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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.
Author Whit Deshner read excerpts from his forthcoming book on my radio show today. It is amazing writing that will inspire your soul, touch your heart, tickle your intellect, and rattle your funny bone:
Want a chance to enter the internationally famous Salt Lick contest and win money? Are you a rancher? Do you raise cows? Here is your chance!
To learn all about the one and only Salt Lick Contest to be held in Baker City, Oregon, watch the video on the follow Oregon Public Broadcasting Link:
For details on this years auction to be held September 24th at the Crosswoods Art center in Baker City, visit Whit Deschner’s website
Funds from the Salt Lick Contest support research on Parkinson’s.
Robert Rodgers, Ph.D.
Road to Recovery from Parkinsons Disease
Below is a research proposal to do a rigorous evaluation of Aquas, a homeopathic remedy that was designed to address dehydration. This effort is being energyzed by John Coleman, a naturopath doctor from Australia, who has advocated the use of Aquas for many years to address the symptoms of Parkinson’s.
If you are on the lookout for sound research projects to support, this research project is well worth considering.
Robert Rodgers, Ph.D.
The neuro recovery foundation inc. has developed a partnership with Deakin University Integrative Health Research Unit and the Lewis Institute for Health and Wellbeing (Dr. Daniel Lewis) to undertake this ground-breaking research in reversing the symptoms of Parkinson’s disease. We need your help in obtaining funding for the research.
John C. Coleman, 03 9850 9048, 0437 771 406, email@example.com.
BACKGROUND TO RESEARCH
Parkinson’s disease is considered to be progressive, degenerative and irreversible. Yet a few people have reversed all their symptoms and become well. To all observable measures, they can be considered “recovered” or “in remission” – that is, they are free from symptoms, need no medication or ongoing treatment, and live normal, healthy lives.
The first person to recover was John Coleman, who developed his own protocol of activities and therapies to reverse his symptoms of Parkinson’s disease (stage IV on the Hoehn and Yahr scale, or 127/199 on the UPDR scale), and early stage Multi System Atrophy. Others using this protocol have reversed their symptoms equally or to a lesser degree, and continue to live healthier lives.
Central to the therapeutic section of this protocol are the Aqua Hydration Formulas, homeopathic remedies designed to hydrate the body at cellular level (www.aquas.us). It is thought that the Aqua Hydration Formulas play a pivotal role in preparing the environment around nerve cells and cells producing dopamine, so allowing and enhancing repair and cell recovery.
The remedies have been shown, in clinical practice, to be safe to use in conjunction with all other medications – Western, Complementary, or traditional Chinese, and free from adverse effects.
This research is designed to show the degree to which the Aqua Hydration Formulas, when taken appropriately, will enhance the process of symptom reduction and health improvement by conducting a double-blind, placebo-controlled study. Participants will be under the care of a Neurologist for definitely diagnosed Parkinson’s disease, and treated conservatively. The only change, during the study period of approximately nine months, will be the introduction of the Aqua Hydration Formulas or placebo at safe levels established in open clinical trials since 1998.
When efficacy is established, the information will be provided freely to all Parkinson’s disease patients, associations, support groups and therapists to assist in improving the quality of life for those living with this dreadful disorder.
There are approximately 6.5 million people with Parkinson’s disease worldwide – around 100,000 in Australia. Any therapy that can improve quality of life for patients, also improves life for family, friends and carers. This research has the potential to help many millions.
The Aqua Hydration Formulas were developed in Australia by Neuro-endocrinologist Dr. Jaroslav Boublik and Natural Therapist Leonie Hibbert. They were designed to assist athletes overcome hydration issues during elite sporting events.
The Aqua Hydration Formulas were first used in treating Parkinson’s disease in 1997 by John Coleman, after he had investigated their properties and felt they could help him improve his health. He discovered that he required tiny doses, rather than the amounts used by athletes. His health notes show improved health status after establishing appropriate dosage, and continuing improvement resulting in freedom from all symptoms by mid 1998.
Two years of clinical observation resulted in a well-established protocol for using the Aqua Hydration Formulas in conjunction with other activities and therapies. Over 2000 people around the world have used this protocol with varying degrees of success in conjunction with synergistic activities and therapies.
This research is designed to show the efficacy of the Aqua Hydration Formulas alone in reducing the symptoms of Parkinson’s disease, when used by people who are being treated conservatively for Parkinson’s disease.
NEURO RECOVERY FOUNDATION
The Neuro Recovery Foundation was established in 2002 to support those diagnosed with neurodegenerative or autoimmune disorders who wished to seek information and/or interaction outside established organisations focusing on Western medicine.
A prime aim was to support and/or establish research in Complementary Medicine that would assist patients to improve their quality of life and mitigate symptoms. The neuro recovery foundation has approached established Parkinson’s disease organisations for assistance in proceeding with this research, but has been rejected because it falls outside the parameters of current pharmaceutical and surgical research.
Therefore, the Foundation has formed a partnership with Deakin University Integrative Health Research Unit and the Lewis Institute for Health and Wellbeing, and has agreed to raise the funds required to conduct this research as quickly as possible.
Professor Sally Walker, Vice-Chancellor, says:
“Deakin University continues to move confidently towards its goal to improve the University’s research performance so that it is in the top third of the Australian higher education sector.
We are doing this by building a critical mass of researchers who will develop a distinctive, broad-based portfolio of high quality discovery, applied and commercial research.
Another central component to Deakin’s innovative work in health and wellbeing is the Clinical Research Facility, the first stage of which was launched in January, 2008. The CRF has been established to provide a much needed state-of-the-art space within the School of Exercise and Nutrition Sciences to support approximately one-third of the School’s research conducted in a clinical setting. It is a multipurpose area capable of supporting both discrete discipline and multidisciplinary activity. The proposed stage two of the research facilities will establish rehabilitation and exercise programming space to provide clinical opportunities for postgraduate students and staff.” (from Deakin University website, October 2009)
DR. DANIEL LEWIS
Dr Daniel Lewis, MBBS(Hons), FRACP, is an experienced rheumatologist (bone, joint and arthritis specialist) who integrates mainstream medicine with natural approaches to health and wellbeing.
He has a private specialist medical practice in Melbourne and has appointments at Monash Medical Centre, Monash University and Deakin University.
He is currently the Director of a musculo-skeletal and Pain Management Program at a Rehabilitation Hospital. He is a Past President of Arthritis and Osteoporosis Victoria.
He is co-director of the Deakin University Integrative Health Research Unit formed in 2007.
In addition, Daniel gives lectures, workshops on a range of medical subjects and has led retreats in Australia and overseas on various aspects of whole person care. He teaches meditation during the Lewis Institute’s More Than Meditation Course which is held regularly throughout the year.
Daniel’s passion is integrating balanced lifestyle practises into mainstream management of bone, joint and arthritis related illnesses.
The Lewis Institute for Health and Wellbeing evolved out of Daniel’s desire to provide a supportive and empowering educational network for individuals with long term arthritis- and other health-related illnesses and for those wishing to prevent illness.
LEWIS INSTITUTE FOR HEALTH AND WELLBEING
Our Philosophy: There are many pathways to health and wellbeing. Understanding this and having a willingness to take the time to explore various paths contributes to wellbeing. Gaining knowledge, skills and life purpose provides access to personal wellbeing.
What Do We Do? In line with our purpose to enhance health and wellbeing, we provide
- whole person education programmes to the public
- education programmes for health care practitioners
- Integrative medical services
- a clinical research programme.
The people who lead our programmes are carefully selected for their expertise and education skills. They are from the disciplines of Medicine, Physiotherapy, Occupational Therapy, Psychology, Nutrition Science and Yoga.
- Our Medical Service is provided by Dr Daniel Lewis.
- Our Research Service is available to Companies, Universities and individuals who want to avail themselves of our expertise in the design and/ or conduct of scientifically-sound clinical trials.
- Our Disability Service is in association with Everycare. We provide access to information about and referral to this organisation. Everycare specialises in computer programmes to assist individuals with severe disability in voice communication.
$35,000 to allow Deakin University to conduct a double blind study to establish the efficacy of the Aqua Hydration Formulas, and publish their findings through appropriate media. The Neuro Recovery Foundation has raised $13,00 so far from subscriptions and donations, but we URGENTLY need the balance ($22,000) to make this exciting research possible.
HOW YOU CAN HELP
- Tell your family, friends and business associates about the urgent need for this research
- Broadcast our need to the public through the media
- Guide us to businesses or funds who can provide us with financial support (or get them to call us)
- Donate to our research fund. Every cent donated will be used for this research project. No administrative costs will be deducted.
Neuro recovery foundation is a registered charity and any donation over A$2 is tax deductible in Australia. Receipts will be provided on request.
Do you have any testimonials from individuals that have recovered from PD using your protocol? Why aren’t you on Larry King or Oprah?
Without validity, your claims are the same as other people. Where are the recovered people?
Thanks so much for your questions. I do not have a “protocol” that I advocate. I am a researcher gathering information from people who are recovering from Parkinson’s.
I do not make any claims to be sure about any approach or remedy or treatment, though many people I interview or who are on my radio program give testimonials about what they are doing to feel a lot better.
I believe the causes of Parkinsons are multifaceted, so different treatments will help depending on the persons individual situation. Let me know if there is a “claim” that I have made or written about. I will need to revisit that writing and clarify the presentation.
The first round of field research is reported in Pioneers of Recovery (www.pioneersofrecovery.com). Two of the people I interview in the book have recovered fully. Others are on the road to recovery. The Pioneers talk about what they are doing to get relief from their symptoms.
I am determined to do a study of 100 persons to track holistic approaches to healing the symptoms of Parkinsons. I totally agree with you that it is important to present evidence that treatments or approaches are effective. That is the road I am taking with my research.
I just released Five Steps to Recovery (www.fivestepstorecovery.com) which is all about thoughts and how they help or obstruct healing. Again,there is no protocol here, just support to people who want to sustain positive thinking about their recovery.
All the best,
Robert Rodgers, Ph.D.
Dr. Jay Alberts, Ph.D., from the Center for Neurological Restoration at the Cleveland Clinic will be my special guest on the Parkinsons Recovery Radio Program at 11:00 am pacific time on Thursday, April 23rd. Dr. Alberts and I will also be talking with Scott Luikart who is participating in the Race Across America this summer to raise money for research on Parkinsons.
Listen to the program over phone by calling 347-945-5358 at 11:00 am pacific time – Thursday, April 23rd or listen in here. I hope you can join us.
Robert Rodgers, Ph.D.
The Race Across America (RAAM), is a solo, 12 day, 3,021 mile bike race. It touches 15 states and climbs more than 100,000 feet. Once the clock starts on the west coast, it doesn’t stop until the racer reaches the finish line on the east coast. Scott Luikart, a 2009 RAAM participant, has chosen to use the RAAM as an avenue to raise much needed funds for cutting edge Parksinson’s disease (PD) research going on at the LRI.
What motivates someone to push their body to the extreme? Ask Scott that question and his answer comes without hesitation. His twin brother Mark was Scott’s inspiration to begin cycling four years ago. Mark was recently diagnosed with PD.
While watching MSNBC one night, Scott heard about the exciting work of Jay Alberts, Ph.D. of the Center for Neurological Restoration at the Cleveland Clinic. About 200 miles into a week long “Pedaling for Parkinson’s” awareness ride on a tandem bicycle, Dr. Alberts noticed the Parkinson’s symptoms disappearing from the patient who was riding with him.
From this experience, Dr. Alberts asked: Could exercise — be therapeutic for PD patients? Initial research is telling us “yes.” Donations raised through the RAAM will go to support this cutting edge work leading to more answers which we feel will have a direct impact on the lives of those living with PD.
[iframe http://www.InstantTeleseminar.com/?eventid=5714760 500 610]
Are you familiar with the approach to
treating Parkinson’s used by the
Australian natural therapist
Noel Batten, detailed on his website
and what is your opinion of that method?
Out of the many people I have talked
with or interviewed, I have not run
across one person who has had any
experience with this particular treatment
I am familiar with the web site and can
offer my reactions based on my impression
of his website.
It appears to me this man implicitly
offers a “cure” in five days. This is
quite ridiculous. No “cure” exists.
People certainly have recovered and are
symptom free today, but the minimum time
I have heard it takes to recover is two
years. The average time appears to be
The sales pitch on the web site involves
before and after videos of people who
received his treatment. What you observe
are marked improvements. This is the norm
for many forms of body therapies.
People often do show marked improvement
after receiving a variety of different
treatments. They often look like
I have interviewed a number of people who
report seeing a therapists of one type of
another (craniosacral, Bowen, energy healing,
drumming, healing touch, reiki, etc.),
who tell me that for a period of time after
the treatment (4 hours, one day, two days –
the time varies) they were totally symptom
free. After the the brief honeymoon however,
The videos on this web site do show the
physical manifestation of trauma to the
physical body. The body becomes contorted
and twisted. Various body therapies
are helpful in releasing the tension that
is held in the body tissues.
The theme of this web site is:
Come to me. I will fix you.
This is not how people recover. The people
who recover wind up figuring out ways to
No one can fix them or cure them. The tone
of the sales pitch on this web site feels
manipulative to me.
My research shows only a combination of
approaches will work. There is no single
answer. There is no holly grail.
There are however two benefits to a search
for the holly grail if you choose to go on
such a journey.
First, you exercise your mind. This
creates new neural pathways and is a good
thing. (Of course there are many other ways
to accomplish the same benefit).
Second, if you physically have to move or
travel to find the people who claim they
will fix you, you will receive the benefits
of physical exercise. This also is a good thing.
Does this man’s therapy help? I certainly can not
I am very impressed in general with the
research on alternative therapies. Study
after study shows that one therapy after
another helps relieve symptoms.
I have stacks of studies for one therapy or
another that report positive findings. Many
studies use small samples, so the results
will never show statistical significance
because of the small sample sizes.
The actual effect sizes reported in
many studies are impressive. In some studies
effects are not large but they nonetheless
reflect improvements. Effects in many of
these studies are also larger than
any effects reported in the drug studies.
My point is that there a many modalities that
provide ways to get symptom relief. The challenge
is to do a little experimentation for yourself
and figure out which ways are most useful
Robert Rodgers, Ph.D.
© 2008 Parkinsons Recovery
Dear Dr. Rodgers:
After reading a number of your helpful articles, I am writing to ask your opinion regarding a difficult case of Parkinson’s disease or similar disorder (as described below, the symptoms are somewhat atypical for classical PD).
The person in question, now 63 years old, was diagnosed in mid-2005. The symptoms include right arm/shoulder pain, which has worsened over time, along with a mild tremor in the right hand. This is accompanied by a feeling of internal tremor or other unpleasant sensations which are difficult to describe but are all the same extremely and increasingly difficult to experience, sometimes like a feeling that his entire body is disintegrating (but he is otherwise healthy).
On observation, he has a slow or shuffling gait and decreased facial expression at rest and mild tremor of the right hand, but otherwise few other noticeable signs to indicate PD.
This person has been on Dopicar (L-dopa/carbidopa combination) for over a year, which helped for the first 3-4 months. However, over a short time the beneficial effects of L-dopa have diminished greatly, so that now it sometimes doesn’t help at all, and when it does, only for a very short period of time (an hour or less).
The present dose of L-dopa varies between 300 and 600 mg 2-3 times daily, depending on the particular symptoms and feelings on a given day. When the effect of the L-dopa wears off, the right arm becomes stiff like a log and very painful (worse than before taking it). This means that most of the day he is feeling bad, with little relief from L-dopa.
He has also been taking Azilect with little noticeable benefit. This was stopped recently after hearing John Coleman’s teleconference, but pain and other symptoms have worsened since that time.
My questions are 1) have you ever seen anyone like this who responds very poorly to medications after such a short period of time, and whose primary symptoms are pain and a very unpleasant internal tremor or other sensation, and if so 2) what helped, or what treatment or other plan would you recommend?
At the top of my response to your fascinating question is a brief explanation of my qualifications. It is true that I am
a doctor, but I am not a medical doctor. I have a Ph.D. and am a researcher. I need to be clear that I am not a medical doctor and so I am not qualified to diagnose or treat any disease.
I regularly interview people with Parkinson’s (like John Coleman) and conduct teleseminars with experts in various modalities regularly, so I am in a position to provide insights based on the research I am doing. Please do not interpret anything I might say as medical advice but rather as simply information. It is always important to check with your doctor or health care provider for taking making any changes to a health care program.
Your questions in order:
Have you ever seen anyone like this who responds very poorly to medications after such a short period of time?
From my research, your report of getting relief from medication after 3-4 months is typical, but at the low end of the range. I do not have enough data now to give you a good estimate, but qualitatively speaking, the average time appears to me to be around 7-8 months. Some people get no relief. Some get good relief for 2 years or more. I hear many reports of good relief for 6 months.
Regardless of the length of the honeymoon, I have not interviewed anyone yet who has been on medication and not had to increase the dose after a period of time. The brief honeymoon suggests to me that the primary cause of symptoms may be rooted in factors that are not directly connected to the level of dopamine in the body.
Have you ever seen anyone like this who whose primary symptoms are pain and a very unpleasant internal tremor or other sensation?
If I have learned anything from my research, it is that each person’s symptoms are entirely unique to them. I interviewed a man recently whose primary symptom was pain. I am currently writing about how to address this particular symptom. So, stay tuned.
Internal tremors are very common among the many people I have interviewed. It is a clue that the neurological system is not functioning at full capacity.
You also mention that his symptoms have been worse after going off the medication. This too is very typical from the people I interview. Some people who try and stop cold turkey without gradually reducing the dosage wind up eventually deciding to start taking the medication again at an even higher dose.
You can probably expect a period of time for the body to adjust. From my research, what has happened to him is very typical and very difficult to deal with.
You also ask what treatment plan would I recommend. I will soon have a very concrete answer for you to see. I have created a web site interface that contains information, exercises and experiences that my research shows is needed for a person with the symptoms of Parkinson’s to feel better.
The honest answer to your question is that a person can begin feeling better slowly and gradually when they make certain changes in how they eat and live. Finding ways to reduce stress and release trauma have also helped many people.
Finding ways to help the body release toxins has certainly helped many people with Parkinson’s. I am beginning a series of interviews with naturopaths and other doctors who offer different approaches for helping people detox their body. I would recommend that you might consider these many different options and see if one calls to you and him.
Another place to look is his digestive system. My guess would be that his digestive system may be compromised. Ayurveda has offered some people with Parkinson’s wonderful relief. Please note that I say some.
I suggest he experiment. Check out what is working for other people. Try out something that calls to him (a herb, a form of body work, a detox method, etc.). If it begins help, stick with it. If not, turn to something else. The people who are having the greatest success with recovery do just this. They are always experimenting.
I might mention that this is precisely what John Coleman did. He experimented with a number of therapies. Some helped and some did not.
Give whatever is tried time to take effect. Most people are not aware they are getting better, so they abandon therapies too early because they falsely convince themselves the therapy is not helping.
We do know now that it takes time for the body to heal from the symptoms of Parkinson’s. The range I now have is a minimum of two years to a maximum of 6 years. Recovery is a slow process.
The one thing that will help him the most is to acknowledge no single medicine or pill exists that can fix the problem. The causes of the symptoms are far too complicated and delicate for this to be true. It takes a dedicated commitment to give the body all that it needs to heal itself.
Robert Rodgers, Ph.D.
© 2008 Parkinsons Recovery
What success have you had with Parkinson’s disease?
We believe the causes of Parkinson’s are multi-faceted and
that the underlying cause for one person may differ from
another. Specifically, the underlying and primary cause for
one person may be heavy metals, another pathogens, and
still another trauma. Some people are unlucky enough to
have issues with all three.
Our research thus far has evaluated only the effects of
energy healing that included craniosacral therapy on the
symptoms of persons with Parkinson’s who chose not to
take medications. Findings of our study showed that 75%
of the symptoms for the 10 persons in the study either
stayed the same or improved.
We concluded that energy work clearly helps, but
that the body also needs additional support like good
nutrition and detoxing to come back into balance.
The study led us to adopt a more holistic approach.
Some of our initial study volunteers are doing quite
well indeed. I hope to have interviews with them soon.
We are gathering stories from people across the country
and elsewhere who are feeling better and finding
relief from their symptoms so others can get a sense
of what other people are doing for themselves to feel better.
It gives hope to many people when they realize that others
with Parkinsons are finding relief from their symptoms.
Some people have fully recovered.
Clearly, there is no cure nor is there any magic formula
that people can use to heal. But it is also clear that many
people have found ways to feel better and get relief from
their symptoms. We are documenting these stories.
I also believe that everything we try must be carefully
documented, so in our initial study I used many research
instruments to track what was happening. Our subsequent
studies will be just as rigorous. We are planning to use
outside evaluators for the First 100 Study.
Robert Rodgers, Ph.D.
© 2008 Parkinsons Recovery