http://www.aarp.org/home-family/caregiving/info-2014/caregiving-muhammad-lonnie-ali-parkinsons.html
Showing posts with label Parkinson's disease. Show all posts
Showing posts with label Parkinson's disease. Show all posts
Sunday, June 05, 2016
Sunday, September 21, 2014
Parkinson's Not The End Of The World
Parkinson’s disease not end of the world - http://www.themalaysianinsider.com/opinion/anthony-sb-thanasayan/article/parkinsons-disease-not-end-of-the-world
Thursday, July 11, 2013
WHEEL POWER: Living Positively With Parkinson's
Columnists
wheel power x
Wheel Power
Published:
Thursday July 11, 2013 MYT 12:00:00 AM
Updated: Thursday July 11, 2013 MYT 9:31:59 AM
Updated: Thursday July 11, 2013 MYT 9:31:59 AM
Coming to terms with Parkinson's
WHEEL POWER BY ANTHONY THANASAYAN
Supportive
spouse: Siti Khalijah Isa is glad that she has more time to spend with
hubby Abdul Majid Abdul Rahman since retiring in January.
Parkinson’s patients need all the support they can get.
WHAT would you do if you suddenly discovered that a loved one has been living with a serious medical condition for nearly a decade? And all that while you and most of your family members were blissfully unaware of what was going on?
This was the nightmarish situation that Siti Khalijah Isa, 56, faced three years ago when she found out that her husband Abdul Majid Abdul Rahman, 60, had Parkinson’s disease. Parkinson’s is a progressive disease of the nervous system marked by tremors and muscle rigidity.
The person who broke the bad news to Khalijah was Majid’s doctor. Majid had a vague understanding that something was wrong with him from as early as 2002. But Majid, an army retiree, did not want news of his health condition to affect his family. He thought that what his family didn’t know wouldn’t hurt them.
Majid continued to live his life as normally as he could. He helped with house chores, and drove his wife and children to and from school. Khalijah was a senior assistant principal in a secondary school in Kuala Lumpur at that time before she became headmistress.
The heavy responsibilities of work kept the headmistress occupied most of the time. However, relatives and friends began to notice the tell-tale signs of Parkinson’s in Majid.
Majid began to have trouble walking. Then his body became weaker, especially on his left side. People started noticing that when Majid walked, only his right hand would swing along with his movements.
This was never discussed with Khalijah or the rest of the family. In fact, Majid did a good job of hiding everything from them.
Whenever he went to see the doctor, he would make sure that he was alone. Either he would drive to his appointment on his own or insist on being dropped off and picked up later.
But soon it became impossible to keep his condition a secret. His worsening physical symptoms forced him to go for a thorough medical check-up. Majid was diagnosed with Parkinson’s.
By then Khalijah knew her husband was on some form of medication. However, she decided to give Majid more time until he was ready to talk about it. Then, one day, Majid asked his wife to accompany him to the hospital.
Today, both Khalijah and Majid are very much aware of Parkinson’s and what needs to be done to tackle it.
Majid now has a wheelchair on standby for those times when he experiences sudden weakness and “freezing moments” when he is unable to move his body.
“Our neighbours are pretty helpful,” says Khalijah. “Whenever my hubby goes jogging around our neighbourhood, our maid pushes his wheelchair next to him. When he experiences a freezing episode, the chair is ready by his side to prevent him from falling. The neighbours also chip in by pushing him home in his wheelchair.”
Since Khalijah retired in January this year, she has been able to spend more time with her husband.
She is also very encouraged by the support she gets from the public when they attend any function.
“People are always willing to help by offering to carry his wheelchair out of the car or simply encouraging us on,” says Khalijah.
Majid is exempted from fasting during Ramadan. This is because he has to take six types of medication, nine times a day for his condition. The dosages start from 7am to 9pm. Some of the tablets have to be taken before food, and others after meals.
Majid and Khalijah take everything in their stride and make it a point to live as normally as possible. They attend breaking fast events and Friday prayers in the mosque.
Then there’s the weekly self-help sessions at the Malaysian Parkinson’s Disease Association centre in Kuala Lumpur where the couple get all the motivation they need to continue their fight against a most insidious disease.
To find out more about the Malaysian Parkinson’s Disease Association, please call 03-7980 6685 (Tuesday to Saturday).
Saturday, October 13, 2012
Blind And Parkinson's Events Today
TWO terrific events are
taking place this weekend involving people with disabilities.
The first is in the morning of
today at the community forest in Kota Damansara in Petaling Jaya, Selangor.
If you think that being blind is
no fun – think again!
As many as 100 blind Malaysians
will be having a time of their lives by taking a walk through the Kota
Damansara Community Forest Park – said to be the oldest in Peninsular Malaysia.
The eager and raring to go group
of all ages and backgrounds will be led by Selangor executive council member
for the environment Elizabeth Wong.
The VIP and her visually
impaired friends will be spending as long as 1½ hours with the forest’s unique
fauna and flora, including its trademark artificial lake.
The event is to commemorate
World White Cane Day (WWCD) which falls on the same day. WWCD is an occasion
for the blind to highlight their concerns to a sighted world.
For most of the blind, it will
be their first experience being so close and personal with Mother Nature.
“Many blind persons have never
been inside a forest. This will be a rare opportunity for them to do so,” says
Yam Tong Woo, 59, who is blind himself.
“Each blind person will be
assigned with a sighted volunteer who will then take them into the forest and guide
them to touch and smell the abundance of the pioneer plants and rare species
there in order to appreciate them,” adds Yam, who is protem president of a
newly registered society called the “Adult Blind Association of Selangor”.
Yam goes on to point out that
one doesn’t necessarily need the gift of sight to be able to appreciate the
forest.
“I know many sighted people who
don’t even stop to admire the forest when they are in it. In fact, it is the
blind who tend to ironically appreciate the greenery more,” says Yam, the
organising chairman of the event.
Saturday’s event which is also
organised by the Friends of Kota Damansara group and the Petaling Jaya City
Council intends to give the blind a sense of independence in the forest.
“The ultimate goal is to show
the blind that they can do virtually anything that the sighted can.” Concludes
Yam.
If you are blind and would like
to take part in the programme which starts at 8am, please contact Yam at 012
305 3853.
Malaysians living in Ipoh,
Perak, meanwhile, will be able to know more about Parkinson’s disease – and how
to stay on top of the condition if they have it.
A public forum to empower
Persons with Parkinson’s (PwP) and their caregivers will be held this afternoon
from 1.30pm to 5pm at Syuen Hotel at 88, Jalan Sultan Abdul Jalil in the
city.
Attendees of the event will get
to hear everything about the insidious disease of the nervous system which
causes the muscles to become stiff and the body to shake, and which gradually
gets worse as a person gets older.
The event will share the latest treatments
as well as knowledge on how to become a more effective caregiver for PwP.
Dr Lim Shen-Yang, a consultant neurologist
and professor of medicine at the University of Malaya will be one of the
speakers.
Prof Dr Lim who lectures locally
and abroad is medical advisor to the national Malaysian Parkinson Disease
Association based in Kuala Lumpur which is organising the Ipoh event.
A second speaker is Mr Tarun
Amalnekar who is physiotherapist and
lecturer in Masterskill Global College in Ipoh itself.
He will share on his expertise
in choosing the best exercise activity for PwP which is crucial in fighting
against Parkinson’s.
Another highlight of the
afternoon session which will certainly prove interesting are stories of
struggles by a couple of PwP themselves.
“Despite having Parkinson’s
myself, I am delighted to be given the challenge to be organising chairman of
the forum,” says Samuel Ng who got the disease five years ago when he was 42
years of age.
“We are targeting about 200
people. We hope PwP will make it a point to attend the event rather than shying
away in their homes,” he adds.
“When I was diagnosed, I found
it difficult to accept that I had become a PwP. But when I started having it
treated – including my depression over it – I started to be able to take
control of my life again and be positive in the face of Parkinson’s.” Concluded
Samuel.
Samuel can be contacted at 012
557 1682.
The End
Friday, October 12, 2012
Parkinson's And Blind Events Tomorrow
Thursday October 11, 2012
Forest walk for the blind
WHEEL POWER
By ANTHONY THANASAYAN
IF you think that being blind is no fun – think again! This Saturday, as many as 100 blind participants will be having the time of their lives as they take a walk through the Kota Damansara Community Forest Park in Petaling Jaya, Selangor. It is said to be the oldest forest reserve in Peninsular Malaysia.
The group will be led by Selangor executive council member Elizabeth Wong. The event is to commemorate World White Cane Day (WWCD) which falls on Oct 15. WWCD is an occasion for the blind to highlight their concerns to a sighted world.
For most of the participants, it will be their first experience being up close and personal with Mother Nature.
“Many blind persons have never been inside a forest. This will be a rare opportunity for them to do so,” says Yam Tong Woo, 59, organising chairman of the event.
“Each blind person will be assigned a sighted volunteer who will guide them as they walk through the park. They will get to touch and smell the plants and rare species to better appreciate them,” says Yam, who is pro-tem president of a newly registered society called the Adult Blind Association of Selangor.
Yam points out that one does not necessarily need the gift of sight to be able to appreciate the forest.
“I know many sighted people who don’t even stop to admire the forest when they are in it.
“In fact, it is the blind who tend to appreciate the greenery more,” says Yam.
The event is organised by Friends of Kota Damansara and the Petaling Jaya City Council.
“The ultimate goal is to show the blind that they can do virtually anything that the sighted can,” adds Yam.
Meanwhile, a public forum to empower Persons with Parkinson’s (PwP) and their caregivers will be held on Oct 13 at Syuen Hotel, Jalan Sultan Abdul Jalil, Ipoh.
Participants will be able to know more about this insidious disease of the nervous system which causes the muscles to become stiff and the body to shake, and which progressively worsens as the patient grows older.
The forum will share the latest treatments as well as knowledge on how to become a more effective caregiver for PwP.
Dr Lim Shen-Yang, a consultant neurologist and professor of medicine at Universiti Malaya, will be one of the speakers.
Dr Lim is medical advisor to the Malaysian Parkinson’s Disease Association in Kuala Lumpur, which is organising the event.
Tarun Amalnekar, a physiotherapist and lecturer at Masterskill Global College in Ipoh, will also be speaking at the forum.
Tarun will offer advice on the best exercises for PwP in their fight against Parkinson’s.
A couple of patients will share their struggles with Parkinson’s.
“I am delighted to be given the challenge to be organising chairman of the forum,” says Samuel Ng, who was diagnosed with Parkinson’s five years ago when he was 42.
“Initially, I found it difficult to accept my condition. When I sought treatment, I started to take control of my life again and be positive in the face of Parkinson’s,” adds Ng.
The blind who would like to take part in the Kota Damansara Community Forest Park walk on Oct 13 can contact Yam Tong Woo at 012-305-3853. Those who would like to attend the public forum on Parkinson’s can contact Samuel Ng at 012-557-1682.
PET+BLOGSPOT is the ONLINE BLOG of the Malaysian Animal-Assisted Therapy for the Disabled and Elderly Association or Petpositive. Our stories are CURRENT, ACCURATE and RELIABLE. We offer both local and foreign news on animals, disability and the elderly. PET+BLOGSPOT was first established in October 2007. Our hits since then are now 150,000 and ever increasing! PET+BLOGSPOT is updated daily. Kindly note that views expressed in PET+BLOGSPOT are not necessarily those of PETPOSITIVE. You may also visit our Webpage by browsing: www.petpositive.com.my You can also find us in Facebook under PETPOSITIVE EMPOWERMENT. Please sign up as a FOLLOWER of this Blog if you haven't done so already in order to show us your kind support for our work. Thank you!
Wednesday, August 22, 2012
Michael J Fox To Return To TV More Powerful Than Ever
BBC ONLINE 21 August 2012
Last updated at 08:49 GMT
Fox set up his own foundation to research a cure for Parkinson's in 2000
Michael J Fox to make full-time TV return
Fox set up his own foundation to research a cure for Parkinson's in 2000
Twelve years after giving up full-time acting to focus on fighting Parkinson's disease, Michael J Fox will star in a new TV comedy based on his illness.
The Back to the Future star will play a father of three dealing with the degenerative nervous system disorder.
NBC television called Fox "utterly relatable, optimistic, and in a class by himself".
In recent years, Fox gradually returned to TV with recurring roles in the likes of Boston Legal and The Good Wife.
However, the new 22-episode sitcom marks his first long-term commitment to a show since he left political comedy Spin City in 2000.
"I have no doubt that the character he will create - and the vivid family characters surrounding him - will be both instantly recognizable and hilarious," said NBC Entertainment Chairman Robert Greenblatt.
Fox made his name in the 1980s TV comedy Family Ties, winning three Emmy Awards for his role as Nixon-loving, Reagan-worshipping teenager Alex P Keaton.
His movie career took off when he played teen adventurer Marty McFly in the Back to the Future franchise and starred in horror spoof Teen Wolf.
In the 1990s the 51-year-old actor's role in TV political comedy Spin City won him an Emmy, three Golden Globes, and two Screen Actors Guild Awards.
Fox won three Golden Globes for his role in political comedy Spin City
Having been diagnosed with Parkinson's disease in 1991, Fox took the decision to semi-retire from acting in 2000 as his symptoms worsened.
He founded the Michael J Fox Foundation dedicated to finding a cure for the disease, promoting the development of improved therapies and raising public awareness.
The Canadian actor continued to guest star in shows including Scrubs and Curb Your Enthusiasm, as well as doing voice-over work for the Stuart Little movies.
Filming for the new sitcom, loosely based on Fox's own personal life, will start this year with the rest of the cast still to be announced.
The actor said he was "extremely pleased" to be working on the show.
In May he told ABC News in the US that a new drug regimen had helped him control the tics that are a result of the disease and could allow him to take on more acting roles.
"To bring Michael J. Fox back to NBC is a supreme honour," said Greenblatt. "We are thrilled that one of the great comedic television stars is coming home again."
The as-yet-untitled series will be broadcast from autumn 2013.
The Back to the Future star will play a father of three dealing with the degenerative nervous system disorder.
NBC television called Fox "utterly relatable, optimistic, and in a class by himself".
In recent years, Fox gradually returned to TV with recurring roles in the likes of Boston Legal and The Good Wife.
However, the new 22-episode sitcom marks his first long-term commitment to a show since he left political comedy Spin City in 2000.
"I have no doubt that the character he will create - and the vivid family characters surrounding him - will be both instantly recognizable and hilarious," said NBC Entertainment Chairman Robert Greenblatt.
Fox made his name in the 1980s TV comedy Family Ties, winning three Emmy Awards for his role as Nixon-loving, Reagan-worshipping teenager Alex P Keaton.
His movie career took off when he played teen adventurer Marty McFly in the Back to the Future franchise and starred in horror spoof Teen Wolf.
In the 1990s the 51-year-old actor's role in TV political comedy Spin City won him an Emmy, three Golden Globes, and two Screen Actors Guild Awards.
Fox won three Golden Globes for his role in political comedy Spin City
Having been diagnosed with Parkinson's disease in 1991, Fox took the decision to semi-retire from acting in 2000 as his symptoms worsened.
He founded the Michael J Fox Foundation dedicated to finding a cure for the disease, promoting the development of improved therapies and raising public awareness.
The Canadian actor continued to guest star in shows including Scrubs and Curb Your Enthusiasm, as well as doing voice-over work for the Stuart Little movies.
Filming for the new sitcom, loosely based on Fox's own personal life, will start this year with the rest of the cast still to be announced.
The actor said he was "extremely pleased" to be working on the show.
In May he told ABC News in the US that a new drug regimen had helped him control the tics that are a result of the disease and could allow him to take on more acting roles.
"To bring Michael J. Fox back to NBC is a supreme honour," said Greenblatt. "We are thrilled that one of the great comedic television stars is coming home again."
The as-yet-untitled series will be broadcast from autumn 2013.
Related Stories
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- 22 AUGUST 2010, ENTERTAINMENT & ARTS
- 26 OCTOBER 2010, ENTERTAINMENT & ARTS
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Related Internet links
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Saturday, June 23, 2012
Struggling With Parkinson's
WEEKEND VIEW: WHEEL POWER
(Start of Article)
SAMUEL NG was the epitome
of health at one time until his whole world suddenly came crashing down.
It happened nearly five years
ago. Samuel was living in his hometown in Ipoh in the state of Perak where he
still resides today.
Then 42-years of age, Samuel was
working for a top pharmaceutical company.
His associates and friends regarded
him as not only one of the most active persons around but Samuel was known for his
good and healthy way of living.
For Samuel, it was always a must
to have a balanced diet. He would exercise regularly and never touched a
cigarette.
He also regarded alcohol as a
major enemy. No one could ever bring him near a bottle.
After all, as the breadwinner of
the family – his lovely wife Chris and his loving teenaged children Gibson, 20
and Rachel, 17, the medical executive, husband and father always thought of his
family as the greatest gifts and treasures in his life.
These alone were motivation and reason
enough to stay healthy in life.
Then one evening after dinner,
everything changed.
“I suddenly started to feel a
sharp pain in my stomach,” Samuel told Wheel Power last week.
“I wasted no time in having
myself checked by a doctor the next morning,” Samuel added.
An ultrasound discovered stones
in Samuel’s gallbladder. They were quickly removed through key-hole surgery.
Samuel thought that that was the
end of his health problems but he was mistaken.
A week after the operation,
Samuel noticed a certain stiffness that had crept up over his left hand. It kept
coming and going off.
That landed him inside the
consultation room of another doctor – this time a neurologist.
After a simple test of walking a
few metres, sitting and standing and raising his hand up and down, he received
a rude shock from the specialist.
“I was told point blank that I
had Parkinson’s disease (PD),” said Samuel.
(Parkinson’s
is a progressive disease of the nervous system that weakens the muscles and
makes the limbs to shake)
“My immediate reaction was one
of denial,” Samuel went on.
“I scoffed at the doctor saying
he must have been seeing too many PD patients. A bright career was just starting
for me at age 42 and this was no time for me to be dealing with this.”
But the doctor paid no attention
to Samuel’s complaints.
Instead, Samuel was given
medications to treat his condition.
But Samuel just threw it away
because of some side effects and went back to work. The stiffness on his hand
got worse and it got more difficult to sleep at night.
In desperation Samuel went for
further consultations with other doctors but they all arrived at the same
conclusion.
“I tried every single thing I
could to make my job work for me because I didn’t want to let down my family
but things just got worse.
“The breaking point came when I
couldn’t wear my shirt by myself and started walking like a robot. I had to
depend on others to do things for me which I could do by myself previously.”
After 16 years in the company, Samuel
finally told his boss about his illness. They had no choice but to let him go.
“It was being at home and doing
nothing that made me start worrying about the future and going into depression.
“Even at that point, I still
refused to accept that I had PD. I felt useless, hopeless and afraid. There
were even moments when I couldn’t control my anger and ended up breaking some
things just to release my frustration.
“The situation was also
especially difficult for my family to take, seeing me in such a way.”
But change came about for Samuel
when he finally met a neurologist in hospital in Kuala Lumpur. The specialist
“tailor-made” a special combination of drugs to tackle each and every of the
symptoms that was troubling Samuel.
Because of this careful
listening to Samuel’s problems, the right kind of medications helped improve
his condition little by little.
Although there is still no cure
for PD, Samuel has learnt other ways to live on top of his condition.
“That includes in going out and
meeting other People with Parkinson’s and their caregivers so that one can
learn from the experiences and challenges of others facing the same disease,”
Samuel, now 47, explained.
“The first step is to accept
your condition. Next, dream big dreams, especially of those where despite our
conditions, we can still play a part in helping other people like ourselves.
“There is no limit to what we
can do: help set up support groups for PD persons, get the government to make
positive changes to help us, educate the public about what PD is about, etc.
“As they say, the sky is really
the limit,” concluded Samuel.
Samuel spent Father’s Day with
his family on Sunday enjoying special dishes made by Gibson who is doing a
degree in hotel management.
THE END
PET+BLOGSPOT is the ONLINE BLOG of the Malaysian Animal-Assisted Therapy for the Disabled and Elderly Association or Petpositive. Our stories are CURRENT, ACCURATE and RELIABLE. We offer both local and foreign news on animals, disability and the elderly. PET+BLOGSPOT was first established in October 2007. Our hits since then are now 150,000 and ever increasing! PET+BLOGSPOT is updated daily. Kindly note that views expressed in PET+BLOGSPOT are not necessarily those of PETPOSITIVE. You may also visit our Webpage by browsing: www.petpositive.com.my You can also find us in Facebook under PETPOSITIVE EMPOWERMENT. Please sign up as a FOLLOWER of this Blog if you haven't done so already in order to show us your kind support for our work. Thank you!
Thursday, April 26, 2012
Finding Cure For Parkinson's/Dementia On The Rise
A COUPLE of significant developments took place last week on the international level where people with disabilities and the elderly are concerned.
I thought it a must to mention
them in my column for this week.
The first was some good news for
persons with Parkinson’s disease and their caregivers.
It was announced on BBC World
Service radio that the world’s biggest research study into the cause of
Parkinson’s disease is to take place soon.
It will be headed by Dr Donald
Grosset, a neurologist at Glasgow University in the United Kingdom.
According to the BBC report, the
brain condition affects almost 130,000 people in the UK.
And Dr Grosset says he hopes the
milestone research will be able to find better ways of both diagnosing and
treating the disease.
In order to do this, Charity
Parkinson's UK is looking for as many as 3,000 volunteers with the condition –
as well as their siblings - to take part in the study.
Parkinson's is a debilitating
condition. Its symptoms include tremors, mood changes, difficulties in movement,
loss of smell and speech problems.
Charity Parkinson’s says it was
investing more than £1.6m in the Tracking Parkinson's study with the long-term
aim of boosting the chances of finding a cure.
The 3000 volunteers who will be
taking part in the study will those who have recently been diagnosed with the
disease. It will also include people diagnosed aged under 50 and their brothers
and sisters.
According to the London-based
broadcaster, the purpose of the research is to identify markers in the blood
which could be used to create a simple diagnostic test for the disease,
something which currently does not exist.
Parkinson's medical experts say early
diagnosis is crucial for doctors to be able to prescribe the right drugs for
people with the condition.
The BBC adds that the responses
to various treatments of those taking part in the study will be closely
monitored for up to five years.
The project will then eventually
be linked up to 40 research centres across the UK.
Dr Grosset says the cure for Parkinson's
disease is a global challenge.
“And all the samples gathered
from our thousands of volunteers will be available for analysis by researchers
the world over,” he adds.
Apart from Dr Grosset’s
involvement, this cutting edge research will collaborate with top researchers
from Scotland, England, Wales and Northern Ireland.
"Finding a cure for
Parkinson's is like building a gigantic jigsaw, but we still have a number of
the pieces missing, says another Parkinson’s expert Dr Kieran Breen, director
of research and innovation at Parkinson’s UK.
"This vital new study will
help us fill in some of the gaps in our knowledge,” he concluded in the BBC
report.
Several Malaysian with
Parkinson’s and their caregivers meanwhile that I spoke to, welcomed the
research news. The development, they
said, has given them more impetus to fight against the insidious disease
through positive living.
Meanwhile, a report from Geneva
on the Voice Of America (VOA) broadcaster has warned the dementia cases are
poised to triple by the year 2050.
The Washington DC-based
international radio station was quoting a new report based on a population of
people with dementia from 36 million to more than 115 million.
The VOA, quoting the report from
the World Health Organisation and Alzheimer’s Disease International (ADI)
pointed out that dementia will be a major problem for people in all countries,
with more than half living in low and middle-income countries.
ADI Executive Director Marc
Wortmann says by any measure the statistics are frightening.
He says a new case of dementia
now pops up in every four seconds when 10 years ago, it was calculated at one
in every seven seconds.
“And if you look into the future
projections, it may be close to one in every second by the year 2050. So, we need to act. We need to do something to
stop this epidemic,” added Wortmann.
According to experts, dementia
is increasing because people are living longer. However, the disease is not a
normal part of growing old. Most older people do not have this condition.
Dementia is a brain disorder
caused by a variety of brain illnesses that affect memory, thinking and the
ability to perform everyday activities.
WHO Mental Health and Substance
Abuse Director Shekhar Saxena says dementia is often not recognized because it
is commonly mistaken for an age-related decline in functioning because it can
mimic age-related problems.
It also progresses slowly and is
not easily diagnosed.
Professor of Epidemiological
Psychiatry at Kings College London, Martin Prince, says dementia is not yet a
huge problem in developing countries, but that is because few people live more
than 75 years.
This is expected to change with
population growth and improved health.
WHO reports more than $600
billion a year is spent in treating and caring for people with dementia and
that figure is expected to rise astronomically.
Health officials call dementia a
ticking time bomb. But only eight countries have dementia strategies in place.
The report recommends nations
set up programs that focus on improving early diagnosis, raising public
awareness about the disease and reducing stigma, as well as providing better
care and more support to caregivers.
There is no cure for dementia,
but health officials say a great deal can be done to support and improve the
lives of people with dementia, their families and caregivers, concluded the VOA
report.
THE END
PET+BLOGSPOT is the ONLINE BLOG of the Malaysian Animal-Assisted Therapy for the Disabled and Elderly Association or Petpositive. Our stories are CURRENT, ACCURATE and RELIABLE. We offer both local and foreign news on animals, disability and the elderly. PET+BLOGSPOT was first established in October 2007. Our hits since then are now 150,000 and ever increasing! PET+BLOGSPOT is updated daily. Kindly note that views expressed in PET+BLOGSPOT are not necessarily those of PETPOSITIVE. You may also visit our Webpage by browsing: www.petpositive.com.my You can also find us in Facebook under PETPOSITIVE EMPOWERMENT. Please sign up as a FOLLOWER of this Blog if you haven't done so already in order to show us your kind support for our work. Thank you!
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