Parkinson's Disease Archives | Experience Life https://experiencelife.lifetime.life/category/health/health-conditions/parkinsons-disease/ Wed, 10 Sep 2025 20:19:13 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.2 Fighting Parkinson’s https://experiencelife.lifetime.life/article/fighting-parkinsons/ Tue, 04 Jun 2024 17:00:17 +0000 https://experiencelife.lifetime.life/?post_type=article&p=99643 We’re in the midst of a Parkinson’s disease crisis. Explore the causes of the world’s fastest growing neurological disorder — and discover the innovative new treatments and functional therapies that can help patients live long and productive lives.

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Vicky Stanich is all suited up, her fists poised in Barbie-pink TITLE boxing gloves; she’s ready to throw a punch at Parkinson’s disease. Stanich is in a St. Paul, Minn., gym among hanging punching bags, squat racks stocked with free weights, two boxing rings, and posters of champion fighters. When the coach gives the go, she lets loose with a left jab, then a right cross, followed by a feint and a bit of fancy footwork before a further one-two of punches. The jaunty taunt of a fellow boxer — Muhammad Ali, who also fought Parkinson’s — comes to mind: “Float like a butterfly, sting like a bee.”

Stanich, 65, is part of a Rock Steady Boxing class, along with 20 other boxers on this day. Each one has Parkinson’s and each one is fighting back against the disease.

Rock Steady Boxing is one of several progressive functional therapies for Parkinson’s disease (PD). Such therapies are based on movement as varied as tai chi, tango dancing, and cycling. A growing body of research shows that exercise is one of the best — and simplest — antidotes for this disease that has no cure.

Vicky Stanish
Vicky Stanich, 65, fights her Parkinson’s disease in a Rock Steady Boxing class in St. Paul, Minn

Movement aids mobility, agility, balance, and strength — motor functions affected by PD. This then boosts nonmotor functions like neuroplasticity, cognition, and mood. And the boxers have to remember sequences of punches and footsteps, which aids memory and eye–hand coordination.

In addition, programs like Rock Steady offer socialization and camaraderie, which can suffer when someone has a neurodegenerative disease. Plus, participants have to get up in the morning, round up boxing togs, and get to class — no small matter for some people with PD. These exercise-therapy classes are like support groups without the chairs.

“I get up in the morning and I’m stiff and hunched over. Then I box and I feel wonderful. I’m a lot more flexible and clear in my mind. Boxing got rid of my tripping when I walked. I have way more energy, and it helps me the rest of the day.”

“I never dreamed I’d be a boxer,” Stanich says, but after she was diagnosed in December 2018, she discovered the Rock Steady Boxing classes. She has been throwing punches now for four and a half years.

“I get up in the morning and I’m stiff and hunched over,” she says. “Then I box and I feel wonderful. I’m a lot more flexible and clear in my mind. Boxing got rid of my tripping when I walked. I have way more energy, and it helps me the rest of the day.”

After a moment to hydrate and catch her breath, Stanich is ready to go another round.

Understanding Parkinson’s

Like an earthquake, Parkinson’s often begins with a tiny tremor.

“I used to be an expressive, high-energy person,” recalls John Clayton. “But about seven years ago I found myself tired, exhausted, and trembling.”

His doctor remarked that his face seemed frozen into a mask and wondered aloud whether he might have Parkinson’s disease. Clayton went to a neurologist for the first of a seemingly never-ending battery of tests.

He was also starting to stumble as he walked. He began to have a difficult time swallowing, which led to drooling. He felt mired in sluggishness. He woke from sleep unrested and still weary.

Worse yet, he suddenly found himself without will — apathetic, lethargic, his only desire a lack of desire, as he describes it. “Sometimes I sit at my desk just looking into space while torpor and self-pity fill me.”

Clayton, now in his late 80s, notes on the first page of his memoir, Parkinson’s Blues, that PD settled on him like “a vulture.”

A novelist and professor emeritus of modern literature and fiction writing at the University of Massachusetts Amherst, he began documenting his experience with PD following his diagnosis. In part, it was to explain to himself and the world what he was going through. It was also to inform us all about living with the disease.

“I’m in a place I’ve never heard anyone describe: both alive and not alive. Like a ghost, I can look from a distance upon my children, my wife, our friends — and love those I look upon. . . . But secretly, inwardly, I’ll be separate, taking in the world without acting in it.”

But his writing had another motive as well. “The most painful part of having PD is what it does to my thinking,” Clayton explains. “Say I’m taking part in a discussion and I have an idea. The idea is clear enough when I start to speak, but at once the idea is gone. I try to get it together, but I can’t. I ask the other discussants to wait and I struggle to find the idea. But I can’t bring it back.”

Writing, too, is tough. But it’s also empowering and liberating — a way to step back into a semblance of his old self. “Paradoxically, writing about disorientation helps orient me,” he notes.

I’m in a place I’ve never heard anyone describe: both alive and not alive. Like a ghost, I can look from a distance upon my children, my wife, our friends — and love those I look upon. . . . But secretly, inwardly, I’ll be separate, taking in the world without acting in it.”

The Parkinson’s Pandemic

Chances are, you know someone with Parkinson’s. Some 1.2 million Americans are living with the disease as of this writing in March 2024; the counter at www.pdclock.org/counter/ updates approximately every seven minutes — the same rate at which a new person is diagnosed with PD in the United States. Ten million people worldwide have PD, according to the Parkinson’s Foundation.

There are a range of what are called “parkinsonian” or “parkinsonism” syndromes that can be caused by a stroke, brain injury, medication use, or infections, resulting in tremors and movement issues. Parkinson’s disease is one of these — and it is the most common cause of parkinsonism. In fact, PD is the second-most common neurodegenerative disease after Alzheimer’s. And no two people with PD exhibit the exact same symptoms, age of onset, rate of progression, or treatment response.

The prevalence of Parkinson’s is “rising exponentially,” says Ray Dorsey, MD, the David M. Levy Professor of Neurology at the University of Rochester and coauthor of Ending Parkinson’s Disease. “Parkinson’s disease is the world’s fastest growing neurological disorder.”

“Parkinson’s disease is the world’s fastest growing neurological disorder.”

This has spurred physicians and scientists to label it a pandemic.

“From 1990 to 2015, the number of people with Parkinson’s disease doubled,” Dorsey and his co-authors noted in a 2018 report in the Journal of Parkinson’s Disease. “Just due to aging, this number is projected to double again by 2040.”

“Today, more than 200 Americans were diagnosed with the disease and another 100 died from it,” Dorsey says.

And a growing aging population means that more people will experience Parkinson’s, he notes.

And sadly, he adds, it’s a largely preventable pandemic.

A Pandemic of Our Own Making

Parkinson’s is a “human-made pandemic,” Dorsey explains. Genetics, family history, and head injuries are among the myriad factors that cause PD. Yet only about 15 percent of all people with the disease have an identifiable genetic risk factor, he says.

The main culprits in Parkinson’s are human-created industrial chemicals, pesticides, herbicides, and solvents that are attacking us via air and water pollution and other chemical contact.

“The evidence for this connection is overwhelming,” Dorsey and his coauthors write. “Countries that have experienced the least industrialization have the lowest rates of the disease, while those that are undergoing the most rapid transformation, such as China, have the highest rates of increase.

“All of the evidence indicates that the full effect of the Parkinson’s pandemic is not inevitable but, to a large extent, preventable.”

“All of the evidence indicates that the full effect of the Parkinson’s pandemic is not inevitable but, to a large extent, preventable.”

The disease was first discerned and described as “the shaking palsy” in 1817 by future disease namesake Dr. James Parkinson in Great Britain at a time when industrialization was beginning to boom. But it wasn’t until recent years that scientists made the connection to industrial pollutants.

Our understanding of Parkinson’s as a disease largely of our own making comes thanks substantially to the trailblazing research of Caroline Tanner, MD, PhD, currently the vice chair for clinical research and a professor of neurology at the Weill Institute for Neurosciences at the University of California, San Francisco.

The first clue was uncovered in 1982. J. William Langston, MD, was then the chair of neurology at California’s Santa Clara Valley Medical Center, an affiliate of Stanford, and he was investigating a garage-brewed version of the opiate Demerol that caused parkinsonian symptoms in users. Langston zeroed in on the chemical MPTP, an accidental byproduct of the synthetic heroin, which was found to kill dopamine-producing nerve cells in the brain.

“Dr. Langston and others realized that this drug caused selective injury to the area of the brain that is also damaged in Parkinson’s disease,” Tanner told Neurology Today. “They figured out that it blocked mitochondrial respiration and caused oxidative stress, and when it was observed that MPTP was structurally very similar to pesticides like paraquat and rotenone, that led to the idea that agents like these might be potentially contributing to Parkinson’s.” (Learn more about the importance mitochondria and how to keep these power houses health at “The Care and Feeding of Your Mitochondria.”)

Tipped off by this connection, Tanner began in the mid-1980s to study the effects of pesticides, herbicides, solvents, and other chemicals. In the 40 years since, she has been prolific and tireless in leading the understanding of the environmental factors now linked to Parkinson’s.

Chemicals linked to Parkinson’s include:

  • Paraquat and other pesticides and herbicides: Also known by the brand name Gramoxone, paraquat is banned in 32 countries but is one of the most widely used weed killers in the United States.Its use tripled between 2008 and 2018.
  • Chlorpyrifos: The most widely used insecticide in the country, it’s sprayed on everything from golf courses to utility poles as well as crops, including almonds, cotton, apples, and other fruits. Other problematic pesticides include rotenone and 2,4-D.
  • Trichloroethylene: An industrial solvent also used in dry cleaning, TCE is found in between 4.5 and 18 percent of the U.S. drinking-water-supply sources that are tested on an annual basis, according to the Centers for Disease Control and Prevention (levels are typically below 30 parts per billion). It’s also a carcinogen.
  • Other industrial chemicals and metals: Polychlorinated biphenyls (PCBs) were used as coolants and insulators in electrical equipment. Although they’ve been banned for several decades, PCBs continue to exist in the environment because of their long half-life.

Welding work has been associated with a greater risk of PD, possibly due to manganese in fumes; exposure to other metals, such as iron and lead, is also believed to increase the risk of PD. And the exhaust fumes from road traffic has also been associated with an increased risk of the disease.

Parkinson’s Pathology

Unlike Alzheimer’s, the pathology of Parkinson’s is well understood. Parkinson’s and other parkinsonian syndromes stem from a loss or impairment of brain neurons that produce dopamine. Dopamine is a neurotransmitter and hormone that plays a role in myriad aspects of our behavior: It governs our thinking, planning, focusing, and striving, and it helps us coordinate our movements. It’s also involved in regulating our sleeping; controlling nausea and vomiting; and facilitating certain cardiovascular and kidney functions.

New research suggests that there may be several subtypes of PD: Some may be caused by pathologies in other brain regions involving nondopaminergic neurons as well.

For some people, Parkinson’s may even begin in the gut. As a study published in the Journal of Gastroenterology and Hepatology Open in 2020 explains, “It has been postulated that gut pathogens and dysbiosis can contribute to peripheral inflammatory states or trigger downstream metabolic effects that exacerbate the neurodegenerative process in PD.”

“Most PD cases likely have a multifactorial etiology, or causes, resulting from the combined effects of environmental and genetic factors,” explains David K. Simon, MD, PhD, a neurology professor at Harvard Medical School and director of the Parkinson’s Disease and Movement Disorders Center at Beth Israel Deaconess Medical Center, and other authors in a 2020 status report on Parkinson’s knowledge.

The decline in dopamine production leads to some of PD’s earliest and most visual symptoms affecting motor activities, which bring on tremors, stiffness, slowness of movement, and balance issues. For this reason Parkinson’s is often called a movement disorder.

But the disease also sparks what are known as “invisible” symptoms: depression, anxiety, apathy, issues with pain processing, memory problems, dementia, and even psychosis. Other nonmovement symptoms include autonomic dysfunction, including constipation, low blood pressure, sexual dysfunction, and more.

These nonmotor symptoms are “the hidden face of the disease” — and they are often overlooked, according to Indu Subramanian, MD, director of the VA Southwest Parkinson’s Disease Research, Education, and Clinical Centers and a clinical professor of neurology at University of California, Los Angeles. “Tremor doesn’t affect quality of life as much as depression or anxiety,” she says, calling for greater awareness of the intricacies of PD among both the public and her fellow doctors.

While multiple factors may be involved in PD’s pathology, the fallout from environmental pollution, industrial chemicals, and synthetic pesticides is clear, according to Dorsey: “People with the most exposure have higher rates of the disease than the general population.”

In recent years, several advances have helped physicians identify Parkinson’s. In 2019, a skin biopsy test became available that detects PD via a misfolded version of the alpha-synuclein protein  in patients’ skin. And in 2023, a biomarker that signals protein dysfunction was found that can help discern Parkinson’s disease in patients.

What causes the degeneration or death of the dopamine-producing brain cells in the first place?

Age-related changes in neurons certainly play a part. Neurons may degenerate as the result of oxidative stress, mitochondrial dysfunction, inflammation, and other causes. Lewy bodies, or abnormal clumps of proteins, may also block dopamine production and transmission. And research published in 2023 suggests that chronic brain inflammation or systematic inflammation or both may contribute to the disease. (Our bodies need inflammation to fight off infection, but too much of it for too long can spur a wide range of illnesses. Learning to manage it effectively is key. Learn more at “How Chronic Inflammation Affects Your Health.”)

While multiple factors may be involved in PD’s pathology, the fallout from environmental pollution, industrial chemicals, and synthetic pesticides is clear, according to Dorsey: “People with the most exposure have higher rates of the disease than the general population.”

PD is a lifelong and progressive disease, and symptoms slowly worsen over time. There currently is no known cure.

The disease itself is not fatal: PD won’t kill you, like a heart attack or stroke can. But it can lead to an increased risk of dying from things such as a fall due to motor issues; pneumonia from progressive problems with swallowing and aspiration; pressure ulcers from immobility; or infections.

As Clayton writes in his memoir, “Parkinson’s won’t kill me. But it’s a preparation for death. A rehearsal.”

Parkinson’s Medications and Treatments

“Although Parkinson’s is a progressive disorder, most people can still live long and productive lives,” says Dorsey. While Alzheimer’s sufferers lack medications that make a meaningful difference, Parkinson’s patients are fortunate to have a drug available that helps many people, called levodopa. Below is a survey of current — and some possible future — medications and treatments.

Medications
There is a range of medications to help with Parkinson’s motor symptoms, the most commonly prescribed being levodopa. The drug is absorbed through the intestine and the brain converts it to dopamine. The U.S. Food and Drug Administration (FDA) approved levodopa as a treatment for PD in 1970. And there are other medications, such as carbidopa, that can help support levodopa and alleviate its side effects.

For nonmotor symptoms, a range of medications, supplements, diet, and lifestyle choices can help. The Michael J. Fox Foundation offers a helpful guide at www.michaeljfox.org/medications-treatments. Talk to your healthcare provider for more personalized advice. (For more on natural supplements to boost your mental health, see “8 Key Supplements to Boost Your Mental Health — Naturally.”)

Deep Brain Stimulation
John Foley of Minneapolis was 65 when he was diagnosed with Parkinson’s, although his doctors believe he may have had it for some four years by that time. Soon after his diagnosis, Foley consulted with neurosurgeon Kendall Lee, MD, PhD, at the Mayo Clinic, and opted for deep brain stimulation surgery. DBS involves making small holes in the skull to embed electrodes into the brain. The procedure also includes implanting a pacemaker-like pulse generator under the skin in the chest that is later programmed to send continuous electrical signals to the brain.

In 2019, Johns Hopkins Medicine researchers found that “deep brain stimulation using electrical impulses jump-starts the nerve cells that produce the chemical messenger dopamine to reduce tremors and muscle rigidity that are the hallmark of Parkinson’s disease,” according to a study press release.

DBS is a complex and “potentially risky procedure,” the Mayo Clinic warns on its website. And it’s not right for all PD patients. Still, it may make a difference for some: “Deep brain stimulation won’t cure your condition, but it may help lessen your symptoms.”

For Foley, DBS has been life-changing. “I just returned from my baseline checkup, and I’m better today than I was two years ago,” he says. He has stopped taking PD medications and he holds his hands out to show that they no longer tremble.

After his PD diagnosis, Foley began doing something he’d never considered before: He started writing poetry. “I began writing poetry as a catharsis for dealing with the disease and treatments,” he explains in the introduction to his collection, No Turning Back, which includes artwork by Mary GrandPré, who illustrated the U.S. editions of the best-selling Harry Potter books.

The book is also his testament to the efficacy of DBS. As he writes in his poem “Aftermath”: “Behind the tremors, behind the verdict, it’s still me. / I’m not lost, just working on a new map.”

Focused Ultrasound
In 2018, the FDA approved MRI-guided focused ultrasound (MRgFUS, or sometimes simply FUS) as a noninvasive treatment that helps some Parkinson’s patients manage tremors. Ultrasound is guided by an MRI to the specific areas in the brain. The high-temperature ultrasound waves destroy brain cells that cause movement problems.

FUS is currently approved for use on only one side of a patient’s brain, so it helps with symptoms on only one side of the body. When done on both sides of the brain, FUS may cause speech, swallowing, or memory issues. Researchers are looking to perfect FUS for both sides of the brain.

Vaccination
Vaccines empower antibodies in the body’s immune system to fight off harmful agents, such as the viruses that cause polio or chicken pox. Vaccines can also be aimed at proteins, which may be the key to developing a PD vaccine: “This is convenient in the case of Parkinson’s because misfolded forms of the alpha-synuclein protein — that major factor in the disease — could be targeted,” explains Dorsey and his coauthors in Ending Parkinson’s Disease.

Vaccine studies began in 2017 and continue today.

Parkinson’s Therapies

In recent years, progressive new therapies are helping those with Parkinson’s like never before. Subramanian calls the new understanding of the benefits of exercise, diet, and social connection “game-changers.” Below is a survey of current therapies.

Exercise and Movement
The power of exercise for people with Parkinson’s disease is remarkable and represents one of the biggest advances over the past 20 years or so,” says movement scientist Gammon Earhart, PT, PhD, associate dean and director of the Program in Physical Therapy at Washington University School of Medicine in St. Louis. “To date, exercise remains the only approach that may modify disease progression.”

Volumes of studies and trials have validated the benefits of exercise as therapy for PD. And while most research focuses on a specific type of movement, in the end it appears that simply moving is the key.

“Exercise has positive effects on movement, mood, thinking, and quality of life, just to name a few.  And it is never too early, or too late, to start exercising.”

Exercise has positive effects on movement, mood, thinking, and quality of life, just to name a few,” Earhart explains. “And it is never too early, or too late, to start exercising.”

Earhart led trials on tango dancing as Parkinson’s therapy. “Tango has lots of features that enable people with PD to practice things, within the context of the dance, that are often challenging for them. For example, starting and stopping, moving at different speeds, walking backward, turning, and multitasking,” she says. “It is also a social activity that allows the person with PD and their partner or friend to participate on equal footing, which helps with engagement as well as motivation and desire to continue.”

PD therapy classes featuring tango and myriad other styles of dance — Zumba, ballet, and more, both in person and virtual, and in several languages — are offered around the country.

A recent long-term study in China on the effects of tai chi as PD therapy found numerous benefits. “Tai Chi training reduced the annual changes in the deterioration of the Unified Parkinson’s Disease Rating Scale and delayed the need for increasing antiparkinsonian therapies,” the authors note. “The annual increase in the levodopa equivalent daily dosage was significantly lower in the Tai Chi group [compared with a control group].”

Davis Phinney is a former professional bicycle racer who won an Olympic bronze medal as well as two Tour de France stage wins. In 2000 at age 40, he was diagnosed with early-onset PD. He cofounded the Davis Phinney Foundation for Parkinson’s with his wife, Connie Carpenter Phinney. One of its key programs is Pedaling for Parkinson’s, with in-person classes using stationary bicycles at YMCAs, community centers, and gyms across the country. The program also offers virtual classes.

“Participants who ride three days a week over eight weeks have shown improvement in their Parkinson’s-related symptoms by as much as 35 percent,” the group’s website states. “Exercise not only improves your general health, but it also has specific physical, mental, and emotional benefits as you live well with Parkinson’s.” (See “The Health Benefits of Cycling” for more about boosting your overall health with a bike ride.)

“The data that physical exercise is beneficial for people with PD is overwhelming,” says Simon, the Harvard Medical School neurology professor. “Some studies suggest more intense physical activity yields the most benefit, but other studies suggest substantial benefits from moderate-intensity exercise. The exact optimal amount is unclear, but generally we recommend aiming for at least 150 minutes per week of at least moderate-intensity exercise. However, even less than this recommended amount likely still has benefits.”

Exercise may even help prevent PD in the first place.

Exercise may even help prevent PD in the first place. Following the publication of a paper in Clinics in Geriatric Medicine on the status of Parkinson’s research, coauthor Tanner, of the Weill Institute for Neurosciences, predicted in the Washington Post that the 90,000 new Parkinson’s cases currently diagnosed annually among Americans age 65 or older could drop by nearly half by 2030 if everyone simply exercised more regularly and vigorously.

One of the next goals in PD treatment is to create guidelines for exercise prescriptions.

“We have long known exercise is good for Parkinson’s patients,” Giselle Petzinger, MD, associate professor of neurology at the University of Southern California’s Keck School of Medicine, tells the Post. “What we are trying to do now is further refine what we already know into practical applications for patients.”

(For more on how exercise benefits the brain, see “How Exercise Benefits the Brain.” And for advice on exercising safely with Parkinson’s, visit “Exercising Safely With Parkinson’s Disease.”)

Motor Skills and Speech Therapy
Lee Silverman was an individual with PD whose speech abilities were affected by the disease. This is a common occurrence, as published studies have found that some 70 to 90 percent of people with PD show some type of speech disorder during the course of the disease. Lorraine Ramig, PhD, now a research professor emeritus of speech, language, and hearing sciences at the University of Colorado Boulder, was called in to work with Silverman in 1987. The speech therapy Ramig and her colleagues developed was named in Silverman’s honor as Lee Silverman Voice Treatment (LSVT) LOUD.

LSVT LOUD retrains soft-talking individuals with PD to use their voice at a more conventional volume. “Key to the treatment is helping people ‘recalibrate’ their perceptions so they know how loud or soft they sound to other people and can feel comfortable using a stronger voice at a normal loudness level,” the group’s website explains.

The group subsequently launched LSVT BIG, offering therapy to recalibrate motor skills, including both small-motor tasks like buttoning a shirt and large-motor skills such as maintaining balance while walking.

LSVT has certified speech clinicians and physical and occupational therapists in its programs in 70 countries.

Nutrition and Psychobiotics
Diet is key to overall health, but certain “neuroprotective” foods may be especially beneficial to those with Parkinson’s. “In PD, there are some foods that may help to ease symptoms and help brain health, while others can affect the way medications work,” states the Parkinson’s Foundation website. “While there are many things about PD that cannot be changed, the informed choice of diet can help people to live better with the disease.”

The foundation offers the following advice:

  • Anti-inflammatory foods are important for brain and overall health. These include oily fish, like salmon, tuna, and mackerel; dark leafy green vegetables, like spinach, Swiss chard, kale, and collard greens; as well as soy products and herbs such as rosemary. Fats like medium-chain triglycerides may also tamp down inflammation: Coconut oil is a good source. (See “5 Rules for Anti-Inflammatory Eating” for more.)
  • Antioxidants in foods can also protect the brain. They fight free radical molecules that can damage neurons and other healthy cells. Purple and red fruits, like blueberries and raspberries, contain a group of antioxidants called anthocyanins, which, according to one study, can increase blood flow to and activate areas of the brain that control, memory, attention, and language. Studies also find that drinking green tea, which has the antioxidant-like catechin EGCG, has both anti-inflammatory and antioxidant effects.
  • Nuts and spices also offer strong neuroprotection. Nuts deliver healthy oils, essential fatty acids, minerals, vitamins, and antioxidants. Among the best are walnuts, pistachios, macadamia nuts, cashews, almonds, and Brazil nuts. Spices include turmeric (which offers the powerful anti-inflammatory curcumin) and Ceylon cinnamon, which in animal studies has shown potential for normalizing neurotransmitter levels and other PD brain changes. (Turmeric is a potent, anti-inflammatory spice with a wide range of promising therapeutic properties. See “The Health Benefits of Turmeric” for more on this healing spice.)

(For more on eating habits and nutrition to support your brain, see “Healthy-Brain Food.”)

The connection between Parkinson’s and the gut microbiome — the trillions of microbes in your intestines — is one of the newest, most innovative fields of PD research. More research is needed, and ongoing trials are looking at probiotics and prebiotics that may affect PD, including helping with side effects such as constipation.

Probiotics are living microorganisms found in fer­mented foods, such as yogurt, kimchi, and sauerkraut, and available in supplement form; they can help create and sustain a diverse microbiome, supporting the intestinal lining and enhancing nutrient absorption, which aids overall digestive health. Prebiotics are types of indigestible, fermentable fiber that help the growth of the beneficial bacteria.

Future therapy may include “psychobiotics” — a combination of beneficial bacteria that can influence your neurological health and mental well-being via the gut–brain axis. (For more on the power of your microbiome to heal and protect your brain, from neurologist David Perlmutter, MD, FACN, ABHIM, see “Healthy Gut, Healthy Brain.”)

Parkinson’s Trends

The prevalence of PD is growing so rapidly it seems difficult to track. A 2022 study by the Parkinson’s Foundation, the Michael J. Fox Foundation for Parkinson’s Research, and the Institute for Clinical Evaluative Sciences shows the incidence of Parkinson’s disease in the United States is about 50 percent higher than previous estimates: In 1978, 40,000 to 60,000 cases were reported annually; some 60,000 to 95,000 Americans are now newly diagnosed with PD each year.

The World Health Organization reported last year that PD’s prevalence around the globe has doubled in the past 25 years. The number of deaths caused by the disease in 2019 was twice the number reported in 2000.

Why the rate of Parkinson’s has grown so dramatically is a larger question. “The reasons for a greater incidence . . . remains to be explained, but could represent either improved ascertainment and clinical recognition of PD or reflect the impact of risk factors for PD,” explain the authors of the 2022 study, published in the journal npj Parkinson’s Disease.

The Parkinson’s Foundation estimates that the combined direct and indirect cost of PD, including treatment, social security payments, and lost income, is currently nearly $52 billion per year in the United States alone. And it’s projected to surpass $79 billion by 2037.

As the incidences increase, so do the economic costs of the disease. The Parkinson’s Foundation estimates that the combined direct and indirect cost of PD, including treatment, social security payments, and lost income, is currently nearly $52 billion per year in the United States alone. And it’s projected to surpass $79 billion by 2037.

There are other, hidden costs as well. Most people with PD are looked after by informal caregivers such as spouses, adult children, friends, or other nonpaid individuals, according to a study published in the Journal of Neurology in 2023. Looking at five European countries plus Japan and the United States, the authors found that 70.4 percent of caregivers were spouses and 71.6 percent were female. The average caregiver age was 62.6 years old, and they had been caring for the person with PD for an average of 4.6 years.

The authors warn of an impending crisis. As the prevalence of PD increases over the next 20 years, a greater burden will fall on healthcare systems and caregivers.

Early-Onset Parkinson’s

Actor Michael J. Fox was just 29 in 1990 when he first noticed a tremor in his pinkie. The trembling wouldn’t stop: It was like his littlest finger was possessed. After rounds of tests and doctor’s visits, he was diagnosed with Parkinson’s, although he didn’t share this with the world for seven more years. In his 2002 memoir, he writes on the first page not of his stellar television and movie career but about PD.

The title of Fox’s autobiography? Lucky Man.

In interviews after revealing his diagnosis, Fox referred to his PD as a “gift” — an epithet that did not please others with the disease. As he clarifies in his book, “If it is a gift, it’s the gift that just keeps on taking.”

Instead, the gift Fox was describing was the personal journey Parkinson’s led him on.

“These last 10 years of coming to terms with my disease would turn out to be the best 10 years of my life — not in spite of my illness, but because of it,” he writes.

“Coping with the relentless assault and the accumulating damage is not easy. Nobody would ever choose to have this visited upon them. Still, this unexpected crisis forced a fundamental life decision: adopt a siege mentality — or embark upon a journey. Whatever it was — courage? acceptance? wisdom? — that finally allowed me to go down the second road (after spending a few disastrous years on the first) was unquestionably a gift — and absent this neurophysiological catastrophe, I would never have opened it, or been so profoundly enriched. That’s why I consider myself a lucky man.”

In the years since revealing his diagnosis, Fox used his celebrity status to make himself the face of PD. And in 2000 he launched the Michael J. Fox Foundation for Parkinson’s Research, which remains one of the primary organizations worldwide dedicated to ensuring the development of improved therapies for those living with PD — and to ultimately finding a cure for the disease.

Age may be a key risk factor for Parkinson’s, but it is not just an elderly person’s disease, as Fox’s story shows. An estimated 4 percent of people with PD are diagnosed before age 50.

Women and Parkinson’s

In the United States, men are between one and a half to two times as likely to get PD than women. But Parkinson’s is in no way an affliction of just older men. In fact, 40 percent of those worldwide with the disease are female, says Indu Subramanian, MD, director of the VA Southwest Parkinson’s Disease Research, Education, and Clinical Centers and a clinical professor of neurology at University of California, Los Angeles. And in Asia, the ratio is equal.

“People think of this white older man who’s bent over with a cane — and that is the picture that has been propagated time and time again,” says Subramanian. And she warns that doctors may even overlook classic PD symptoms if they present in young people, women, BIPOC, or members of the LGBQTIA+ community.

Subramanian and her coauthors outlined such disparities in diagnosis and treatment in a report published in 2022 in the journal Movement Disorders, entitled “Unmet Needs of Women Living with Parkinson’s Disease: Gaps and Controversies.”

“There’s a huge gap in advocacy as well as research,” she explains. “You look at trials: Most of them are of white, affluent men whose wives bring them in for study visits.” In fact, clinical trials haven’t always needed to collect or report data on biological sex. It was only in 2016 that the NIH began requiring researchers with NIH funding to report results by sex, which means it can be impossible to know who was involved in certain studies conducted before that. Then, Subramanian adds, trials data is extrapolated to others in a “cookie-cutter approach.”

Women may endure a faster progression of the disease and a higher mortality rate. Many women have less body weight than men and metabolize PD drugs differently. Women’s symptoms can differ and present differently as well.

Women may endure a faster progression of the disease and a higher mortality rate. Many women have less body weight than men and metabolize PD drugs differently, Subramanian says. Women’s symptoms can differ and present differently as well.

“One of the things that is often not said is that women who get Parkinson’s disease often have shame about their diagnosis,” she notes. “They have a huge stigma about having the disease and they feel that it might have been something that they did; they don’t want to tell people. They have low self-esteem since much of what determines their own sense of self is their ability to be a caregiver for others such as their children, grandchildren, or husbands.”

She calls for a “rebranding” of Parkinson’s because it affects “everyone across the globe — no one is spared.”

Ending Parkinson’s

In their book Ending Parkinson’s Disease, four leading experts — Ray Dorsey, MD; Todd Sherer, PhD; Michael Okun, MD; and Bastiaan Bloem, MD, PhD — offer a prescription for curtailing the disease. Their action plan is summarized in the acronym PACT.

Prevent:

  • Ban herbicides and pesticides like paraquat and solvents like trichloroethylene. Reduce your risk of exposure if you work with such chemicals by wearing masks, gloves, and protective clothing. Accelerate the cleanup of contaminated sites.
  • Eat healthy. Buy organic when possible and avoid foods that may be contaminated with herbicides and pesticides. Wash your produce thoroughly. Eat a Mediterranean or similar low-carb, plant-based diet.
  • Drink clean water. Test your water and use water filters to reduce exposure to chemical contaminants.
  • Exercise. There is no exact optimal amount of exercise, but David K. Simon, MD, PhD, a neurology professor at Harvard Medical School and director of the Parkinson’s Disease and Movement Disorders Center at Beth Israel Deaconess Medical Center (who was not involved with the book), generally recommends at least 150 minutes per week of at least moderate-intensity exercise. Still, even less than this recommended amount likely has benefits, he says.
  • Protect your head. Avoid activities with a high risk of concussion or wear a protective helmet.

Advocate:

  • Share your story: Attend a Parkinson’s support group in person or online.
  • Call your government representatives and push for more research funding via the National Institutes of Health.
  • Donate to Parkinson’s foundations and stay informed.

Care:

  • Get the care you want and need by going to a medical center that specializes in Parkinson’s.
  • Advocate for training of more specialists and clinicians in PD care.
  • Expand access to care. Ask your government representatives to request ongoing Medicare coverage of telemedicine so Parkinson’s care is available to more patients.

Treat:

  • Consider genetic testing to assess your family history regarding Parkinson’s.
  • Join a clinical study. As Jim Hunt, who has Parkinson’s, explained during a break in a Rock Steady Boxing class, “I’m a research subject volunteer. It’s not going to help me, but it may help the next generation.”

About John Foley 

John Foley of Minneapolis was 65 when he was diagnosed with Parkinson’s. Following his diagnosis, he began writing poetry as a catharsis for dealing with the disease and treatments. His collection, No Turning Back, included artwork by Mary GrandPré, who illustrated the U.S. editions of the best-selling Harry Potter books.

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PUMPING IRONY: Life in the Slow Lane https://experiencelife.lifetime.life/article/pumping-irony-life-in-the-slow-lane/ Tue, 14 May 2024 17:00:32 +0000 https://experiencelife.lifetime.life/?post_type=article&p=98431 While researchers hunt for the causes of age-related mobility issues as a way to address Parkinson’s and other diseases, I find myself embracing a mindful slowness.

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Among the more intriguing aspects of the aging process that I’ve been noticing lately is how much more slowly I move now than in my younger years. Climbing in and out of the shower, navigating a staircase, even clearing dishes from the dinner table, I tend to travel from point A to point B with what sometimes strikes me as an odd sort of deliberation.

I like to think of it as a kind of mindfulness practice, one that may help me avoid an inadvertent tumble. Falling, after all, is a major cause of debilitating injury among the Medicare set. And, as I occasionally remind myself: What’s the hurry, anyway?

It’s not all about a particular mindset, obviously; there are physiological factors that slow us down as we grow old. Creaky joints, overtaxed muscles, and unreliable equilibrium all conspire to impede our speed. And as researchers at the University of Colorado Boulder recently noted, certain parts of our brains may play a role as well.

It’s no secret that our aging muscles work less efficiently — burning more calories — than those of younger people when performing the same task. By slowing our movements, seniors conserve energy. But Alaa Ahmed, PhD, and her team wondered whether older brains, which produce less dopamine than their younger counterparts, would cause seniors to respond less energetically to rewards. If you’re not feeling much of a dopamine rush, in other words, you’re less likely to move more quickly to trigger one.

The question, as Ahmed recently posed it in the Journal of Neuroscience, is a fairly straightforward one: “Is age-related slowing principally a consequence of increased effort costs from the muscles, or reduced valuation of reward by the brain?”

Her team recruited 80 study participants and separated them into two age groups: a younger cohort (18 to 35) and an older one (66 to 87). Stationed in front of a computer screen, each participant was instructed to move the cursor toward a target by manipulating the handle of a robotic arm. Some of the targets would explode with a bing bing sound when hit, and the study subjects would earn points.

Both groups hit the exploding targets more quickly than those lacking such a “reward,” but the younger participants did it by moving the arms faster while the seniors relied on their ability to anticipate the arrival of the targets. When researchers added an 8-pound weight to the robotic arms used by the young folks, it negated their speed advantage. So, they mimicked the seniors’ anticipatory strategies.

“The brain seems to be able to detect very small changes in how much energy the body is using and adjusts our movement accordingly,” explains study coauthor Robert Courter, PhD. “Even when moving with just a few extra pounds, reacting quicker became the energetically cheaper option to get to the reward, so the young adults imitated the older adults and did just that.”

All of which seems to suggest that it’s the increased “effort costs” of moving that slows us down as we age. But Ahmed admits that the brain’s reward centers cannot be dismissed as a potential influence. More research, as they say, will be required before we’ll have a clearer picture of the forces governing our movement challenges — and potential breakthroughs in the diagnosis of Parkinson’s, multiple sclerosis, and other similar diseases.

“Why we move the way we do, from eye movements to reaching, walking, and talking, is a window into aging and Parkinson’s,” she says. “We’re trying to understand the neural basis of that.”

While Ahmed and others delve more deeply into the mysteries of movement, I find myself less anxious for the next scientific breakthrough than with my ability to consistently embrace my slowness. Wherever I’m headed, I’ll get there eventually — and arriving safely is an ample reward.

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How to Keep Your Brain Healthy as You Age https://experiencelife.lifetime.life/podcast/how-to-keep-your-brain-healthy-as-you-age/ Tue, 05 Sep 2023 10:00:40 +0000 https://experiencelife.lifetime.life/?post_type=podcast&p=82052 The post How to Keep Your Brain Healthy as You Age appeared first on Experience Life.

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Can Exercise Mitigate the Effects of Parkinson’s? https://experiencelife.lifetime.life/article/can-exercise-mitigate-the-effects-of-parkinsons/ https://experiencelife.lifetime.life/article/can-exercise-mitigate-the-effects-of-parkinsons/#view_comments Tue, 18 Jul 2023 13:01:48 +0000 https://experiencelife.lifetime.life/?post_type=article&p=76151 Bouts of high-intensity exercise may ease the effects of this common neurodegenerative disease, according to a recent study.

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A bicycle trip across Iowa 20 years ago sparked Jay ­Alberts’s interest in the power of exercise to treat Parkinson’s disease. After riding a tandem with a Parkinson’s patient, he was struck by the improvements in her handwriting after several days of pedaling. “It was a real aha moment,” he tells the Washington Post. “It got me thinking that maybe something was changing in the brain.”

Alberts, a PhD and Cleveland Clinic neuroscientist, has been studying the connection between exercise and Parkinson’s ever since. He suspects that a solid fitness regimen ramps up the production of proteins that boost brain-cell growth. “They don’t produce dopamine, but they may reduce the effects of whatever is causing the loss of dopamine,” he explains.

He points to a recent study involving Parkinson’s patients who pedaled stationary bikes at a high intensity three times a week for eight weeks. Researchers tested the participants’ ability to react to a timed task prior to the study and again after the two months of workouts. The improvements they noted, Alberts believes, “could aid in the performance of activities of daily living.”

Other research suggests that the secretion of the hormone irisin during endurance exercise may reduce the production of alpha-­synuclein, a protein associated with the development of Parkinson’s. And Caroline Tanner, MD, PhD, a neurology professor at the University of California San Francisco, argues that regular workouts may ease chronic inflammation, which has been linked to neurological disorders.

Indeed, Tanner predicts that the 90,000 cases of Parkinson’s currently diagnosed each year in the United States could fall by almost half by 2030 if we simply exercised more regularly and vigorously. “This could have amazing public-health consequences,” she tells the Post.

The anecdotal evidence supporting this view is compelling. Take the case of Bob Sevene, 79, who struggled to stand upright and needed a back brace and walker to get around following his 2019 diagnosis. In 2021, Sevene began a noncontact boxing regimen designed for Parkinson’s patients, as well as a daily high-intensity fit­ness routine that includes 25-minute cycling sessions on a stationary bike and brief sprints in the hallway outside his apartment. The results have been transformative: He no longer needs the back brace or walker.

“My doctors have run strength, balance, and gait tests, and everything has improved,” Sevene says. “They decided to not up my medicine. I’m convinced exercise is the reason.”

Ryan Cotton, DHSc, CEO of Rock Steady Boxing, a program created for people with Parkinson’s, tells the story of a retired military officer who donned the gloves six years ago when he needed a walker to steady himself. “He took out all his frustrations on the bag,” Cotton recalls. “Six months later, he was walking independently and later ran a half-marathon. Today, someone seeing him on the street wouldn’t even notice he had Parkinson’s.”

1 Million
Number of Americans living with Parkinson’s, making it the second-most common neurodegenerative disease after Alzheimer’s.

And Sherri Woodbridge, writing in Parkinson’s News Today, describes how she’s benefitted from the LSVT BIG program, a physical therapy regimen designed to enhance movement. “The BIG treatment improved my walking in general, and I gained confidence with ‘stairstepping,’” she notes. “I no longer take each stair sideways, with extreme caution, and slower than molasses. The program helped me to be more intentional in my ­activities and how I carry them out.”

More research will certainly be forthcoming, but Tanner and others caution those with Parkinson’s against waiting for more evidence before they begin a workout regimen. “There already is enough excellent evidence to suggest this is a very good thing to do if you are a person with Parkinson’s,” she says.

This article originally appeared as “Can Exercise Mitigate the Effects of Parkinson’s?” in the July/August 2023 issue.

Go Deeper

Explore the causes of the world’s fastest growing neurological disorder — and discover the innovative new treatments and functional therapies that can help patients live long and productive lives at “Fighting Parkinson’s.”

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Exercising Safely with Parkinson’s Disease https://experiencelife.lifetime.life/article/exercising-safely-with-parkinsons-disease/ Thu, 13 Apr 2023 13:00:35 +0000 https://experiencelife.lifetime.life/?post_type=article&p=75361 Consistent exercise can help slow the progression of Parkinson’s. Experts weigh in on how to get the best results.

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Nearly 1 million people in the United States are living with Parkinson’s disease, making it the second-most-common neurodegenerative disorder, according to The Parkinson’s Foundation. This condition of the nervous system involves tremors, muscle rigidity, and slower movements. Symptoms can start slowly and get worse over time. Age is a key risk factor, with most people diagnosed at age 65 or older. And while there is currently no cure for the disease, there is hope in slowing the progression of its symptoms.

“Parkinson’s may be a chronic and progressive disease, but daily exercise increases neuroplasticity,” says Tara Sayer, RN, BSN, MSCN, CPT, CES, Dynamic Personal Trainer at Life Time in Des Moines, Iowa. “Consistently exercising can help your brain ‘rewire’ itself and strengthen the communication between neurons to prevent and protect your body from Parkinson’s symptoms for a longer period of time.”

Because exercise is so important in ensuring a higher quality of life for those with Parkinson’s, we spoke with two experts for advice on how to safely reap the benefits.

Meet Our Experts

Tara Sayer, RN, BSN, MSCN, CPT, CES

Sayer is certified in advanced Parkinson’s disease specific training. She works with individuals who have Parkinson’s disease, multiple sclerosis, paraplegia, and other neurological disorders.

Robert Murphy, M.S., CPT, PES, MMACS

Murphy is an ARORA-certified Dynamic Personal Trainer and group training coach at Life Time in Novi, Mich. He has worked with hundreds of individuals with Parkinson’s disease at Life Time and as a certified coach with the Rock Steady Boxing organization.

Before You Start a Workout Program

If you’re diagnosed with Parkinson’s or are experiencing symptoms, it’s important to note that no two cases are the same.

“There’s a popular saying for Parkinson’s coaches: ‘If you’ve met one person with Parkinson’s — you’ve met one person with Parkinson’s,’” says Murphy. “Essentially, no two people will display or experience symptoms the same.”

“Parkinson’s is often referred to as a ‘snowflake disease,’” Sayer adds. “Each person presents uniquely and differs in past medical history, previous workout experience, symptomology, psychology, and ability. The exercises that can benefit a person also depend on their day and how they’re feeling at that moment.”

Before you begin a workout program, consult with your physician or neurologist to discuss your treatment options and recommendations for exercise. “A comprehensive assessment of your past medical history and risks is vital to ensuring safety for anyone with Parkinson’s disease,” says Sayer. “If you’re working with a personal trainer, they’ll need this information as well as an emergency contact for you.” 

5 Tips for Exercising with Parkinson’s Disease

1. Create a safe workout environment.

A safe training space for those with Parkinson’s is essential. “All bags and equipment must be placed on the perimeter of your training space,” Murphy advises. “Be sure to have a chair or mat nearby in case you need to sit or take a break.”

Clothing choices are also important, according to Murphy. “In my opinion, one of the most important pieces of equipment for a Parkinson’s athlete is their shoes,” he says. “Investing in a pair of well-fitting, quality training shoes — think cross-training, not running — will go a long way. I also recommend working out in loose, comfortable athletic gear and having layers for when you heat up or cool down throughout your workout.”

2. Practice balance daily.

One of the most important skills to work on when battling Parkinson’s disease is balance. That’s why Murphy recommends practicing basic balance exercises at least once per day.

“I encourage the people I work with to do balance work for 10 to 12 minutes every day,” says Murphy. “It’s not a lot of time to invest for a lot of benefits.”

Sayer adds that balance work doesn’t have to be complicated. “You don’t need fancy equipment. Balance exercises can be completed at home with minimal or no equipment,” she notes. “Simple, consistent movements like standing on one leg while you brush your teeth or wash the dishes can improve balance significantly. Standing on a pillow, Airex balance pad, or even just while closing your eyes can all be little ways to improve your balance.”

3. Try something new.

There are many different types of exercises that can help slow the progression of Parkinson’s, including the following:

  • Water workouts can help with circulation while creating sustained resistance, which allows you to increase intensity without impact. ARORA Aqua classes are a safe option for enjoying time in the water while also working on coordination, strength, cardio, and mobility.
  • Tai chi brings together the body and the mind, which is why it is is generally recognized as a highly effective modality to slow Parkinson’s symptoms.
  • Noncontact boxing involves gross motor skills and cognitive exercises, along with balance and core strength work. Studies show that this kind of intense movement may be neuroprotective.
  • Dance classes can help you work on balance, coordination, and cognition — while offering the benefits of community and fun.
  • Yoga can help reduce tremors and other motor symptoms by encouraging functional mobility and stability.

“If you find one of these modalities that you enjoy, keep at it!” Sayer advises. “You’re more likely to continue to exercise if you’re doing something you enjoy and look forward to. That is key in any workout program.”

4. Stretch every day.

Flexibility and mobility are crucial to being able to move independently. In combination with exercise, stretching can improve joint and muscular capabilities for those with Parkinson’s.

“Given that many folks battling Parkinson’s will endure stiffness, rigidity, and skeletal muscle discomfort, a daily routine that includes flexibility work is highly recommended,” says Murphy. “Just like balance work, stretching is an important daily habit for individuals with Parkinson’s. Yoga, barre, and stretch workouts are all fantastic modalities to reduce stiffness, move better, and live well.”

5. Lean on your community.

Fighting Parkinson’s is never something you have to do alone. “Look to your personal circle of people who care about you and are ready to fight with you,” says Sayer. “Life Time is also a large community of people who can join your circle. Working with a personal trainer can help you find a workout program that’s right for you, whether that’s one-on-one dynamic personal training or in a group or a class. There are passionate fitness professionals who will not only meet you where you’re at, no matter where you are in your journey, but also be there as part of your support system.”

Sayer also suggests bringing your loved ones to work out with you. “Feel free to bring your spouse or care-partners,” she adds. “I always encourage their presence and love to see my clients working out with people they love!”

Nutrition and Parkinson’s Disease

Nutrition is a crucial factor in maintaining a healthy brain and nervous system, according to Sayer. Nutritious foods also help fuel your workouts and improve your muscle function. She offers the following tips to complement your workout routine.

Eat your omega-3s.

A diet high in omega-3s can be neuroprotective. Research shows its antioxidant properties can protect against free radical damage, which increases risk for diseases. Together with phospholipids, omega-3s also form the basic structure of all cell membranes, and healthy cell membranes are important for brain function. Try seed sources including flaxseed oil or ground flaxseed, chia seeds, hemp seeds, and pumpkin seeds, or other options such as wild-caught salmon, herring, mackerel, and trout. A high-quality fish oil supplement is also a reliable and consistent source.

Prioritize fiber.

High-fiber foods help improve bowel health and nourish the lining of the gut, which leads to better nutrient absorption. The gut and brain are intricately related; to support a healthy brain, you need to support a healthy gut. Most individuals benefit from an intake of at least 30 to 35 grams of fiber per day. Wheat bran, psyllium husk, pears, beans, lentils, broccoli, berries, avocados, apples, nuts, chia seeds, ground flaxseeds, and whole grains like oats can all be helpful sources of fiber. A diet high in insoluble fiber can also help reduce or eliminate constipation, a symptom people with Parkinson’s disease may experience.

Go for anti-inflammatory foods and avoid refinded sugar.

Anti-inflammatory foods and herbs can help prevent cellular stress for a healthier nervous system. Aim for more berries, fatty fish, green leafy vegetables, mushrooms (like lion’s mane, chaga, reishi, and cordycepts), avocados, extra-virgin olive oil, cabbage, onions, garlic, cocoa, and elderberries. Sayer also recommends avoiding sugars and refined carbohydrates such as white flours in bread or pasta, crackers, and other processed products.

Supplement when needed.

CoQ10, creatine, N-acetylcysteine, vitamin D3, and vitamin B6 are all nutrients that can be especially helpful forindividuals with Parkinson’s disease, assisting with energy levels, workout recovery, immunity, and more. Botanicals like Mucuna pruriens (an Ayurvedic herb) and turmeric also have anti-inflammatory properties. Check with a healthcare professional before taking any new supplements.

Consider a moderate dose of caffeine.

Studies show that a moderate amount of caffeine can help with movement symptoms for those with Parkinson’s disease. A cup of green tea is an option for consuming a small amount of caffeine with added anti-inflammatory benefits.

Sayer notes that it’s important to consult with your healthcare team when it comes to nutrition. “Be sure to discuss your medications and timing of eating with a nutrition professional,” she says. “Certain types of eating patterns can help with insulin transport and dopamine synthesis. It’s also important to know how your food may interact with your medications.”

Go Deeper

Explore the causes of the world’s fastest growing neurological disorder — and discover the innovative new treatments and functional therapies that can help patients live long and productive lives at “Fighting Parkinson’s.”

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PUMPING IRONY: Every Breath You Take https://experiencelife.lifetime.life/article/pumping-irony-every-breath-you-take/ Tue, 28 Feb 2023 18:00:29 +0000 https://experiencelife.lifetime.life/?post_type=article&p=72919 While air quality nationwide has improved markedly since the turn of the century, recent research highlights the cognitive damage that even low levels of pollution can exact on the aging brain.

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As much as I’ve come to accept that life as a septuagenarian is a bit of a crapshoot, what with random cellular mischief occasionally complicating basic bodily functions, there are moments when my cautious optimism can’t help but descend into murky fatalism. Last week, for instance, I stumbled upon a raft of new research suggesting that all the health-affirming habits I’ve established over the years may be undone by a force over which I have very little control: the air I breathe.

We’ve known for decades what air pollution can do to the lungs, and more-recent research has revealed its harmful effects on the cardiovascular system. But fresh revelations are particularly noteworthy — and disturbing — for older adults. They link poor-quality air to a higher risk of Parkinson’s disease, late-life depression, and dementia.

In a paper to be presented at the American Academy of Neurology’s annual meeting in April, lead study author Brittany Krzyzanowski, PhD, a post-doctoral researcher at the Barrow Neurological Institute, and her team identified 83,674 seniors diagnosed with Parkinson’s in 2009 among more than 22.5 million Medicare beneficiaries involved in the study. When they plotted the addresses of all participants on a map showing average air pollution exposure levels, and they adjusted for a variety of health and lifestyle factors, the team found that those living in places with the highest exposure to fine particulate matter were 25 percent more likely to develop Parkinson’s than those living in the lowest exposure areas.

“By mapping nationwide levels of Parkinson’s disease and linking them to air pollution,” Krzyzanowski explains, “we hope to create a greater understanding of the regional risks and inspire leaders to take steps to lower risk of disease by reducing levels of air pollution.”

“By mapping nationwide levels of Parkinson’s disease and linking them to air pollution,” Krzyzanowski explains, “we hope to create a greater understanding of the regional risks and inspire leaders to take steps to lower risk of disease by reducing levels of air pollution.”

Xinye Qiu, PhD, of the Harvard T. H. Chan School of Public Health, and Liuhua Shi, ScD, of Emory University, took a similar approach in a study published recently in JAMA. Their team of researchers mapped the addresses of more than 1.5 million Medicare enrollees who were diagnosed with late-onset depression between 2005 and 2016. They found that long-term exposure to fine particulate matter, nitrogen dioxide, and ozone increased the risk of developing the condition — even when pollution levels were lower than government-regulated mandates.

It’s been nearly 10 years since researchers first suggested a link between cognitive dysfunction and air quality, but two recent studies offer both some validation of those earlier findings as well as some promise of mitigation. A January 2022 report, published in Proceedings of the National Academy of Sciences, noted a significant reduction of dementia risk among older women living in areas where levels of nitrogen dioxide and fine particulate matter had dissipated over a 10-year period. And a second study, published in the February 2022 issue of PLOS Medicine, corroborated those findings, noting that lower levels of pollutants resulted in a slower rate of cognitive decline among study participants.

As Judith Graham reports in Kaiser Health News, older adults are particularly vulnerable to fine particulate matter, which can migrate from the nasal cavities to the lungs and brain, triggering inflammation and exacerbating chronic conditions such as heart disease and respiratory illnesses. Graham cites the work of University of Southern California neurobiologist Caleb Finch, PhD, whose research team is embarking on a five-year study to dig deeper into the threat air pollution presents to the aging brain and determine how to most effectively respond.

“The main point is we now realize that Alzheimer’s disease is very sensitive to environmental effects, including air pollution,” Finch says.

“The main point is we now realize that Alzheimer’s disease is very sensitive to environmental effects, including air pollution,” Finch says.

That’s a view shared by The Lancet’s Commission on Dementia Prevention, Intervention, and Care, which in 2020 listed air pollution as one of the risk factors for dementia. Addressing these risks could prevent or delay as many as 40 percent of global dementia cases, the commission notes.

And while air quality has steadily improved over the years — average U.S. annual levels of fine particulate matter, for instance, dropped by 43 percent between 2000 and 2019 — research suggests that seniors remain particularly vulnerable. “With older adults, there really is no level at which air pollution is safe,” argues Jennifer Ailshire, PhD, an associate professor of gerontology and sociology at the University of Southern California.

Ailshire says she’s “hopeful” that air quality continues to improve, but she cautions seniors to check pollution levels before embarking on any outdoor activities. “If it’s a high-risk day,” she warns, “that might not be the day to go out and do heavy yardwork.”

There’s about three feet of snow obstructing my carriage walk after snowplows yesterday cleared our side of the street. Shoveling that out was on my to-do list today, so I checked the weather app on my phone and learned that the quality of the air outside was only moderately risky. That seems to generally align with life in my eighth decade, so I guess I’ll grab my shovel and take my chances.

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What Are the Risk Factors and Triggers for Functional Neurological Disorders? https://experiencelife.lifetime.life/article/what-are-the-risk-factors-and-triggers-for-functional-neurological-disorders/ https://experiencelife.lifetime.life/article/what-are-the-risk-factors-and-triggers-for-functional-neurological-disorders/#view_comments Thu, 26 Jan 2023 12:00:00 +0000 https://experiencelife.lifetime.life/?post_type=article&p=68427 It turns out there are a variety of different triggers, say experts.

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For Functional Neurological Disorders (FND), David Perez, MD, MMSc, director of the Functional Neurological Disorder Clinical Unit and Research Program at Massachusetts General Hospital says, it’s important to investigate potential risk factors and triggers that can also perpetuate the disorder. Yet, for each patient, these elements might be unique and interact differently.

Adverse early life experiences, such as abuse or neglect, can be a risk factor for FND. So can a history of depression, anxiety, and trauma symptoms. But these are far from universal among FND patients, and an assumption of their centrality to the condition has contributed over the years to neglected and misunderstood patients.

“Some FND patients do not report adverse life experiences and have never been in therapy,” Perez says. “They’re used to pushing through and doing 120 percent. For reasons that might be personal to each case, that person with high-achieving tendencies can also develop FND.”

Using a brain-as-computer analogy, Perez notes that there are many ways that software can crash. “That’s why a one-size-fits-all formulation falls flat in the FND population.”

FND tends to be triggered by something that draws attention to the body. That might be a common event, such as a minor physical injury, a viral illness, or even a vaccination. “The physical triggering event is usually something that would be expected to get better,” explains St. George’s, University of London, neurologist Mark Edwards, PhD, on the website FND Hope.

“Some FND patients do not report adverse life experiences and have never been in therapy,” Perez says. “They’re used to pushing through and doing 120 percent. For reasons that might be personal to each case, that person with high-achieving tendencies can also develop FND.”

“For example, a flu that would be expected to go [away] after a few days’ rest, but instead symptoms continue and functional symptoms emerge. Sometimes this process can be very quick and dramatic or sometimes much slower.”

It’s not the injury, illness, or event itself that triggers FND, but the attention, awareness, emotion, and meaning-making that accompanies it. If someone has an injury to their leg, they might then fixate on it, says London-based psychiatrist Alastair Santhouse, MA, FRCP, FRCPsych, author of Head First: How the Mind Heals the Body. “They notice the sensations in that part of the body, they’re hesitant to use it, and the symptom develops further. By the time you see them in the clinic, they may already be walking with a limp or using walking aids.”

Paying attention to the body is not inherently dangerous, notes Gavin Martin who was diagnosed with an FND in 2010 (learn more about his story here). But attention can amplify signals and give form to ambiguous feelings in a way that isn’t always helpful. “Imagine I’m walking through a field and feel the tickling of the grass on my legs, and I suddenly encounter a spider and it freaks me out: In the future, my brain at a subconscious level will be more likely to associate the ambiguous feeling of grass on my legs with the presence of a spider.”

In this way, FND isn’t caused by physical or psychological factors alone, but by the way they interact in the brain. “They’re both converging on a common system in the brain, where all these things are processed together. To some extent, they become indistinguishable,” he explains.

This process is not voluntary and can result in symptoms that are very real. It also helps explain why postconcussion patients or people with “organic” neurological disorders such as Parkinson’s, epilepsy, or MS are particularly vulnerable to developing functional-neurological symptoms in addition to those caused by their primary condition.

As Martin describes it, “The brain learns the injury, absorbs it, and then reenacts it.”

“We are not talking about personal flaws or weak-willed patients wishing to be sick,” Perez stresses. This understanding is crucial for providers to deliver a diagnosis of FND clearly and empathetically — and to point patients toward helpful treatments.

This was excerpted from “What Is a Functional Neurological Disorder?” which was published in the January/February 2023 issue of Experience Life.

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PUMPING IRONY: A Parley With Parkinson’s https://experiencelife.lifetime.life/article/pumping-irony-a-parley-with-parkinsons/ https://experiencelife.lifetime.life/article/pumping-irony-a-parley-with-parkinsons/#view_comments Tue, 17 Jan 2023 18:00:20 +0000 https://experiencelife.lifetime.life/?post_type=article&p=70463 While I only occasionally wonder whether Parkinson’s awaits me somewhere down the road, recent research provides some calming evidence that lifestyle changes may help keep the disease at bay.

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I’m reasonably confident that I don’t have Parkinson’s disease, though my old pal Leo, who does, often likes to call attention to a slight tremor in my left hand when we’re kibbitzing at the coffee shop. “It’s just the caffeine,” I assure him (and myself) — nothing to worry about.

None of the other symptoms — slowed movement, rigid muscles, impaired posture, or speech problems — seem to have surfaced, which makes me think I’m mostly in the clear. Then I notice how my handwriting sometimes crumbles into gibberish, which seems vaguely disconcerting. I’ve never been one to “catastrophize” these sorts of things (sign above my desk: “Learn to love not knowing.”), but such incidents do give one pause.

So, it’s been interesting — OK, reassuring — to learn about recent advances in Parkinson’s research that suggest lifestyle changes may help mitigate the physical and mental toll this currently incurable disease can exact.

Diet — as it affects the gut microbiome — may play a role, according to the results of a study published last week in Nature Communications. Neurologist Haydeh Payami, PhD, and her team of researchers at the University of Alabama at Birmingham analyzed stool samples from 490 people living with Parkinson’s and found an overabundance of certain inflammatory pathogens and toxic molecules, as well as a specific bacterial product called curli. The resulting imbalance in their gut microbiomes, Payami suggests, causes the dysregulation of neurotransmitters that characterizes Parkinson’s.

“We found that over 30 percent of the micro-organisms and bacterial genes and pathways tested have altered abundances in Parkinson’s disease, which indicates a widespread imbalance,” she says.

To hear Payami tell it, ongoing research in this field, known as metagenomics, will likely reveal more about how diet may effectively rebalance the gut microbiome and perhaps reduce the risk of Parkinson’s: “We anticipate that in the near future we will have the tools and the analytic power to use metagenomics as a new approach to study Parkinson’s disease heterogeneity, search for biomarkers, delve deeper into the origin and progression of Parkinson’s disease subphenotypes, and investigate the potential in manipulating the microbiome to prevent, treat, and halt the progression of Parkinson’s disease.”

Payami’s study doesn’t offer much in the way of dietary recommendations, but there’s plenty of research touting the value of adding certain types of food to your diet when experiencing bacterial imbalances in the gut microbiome. I suspect she’d be leaning more toward manipulative processes such as fecal transplants, which have already been shown to be an effective rebalancing tool. And, while certain aspects of the procedure tend to diminish my enthusiasm — despite its salutary effects — I can imagine it could prove incrementally more attractive should I eventually find myself beset by Parkinson’s more debilitative symptoms. Meanwhile, there’s always yogurt.

And exercise!

Caroline Tanner, MD, PhD, a neurology professor at the University of California San Francisco, predicts that the 90,000 cases of Parkinson’s currently diagnosed each year could fall by almost half by 2030 if we simply exercised more regularly and vigorously.

Caroline Tanner, MD, PhD, a neurology professor at the University of California San Francisco, predicts that the 90,000 cases of Parkinson’s currently diagnosed each year could fall by almost half by 2030 if we simply exercised more regularly and vigorously. “This could have amazing public-health consequences,” she tells Marlene Cimons in the Washington Post.

The anecdotal evidence supporting this view is certainly compelling. Cimons cites the case of Bob Sevene, 79, who struggled to stand upright and needed a back brace and walker to get around following his 2019 diagnosis. Last year, Sevene began a noncontact boxing regimen designed for Parkinson’s sufferers as well as a daily high-intensity fitness routine that includes 25-minute cycling sessions on a stationary bike and brief sprints in the hallway outside his apartment. The results have been transformative; he no longer needs the back brace or walker.

“My doctors have run strength, balance, and gait tests, and everything has improved,” Sevene tells Cimons. “They decided to not up my medicine. I’m convinced exercise is the reason.”

Ryan Cotton, DHSc, CEO of Rock Steady Boxing, a program created for Parkinson’s patients, tells the story of a retired military officer who donned the gloves six years ago, when he needed a walker to steady himself. “He took out all his frustrations on the bag,” Cotton says. “Six months later, he was walking independently and later ran a half-marathon. Today, someone seeing him on the street wouldn’t even notice he had Parkinson’s.”

A bicycle trip across Iowa 20 years ago sparked Jay Alberts’s interest in the power of exercise to treat the disease. Riding a tandem with a Parkinson’s patient, he was struck by the improvements in her handwriting after several days of pedaling. “It was a real ‘aha’ moment,” he recalls. “It got me thinking that maybe something was changing in the brain.”

Alberts, PhD, a neuroscientist at Cleveland Clinic’s Neurological Institute, has been studying the connection between exercise and Parkinson’s ever since. He suspects that a solid fitness regimen ramps up the production of proteins that boost brain-cell growth. “They don’t produce dopamine, but they may reduce the effects of whatever is causing the loss of dopamine,” he explains.

The more vigorous the workout, the more protein the body produces, Alberts says, but any amount of activity is better for the brain than none at all.

He points to a recent study involving 50 Parkinson’s patients who pedaled stationary bikes at a high intensity three times a week for eight weeks. Researchers tested the participants’ ability to react to a timed task prior to the study and again after the two months of workouts. The improvements they noted, Alberts believes, “could aid in the performance of activities of daily living.”

Other research suggests that the secretion of the hormone irisin during endurance exercise may reduce the production of a protein, alpha-synuclein, associated with the development of Parkinson’s. And Tanner argues that regular workouts may ease chronic inflammation, which has been linked to neurological disorders.

More research will certainly be forthcoming, but Tanner and others caution Parkinson’s sufferers against waiting for more evidence before they begin a workout regimen. “There already is enough excellent evidence to suggest this is a very good thing to do if you are a person with Parkinson’s,” she says.

And probably even if you’re pretty sure you’re not.

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What Is a Functional Neurological Disorder? https://experiencelife.lifetime.life/article/what-is-a-functional-neurological-disorder/ https://experiencelife.lifetime.life/article/what-is-a-functional-neurological-disorder/#view_comments Mon, 09 Jan 2023 12:00:16 +0000 https://experiencelife.lifetime.life/?post_type=article&p=67673 Hybrid disorders of the brain, mind, and body once confounded physicians and researchers. Today experts are beginning to uncover the conditions’ complexities — and how to treat them.

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In 2010, Gavin Martin suffered a series of injuries at his workplace. None of them were terribly serious, and they healed on their own. But Martin (not his real name), who was in his mid-20s, found that the resulting disabilities — shooting pain, weakness, and speaking difficulties — persisted. Then they began to spread.

During the next few years, Martin lost function in his vocal cords and his limbs. “At my most disabled, I was in a wheelchair, unable to walk. I couldn’t use my hands for more than grasping weakly,” he recalls. “There were months at a time when I couldn’t speak.”

His quest for a diagnosis took him to neurologists, rheumatologists, allergists, and immunologists. He visited five major medical centers, but no one could figure out what was wrong. Some of the doctors thought he might have an undiscovered genetic condition that could prove fatal, a hypothesis that only increased Martin’s alarm.

“Eventually, I ran out of places to go,” he says. “I just could not get referred anywhere else.”

In a last-ditch effort, he applied to the highly selective National Institutes of Health Undiagnosed Diseases Program, and was accepted in 2017. A team of specialists from multiple disciplines examined him.

Their diagnosis was clear: Martin had functional neurological disorder (FND).

“I think their team actually knew what I had just by looking at my application,” he says.

The FND-affected brain looks healthy on MRI studies or CT scans. But the way it communicates — with itself, the body, and the outside world — has gone awry. It’s not a “hardware” problem, as in stroke or multiple sclerosis (MS). Structurally, the brain is healthy.

Imagine the brain as a computer;
with functional neurological disorders, it’s running faulty Software.

Yet FND does represent “changes in the software circuitry of the brain,” says Jeremy Schmoe, DC, DACNB, director of the Functional Neurology Center in Minnetonka, Minn. Imagine the brain as a computer; with FND, it’s running faulty software.

Therein lies the conceptual challenge of the disease: It is rooted in the brain, but the brain is healthy; it’s a signaling problem, not a structural one.

“I hit a real emotional low point,” says Martin. “I thought they were saying I had a delusion of illness — like I had inflicted it on myself or there was no substantial disability beyond me thinking that I had one. It was incredibly unnerving.”

Yet as Martin researched FND, he started to understand the condition in a new way. He also gained access to emerging insights and treatments that have made a world of difference to his recovery.

Complicated Signals

Through the centuries, FND has been given various names, including “conversion disorder” and “hysteria.” Stigma has often followed it.

“People thought these patients were constitutionally weak, exaggerating their symptoms, or making it up,” says London-based psychiatrist Alastair Santhouse, MA, FRCP, FRCPsych, author of Head First: How the Mind Heals the Body. “We have a far more sophisticated understanding now of what this is. These symptoms are not made up or imagined.”

Symptoms of FND can include weakness or paralysis, abnormal movements, changes in speech, difficulty swallowing, seizures, numbness, and sensory challenges, such as difficulty seeing, smelling, or hearing. Many of these symptoms are also present in other neurological conditions, such as Parkinson’s, MS, epilepsy, or stroke, but the underlying causes are different.

Back when it was known as conversion disorder, FND was thought of as a diagnosis of exclusion, made only when tests had ruled out all other possible diseases. The diagnosis also required a connection to a psychological stressor.

“It was thought that some psychic distress was being converted into a physical symptom,” explains Santhouse. For instance, if someone had seen something upsetting, the belief was that they might develop blindness in response.

But functional symptoms are rarely that literal. And although many people diagnosed with FND do have a history of traumatic or stressful life events, not all do.

Different brain areas communicate in a way that allows us to move around and think and sense things.” When someone has an illness, injury, or upsetting experience, it can change the way these brain areas talk to each other.

Neurologists can now confidently diagnose FND using specific neurological examination features, says David Perez, MD, MMSc, director of the Functional Neurological Disorder Clinical Unit and Research Program at Massachusetts General Hospital. By the time the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) was published, in 2013, the disorder had been reframed as a “rule-in” diagnosis — which means a specific list of criteria must be met rather than ruled out — and renamed FND.

Some of the positive signs used to diagnose FND include Hoover’s test for functional weakness, in which a person may have significant weakness in one leg when they consciously try to move it but find that their strength returns to normal when movement is triggered in a different way. Or someone might be unable to walk or turn, but if they’re distracted, mobility returns.

Estimating the prevalence of FND is challenging because of how the definition has changed over time. But a 2010 multicenter study in Scotland found that functional/psychological disorders were the second most common diagnosis category in outpatient neurology clinics, behind only headaches. And an investigation published in JAMA Neurology in 2021 estimated annual spending for FND-related emergency-room visits and inpatient care to be more than $1.2 billion per year.

FND and the Brain

“FND is a condition that lives at the intersection of neurology and psychiatry,” explains Perez. It falls under a larger category of hybrid brain–mind–body conditions that are often referred to as functional disorders — a category that can include conditions such as irritable bowel syndrome (IBS) and fibromyalgia, which are distinguishable mainly in their effects.

Functional disorders are contrasted with “organic” diseases, such as MS or cancer, which are diagnosed based on biological changes in the body.

What makes FND unique is the way it rewires the brain to produce neurological symptoms. In FND, the amygdala (part of the limbic system that’s involved in the stress response) is hyperactive, while the brain’s frontal lobe (which plays a role in calming the amygdala) is underactive, explains Stanford University neuropsychiatrist Sepideh Bajestan, MD, PhD.

“This is what we see in PTSD and panic disorder also,” she says. But in types of FND that involve abnormal movements, the limbic system is also hyperconnected to the parts of the brain that control movement. This means that bodily movement can be affected by current or even past stresses. (Imagine the way your hands might involuntarily shake after narrowly avoiding an accident. Now imagine if that state didn’t pass.)

Functional ­symptoms for which no ­physical cause can be found — headaches, stomach­aches, back pain, ­fatigue, dizziness, or chest pain — are ­incredibly common.

“Think of the brain as an ensemble,” says Martin. “Different brain areas communicate in a way that allows us to move around and think and sense things.” When someone has an illness, injury, or upsetting experience, it can change the way these brain areas talk to each other.

“Certain parts of the brain, like the amygdala, can influence the operation of everything else because they’re highly interconnected with other parts of the brain,” he explains. “All of a sudden you have one part of the brain that’s yelling at everyone else, and the other parts of the brain respond to that.”

Functional symptoms for which no physical cause can be found — headaches, stomachaches, back pain, fatigue, dizziness, or chest pain — are incredibly common. In one study, a physical cause was shown in only 16 percent of the 567 new complaints of common symptoms presented to U.S. primary-care practices over a three-year period.

Anyone who has experienced a tension headache or nervous stomach in a stressful moment knows that our emotions can lead to physical symptoms. “The difference between FND and some other more passing functional symptoms is that in FND, these patterns get stuck,” says Martin. “The brain has the ability to learn and change, and sometimes it doesn’t go back.”

Functional disorders like fibromyalgia are likely driven by at least some different mechanisms than FND. But commonalities that might underlie the broader category of brain–mind–body conditions are an active area of research. “A subset of patients with FND also have fibromyalgia or IBS — what we think of as functional somatic disorders,” Perez says. “The increased coexistence of these conditions in one population potentially suggests some shared mechanisms.”

This means that as research into FND progresses, people suffering from other chronic brain–mind–body disorders also stand to benefit. Advances in understanding FND also start to erase the often arbitrary distinction between mental and physical health, he notes.

“In fact, maybe with the challenges of the pandemic and everything else going on, we’re realizing that physical health and mental health are interconnected — that one’s mental health is one’s physical health.”

Risk Factors and Triggers

For FND, Perez says, it’s important to investigate potential risk factors and triggers that can also perpetuate the disorder. Yet, for each patient, these elements might be unique and interact differently.

Adverse early life experiences, such as abuse or neglect, can be a risk factor for FND. So can a history of depression, anxiety, and trauma symptoms. But these are far from universal among FND patients, and an assumption of their centrality to the condition has contributed over the years to neglected and misunderstood patients.

“Some FND patients do not report adverse life experiences and have never been in therapy,” Perez says. “They’re used to pushing through and doing 120 percent. For reasons that might be personal to each case, that person with high-achieving tendencies can also develop FND.”

Returning to the brain-as-computer analogy, Perez notes that there are many ways that software can crash. “That’s why a one-size-fits-all formulation falls flat in the FND population.”

FND tends to be triggered by something that draws attention to the body. That might be a common event, such as a minor physical injury, a viral illness, or even a vaccination. “The physical triggering event is usually something that would be expected to get better,” explains St. George’s, University of London, neurologist Mark Edwards, PhD, on the website FND Hope.

“Some FND patients do not report adverse life experiences and have never been in therapy,” Perez says. “They’re used to pushing through and doing 120 percent. For reasons that might be personal to each case, that person with high-achieving tendencies can also develop FND.”

“For example, a flu that would be expected to go [away] after a few days’ rest, but instead symptoms continue and functional symptoms emerge. Sometimes this process can be very quick and dramatic or sometimes much slower.”

It’s not the injury, illness, or event itself that triggers FND, but the attention, awareness, emotion, and meaning-making that accompanies it. If someone has an injury to their leg, they might then fixate on it, says Santhouse. “They notice the sensations in that part of the body, they’re hesitant to use it, and the symptom develops further. By the time you see them in the clinic, they may already be walking with a limp or using walking aids.”

Paying attention to the body is not inherently dangerous, notes Martin. But attention can amplify signals and give form to ambiguous feelings in a way that isn’t always helpful. “Imagine I’m walking through a field and feel the tickling of the grass on my legs, and I suddenly encounter a spider and it freaks me out: In the future, my brain at a subconscious level will be more likely to associate the ambiguous feeling of grass on my legs with the presence of a spider.”

In this way, FND isn’t caused by physical or psychological factors alone, but by the way they interact in the brain. “They’re both converging on a common system in the brain, where all these things are processed together. To some extent, they become indistinguishable,” he explains.

This process is not voluntary and can result in symptoms that are very real. It also helps explain why postconcussion patients or people with “organic” neurological disorders such as Parkinson’s, epilepsy, or MS are particularly vulnerable to developing functional-neurological symptoms in addition to those caused by their primary condition.

As Martin describes it, “The brain learns the injury, absorbs it, and then reenacts it.”

“We are not talking about personal flaws or weak-willed patients wishing to be sick,” Perez stresses. This understanding is crucial for providers to deliver a diagnosis of FND clearly and empathetically — and to point patients toward helpful treatments.

Treating FND

Educating patients about FND is the first step in treating it. “The starting point is to come to a shared understanding of what’s causing the symptoms,” Santhouse says. “Then you can start to treat them.”

Like many chronic conditions, FND benefits from a multidisciplinary approach. “The two mainstays of treatment are physical rehabilitation — including physical therapy, occupational therapy, and/or speech and language therapy — coupled oftentimes with psychotherapy,” Perez says.

For Martin, the most successful treatment was physiotherapy that got him out of his wheelchair, and then off a cane, until he was walking normally again. He has also benefited from mind–body techniques, such as body scanning, awareness exercises, and progressive muscle reaction, and an app to help deal with chronic pain.

Physiotherapists can also work with patients to retrain particular movements, usually using some kind of diversion so the patient isn’t actively focusing on the body part in question.

For instance, some patients who can’t walk as they once did are able to run or walk on a treadmill. Using music or automatic movements from learned dances can also help improve movement.

Researchers conducting a pilot trial of 60 patients who’d had FND symptoms for more than six months found that after five days of specialized physiotherapy intervention, 72 percent of patients reported symptom improvement, compared with 18 percent of patients in the control group who received standard physiotherapy.

The combination of movement retraining, cognitive behavioral therapy, and limiting overwhelming stimuli was transformative for Martin. (For some FND patients, symptoms are triggered by sensory overstimulation — a hypersensitivity that’s like what people with autism experience: Lights can feel too bright, touch can be uncomfortable or painful, and smells or sounds can feel overpowering.)

“It took time and many false starts, but my symptoms began to stabilize, and then to recede,” Martin recalls. “I found I could walk for longer and work more consistently, and I felt less pain. When a limb started to twitch, I’d pull my attention off it, occupy myself with other movements, or moderate my pain with deep breaths.”

In 2018, he had more than 150 days of headache and was hospitalized multiple times. In 2019, the benefits of his persistent healing work became evident — he had only three headaches and recovered at home.

Perez says that patients with FND have reason for hope, but he also cautions that more research into additional therapeutic interventions is needed. “Out of the first 100 patients that come through our clinic, about 40 to 50 percent saw at least some degree of improvement. A similar 50 percent or so continue to be significantly impaired by their FND.”

Schmoe finds that some of his FND patients benefit from hypnosis and eye movement desensitization and reprocessing (EMDR) — practices that aim to access and calm deep limbic areas of the brain.

And interest is growing in the potential of psychedelics to treat a range of challenging neuropsychiatric conditions, including FND. (Research on the use of psychedelics to treat FND is ongoing in the United Kingdom.)

Other potential novel therapies might include neuromodulation (such as vagus-nerve stimulation) or transcranial magnetic stimulation, which uses magnetic fields to stimulate nerve cells in the brain.

“Patients with FND keep us on our toes in a variety of ways. A rich and varied toolkit is likely to be needed.”

Building an evidence base for effective treatments is challenging for conditions, such as FND, that benefit most from highly individualized treatments, Perez notes. “Patients with FND keep us on our toes in a variety of ways. A rich and varied toolkit is likely to be needed.”

Much work remains to be done for people with functional seizures, which have proven tough to treat. But here, too, there are hopeful signs. A recent small pilot study of children with functional seizures trained those patients to reinterpret their body signals and engage in movements to counteract the onset of seizures. Every one of the kids in the treatment group was seizure-free after one week, and 82 percent remained seizure-free two months later.

For now, FND treatment can be difficult to access, with only a limited number of multidisciplinary centers and specialized clinics. Perez hopes that eventually all major neurology outpatient clinics will be able to offer integrated, multidisciplinary care, not only for FND, but for a range of brain-based conditions across neurology and psychiatry.

Martin envisions a day when it won’t take specialists to offer this kind of support. “A sports-medicine clinic already has physical and occupational therapists, sometimes an osteopath, and sometimes a physiatrist,” he notes. (Physiatrists are physicians who specialize in rehab involving the brain and spinal cord.)

“If those people were able to offer psychologically informed treatment as well, then we could see FND treatment in the community.” (Martin shares emerging insights into FND on Twitter under the handle @FndPortal.)

Today, Martin has recovered more than most people with FND. He still has weakness in his arms and legs, plus occasional headaches and voice problems. But his symptoms have receded enough that they no longer dominate his days.

“FND is still there,” he says. “But I’ve carved out enough recovery that I can live my life again.”

This article originally appeared as “Understanding Functional Neurological Disorders” in the January/February 2023 issue of Experience Life.

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PUMPING IRONY: Parkinson’s: The Next Pandemic? https://experiencelife.lifetime.life/article/pumping-irony-parkinsons-the-next-pandemic/ https://experiencelife.lifetime.life/article/pumping-irony-parkinsons-the-next-pandemic/#view_comments Mon, 17 May 2021 20:09:35 +0000 https://experiencelife.lifetime.life/?post_type=article&p=41579 Cases of the debilitating neurological disease have been surging in recent years and some researchers suggest COVID-19 may accelerate the trend.

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Dire warnings about the “next pandemic” have been circulating almost from the beginning of our current struggle with COVID-19, as epidemiologists argue that it’s not a matter of if but only of when a new virus emerges to test our public-health (and political) systems. Some research, however, suggests that it’s already arrived — and it’s only tangentially linked to a bug.

And, of course, it’s hitting those of us here in Geezerville the hardest.

Parkinson’s disease (PD) is the world’s fastest-growing neurological syndrome, increasing by 35 percent in the last 10 years in the United States and expected to strike more than 12 million people worldwide by 2040. And, to hear neuroscientist Leah Beauchamp, PhD, and her team of Australian researchers tell it, COVID is likely to accelerate that trend.

Writing in the Journal of Parkinson’s Disease, Beauchamp describes the neurological toll the novel coronavirus exacts on its sufferers and notes similar patterns and outcomes during other major influenza outbreaks, including the 1918 pandemic. In each of these cases, scientists documented instances in which the virus entered the brain and triggered the kind of neuroinflammation thought to play a role in the onset of Parkinson’s.

“A single pathogen is unlikely to be responsible for the entire pathogenesis of PD, but there is some evidence that certain viral infections may increase the susceptibility of PD and parkinsonism,” she writes. Some research suggests that the virus delivers a “first hit” that activates certain cells that make the brain more predisposed to damage from a later second strike.

Beauchamp cites recent research showing neurological damage in COVID-19 patients and notes that, despite the lack of a control group in these studies, certain symptoms — especially an inability to smell — may point to a link between the virus and PD. “One of the commonest causes of impaired olfactory function are the neurodegenerative disorders of Alzheimer’s and Parkinson’s disease,” she notes. “Patients with PD who exhibit decreased olfactory ability appear to have a significant increase in their risk of progression in the disease.”

Much more research will be needed to solidify such a hypothesis, Beauchamp admits, but with Parkinson’s cases already surging, the potential COVID link does little to calm fears of another major public-health issue. “With more than 23 million people infected with COVID-19 worldwide,” she notes, “the potential increase in the number of cases of parkinsonism in the coming years is going to have serious ramifications for the healthcare systems of many countries, and a well-considered proactive response should be implemented.”

Ray Dorsey, MD, a neurologist at the University of Rochester, shares Beauchamp’s concerns about the surging Parkinson’s rates, but he suggests that the proper response is more environmental than epidemiological. “Numerous byproducts of the Industrial Revolution, including specific pesticides, solvents, and heavy metals, have been linked to Parkinson’s disease,” he noted in a 2018 study. “Countries that have undergone the most rapid industrialization have seen the greatest increase in the rates of Parkinson’s disease.”

The primary culprit may be trichloroethylene (TCE), a chemical found in numerous household products and also used in dry cleaning and industrial degreasing operations. A 2011 study in the Annals of Neurology linked TCE exposure in the workplace with a six-fold increase in risk of developing Parkinson’s and sparked a U.S. Department of Labor warning of its dangers. The European Union has banned the use of the chemical, as have lawmakers in Minnesota and New York.

Still, the EPA estimates some 250 million pounds of TCE are deployed annually in the United States and the chemical is present in about 30 percent of the nation’s groundwater. “We are undersampling how many people are exposed to TCE,” University of Alabama toxicologist Briana de Miranda tells The Guardian. “It’s probably a lot more than we guess.”

And Dorsey believes it’s not just TCE that may be driving the growth in Parkinson’s cases. “Numerous studies have linked well water to Parkinson’s disease, and it’s not just TCE in those cases,” he says. “It can be pesticides like paraquat, too.”

Part of the trend, Dorsey admits, may be linked to increased lifespans, as the condition primarily descends upon seniors. He also points to a dramatic drop in smoking in recent decades as a possible link. Smokers, ironically, are 40 percent less likely to develop the disease than non-smokers, though it’s tempting to note that smokers tend to expire earlier. Scientists have thus far fallen short in their search for a cure, though some medications may slow the advance of the disease.

I mentioned some of this over coffee the other day with my old pal Leo, who has been gamely coping with Parkinson’s for a few years. He listened patiently.

“It’s too bad you never took up smoking,” I quipped. “Maybe it’s not too late.”

He rolled his eyes.

“And I read somewhere that there’s a boxing gym in town that specializes in training Parkinson’s patients in the pugilistic arts,” I added. “Intense exercise is supposed to mitigate its effects.”

“I climb 150 steps in my apartment building every day,” he countered. “That’s intense enough for me.”

The conversation soon drifted off toward more pleasant topics, but as we were getting ready to leave, he pointed a shaky digit finger at my left hand, twitching slightly as I reached for my coffee cup. “I’m worried about that tremor, Boss,” he noted.

“You’ve got enough to worry about, Leo,” I said. “It’s probably just the caffeine.”

“I sure hope so,” he sighed.

“Me too.”

Go Deeper

Explore the causes of the world’s fastest growing neurological disorder — and discover the innovative new treatments and functional therapies that can help patients live long and productive lives at “Fighting Parkinson’s.”

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