Parkinson's Disease, Parkinson's exercise, Research

Research News About Boxing Therapy

News that Rock Steady Boxing works for PD patients

The Miami Herald wrote a feature story about a local Rock Steady Boxing program. Deep in it was real news about research confirming the program’s effectiveness. Here is the nugget:

“Stephanie Combs-Miller, associate professor at the University of Indianapolis’ Krannert School of Physical Therapy, recently conducted the first major study on the effects of boxing therapy on Parkinson’s. Over a two-year period, 88 volunteers, half of whom participated in Rock Steady Boxing, were tracked every six months using physical therapy assessments.
“’We found that people who exercise in a boxing program demonstrated a higher level of function,’’ she said in a release about a lecture she was giving on the subject.
“The theory is that the combination of activities connected to the boxing helps develop strength, agility, endurance and flexibility. Over time, the participants who did the program demonstrated significantly better balance and walking function, compared with Parkinson’s patients who chose other forms of exercise.”

Combs-Miller’s study has not yet been published in a scientific journal. There has been widespread scuttlebutt that the results were positive,

On a personal note, I continue the training three times a week and have improved balance, agility and coordination. My off days are way down. An informal poll of my exercise mates confirmed my experience was also theirs.

A Beautiful You Tube video on participatory medicine

Don’t miss this video on the benefits of a collaborative relationship between doctor and PD patient. It goes to the heart of the argument for a revolution in the continuity of Parkinson’s care.

A Deserved knock on PD treatment nostrums

My friend and fellow retired editor Doug Clifton has written a lovely essay on the dangers of nostrum remedies for PD. Check it out.

PDF Help Line

The Parkinson Disease Foundation offers a reminder about its help line. Someday I hope to have a local version for Tampa Bay.

Do you have questions about Parkinson’s? PDF’s HelpLine team is ready to be a resource for you, your loved ones and patients. Our information specialists
are available Monday through Friday, 9:00 AM to 5:00 PM ET at (800) 457-6676 or info@pdf.org. They can answer questions about PD, point you toward local doctors, support groups and resources, and send free educational materials.

.

Palliative Care, Parkinson's Disease, Parkinson's exercise, Research

TAMPA SEMINAR, BOXING UPDATE, RESEARCH MORSELS

FOX SEMINAR ON PD IN TAMPA FEB. 6

Partners in Parkinson’s is coming to Tampa on Saturday, February 6. The event features a full day of panel discussions, breakout sessions and a resource fair to connect you with clinicians, support and exercise groups and other resources right in the Tampa community.

WHERE:
Hilton Tampa Downtown
211 North Tampa Street
Tampa FL 833602

WHEN:
Saturday, February 6, 2016
8:00 a.m. – 3:30 p.m.

Partners in Parkinson’s events cover topics related to all stages of Parkinson’s disease. Whether you’re newly diagnosed or have been living with Parkinson’s for years, you will learn:
• How Parkinson’s impacts everyone differently, and how to tailor a care team that meets your specific needs
• What to know, ask and expect at an appointment with a movement disorder specialist
• Updates on the most promising Parkinson’s disease research
• How to live well with PD by incorporating diet and exercise into your lifestyle
• The benefits of staying connected to loved ones and to the community
Registration opens at 8 a.m. and a continental breakfast and lunch will be provided.

Visit http://partnersinparkinsons.org to learn more or RSVP today.

MY WEEK FOUR REPORT ON ROCK STEADY BOXING
After four weeks of Rock Steady Boxing experience, I am an even bigger fan. Working out 3x a week has improved my balance markedly and decreased blah days. My training mates offer the same positive assessment Do it if you can. See my earlier post for details.

AARP PRESIDENT BOOSTS PALLIATIVE CARE

Palliative Care, often the missing link in PD management gets a boost from the heavy-hitting AARP.

http://www.aarp.org/politics-society/advocacy/info-2015/palliative-care-living-with-dignity-english.html


IS GOLDEN OLDY ASPIRIN GOOD FOR PD?

Have a look at http://www.pdf.org/en/science_news/release/pr_1450710960

UPDATE ON NILOTINIB

My support group friend Doug Dear passes along these intriguing reports on the anti-cancer drug Nilotinib and its possibilitise for PD treatment:

http://www.npr.org/sections/health-shots/2015/10/17/448323916/can-a-cancer-drug-reverse-parkinsons-disease-and-dementia

Cancer Drug Improved Cognition and Motor Skills in Small Parkinson’s Clinical Trial

Nilotinib (Tasigna) for Parkinsons: Questions and Answers

Palliative Care, Parkinson's Disease, Parkinson's exercise, Research, Uncategorized

TRAIN YOUR BRAIN WITH COMPUTER GAMES

The scientific journal Neurology has editorially endorsed computerized training as a way to slow or prevent cognitive decline in Parkinson’s. The endorsement is somewhat tentative but definitely a boost for Brain Hq-like computer training: “…… cognitive training is modestly effective for improving cognitive function in people with PD.” The editorial concludes: “Given that PD is more than just a movement disorder, cognitive training may be an important option for improving cognitive function in patients with PD.” USF’s School of Aging Studies has a computerized cognitive study underway of PD and is seeking volunteers. The principal investigator is Dr. Jerri Edwards. For more information call USF’s Cognitive Aging Lab at 813-974-6703.

Tampa JCC Wellness Program Launches Jan. 23

The Shuffling Editor has gotten more information on the Tampa Jewish Community Center/USF Health wellness program for Parkinson’s. Exercise classes begin Jan. 26, run for 12 weeks and cost $120.

Tuesdays from 11:30 AM to 12:30 PM is Nia, a new term to me. Wikipedia describes Nia thusly: “Nia dance cardio fitness classes are taught by instructors licensed in the Nia Technique. Each class includes mindful movement guidance and somatic education; class cycles include warm-up, sustained non-impact aerobic conditioning, strength training, cool down and stretching. Nia Fitness classes are taught to music, including pop, electronica, jazz, Latin, New Age, Indian and hip hop. They employ 52 basic movements and techniques that draw on a combination of Jazz, Modern and Duncan Dance styles, Tai Chi, TaeKwonDo and Aikido; and the body mind healing arts of Feldenkrais Method, Alexander Technique and Yoga.”
Thursdays, same hours is chair-based strengthening.
Fridays from 1:30 PM to 2:3 0 PM is Tai Chi.
The Caregiver Support Group begins Jan. 29. It is free and runs for12 weeks on Fridays from 1:30 PM to 2:30 PM. A community event is scheduled Jan. 23, 7-9 PM. The topic is Keep Moving Tampa! For background and contact information see my earlier post: https://shufflingeditor.wordpress.com/2015/10/01/tampa-gets-grant-for-parkinson-wellness-program/

Rock Steady Boxing and Me

I am into the second week ( 3x times a week) of this slightly misnamed program. Of a 90 minute training session, no more than 30 minutes is devoted to punching hanging and big bags. The remaining 60 minutes is spent in floor, strengthening exercises, weight training and Balance exercises such as skipping, sidestepping, butt kicks, monster steps and backwards walking.

Two early observations of the program: I had not realized how degraded my hand-eye coordination had become. That sure explains why my golf swing left me. Second observation. I end sessions more energized than tired. Whether coincidence or not, I have not had a “bad” PD day since starting the program. Bad days are when you feel like you have the flu. I am accustomed to having them one day in five.

Huffington Post had a recent piece on the program: http://www.huffingtonpost.com/jonathan-j-doll-phd/rock-steady-boxing-for-people-with-parkinsons-symptoms—-a-national-perspective_b_8646972.html
The Largo program has no plans for a move into Hillsborough. But I have talked to a person who is seeking to put a franchise location in Channelside.

AN INVALUABLE RESOURCE GUIDE FOR THE NEWLY DIAGNOSED

My friend Kirk Hall has updated his information guide for those new to PD. It is pure gold and is a byproduct of the national research project on palliative care in PD. http://www.shakypawsgrampa.com/index.php/new-blog/entry/parkinson-s-education-resources-1-years-since-diagnosis

SPEAKING OF PALLIATIVE CARE

None of us likes to think our journey will end with dementia. In upwards of 50% of PD cases it does. The financial impact of dementia can be devastating. Money magazine has a helpful review of available options at Money.com/dementia.

Parkinson's Disease, Parkinson's exercise

I’m Boxing Against My Parkinson’s

I now have boxing gloves. Red ones.

I have signed on to a rigorous exercise program called Rock Steady Boxing. It is offered in Largo, FL at Bodyssey gym on Walsingham Road not far from the beach.

For now, the Largo location is the only one in the Tampa Bay area. That’s a 70-minute haul from our Hillsborough manse, in the best of traffic conditions. If the franchise program is as good as its press and promise, I bet it will soon jump the bay into Tampa.

Rock Steady has received a great deal of positive, anecdotal notice lately on CBS TV, local TV and in the Tampa Bay Newspapers (TBN) weekly group. From my two visits, I think the Rock Steadiers are on to something very promising.

TBN reporter Chris George got there before I did. Gym owner Tara Schwartz pitched program benefits this way to George: “ The studies have shown that forced intense exercise has slowed the progression of Parkinson’s. Parkinson’s slows the conduction of the nerve to the muscle, so everything slows down. Boxing does the absolute opposite of that. And it’s a non-contact form of boxing.”

Good elevator speech, Tara. I watched one day. Signed up and worked out the next. Ninety intense minutes to pulsating music and demanding, disciplined but supportive instructors: “elbows up…jab, jab, hook…chest out, stomach in…just 10 more seconds.”

By coincidence, I just ran across this article about intense exercise and how it relieves Parkinson’s symptoms. It talks about yoga but the principles also apply to boxing.

Schwartz’s class typically has 12 to 15 participants who work out ideally at least three days a week. Said Schwartz: “While focusing on overall fitness, strength training, reaction time and balance, workouts include: ring work, focus mitts, heavy bags, speed bags, double ended bags, jump rope, core work, calisthenics and circuit weight training. No boxing experience is necessary and people of all ages are invited to participate.” For more details, check out her website, including fees.

The session I attended ran 90 minutes and had 30 minutes of stretching exercises, 30 minutes of weight training and 30 minutes of working on the punching bags. I intend to give you periodic updates on my progress and impression of the program as I go forward.

One follow up to the palliative care conference in Denver follows:
http://blog.pdf.org/2015/11/30/improving-palliative-care-throughout-the-pd-journey-qa-with-kirk-hall-and-gil-thelen/

Palliative Care, Parkinson's Disease

It’s Time for a Tampa PD Helpline

Science writer and Parkinson’s patient Jon Palfreman sets out this concise description of the disease that over one million Americans live with …and die from:

“… people with Parkinson’s progressively lose core pieces of themselves. We forget how to walk. Our arm muscles grow weaker. Our movements slow down. Our hands fumble. Simple fine-motor tasks like buttoning a shirt or balancing spaghetti on a fork become a challenge. Our faces no longer express emotions. Our voices lose volume and clarity. Our minds, in time, may lose their sharpness…and more.”

The “more” varies, widely from patient to patient, writes reviewer Doug Clifton, former editor of the Miami Herald and PD patient. Some lose the sense of smell. Some shuffle instead of stride; freeze in place as they try passing through a doorway. Some drool. Some have all the symptoms, others just a few. Some are dramatically helped by the drug regimen prescribed; others continue to struggle as the regimen gets tweaked.

How aware of their disease are PD suffers? According to a 2014 Harris survey:
57% feel informed about how PD progresses.
46% feel informed about treatments for non-motor symptoms of their disease.
54% feel informed about treatments for motor symptoms.

In other words, stunningly few PD sufferers understand what’s in staring them in the face today and what’s ahead for them.

I am not blaming doctors for this patient ignorance. Doctors are compensated for diagnosing disease and prescribing remedies. They have no financial incentive, much less the office resources, to educate patients about PD and answer everyday questions from patients.

Patients are asking questions but finding few answers, especially close-to home answers.

Where do I locate the physical therapy that doctors often suggest? How do I find a personal trainer who specializes in PD? Who can help me make my home safe from falls? Where do I enroll in recommended Tai Chi classes? Is anyone local offering that boxing therapy I saw on Sixty Minutes? Is there a young-onset support group in our area?

In most locales, there is no one place to find answers to those and dozens more local questions. National PD foundations effectively provide broad stroke answers, not geographic specific ones.

Why not provide a Tampa Bay answer line to recommend local resources PD patients nee to address their specific concerns and questions?

This multimedia clearinghouse, call it the Parkinson Connector, would be a one-stop shop for solutions. It would assemble lists of certified and licensed providers of care and share those lists with patients.

Patients, in turn, would be obliged to “own” their disease and make decisions and take action based on the provider lists. The Tampa Connector would not be a treatment provider. It would be a crucial link between doctors and the needs of their patients.

Physicians could recommend the connector to patients. At diagnosis, doctors would provide patients a succinct and jargon-free brochure that answers initial questions and concerns and directs patients to the connector for more information.

Imagine Rotary International providing seed money for this start up. District clubs would make it a priority project and spread the word in the community. If successful, the model could be duplicated in other Rotary locations.

The ideal connector is an existing, non-profit medical care organization with the infrastructure and patient experience to integrate the PD initiative into existing operations. Supplemental resources, of course, would come from a grant.

The connector proposal addresses real needs with the promise of great service to people who deserve guidance, direction and validated information.

This proposal is bold and complicated in operation, especially the marketing and public information aspects. But it is simple in strategic concept: connect people with daunting challenges in everyday living with existing local resources to meet those pressing needs.
*******************************************************************************************(

NPF response from Leilani Pearl, Vice President, Marketing & Communications, National Parkinson Foundation:
“I saw you new blog post this morning. As I mentioned on the phone, we do have a national Helpline to help people find resources in their area, including Tampa. The # is 1-800-4PD-INFO (473-4636) and the link to search by state is here: http://www.parkinson.org/search.

Parkinson's Disease

More on “Brainstorms” book and more on Exercise

I have touted this book in a previous post. My former newspaper colleague Doug Clifton adds perspective in this insightful review for the Miami Herald.

What happens when an award-winning science writer is struck by a disease he would ordinarily be writing about? Jon Palfreman’s Brain Storms: The Race to Unlock the Mysteries of Parkinson’s Disease is the answer.

Diagnosed with Parkinson’s in this book 2011, Palfreman set out to learn all he could about this mysterious ailment that defies simple description.

His one-paragraph attempt comes close:

“… people with Parkinson’s progressively lose core pieces of themselves. We forget how to walk. Our arm muscles grow weaker. Our movements slow down. Our hands fumble. Simple fine-motor tasks like buttoning a shirt or balancing spaghetti on a fork become a challenge. Our faces no longer express emotions. Our voices lose volume and clarity. Our minds, in time, may lose their sharpness . . . and more.”

The “more” varies widely from patient to patient. Some lose the sense of smell. Some shuffle instead of stride, freeze in place as they try passing through a doorway. Some drool. Some have all the symptoms, others just a few. Some are dramatically helped by the drug regimen prescribed, others continue to struggle as the regimen gets tweaked.

Parkinson’s affects 1 million Americans, 7 million worldwide. It is a disease that disproportionately strikes older people, so it is projected to touch even more as the population ages. For reasons unclear, the brain’s natural production of dopamine — a neurotransmitter that sends signals to other nerve cells — comes under attack and Parkinson’s symptoms are set in motion.

Palfreman treats his readers to a complex but cogent explanation of how the process works — or, more accurately in PD — doesn’t.

Like many PD sufferers — actor Michael J. Fox once among them — Palfreman wouldn’t, at first, disclose his ailment. He soon overcame that reluctance and plunged into his research. What resulted is a deftly crafted and authoritative literary journey that takes his reader from James Parkinson’s 1817 discovery of the “shaking palsy” to a worldwide Parkinson’s symposium nearly 200 years later — with many stops between.

Among them dancer Pamela Quinn, NBA player Brian Grant, cardiologist Thomas Graboys, each a PD sufferer, each a profile in courage and optimism. They share billing with an array of biologists, clinicians, researchers and doctors whose work he introduces a chapter at a time.

Parkinson’s is a neurodegenerative disease that so far has proved to be irreversible. Because the disease is slow to develop, its diagnosis often comes years after onset. Early signs are loss of smell, REM sleep disorder and constipation, all easy to overlook in older people. By the time tremors start— if they start at all — the disease may have progressed into its third or fourth stage.

Palfreman does a superb job of describing the torturous search for a cure or, at a minimum, an effective treatment to arrest PD’s progress or diminish its symptoms. Research is slow by its nature, but regulatory obstacles and drug company profit concerns slow it further.

For example L-dopa, the drug used in PD treatment since the late ’60s is marginally effective because so little of it gets to the brain, 5 to 10 percent, Palfreman says. Some current research suggests that rate could be substantially improved if research money were available to develop new drugs. That’s not likely, given the cost and slowness of research and urgency of need to combat more immediately lethal diseases.

Brain Storms is alternately optimistic and unapologetically realistic; PD is irreversible. The best hope is early detection and treatment, but early detection is rare and treatment seems to be marching in place. Still, exercise seems to help. A positive attitude goes far. Researchers are toiling harder than ever. And giving up just deepens despair.

As a PD sufferer myself, I found Brain Storms both uplifting and deeply informative. But if at bottom, what you want out of a science book is clean prose, clear thought and fascinating stories, Palfreman delivers.

Doug Clifton is the former executive editor of the Miami Herald, and former editor of the Cleveland Plain-Dealer.

*********

Exercise

Dr. Juan Sanchez-Ramos, medical director of the Parkinson Research Foundation, offered this clear sighted advice on exercise in a foundation publication.

Exercise and Parkinson’s Disease Many patients ask if exercise is beneficial for Parkinson’s disease. Research studies have demonstrated that exercise reduces stiffness, improves mobility, promotes better posture and benefits balance and gait. What is less clear is which form of exercise is best and how long and frequently the exercise should be done.

Aerobic exercise that increases the flow of oxygenated blood to the brain is the first and perhaps most important form of exercise. Even better is the combination of aerobic exercise with learning-based exercises. This kind of exercise will improve mobility, posture and gait, and might be neuro-protective in Parkinson’s disease. Aerobic exercises that challenge the individual to change tempo, activity or direction are optimal. For example, exercises that require balance and preparatory adjustments of the body such as dancing, skipping and cycling are highly beneficial. Other examples include: marching to music with big arm swings, sports (tennis, volleyball) and aerobic/jazzercise classes. Exercises that are especially beneficial because they promote cardiopulmonary fitness and motor learning include fast walking (including treadmill walking at different speeds and different inclines), cycling at varying speeds and cadences and swimming with different strokes with eyes open and closed.

Exercises that don’t challenge motor learning include riding a stationary bicycle at a constant speed without doing other activities and treadmill walking at a slow, constant speed. Exercises for cardiovascular, endurance and strengthening can be enriched by performing simultaneous activities such as reading, singing, or watching the news while pedaling on an exercise bike. Exercises that demand attention, repetition, progression of difficulty with spaced practice over time are the best exercise routines to promote motor learning.

Weight lifting alone is not the best choice of an exercise program for people with Parkinson’s disease especially if it’s the only exercise activity. Strengthening exercises should be done in a way that does not further increase the intrinsic muscle rigidity of PD. Weight training should be with light weights and frequent repetitions with plenty of stretching. Muscle mass decreases with aging, so it is important to exercise more to maintain muscle mass and strength. Strengthening postural muscles may help maintain a more upright posture. Integrative, functional exercises other than weight training may strengthen muscles in ways that are more beneficial to individual with Parkinson’s disease. So instead of weight lifting the patient can perform the following exercises: repeatedly rise up on ones toes, modified squats, repetitively rising and sitting from a chair, wearing ankle and wrist weights around the house or when walking outdoors. These kinds of exercises are just as effective in maintaining muscle tone and don’t increase stiffness as much as heavy weight workouts. Swimming is an excellent exercise providing good cardiopulmonary training and maintenance of muscle strength. Lap swimming doesn’t challenge balance, but because it involves a variety of movements of the arms and legs and head, it may increase coordination. The resistance of the water increases stiffness in some people but it decreases stiffness in others.
Some individuals with Parkinson’s disease have difficulty breathing while swimming, so it may not be a comfortable aerobic exercise. Swimming is best for people who have enjoyed swimming in the past before they developed Parkinson’s disease.

Exercises to lessen muscle stiffness require large rhythmical movements through a full range of motion. For example a program of aerobic exercise using music will reduce rigidity significantly. Yoga and TaiChi classes are also recommended because of increasing demands on postural mindfulness, balance and movement of all parts of the body. Other ways to decrease stiffness is to decrease stress by having fun, having a positive attitude and participation in socially engaging and learning-based activities.

One should chose a regular time in the day to exercise but more importantly one should exercise after taking a dose of medication, when motor function and mobility is best. This usually occurs about an hour after a dose of levodopa/carbidopa but this may vary in different individuals at various stages of the disease. The frequency of exercise is also important. Exercising should be done around 4 to 5 times per week for at least 30 minutes. One should strive to attain a heart rate goal that is 80% of the patients maximum heart rate adjusted for age. This is calculated as 220 minus age multiplied by 80%. So a 70 year person should target 120 beats per minute (220-70 times 80%). Exercise is much more fun if it’s done in a group, so it is recommended that patients become involve in group exercises such as dancing groups, Yoga and TaiChi clubs. Exercising with other people can make it much more enjoyable and will enhance compliance with the program. Finally, the PD patient should not forget a cool-down period after exercise. This will result in a slowly decreasing heart rate, allowing the muscles time to cool down gradually so they don’t become excessively stiff after the exercise. A cool-down period consists of the same exercise activity, but at a progressively slower rate. During the cool-down, all muscles need to go through a slow, full range of motion.

Article prepared by J. Sanchez-Ramos, with emphasis on the information provided to patients by the UCSF PD Center in San Francisco.

For more detailed information go to:
http://pdcenter.neurology.ucsf.edu/patients-guide/exercise-and-physical-therapy

Goodwin et al, “Effectiveness of Exercise Interventions for People with Parkinson’s disease: A systematic review and meta-analysis” Movement Disorders 23:631-640, 2008

Palliative Care, Parkinson's Disease

If Cardiologist Tom Graboys Had Instead Been a Neurologist

Thomas Graboys, M.D. was a beloved Boston cardiologist who struggled for many years with dementia connected with Parkinson’s disease. He died with it this year.

He famously wrote a book, “Life in the Balance: A Physician’s Memoir of Life, Love, and Loss with Parkinson’s Disease and Dementia.” It bared his innermost thoughts and emotions about what Parkinson’s and advancing dementia feel and look like.

I reread the book recently. I imagined how he would break the news of a Parkinson’s diagnosis if he were a neurologist and not a cardiologist.

All of us end up in the neurologist’s office with a variety of seemingly unrelated problems. That’s one of the many things that makes PD so frustrating. Like
snowflakes, each case of is different.

When the doctor’s verdict is rendered, Parkinson’s disease, it is the day we will never forget. For some like me, there is a momentary sense of relief that the accumulating symptoms have a cause and a name. For others the reaction is terror, shock and confusion.

We ask what does this mean for us? A brusque answer one of us received was “your symptoms will only get worse.” In my case, the answer was “at your age of 75 something else will kill you first.” Few of us received information beyond the diagnosis that day.

Commonly, we leave the doctors office with a pill prescription and instructions to return in three months. We are on our own. We get no literature explaining what Parkinson’s disease is, what we can do about it and what our future holds.

What if Tom Grayboys had had been the one delivering the news? He would have taken the time to give us a short explanation about the disease, encouragement about the therapies available to treat it, some information about the importance of exercise and diet.

He also would have given us a set of instructions about exactly where on the Internet we could find reliable information, where exactly and what specific exercise we should seek, and information about support groups in our area. He would tell us that patients who do well with the disease don’t let it own them—they own and control it. You don’t have to do this alone, he would say.

Graboys would not have done this from behind his desk but sitting close to us in a reassuring matter. He would have written down on a piece of his stationary his home phone number and told us to call anytime we needed help. He would not have said to return in three months but in one month. Then we would discuss what we had read and the questions we had concerning it.

Graboys would also explain at that next meeting how there was an organization we could join that would have regular educational seminars about PD, special programs for caregivers and recommendations on finding the physical and other therapists who could attend to her needs. He said he would work closely with the organization to see that care provision was modified as needed for each of us.

The Graboys approach would reduce our anxieties and provide an organizational anchor point.

Graboys would write out the medications he was recommending and what they were for. He would ask the patient what he or she thought was a reasonable exercise regimen within their abilities. We would discuss dietary and other lifestyle changes that would help us enhance our life. He would call it the plan.

It was the “contract” between Graboys and the patient that, if adhered to, would help ensure a positive outcome. And because the plan was personal to each patient, it was more likely to be honored. Just leaving the office with that plan in hand inspired hope because implicit in that plan was the message that there were things the patient could do to take control of their illness. Indeed, while there may have been three hundred words on that page, it really was just one: “hope.” The written plan inspired hope that by following the instructions we could enhance our chances of living out a fairly normal life.

Must Read, Palliative Care, Parkinson's Disease

A Resource Guide For The Newly Diagnosed Parkinson Patient

This authoritative guide was created by my colleague Kirk Hall and  first published on his blog shakypawsgrandpa.com. It is a wise and comprehensive list of existing resources. His advice deserves widespread attention.

This resource guide has been assembled by an experienced patient/caregiver group and members of the Parkinson’s disease (PD) medical/research community who share a common goal, which is to improve quality of life for people with Parkinson’s (PWPs), care partners, and their families.  A common concern of the newly diagnosed is how to find the information that they want and need.  In this brochure are links to resources that will provide helpful basic information regarding Parkinson’s, including young onset.  In the future a comprehensive guide will be available that will allow you to access a wide range of additional information.  If you are unable for any reason to obtain information you seek, there are services that will enable you to speak directly with someone who can help.

But first, our PWP/care partner members want to share a few things they have learned that are important for you to know:

  1. Give yourself some time to “process” your diagnosis.  This is a major unanticipated change in your life.  Do not give in to feelings of fear or anxiety!  Yes, your life will be different, but you will be surrounded by many people in support groups, PD organizations, and the medical community who are dedicated to making your life better!  Not to mention the support of family and friends (the same people you would support if they were going through something like this).  As soon as you are ready:
  2. Your #1 priority is to be sure you are working with a doctor that has appropriate experience, training, and education for your condition.  Do not assume that your doctor, no matter how much you may like him or her, meets this description!  Not all neurologists, for example, have movement disorder expertise that will enable them to recognize the subtle symptoms of PD and recommend appropriate medications and/or therapies.  If your doctor is not a good fit for you, or even if you are not sure and want a second opinion, we will provide information in our resource guide to help you locate a movement disorder neurologist in your area.
  3. Your #2 priority is to understand that exercise has been proven to be the single most important thing you can do for yourself to improve your condition and how you feel as well as potentially slowing the progression of the disease.  It will help you stay positively engaged and fight off the apathy that some of us experience.
  4. Your #3 priority is to take ownership of your situation by learning about PD and how you can live well with it.  This will enable you and your care partner to take an active role in the management of your condition, including providing information about your symptoms, any changes you have experienced, things that concern you, medications you are taking, other conditions you may have and more.  If you have concerns, ask questions!  If your doctor consistently does not take the time to answer your questions, find a new one!  Your obligation is to yourself and your family!
  5. Your #4 priority is to locate and join a PD support group.  “Test drive” one or two, if necessary, to find one that is comfortable for you and your care partner.  Get involved!
  6. If you are in a remote area, your options may be limited.  We know people who have teamed with a local neurologist working in conjunction with a movement disorder specialist that you can visit occasionally.  Another option is telemedicine, which allows you to receive care using communication technology.  Explore these options with your doctor to find an arrangement that works for you.
  7. Stay engaged!  The steps above will get you moving in a positive direction.  It is OK to have a bad day here and there, but own it and don’t let it turn into a bad week.  You do not have to go through this alone!

 

Help locating a movement disorder neurologist and why this is important

Exercise information

Newly diagnosed information

Young onset information

Help locating a support group (PWP & care partner)

Help locating a caregiver support group

Talk directly to a person who can help

 

Parkinson's Disease

Upgrading PD Patient Care

I have previously written about plans for a Denver meeting of neurological experts and specialists to discuss Parkinson’s disease and palliative care. It occurred Oct. 3-4 sponsored and funded by the Parkinson’s Disease Foundation. I was privileged to take part as a patient presenter of the plan I outlined in my Sept. 26 post.

You will recall palliative care focuses on providing maximum comfort to patients. Kirk Hall, my co-author, and I prefer to call it the Life Enhancement plan for Parkies at all stages of their disease. (See below for Kirk’s fuller explanation of palliative care.)

I was one of several patients who told our stories about living with Parkinson’s disease in its various phases of progression. The stories were enormously powerful and the feedback from the professionals wtion.as supportive and enthusiastic. Our narratives ranged from the shock at diagnosis to how alone and confused we felt after learning that we had a progressive and incurable neurological disease—a disease that affects not only the neuro-muscular system but many other functions such as digestive, smell, sleep and thinking (cognition).

My first impression of the experts in the hotel meeting room was how young they looked. Here we were, a group of 60-plus-year-old patients and caregivers, talking to aces who could be our grandchildren. And these were awfully smart and dedicated young people whom I quickly came to respect for their dedication and knowledge.

The primary difference between we patients and caregivers and the various neurological pros was our focus on qualitative actions versus their need to validate results by quantitative measures.

The patients favored action steps, such as one-stop shop for authoritative information for patients and caregivers.

By contrast our audience lived in a far more quantitative world that is required by their disciplines. Life experience truths were not sufficient for the work they needed to do in their world of high-powered measurement and proof.

It was clear to me and the other patients that an organized and efficient system of treatment utilizing the right professional at the right time in disease progress was a no-brainer to establish. The researchers, by contrast, even if they agreed with us, bore the burden of proving with bullet-proof data that the new system would produce better results for patients than the current system (or better, non-system).

Nonetheless at the conclusion of the two-day meeting, there was a remarkable accord about next steps in moving toward a new system of organized care.

To give you some examples, one of the tasks the group will undertake is “theoretical model and practical next steps for caregiver research and support.” A second was “an outcome measures working group including review paper summarizing state of evidence with recommendations.” On the qualitative side was a recommendation to publish in a neurological journal a letter suggesting what neurologists should be doing better for patients. One very ambitious recommendation was “categorizing, summarizing and critiquing what resources are currently available for patient education…”

There were other recommendations to create new committees and coordinating bodies to make permanent the palliative (“Life Enhancement”) movement with an ongoing series of caucuses and professional interest groups.

My colleague Kirk Hall describes an ongoing next step: “A new clinical research study titled ‘Does outpatient palliative care improve patient-centered outcomes in Parkinson’s disease?’ has begun at University of Colorado Hospital Anschutz Campus and is actively seeking interested individuals over the age of 40 that have been diagnosed with probable Parkinson’s disease and their care partners. Dr. Benzi Kluger is the principal investigator for the study, which is being funded by the Patient-Centered Outcomes Research Institute (PCORI) and will take place over a period of three years. There are two additional sites at the University of Alberta and the University of California San Francisco. Information regarding this study is available on the Fox Trial Finder site: https://foxtrialfinder.michaeljfox.org/trial/4202/.

“Many people are confused by the term palliative care. It is a treatment approach focused on improving quality of life by relieving suffering in the areas of physical symptoms such as pain, psychiatric symptoms such as depression, psychosocial issues, and spiritual needs for PWPs, care partners, and families at all stages of PD. Hospice and palliative care are not the same thing. Hospice can be an extremely valuable end-stage service and is an under-utilized subset within the palliative care spectrum. This study plans to learn more about the effect of palliative care on patients with Parkinson’s Disease and their care partners.”

To summarize, through the leadership of Dr. Kluger, who organized the Denver conference, a very large ball in the treatment of Parkinson’s has begun rolling. There is no reason that parts of the larger three-site study can’t be implemented now in other cities.

Parkinson's Disease

Parkinson’s Life Enhancement Proposal

Parkinson’s Life Enhancement Proposal

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Kirk Hall and I  are Parkinson’s patients who are members of a patient/caregiver council participating in a PD Palliative Care clinical research study as stakeholders providing ideas, input, and feedback to researchers.  The study is just getting ready to start recruiting patients and caregivers in Denver, Edmonton, and San Francisco who are approaching late stage and value the idea of assistance and support in making plans that will meet their needs and wants.  Check for details at https://foxtrialfinder.michaeljfox.org/.

The proposal below was developed by patients who live with PD and would like to assist the medical community in developing programs that will improve the lives of patients and caregivers at all stages of the disease. This post originally appeared on Kirk’s blog shakypawsgrandpa.com.

Comments or feedback will be appreciated!

Patient Perspective Proposal for PD Palliative Care

Kirk Hall & Gil Thelen

August 3, 2015

Patient/Caregiver/Family Proposal

Overview

A key question is how this new, improved approach to Palliative Care (PC) might be structured.  We are recommending a “three-legged stool” approach:

  • Patient’s primary neurologist/PC team
  • Patient PCP
  • PD support entity (in Denver Parkinson Association of the Rockies– PAR)
  • The “three legs” provide support for patients, care partners, families

For the purposes of this discussion, the PC spectrum will be divided into three stages:

  • Early: Diagnosis-5 years (typical honeymoon period)
  • Middle: 5 years-Advent of symptoms that substantially affect daily living
  • Late:  Advent of symptoms that substantially affect daily living/hospice – death/bereavement

Recommendations for each stage:

Early stage

  1. Rebrand PC as PD Life Enhancement or similar to address pervasive confusion about what palliative care is.
  • Proposed definition: A comprehensive, coordinated approach by the medical and PD support communities designed to maximize the quality of life for PD patients and caregivers.  Also minimizes stress for the patient, caregiver, and their families for the duration of the disease and bereavement period.
  1. Program starts at diagnosis.
  2. After diagnosis, doctor explains what the Life Enhancement program is and how it was designed to help them.
  3. Key points to communicate during appointment during which diagnosis occurs:
  • PD is a challenging disease for patients, care partners, and families
  • Patients who do well with the disease don’t let it own them—they own and control IT.
  • Here is a simple brochure that explains the disease.  It discusses telling your family and others about your diagnosis.  It provides a guide to local support groups and educational resources regarding Parkinson’s, nutrition, and exercise.
  • You don’t have to do this alone.  We will help.
  • Let’s schedule a follow up session at my office for a month from now to answer any questions and discuss next steps.
  1.  Key points to communicate during second appointment:
  • We have designed a cooperative Life Enhancement program with (PD support entity) that is available to provide education, assistance, and resources to make patients and care partner’s lives with PD better.
  • Here is a SECOND brochure that describes the Life Enhancement program, including how to manage the weeks and months following your diagnosis.
  • The first step is to attend one of the orientation sessions that are held on a regular basis at a convenient location. Transportation to the session you choose to attend is available, if needed.
    • It is extremely desirable that both PWP and care partner attend a session like this where they can interact with other PWPs, care partners,  and (PD support entity) staff to get them off on the right foot, hopefully precluding/reducing issues related to denial, apathy, depression, anxiety, etc.  A backup to this, if there is resistance (unwilling or unable to attend), is a DIY self-education program with comprehensive list of resources, step by step list of recommendations, etc.
    • I see that there is a session coming up on _________ in your area.  Would you like me to make a reservation for you?  I understand you may need time to process all this, so there is a number on the brochure you can call to make a reservation.
  • We can’t do this for you, but we will do it with you.  We are prepared to provide you with the tools you will need to take ownership of your future with PD.
  1. Orientation Program*
  • Conducted by PD support entity (participation by “experienced, knowledgeable patients is desirable)
  • Address needs of patients, caregivers, and families
  • Media advertising (free public service) will be needed to reach patients (and their caregivers) who are diagnosed by doctors (non-MDS) who are unaware of this program
  • Preferably live to allow interaction (some elements could be videotaped)
  • Connect them with a support group tailored to their needs (young onset, newly diagnosed, and more)
  • What Do I Do Now presentation (including what is the PC/Life Enhancement program and how will it help me/us):
    • Desirability of working with a movement disorder specialist (MDS)
    • List of MDSs in my area
  • PD 101: Comprehensive PD information (what is it, symptoms, progression, etc.)
  • Partners in Parkinson’s (https://www.partnersinparkinsons.org/parkinsons-advocate-program)
  • Davis Phinney “Importance of Exercise” presentation
  • Patient to Patient program:  offer to connect them with an “experienced” PWP who has “been there/done that”.  Could be called a “shepherd”.  Shepherd is a volunteer who is willing to be available to talk on the phone, meet in person to provide suggestions/guidance.
  • Participation in clinical research studies (why & how)
  • Resource handout
    • Recommended information websites
    • Recommended webinars
    • List of available medical devices for borrowing
    • Tremble clefs, dance, yoga/exercise programs
  1. Continue with ideas up to approximately 5 years including learning about what they will need to do in the middle stage and why it is important.
  2. Develop a plan to make as many of these services as possible available to patients and caregivers in remote/rural areas (possibly record programs and post on you tube).      

*This will require significant new sources of funding as well as a great deal of planning/coordination.

Middle stage

This stage can and should be a crucial stage because it is a time when learning can take place relative to late stage and plans/decisions made that will make this stage easier for patients, care partners, and families.  Wrestling with these issues including faith has the potential to create acceptance and peace of mind for all involved, making the last stage of the journey far less stressful.

  • Developing a personal plan for taking ownership including the possibility of financial challenges
  • Develop end of life wishes list & legal documents
  • Discuss with doctor what his/her role will be in end stage
  • Discuss options like hospice, staying at home, preferred death choices, brain donation, and more with doctor
  • Faith issues/choices
  • Evaluate in home services options, assisted living/nursing homes, etc.
  • Consider what would trigger move out of home choice

Late Stage

Ideally, late stage will become a matter of implementing plans/preferences identified in middle stage.  If the plan includes contingencies based on nature of specific health issues as they unfold, there can be “course adjustments” as opposed to confusion and stress related to confrontation of unanticipated issues.  Bereavement would be easy to overlook, but if we are to commit ourselves to fulfilling the PD Life Enhancement “mission” as defined, we must be mindful of the needs of the caregiver and families following the death of the patient.

Medical Community Proposal

There is a need for a fundamental shift in the mindset and training of doctors (see references):

  • Starting with med school, the ethical aspects of working with patients (and not referring them appropriately) who would be better served elsewhere must be addressed.
  • Get to know patients and caregivers to a degree that enables them to be one of the “legs” of the “three-legged stool”.
  • Their role does not end when they are no longer able to prolong the life of their patient.  In this new model, they are likely to be the one patients and caregivers (and their families) will most depend on to ensure a “successful transition to death.”
    • One where the caregiver and family (and medical team) can feel at peace because they did everything possible to honor the patient’s wishes about how he/she wanted to die.
    • This is not the current mindset of many doctors due to accepted practices and training starting in medical school.  With that in mind, PC needs to become part of med school curriculum.  Create and implement program for changing orientation of existing doctors.
  • Develop telemedicine capability that would allow palliative care services to be made available to patients and caregivers in remote/rural areas.

Unmet Needs

Upon review, it seems that none of this is the norm in our current system, so everything here is an unmet need, in our opinion.  Some of it ends up happening with some patients and caregivers (based on their personal research, recommendations from others, church counseling or other), but not based on an intentional, organized PC program.  The goal here is to achieve the outcomes described for as many as possible, not just for the fortunate few.

That said, Rome wasn’t built in a day.  Priorities will need to be established.  Programs that attempt to achieve too much too fast typically fail. We would recommend choosing priorities that have the greatest potential to positively affect the overall PC experience for patients and caregivers.  Here is a description of actions to pursue in the short term concurrently, if possible:

  1. Changes in medical school curriculums and related training.
  2. Create a PC team (similar to the UCH model) and focus on the middle stage educational piece/plan development.
  3. Track status of each patient/caregiver in late stage to ensure plan is being followed.  Assist/support/intervene as necessary.
  4. Develop and implement standard practices for initial diagnosis appointment (including rebranding).
  5. Develop telemedicine capability to reach the PD population in remote and rural areas.