Category Archives: Exercise and Parkinson’s

Yoga

Exercise is a proven way of helping people with Parkinson’s reverse their symptoms. Many people think yoga is reserved for athletic types, but a dedicated group of individuals with Parkinson’s have found a program tailored to people of all levels and now practice yoga on a regular basis. Three members of the Yoga for People with Parkinson’s classes in Seattle, Washington tell their stories about how yoga has provided them with remarkable relief from their symptoms.

Is yoga a therapy that is right for you? Listen to these incredible student testimonials and decide for yourself. Yoga is a time-tested, natural therapy and if practiced on a regular basis you can expect often dramatic improvements in flexibility, strength, balance and peace of mind. That formula is hard to beat.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery
Rock Solid Walking

Update from Christian Hageseth

Robert and I have recorded interviews three times in the past:

  1. September 2016: Five years no medications. Parkinson’s improving. How I had gone for 5 years without meds and was doing well using exercise and yoga
  2. January 2017: Wholistic (or holistic) how different PWPs approach their treatment.
  3. October 2018: Shifting the Parkinson’s disease mindset.
  • This is my fourth appearance on the show today, and I still hold to my beliefs.  
  1. EXERCISE. EXERCISE, EXERCISE. I cannot exercise as hard as I did before. Gradually I had to walk more and jog less. Could only 3 – 4 miles.
  2. More convinced than ever that MINDSET/ATTITUDE is the key, PARKINSON’S IS A CHALLENGE, NOT A CURSE.  When I was formally diagnosed, I was 70 years old. Life expectancy for me was 84.1. Well, now I’m 82.4. In a year and a half, I will have reached my life expectancy.
  3. YOGA remains critical.
  4. WAIT UNTIL you really must take Levodopa. Levodopa induced dyskinesia (LID) is a real deal and can be disabling. Google it on YouTube. 
  • Let’s look at my life since we last met, year by year.

2018 – I shot a video titled So High So Low for the “I HAD A DREAM PROJECT” where I hiked a three mile walk trail and climbed a thousand feet. 

Link: https://www.ihadadreamproject.com/i-had-a-dream-project-videos 

That year I also went to Uganda to demonstrate the practices I used to manage so long without meds. (Robert, this is quite a tale, plus I have pictures.)

  • 2019 – After directing the local Parkinson’s support group, I resigned so new blood could take over.

BUT: New symptoms emerged that I didn’t know about:

  1. Anomia: a language specific disturbance arising after brain damage whose main symptom is the inability of retrieving known words. But it’s not dementia!
  2. Pseudo Bulbar Affect Crying or laughing excessively upon feeling any deep feeling.
  3. Dysphagia: difficulty or discomfort in swallowing as a symptom of disease. It starts out with mucus as postnasal drip. Get to an OT!
  4. Oily, flakey skin
  5. Sleep disturbances. Fall into deep sleep in the middle of the day. And then don’t sleep well at night.
  6. Pain in bed at night. Interfered with sleep.
  • 2020 – It was a remarkable and horrific year. PANDEMIC!

No more yoga classes! No gym with weightlifting. Social interaction approached zero. 

  • 2021 – Then, a condition worse than Parkinson’s emerged: Major Depression.

March 2021 – Fell and shattered right knee – 16 days in hospital.

July 2021 – Fell and broke my right hip.

August – Severe depression, I became suicidal.

September – Chose to have a course of electro-convulsive therapy (ECT)

October- It worked, and my PD improved a lot.

The falls were due to the antidepressant I was taking may increase fall for people with Parkinsons.

LESSON: Make sure you MD goes through all meds in case a med might make falling more likely

My story with Depression

Family history is strong.

Parkinson’s did not cause my suicidal depression, genetics and environment did.  Antidepressant medication failed to work and led to my falls!

2022 – I returned to my new normal. And that’s where I am today. I just have more symptoms and feel weaker.

I followed up with PWPs who I have advised in the past.

It became clear to me: I want to coach people with PD. 

I HAVE A LOT TO OFFER!

Teach PWPs how to become a “Bad Ass with PD.” 

No more withdrawal and depression.

My PD website: www.makemostofpd.com  

Robert, I want to come back with a program I have just developed to make being a person with PD and their caregiver have a better relationship. 

New website www.the-kindness-dialogue.com 

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery
https://www.parkinsonsrecovery.com

Ketone Esters

I have included my full interview with Bill Curtis on Parkinsons Recovery Radio with this post. He provides a remarkable summary of his customized treatment protocol involving ketones, fasting and exercise which has quieted his symptoms for many years now.

You having to take more and more medications to achieve relief? Bill has been taking five (5) prescription medications for many years with no requirement to increase dosages.

In summary I promise you will not regret taking 45 minutes out of your day today to listen to Bill’s remarkable story. His customized protocol is worth taking seriously!

Bill Curtis developed Parkinson’s symptoms at the age of 45 in the year 2000. He  discusses his experience with using ketones and other therapies.

Ketone Ester available at: https://www.ketoneaid.com/pr

Have questions? Email Frank at: frank@ketonaid.com

 

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery
Road to Recovery from Parkinsons Disease
https://www.parkinsonsdisease.me

Physical Therapy and Parkinson’s Disease

Walter Mady discusses the importance of Physical Therapy for the Parkinson’s disease patient and the factors that have made the biggest difference in addressing his own Parkinson’s symptoms.

  • Walter Mady has been a Physical Therapist for 28 years in the private sector.  Physical Therapists are healthcare specialists utilizing their knowledge of anatomy and physiology, therapeutic exercise, and ADL modifications when treating the Parkinson’s disease patient.
  • He specializes in manual therapy, orthopedic physical therapy, and is a specialist in exercise recreationally and therapeutically
  • Walter was diagnosed in 2008 with Parkinson’s Disease..
  • He will discuss and stress the importance of nutrition and exercise.

Walter Mady [wmady@comcast.net]

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease
https://www.parkinsonsdisease.me

Macrobiotics: Natural Medicine for Parkinson’s Disease

My guest on Parkinsons Recovery Radio today was Warren Kramer from Macrobiotics of New England who discussed what is involved with a successful macrobiotic practice for Parkinson’s and why it is so powerful in improving one’s health. Click on the arrow below to hear this useful and amazing interview today:

 Macrobiotics Natural Treatment of Parkinson’s
Warren discussed how to tailor the macrobiotic approach to address symptoms of Parkinson’s disease. He also previewed what foods are best to avoid and to incorporate. Interested in natural remedies to address your symptoms? He offers several natural home remedies and lifestyle factors to consider.
  • Do you have tremors? Warren has some awesome suggestions for  you.
  • Do you have mobility issues? Warren also has some awesome suggestions for you too.

Topics discussed during the interview included:

1) Where does macrobiotics come from?
2) What is the difference between what a dietitian would suggest and you?
3) Why is macrobiotics effective in healing?
4) How do lifestyle factors play a role in healing?
5) What are the most important foods that a person with Parkinson’s should avoid?
6) What foods to include?
7) What are natural home remedies? What can help Parkinson’s?

Robert Rodgers PhD
Olympia Washington
Parkinsons Recovery
Road to Recovery from Parkinsons Disease
877-526-4646

Solutions for Parkinson’s Symptoms

On Parkinsons Recovery Radio today. Fred Phillips offered his insights into how he gets immediate relief from a variety of his Parkinson’s symptoms.  His solutions for Parkinson’s symptoms are novel and profound. Do you ever have difficulty when walking with:

  • Freezing?
  • Standing up?
  • Shuffling?
  • Slowness?
  • Leg Cramps?

If so, I strongly recommend that You listen to my interview with Fred today. Click the arrow below to hear the replay. Fred has discovered some powerful, yet simple solutions to these
symptoms that have helped him enormously.

One of now over 70 pioneers of recovery I have hosted on Parkinsons Recovery radio, Fred also previews his 10 step protocol for recovery.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

 

 

 

Process of Recovery from Parkinson’s Symptoms


I interviewed Tom House today on the radio show.  He was diagnosed with Parkinson’s disease about five years ago. Tom has a unique perspective on the “process” of recovery. Note that I used the word “process” not “outcome”. Tom explains that when athletes focus on the “outcome” they want – i.e., winning the game – their performance sinks and they are more likely to lose.

The outcome is not what matters, but the process. Of course people diagnosed with Parkinson’s want to see all symptoms dissolve. To make that happen however, the focus needs to be on the present moment activities and behaviors that in the end make that outcome possible.

This is why mindfulness programs are so successful for people with Parkinson’s.  They focus on process rather than outcomes.

My Interview with Former Major League Pitcher Tom House

P.S. Have you heard? I  just released the 2017 update to Road to Recovery from Parkinsons Disease.

Robert Rodgers PhD
Parkinsons Recovery
https://www.parkinsonsrecovery.com

 

 

P

Slightly Used Theracyle for Sale

Here is a notice about a Theracyle for sale. COntact Bob Jones if interested.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease 

“My wife has Parkinson’s, and to help her stay in fighting shape, we purchased a brand-new Theracycle 200 less than a year ago. But in the meantime, her lower back problems became more serious, so now we’re looking for someone to take the Theracycle off our hands. The bike is fully operational, and has hardly been touched. We’re asking $2500. I’d be very grateful if you were willing to share this information with your friends there on the internet.”

Thanks very much.

Bob Jones
stoic1@me.com

Exercise and Parkinson’s Disease Tips

How often should I exercise and what type of exercise is best for persons currently experiencing symptoms of Parkinson’s Disease?

Hear my response to this question which was posed on the Sunday Connections Program sponsored by Parkinsons Recovery by clicking on the purple arrow below.  It is now well established that exercise is beneficial for the general population. Exercise has all of the same beneficial effects of people with Parkinson’s disease as it does on healthy individuals. In addition, it can help to alleviate some of the negative signs and symptoms of the disease such as bradykinesia. It can also reduce tremor.

The radio show that I mentioned in my response to this question was with Dr. Daniel Corcos, Ph.D.  who is Chair of the Graduate Program in Neuroscience at the University of Illinois at Chicago (UIC) and Director of the Neural Control Of Movement Laboratory at UIC. On the radio show Dr. Corcos discusses  the various forms of exercise that are ideal for persons currently experiencing Parkinson’s symptoms.

Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease


Exercise and Parkinson’s Disease Tips

 

Best Exercise for Parkinson’s Disease

What is the Best Exercise for Parkinson’s Disease?

Everyone by now has heard that exercise provides welcome relief from many of the symptoms associated with Parkinson’s disease.  Most people want to know more. What is the best exercise for Parkinson’s disease? Is it aerobics which involves activities like spinning, running on a treadmill or a track? Is it resistance exercise through lifting heavier and heavier weights? Is it Tai Chi or Qigong which improves balance?

I am out of breath just listing the choices and I am just sitting right now! To make the decisions even more challenging, how much of each type of exercise should you do every week?

This week’s guest on  my radio show was Dr. Daniel Corcos has seasoned answers to these questions. Dr. Corcos has studied the impact of exercise on the symptoms of Parkinson’s disease for the past several decades. He recommends that doing all three types of exercise during the week will yield the most impressive results.

Yes, it takes a little extra time every week. Yes, it can be  tiring. And yes, it will help you feel a lot better. The recent study just published by Dr. Corcos reports a dazzling improvement in symptoms as a result of resistance exercise.

I encourage everyone to take 45 minutes out of your week to hear my radio show interview with Dr. Corcos:  www.blogtalkradio.com/parkinsons-recovery

Exciting Research Opportunity

During my radio show this week Dr. Corcos announced an exciting opportunity for people to participate in a research study which will evaluate the effects of exercise on Parkinson’s symptoms. He is recruiting volunteers who have never taken medications that happen to live in Chicago, Pittsburgh or Denver. Please help us spread the word. This is a spectacular opportunity for people to help themselves as well as others who currently experience the symptoms of Parkinson’s disease.

Contact Dr. Corsos to apply: Daniel Corcos [dcorcos@uic.edu]

Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease
www.parkinsonsdisease.me
Olympia, Washington

P.S.:: Only one day left to claim your 25% discount on orders of the Parkinsons Recovery Summit videos of the Santa Fe Presentations in February, 2013
www.summit.parkinsonsrecovery.com

 

Exercise and Parkinson’s – What Type is Best?

Everyone knows by now that exercise and Parkinson’s is a  healthy formula. Exercise helps alleviate the symptoms that are associated with a diagnosis of Parkinson’s Disease. I have hosted a series of renown researchers on the Parkinsons Recovery Radio Show over the past five years who have exposed on its benefits and virtues. It is clear you will see improvements in your health on some level when you exercise. Everyone needs to exercise if they are serious about recovery.OK. But …

Let’s get down to practicalities here. What type of exercise is best for people who currently experience Parkinson’s symptoms? Is it aerobic exercise which strengthens the heart and immune system? Or, is it resistance exercise that involves lifting weights? Is it advisable to lift heavier and heavier weights? Or, is exercise that improves balance the best option for people with Parkinson’s symptoms through accessing a modality like Tai Chi or Qigong or dance?

How often should you exercise – every day? Or, every week? Or …? When you really get down to practicalities it gets complicated.

Daniel Corcos, Ph.D., is my guest on the Parkinsons Recovery Radio show this Wednesday (May 22nd). Dr Corcos answers all of these questions and more! After three decades of conducting research on exercise and Parkinson’s he is one man who has the answers to all of these questions.

Listen to the show live Wednesday or listen to the recording later. All of my radio shows from the past five years are archived and free to access at anytime of the day or night. This is one of the many free services that are sponsored by Parkinsons Recovery. The radio show page is:

www.blogtalkradio.com/parkinsons-recovery

OK – so you have never liked to exercise? Dr. Corcos has some suggestions for you too!

Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease
www.parkinsonsdisease.me
Olympia, Washington
877-526-4646

 

Foot Whispering or Fitness Program?

Do you elect to access recovery through Randy Eady’s foot whispering or through the Delay the Disease fitness program? You will have to make a choice at the Parkinsons Recovery Summit regarding which of these two options you will learn much more about. As you can see below, they are offered at the same time!

http://www.summit.parkinsonsrecovery.com

        2:00 – 3:30

Randy Eady
          Florida
        Kentucky
$15

 

 Barefoot Doctoring:  The Heart of Foot Whispering and Perfecting Posture

Experience the subtle energy elements in Ancient Walking to Primal Rhythms that helps to
release toxins and enhance overall health

       2:00 – 3:30

 Jackie Russell
Ohio
Kroger

$15

 

         A Parkinsons Specific
Fitness Program

Parkinson’s specific fitness
program, Delay the Disease, will be an interactive demonstration with tips for the caregiver to help with functional fitness

 

Parkinsons Recovery Happens Day By Day: People Get Better

Parkinsons Recovery– People Get Better

I am a recently joined member from England. I am so excited about finding your web site and want to thank you from the bottom of my heart. There are no words to express my gratitude and excitement. I am really going to enjoy my recovery as it happens day by day. I have always had a little place inside me that says “I will figure this out”.  Now I have found the way with your help and I have regained my drive.  It is fantastic!

I have had definite symptoms for 12 years though I have been burdening  my mind and body with severe stress for years, mistakenly believing I could handle anything. Then the oak tree collapsed: I was totally exhausted and had no idea. I have been taking requip for 5 years and sinemet for 18 months and am determined to get free of them. I know I will though I don’t know details of the how yet. Don’t worry I shall be very careful and I have a lot of support. I have learned that relationships are even more important than health.

The things I am doing NOW are:

listening to your radio shows lots of exercise,  my dog gets 2 1hr walks per day in beautiful woodland exercise bike stretches and balancing listening to guided meditations really clean healthy diet lots and lots of water singing class nintendo wi writing out and reading poetry aloud eft feldenkrais recording my progress and activities and goals. my writing is loads better already hot and cold showering every day. The EFT Deft is HUGE for me.

I am not the person I was before my symptoms came along. The changes are quite staggering that actually I am a bit overwhelmed and confused. It has helped uncover something of the pay- off I get from having my symptoms – a mega breakthrough.

I found your site, actually the radio downloads on itunes 5 weeks ago and have improved so much already ( from really quite a bad place as the drugs were beginning not to work. They work well now. I have only stared eft in the last week

I was doing something of the above list before but now I have designed myself a programme which is a little bit strict and a little bit flexible. I have decided to stick to working with  this before I look at supplements and more complex things. I want to give my body some time on the basics  – good food, fresh air, mental stimulation, relaxation, fun etc. I have realized how sensitive I am at last. And I forgot to mention I have started detoxing  my environment – so far I have junked all my toiletries for natural ones, and only have about 1/8 what I had before! Now I am working through the cleaning stuff. It feels so good.

I am 55 years young, have a great husband who doesn’t give me too much sympathy and does his own thing, yet is fantastically caring and I have 2 fantastic sons aged  24 and  27. I have a brother who I would do anything for and a sister that I value  and love though I don’t have the same rapport with her.

I have just joined your membership pages today to continue my parkinsons recovery and it is great to get your emails. Encouragement is fab.

The crucial thing you have given me is the knowledge  PEOPLE GET BETTER. Now I know that I am on my way.

With heartfelt thanks

Fiona

Ride With Larry

Andrew Rubin, Co-director/Producer of the documentary currently being produced titled Ride with Larry, called me today to explain his exciting project to make a documentary about Larry who has the symptoms of Parkinson’s. Be sure and watch the video posted here. It is truly inspiring.

Andrew is seeking donations to support the project. With only 15 days to go, please consider making a donation. Even $1 helps. Andrew sent me a description of the project which follows:

Robert Rodgers, Ph.D.
Parkinsons Recovery

Ride with Larry, an inspirational Parkinson’s documentary to start a movement, and it needs your help.

A team of advocate filmmakers, who all have loved ones with Parkinson’s, want to uplift the Parkinson’s community today while fighting for a cure tomorrow. They are creating the first film for the Parkinson’s community, by the Parkinson’s community that will help spark an international movement for research, awareness, and inspiration.

The documentary focuses on Larry Smith, a retired police captain, beloved small-town baker, and avid cyclist who has had Parkinson’s for the last 20 years. This spring filmmakers will follow him as he bikes across his state of South Dakota to raise awareness about the benefits of cycling, keeping your body active and mind positive.

As Larry’s wife Betty states:

“if you love life, you’ll fight for it.”

Please take several minutes to watch their incredibly moving trailer and you’ll find out why this film is worthy of our and hopefully your support:

They are asking for contributions through Kickstarter, a site that allows artists to fundraise online through Amazon. The funds will allow them to travel around the world to interview researchers and tell Larry’s inspirational story. However, Kickstarter’s rules state that they must raise all their money by February 1st or all pledges will be refunded. Please help them reach their goal; they are so close!
If everyone gives what they can, they will quickly surpass their required amount and make a film that will ultimately give back to the Parkinson’s community ten-fold.

To find out how to make a tax-deductible donation click the following icon below:

They are endorsed by a team of sponsors that includes Parkinsons Recovery, the Davis Phinney Foundation, the National Parkinson Foundation, LSVT Global, and more.

The Ride with Larry team is overseen by Executive Producer Stephen Nemeth, whose socially conscious documentary credits include War/Dance (2008 Academy Award Nominee – Best Documentary), Flow (screened at both Democratic & Republican Conventions), and Fuel (Audience Award – 2008 Sundance Film Festival).

Beyond Parkinson’s disease, anyone facing a life altering illness can find true inspiration in Ride with Larry.

For more information about the project, visit http://ridewithlarrymovie.com.

For updates and to join the conversation, follow us on Twitter (@ridewithlarry) and join our community on Facebook (facebook.com/ridewithlarry).
###
CONTACT INFORMATION:
Andrew Rubin, Co-director/Producer
760-390-1426
ridewithlarrymovie@gmail.com

Symptoms Getting Worse – What Can I Do?

Question:

I have been suffering from PD for last four years (Started at the age 50). Currently I am on Apo_Pramipexold 3x1mg and Azilect 1x1mg. Tremor is under control and can walk easily but the problem I am facing now is that when I wake up its very difficult to get out of bed. I tried Acupuncture, Physiotherapy, Massage therapy but situation is going to worsen day by day.

Any suggestion of exercise or home remedy may be welcomed

I Abbasi

Response:

My hunch is that movement will help the most right now – any movement be it dance, walking, swimming, weight lifting, forced exercise – you name it. Perhaps your physiotherapist might have some great recommendations on exercise that might help you in particular.

I received a call yesterday from a women who was diagnosed about the same time as you. She tells me she is doing great. No one would ever know she had Parkinsons given her symptoms are not evident to anyone.  How does she do it? She explains – exercise! The more the better.

My initial reaction is to suggest that you begin to move your body as often as possible – every day. Most of the therapies you have explored require passive participation on your part. Why not become more active?

What else might I recommend? The therapies you have considered so far represent a very small number of the natural and safe therapies you can consider in addition to the medications.  I have now documented 44 therapies that have given people currently experiencing the symptoms of Parkinson’s relief in one form or another. I discuss these many therapies in my book, Road to Recovery from Parkinsons Disease.

Parkinsons Recovery is sponsoring a Summit March 7th. Why not join us? You will hear directly from people stories about what they are doing to recover.

Robert Rodgers, Ph.D.
Parkinsons Recovery
www.parkinsonsrecovery.com

Parkinsons Disease Treatment Options

Angela Wensley was a guest on my radio show on October 28, 2010. You can listen to the show by visiting http://www.blogtalkradio.com/parkinsons-recovery.  Angela wrote a thorough update describing the treatment options she has pursued. Her update is posted below. Robert Rodgers, Ph.D.

This update is intended not only for my friends and family, but also for people who have been diagnosed with Parkinson’s disease (PD). Please feel free to pass this on to anyone that you may know who has a diagnosis of PD as they may find some of the information helpful. I was diagnosed with the symptoms of PD in May 2007, over 3 1/2 years ago at age 59. At the time of diagnosis, I was informed that not only was the cause unknown (“idiopathic”), but also that it was irreversible and progressive. Initially, I questioned the diagnosis but any doubts were resolved when I traveled to Los Angeles in September 2007 for a PET scan that confirmed (in medical-speak) that there was: moderately decreased dopamine accumulation into the posterior putamen on the left side of my brain, consistent with PD. Since then, I have come to accept the diagnosis as my symptoms have become rather “classic”. In particular, I have tremours in my right hand and these have become increasingly worse as the years have progressed.

The progression of my PD symptoms has not been linear, but instead I experience it in waves with definite peaks and valleys. The symptoms can be pronounced for a number of days interspaced by days of calm where I am almost symptom-free. Over time, however, the general trend has been a gradual progression downward (probably corresponding to dopamine depletion in the part of my brain responsible for motor activities) with the valleys becoming more savage and the peaks becoming shorter. In addition, there can be variations in my tremours during the day. When I am relaxed, I have no tremours. When under stress, or excitement, or cold, the tremours become more pronounced.

The worst situation is “White Coat Syndrome” whenever I visit a medical doctor or a neurologist. On those occasions, my tremours are effectively out of control. Other PD symptoms such as impaired arm swing, problems with gait, problems with balance, and constipation are so far in the mild category. Besides tremour, the other most bothersome PD symptom for me has been “micrographia.” As I can no longer move the fingers on my right hand, my ability to write has decreased to the point where I have ceased keeping a daily journal, something that I had been doing since the 1980s. Also, typing has become difficult and slow. Luckily, Dragon voice-activated software has come to my rescue and I now dictate most of my communications (such as this update).

I plot the progression of my PD every three months using the Parkinson’s Disease Rating Scale (PDRS) from 0 to 100 on the website www.PatientsLikeMe.com where my patient name is “Dawn Angel”. My current rating is 7. It has been as high as 14. My human tendency is to self-evaluate when I’m feeling good so it is possible that my PDRS is higher at some times.

So far, I have avoided taking any of the Parkinson’s medications (with a brief exception of one month after I was first diagnosed when I took Mirapex, a dopamine agonist that for me had dreadful side effects). To me, the PD medications are a last resort. Since they will only provide a certain number of years of effectiveness it seems reasonable to forestall taking them until it is absolutely necessary, that is, when having the symptoms is no longer preferable to the side effects of the meds. I have been able to work for three years post diagnosis but I’m at the point where it may not be possible to continue working as a freelance consulting engineer. I haven’t had any jobs since June 2010, so it is difficult to say if it is time for me to retire.

RESOURCES

I am fortunate to have two outstanding neurologists on my side, Andrew Wolfenden and Jon Stoessl, although I only see them once a year. Stoessl is the director of the Pacific Parkinson’s Research Centre. I see him at the Movement Disorders Clinic at the University of British Columbia in Vancouver. With Western medicine offering only drugs that mask the symptoms of PD and unable to otherwise treat the condition, it is inevitable that a person diagnosed with PD will seek out alternative forms of medicine. My naturopath Caleb Ng

www.mountainviewwellnesscentre.ca/

is a valuable part of my team. Ideally, a person diagnosed with PD should have a team of practitioners, including at least one neurologist, their GP, a naturopath, a physiotherapist, an herbalist, a massage therapist, a personal trainer, a psychotherapist, and others. The reality, however, is that no “team” really exists. My personal trainer may know my chiropractor, and my naturopath may have met my neurologist, but this is not team behaviour. The cold truth is that each patient is pretty well left to their own devices. So one must be proactive and become better informed, often more so then their practitioners. We are the keepers of the complete story.

There are many very good publications on PD available in book form. Some that I have found to be exceptional are:

1. Jill Marjama-Lyons and Mary J. Shomon, “What Your Doctor May Not Tell You About Parkinson’s Disease,” Warner Books (2003).

2. Gretchen Garie, Michael J. Church, and Winnifred Conkling, “Living Well With Parkinson’s Disease,” Collins (2007).

3. David A. Grimes, “Parkinson’s: Everything You Need to Know,” Firefly Books (2004).

4. Geoffrey Leader and Lucille Leader, “Parkinson’s Disease: Reducing Symptoms with Nutrition and Drugs,” Denor Press (2009).

5. Laurie K. Mischley, “Natural Therapies for Parkinson’s Disease,” Coffeetown Press (2010).

6. Abraham Lieberman, “100 Questions and Answers about Parkinson’s Disease,” Jones and Bartlett (2003).

7. David H. Anderson, “How to Tame Parkinson’s by Keeping Fit,” Authorhouse (2005).

8. John Ball, “Living Well, Running Hard,” Authorhouse (2005).

9. Arthur W. Curren, “Dumb Bells and Dopamine,” Authorhouse (2006).

Downloadable books from the Internet include:

1. John C. Coleman, “Stop Parkin’ and Start Livin’: Reversing the Symptoms of Parkinson’s Disease,” available for a fee from www.returntostillness.com.au

2. Robert Rodgers, “Road to Recovery from Parkinson’s Disease,” available for a fee from www.parkinsonsdisease.me

3. Janice Walton-Hadlock, “Recovering from Parkinson’s Disease: Understanding its Cause and Mastering and Effective Treatment,” available for free from www.pdrecovery.org/ (I do not necessarily endorse the concepts or opinions of the author but found it a compelling and worthwhile read; too bad she won’t converse with anyone that has been on PD meds such as Mirapex for a month!)

There are almost unlimited resources available on the Internet. By far the best PD website is www.PatientsLikeMe.com that has over 5000 members with PD.

My “Dawn Angel” profile there has been browsed over 7000 times at the time of writing this update.

PD PREVENTATIVE MEASURES

The various measures I have taken in my attempts to slow the progression of PD are listed below in approximate order of effectiveness (my perception). The regimen I am on is constantly changing but the overall goal remains the same: to feel as good as I can.

1. Exercise.

2. Physiotherapy

3. Neuroprotective supplements

3. Diet

4. Chelation

5. Brain therapies

Exercise

The initial diagnosis of PD scared me so much that I decided I had to get into the best possible physical shape to be able to combat the progression of PD. I also engaged a personal trainer, Julie Beenham, to keep me honest. I have seen Julie since June 2007 and would consider our sessions the single most effective measure I have taken against my PD. Within a few months, I had dropped over 40 pounds through a regimen that included running every morning for 5 miles (running for my life) plus extensive workouts in the gym in the afternoon in addition to my sessions with Julie. While my initial reasoning was correct in terms of my being better prepared to withstand the ravages of the disease, I have since found out that intense physical exercise can also have neuroprotective benefits. All the more reason to keep it up. I counsel other people with PD to start exercising and keep at it even when they don’t feel like it.

My exercise regimen has varied significantly over the years, particularly with the seasons, but exercise still remains the most effective method I have found for relief from the symptoms of PD. I have also had to accommodate changes to my body thanks to Mr. Parkinson. For example, I have nearly-constant pain in my right hip that now prevents me from running or from using certain equipment in the gym. When I find I can no longer do one thing (use an elliptical training machine) I do whatever I can to keep that it. A “toe crest” helped keep the toes on my right foot from curling under; I still use toe sleeves to prevent the formation of corns. When these measures weren’t enough I found something else that I could use: a stationary bicycle. I will continue with this practical approach as long as I am able. Whenever possible, I indulge in two of my favourite sports, tennis and kickboxing. Not bad for someone who’s 63 years old!

Gym

Currently, my gym workouts consist of roughly 30 minutes of cardio, 30 minutes of weight training, and 30 minutes of stretching. As mentioned above, the cardio originally was done on an elliptical machine but now I use an upright bicycle. Weights involved a number of machines but also free weights (dumbbells). I have found that stretching is an important component of any exercise regimen and worth the time taken for it.

Personal trainer

I see my personal trainer Julie twice a week for one hour each time. In our ever varying routine, she has me attempt a number of balance exercises. I can balance on my left leg very well but balance on my right leg is problematic. Standing on a wobble board is possible but is becoming an increasing challenge for me. We do part of each session with my eyes closed which seems to be helpful. Each session ends with stretching, the best part!

Tennis

I had given up playing tennis in 2005 after a rotator cuff injury made it impossible for me to raise my right arm (I am right-handed) out to the side and overhead. Little did I know that a “frozen shoulder” is often a sign of PD. In 2008, on the advice of a friend who had seen an amputee play tennis again after switching to his left arm, I resumed playing tennis as a lefty. When my right arm finally came around in 2009, I morphed into an ambidextrous player with both right and left handed forehands. We bought a condo in a tennis community in Delray Beach, Florida that we visit twice a year for a month each time and were I can indulge my tennis habit. Back home in the relatively cold Northwest I see a tennis coach on a weekly basis and play indoors during the winter.

When I play tennis, my PD symptoms also take a vacation although videos show that I am clearly compensating for any impaired movement. Nonetheless, my footwork is good as is my ability to run and make shots from either side of the court. Why this is so is not really clear to me. Perhaps doing something that one really loves is conducive to generating dopamine, the neurotransmitter in short supply in the brains of people with PD. I suspect that it has something to do with the repetitive nature of the game and the delightful sense of vibration when the ball is well struck. For this reason, I prefer “tennis therapy” with a coach feeding me shots, to actually playing a game. I have noticed that on those rare occasions where I summon up extra energy through adrenaline (which consumes dopamine) I pay for it later in terms of a short-lived exacerbation of my PD symptoms. The trick is to learn how to stay relaxed while playing the game.

Kickboxing

It was Julie my personal trainer who introduced me to kickboxing. The kickboxing I do is not in the ring (!) but rather with a partner holding pads or in a gym with a kickboxing circuit. In the summer I am able to set up a punching bag outdoors in the carport but most of the time I now go to “30 Minute Hit”, a local kickboxing circuit. There is something about the contact and the vibrations from the punches that help calm the symptoms of PD. Besides, it just feels good to hit someone! There is clearly some adrenaline production involved with kickboxing as my tremours are usually set off for several minutes after I complete the circuit.

Physiotherapy

Since my diagnosis with PD, I have seen a number of physiotherapists. I am relatively good at following orders and did whatever exercises they recommended, with satisfactory outcomes. Initially, my focus was to regain the use of my right arm. More recently, I have been addressing the progressive effects of PD on my body.

Prolotherapy

As mentioned above, I had given up playing tennis in 2005 after a rotator cuff injury. After my diagnosis with PD in 2007, I worked very hard on regaining the function of my right shoulder. I underwent two months of prolotherapy from a naturopath where dextrose was injected into my tendons (hurt like hell) to promote improved blood supply and healing. In this regard, the prolotherapy was very effective, although I still had to follow up with more than a year of intense physiotherapy. There is still some residual pain in my right shoulder and a tendency for the femur to sit outside of its socket, but for all intents and purposes I have regained a full range of motion. I continue to receive physiotherapy on my right shoulder.

Intramuscular stimulation

In 2009, I began to see Dan Sivertson, a physiotherapist who practices “Intramuscular Stimulation” (IMS), a therapy developed in Vancouver BCwww.istop.org/. IMS is a form of “scientific acupuncture” where the needles are inserted into the problem area such as tight or shortened muscles, without application of electric current (I have little time for non-scientific or traditional acupuncture that relies on mythical meridians to determine where the needles should be placed.). The results of IMS have been amazing and muscles that I thought had been irrevocably tightened have loosened up. There has also been a significant reduction in pain, especially in my right hip. IMS must be considered as part of a complete physiotherapy package that includes myofascial release and massage.

Currently, Dan and I are working on improving my posture. One of the progressive features of PD is the gradual tightening of muscles that progressively cause a stooped posture. With weekly sessions of physiotherapy and daily posture exercises we are keeping the ravages of PD to a minimum at least as they affect my posture and mobility.

Chiropractic

While some people regard chiropractic as a pseudoscience, my experience has been that it is very effective for treating lower back pain. I have had lower back pain for at least 30 years, well before my diagnosis with PD. Whenever I put my back “out” I see a chiropractor as soon as possible and usually a few adjustments set me right. In the past, I used to go for physiotherapy and it took over a month to get any benefit. Chiropractic is faster and more effective than physiotherapy for relief of lower back pain, in my opinion. In addition to chiropractic, exercises to strengthen my “core” help me to recover quickly from recurring back injuries.

Myofascial release

Deep tissue massage is another form of physiotherapy that I have found to be beneficial for PD. In 2010, I had a package of 10 sessions of Hellerwork. Over a couple of months, my Hellerworker Melissa Patton accessed and massaged all accessible fascia of my body. Despite the intensity of the bodywork, the sessions were soothing and felt heavenly.

Air splint

I am currently experimenting with an inflatable splint of the kind used for retraining of stroke patients by immobilizing spastic limbs. The splint is used to straighten my right arm and eliminate the crook in the elbow. I use it three times a day for 10 minutes at a time. It feels good to have my arm straightened.

Minimal contact therapies

There are a couple of therapies that have reportedly had good effect on people with PD. One of these is Bowen Therapy. I have had several sessions of Bowen and found them very relaxing but did not experience any lasting effects. I did, however, find that osteopathy was effective. I have seen in osteopath in New Zealand on a few occasions when I was working there and found his techniques to be effective in reducing lower back pain as well as being very relaxing. If there was a local osteopath, he or she would be in my “team” of caregivers.

Neuroprotective supplements

Neuroprotective supplements are also referred to as “anti-aging” supplements or “mitochondrial enhancing agents” and are taken in addition to the conventional antioxidants (such as vitamin C, beta carotene, vitamin E, and selenium). Most of these supplements are taken orally; the very powerful antioxidant glutathione must be taken intravenously. While I am normally very skeptical of practices that come across as pseudoscience, I can appreciate the rationale for taking supplements that could protect the brain.

The first neuroprotective supplement I began taking (in 2007) was co-enzyme Q-10 after I read that a small clinical trial had revealed that it slowed the progression of PD. Subsequent, larger, studies have not found any beneficial effect on PD but I was willing to go with at least the chance of a good result. I have since learned that the ubiquinol form of co-enzyme Q-10 is superior to (and more expensive) the ubiquinone form.

In 2008, I chanced upon “The Better Brain Book” by neurologist David Perlmutter http://renegadeneurologist.com. The book contains a chapter on maintaining brain function using antioxidants and other compounds that facilitate the functioning of existing neurotransmitters. The protocol recommended by Perlmutter for PD patients is more extensive than that recommended for normal people who simply wish to improve their brain function.

I am currently taking the following neuroprotective supplements:

– Alpha lipoic acid* (time-release) 1200 mg per day.

– N-acetyl cysteine* 600 mg per day.

– Phosphatidylcholine 420 mg per day.

– Phosphatidylserine* 100 mg per day.

– Acetyl l-carnitine* 500 mg per day.

– Co-enzyme Q-10* (ubiquinol) 600 mg per day.

– NADH 5 mg per day.

– DHA + EPA (omega-3*) 660 mg +330 mg two times per day.

– Glutathione* (intravenous) 2500 mg per week.

* Recommended by David Perlmutter.

The glutathione IVs are administered by my ND, Caleb Ng. The protocol is that recommended by David Perlmutter. By the way, there is a video with David Perlmutter showing the near-miraculous effects of glutathione injections on people with PD http://www.glutathioneexperts.com/benefits-glutathione.html that to me seems to be a startling example of the “placebo effect.” I have never experienced anything even remotely resembling the improvement rapidly shown by the people in the video but again, my PD symptoms are not as advanced as those shown in the video. If glutathione has any effect on my symptoms, I believe that glutathione has produced a small (1-2) decrease in my PDRS.

In addition to the special mitochondrial enhancing supplements, I take vitamin C in both in time-release form and also as mixed ascorbates (total 4800 mg vitamin C per day), vitamin D drops (4000 IU per day), selenium drops (260 mcg per day), and zinc drops (30 mg per day) and others. I have my blood work checked regularly and have near-ideal results (all parameters within reference ranges). For years my cholesterol was chronically high and required meds for regulation; now it is excellent (high HDL and low LDL) without meds. Also, I used to be on meds for high blood pressure; now my blood pressure is close to ideal (typically 110/65) and I no longer take meds.

Although it is difficult to say whether all of these supplements are having any effect on my PD, I figure that at least I am extending my life!

Diet

The first alteration to my diet was to eat mostly organic foods to minimize the amount of pesticides that I was incidentally ingesting. Pesticides have been implicated with PD in some cases so I was not about to take the chance that my PD was unrelated to pesticides. I also began eating more fish and less red meat. In 2009, I heard about Donnie Yance, an herbalist in Ashland, Oregon, who had a protocol for treating patients with PD. I read his paper, “Parkinson’s Disease and the Use of Botanical and Nutritional Compounds” and was impressed withhis knowledge. In July, 2009, I traveled to Ashland and saw one of his associates, Jason Miller who has become my herbalist.

Botanicals

Jason provides me with a number of proprietary botanical formulations marketed under the Natura brand from the Centre for Natural Healing in Ashland, Oregon www.centrehealing.com. These contain botanicals that have been known to have a beneficial effect on PD, including:

– Mucuna pruriens (a natural source of levodopa)

– Hyoscyamus niger (henbane)

– Withania somnifera (Ashwagandha)

– Turmeric

– Green tea extract

– Piper methysticum (kava kava)

– Panax ginseng

– Bacopa monniera

– Scutellaria lateriflora (skullcap)

Of these botanicals, the first two on the list are perhaps the most potent. Mucuna pruriens is a natural source of levodopa and has been found to be more effective than synthetic levodopa in clinical trials. I have experimented with not taking the Mucuna and not noticed any difference, although perhaps I am not yet at the stage of my PD were levodopa is necessary. I am currently in a trial of titrating in with Hyoscyamus niger that is supposed to be effective against the tremours of Parkinson’s. So far, at 30 drops a day of a 1:10 tincture, it seems to have appreciably mitigated my tremours but it is too early to confirm it as effective at this time. Any beneficial effect is overwhelmed if stress rears its ugly head. Stress trumps hyoscyamus every time in the tremour department.

In addition to the above botanicals I also use products such as Natura “Beyond Whey” and “NanoGreens” that, amongst a host of other ingredients including frozen blueberries, make up a morning smoothie that I make every day. The Centre for Natural Healing also prepares a custom “tonic for me that I take twice a day. The tonic contains ginkgo, gotu kola, milk thistle, orange peel, kava kava, liquorice, skullcap, and other botanicals.

Gluten-free, dairy-free, and sugar-free diet

In 2009, I traveled to Melbourne Australia where I met John Coleman, a naturopath who has recovered from PD. Of course, I was very interested in doing whatever he did to recover. Amongst his recommendations was a change in diet to gluten-free, dairy-free, sugar-free (and others). I saw John again in 2010 and he said that I was doing well and to stay the course. He said the last of his symptoms to go was the tremour. This gives me some heart as tremour is the most bothersome of my symptoms.

In their book, “Parkinson’s Disease: Reducing Symptoms with Nutrition and Drugs,” Geoffrey and Lucille Leader advocate a gluten-free and dairy-free diet for people with PD. I am not lactose-intolerant nor do I have a gluten intolerance (this has been confirmed by genetic testing with www.23andMe.com) but their reasoning is compelling. It is possible that people with neurological disorders such as PD are much more sensitive to lactose and gluten than are people without those disorders. Luckily for me, we live in an age where it is possible to btain gluten-free and dairy-free foods readily. My favourite gluten-free bread is “Udi” available from Whole Foods in the US (but alas not in Canada). I substitute almond milk for regular milk. Dining out can be a problem; however, I travel a lot in my work and have found that the chefs in hotel and other restaurants are more than willing to meet my dietary requirements.

Adrenal support

In early 2010 I had a saliva test to determine my free cortisol rhythm. Samples were taken at 8 AM, noon, 5 PM, and at midnight. My cortisol levels for morning, noon, and afternoon where all markedly depressed (only the midnight sample was normal), indicating (according to the report) marginal HPA (hypothalamuspituitary-adrenal) performance. I purchased an excellent book, “Adrenal Fatigue,” by James Wilson that help to explain the significance of my results. Low cortisol, or hypoadrenia, is normally characterized by fatigue, difficulty rising in the morning, a desire for caffeine, feeling run down and stressed, etc. Other than perhaps a desire for a daily cup of coffee, I have none of these symptoms. Indeed, I seldom experience fatigue and still consider myself as a high-energy person. Yet, people with hypoadrenia have a reduced ability to cope with stress. Interestingly, people with PD report that their symptoms are aggravated in times of stress. There has to be some sort of connection between the symptoms of PD and impairment of HPA performance, but so far discussions with my neurologist and endocrinologist have not revealed any knowledge by them of any connection.

The danger is that people with hypoadrenia are on the borderline of having adrenal fatigue (no cortisol). When cortisol reserves are too low, and a stressful situation occurs, one may not be able to produce enough cortisol to handle it. Adrenal fatigue has been responsible for high-performing individuals “crashing” and becoming effectively bedridden for months or years, too fatigued to do anything. Not wishing to come down with adrenal fatigue, I have begun taking an adrenal support botanical supplement (“Restorative Formulations Adrenal Px LOPB”) and have also tried adrenal cortex extract (“Adrenal Stress End”).

Hydration

I have tried the Aquas formulas available from John Coleman in Australia. These homeopathic remedies are supposed to enhance cellular hydration. I have a problem with homeopathy. If an infinitely diluted amount is good for me, then not taking it all should even be better! Yet, John Coleman swears by the Aquas and he has recovered from PD, so there may be something to it.

Red wine

Geoffrey and Lucille Leader recommend elimination of alcohol from the diet. John Coleman, sensible man that he is, recommends 1 to 2 glasses of vintage red wine a day. I am on John’s side. Drinking fine red wine has been a passion of mine since the 1970s and one that I am loath to give up especially since I have a wine cellar containing approximately 2000 bottles! Of course a big part of the enjoyment of red wine is the bouquet. Reportedly, loss of the olfactory sense is a common complaint in people with PD and is liable to occur early in the progression of the disease. I noticed no such impairment (and can still guess in a blind tasting that a bottle of Bordeaux is a fine old Burgundy!). For now, I enjoy each bottle of fine wine as if it were my last. To me, joy = dopamine. Also, there must be some benefit from the resveratrol!

Constipation

As PD also affects the autonomous nervous system, constipation can be a severe problem. Since my diagnosis with PD I have had some problems in this regard especially when I travel over multiple time zones and upset my daily rhythms. Currently, I have it under control with the simple addition of one or two rehydrated prunes to my morning smoothie plus a level teaspoon of organic psyllium fibre. These seem to be enough to keep me regular.

Hedonism

I stayed strictly on my gluten-free and dairy-free diet for over a year, but recently had the opportunity to travel to France for a combination of business and pleasure. I temporarily abandoned my diet and indulged myself for a full week in French gastronomy, eating foie gras, croissants, baguettes, rich cheeses, and just about everything else that the French are famous for. The consequence was that I had not felt better in over three years! Now, I am not so strict about my diet and allow myself the occasional indulgence.

Chelation

In 2008, a urine test for heavy metals revealed excessive concentrations of lead and mercury and other metals such as manganese. I have been undergoing chelation off and on since then and currently receive one treatment per week from my ND Caleb Ng. The treatments involve a small IV of EDTA solution. For any benefits to be realized, numerous treatments are necessary. Heavy metal poisoning (especially manganese) has been implicated in PD and welders are one profession that is at higher risk for PD. Since I spent many years working closely with welders and breathing welding fumes, I have no doubt ingested my fair share of iron, manganese and other metals. Interestingly, a CT scan of my brain failed to reveal any abnormal concentration of manganese. Note: the claimed benefits of chelation for PD have yet to be established through rigorous clinical trials.

Brain therapies

This section covers a number of therapies that may be useful for maintaining mental functioning and postponing the dementia that may occur as PD progresses.

Positive attitude

It is difficult to remain positive when confronted with a disease of no known cause and inevitable progression, yet this is precisely what must be done. Depression is one of the predominant symptoms of PD. If necessary, it may be necessary to take an antidepressant. One that has been recommended to me is duloxetine.

Body-mind psychotherapy

For several years in the 1990s, I had training in Hakomi body-mind psychotherapy arising out of the deep desire to know myself. I still keep in touch with my teacher, Ron Kurtz http://hakomi.com/. I regularly see a therapist,Mahmud Nestman, a Sufi who is familiar with the methods of Hakomi. In our explorations one useful technique is called “taking over”. In one session I had Mahmud take over (literally, with his hand) a tightness I felt around my heart.

When he did so, I was able to go in deeper into my own unconscious and to gain some valuable insights as to why the tightness was there in the first place. I have invariably noticed that during our sessions my tremours at first become almost uncontrollable but then they disappear, leaving me in a most serene and quiet and still place. Stillness is priceless.

The science of happiness

For several years I was an active member of the Ken Keyes community based in Coos Bay, Oregon. Ken was the author of the “Handbook to Higher Consciousness,” “The Power of Unconditional Love,” and many other books. For a number of years, I taught “Living Love” workshops in the US, Canada, and New Zealand. These teachings have served me well, particularly now that I have the symptoms of PD. I take responsibility for my own feelings. Nothing or nobody has ever made me upset are unhappy: I do it to myself. This is good news as the only person I am capable of changing is myself.

Neurofeedback

I have had six sessions of neurofeedback, also referred to as biofeedback from Mike de Jong, a PhD psychologist. During the first session and EEG was done to determine those parts of my brain that had abnormal brainwave patterns. Mike determined that my dorsolateral prefrontal cortex was deficient in theta wave output. Subsequent sessions (one hour each) involved application of a single electrode at the position on my head corresponding to the dorsolateral prefrontal cortex. I was provided with headphones to listen to the sound of surf while my eyes were closed. Whenever my brain produced Theta waves I could hear the surf; when no theta waves were being produced all I heard was static. At first, I struggled to hear the surf, but later just let my brain do all the work of figuring it out. After six sessions, some progress is being made. If I didn’t think there was some benefit to this I wouldn’t continue. Typically, it takes 20 sessions to realize any permanent benefit, so I have some time to go.

Meditation/relaxation

For many years, I was an adept meditator and meditation was the most important part of my day. Since my diagnosis with PD, however, I have found it very difficult to get into a meditative state. Sitting cross-legged is agonizing. Instead of stillness, I have tremours. By re-casting meditation as relaxation, I can derive some of the benefits, primarily reduction in tremours and tension. I have found that electro-cranial stimulation (see below) is a good substitute for meditation.

Electrio-cranial stimulation

In electro-cranial stimulation, a small electric current is passed through electrodes attached to my earlobes that produces a mild tingling sensation. Sessions are either 20 minutes or 60 minutes and are very relaxing, almost to the point of putting me to sleep. Tremours also appear to take a nap.

Neurocognitive screening

In 2010, I participated in a neuropsychological screening evaluation at the Movement Disorders Clinic at the University of British Columbia. These tests revealed that my cognitive functioning was “broadly average to superior” depending on which test was being administered. I take this as a sign that I have experienced some cognitive impairment as I would have expected all the tests to result in a “superior” rating!

Defiance

If I had one final piece of advice for anyone who has been diagnosed with PD, it is to defy it. If it is a fight that Mr. Parkinson wants, it is a fight that he will get. The worst thing one can do is to deny it. As long as one remains in a state of denial, the PD will continue to progress. But as soon as you turn to face your tormentor and fight back, the PD will lose its grip over you. Mr. Parkinson may win in the long run but it will be a protracted fight and you will win many of the rounds. And, who knows, you may just beat him!

Afterward I hesitate to call this section “Conclusions” as my protocol is very much a work in progress, and the effectiveness of many of the measures has not yet been verified. I do not have time to wait for the development of a “cure” from conventional Western medicine. I will be dead long before any such treatment has passed through all the hoops and clinical trials necessary for its approval.

Currently, the treatment of last resort for PD is Deep Brain Stimulation (DBS) but it is only done when a PD patient is essentially incapacitated with an advanced form of the disease. How humiliating! For people with tremour-dominant PD the option is thalamic surgery, either in the form of thalamic DBS or thalamotomy. Canada’s medical system is unable to cope with the (growing) numbers of PD patients, so in the meantime I will do everything I can to prevent the progression of my PD to the point where surgery is even an option.

I am doing the best that I can to not be a burden on the medical system. What I am doing is also expensive. Canada’s medical system pays for my neurologist visits and little else. The PET scan, physiotherapy visits, naturopath visits, botanicals, and supplements are not covered. Yet if there was ever a time to start spending what I have saved, it is now. I would rather have quality of life than a fat bank account anyway. I’m currently working my way through my “bucket list” and having the time of my life.

Angela Wensley

Full Recovery from the Symptoms of Parkinson’s

Hi Robert,

You have been incredibly on point with regard to healing and recovery, although I am not one hundred percent sure how it is I recovered. I know that you have recently expressed the direction I went. I think the study of neurophysiology and quantum mechanics as it applies to neurology forced me to go back and re-learn the mathematics necessary to visualize quantum theory. Furthermore when I would go walking I would of course contemplate these principles. This is a little difficult to explain but it was like a light came on. This event was not sudden but involved significant time with daily study and contemplation although that is not what I intended.

In those days the talk of any sort of psychic change or shift in consciousness would have been met with laughter, however those concepts are steadily becoming more talked about especially from evolved teachers like yourself. Although not advised I quit taking all of my PD meds which included a lot of sentimet and mirapex. It was difficult for a few days and I was still shaky.

I applied a lot of other things that I had learned including detox, no refined foods, organic fruits and veg’s and a great deal of exercise. Then the symptoms dissipated completely.

Robert I think if there is an effective way to release our minds from the conditioned way of perceiving information or reality as we have learned it is much easier to experience more constructive thoughts. Our new found way of experiencing life is where healing and recovery reside because there is this all important element of belief that plays a vital role.

Bobby

What Helps Parkinsons Disease

Dear Robert,

I want to thank you for all of the help you have offered during this time of struggle with Parkinson’s.  My husband did pass away two weeks ago. I know that we learned a lot from your newsletter here and with prayers and the Theracycle and CoQ10 (up to 1200 units a day) and many of the other suggestions from your readers my husband walked (even without the walker around the house) until the day he passed away.  He was able to eat by himself at the table.

By the way we also saw improvement with Prevagen. After 3 months we were advised by the Prevagen people to up the dose to 2 caps a day.  We did see a very good improvement.  Also we tried GLUCOSAGEN from Health Freedom Nutrition and saw a good improvement in moving. Each person must try for himself. I feel very confident in recommending these however they were all part of a larger supplement program we had worked on for years.

My very best to all who are working through this illness.

We cannot change the hour of death but we can make a difference in the quality of life. I wish you all the best of health and comfort. And I do hope all who suffer with these Parkinson’s symptoms will find access to your  newsletter.

Best regards,

Karima

To subscribe to the free Parkinsons Recovery newsletter enter your e mail address in the field provided on the main website at http://www.parkinsonsrecovery.com

Robert Rodgers, Ph.D.
Parkinsons Recovery

Angela’s Story

Angela is my guest on the radio show this week. As you can ascertain from her story below, she has had a fascinating journey on the road to recovery.

Angela will be available to answers questions from listeners on Thursday from 11:00 am – 12:30 pm pacific time.  Call the following toll free number to talk with her:1 (877) 590-0733 or visit the Parkinsons Recovery radio page here:

http://www.blogtalkradio.com/parkinsons-recovery

Angela’s History

Work as a freelance professional engineer in the pulp and paper industry. Based near Vancouver BC but work mainly overseas, particularly in Chile and in New Zealand.

In 2009, I won the Beloit Prize, the highest honour for engineering in the pulp and paper industry.

Have had previous training as a therapist in Hakomi body centered psychotherapy.

Was a trainer in “Living Love” method as described by Ken Keyes Junior in his book “The Power of Unconditional Love” and others. Ken taught that true happiness is uncaused, that no one or nothing is ever made us upset are unhappy. This is really good news since I realized I could change myself whereas it is impossible to change anyone else.

Living Love has really helped me with my PD. I don’t have to demand that I not have it, with all the attendant negative emotions. I can prefer to be PD free and work to that goal without negativity.

For many years, was an adept meditator. Spent much of my spare time on the spiritual journey visiting spiritual communities around the world.

My hobby and passion is fine wine. I am a past president of the American Wine Society. I know that many people with PD have lost their ability to smell but I still have mine. The result of long, intense training?

My outlook on life is decidedly optimistic. I am a “reverse paranoid” as I believe that everyone is out there to make me happy!

2006

First symptoms 2006 at age 59: cramped handwriting and frozen right shoulder.

Over the years my handwriting has remained cramped but my right shoulder has thawed. The tremor in my right hand has increased from virtually nothing in 2006 to intermittently bothersome in 2010.

Saw a neurologist in December 2006. Possible Parkinson’s. I rejected this out of hand as it was obvious that I have a “pinched nerve”.

Part of me still wants to believe the pinched nerve theory.

2007

Went for a second opinion. Saw another neurologist in May 2007. Diagnosis: idiopathic Parkinson’s disease. This was a terrible moment in my life as the urologist was almost gleeful when he told me what I had, as if he had solved some great mystery. I felt like I had been shot with a cannon.

On the recommendation of my neurologist, I started on Mirapex, a dopamine agonist. Dreadful side effects: somnolence, insomnia, nausea. Just about everything except compulsive gambling. I stopped taking Mirapex after four weeks and vowed to never again take a Parkinson’s medication.

It is as if the Mirapex put a “hole” in my brain. It took over three years for this to be repaired. I would classify Mirapex is a neurotoxin.

Desired third opinion. Had a PET scan at the Inglewood imaging center in LA. Supported diagnosis of idiopathic Parkinson’s disease. Finally accepted that I had PD and decided to defy rather than deny it.

Having read that exercise is the “best medicine” for PD decided to get serious about it. Started running. Started going to the gym. Hired a personal trainer. Within four months I had lost nearly 50 pounds and became a lean, not-so-mean, fighting machine.

I exercise regimen at the gym typically consists of 30 min. of cardio (upright bike), 30 min. on the weights, and 30 min. of stretching.

My personal trainer concentrates on keeping all of my muscle groups functional. She also includes many balance exercises. Balance on my right leg is not as good as on my left but at least I still have it.

I regained use of right shoulder by numerous injections of prolotherapy, although my right arm remained significantly impaired.

Prolotherapy is merely the injection of dextrose into the tendons. This irritates the tendon and stimulates blood flow to the area. It really hurts! But after two months I could raise my arm that was formerly just hanging at my side.

I was introduced to kickboxing by my personal trainer. Found that I enjoyed it very much.

They usually have 2×30 min. sessions of kickboxing a week. Kickboxing also feels good and I believe it is the cyclic vibrations from alternating job-crosses, right hooks-left hooks, right kicks-left kicks, that keep my movements stabilized. I particularly like hitting a dummy that I have named “Mr. Parkinson”.

On the recommendation of a friend, I started playing tennis again (I had to stop due to my frozen shoulder) using my left arm instead of my right. Soon after, however, I regained the use of my right arm. Now, I have two forehands and a left-handed serve.

I now visit Florida for two months each year where I engage a tennis coach every other day to put me through my paces. When I am on the court, I can run like the wind, and have no problems moving sideways or forwards or backwards or running. As soon as I leave the court, my PD symptoms return. I wish I could play tennis 24/7.

2008

Saw Jon Stossel, Canada’s top PD researcher at the University of British Columbia. With him, I feel that I am being provided with the best service available from standard Western medicine.

I see Jon Stossel once a year.

Became a patient of ND Caleb Ng of Mountainview Wellness Center in Surrey BC. Introduced to protocol of Dr. David Perlmutter, the “renegade neurologist”. Embraced Perlmutter’s protocol of supplements for neuroprotection of Parkinson’s patients. This included co-enzyme Q10, omega-3, B-complex, N-acetyl cysteine, alpha lipoic acid, phosphatidylserine, and others.

I have been taking intravenous glutathione once or twice-weekly. I began with 1400 mg but am now taking 2500 mg each time. Quite frankly, I have never noticed any of the miraculous improvements shown in Perlmutter’s videos.

Caleb also started me on chelation therapy as urinalysis revealed high contents of lead and mercury. I had about a dozen sessions but then have stopped. I understand that dozens of sessions are necessary for any improvement to be realized.

2009

While visiting my Hakomi teacher in Ashland, Oregon, I found out about the Center for Natural Healing in Ashland where herbalist Donnie Yance had a botanical protocol for PD. In late July, 2009, I commenced his protocol for botanicals and supplements. Botanicals included Mucuna pruriens, Withania somnifera, turmeric, and others. Additional supplements included vitamin D3, zinc, selenium, and others.

After one year on the Donnie Yance botanical protocol, I decided to stop taking Mucuna and NADH as neither of these appear to offer any therapeutic benefit whatsoever.

I am about to start using henbane, a botanical anticholinergic, in an attempt to reduce the tremors. The grand experiment is yet to begin however.

In June, 2009, I became a member of PatientsLikeMe.com (patient name: Dawn Angel). I also joined 23andMe.com where I learned that I did not have the LRRK gene for Parkinson’s.

In September, 2009, I visited John Coleman in Australia. The recommended that I go on a strict diet: gluten-free, dairy-free, coffee-free, sugar-free, peanut-free, cashew-free, and so on. He also recommended that a begin taking the Aquas. For therapy, he recommended Bowen.

I have recently stopped taking the Aquas as I have never noticed any benefit from it.

I had several sessions of Bowen therapy. Very relaxing. Not as effective as IMS (see below).

While working in New Zealand, I found a very good osteopath who was able to effect incredible improvement in my tremors.

Osteopathy is mostly hands-free bodywork. I have no idea how or why it works, but it does.

In December, 2009, I attended Robert Rodger’s “Jump Start to Wellness” in Olympia Washington. This is where I first learned that there were other people interested in getting well.

2010

A check of my free cortisol rhythm revealed that my cortisol levels were very low throughout the day. This is characteristic of “adrenal fatigue”. The only problem was, I remained high-energy and was not fatigued in the least, however, I began taking the supplement called “Adrenal Support”.

In January and February of 2010 I had a 10-session course of Hellerwork, a form of myofascial release. Very good.

Hellerwork is closely related to Rolfing. Over the 10 sessions my practitioner literally massaged all the fascia of my body. It felt great to have stiffened muscles worked upon. I return for an occasional tune-up.

I found a practitioner of intramuscular stimulation (IMS), who has been able to read awaken muscles that had become shortened due to disuse. This has been the most effective therapy of all for me.

IMS involves needling as in acupuncture but the needles are applied to the tendons instead of to fictional meridians. The benefits of IMS are immediate and last for at least several days. I see my physiotherapist weekly.

Despite improvements in my mobility and strength, the tremors in my right hand had become noticeably worse, especially when I visit either an M.D. or a neurologist. The tremors would go away as soon as they left their offices. This is clearly a manifestation of “white coat syndrome”.

I revisited John Coleman in May, 2010. He commented that tremors were the last symptom to go away for him.

After hearing about the possible benefits of neurofeedback for PD, I had a EEG done and found that my dorsolateral prefrontal cortex was not producing theta waves. I have since had six sessions of neurofeedback and have noticed improvement.

In a session, an electrode is applied to my scalp in the location of the dorsolateral prefrontal cortex. I listened to soothing sounds through headphones. When that part of my brain is active I hear the sounds. When it is in active, I hear only static. The reward is the sound and the brain actively creates the ability to hear the sound without intervention on my part.

I purchased a small unit for cranial electrostimulation (CES). This applies a very small current through my head by means of electrodes clamped to my earlobes. I find it very relaxing; indeed, it is a form of meditation. Since my diagnosis with PD, meditation has not come easy to me.

In October, 2010, I visited France where I completely abandoned my dietary protocol and gorged myself on foie gras, croissant’s, baguettes, rich cheeses, exotic desserts, café au lait, and other forbidden foods. After one week I felt better than I have in three years. Go figure, who would’ve thought there was such a thing as the “French Cure”! Vive la hedonism!

Angela