata
There has been a surprising outbreak of the use of the c-word among medical researchers over the past few days. Normally cautious in their language, they have nevertheless been wielding the term “cure”…
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#Alzheimer&039;s#Article#Biology#Comment#Cystic fibrosis#Dementia#Genetics#Huntington&039;s disease#Main section#Medical research#Opinion#Robin McKie#Science#Society#The Observer
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Stunning gene therapy breakthroughs are a riposte to our truth-tarnished times
This article titled “Stunning gene therapy breakthroughs are a riposte to our truth-tarnished times” was written by Robin McKie, for The Observer on Sunday 17th December 2017 05.35 Asia/Kolkata There has been a surprising outbreak of the use of the c-word among medical researchers over the past few days. Normally cautious in their language, they have nevertheless been wielding the term “cure”…
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#Alzheimer&039;s#Article#Biology#Comment#Cystic fibrosis#Dementia#Genetics#Huntington&039;s disease#Main section#Medical research#Opinion#Robin McKie#Science#Society#The Observer
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Local authorities failing to meet dementia care targets | Care Industry News
Local authorities failing to meet dementia care targets | Care Industry News
Today, Healthwatch England has published new data showing that overstretched councils across England are struggling to meet key legal duties in social care services for people with dementia.
The Care Act, which came into force in April 2015, says that councils must ensure that their social care services are responsive to people’s specific needs. To do this, they must review people’s care plans at…
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#Alzheimer&039;s Society#Care#Decades of squeezed Government funding has left the social care system on its knees#dementia#dementia support services#Healthwatch England#Healthwatch England has published new data showing that overstretched councils across England are struggling to meet key legal duties in soc#Jeremy Hughes CBE Chief Executive Officer of Alzheimer’s Society#Local authorities failing to meet dementia care targets#NHS Digital#reassessments#Social Care#social care responsibilities
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Seize the day! Sign up for Exeter Memory Walk
Seize the day! Sign up for Exeter Memory Walk
Andrea’s mum, Jean, with two of her grandchildren. Thousands of people are being called on to unite against dementia by signing up for Alzheimer’s Society’s Exeter Memory Walk. (more…)
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