Category Archives: chiropractic Treatments

Does Chiropractic Therapy Offer Relief from Parkinson’s Symptoms?

I have your book and have spent some time on your website, but so far I haven’t seen any reference to possible relief provided through chiropractic therapy.

I recently met an upper cervical chiropractic specialist who claims to have helped many people with Parkinson’s reduce or eliminate their requirement for medication. Of  course, he wants me to sign up for a year of treatment which is quite costly and no guarantee of results. I had to stop working a year and a half ago, so the cost is really only affordable if it would enable me to go back to work.

I have requested a list of references from people he has helped, but while I’m waiting I thought I would ask you if you have heard of this. I would greatly appreciate any information or insights you can offer.

Thanks,

Bob

Response:

First, you can review a rich discussion on this blog about chiropractic treatments as they address symptoms of Parkinsons Disease. Click on the category to the right entitled “Chiropratic Treatments.”

Second, I have not found chiropractic treatments to be high on the list for people with symptoms of Parkinsons. Some people report that the adjustments are too invasive, creating problems rather than solving them. Of course, the treatments depend greatly on the chiropractor. There are many approaches that are used.

Third, I want to offer a reaction to the requirement you would have to sign up for a year of treatments. Hummm – why a year? Why not six months or one month or one week? I do not understand how anyone would understand your body well enough to know that it would take a year for results to be seen.

Fourth, I note that the promise is to reduce medications. Huuumm – what about symptoms? The idea of pursuing options is to see sustained relief from symptoms. It seems to me you are not getting much return for your money if the only benefit is a reduction in medications  without any resultant impact on symptoms.

Fifth, if cost is an issue – I suggest you investigate many of the free treatment options that are readily available and are helping people recover. It is surprising how many free things you can do that will make a huge difference (e.g.: exercise, eat live food, etc.)

Sixth, it may come as a surprise, but I have found most options result in some benefit. Isn’t that interesting? The reality is, however, that some options will be far more beneficial than others. You just have to discover which ones will help you the most. Have you really considered some of the other options? There are so many that are helping people.

Seventh, notice that I used the word “öptions” which is plural. From my research, it is rare for a person to have a sustained reversal of symptoms without using multiple approaches. More than one approach/therapy/treatment is usally necessary. In your question, you are relying on only one treatment to do the trick so to speak. I do not care what the treatment is, it is likely that using only one will disappoint.

Eighth, I am posting a video clip that was filmed at last year’s Parkinsons Recovery Summit. The suggestion that is offered responds to a question I asked for reports of any and all therapies people found had been helpful and effective. This explanation centers on a spine stretch that is treated with special equipment by a chiropractor.

The machine that was used by the chiropractor to do the adjustments that is referenced in this discussion is a DRX9000C. As you will discover from the discussion, this therapy was very beneficial.

[flashvideo filename=videos/spinestretch.flv image=videos/spinestretch.jpg /]

Finally, you ask me whether you should pursue this therapy. Why not ask your own body? It will give you the answer you need. Muscle test it! I honestly do not know if this would be  a  good option for you or not but your body does know the answer.

Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease
http://www.parkinsonsdisease.me

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Resources for Recovery from Parkinsons in France and Great Britain

Dear Robert,

I have been given your address, after being diagnosed with early Parkinson’s Syndrome, by a friend after discussing my general state of health with him. After exhaustive tests and the most frightening stay in hospital, a number of health issued raised their ugly heads.

I am just coming to my 56th birthday in June, to be told I had a liver virus, gall stones, depression (I have suffered with this after a nervous breakdown in 1994, but have been taught to control the effects through non-medicinal methods). I am in constant lower back pain and my specialist finally dropped the bomb shell that she believed I had the early symptoms of Parkinson’s.

I have been on a ‘light’ cocktail of drugs which have helped, but I do find it difficult to write now and hold a glass – it can suddenly fall from my hand for no reason. Walking is difficult, and I have had to give up driving, move into a friends apartment after falling and being unable to contact anyone for two days.

After going through your excellent site and information, I am writing to ask if you have :

  • Any knowledge of someone I can contact in France as this is where I live (or the UK)
  • Can I receive information you have on your site here

And finally, I want to be able to not be classed as disabled (which is what the French Health Service currently have me registered). It was hard work learning how to deal with my depression, but I learnt, I’m sure I can do it with the tools you have in your arsenal ! I am not a religious person, but I do believe in the power of the mind and the importance of a balanced spirit. If I could get to Bali, I know who and where I could go to get this positive / negative energy balance.

Thank you for your time,

Best regards

Rigby

Response:

Sounds like it is indeed a good time to get serious about considering other options! You have certainly come to the right place to get information about options that are helping people reverse symptoms that are similar to yours.

You ask about resources that might be available to you in France or the UK. There just happens to be one wonderful resource which has helped me personally and has helped many other people who currently experience the symptoms of Parkinson’s: Simon King. Simon, located in the United Kingdom, is a chiropractor who has has discovered the debilitating role that metal and crowns in our teeth can play on our neurological  system.

Why not first listen to my radio show interview with Simon King to evaluate whether you might want to make an appointment with him. His show aired April 9, 2009. To listen, visit:

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

Be sure to keep scrolling back since the most recent shows are listed first. Of course, all shows are free to download and listen. Simon’s website is:

http://www.proprioception.co.uk

You ask about other resources. My answer here is really quite simple. Start listening to some of the other Parkinsons Recovery Radio shows! There is a wealth of information in each show that I have aired. Read posts here on the Parkinsons Recovery blog too. If you have ever had any doubt about the prospects for recovery, those doubts will soon dissolve after you have listened to a few of the radio shows and had a chance to realize the wealth of information on the blog. Recovery is happening for more and more people.

Finally, if you want to get serious about identifying options, one incredible resource Parkinsons Recovery is making available in 2012: the Parkinsons Recovery Summit which will convene in Cincinnati, Ohio June 22 and June 23. I fully realize this is a long trip for you and would mean you must cross the ocean. I can assure you, however, that the trip would be well worth the effort.  You will encounter an incredible diversity of resources that are transforming many lives.

For more information about the Summit, visit:

http://www.summit.parkinsonsrecovery.com

Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease
http://www.parkinsonsdisease.me

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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

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Chiropractic Adjustments as Therapy for Parkinson’s Symptoms

Hello Dr Rodgers

I appreciate your work & I bought several of your programs which I follow: 5 Steps to RecoveryRoad to Recovery … After reading the Book from Dr J. COLEMAN, [Stop Parkin’ and Start Livin’] I postponed starting chiropractic Treatment.

Recently I found a GENTLE chiropractor & not a “bone crusher” (tried once) & I was convinced  to try chiropractic adjustments 3 times / week for neck & back pain.For the last 3 weeks, I haven’t seen any improvement BUT EVERYBODY SAYS IT IS A SLOW RECOVERY COMPARING the same way we wear braces for the teeth.I know the Healing is from the INSIDE OUT as Dr John SARNO  explains in his book: the mind body prescription.(Healing the body healing the pain)

There is no specific program one size fits all but we want to benefit from those who tried these modalities.Of course I follow a diet from Dr COLEMAN & DR L. MISCHLEY, I take the supplements, I exercise, bodywork ( Bowen + CST) meditate, clear my heart with healthy beliefs etc…

My first question:

Is chiropractic beneficial or no in the long run?

Response:

I would not place chiropractic adjustments in the list of preferred therapies that people with the symptoms of Parkinson’s say has helped them the most. I suspect the problem lies in the fact that the muscular restrictions found with many symptoms of Parkinson’s create an inflexibility that makes adjustments painful for many people. In some cases, the body will respond by tensing up more which of course is the reverse of what the chiropractor intends. Chiropractors who use gentle touch are more likely to get better results.

Every one’s body is different. We cannot make a list of good and bad therapies for people with the symptoms of Parkinson’s because the conditions that create the neurological challenges are different for each person. Listen carefully to how your body responds to a therapy such as chiropractic adjustments. Your body will tell you loud and clear whether the therapy is helping or not.

The best approach I think is to use your own good intuitive insights and give it a try if you are called to explore the therapy as a possibilty. I should say however that my research shows there are other therapies that show up more often as beneficial in reducing symptoms.

2nd question:

Bowen is helpful but we are limited by no bodywork 4-5 days before & after.

As I understand this question – you are saying that your Bowen therapist recommends a time when the body can integrate the work. This is a common recommendation after work is done, though I am not familiar with the idea that you have to do nothing 4-5 days before the therapy is administered.

Again, I do not think any static rule needs to be followed here. Just listen to your body. If it tells you it needs the therapy, go for it.

Last question for now

GLUTATHIONE is a strong anti-oxidant & IV administration is not practical & the nasal spray is yet to come BUT I found a respected Canadian company selling IMMUNOCAL based on WHEY Protein (cow dairy product) supposed to increase significantly the Glutathion in the body.This product is registered in the US & Canadian medicine compondium as a booster of immunity. My problem is the dairy origin of IMMUNOCAL & we have to stay away from dairy products in PD.

Response:

How interesting! Your doctor can obtain the nasal Glutathione through a company in Seattle called Key Compounding Pharmacy. Listen to my radio program interview with Dr. Laurie Mischley on June 17th. She has been prescribing the Glutathione nasal spray for her patients for several years and has been getting great results overall.

I will follow-up on your tip. Sounds interesting! Perhaps I can interview a representative of the company and air the interview on my weekly radio show.

Thank for all your work & Bless you all

Abi

I assure you it is a pleasure for me to serve.

Robert Rodgers, Ph.D.
Parkinsons Recovery

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Books
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Parkinson’s and Chiropractic

Question:

Noel Batten from Australia makes impressive  claims with regard to Parkinson’s Disease and has an interesting website: http://info.noelbatten.com/testimonies_and_cases.html

Did you hear about him?

If his claims are right, then I would get an x ray for my wife and let a chiropractor re-align the vertebrae.

Response:

I have known about this particular website for several years but have received no feedback from anyone who has used his service. Noel Batten presents case studies  on his website of people with a wide variety of diagnoses including carpal tunnel, cancer, MS, autism and Parkinson’s Disease. He shows videos before and after his treatments which reveal improvements. Keep in mind he does not show his videos of people who did not experience improvements.

In my research, we find that any specific therapy or modality will help some, perhaps many, but not everyone. I will invite Noel Bratten to be a guest on my radio program so we can all learn more about his approach. I hope he accepts my invitation.

I examined the testimonials on his website and have a sense that his five day program involves a little in the
way of chiropractic adjustment and a lot in the way of physical exercise. The research is very clear with regard to physical exercise. If a  person engages an exercise program for five straight days they are vitually assured of seeing some improvements in their symptoms, particularly those related to mobility. The case studies he
has on the website show people who clearly have inflammation. My hunch is that the exercise and his treatments probably help relieve the inflammation.

I would point out that the video testimonials involve a taping just before the five day treatment program began (showing the person has difficulties of one type or another) and a taping immediately after the end of the treatment (at day four or day five of his treatment program). These results are typical of what we see when people exercise regularly or when they get body work in one form or another (e.g., cranio sacral work, energy healing, etc.).

Of course, you can also see similar improvements that are just as dramatic when medications are “on” or working as opposed to “off” or not working. We do not know how medications might have confounded what we are seeing in the videos.

If the person did not continue with their exercise program, I suspect a video of them a week after their treatment ended would reveal they had reverted back to their baseline (when they were shown as being significantly challenged from a mobility perspective). It would be wonderful news if a five day program resulted in permanent improvement, but we see no evidence of that on the website. Of course, temporary improvement can be a blessing to many people.

What we want to see from a research point of view is sustained improvement over months and years. Speaking intuitively, this is not likely to happen with a few chiropractic adjustments or with five continuous days of exercise. The underlying factors that put the spine out of alignment in the first place need to be identified and addressed.

I should also report that I always ask the persons I interview with Parkinson’s  what treatments or therapies have helped them.  Chiropractic adjustments are mentioned by a few people, but they certainly do not float to the top as being one of the therapies that helps people the most. Exercise does float to the top as a helpful therapy,
so to the extent that his program includes exercise, it may indeed be helping over the long term if his clients  continue with the exercise program.

If anyone has direct experience with his five day program, please let us all know.

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What Therapies Do Not Help Relieve the Symptoms of Parkinson’s?

I had a fascinating interview
with Dr. John Coleman, ND,
this week. John was diagnosed
with Parkinson’s in 1995, but
after experimenting and trying
a wide variety of healing modalities
he is symptom free today.

I was curious about what
approaches and therapies John
tried – and he experimented with
many modalities – that did
not work for him. Here was
my question:

Robert Rodgers: “Which therapies
and approaches did not help relieve
your symptoms? 

John Coleman: “There were a lot.
In general, any form of body work
that was firm or hard. Deep
tissue massage, sports massage –
those sorts of massages – created
extra pain. Vigorous therapies
like chiropractic and other
manipulative therapies also
tended to increase my
symptoms and create pain.”

“Excessive intake of nutritional
supplements tended to have no
effect or make me nauseous or
simply be a waste of money. I
had to be very careful about
homeopathic remedies because
the normal approach in selecting
potencies and frequencies seemed
to aggravate me where a very
gentle, a very cautious approached
worked.”

“Many counseling modalities helped.
Psychiatry did not. I am sure there
are good psychiatrists out there,
but I saw four and none of them
helped me at all. Antidepressant
therapy did not work.”

“I choose not to take pharmaceuticals,
but other forms of herbal, vitamin
homeopathic remedies for depression,
but I realized I actually was not
depressed. I was certainly anxious,
but the antidepressant therapies were
just no good for me.

“I needed to be active and proactive
in my approach. In general, anything
that was too hard, too vigorous, too
enthusiastic didn’t work, and gentle,
cautious, loving therapies worked.”

John offers a powerful 12 Step
Parkinsons Recovery Program
that is designed for anyone with
Parkinson’s who is looking for 
ways to get relief from their
symptoms. 

Robert Rodgers, Ph.D.
Parkinsons Recovery

© 2008 Parkinsons Recovery

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