Natural Options that Reverse Symptoms

Author: manabunnow4zph (Page 33 of 37)

Story of Recovery from Parkinson’s Disease by Detoxing Lead, Arsenic and Mercury

Joan has given me permission to post her most remarkable story of recovery from Parkinson’s disease by detoxing lead, arsenic and mercury.

Parkinsons Recovery was founded in 2004 to provide information, support and resources to persons diagnosed with Parkinson’s disease and their family interested in exploring natural therapies that offer symptom relief.

Robert Rodgers, Ph.D.
Parkinsons Recovery

Hello Robert,

It has been a while since we communicated but with reasons. Shortly after you were here in Lexington, I went somewhere into a tremendous panic situation finally diagnosed as Panic Disorder. As usual, I wanted NO DRUGS and it took a bit to locate natural products to manage and stop this thing! It was not a kind place to be and it took a grave toll on me. So………I got SERIOUS! I wanted NO MORE OF THIS AND NO MORE PARKINSON’S DISEASE!

I searched for and found a Medical Doctor who practiced natural therapies……yes cures and recoveries! Thank God he is only a short 30-minute drive from me in a lovely small town called Midway, Kentucky. His clinic is Midway Center for Integrative Medicine, 129 Winter Street, www.themidwaycenter.com . He has helped me, Robert!

I went to him with HOPE and came away with real facts for recovery. He diagnosed me with LEAD, ARSENIC, AND MERCURY poisoning in my whole nervous system from simple blood tests and I am NOW ON MY WAY TO RECOVERY!! When I said to him,

You mean I do not have Parkinsons?

His reply was direct and loaded with impact! His reply,

Don’t put a label on it!

He placed me on a full detox program with nutritional supplements to increase my health that had been so damaged by doctors who only treated my SYMPTOMS and never the CAUSE!! I have seen seven neurologists in seven years of dealing with this horrid disease who all ended up with the same position. MRI, Cat Scan, and diagnosis of Parkinson’s Disease. When I finally asked the last one at the University of Kentucky Neurological Institute to do a toxicology test, she refused saying it would do no good because I have the disease. THIS IS SAD!! So many people……..such a dastardly disease……….and with doctors who won’t even TRY to step outside their boxes of comfort and paychecks!!

On March 23 I went to Dr. Roach the first time. He did blood work and diagnosed the CAUSE of my nervous system that was a mess from being attacked by poisons. He started me on certain few supplements ahead of getting the results back from the Lab and I began to FEEL BETTER inside a week! Just FEELING BETTER increased my HOPE and my TRUST in a Doctor was finally beginning to grow. See the comparisons listed here in less than two months recovery!!!

Joan’s Story of Recovery from Parkinson’s Disease – Comparison of Pre versus Post Symptoms

March 23 SYMPTOMS

  • Wheelchair bound and I was seriously considering a nursing home
  • Basic frozen body, total weakness, inability to move at all most times
  • Severe toes spasms and cramps
  • Tremors so massive my body, at times, would violently shake to almost injury
  • Slurred speech and drooling
  • Unable to stand or walk beyond 10 feet
  • Been to emergency room for panic attacks and inability to move while standing three times since September 2009
  • Disinterest, not able to even go to Christmas with my family
  • All the other stuff that goes along with this disease

APRIL 30 SYMPTOMS

  • No wheelchair since April 20! Though for very long days I take it in case of need
  • Freezing gone……….some minor feelings come and go throughout the day and getting better 
  • Toes improved 60%
  • Mild weakness
  • Tremors down to ZERO!
  • No slurred speech
  • No drooling

I walk everywhere……….even though it is often painful and at times I have to sit a bit longer than I want to give my body time of recovery from the minor freezes. On my first visit, Dr Roach told me (on my 3rd visit) that he thought my IQ was really low………but on this 3rd visit April 20, he said my  brain is just fine!

I told him about you, Robert. He would very much like to communicate with you! I hope you can as THIS IS THE KIND OF DOCTOR NEEDED IN THIS PROFESSION WHERE NO SCIENCE-BACKED M.D. HAS A DESIRE TO TREAT THE CAUSE AND NOT JUST SYMPTOMS OF ALL DISEASES!

Robert, he says 6 months to two years should see me recovered! I WILL TAKE THIS DIAGNOSIS ANY DAY!!

Joan

Many thanks to Joan for sharing her remarkable story of recovery.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

Myofascial Release and Parkinson’s Disease

I was so happy to listen to your radio segment with David Howell on Myofascial Release. I’ve been using it on myself for over 4 years. I am diagnosed with PD symptoms for 5 yrs but probably have had symptoms for 8.

I developed trigger finger in my thumb, and was interested in a therapy I could do myself other than the usual icepack, cortisone, etc therapy the doctor prescribed. I wanted to know and understand the root cause. I ended up on the internet of course and typed in “trigger finger” and saw a book called “The Trigger Point Therapy Workbook Second Edition, Your Self-treatment Guide For Pain Relief. by Clair Davies, NCTMB“.

“Trigger Point Therapy” is another name for Myofascial Release. The book is very user friendly and well written.  I’ve also self-treated myself for stiff neck and shoulder pain, so common with PD, and just recently a groin pull. I am not a massage therapist. I can understand better after reading this book how PD, emotional and physical stress could breed trigger points very easily.  PDr is constantly out of whack (tense muscles)  and one unbalanced area puts severe strain on another part of your body you might think is in no way connected.  They call this “referred” pain.

For instance, you may have excruciating wrist pain (Referred Pain), but the cause (Trigger Point) is further up your arm and even the muscles in the base of the neck. I don’t like to wait for the PD stiffness to evolve to jammed up trigger point aches and pains. I combat muscle stiffness so I don’t have to use trigger point therapy with daily at home simple yoga, tai chi, and 3lb dumb bells. Also I do walking and breathing meditation. Knock on wood, I am without any pain on a daily basis. So thank you from the bottom of my heart for featuring this not well heard of therapy in the PD community.

Monica

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

Heavy Metal Chelation for Parkinson’s

Just wanted to let you know that I have been testing for heavy metal for over 7 years now and nothing ever showed up on lab tests. I kept having a nagging feeling that a big part of my symptoms were caused from heavy metal poisoning, but I couldn’t get anyone to prove it. I have always believed there is a benefit of  getting heavy metal chelation for Parkinson’s.

I kept searching and found a naturopathic doctor who consented to another urine test, but this time he used the chelating agent MDSA to pull the metals out of my tissues.

The results confirmed my feeling of years. Extremely high levels of Mercury, Lead and Uranium. He said in all of his practice, he has never seen such high levels and promptly started me on a heavy metal chelation. I’m now on a two week regimen to support my organs from permanent damage prior to the chelation.

He said that while he can’t promise a definite correlation of symptoms and heavy metals, he does feel there is a huge relationship. He also so that he can’t promise complete relief of symptoms after chelation and removing these heavy metals from my body, but he said he feels confident that my symptoms will improve, and my symptoms shouldn’t worsen and my body should be allowed to heal, once the mercury is gone. He said that with my levels of metals, it may take up to a year to completely chelate.

I will keep you posted. I just thought you might be interested in knowing my most recent finding, and possibly an option for some of your other followers.

Again, thanks for all you do and continue to do. You are amazing! Such a gift to humanity, not only those with a PD diagnosis.

Take care,

Melanie

Thanks for the update Melanie on heavy metal chelation for Parkinson’s. I have my fingers crossed your symptoms will gradually improve.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

Road to Recovery from Parkinsons Disease

Hi  Robert: First let me say that I just finished reading your book on Parkinson’s: On The Road To Recovery from Parkinsons Disease AND IT WAS WONDERFUL!!!

We have corresponded before. I live in Victoria BC. My name is Linda Ralph. I have had symptoms of PD for 12+ years now. I wanted to send you my review of Road to Recovery from Parkinsons Disease. 

I loved the way you presented it in a clear, concise, easy – to- read fashion, so that even I could understand it from cover to cover.(Ha.) At last a hands- on reference book for Parkis that is useful. Yeah!

Because of the chosen format, the wealth and variety of information, the adaptable index and contents, readers like myself, can access pertinent information readily, or, if not, be shown alternative ways to gain such information. Good stuff.

I really enjoyed the inclusion of the anecdotes of others who had/have this condition. Reading their stories, as well as listening to the guests that are featured on your radio show, have provided me with some new ideas and strategies that I would like to try. And hearing the success stories of those who are completely free of the symptoms of Parkinson’s – well – that’s my kind of reading. Yes!

The Q. and A. section was personal and informative and reminded me, and probably other readers as well, of some of the same questions that we too have pondered at some time or another along our way. Such questions are real.

Most importantly I think that your book provides Parkis and their family members with some HOPE in a society where doctors are still professing, even today, much gloom and doom to the newly diagnosed. And, HOPE where there is depression, anger, resentment, pain and lack of understanding about this condition.

I have already lent my book to a newly diagnosed friend of mine. I just wish that I had been given a copy way back in 1998 when I was first diagnosed. Perhaps my bout of depression, brought on by: fear, hopelessness, misinformation, and by the way my doctors treated me at that time could have been avoided. (Who knows?)

What you ARE NOT  providing for those of us with this condition is a cure. And some may say,”Darn.”(or maybe something a wee bit stronger.) But what I am saying that you ARE providing, is something to hold onto. Something tangible that Parkis can use to fight their symptoms right now and in the future, a reference book that those of us with the symptoms of Parkinson’s and our families can pick up, look inside and maybe  find an idea or two that may just work. And dare I say maybe glean just enough information, and try just hard enough, to recover completely from this condition.

Thank you so much for this book. And thanks to your staff, who worked alongside you to help you reach your goal. And thanks to you for all the work that you have done and continue to do  for those of us with this condition.

You are appreciated!

Linda Ralph

Linda gave me permission to post her review of my book here on the blog. You can find more details about Road to Recovery from Parkinsons Disease by visiting: https://www.parkinsonsdisease.me

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

 

Can-C Eye Drops

Are you having issues with your eyes? Perhaps dry eyes. Perhaps double vision. Perhaps jittery eyes. This post is about antioxidant Can-C eye drops.

My uncle Gordon Ward developed advanced cataracts 15 years ago. A former college president and Wyoming State Legislator, Gordon loved to play tennis, read books and write about history. Cataracts made it so difficult to read that Gordon reluctantly decided to have cataract surgery, one eye at a time. There was no other good options at the time.

Cataract surgery on his first eye healed beautifully. Surgery on the second eye was a miserable flop. Gordon developed double vision and was essentially blinded. He could not read. He could no longer play tennis. It was all a horrible shock.

My Aunt Betty said that the stress of cataract surgery caused Gordon to begin experiencing the symptoms of Parkinson’s. He was diagnosed shortly after his failed surgery. Had Gordon been able to see, I believe he would still would have been able to continue playing tennis and enjoying life to the fullest.

As part of my work to identify natural remedies, I am excited to report that I have located the source of a natural anti-oxidant eye drop that addresses eye problems caused by inflammation.

The discovery of this remedy originated with the work of a Russian medical researcher Dr. Mark Babizhayev, Ph.D. who made the simple but profound observation that people who had no cataract problems had sufficient levels of N-Acetyl-Carnosine in their eyes. This substance happens to be a natural antioxidant. People with cataracts had insufficient levels of N-Acetyl-Carnosine in their eyes.

Dr. Babizhayev took his research to the second level by developing eye drops that contained N-Acetyl-Carnosine. He then began doing research to see if the new antioxidant eye therapy worked.

Studies confirmed his hypothesis. Add N-Acetyl-Carnosine to the eyes and the eyes heal themselves. Cataracts are reversed. Most eye problems are caused by inflammation. The eye drops thus help reverse many eye problems. Isn’t that totally cool?

In addition, the eyes are physically located next to the part of the brain that is responsible for manufacturing dopamine. I am wondering if healing eye problems might have an indirect, but positive impact on Parkinson’s symptoms in general. The jury is still out on that one, but you never know. You can find more information about Can-C eye drops by visiting : https://www.can-c.me

Robert Rodgers, Ph.D.
Parkinsons Recovery

Tai Chi for Parkinsons

The inspirational e-mail posted below about tai chi for Parkinsons was sent by Danny Loney

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

Hi Robert. This past week concluded the conference of the Israel Parkinsons Association held at the Dead Sea. I spent most of the last night of the conference laying in my bed with tears in my eyes as I thought about the experiences that I had encountered over the previous four days. For me personally, it was emotionally overwhelming as I did not expect to experience such an outpouring of warmth, acceptance, and love. Most of the participants I had known from past conferences and other Parkinsons events, but this time I was able to connect to others and get to know them in a very personal way. I felt like a lost puppy that had found a warm and accepting home.

I was amazed at the many compliments that I received from my tai chi workshops and felt a bit uncomfortable with all of the attention. There is a tremendous amount of creative talent in our Parkinsons Association, whether it be paintings, woodwork, organizational skills, poems, music, counseling, or just a word of encouragement and a warm smile. And I am only one of many who want to make a contribution; a guy uses tai chi for Parkinsons to help a few other people with Parkinsons  improve the quality of their lives.

Danny

Loss of Smell

A pre-diagnosed Parkinson symptom was the loss of smell. It rarely appears on medical information forms, and if brought up during  examination noted but never gone further in discussion.

I wonder about this. If it was a matter of loss of touch, hearing or sight, would this be treated differently? Why is it downplayed? Are there any known recovery methods, studies or treatments concerning this condition?

Thanks, any information will be appreciated.

Daniel

Researchers have known for at least 30 years that persons with the symptoms of Parkinson’s have a loss of smell. Several studies have confirmed the link. The impairment in ability to smell involves more than being able to take in the full essence of a scent. Individuals with the symptoms of Parkinson’s have greater difficulty distinguishing one order from another or are unable to detect any odor whatsoever.

There is currently considerable research interest in the link between Parkinson’s symptoms and the loss of smell now that it has become clear that the two are inextricably linked. Loss of specific smells in particular have also been linked to Parkinson’s symptoms, which is interesting in itself.

Some researchers are currently working on designing a diagnostic smell test for Parkinson’s. There is no definitive test at present that gives a clear indication of Parkinson’s. A smell test will also not be definitive, but it can be used in conjunction with other evidence. I suspect such tests will soon be routinely offered to patients.

The Pennsylvania Smell Identification Test is often used by many neurological clinics to evaluate neurological imbalances. This test evaluates a person’s ability to detect 40 scents. People who take the test can are able to identify on average 35 of the 40 odors correctly. Parkinsons patients can identify 20 of the 40 odors or less.

Researchers predict that people with seriously impaired olfactory functions have five times the risk of developing Parkinson’s than those with the highest olfactory function.

In light of your interest in this question, I will set my intention to interview some of the researchers who are currently conducting studies to evaluate the connection between the ability to smell and the symptoms of Parkinson’s. To be sure, it is an interesting line of inquiry which may lead to understanding the underlying factors that are at play.

Robert Rodgers, Ph.D.
Parkinsons Recovery

 

 

Dental Detox and Parkinsons

What follows is a rich explanation of dental detox and Parkinsons as a critical factor in the overall health and well being of persons with neurological challenges which was submitted by Brad:

Robert Rodgers Phd
Founder 2004
Parkinsons Recovery

Much has been written about the presence of toxic metals in dental work, but there is another source of toxins in our mouths that should not be overlooked. Naturally occurring bacteria are present between the teeth and gums that can cause bleeding gums and in severe cases, loss of teeth. The bacteria produce potent foul-smelling toxins.  As the toxicity becomes chronic, the gums become inflamed and recede over time.  This is known as “gingivitis” or “periodontal disease”.  If your gums bleed, even a tiny bit, you have it. As the condition worsens, “pockets” form deep around the tooth, further harboring the toxin-producing bacteria and absorbing the toxins directly into the bloodstream.

I have not seen research linking these toxins to Parkinson’s, however, the mouth is very close to the brain and any toxic stress is bad for PD. There IS research linking periodontal disease to heart disease and other maladies.

Gingivitis can be mild and persist for years without pain or obvious symptoms. Regular dentists do not usually treat this condition, referring patients to periodontists who specialize in gum conditions. If the condition is advanced and the pockets are deep, the periodontist may recommend gum surgery, which is obviously costly and more traumatic than prevention.

Prevention or recovery from mild cases is simple and inexpensive. Merely following routine oral health practices (brushing, flossing, rinsing, use of anti-bacterial mouthwashes, etc.) religiously will destroy the bacteria and toxins before they can reach your bloodstream are sound steps for a dental detox and Parkinsons This must be done at least once or twice daily, though. Regular dentists or periodontists can give advice and judge the effectiveness in this regard.

Brad

There is Nothing Wrong With You

Below is a follow-up correspondence from Brad.

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

I got “PD’ed” at church today. I was a visitor and had no sooner entered than I was greeted by a young man with very obvious Down Syndrome. He instantly spotted my shaking hand and said with a big smile,

“Don’t worry, you don’t have to be nervous, it’s only Ash Wednesday. Or perhaps you’re very excited because you have such a beautiful wife!”

From his perspective there was absolutely nothing “wrong” with me; to the contrary everything was “right” with me. My partner and I agreed that there was a profound lesson to be learned from this man’s innocent and perceptive observation.

Brad

Alternative Therapies for Parkinson’s Disease

What follows is a fascinating e mail I received from Brad about alternative therapies for Parkinson’s disease . He has kindly given me permission to post it here.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery
www.parkinsonsrecovery.com

I am still “in the closet”, so to speak, that is to say I have not publicly discussed my diagnosis. I am very new to this discovery as I received my diagnosis one year ago (at age 52). Sometimes I get “PD’ed” by strangers who notice my symptoms and ask (or tell) point blank that I “have Parkinson’s”, which I cannot evade. The only purpose for taking the currently available meds is to hide the condition from others during, say, public speaking or other event which might lead to  or embarrassment. The meds serve no other purpose, they do not treat any underlying condition whatsoever. I suspect this denial, or hiding from PD symptoms, is very psychologically damaging (Michael J. Fox treats this in depth in his books). It leads to over medicating and adds stress, thereby worsening the condition.

In my case, I was lead to believe that the use of L-Dopa would provide dramatic relief and thereby confirm the diagnosis (remember that PD is a “negative” diagnosis, that is, it is indicated by ruling out all other possible explanations, however, in reality this is impossible to do. So PD is labeled “idiopathic”, or of unknown causation). Instead of relief, absolutely nothing happened, except that I immediately worsened and developed new symptoms in addition to a multitude of side effects. My brain has resisted L-Dopa therapy over these twelve months. L-Dopa is only sporadically effective and is very hard to predict. It takes very high doses to alleviate all symptoms (briefly) and during periods of high stress (particularly social stress) it does not work at all. So I have made a conscious decision to minimize my use of L-Dopa and seek alternatives right from the start. Sometimes I go for days without medicating at all and my symptoms usually stay about the same or sometimes better.

Things I am doing that seem to help:

Continue to ride and race bicycles  I have had to give up certain types of racing that require extremely fine motor skills, but I ride with accomplished groups regularly, at least 5,000 miles per year. Balancing a bicycle utilizes different neural circuits from your center of gravity than balancing on your feet, so I actually cycle better than I stand or walk. Some medication is required to control dystonia and keep my “slow” leg in sync with my “fast” leg, but I have experienced symptom-free rides occasionally.

Continue serious weight training. Since lifting weights does not involve high speed movements, it is largely unaffected by the symptoms. I have always been very strong and have become even stronger with pd symptoms than I was previously.

All other forms of physical activity, such as stretching, hand and finger exercises, table tennis, hiking, walking, basketball, anything that involves motion.

Healthy food, water, and sleep/rest. Avoid all trauma and toxins insofar as possible. Drama-free social life, mental engagement and exercise, healthy spiritual practices. These seem to be so “common sense” that they may be overlooked, but the proof is in disrupting any one of these and the symptoms immediately worsen. Improve them, and they immediately get better. Simple.

Alternative therapies for Parkinson’s disease that I am trying or considering include mercury detox. This is very dangerous, because disturbing mercury in dental work and/or chelating mercury that has been bound to brain tissues for a long time can worsen matters by “stirring up” heavy metals that may then be reabsorbed or recirculated prior to elimination. A personal decision has to be made balancing the risk/possible benefits of this approach. It is too early to tell what impact this decision will have on me because I have only had mercury-free teeth for less than thirty days after more than thirty years. I do believe eventually mercury will be banned in dental work. There are better alternatives available. My dentist conceded only after agreeing that having already developed pd symptoms, the levels of mercury that may be safe for a normal healthy adult might not be appropriate for me.

Hypnotherapy is showing great promise. If nothing else, achieving relaxed states reduces stress. However, even western medicine recognizes “psychogenic Parkinson’s”, from which full recovery is possible. It distinguishes this from “real” or “organic” Parkinson’s which by definition precludes recovery. So if you recover, it must have been psychogenic and vice-versa, if you don’t recover it’s not psychogenic. This is circular reasoning. Self-observation proves that all PD is at least partially psychogenic. Besides, it is a Western assumption, wholly based on faith, that there is any real difference between the mind/spirit and body at all. There is plenty of evidence, including in Western science, that there is no difference. One cannot exist or be healthy without the other. During hypnotic states (basically that relaxed dreamy state just before falling asleep), observable symptoms abate. What more proof that these symptoms are controlled by mental states (or brain waves, if you will) is needed?

Long held attitudes and “belief systems” are hard to change but they clearly play a role in recovery. At home, we avoid using the term “disease” or even “Parkinson’s”, instead referring to “Mr. P” or “my condition” or “symptoms” because one thing is for sure, if for one minute, you believe that you will not recover, your prophecy will be self-fulfilled. On the other hand, if you believe improvement or recovery is possible (not guaranteed), then that will be true also. Cancer victims refer to “fighting” cancer, PD’ers often talk about “accepting” PD. While “accepting” oneself as one is or accepting the public acknowledgement of your symptoms may be helpful, the will to live (not mere survival, but living well) is the driving force behind recovery from any illness.

On the drawing board when it comes to alternative therapies for Parkinson’s disease is acupuncture. The brain is an electrical system. Western science proves this through DBS. DBS, however, is a crude and intrusive means of maintaining that system. Again, the website mentioned above details how electrical disruptions in other parts of the body (particularly the foot or ankle) may affect the brain. I had such a traumatic injury in which the tibia was fractured and did not “knit” after 99 days in a cast. Subsequently, a “TENS” unit was utilized passing an electrical current, night and day, for several months through the fracture. While this did cause an 80% “healing” of the bone to occur, there may have been electrical side effects unbeknownst to me from this therapy.

I realize that this is rather lengthy, but PD is a vastly complex and mysterious condition. This means there are a variety of alternative therapies for Parkinsons disease which can offer symptom relief. The mere lack of dopamine is neither its cause nor solution. I agree with you that the current scientific research will never result in a “cure” because there are a multiplicity of causes and therefore a multiplicity of “cures”.

I appreciate this opportunity to share my thoughts about alternative therapies for Parkinson’s disease. It has helped me be a little more organized in my own research and thinking. I do not yet know in what way my experience may be used to help others, but I will consider your idea. Thank you for your time and the work that you are doing.

Brad

Liver Detoxes

Toxin buildup in the body is one of the probable causes of PD. As we know, the liver is our body’s major waste converter. What do we do to keep the liver in top shape? What are good liver detoxes? Also, what is the best supplement to give the liver especially when one has PD?

Thank you,

Arsenio

The question you raise about good liver detoxes is critically important for persons with Parkinsons. Research has definitely shown that heavy metals and pesticides have a direct impact on the symptoms of Parkinsons. As you point out, the liver plays a huge role in this drama. The bowels and kidneys are also lead actors. I like to think of detoxing from the perspective of all the body’s elimination organs.

Perhaps the most important factor to a successful detox is better hydration. Many people are unaware they are dehydrated. If cells are not adequately hydrated, waste does not have a prayer of being eliminated regardless of the detox method you use. John Coleman, ND recommends people used Aquas (www.aquas.us), a homeopathic remedy designed to help the body take in water and distribute it to the cells. Clearly, the intake of sufficient quantities of water is important.

I believe many people underestimate the value of colon cleanses. Regular colon cleanses can take the burden off the shoulders of the liver and kidneys.

Eating unprocessed foods also takes a huge burden off the liver. Fresh vegetables and pure water can do wonders for the liver. Some people with Parkinsons use a brief fast to cleanse the liver, though these decisions should of course be pursued under the close consultation of your doctor.

In part, the best detox method depends on the type of toxins that are present in the body. Testing can be done by a naturopath doctor or medical doctor to pinpoint the specific toxins that are present in the body. Naturopath Ivy Faber uses bioenergetic testing which scans the body for toxins and other problems :

Doctors also have tests to identify the presence of specific toxins that may be causing the symptoms. There are specific detox methods for specific toxins, so it really depends on the specifics. This is such a specialized area that some medical practices specialize in helping people detox their bodies.

By way of example, one detox method that can successfully remove heavy metals according to my interviews with doctors and other health professionals is zeolite, a substance that is derived from the ashes of volcanoes.

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

 

 

Is Sinemet necessary for Recovery from Parkinson’s

Is Sinemet necessary for Recovery from Parkinson’s? John Coleman, ND mentioned in his book Stop Parkin’ and Start Livin’ that Aqua Hydration Formulas (www.aquas.us) comprise 60% of the therapy, while Bowen therapy 25%.

What makes up the remaining 15%? Does Sinemet (or herbal like Mucuna) fit into it? If so, does it go to say that we cannot recover from Parkinson’s without including Sinemet in the regime?

Thank you,

Arsenio

Dr. John Coleman ND has offered the fascinating estimates you note above based on his personal experience with recovery and with treating others with Parkinsons in his capacity as a naturopath doctor. Simply summarized, his experience is that when the body is properly hydrated and trauma is released using Bowen therapy, the body is in a position to heal itself. Better hydration is of course also plays a critical role in detoxing heavy metals and pesticides from the tissues of the body which have a clear and direct impact on symptoms.

In my conversations with many people who are on the road to recovery, some have an immediate, positive response from beginning to take the Aquas homeopathic remedy designed to hydrate the body. Other people must continue taking Aquas for several months before relief is detected. Others see improvement, but not in the range of the 60% that John reports. And of course a few do not observe any detectable result.

The bottom line for all therapies is this: They work beautifully and profoundly for some people, but not others. I believe the underlying factors that cause the symptoms and multifaceted and vary considerably from person to person.

Permit me to extend my explanation further by reference to Sinemet (which must be prescribed by a neurologist) or mucuna or fava beans which are natural sources of dopamine and do not require a doctor’s prescription. Some people report that the quality of their lives improves markedly after taking either Sinemet or fava beans or mucuna. Other people report trying them but see no positive impact. Some people who take Sinemet feel worse from the side effects.

In the end, it depends on the underlying reasons for the person’s symptoms and on the body’s response to whatever treatment is being tendered.

In specific response to your question,

Is Sinemet Necessary for Recovery from Parkinson’s

The answer for some people is no and for other people it is yes. Believe me when I say I do not mean to waffle here. It is the simple truth. I interviewed people in Pioneers of Recovery who took no Sinemet but are symptom free today. Other people take dopamine supplements of one form or another and do better on them than off.

The good news of the day is that anything is possible. As I document on this blog and in my books such as Road to Recovery from Parkinson’s Disease, there are many therapies that help people get sustained relief from their symptoms. Sinemet and the other dopamine enhancing supplements provide a source of relief, but they are only one among many other options.

In conclusion, the factors that contribute to the symptoms are extremely complex. If you hold the belief that a rigid formula will help you recover, I suspect the chances are pretty good that you will be disappointed with the outcome. There are certainly some people who might lead high quality lives from taking [Aquas + Bowen therapy + Sinemet], but that happens to be the solution set that works well for them. It may do little for you.

Dr. Coleman, ND never actually took Sinemet himself, but is symptom free today. Depending on personal circumstances, he does prescribe Sinemet to some of his patients.

I believe Parkinson’s is the most complex and multidimensional illness that exists in our world today. The answer to your question Is Sinemet necessary for Recovery from Parkinson’s is: it depends. Commit to a personal path of recovery and you will begin to feel better with each passing day. Chances are good that your solution set will be unique to your needs and the requirements of your body.

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

Five Steps to Recovery

Negative Thoughts Equal Instant Failure

Below is an e mail I received from Rose with encouraging news of recovery from the symptoms of Parkinson’s from a “healing.”

YOU ARE SO RIGHT ON! NEGATIVE THOUGHTS EQUAL INSTANT FAILURE! BAH! HUMBUG!

THERE IS THIS OTHER BOOK, CALLED “THE SECRET”..POSITIVE PEOPLE ATTRACT POSITIVE PEOPLE = SUCCESS…WORTH READING.

I WENT TO MY HEALER FOR THE FIRST TIME HERE IN NASHVILLE. SHE WAS WONDERFUL. WE FOCUSED ON SOME BAGGAGE I’VE BEN CARRYING….NOT THE PARKINSON’S DISEASE…AND WE IDENTIFIED SOME OF THE BIGGER PIECES AND I ‘GAVE’ THEM TO OTHERS AS IT WAS THERE iS TO HANDLE.

MY TALKING SPEED WAS VERY MUCH IMPROVED THE NEXT COUPLE OF DAYS! I STILL HAVE A WAYS TO GO, BUT I AM EXCITED ABOUT THE RESULTS WITH JUST ONE SESSION AND WILL SEE HER AGAIN IN MARCH.

ROSE

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery
Five Steps to Recovery

 

Table Tennis and Parkinsons

Looking for a new exercise venue that is fun and has the potential to offer sustained relief from the symptoms of Parkinson’s? Brad has a novel suggestion that works for him: table tennis.

I wanted to mention a new idea for Parkinson’s Disease exercise: table tennis. I am talking serious, competitive table tennis. I have not played for 25 years, but I just spent 3 hours playing with NO symptoms (I have not medicated for a few days). I’m pretty rusty, but I was able to execute high-speed movements, with eye-hand coordination, and no tremor for the duration.  Also, this level of play works up a pretty good sweat and cardio rate.

Brad

Robert Rodgers, Ph.D.
Parkinsons Recovery

 

Parkinsons Relief Through Better Hydration

A letter about Parkinsons relief thorough better hydration from Mary follows. Mary  gaveAquas relief through better hydration me permission to post here on the Parkinsons Recovery blog.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

I am enjoying reading your new book [Road to Recovery from Parkinsons Disease: https://www.parkinsonsdisease.me] and look forward to trying some new things for myself that are mentioned in there.

I know that the dehydration thing is right on for me. I started drinking lots more water this past summer at my friend’s insistent urging. And it has really been so helpful. I already have the Aquas [http://www.aquas.us] and will start doing those again in the morning and evening and see what happens. Parkinsons relief through better hydration is possible. 

I had remembered that in 6-08 and 12-08 after two surgeries I had felt much better. I had thought that it could have a couple of things that made me feel better. One was the O2 that I received during the surgeries. I have sleep apnea and having 02 might have made a difference. I also thought that it could have been the IV’s hydrating me.

Well I went into the hospital in Oct. 09 and stayed there for three days, recovering from a kidney infection . I slept and rested for three days (admitted through ER with 104 degree fever) and had an IV 24/7 all those days. What a difference!

Mary

Robert Rodgers, Ph.D.
Parkinsons Recovery

 

Dynamic Energetic Healing

My radio show interview with Dr. Steve Fenwick on dynamic energetic healing was indeed fascinating. Are you aware of ways that you sabotage your own recovery from the symptoms of Parkinson’s?

We all sabotage ourselves, but sabotage is serious when it impedes our ability to recover from symptoms that are debilitating. As a psychologist, Dr. Fenwick helps people heal from the inside out.

Listen to a replay of my interview with Dr. Fenwick below.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

 

 

Do Doctors Prescribe Fava Beans for Parkinsons

The following are questions I asked Sandra who grows her own fava beans for Parkinsons and harvests them herself to treat the symptoms of Parkinson’s.

Can fava beans be used in conjunction with other medications?

They do not appear to conflict with sinemet, but there is a fine balance between not enough l-dopa and too much. If my friend eats too many beans with her Sinemet dose..she appears to be drunk and tends to fall.

It would be great if each person’s body metabolism were the same and a clear dose could be established, but it doesn’t work that way. It has been our experience that most doctors are not familiar with fava beans and other natural remedies, and will likely advise Sinemet or other PD meds. I have chosen to stay away from synthetic l-dopa & stick with what I know and consider natural, so that my body can stay at it’s optimal health.

Do doctors prescribe fava beans??

In Europe, people have used favas for PD therapy for a long time. Favas are also a very popular food in Europe. In the United States, most people have never heard of favas. However, there is a product called Balance D that is available in the US, a supplement containing fava, by Neuroscience. It was recommended to my friend by her doctor.

Do you have a website that would help people understand the use of fava beans and how to grow them?

There is a man in Canada, Ken Allan, who has been so much support to me in this adventure with the favas. He also has PD and has grown and used them to supplement his sinemet for several years now.

Parkinsons Recovery has also set up a website specifically for fava beans: https://www.favabeans.parkinsonsrecovery.com

Is there a fava bean support group where people can get answers to their questions about growing and using the beans?

No, not that I am aware of, but it is a great idea. Could Parkinsons Recovery start an online support group where people could share valuable information about fava beans and their uses and how to grow them?

I am happy to share the little bit of information that we have gleaned over the past 12 months. I pray that many of your listeners will be encouraged to grow their own favas and that we will find people interested in doing valuable research on these amazing fava beans. May God Bless You. Sandra

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

 

Are Fava Beans Hard to Grow?

The following are answers to the question: Are fava beans hard to grow – by Sandra who grows her own fava beans as a remedy for the symptoms of Parkinson’s.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

About Fava Beans

They were a pleasure to grow for me, but some people would consider them difficult. Some of the plants become tall, depending on the variety of fava and on the composition of the soil. Ours had to be staked to prevent them from falling over when they reach about 4 foot. (Falling over can break the plant/ or they sometimes start getting discolored leaves and beans because of close contact to the ground..neither of which I wanted). So, I hammered stakes in each row with about 6 plants in between, and did what is called a Florida weave to secure them in upright position.

I learned to do this when growing a field of tomatoes one year. When done properly, a whole field can be tied in a very short time. A couple of weeks later. A second level of string is used to envelope the plants as they grow taller.

The biggest time consumer is hammering stakes if you grow a large crop. The plants are very hardy and ours survived temperatures down to 26 degrees here in Tennessee. When it dropped lower, they were hit hard……though it looks like they may come back from the roots possibly if the weather ever warms up again.

This is the coldest winter I have seen here. Favas like cool weather. They are actually in the pea family/ and not a bean. They do not tolerate very hot weather. I plan to plant my spring crop, Lord willing, in the end of February or first of March. Once you look at the beautiful, and prolific flowers on the plants, you will see why the bees and other insects migrate to your favas…they are amazing.

I found that soaking the seeds for about 2 days, until they begin to sprout, is best and then setting them directly out into the soil about 10 inches apart and 1 1/2 to 2 inches deep. Once they have developed their first 2 leaves, the root is close to a foot long. They are a good soil builder and bring a lot of nutrients up to the surface from deep in the ground. They are used as “cover crops” in some places plowed under to fertilize the soil, and then the area is replanted.

Where can a person get fava beans if they cannot grow their own?

We have not yet located a source for young/ green/ immature pods. I have come across dried beans in several markets, and even full sized bean pods in Earth Fare…but neither of these will give the l-dopa we need for PD.

You may find a local farmer who would be willing to raise a crop for you. You would have to specify the length you want the beans / or go pick them yourself & come home & process them immediately… so as not to loose the medicinal qualities of the beans. It is best to grow/ harvest & process your own and this will be a priority for me as long as I am able.

The beans (seeds) themselves , whether green or dry, contain very little levadopa….it is the leaves, stems, and the pods surrounding the bean seeds that contain the levadopa.

Fava Bean Tincture Q&A

What follows is Sandra’s answer to my question about how she goes about preparing her fava bean tincture.

I have found that picking the immature pods at about 2 1/2 inches is the best for us. They have a great buttery taste and no strings. We steam them for about 6 minutes, then freeze them on cookie sheets for about 15 minutes, then place them in freezer bags and return them to the freezer. My friend enjoys them the right from the freezer…2-4 pods with her sinemet dose .. Bean chips & cookies were made by putting large favas (past the stage of eating the pod) through a Champion Juicer, which takes out all the indigestible fiber, etc. ..and using that juice to make tasty l-dopa treats. We keep our “treats” frozen and use them to ward off symptoms. They are great also for car trips, just to carry along if needed. The possibilities are endless.

You prepare a tincture from the fava beans you grow in your grow. Tell us more about how you make your tincture

I wanted something that would capture the essence and l-dopa of the plant, and preserve it. Mainly, because there is the problem of having to grow a year’s supply of pods and freeze them. There is always a possibility of a power outage and a years supply would be lost. Since I have been making Echinacea tincture for years from my garden I wondered,

Could I formulate a fava bean tincture from the fava bean plant?

A specific part of the plant captured my attention, so I went through-out the garden harvesting these little “tops”…a little hidden, protected part of the plant. They were placed in a dehydrator to dry and then into a jar with brandy. This was shaken for a month, several times a day. Then, it was strained.

It looked good, and I played the part of a white experimental rat and took several drops to see what would happen. I didn’t see any change right away, but later, went outside and was coming up the steps and noticed that I didn’t halt on my right hip/leg like I always did. I went back down & climbed up the steps again. It wasn’t my imagination. Started trying other things that I usually couldn’t do…and kept noticing other improvements…..it was easy to drive the car, my reaction time was much improved. The list went on on.

I decided to take another drop at bedtime…and actually got a good night’s sleep. I have been using the tincture now since October 9th. Still no side effects, besides lack of Parkinson’s disease symptoms. If I feel symptoms starting…I just take a couple of drops and in about 15 minutes I don’t notice them anymore.

Ken Alan…a fellow PD patient has been growing favas for a few years. I sent him some of my fava bean tincture and he “kitchen tested it”. He wrote back that there was approximately 1 mg levadopa in 2 drops tincture. I have been taking this small dose 3 to 4 times a day to alleviate my symptoms.

Can you provide your fava bean tincture to other people?

No. I feel that much research needs to be done on the tincture, and perhaps a better base can be found to draw out even more of the levadopa than brandy. I plan to experiment in the spring with wine vinegar for tincture. But, I cannot test for levadopa and each batch will be slightly different, because of the soil area in which the favas are grown / the time of year the top is harvested/and the chosen liquid base for the tincture.

I want to make a plea for someone, or perhaps a medical school to take on the fava project that I started. I will help in any way I can to make this valuable way of using favas available to other people with Parkinson’s disease who would benefit from it, as I have.

A free download of Aunt Beans Fava Bean recipe is available at: https://www.favabeans.parkinsonsrecovery.com

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

 

Five Steps to Recovery

Perhaps the most formidable challenge for everyone on the road to recovery is to persist, stay on track and maintain the commitment that is needed to recover. This I must say is no minor challenge. Five steps to recovery are critical for success to manifest.

People tell me consistently that when they take a vacation from eating healthy food, exercising or abandoning therapies that help them, symptoms worsen. Guaranteed.

How does anyone maintain the focus that is needed to stay on track? It certainly helps to have a daily infusion of hope which is why I invented the  Parkinsons Recovery Membership.

Affirmations can certainly help us all sustain the discipline and commitment that is so critical to a recovery program.

Five Steps to Recovery lays out the steps necessary to transform negative thought forms into positive ones. When we hold positive thoughts moment to moment, day in and day out, we can manifest whatever our heart desires – health, wellness, abundance, happiness, joy – you name it.

Discover more about Five Steps to Recovery by visiting: https://www.parkinsonsrecovery.com/five-steps-to-recovery

Robert Rodgers, Ph.D.
Parkinsons Recovery

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