Rigorous Exercise Proving to Fight Back Against Parkinson’s

Researchers studying Parkinson’s disease are spending more time on what the effects of exercise is having on fighting back against the disease. It is becoming clear that working out does reduce symptoms, but it appears it has to be strenuous. The below article by Alice Reid of the Washington Post confirms much of the same that has been repeatedly stated here at Attitude Fitness Wins on numerous posts including our first post ever on September 22, 2011, My Story.

Well before sunup, Chuck Linderman launches his daily workout at the Alexandria, Va., boat house: 30 minutes pulling hard on a Concept 2 rowing machine, an equal stint lifting free weights and 30 minutes pedaling a stationary bike. He drives himself to sweaty, breathless exhaustion, for Linderman is training for the race of his life — a race against Parkinson’s disease.

Exercise of any sort has long been known to be helpful for Parkinson’s. Before the development of effective drug therapy in the ’60s, patients often improved with any exercise, even the act of folding laundry, according to Michael Okun, national medical director of the National Parkinson Foundation, which emphasizes exercise as an important tool to fight the disease.

Much of Linderman’s regimen — daily cycling and hard rowing, plus weight training twice a week with a personal trainer — is just the sort of workout that is intriguing researchers. There is evidence that challenging the muscles through repetitive resistance motion far beyond one’s comfort zone can diminish some symptoms.

Preliminary studies show that after eight weeks of cycling three times a week at a pace high enough to break a sweat and raise the heart rate, some patients can recoup much of their mobility for nearly four weeks. After that, gains disappear unless the patient resumes exercising. While it cannot cure Parkinson’s, heavy-duty exercise shows promise for countering, even delaying, the inability to move that the disease causes.

The Michael J. Fox Foundation for Parkinson’s Research has funded close to $3 million in exercise research. And Okun of the Parkinson’s Foundation said the focus is on finding the most effective exercise. “We know you need to sweat,” says Okun. “But we don’t know exactly what kind of exercise is most effective, its optimum frequency or what the long-term benefits are.”

Jay L. Alberts, a Parkinson’s researcher at the Cleveland Clinic, discovered how good intense cycling could be quite by accident eight years ago, as he rode a tandem bike across Iowa with a friend who has the disease. The purpose of the trip was simply to show that with Parkinson’s you can live an active life,” says Alberts. But something surprising happened. Although the disease had already robbed his friend of her ability to write legibly, she could suddenly write her name clearly after the first day of strenuous cycling.

For five years Alberts has been researching the effects of strenuous cycling on patients. With $1.5 million in grants from the National Institutes of Health and the Department of Veterans Affairs, he has finished a 60-person study and has just launched another for 100 patients. Although no final answers are in, Alberts’ work has sparked interest in the Parkinson’s world. Indoor cycling programs have sprung up at YMCAs in Seattle, Cleveland and Sarasota, Fla., with another in the planning stages in Los Angeles. A nonprofit called Pedaling for Parkinson’s is affiliated with the YMCA.

For Alberts’ just-completed study, patients rode indoor bikes. First he tested them to determine the pace at which they were comfortable, which was about 60 pedal revolutions per minute. Then they were required to pedal 35 percent faster. After three-times-a-week sessions, nearly all patients showed improvement in mobility and small motor skills, and not one dropped out of the rigorous program. And although cycling involves the legs, mobility improved elsewhere as well — “in manipulation — the ability to open a jar, for instance. Something global was happening in the brain,” Alberts says. When Alberts did brain scans on his research subjects they showed that exercise sparked blood flow and brain activity as effectively as the medications routinely prescribed for Parkinson’s.

“One of our goals is, can we delay the onset of symptoms. This is a neurodegenerative disease,” Alberts says. “If we can alter the slope of that progression, there is tremendous value here. You want to make sure the person is really doing something. They must actively participate,” he says. By cycling intensely, Alberts speculated, “you have information about a (muscle) movement going back to the brain. So if you can increase the quality and the quantity of that information, it may trigger biochemical changes in the brain.”

Another researcher, University of Florida neuroscientist David E. Vaillancourt, has been comparing how patients do on two exercise programs, the Parkinson’s Foundation’s “Fitness Counts” and Progressive Resistance Exercise, which is directed at lifting increasingly heavy weights.
“My colleagues and I believe that pushing the patients to work out hard is the key to exercise training in Parkinson’s disease,” he says. Told of Linderman’s workouts, he added, “It sounds to me that Mr. Linderman has figured this out on his own.” Linderman, for his part, said fighting Parkinson’s with exercise has many benefits. “And,” he adds, “it beats taking a whole lot more pills.”

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AttitudeFitnessWins.com Recognized by PAN

Good things are happening at AttitudeFitnessWins.com in 2012. For those of you not aware of PAN (Parkinson’s Action Network), PAN is the unified voice of the Parkinson’s community, advocating for more than one million Americans and their families for treatments and a cure. PAN is a public policy organization, representing other national Parkinson’s organizations (such as Parkinson’s disease Foundation, National Parkinson Foundation, Michael J. Fox Foundation, etc.) in Washington DC.
Earlier in January PAN became aware of AttitudeFitnessWins blog and contacted me regarding becoming an Assistant State Director of Nevada for PAN. As an Assistant State Director, I would work with our state’s grassroots leadership, communicate with our Members of Congress and build relationships within our community. PAN is passionate about raising awareness of Parkinson’s disease (PD) and finding a cure.
After submitting information about myself and taking 2 training classes, I was officially appointed the Assistant State Director of Nevada and with great honor I accepted the challenge. My first charter at PAN is to encourage as many as possible to join PAN as we rely on advocates across the country to help us raise awareness and educate elected officials about the need for strong federal policies and funding for Parkinson’s research and support.
If you have Parkinson’s and are not aware of PAN, I strongly recommend you stop and educate yourself on PAN. Once you complete your research, I’m sure you will agree that becoming a member of PAN is a must. 2012 will be another high-gear political year in Washington DC. It is our collective responsibility to ensure politics does not impede the Parkinson’s community’s efforts to fight for better therapies and a better quality of life for people living with Parkinson’s. As always, I thank you in advance for your support. For more information please view below video.

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Goals and Aspirations for 2012

(Versión en español de blog AQUÍ)

Happy belated 2012 to all!  I can already feel it.  2012 will be one for change.  To be successful in adapting to change no matter what the situation and/or endeavor, you have to have a conviction and passion to what you are trying to achieve.  Change is inevitable and we all need to learn how to embrace it and use it to our advantage. Thus, setting new goals or modifying past goals you have made in life is essential and there is no better time to make that commitment to change then the ringing in of a new year.

My TOP 10 goals for 2012 are as follows and not really in any particular order except my #1 goal each year since being diagnosed with Parkinson’s stays the same:

  1. Fight back the progression of PD in any way shape or form possible until we find a cure.
  2. Be more thankful for what you have because one morning when you wake up it may be gone.
  3. To have an impact on others in helping them achieve their dreams.
  4. Continue working out 7 days per week for good health, fitness and to slow down or stop the progression of PD.                                                            
  5. Don’t Give Up, Don’t Ever Give Up”.  ATTITUDE matters. One common response to some of my previous posts regarding fighting back against Parkinson’s is what a difference a positive attitude can make if you really believe in it.  Talk is cheap, action with attitude wins.
  6. Truly enjoy life to its fullest.  Tell your wife or significant other you love them every day.  Stop and take the time and listen to your family on what is important to them.  Just listen.  Do not try to guide them in a different direction or mention a fix to what maybe a problem, JUST LISTEN…
  7. Make contact and build relationships with other Parkinson’s foundations to all work together to find a cure in our lifetime.
  8. Meet face-to-face with Michael J. Fox and Mr. Ali with purpose to increase awareness worldwide of the myths of Parkinson’s.  Convince both to do more in our fight against PD by being more outspoken.
  9. Stay in better touch with your life-long friends.  The ones that you lift up and in return lift you up when you talk or exchange emails or texts.
  10. I know it sounds corny, but it’s simple.  Be the best you can be at whatever you choose to do.

So, if you have not already set your goals for 2012, what are you waiting for?  It is important to write them down so you can look back each year to see how successful you were in achieving your goals. Share your goals with your family and close friends too.

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Housekeeping:  Over the past month I have moved my AttitudeFitnessWins blog from a Word Press hosted site to a self-hosted site. This has taken a good deal of my time and is one of my main excuses for not having more frequent blogs.  Now that I have most of the bugs out, my promise to those that have followed me will be to have a new post every week on either Tues. or Weds.  Thanks for your patience and understanding.

Note:  If you signed up as a subscriber on my Word Press hosted blog, please take the time to re-subscribe on my new site www.attitidefitnesswins.com .  My new Attitude Fitness Wins site is easily recognized as the header photo is of the greatest of all time, Mohammad Ali.  Thanks again.

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Attitude Fitness Wins Fights Back with Exercise

For those that have not followed AttitudeFitnessWins.com blog and are new to the site, its main purpose emphasizes the goal to slow down the progression of Parkinson’s by the commitment to a positive attitude and a fitness routine. Embedded in this post is a video featuring my workout routine in fighting back against PD.  Click on the arrow to start the video.

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AttitudeFitnessWins takes on NEW LOOK

No one ever has exemplified the positive Attitude, the ultimate in Fitness and being a Winner in every sense of the word more than Mohammed Ali. That, along with the fact, he is arguably still the most recognizable face in the world, and just happens to have Parkinson’s, makes it an honor to feature Mr. Ali on this website.

Mohammed Ali was one my heroes growing up and remains to be a man I look to for strength in fighting PD. He continues to put himself out there for the public to see despite being in the latter stages of the disease. Seeing him light the torch at the Olympics was a sight I will never forget.

“It’s the repetition of affirmations that leads to belief. And once that belief becomes a deep conviction, things begin to happen.”    -Mohammed Ali

In 1988 I went to the Rose Bowl and we visited the area where all the floats were being built the day before the big parade.  Mohammed was there as he was scheduled to be on one of the floats in the parade.  I caught his eye from a distance and shouted out, “Mohammed, you still pretty.”  He looked back at me and said in a very soft spoken voice, “you pretty too.”

Mohammed Ali continues to be an inspiration in my life and I thank him for his ongoing support in fighting Parkinson’s with the strong conviction that we will find a cure someday soon.

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Unintentional Disrespect

On this day of thanks I feel it necessary to apologize to those that are in the advanced stages of Parkinson’s.  As I look back on my blogs there is a constant message to fight back against the disease with the power of thought, attitude and physical exercise.  After what happened last week, I feel the need to reach out to not only those like me, but also be empathetic to those who suffer daily from chronic illnesses that are much worse than me.

I am a partner in a company called HiTechSeniors.com.  What we do is provide 55+ adults with the opportunity to learn the basics with computers, the internet, cell phones and more in hopes of improving their quality of life.

HiTech Seniors Unite

Last week after making a presentation to a group of seniors at an adult living community here in Reno, something very special happened.  After the presentation a woman named Linda came up to me and gave me a VHS tape that was all about DBS (Direct Brain Stimulation) treatment of PD.  She explained she has had Parkinson’s for 21 years and at one time was in a wheel chair and would struggle everyday with severe symptoms of PD.  That all changed for her when she decided to have the DBS surgery.

I thanked Linda for sharing and gave her a big hug for coming forward.  She explained she had undergone the DBS surgery and it had turned back the clock for her many years.  She was no longer in a wheelchair and in my short conversation with her I could not even tell she had Parkinson’s.

Upon returning to my office I placed the VHS tape on my desk where it sat for a week untouched.  My reluctance to watch the tape stemmed from my fear of seeing PD patients that were further along in the progression of the disease, which scares me. This past weekend I finally watched the tape.  My emotions went from tears to joy as it showed before and after surgery footage of numerous PD patients that have had the DBS procedure.  This dose of reality enlightened me to the fact all those with PD are not capable of just turning back the clock as I have preached in some of my previous posts.

So, on this day of thanks if we could all join together in a big virtual hug with goals and aspirations to fight all chronic illnesses until there is a cure.  Raise your glass.

Happy Thanksgiving to all.  Steve

 

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The Power of Thought Alone

Question: How many years until we see the same digit 6 times in our date 11/11/11?  Hint: I will definitely not be around.

A study in the UK is proving that by thought alone (The Power of Positive Thinking and/or Positive Attitude) we can improve movement by 1/3rd. Who out there with PD does not want to improve their movement by 33%? Improve movement by 1/3rd and quality of life would naturally go up.

I realize this is a small sampling and the study is still in the initial stages, but this is very close to validation of what I have been practicing for the past few years, and emphasizing on this blog since I started it approximately a month and a half ago.

Who knows, I may not be crazy after all…  See article below:

Cardiff University new Parkinson’s therapy hope

A brain scan of a patient with Parkin

son’s disease. The blue box highlights a damaged region.                                                                               

A new technique could improve the quality of life for patients with Parkinson’s Disease, according to research led by Cardiff University. Patients with the early stages of the disease were trained to control areas of the brain associated with movement by using the power of thought alone.

A clinical evaluation later found their movement had improved by up to a third. The charity Parkinson’s UK described the research as “exciting” but stressed “these are very early days”.

The study, published in The Journal of Neuroscience, involved ten patients with the disease that affects the brain and results in slow movements and a tremor. Five patients received the brain regulation feedback technique and five acted as a control.

Activity mapping “We wanted them to activate the brain regions associated with movement through the force of their mind.”

Quote Professor David Linden Cardiff University

Patients undergoing the training were placed in a Magnetic Resonance Imaging (MRI) scanner in Bangor, Gwynedd. At first, they were asked to squeeze a hand as the team mapped the regions of the brain responsible for controlling movement.

Then, in real time, the subjects were shown the level of activity in these regions displayed on a gauge above them. They were asked to imagine making complex movements in order to activate the brain centers, and saw a corresponding increase on the gauge. With practice, they were able to increase and decrease the level of activity at will, through thought alone.

Prof David Linden from Cardiff University, who led the research, described the process as “real-time neural feedback”.

Motor function  ”Self-regulation of brain activity in humans based on real-time feedback is emerging as a powerful technique,” said Prof Linden. Patients experienced a feedback effect as they learned to control motion centers in their brain. “In this study we assessed whether patients with Parkinson’s disease are able to alter their brain activity to improve their motor function. We wanted them to activate the brain regions associated with movement through the force of their mind,” he explained.

The professor stressed that the technique did not offer a cure but he said that improved function could lead to a better quality of life.

“We found that the five patients who received neuro feedback were able to increase activity in brain networks important for movements and that this intervention resulted in an overall improvement in motor speed – in this case, finger tapping,” said Prof Linden.

“The training resulted in clinically relevant improvement of motor functions – so assuming patients can learn to transfer the strategies used during neuro feedback into real-life settings, it might also become possible to sustain the clinical benefits,” he added. The research team said the study was a small scale proof of principle and they now hope to stage a larger, randomized, clinical trial. “While these results are exciting, these are very early days”

Quote Claire Bale Parkinson’s UK

‘Amazing’ brain    Claire Bale, senior research communications officer at Parkinson’s UK, said: “This study showed that people with Parkinson’s were able to alter their own brain activity to improve their movement symptoms using neuro feedback from brain scans. This highlights the amazing ability of the brain to change and adapt”.

“While these results are exciting, these are very early days. We need much larger, in-depth studies to help us understand the potential these techniques may have to tackle some of the symptoms of Parkinson’s,” said Ms Bale.

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Fight Back to Maintain Motor Skills

In keeping it lite today I thought I would show you one of the many exercises I do on a daily basis to hopefully maintain my motors skills as long as possible.

This will be one of the first videos I post actually showing what I do in the way of agility drills to keep me at peak performance.  I in not way shape or form want to come across as if I am bragging about my ability to do what you are about to see on this video.  Please keep in mind though I am 55 years old and have had Parkinson’s for 7 years.

The main point I am attempting to show is that you can trick your mind and actually do things with your body that you do not think are possible any more.  The power of positive thinking is endless.

So click on the link below to view me performing some basketball drills that I believe are helping me fight back against the symptons that Parkinson’s inflicts on us daily.

Hang with me though the entire video as I attempt a trick shot that comes toward the end of roughly a 90 second video.  How about spin the basketball on one finger, throw it up in the air, hit it off my head, it goes off the back board and nothing but net all on the first try!!!

 

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Success against the Progression of Parkinson’s

A very valuable website for many of us that have Parkinson’s called PatientsLikeMe has created a somewhat objective way to track the progression of the disease called the PDRS.  Your Parkinson’s Disease Rating Scale (PDRS) Score is a quick and easy way to track your progress. Simply answer a few questions about the impact of Parkinson’s Disease on your day-to-day life.  PDRS then calculates a score between 0 and 100 (100 being worse) based on your answers to the questions.

My first PDRS test and score was a 7 on Nov. 2, 2007.  For the next 4 years I took 10 PDRS test and averaged a 13 with the highest score coming in at 22 on May 28, 2011.  A little over 2 weeks ago, Oct. 18th I scored a 10.  Obviously I must be doing something right.  Turning back the clock on Parkinson’s is rare. I attribute my success to the following:

  1. Daily workout routine of approximately 90 minutes  incuding agility drills in hopes of hanging on to my motor skills as long as possible.
  2. Push back on symptoms by making your body do what it was like prior to being diagnosed with PD.
  3. Positive attitude that PD is not going to affect my daily life and keep me from my dreams.
  4. Proper diet – I’ve been on the Paleo diet since April 16, 2011.  Since on this diet I feel much stronger and I’ve lost 20 lbs.
  5.  Lastly, but certainly not least are my medications.  My daily meds and supplements are as follows:
    1. Azilect – two 1 MG tablets every morning
    2. Mirapex – one 1.5 MG tablet 3 times per day
    3. Carbidopa-Levodopa – one 25-100 tab 3 times a day
    4. CoQ10 supplement – 800 mg daily

I know that what I do will not work the same for others.  However, I cannot help but think it could help a few  if not many.

So, for those reading this, please do me a favor and send a link to this blog to someone you know that has been affected by the disease. Who knows it may help them; Thank you.

PS.  Link to PatientsLikeMe:

http://www.patientslikeme.com/home

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