Category Archives: Parkinsons Disease Treatment

Cure for PD

Two questions which a similar theme follow:

Hello Robert,

I have just listened to your podcast “what is the biggest roadblock to recovery“. You talk about reversing symptoms or finding compelling relief of symptoms ~ Would you liken this to a cure for PD?

I am writing because my husband, 44 yrs old has a hand tremor & we are concerned that he has PD. We are in the process of finding a neurologist to evaluate him and give us some direction. This is an absolutely frightening experience for him/us. I appreciate any information you can provide.


I am suffering from Parkinson’s disease since 8th year. How can the the Parkinson’s disease be cured?


Speaking as a researcher who focuses on identifying the factors that cause neurological symptoms and natural therapies that help to reverse them, I never think in terms of a “cure” for anything. In general, this term is typically used when a treatment resolves the symptom completely. I know of no such intervention that works this “magic”.

The term “cure for PD” conveys a static condition. If the body is “cured” it is set in “concrete” so to speak. Once “concrete” is cured – it is hardened. The body is fluid and dynamic. Symptoms come and go for everyone – those with Parkinson’s symptoms and those who do not have symptoms of Parkinson’s disease.

The body is always communicating to us what is out of balance. Instead of thinking of tremors as a “problem”, think of them as a message your husband is receiving from his body. In many cases, the body is simply releasing trauma – which it does successfuly by shaking (or tremoring).

You can certainly suppress tremors with medications which is an option many people prefer. There are also natural therapies that are helpful in suppressing tremors which I have document in my recent book “Treatments for Tremors“.

As you already know from listing to my recent radio show What is the Biggest Roadblock to Recovery? I believe the most formidable roadblock to recovery is a failure to recognize the impact of trauma has on the ability of the sensitive neurological system to function.

Robert Rodgers PhD
Parkinsons Recovery

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Do You Have a Systematic Recovery Program?


Do You have a systematic recovery program? 

Is a Recovery Program Realistic?

Our experience in working with persons who have Parkinson’s has convinced us that there is no standard protocol that is the panacea. Of course, there is no “cure.” Factors that cause the
condition are multi-faceted so it depends.

We do know from a thorough review of the research that the symptoms can be caused by heavy metals, pesticides, chemical toxins, pathogens, trauma and stress. A variety of natural therapies are available to address each of these threats to the healthy function of the body.  We encourage each individual to investigate the therapies that are available
depending on their own individual needs and preferences and the primary factors that are causing their symptoms. 

  • Whole body detoxes are critical.
  • Strengthening the immune system is a must.
  • Reducing inflammation is important.
  • Nutrition is essential.
  • Adjusting the hormonal thermostat is important.
  • Exercising the body and the mind makes a huge difference.
  • Laughter every day helps.

Robert Rodgers, Ph.D.
Parkinsons Recovery


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The First Secret to Reversing Parkinson’s Symptoms

I have been focused as a researcher for the past decade on discovering the causes of Parkinson’s symptoms and, just as importantly, discovering the therapies that help reverse them. I must confess that what I believe now to be the ways to reverse Parkinson’s symptoms are very, very different from what I thought a decade ago.

For starters, most people who currently experience the symptoms of Parkinsons Disease focus on what substances they can put into their body to ease the symptoms. There are loads of choices of course, ranging from prescription medications which must be prescribed by a medical doctor to natural herbal remedies and supplements that you can obtain from a health care practitioner or from your health food store.

There is certainly nothing wrong with any of these approaches. I cover them in detail in Road to Recovery from Parkinsons Disease. They may give you your life back.

The first secret of seven that I discuss in Seven Secrets to Healing is that it is much smarter at the outset of your journey down the road to recovery to focus on getting the “bad stuff” out of your body rather than putting anything else in (no matter how “good” the stuff might be).

Please do not feel as though you are being singled out because I am saying you have “bad stuff” inside your body. Everybody does! We live in a toxic world. Everyone has heavy metals, pesticides and bacteria inside their body. The miracle of the body is that it is able to eliminate enough of the bad stuff to keep our delicate organs and other body equipment functioning. When the neurological system becomes challenged, it is more likely the case that there is an overabundance of bad stuff that has accumulated inside the tissues of the body.

The capacity of the elimination organs is constrained.  It cannot eliminate a pound of mercury in a day – obviously! Further, a component of whatever we put into our body – whether a medicine or a supplement or a food – has to be eliminated no matter how “good” we are convinced the “stuff” is that we are ingesting.

When Parkinson’s symptoms are present, I have concluded that the body is already overloaded with too much “bad stuff” that it is desperately trying to get rid of through one of the elimination organs: the kidneys, liver, spleen and colon.

The better choice is to set the intention to get the “bad stuff” out through detoxes and other methods before putting anything else in, One of the seven secrets to recovery from any chronic condition including Parkinson’s Disease is to purge first.

Robert Rodgers, Ph.D.

Olympia, Washington
Parkinsons Recovery
Road to Recovery from Parkinsons Disease
Seven Secrets to Healing

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Parkinson’s Disease Treatment

I am a subscriber to your Parkinsons Recovery emails.  I want to thank you for your innovative thinking about Parkinson’s disease treatment and I really appreciate your effort on our behalf.

I am 57 years old and was diagnosed with Parkinson’s disease at age 35.  I had this dis-ease for 22 years.  During this time, I have tried many, many natural modalities and I keep trying new ones all the time. The great news is that In still ride my horse, drive my car, hike, volunteer with a disability-awareness education group and keep on movin’. I did have a DBS implanted in 2003 which has really helped me.

As far as coconut oil – I tried it for 6 weeks but I did not notice any positive cognitive or physical improvement.  However, it did have a negative affect on my bowels.

Thank you for you positive message, Robert.



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Levodopa Medication

A friend directed me to this Blog because I Have PD with tremors in my right arm. I have been taking Carbidopa-levodopa for two weeks and so far I have not noticed any significant difference.  Am I being too impatient?  



This is certainly a question that others might shed some light on. I have heard a wide variety of reports on the outcomes of taking this medication. Some people report feeling better within days. Others report it does take time. Still others report that the medicine had no effect whatsoever.

Huummm … what is going on here you are wondering? The factors that contribute to the neurological symptoms associated with Parkinsons Disease are multifaceted, so depending on the primary causal factor that is involved in your case, this medicine  may or may not help.

Neurologists get a lot of information on your response to the medication so they are certainly a valuable resource to get an answer to your question. Clearly, your neurologist is the best guide here.

If you are interested in exploring other options that can be pursued (with or without taking medications) I invite you to explore the many fascinating topics that will be presented at the Parkinsons Recovery Summit this summer in Cincinnati. People are reversing their symptoms using a wide variety of approaches. A number of the contributors to Pioneers of Recovery who have reversed their symptoms will be offering workshops at the Summit.  The workshop topics reflect a wide variety of fascinating and very different approaches that are helping people with Parkinson’s recover.

The approaches that tend to succeed usually address the reasons for the symptoms in the first place. My research has uncovered there are many factors involved. The body is not a simple mechanism.  It really does know how to heal itself. It just needs a little extra help sometimes.

The people who are recovering are exploring a combination of treatments, therapies and modalities. If you have elected to explore one and only one therapy, I would recommend that you consider others as well. And of course, determining the root cause of the symptoms helps tremendously in identifying the treatments options that will help your
body heal.

Robert Rodgers, Ph.D.
Pioneers of Recovery

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Natural Therapies for Parkinson’s Disease


What other therapies do you recommend aside from the food aspect?


The thrust of my research has been to cast a wide net to identify any and all therapies that help persons who currently experience the symptoms of Parkinsons. After five years of a focused search, I am happy to report that I have succeeded in identifying dozens and dozens of natural, safe and nonintrusive therapies that people with Parkinson’s symptoms tell me help them immensely. To my surprise, I have not found very many therapies that do not have a positive impact to some degree.

The nature of your question is tied to several underlying assumptions. First, you assume that Parkinsons disease is caused by one and only one imbalance in the body. I disagree. There are a multitude of factors that create neurological symptoms associated with a diagnosis of Parkinson’s disease. For many people, more than one  factor is present. The particular therapies that can help will be driven by the conditions that are causing  the neurological symptoms. There are no easy solutions of fixes.

Many potential therapies exist that will and do help depending on the circumstances that are present. This was the motivating impetus to sponsor the Parkinsons Recovery Summit last week in Vancouver, Washington which was free.

Twelve different therapies were represented. Therapists volunteered their time to give free treatments and consultations to all who attended. It was a historic event for all persons currently experiencing the symptoms of Parkinson’s.

Second, you assume that I have a list of therapies that people should pursue if they expect to get well. That is, you assume that I promote a program of recovery. I am well aware that some medical professionals offer a very  specific protocol to treat the symptoms and that some of these programs are successful.

I am not a medical care professional. I am a researcher. As such, my job is to find the people who are figuring out solutions that are working for them and let others know about it.

I have just finished updating my book, Road to Recovery from Parkinsons Disease. The book offers a detailed description of the many therapies that are helping people who currently experience the symptoms of  Parkinson’s. If I were to offer a full and complete answer to your question I would now be writing a post that is 330 pages long – which is the length of the 2011 edition of Road to Recovery from Parkinsons Disease.

Yes – there are many opportunities to get well. Seize the opportunities and you will begin to feel better day by day.

Robert Rodgers, Ph.D.
Parkinsons Recovery

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Copper and Symptoms of Parkinson’s Disease

Lori sent me several messages from her i-phone about her remarkable recovery from the symptoms Parkinson’s disease. With her permission I am posting her correspondence to me below. Robert Rodgers, Ph.D.

My symptoms are currently reversing. My sons, myself and my sister tested very high copper levels.  Found out once started prenatal vitamins started improving almost gone after nine months .
Neurologist confirmed marked improvement! Work out alot. Eating better. Cut out diet coke addiction. Pray alot! My sons and I take zinc to chelate copper. Water tested positive copper. Copper pipes leaching copper.

It’s so weird! You have been so positive for me. Footdrop gone. Cogwheeling gone. Smile back:) Bradykinesia almost gone. Just action tremor.

They tell me I don’t have Wilson’s disease because cervoplasmin high too. They thought copper was elevated because of bc pills. But off them ordered own serum copper, i’m an OD, still high! My husband md, always said no resting tremor and he would notice it. Five doctors confirmed. Even went to cleveland clinic. Raised 7000 dollars for mjff.  Acceptted it. Something kept telling me have another baby. Got off meds. Started prenatal. Bam – got better. I’m supposed to be in that big mjff study. Called Cleveland. They said pd never gets better. Must be ingesting something.

I kept telling neuro that thought copper toxicity due chronic green hair when moved into house with copper pipes five years ago. Peds doctor helped me most because tested sons and high so he called toxicologist geneticist and metabolic.

I’m so scared it’s going to come back but I don’t think God does partial miracles.  My sister was higher than me. Currently get lots blood tests but say not Wilsons!

Thanks for positive vibes. Pd is so gloom doom. No hope awful, I think no one should not be given hope. People forget the God factor. Please post because if it happened to me it can happen to others.  My husband always thought h1n1 did it. But he sees what vitamins are doing for me, vitamins with no copper.

My handwriting is no longer small. Still trembles but so much easier.  I wrote and dated a journal so I can see the change.

Mirapex never really helped. It really only made a slight improvement in handwriting.  Never helped foot, smile cogwheeling or tremor. My doctors sill say I have PD and haven’t seen all improvement – think I’m nuts!

But pharmacy assured me mirapex er out of system. Completely done with it Nov 1, started to taper it Oct 21. started prenatal vitamins Oct 21. Noticed improvement. Started documenting it all on Nov 16th.  Haven’t seen neuro since nov 18th. I think they are going to be shocked!

Movement specialist said she never doubted my diagnosis, doesn’t want to see me til Feb. I’ve learned I have wrong doctors and the best peds doctor.

The thing that worried me was at 6 year old son started getting breasts. Doctor documented this. I researched crap out of it. It would come and go. Told peds everything, in youth elevated copper secondary sex characteristics. I started boys on vitamins. Youngest would not take them. I told doctor the oldest sons will be lower because been on vitamin. This turned out to be true. My husband’s copper level is normal.

I feel God put me thru this to help my boys! I’m planning to get prego once all gone . It will be miracle baby! It sounds unbelievable!

We have bottled water. Looking to get copper filter for shower! I would love to move but houses not selling.  We have a really nice house but I hate the copper pipes!


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A Clever Solution to Walking and Parkinson’s Disease

Hans de Rijke from The Hague in Holland called in during one of my shows and told us all about how he overcomes any and all challenges with walking by bouncing a ball. Isn’t that clever?

Hans sent me a video demonstrating how this simple technique works. You are going to have to turn you head to the side to watch. Just count that as part of your day’s exercise program.

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

Do you have a ball hanging around at home? Why not give it a try? Hans explains that no one takes notice of a man bouncing a ball down the street.  It  helps make you feel a lot younger than walking down the street with a cane.

The Parkinsons Recovery Jump Start to Recovery program is all about helping you figure out ways you can get sustain relief from your symptoms. Join us in San Diego October 18th-20th.

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Problems with Balance, Walking, Talking and Sweating


I have had Parkinson’s  since 2008. I am now taking amantrel-100 2 tab and pramipex-0.5 2 tab daily.

I still have a balance problem, a walking problem. Turning is also a problem – especially to the left, dryness in mouth, problem of pronunciation of some words while talking. excessive sweating at the left side of forehead is remarkable since 2005.  I also feel pain at neck below head backside of ears.

Kindly help,



You have a series of symptoms which is typical of people who are diagnosed with Parkinson’s Disease. It is likely that the cause is multi-faceted.

First, there is an Ayurvedic doctor in India, Dr. Paneri from Gujarat, who sees people with Parkinson’s exclusively and is getting remarkable results. His website is:

Second, check the side effects of the drugs you are taking. It is likely some of the problems you are experiencing may be simply the side effects of the drugs. You may want to talk with your doctor about adjusting your medications.

Third, I suggest that you focus your attention on finding doctors and health care practitioners who can help you detox the toxins in your body, I am guessing that toxins are a primary cause of your symptoms. You may well have an abundance of heavy metals and pesticides that have accumulated in your body.Once they are removed your symptoms may well subside.

There are many ways to detox – just check around and find an approach that appeals to you. I have been using
zeolite personally with great success – but there are many other excellent methods that are effective as well.

You can get a wide variety of suggestions on detoxes from my new book which is described at:

Know always that the body knows how to heal itself. We just have to give it a little extra loving kindness and attention sometimes.

Robert Rodgers, Ph.D.
Parkinsons Recovery

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Intoxication with Heavy Metal as a Possible Cause of Parkinson’s Disease

A neurologist recommended in the year 1998, that I should be medicated against my tremor, but I said no thank you to his offer, as I preferred to be better diagnosed before starting medication.

The following year my symptoms increased, as I became more rigid and my tremor got worse and I therefore was easy to persuade by a new neurologist to try anti-Parkinson medication. Shortly after, I was scanned for Parkinson’s disease and the result was compatible with the diagnosis of Parkinson’s disease in the early stage.

Anti-Parkinson medication helped to decrease the symptoms, but soon I experienced more severe symptoms. At first I thought that it was the disease becoming more severe and this was confirmed by my neurologist who told me that it was unavoidable.

After one year on medication my neurologist recommended that I stopped medication before the next consultation. This became the start of a new phase in the way I coped with my disease, as without medication, I experienced that:-

–     The medication can result in abstinences when the medication is stopped.

–     Many of the symptoms, that I thought were Parkinson’s symptoms, were in reality side effects of the medication.

Therefore I decided to accept the symptoms of the disease instead of being burdened with adverse side effects of the medication. The outcome of this choice forced me to search for factors, which had influenced my symptoms.

In the year 2001 I was tested for Heavy Metal Toxicity in a private clinic in Aarhus, Denmark by Dr. Bruce Kyle ( and I was diagnosed with a combined toxic overload with mercury and copper.

I was treated at Dr. Bruce Kyle’s clinic with the Chelating Agent DMPS, with Vitamin-C infusions and different kinds of antioxidants and nutritional support. At the same time I had my amalgam fillings removed and had non-toxic, non-metal composites instead. This was done by a dentist with extra education in safe removal of amalgam. I also use saunas, which help detoxification by sweating out the toxins through my skin.

After some years of undergoing detoxifying treatments, I had fewer tremors and was less rigid, but I still suffered from fatigue. Allergic reaction against metals was suspect, and I undertook a MELISA-test.  (

My test showed an allergic reaction against gold, nickel and cadmium and treatment protocol was removal of a dental gold crown, which was replaced with plastic.  Now, I try to avoid nickel and to eat more organic food to avoid cadmium. Luckily I have been rewarded for my efforts as my fatigue has decreased.

Today I can honestly say that testing and treatments for my chronic cumulative toxicity has been successful for revealing some of the causes of my Parkinson’s disease. However, I still have slightly high levels of copper left and in Autumn 2006 and Spring 2008 tests show that I am also burdened with lead and aluminum.

I do not dare to think about how my life would have been without detoxifying treatments!  When I look at other patients with Parkinson’s disease who are getting worse, I have even more reasons to be thankful for my health, which continues to improve as time goes on.

Where do these Heavy Metals come from?

In my case, mercury and copper were likely to have come from my amalgam fillings. Copper-amalgam contains a high percentage of copper and I had many fillings in my milk teeth. Even later in school I had many cavities, which were restored with amalgam. The dentist said that I had weak teeth.

As an adult, I have only had one cavity, so I might think that my parents were not good at helping me with tooth brushing and perhaps also the school dentist has been tempted to do fillings, which were not necessary as she was paid for the amount of pupils’ cavities that she restored.

In addition I have in my job as a veterinarian, been exposed to many thermometers, which sometimes break and where the mercury ended up in the bottom of the car. Veterinarians were not properly informed that this could constitute a health hazard at that time.

Moreover Mercury can come from vaccinations containing the preservative Thiomersal (ethyl-mercury). Mercury might also come from environmental pollution and intake of fish. Copper might come from use of copper spiral (anti contraceptive) and from drinking water and food. The Danish Agriculture Production uses 200 tons of copper yearly and this copper could be assumed to spread to the environment and end up in drinking water and food.

When a person is burdened with mercury toxicity, then the excretion of copper is decreased.

My toxicity burden with lead might perhaps come from common environmental pollution. My toxicity with aluminum probably came from years of injections with aluminum containing products against dust mite allergy.

My nutrition today contains more antioxidants (nutrients which protects the body against free radicals and oxidation), more vegetables (raw vegetables are chosen) and more fruits.
I have stopped eating unhealthy fats such as margarine, hard fats, corn oil, soy, sunflower etc. I try to eat more of the healthy fats such as fat fish (salmon), linseed, olives oil, nuts etc.

I take antioxidants as nutritional supplementation, also a multivitamin mineral pill without iron and copper, extra vitamin C and E, Lipoic acid, N-acetyl-cysteine, Echinacea, Ginkgo Biloba and Coenzyme Q10. I also use DMSA for mercury, copper and lead chelation.

Concerning the nutrition I would recommend the book by Jean Carper – “Your Miracle Brain.”

Physical activity has been an important part of my life. At the beginning of my disease I walked without swinging my right arm and I stumbled rather often. After years training trying to walk normally with swinging my right arm, I have succeeded, but only when I am not too stressed or exhausted. The principle is like this, if I can walk one step with swinging the arm, then I can also walk 3 steps….. or also walk 5 minutes…or 5 kilometres and so on.

I also use visualization when training my movements.

People, who do not realize the effects that Parkinson’s disease has on their own body, often have problems understanding how demanding it is for a Parkinson patient to cope with conscious movements. Even something as banal as cleaning your shoes on a doormat is not necessarily functioning automatically but needs mental work, like steering a toy car with a joystick.

It is very common that a Parkinson patient with time develops a forward bending posture and some years ago I had thoracic Kyphosis and could not wear any of my shirts anymore. A physiotherapist has taught me some physical exercises, which I since have done every day.

Today my back is straight again, which makes me happy. People, who are happy, often have a straight posture, while sad and grieving people often have a crooked posture. By choosing body posture you can also indirectly choose your emotions.

I enjoy sending a signal that I am bubbling with joys of life.

I try to avoid, if possible, all kind of stress. Now I choose calm classical music instead of rock; I value tight relationships instead of having a circle of acquaintances with ‘small talk’ and I love being out in nature instead of taking city walks. It is a pleasure for me to do meditation and to sing.

I have also improved at listening to the signals from my body and I take care to rest and sleep when needed.  I have also improved at learning to avoid doing things, which I dislike and instead I do things that make me happy.

When being diagnosed with a chronic disease the patient often goes through a life crisis and so did I. The crises made me more religious and I learned to pray to my God from the bottom of my heart – this has given me spiritual power to cope with life and the new circumstances.

‘Where there is willpower, there is a way to go.’ This phrase was said about me by a good friend, as a way to express how I cope with my disease.

Years ago the neurologists said several times that I had got Parkinson’s disease and that this disease is chronic, impossible to cure and progressive. I thought that it might be like this for other patients, but that it would not be like this in my case. By working and studying a lot and sometimes by choosing blind paths, I have succeeded in finding a tiny little path out of my disease. Today I have fewer symptoms than in the year 1998, which means that the expression ‘progressive’ cannot be used generally about all patients with Parkinson’s disease.

I retired in the year 2001 when I was 44 years old and although it was really a hard time, today I feel that I have a good life. To my co-patients I will say:-  “Search for knowledge and keep on trying to search for new possibilities.”

Generally I recommend neurological patients to be tested with a chelating agent for chronic toxicity with heavy metals. If this is diagnosed, then it is possible to de-toxify, which can give hope to a future of increased health and decreased neurological symptoms.

If you want more information about toxicity with heavy metal and Parkinson’s disease then use the Internet.

Thank you for reading my case-story and I wish you all the best.

Hanne Koplev

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