WELCOME TO OUR PARKINSON'S PLACE!

I HAVE PARKINSON'S DISEASES AND THOUGHT IT WOULD BE NICE TO HAVE A PLACE WHERE THE CONTENTS OF UPDATED NEWS IS FOUND IN ONE PLACE. THAT IS WHY I BEGAN THIS BLOG.

I COPY NEWS ARTICLES PERTAINING TO RESEARCH, NEWS AND INFORMATION FOR PARKINSON'S DISEASE, DEMENTIA, THE BRAIN, DEPRESSION AND PARKINSON'S WITH DYSTONIA. I ALSO POST ABOUT FUNDRAISING FOR PARKINSON'S DISEASE AND EVENTS. I TRY TO BE UP-TO-DATE AS POSSIBLE.

I AM NOT RESPONSIBLE FOR IT'S CONTENTS. I AM JUST A COPIER OF INFORMATION SEARCHED ON THE COMPUTER. PLEASE UNDERSTAND THE COPIES ARE JUST THAT, COPIES AND AT TIMES, I AM UNABLE TO ENLARGE THE WORDING OR KEEP IT UNIFORMED AS I WISH. IT IS IMPORTANT TO UNDERSTAND I AM A PERSON WITH PARKINSON'S DISEASE. I HAVE NO MEDICAL EDUCATION,

I JUST WANT TO SHARE WITH YOU WHAT I READ ON THE INTERNET. IT IS UP TO YOU TO DECIDE WHETHER TO READ IT AND TALK IT OVER WITH YOUR DOCTOR. I AM JUST THE COPIER OF DOCUMENTS FROM THE COMPUTER. I DO NOT HAVE PROOF OF FACT OR FICTION OF THE ARTICLE. I ALSO TRY TO PLACE A LINK AT THE BOTTOM OF EACH ARTICLE TO SHOW WHERE I RECEIVED THE INFORMATION SO THAT YOU MAY WANT TO VISIT THEIR SITE.

THIS IS FOR YOU TO READ AND TO ALWAYS KEEP AN OPEN MIND.

PLEASE DISCUSS THIS WITH YOUR DOCTOR, SHOULD YOU HAVE ANY QUESTIONS, OR CONCERNS. NEVER DO ANYTHING WITHOUT TALKING TO YOUR DOCTOR FIRST..

I DO NOT MAKE ANY MONEY FROM THIS WEBSITE. I VOLUNTEER MY TIME TO HELP ALL OF US TO BE INFORMED.

I WILL NOT ACCEPT ANY ADVERTISEMENT OR HEALING POWERS, HEALING FROM HERBS AND ETC. UNLESS IT HAS GONE THROUGH TRIALS AND APPROVED BY FDA. IT WILL GO INTO SPAM.

THIS IS A FREE SITE FOR ALL WITH NO ADVERTISEMENTS

THANK YOU FOR VISITING! TOGETHER WE CAN MAKE A DIFFERENCE!

TRANSLATE

Friday, February 19, 2016

Fox speaks on Parkinson’s disease, acceptance, family



February 18, 2016 4:06 PM

Michael J. Fox spoke to a full house at Bridges Auditorium last Friday about life, before and after being diagnosed with Parkinson’s disease.
The celebrated actor learned he had Parkinson’s, a degenerative disorder that affects the brain cells responsible for planning and controlling body movement, when he was 29. While medication offers some relief, his symptoms—which include uncontrollable shaking and twitching—have gotten progressively worse over the years.
It sounds pretty tragic. And yet, the actor insists his life is better than it would have been if he never got sick.
One of the biggest lessons Mr. Fox has learned from from Parkinson’s is how to relinquish control, a scary but necessary proposal. It can be surprisingly liberating.
“What I couldn’t do was more freeing than what I could do. I realized I could play anyone, as long as he had Parkinson’s,” he joked.
The appearance by Mr. Fox, who has a daughter attending Pomona, coincided with the school’s annual parents weekend. He covered a lot of ground in his hour-long talk, during which he fielded questions first by neuroscience professor Nicole Weekes and then by students. 
When Ms. Weekes asked if he supports the idea of universal health care, he noted that he was born and raised in Canada, a country where citizens are afforded medical coverage as a right. He can hardly be blamed for finding the notion both familiar and feasible. He asserted that all it would seem to require is for the very rich to pay a bit more in taxes.
“I’ve been to the Hamptons—I’ve seen the yachts. I just think they can kick a little in,” he said.
He then talked about his experiences as an advocate for Parkinson’s research, which have been by turns rewarding and frustrating.
In 1998, Mr. Fox testified before congress on the importance of stem cell research. He was surprised by the vehemence of the opposition.
The stem cells in question were from frozen human embryos that were scheduled to be disposed, he noted. Rather than treating them as refuse, he argued, why not use them for research with enormous potential to help people with conditions like paralysis, Parkinson’s and cerebral palsy? “We’re talking about people’s lives here,” he said.
Instead, the George W. Bush administration characterized stem cell research as an assault on human lives, referring to the embryos as “snowflake babies, which was such a George Bush thing to say,” Mr. Fox marveled.
One of the most colorful moments of the stem-cell fight was when conservative talk show host Rush Limbaugh imitated Mr. Fox, jerking his body around as he insisted that the actor’s display of symptoms was “purely an act” put on for congress.
“I wasn’t offended,” he said. “I just figured I must have really pissed him off.”
President Bush implemented a policy in August of 2001 severely limiting federal funding for stem cell research. For the remainder of his tenure, he used his veto power to override any legislative attempts to loosen that policy. 
In 2009, in one of his first executive acts, President Barack Obama rescinded the legislation limiting federal funding for human stem cell research. “In the end, I’m proud of my work,” Mr. Fox said.
Ms. Weekes shared some numbers that should also fill the actor with pride. His Michael J. Fox Foundation has garnered an astonishing $450 million towards Parkinson’s research, making it the largest nonprofit funder of Parkinson’s disease research in the world.
Stem cell research may yield a treatment for Parkinson’s, but that treatment will do little good if it’s tendered only after the signs of the disorder present themselves.
Mr. Fox started showing symptoms of early-onset Parkinson’s, beginning with a single, trembling finger, in 1991 when he was on the set of the movie Doc Hollywood. By the time he was diagnosed a year later, 80 percent of the neurological function controlling body movement had been compromised.
Since 2010, the Michael J. Fox Foundation has focused on discovering biomarkers that can help people determine if they are genetically predisposed to develop the disease. He and the scientists at work hope the research will lead to the kind of early intervention Parkinson’s requires.
A lady had a baby in a tree
Mr. Fox’s story is a well-known one. He rose to fame playing whip-smart Republican teen Alex P. Keaton in the long-running sitcom Family Ties. Film success followed, including his starring turn in the Back to the Future franchise.
Throughout the 1980s, he pushed himself hard and partied even harder in a search for fulfillment and success. Fast cars, booze and all manner of ‘80s-style excesses were the order of the day. “I was the prince of Hollywood and digging it,” he said.
He began to get some perspective after Tracy Pollan, who played his girlfriend on Family Ties, pointed out that his lifestyle was putting his career and health in danger.
Ms. Pollan, who he married in 1988, said, “What are you doing? You’re killing yourself.’”
Romance emerged from their longtime friendship, and Ms. Pollan was pregnant within a month of their marriage. The couple went on to have four children. It took a while for Mr. Fox to achieve balance, trading compulsive work for introspection and engagement and curtailing the drinking that initially ticked up after his diagnosis.
Family has since become all-important to Mr. Fox, who shared a few chestnuts of parenting wisdom. One of these can be encapsulated in the phrase: “A lady had a baby in a tree.”
After the Fox family welcomed three girls, he learned something about the estrogen-charged quibbling that ensued. “When you hear your wife and your daughters arguing in the kitchen, don’t go in there,” he said to boisterous laughter from the audience. 
When his girls were younger, they would sometimes approach him with issues that seemed as inconsequential as they were highly charged. “They’d come to me with these things, and I didn’t know how to answer them,” Mr. Fox shared.
Then, he came across a news article that offered a perspective on the kind of troubles that humans can face and overcome.
“A village had been flooded and there was torrential flooding sweeping up animals, livestock and buildings and people,” he said. “What happened was a lady had been swept up and was carried at a raucous pace seaward. She was pregnant and she somehow managed to grab onto a tree branch.”
“She got up in a tree and actually delivered her baby,” he continued. “She was rescued some hours later nursing the baby. Now whenever the kids come to me with issues, I say, ‘A lady had a baby in a tree.’”
Mr. Fox feels it’s important to note that, when he’s not medicated, he’s a wreck. It’s a reality of Parkinson’s and it’s the reason why it’s essential that a cure be found.
Just getting up in the morning is a challenge. He wakes up and his feet are cramped. He has to put on hard shoes to get his feet to conform. Next, he shuffles to the bathroom where he takes a shower, sitting on a little bench, and negotiates the difficulty of washing his hair. Mundane tasks like brushing his teeth have become laborious.
Then he shuffles into the area where he gets dressed, which is dominated by a mirror. “For a minute, I’ll look at myself, kind of all crumpled up, shaking and wet, and say, ‘What are you smiling at?’”
Mr. Fox can sometimes rue the trivialities of daily life—a transaction at a grocery store can seem overwhelming. Simply reaching into a wallet and presenting a credit card can often be hindered by tremors.
“I hate transcactions,”? he said. “When my kids are with me, I tell them, ‘You can get anything you want, as long as you handle the transcaction.’”
Luckily, medication helps him to continue to speak to people, as an advocate and an inspiration. He is still handsome and youthful in appearance, and his speech—if occasionally slurred or halting—is marked by his off-the-cuff wit.
It’s all about attitude, the thing that has kept him going since, 26 years ago, he was told that his career would be over in a decade and, soon after, he would be wheelchair-bound. “It’s not projecting into a grim future that has made my present so wonderful,” he said.
Students proceeded to pose several questions to Mr. Fox, one of which was pure, delicious silliness: “If you were a superhero, what would your powers be?”
Mr. Fox pondered the question as thoughtfully as any others at his Bridges appearance.
“I think I’d be a dog superhero. My ability would be to save dogs in peril,” he said.  And then he sang: “Here, I’ve come to save the day.”
—Sarah Torribio
storribio@claremont-courier.com
 https://www.claremont-courier.com/articles/news/t18311-fox#sthash.WZAJ8nMB.dpuf

Thursday, February 18, 2016

What Richard Sees: Insight into Lewy Body Dementia Hallucinations

FoxFeed Blog

Posted by  Ava Butler, February 18, 2016

Ava Butler, a member of The Michael J. Fox Foundation community, shares what her husband's diagnosis of Parkinson's disease and Lewy body dementia has taught her — which she takes to heart at home, and in her career.
Lewy body dementia (LBD) is not as well-known as Alzheimer’s, but it is the second most common form of dementia. More than 1.3 million Americans are impacted by LBD, but little public attention is paid to this -known disorder.
Lewy body dementia a progressive neurodegenerative dementia closely associated with Parkinson’s disease. My dear husband, Richard has both. (Editor’s note: LBD is a progressive neurodegenerative dementia that is also a form of Parkinsonism, meaning that it includes some of the motor symptoms of Parkinson’s disease, too. While most people with Parkinson’s do not also develop Lewy body dementia, studies suggest that having Parkinson’s increases your risk.)
Persistent and recurring visual hallucinations are often an early symptom of LBD. This was true for Richard. Not all LBD hallucinations are fear based, but Richard’s were. His ability to communicate clearly has been impacted and sometimes words come out in an unusual and poetic way. 
Between 2013 and 2014 I documented, as clearly as I could, exactly what Richard told me he saw. I share what he told me as a way of providing insight to those whose lives are also impacted by LBD. Here are examples of what Richard has experienced as written from his own words:
Occasionally people come in the house at night, but they go away when we turn on the lights and look around for them. 
The plants on the south balcony turned into little children again. Today they are musicians and they played for everyone down below. People danced to their music. 
Today Richard has forgotten my name. He thinks it’s James Stephen Ping, his brother’s name. Then he calls me Damaged Portilla. He forgot his name too. “My name? How would I ever know that?” he says baffled by the thought of it.
“You're making this up,” I say. “No,” says Richard, “that would be immature.”
At the time, we knew he had Parkinson’s, but knew nothing about LBD. At first, the hallucinations and dementia were far more difficult to manage than his physical symptoms. Now that his disease has progressed, his hallucinations have become more manageable and less frequent. But LBD remains our biggest challenge. 
When Richard is having hallucinations, I:
  • Respect what he sees. Dismissing his reality is not helpful, and can actually make it appear that I am not trustworthy.
  • Remind him that we are safe, and that everyone is on our side
  • Ask him to look in my eyes. This can help ground him. Remind him that I love him and secure. However, if I’m part of the hallucination and am perceived to be involved in some conspiracy, I need to back off and give him space.
  • Ask him to describe what he sees. Sometimes this causes him to focus a bit more. What he sees can give me insights into how he is feeling. Anxiety produces scary hallucinations. If he is calm and secure, the hallucinations tend to be positive.
  • Improvise to turn the negative situation into one with a positive outcome. For example, “It first looked like it was a bad guy, but he’s actually very friendly and on our side,” or “I saw that guy before and he’s harmless and is actually here to help keep us safe.” 
  • Tell him that he can instruct the people to leave him alone.
  • Walk slowly towards the hallucination and tell the people it time for them to go away now.
  • Move and talk slowly and calmly. Fast movements cause higher anxiety.
  • Be mindful of my own emotions. My own frustration, anger or stress will make things worse. https://www.michaeljfox.org/foundation/news-detail.php?lewy-body-dementia-hallucinations

IRON ACCUMULATION IN PARKINSON'S DISEASE


18th February 2016 
Iron Pills


Previous studies have claimed that there is an accumulation of iron in the brains of people with Parkinson's Disease This study was designed to explore the progressive pattern of iron accumulation at different stages of Parkinson's Disease. They were able to confirm a regionally progressive pattern of iron accumulation in the different stages of Parkinson's Disease.

The substantia nigra pars compacta, which is the primary area of the brain affected by Parkinson's Disease, showed significantly increased iron levels in people with early Parkinson's Disease. In people with advanced Parkinson's Disease, the regions of the brain with higher concentrations of iron spread to other areas of the brain (substantia nigra pars reticulata, red nucleus, globus pallid us).

Iron accumulation occurs in Hereditary Hemochromatosis. If iron accumulation caused Parkinson's Disease people with Hereditary Hemochromatosis should also have Parkinson's Disease. However, very few people with Hereditary Hemochromatosis have it. Instead of causing Parkinson's Disease, higher intake of iron is associated with a reduced risk of Parkinson's Disease. Iron is essential for the formation of dopamine, which is deficient in Parkinson’s Disease. It is a common compensatory mechanism for a cofactor such as iron to accumulate when the substance it facilitates the formation of is deficient. 
So instead of iron accumulation causing Parkinson's Disease, Parkinson's Disease causes iron accumulation.


Reference : NMR in Biomedicine [2016] Feb 8 [Epub ahead of print] (X.Guan, M.Xuan, Q.Gu, P.Huang, C.Liu, N.Wang, X.Xu, W.Luo, M.Zhang)
Complete abstract : http://www.ncbi.nlm.nih.gov/pubmed/26853890


http://www.viartis.net/parkinsons.disease/news/160218.pdf mail@viartis.net
©2015 Viartis


http://www.viartis.net/parkinsons.disease/news/160218.pdf

This glove could make eating easier for those with Parkinson's disease

Feb. 18, 2016: The Washington Post


The GyroGlove naturally steadies itself, reducing the impact of tremors. (GyroGear)
Eating can be difficult and embarrassing for those with tremors, but GyroGear thinks it has a solution for patients suffering from Parkinson’s disease or essential tremor. The start-up has created a glove that steadies a person’s hand, making it easier to complete everyday tasks such as eating.
The glove’s power lies in a bronze disc on the back of the hand, which weighs about as much as a roll of nickels. It spins at up to 20,000 rotations per minute, providing a steadying force. The force of the battery-powered disc is akin to putting one’s hand in molasses. While moving is not as easy, the benefit is that much of the shaking is naturally filtered out.

GyroGear is aiming to reduce tremors by 70 percent. In one lab test, the London-based researchers say, it reduced a tremor by 90 percent.
GyroGear founder Faii Ong was inspired by a 103-year-old hospital patient who couldn’t eat without spilling food. While cleaning her up, the medical student at Imperial College started to brainstorm solutions.
Ong cautions that there’s still work to be done. The glove hasn’t been tested by outside parties, but they plan to publish their findings in a peer-reviewed journal by the end of the year. They also hope to begin selling the product by year’s end and are raising funds from investors.
“The idea of simple, wearable devices to treat tremor and to avoid the side effects from medications or alternatively the dangers of surgery is very appealing to patients and health care providers,” said Michael S. Okun, medical director of the National Parkinson Foundation. “The GyroGlove is an interesting idea, however many of these types of devices fall short of the expectations — especially when faced with very severe and disabling tremor.”
There are other efforts to use mechanical solutions to aid those with Parkinson’s disease. Lift Labs, a start-up that Google acquired in 2014, has devised a vibrating spoon and fork to counteract tremors and make eating easier. While having shown promise for mild tremors, Okun said it hasn’t proven the most effective solution for more severe cases.
In the long term GyroGear is interested in adapting its glove to other uses, such as for surgeons, physical therapists, photographers or anyone seeking to keep a steady hand.

The glove is designed to work for two or three hours a day. (Gyrogear)

 https://www.washingtonpost.com/news/innovations/wp/2016/02/18/this-glove-could-make-eating-easier-for-those-with-parkinsons-disease/

Japanese team finds new way to create, research Parkinson's stem cells

Researchers from Juntendo and Keio universities have come up with a quicker and easier way to generate iPS cells from people with Parkinson’s disease, a discovery they claim will go a long way in developing a cure for the neurological disease.



Japan Times NewspaperFeb. 19, 2016

In a paper published Friday in the journal Stem Cell Reports, researchers led by Nobutaka Hattori and Hideyuki Okano report they have established a technology to study a large number of patients by using iPS cells derived from their blood. The key lies in their success in turning the cells into neural stem cells more efficiently, which lets them monitor how the disease progresses in test tubes. They can also study how they react to chemicals, bringing a cure closer.
“This method will allow us to use iPS cells derived from several thousand Parkinson’s disease patients treated at Juntendo University in order to study the disease mechanism,” the universities said in a statement. “We aim to create a ‘Parkinson’s Disease iPS Cell Bank’ at a scale never seen anywhere else in the world.”
Induced pluripotent stem cells are traditionally made from skin cells, requiring patients to go through a biopsy. Taking blood samples is less invasive as it leaves no scars, but blood-derived cells are harder to convert to neurons.
The researchers said they overcame this by culturing the iPS cells under certain conditions, such as in a low-oxygen environment, and converting them to neurons more efficiently. While traditional methods require 30 to 50 days for iPS cells to become neurons, the new method can achieve this in a week or two, said Wado Akamatsu, a professor at the Center for the Genomic and Regenerative Medicine of Juntendo University.
According to the Japan Intractable Diseases Information Center, 100,000 people in Japan have Parkinson’s, and the number is expected to surge as the population grays. While a tremor is the most typical symptom, the disorder is also known to cause stiffness and slow movement.
Although there are many theories about the causes, none has ever been proved and many mysteries remain. Around 10 percent of the disorder is genetic, while the rest is caused by environmental factors, Juntendo’s Hattori said.
http://www.japantimes.co.jp/news/2016/02/19/national/science-health/japanese-team-finds-new-way-create-research-parkinsons-stem-cells/?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+japantimes+%28The+Japan+Times%3A+All+Stories%29#.VsY1A8e1WoN

Frailty, falls, and hip fractures may be early predictors of Parkinson’s Disease

Thursday 18 February 2016

New research suggests that people who develop Parkinson’s Disease are at increased risk of falling and injuring themselves in the years leading up to their diagnosis

 X-ray showing a hip replacement. Image by Voisin/ Phanie/ Rex Features

People who are prone to falling and injuring and injuring themselves in middle age are at significantly increased risk of developing Parkinson’s Disease decades later, according to a new study by researchers in Sweden. The findings, published earlier this month in the open access journal PLoS Medicine, suggest that frailty – and especially an increased risk of falling and fracturing one’s hip – could be a marker for degenerative brain changes, which may occur decades before disease symptoms appear, and possibly aid in early diagnosis.
Parkinson’s Disease is a progressive neurodegenerative disease characterised by the death of dopamine-producing neurons in a region of the midbrain called the substantia nigra. This causes the three main symptoms of tremor, muscle rigidity, and slow movements, which typically appear at around 60 years of age, and progress at varying rates. Although widely considered to be a movement disorder, Parkinson’s is also associated with cognitive impairments, which in severe cases can develop into full-blown dementia.
Last year, Peter Nordström of Umeå University and his colleagues published the results of a large population study, in which they examined the medical records of all the approximately 1.35 million Swedish men conscripted at age 18 for compulsory military service between the years of 1969 and 1996. Looking specifically at measures of muscle strength, they found that those who scored lowest on handgrip and elbow flexion strength at the time of conscription were significantly more likely to develop Parkinson’s 30 years later.
The researchers therefore speculated that the reduced muscle strength they observed in adolescents who went on develop Parkinson’s in later life might indicate neuro-muscular deficits that increase the risk of falls and fractures long before a diagnosis of Parkinson’s.
To investigate, they again turned to the Swedish National Patient Register, and compared the medical records of more than 24,000 people, aged 50 and over and diagnosed with Parkinson’s between 1988 and 2012, with those of more than 243,000 matched controls, and the records of 622,000 patients admitted to accident and emergency departments with an injurious fall during the same period with those the same number of matched controls who had not.
Analysing these records, they find that 18% of the Parkinson’s patients had at least one injurious fall, and 7.8% had fractured a hip, up to 10 years before diagnosis, compared to 11% and 3.2% of the age-matched controls, respectively. In the second cohort, they find that 0.7% of those who had experienced an injurious fall were subsequently diagnosed with Parkinson’s, compared to 0.5% of those who had not.
The differences may seem small, but the large number of participants involved makes them meaningful. Overall, the risk of experiencing an injurious fall increased dramatically in the years leading up to diagnosis. The association with hip fractures was even stronger, with Parkinson’s patients being at significantly increased risk for more than 15 years before diagnosis, and almost twice as likely to suffer a fractured hip in the four years preceding diagnosis.
Nordström and his colleagues believe theirs is the first long-term study to assess the risk of injurious falls prior to the clinical onset of Parkinson’s Disease. They point out, however, that diagnoses of dementia, depression, and diabetes were also more common in the Parkinson’s patients than in the controls, and that all of these may also contribute to an increased risk of falling prior to diagnosis. They also note that their results are limited by a reliance on medical records, as opposed to clinically confirmed diagnoses. They also failed to take information about smoking and educational achievement, both of which are known to modify risk for Parkinson’s, into account.
Roxanne Sterniczuk, a neuropsychologist at Dalhousie University in Nova Scotia, who studies theinks between dementia, sleep and frailty, points out another potentially important confounding factor. “They don’t appear to have controlled for the effects of physical activity or exercise, which is one of the most important neuroprotective factors for healthy aging,” she says. “It’s well established that lack of physical activity is a strong risk factor for neurodegeneration, and lack of exercise is directly linked to lower bone density and muscle mass, which in turn increases risk of falls and subsequently fractures.”
Sterniczuk adds that while the results warrant further study, an increased risk of injurious falls may not be enough for accurate and early diagnosis. “Each person has a unique threshold for the onset of disease, and it’s theorized that we become more frail as deficits accumulate, so that eventually our defense mechanisms will be overridden and disease will take over,” she explains. “We know that other changes, such as a worsening sense of smell and sleep disturbances, can occur up to 20 years prior to a Parkinson’s diagnosis, so it’s possible that combining these deficits, including a history of falls and fractures, may serve as a valid preclinical diagnostic measure, and could aid the development of novel interventions at the earliest stages of the disease.”

References

Nyström, H., et al. (2016). Risk of Injurious Fall and Hip Fracture up to 26 y before the Diagnosis of Parkinson Disease: Nested Case–Control Studies in a Nationwide Cohort. PLoS Med. 13(2): e1001954. DOI: 10.1371/journal.pmed.1001954 [Full text]
Gustafsson, H., et al. (2015). Low muscle strength in late adolescence and Parkinson disease later in life. Neurology, 84: 1862–1869. DOI: 10.1212/WNL.0000000000001534 [Full text]
https://www.theguardian.com/science/neurophilosophy/2016/feb/18/frailty-falls-and-hip-fractures-may-be-early-predictors-of-parkinsons-disease?