About Parkinsons Disease

Natural Options that Reverse Symptoms

Category: Parkinsons Disease Symptoms

Research studies document a variety of factors can cause the symptoms associated with a diagnosis of Parkinson’s disease. Researchers describe Parkinsons as a garbage can diagnosis which means there are a variety of reasons that can cause the variety of symptoms that are experienced.

Healing Parkinsons

October 18, 2024 / / 1 Comment

Hello, I am so happy to have received the link to this website..VERY INSPIRATIONAL!!
I am an Energy Practitioner and Motivational Coach. I am presently healing Parkinsons with 2 clients who have been diagnosed with PD.

My 1st client, after 3 years since diagnosed, he has been doing incredible work/ inner work on himself and is transforming and shifting to a higher level of consciousness, awareness and spirituality- which is bringing him much trust, faith and hope in his recovery. His attitude is very Positive and he is feeling GOOD more than not!!! NO DRUGS!!! HE IS RECOVERING!!

On the other hand, my second client , also has been about 3 years since diagnosed.. still very depressed and closed to any new thing that I bring to him to help his attitude to guide him in the right direction of his recovery. I have directed him to this website, the blog etc.. He refuses.. but every week I continue to see him to do energy work, massage and coaching.

There are times that he gets very inspired and makes a couple of steps forward, but the majority of the time, he goes backwards. He is not getting any support or encouragement from his family- and lives in a very stressful household. I am getting frustrated as a practitioner but know only too well that everyone chooses to either heal or not.. It is in their own time and I can not force anything..

Do I continue with my therapy healing Parkinsons? I have been working with him now for about 1 1/2 years. He said that he was going to give himself til November 2008, with doing alternative work before he chooses medication.

His family wants him to go on medication, he really does not want to go on medication but does not want to do the work that will get him on the path to recovery. He is resistant to healing Parkinsons. It is a catch 22- He does not feel good, there fore he does not have the energy or motivation to do the work- but not understanding that if he does the work (yes- will be hard at first) but by continuing, he will feel better. He eats well and takes all of the supplements that is suggested but not moving his body and has become VERY STIFF AND SORE- CAN NOT MOVE.

Can you offer to me any words of advise or encouragement or support for me. If the only thing that I can do at this time is just to be there for support for him, then that is what I will continue to do, but it is frustrating watching this 36 year old man going down hill when he does not have to be. He wants to see PROOF.. Like I said, I have directed him to this website for proof but he is not looking.

Choices for Healing Parkinsons

Warm congratulations to the one client of yours who is feeling so much better. He is clearly on the path of recovery. It is a bumpy ride, so having you there will make all the difference in the world.

Your deep concern of course lies with your second client who is getting worse. Your question is : how do I help him? Your experience is very similar to my experience. Some people are deeply committed to heal and are willing to experiment until they find what approaches work for them. They do get better. I can assure you and your clients that there are many people on the path to recovery.

The second person would prefer to have someone fix them, to make the symptoms magically vanish. I don’t blame them one bit. When I have an ache – I feel the same way. Of course – no such “cure” exists with Parkinson’s, yet many people prefer to believe it will happen to them.

There are many very deep, unconscious reasons why your second client will not do anything to help himself. On the most basic level he does not have the energy to do anything but see you. A nutritional IV can help persons in such situations.

A nutritional IV is a direct infusion of essential vitamins and minerals directly into the body. It is not a chelation. It is mainlining food the body is not getting. Some naturopaths and medical doctors specialize in nutritional IV’s. It helps people get back on their feet and give a much needed burst of energy.

Second, I would recommend you suggest to him that the reasons for his symptoms may in part lie in the area of toxins. There are many gentle ways to detox the body. It sounds like to me he is not ready to address any of the stresses in his life or traumas which sound like are a key reason for the symptoms from your description. He may be open to doing a little detox work.

Third, some people – and he may be one of them – take on a condition from another family member out of love. Sometimes it is a parent or a grandparent. Sometimes it is a brother  or sister. It depends. This is an unconscious entrapment into disease (his happens  to be Parkinson’s). This is a larger family system issue that keeps people sick until they address the issue. He is unlikely to go there now, but maybe later.

Fourth, when people get stuck in the mud so to speak, I have a very counterintuitive suggestion to make. Give him a mantra to say three times a day for a week. The mantra is

I refuse to get better. I like my life just the way it is.

If he can connect that that place within himself  that refuses to heal, he may be able to move forward.  We all get stuck sometimes.

Why might he resist healing Parkinson’s? There may be negative pleasure in having the debilitating symptoms. This too is unconscious. He is not doing anything about his situation because having the disease gives him something.The condition defines his role in his family and the roles of all the other family members. If he gets better, it puts all of that delicate balance out of whack.

The point here is to make explicit his moment to moment choice to feel worse and worse.   You can talk about all the things that will happen like nursing homes and wheel chairs so the truth is spoken out loud. We all make choices in our lives. Maybe the truth of the matter is that his true (though unconscious) choice is to check out of living and die.

Having said all of this, I think the job of a therapist is to honor whatever choice a client makes. Who is to judge that his choices are not the best for him, whatever they may be? When you ask what you can do for him, I would suggest you now put this back on him.

Ask him what he needs from you. Is he interested in healing Parkinson’s? Then give it to him in a loving way – honoring whatever choices he makes. You can facilitate his journey on whatever path he choices to take. Sometimes the most loving thing to do for a client is to honor their choice to get worse.

Keep up the wonderful work healing Parkinsons.  Know in your heart that you are the perfect healer for him at this time in his life.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

© 2024 Parkinsons Recovery

Stress and Parkinson’s Disease

October 18, 2024 / / 0 Comments

I know stress and Parkinsons disease is a major player in my symptoms. I have chronic pain and suffering from a surgery to my face that developed into what is referred to as a central pain disorder. Meaning, the central nervous system has become involved. I think it interesting that where this takes place is in the vicinity of the Substantia Nigra area of the brain where Parkinson’s develops. I’ve always thought there might be a connection.

I take 2 anti-epileptic (dangerous) drugs in order to function but this still leaves me with unbelievable discomfort that registers on my consciousness at all times. This, I see, as one of my greatest challenges to any kind of recovery. The others are :

    1.  Subtle stress in most everything I do (I just realized this) and
    2.  Negative thought patterns even though I see myself as a positive person.

I had childhood trauma and trauma as a young woman. I developed an autoimmune disease at age 22 that most often is not manifested in anyone younger than 50. I attribute this to a sensitive body that could not handle the devastation of estrogen packed birth control pills manufactured in the early 70’s.

Anita

My research concurs with both of your observations. Reducing anxieties and transforming negative thoughts offer welcome relief from symptoms of Parkinson’s disease.

Stress and Parkinson’s Disease

After conducting extensive research on methods that quiet symptoms, I have concluded that there is one step that helps the most. When anxiety and anxiety attacks are shut down, symptoms are significantly reduced. When anxiety flares its ugly head, symptoms become problematic. This is why I developed a three month online course to shut down anxiety so that symptoms become far less problematic.

My online course Shut Down Anxiety  introduces methods, strategies and techniques that have been proven by research and practice to reduce anxiety. They turn down the volume of the overactive flight-fight  sympathetic nervous system that inflames neurological difficulties.

I did not invent these techniques. They have been extracted and simplified from an extensive body of contributions by experienced practitioners and researchers. So, check out the online course and begin taking action on the methods suggested. They really will make a huge difference. Enrollment in the course is available here: Shut Down Anxiety.

Negative Thoughts Fuel Symptoms

The first online course I created focused on the transformation of thoughts that are not in our best and highest good. An explanation of the course and enrollment is available at:
Five Steps to Recovery.

Stress and Parkinson’s Disease Summary

Of course symptoms of Parkinson’s can be suppressed with medications and supplement.  A more direct approach that does not trigger the cost of side effects is to Shut Down Anxiety which it flares up. It also pays handsomely to transform negative thoughts that road block any recovery program by taking Five Steps to Recovery.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

 

Symptoms and Treatments for Parkinsons

October 16, 2024 / / 0 Comments

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 and treatments for Parkinsons 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 interviews 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.

Symptoms and Treatments for Parkinsons Questions

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 at least 6 months. Everyone is different.

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 on symptoms and treatments for Parkinsons,  it is that each person’s symptoms are entirely unique to them. I interviewed a man recently whose primary symptom was pain. 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  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 on symptoms and treatments for Parkinsons, what has happened to him is typical and very difficult to deal with.

You also ask what treatment plan would I recommend.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 exercise. 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. Research studies point to the problems with Parkinson’s originate in the gut. 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. He continued with the therapies that were helpful and ditched those which did not help.

Give any option 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. If a therapy like detox is succeeding, a person may feel much worse before they feel better.

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 therapy, 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.
Founder 2004
Parkinsons Recovery

© 2024 Parkinsons Recovery

Parkinsons and Anxiety

October 12, 2024 / / 2 Comments

Robert :I spoke with you several weeks ago
and I am having difficulty with Parkinsons and anxiety.
 Would sure like some advice.

Norma

Parkinsons disease and anxiety go hand in hand. When anxiety rears its ugly
head, symptoms inevitably flare up. A wise step that offers relief from symptoms is to embrace methods, therapies and techniques to get anxiety under control.

People with Parkinson’s experience anxiety in part due to the unpredictability of their symptoms and the challenges of living with a chronic condition.

Everyone knows when they have anxiety. Familiar symptoms of anxiety in people with Parkinson’s include:

  • Excessive worry
  • Restlessness
  • Difficulty concentrating
  • Physical symptoms like increased heart rate or sweating

When it comes to finding relief from anxiety, Craniosacral
therapy and Bowen therapy can be very beneficial. They both invite
traumas that are embedded in the body at the cellular level
to release. Once released, the potential for anxiety is brought under
control.

I have also developed a three month Shut Down Anxiety
online course that covers proven methods and therapies that
covers proven methods and therapies that
do in fact shut down anxiety. Visit the link below for
more information about Parkinsons and anxiety and to register.

Shut Down Anxiety

Once anxiety is under control, a welcome reduction of
symptom severity follow.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

© 2024 Parkinsons Recovery

Essential Oils for Parkinsons

August 10, 2024 / / 44 Comments

Last Friday I interview Jean Oswald fromessential oils for Parkinsons
Rochester, New York who is a certified
aroma therapist and a registered nurse.
Jean provided a wealth of useful information
about how essential oils for Parkinsons can be used to
provide relief from its symptoms.

Essential Oils for Parkinson’s that Offer Symptom Relief

Here is her answer to two of my questions:

What if an individual has problems with rigidity of their muscles and it is very difficult for them to move with ease. What is an essential oil that might help relieve that particular symptom?

There are a few essential oils that could
be most beneficial for muscle rigidity.
Essential oils like Cedarwood, Frankincense
and Sandalwood are high in Sesquiterpene.
They cross the blood brain barrier. They are
going to be carrying more oxygen throughout
the body and helping with firing neurons and
relieving neurological symptoms.

Muscle rigidity in connection to that is
helped by Marjoram essential oils which are
very relaxing to the muscles and Basil which
is an anti-spasmodic.

Use them in a massage or put them directly
on the skin over the spine, on the soles of
the feet and specifically on areas of the skin
where the tension itself is present in the muscles.

I would recommend a blend, a lotion that
combines the Marjoram, Basil and other essential
oils.

How about the problem of tremors? What essential
oils for Parkinsons tremors might be recommended to relieve that symptom?

I would say Basil or Frankincense, the
anti-spasmodic oils.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

© 2024 Parkinsons Recovery

What causes Parkinson’s symptoms?

February 5, 2023 / / 0 Comments

There exists a wide variety of factors that can inflame Parkinson’s symptoms.  Of course, everyone knows dopamine is often deficient, but what is the cause of this? The most important reason that symptoms flare up is unrelenting anxiety caused by stress.

Members of my global audience consistently say they had to deal with extremely stressful situations  before their symptoms became problematic. Reports vary but always involve challenges in their life that result in high anxiety and stress.

  • Perhaps their business confronted financial or legal problems.
  • Perhaps a family member died.
  • Perhaps a child became addicted to alcohol or street drugs.
  • Perhaps there was a stressful divorce.

Regardless of the specifics, anxiety persists day in and day out, week after week.  The stressful circumstances do not let up. Relaxation is not an option. Worry is constant. The neurological system becomes locked on overdrive.

Feelings triggered by the continuous onslaught of stressful circumstances get stuck in the body like super glue. To celebrate a relief of symptoms, any and all trauma that has been  trapped in the cellular structure of the body has to be released.

  • Is your body rigid?
  • Are you often anxious?
  • Is stress unrelenting?

The best way to calm and even eliminate symptoms  is to address and release traumas from the past including childhood. In doing so the body  becomes flexible, calmer and less stressed.

I have developed a free course which offers ways to release the traumas that are trapped in your physical body. Click on the link below to register:

Jump Start to Recovery Crash Course  

Robert Rodgers PhD
Founder
Parkinsons Recovery

 

Food for Parkinsons Disease

October 18, 2015 / / 1 Comment

Glen Pettibone  discusses his ongoing progress applying the diet and exercise approaches he uses to treat his Parkinsons disease, as featured in his book “Powerful Food And A Walk In the Sun“. He will touch on some of the newer approaches he has discovered about food for Parkinsons disease that are featured in his blog atpowerfulfoodandawalkinthesun.blogspot.com.

Glen Pettibone started developing Parkinson’s Disease symptoms in 2008. In 2011 he was diagnosed.  It was going fast and he could not tolerate most of the drugs.  In January of 2013 when off meds due to food poisoning, he shook so bad he could not walk. He was taking very high doses and at the “end of the algorithm”.  His doctors were suggesting Deep Brain Stimulation (DBS) surgery.

He did not like the high risk and marginal results he saw regarding the surgery So, he drew upon his scientific and engineering background and started reading every paper he could find.

He developed a diet combining Solanaceous vegetables, featuring eggplant juice, green tomatoes, and peppers with perhaps every other suggested dietary element and suggested supplement already discussed in the Parkinson’s community.   Also other nutrient dense foods. Dr. Mischley’s book was inspirational and helpful to him. He added more elements.  He has been under her care for 6 months or so.  She added intranasal glutathione which has helped.

Glen is now off more than 93% of his Parkinson’s disease medication. He completely cured his acid reflux, asthma, allergies and moderated his cholesterol. He regained color vision and acuity, his hearing and sense of smell are improving.  His skin has tanner color and healthier texture. He has more energy, strength, and stamina.

He is in the top 5 consulting employees in his company every month; sometimes number 1.  Also, prior to a car accident last summer, he was off all medication for 3 months. This spring he thinks he will be again.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

 

 

Cure for PD

October 6, 2015 / / 1 Comment

Two questions which a similar theme follow which both ask whether they will ever be a cure for PD

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.

Sir:

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
Founder 2004
Parkinsons Recovery
robert@parkinsonsrecovert.com

Do Parkinson’s Symptoms Come and Go?

January 17, 2011 / / 0 Comments

Do other PD people notice a change/worsening of symptoms seasonally? Do Parkinson’s symptoms come and go? I just realized that for several years now my symptoms seem to increase about Dec or Jan or there about. This time period is when I have been starting or changing or increasing medications.

Susan

Yes – my experience is that many people experience a flare up of symptoms during the winter. I suspect there are several reasons:

  • Diet – the holidays trigger unhealthy eating.
  • Lack of exercise – the winter months can mean colder weather with more rain and snow.
  • Lack of sunshine – Although you live in a rather hot climate, vitamin D3 may not be an issue – but Naturopath Doctor Laurie Mischley finds most people with Parkinson’s symptoms have severe vitamin D3 deficiencies. If there is less sunshine – your body will be getting less D3 the natural way.
  • Change or addition of medications – If you have been adding new medications or increasing the dosage, that could also be a possible cause of a symptom flare up due to interactions and side effects.

All in all – there are a multitude of factors that can potentially contribute to shifts in symptoms seasonally.  So the answer to the question do Parkinson’s symptoms come and go is yes. Since there are typically fluctuations – you can always celebrate improvement down the road.

Robert Rodgers, Ph.D.
Parkinsons Recovery

Books
Road to Recovery from Parkinsons Disease
Pioneers of Recovery
Five Steps to Recovery

Resources
Dehydration Therapy: Aquas
Parkinsons Recovery Membership
Eye Drops for Cataracts

 

Copper and Symptoms of Parkinson’s Disease

January 6, 2011 / / 1 Comment

Lori sent me several messages about her remarkable recovery relevant to copper and symptoms of Parkinson’s disease. from the symptoms Parkinson’s disease. With her permission I am posting her correspondence to me below.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

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. Cog wheeling gone. Smile back:) Bradykinesia almost gone. Just action tremor.

Copper and Symptoms of Parkinson’s disease

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. Accepted 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 cog wheeling 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!

Lori

Genetically Modified Organisms (GMOs)

January 6, 2011 / / 0 Comments

Sharry Edwards has identified a shocking connection between Genetically Modified Organisms (GMOs) and symptoms of Parkinsons that she personally experienced. Sharry has given me permission to post her full research article here.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

Study finds Link between Genetically Modified Organisms (GMOs)
and Current Health Care Crisis
by Sharry Edwards, MEd, Director
Institute of BioAcoustic Biology

The August 14th, 2010 issue of Science News, Separating wheat from chaff in celiac disease, reported that a research team led by gastroenterologist Robert Anderson of the Walter and Eliza Hall Institute of Medical Research in Parkville, Australia, had identified specific triggers (gluten sensitivities) associated with celiac disease.

Since our research efforts often evaluate clients who exhibit gluten sensitivity and a myriad of associated diseases, it was imperative that this important information be added to our software databases. I translated the three proteins into BioAcoustic bio-frequency (biomarkers)* and was immediately inundated with an avalanche of novel data showing that the metabolic pathways influenced by these proteins were linked to nearly all systems of the human body; causing immune distortion, acute cellular inflammation and disruptions in cell communication.

The article listed three proteins, w-5 gliadin (wheat), g-3 hordein (barley) and g secalins (rye) that were implicated in the production of the specific anti-gliadin antibody reactions. These proteins, which have been proven to be responsible for allergic reactions, are associated with grain glutens from which they are derived.

Patient records indicated the grains involved are clones developed in a laboratory by Monsanto, a multinational agricultural biotech conglomerate. This would confirm that the present day epidemic of gluten sensitivities/allergies stem from laboratory created grains. These gluten-distorted, allergy causing grain clones are being used to create foods that we eat everyday; bread, cereals, crackers, pastry, seasonings, even some packaged chip products contain wheat. As I developed the BioAcoustic correlations I was aghast with the realization of how thoroughly our health is being negatively influenced by these genetically modified organisms (GMOs).

Further investigation revealed that the cloned genes contained two substitutions that distorted the way the body processes two sulfur rich amino acids: proline and glutamine. Disturbances in these amino acids substitutions result in the impedance of the methylation of these two essential nutrients.

BioAcoustically Speaking, Glutamine distortions seem to be the most destructive. The enzyme required to utilize glutamine is glutamate decarboxylase (GAD). Glutamate is a key molecule in cellular metabolism and the most abundant excitatory neurotransmitter in a vertebrate nervous system.

In mammals, GAD exists in two isoforms encoded by two different genes – Gad1 and Gad2. GAD1 and GAD2 are expressed in the brain where GABA is used as a neurotransmitter; GAD2 is also expressed in the pancreas. This led to an evaluation of the GAD genomes and what happens when these genes are activated:

Glutamate decarboxylase aka glutamic acid decarboxylase (GAD) is an enzyme that catalyzes the decarboxylation (part of the process of breaking down for use by the body) of glutamate to GABA (gamma aminobutyric acid) and CO2.

GABA is a natural tranquilizer and an important inhibitory neurotransmitter that helps regulate neuron activity and the bodys nanosensors. Starting with the GAD enzyme response and moving toward GABA in conjunction with the active form of B6 (PLP), the nanotransmitters of the body are created and regulated. The movement of electrical energy and hence magnetic potential within the body are controlled by these nanotransmitters.

GAD uses PLP (pyridoxal 50-phosphate) as a cofactor. PLP was granted a patent by the US government patent office to the Canadian company, Medicure. PLP is now under the control of the pharmaceutical industry and its lack is often associated with blood clotting distortions, migraines, neural disorders and seizures.

Nanotransmitters produced in conjunction with GAD metabolism show direct associations with a multitude of diseases: diabetes, autism, arthritis, Parkinson’s, ALS, Multiple Sclerosis, joint pain and deterioration, auditory disorders, Celiac Disease, Crohns, Irritable Bowel syndrome, diverticulitis, schizophrenia, bipolar and anxiety disorders, aspartame sensitivity, MSG reactions, Lupus, Fibromyalgia, depression, seizures, brain signaling, the use of calcitonin (cancer related), histidine function (seasonal allergies), cellular inflammation and vaccination reactions.

Of particular importance is GADs involvement with cancer via Calcitonin, a 32 amino-acid peptide/hormone that participates in calcium and phosphorus metabolism. BioAcoustically Speaking, calcitonin is a major player in the role of how the body handles any cancer threat.

Parkinsons is an incurable, debilitating disease that also shows GAD involvement. The activity of glutamic acid decarboxylase (GAD), the enzyme involved in formation of the inhibitory neurotransmitter γ-aminobutyric acid (GABA), was studied in autopsy brain samples from six Parkinson’s patients and 13 controls. The activity of GAD was significantly reduced in brain samples of patients with Parkinsons disease, being about 50 percent of that in controls. Moreover, levodopa treatment showed a tendency to increase the activity of GAD. The results suggest the involvement of GABA neurons in Parkinsons disease.

A search of the GAD literature stated that acetylcholine, γ-aminobutyric acid, dopamine, calcitonin gene-related peptides, choline acetyltransferase and enkephalins are involved with the metabolism of GAD. It would be important to include these biochemicals when testing subjects for GAD presence and methylation.

Glutamate is the same Frequency Equivalent* as aspartame and is part of MSG (mono-sodium glutamate). James Oschman in his publication, Energy Medicine, states that cells emit frequency-based signals as a request for needed biochemicals to gather at the site where they are needed. Since Glutamate and Aspartame are the same frequency, this may explain why Aspartame has been implicated in so many muscle and joint disorders.

These observations are based on the mathematical matrix of BioAcoustic Biology developed over the last twenty years by the Sound Health Research Center located in Albany, Ohio, USA. The system allows for the evaluation of any item associated with the body in terms of numeric mathways. Sharry Edwards, the recognized pioneer of this emerging technology states, I expect this information will be the impetus that opens the world to the potential of BioAcoustic Biology and the hope of allowing access to Self Health care; even after the appearance of a disease process

From the original Science News article:

Three protein fragments are looking like the guilty parties in celiac disease, an intestinal ailment that affects as many as one in 133 people in the United States. These partial proteins, or peptides, are the part of gluten in wheat, rye and barley that triggers the immune systems of celiac patients, damaging the small intestine. An Australian research team reports the new findings in the July 21 Science Translational Medicine.

This is an impressive and very comprehensive study, says immunologist Ludvig Sollid of the University of Oslo. The authors find that most celiac patients make a response to these three gluten peptides.

Are producers of Genetically Modified Organisms (GMOs)  aware of the damage to health that is being caused? Why are GMO producers and the US government boldly attempting to prevent package warnings that would notify people that they were eating GMO products? Is it greed, ignorance or a misguided attempt to improve our food supply that is in fact poisoning our food, our population, and our genetic pool? Is this assault on our food supply intentionally creating a future that will keep us ill and medication dependent?

Sharry Edwards
https://www.soundhealthoptions.com

 

Lyme Disease and Parkinsons Disease

December 22, 2010 / / 3 Comments

I was tested and treated for Lyme disease (including intravenously) 3 times last year. In January 2010, I was diagnosed with PD.Is there a relationship between Lyme disease and Parkinsons disease?

Have you seen the same thing with many of your bloggers?

Joanne

There is an overlap between the symptoms of Parkinson’s and Lyme Disease. The research suggests that some people are misdiagnosed with Parkinson’s Disease when in fact they have Lyme Disease. From how I see it, this is a possibility that is often overlooked. The symptoms are very similar.

Of course, the recommended treatments are vastly different. This is one of the reasons I talk so much about strengthening your immune system regardless of the diagnosis.

Most of the cases involve a process that is reversed from yours. The diagnosis of Parkinson’s is given. No treatments seem to help. The person searches for other solutions. They eventually discover that they have Lyme disease, not Parkinson’s.

About Lyme disease and Parkinsons disease

Your question elicits a larger issue. I believe that many of the symptoms associated with Parkinson’s are actually caused by bacterial infections. Lyme is only one of the culprits. Some of the bacteria do not have cell walls and thus defy detection by standard diagnostic tests.

If you had three separate treatments last year, you must have a deep respect for the resiliency of the Lyme infection. It is only one of hundreds that can create havoc in the neurological system. Most bacterial infections these days are very difficult to treat successfully.

Robert Rodgers, Ph.D.
Parkinsons Recovery

Books
Road to Recovery from Parkinsons Disease
Pioneers of Recovery
Five Steps to Recovery

Resources
Dehydration Therapy: Aquas
Parkinsons Recovery Membership
Eye Drops for Cataracts

Heavy Metal Chelation for Parkinson’s

April 17, 2010 / / 2 Comments

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

Parkinson’s Symptoms and Medications

September 8, 2008 / / 0 Comments

My Parkinson’s symptoms and medications are going on with me now for
4 months and the strongest is my slowness of movements,
speech and the way my face looks so sad. Today I just felt
fatigued and some feeling in my brain like a flush or a wave of slowness.

I am seeing a neurologist for the second time for
further evaluation. I have yet to be formally diagnosed
with Parkinsonism. In a small corner in my mind I carry
he thought that these symptoms are temporary and it is
not Parkinson’s. Do others that you may know of have
similar symptoms like my self that turn out not to be Parkinson’s
and they are well again?

Thank you for letting me update you on what is going on
with my health. I am reaching out as far as I can for help
and guidance on all I can do. My life has changed l00%
this past 4 months.

I was taking SAMe for three months for depression.
It elevated my mood and I was feeling 80 percent better
so I stopped taking it one week ago. I weaned myself off
in a week.  Now I am wondering if stopping SAMe is
the reason I do not feel so good now.
Are you familiar with SAMe?

Well – you have been on a roller coaster these past few months.

The question you ask is: Do I know of people who have symptoms like
yours who have been able to recover or feel better?

The encouraging answer is yes! I interview people all the time with symptoms
like yours – give them any name you wish – who have figured out ways to feel
better.I just finished an interview with John Coleman, a naturopath doctor
from Australia who had Parkinson’s in 1995 but who has fully recovered today.

You can hear a replay of his interview by clicking on the link below:

About Parkinson’s Symptoms and Medications

I personally believe there are two basic ways to
approach problems like yours. First, many people
spend a great deal of energy and time trying to figure
out what is wrong. From my experience, this approach
tends to sustain a great deal of fear and makes sure that
you will experience the symptoms of Parkinson’s because
fear triggers hormonal imbalances in the body.

The second approach is to say – OK – my body is giving
me some information. It is working perfectly – as it always does.
It must be the case that my body needs something I am not
giving it – perhaps good food, exercise, mind challenges,
levity, relaxation, detoxing, etc., etc.). With this approach
a person can begin to make some changes in their life and
eventually turn their health around. It does take time and trust. 

As for tests revealing problems with lesions and tumors and
cancers and – you name it – my personal feeling is (and remember
this is only my personal feeling) – everyone has things like this
in their bodies. Everyone has cancers in their body at one time or
another. Most people have lesions of one type or another. Etc.

Clearly it is a good idea to get things checked out by doctors
and consider their recommendations. Medicine sometimes
works miracles for people.

The challenge for anyone in a situation like yours is that
if you spend most of your time focusing your attention on
what is wrong with your body – if those thought forms
dominate your thinking – you will be guaranteed to manifest
something wrong. Our thoughts create our reality.

As for the drug you asked about – I stay away from making
any comments about drugs since I am not a medical doctor
and I am not qualified to do so. 

I am hoping for good news from the doctors for you…

All the best,

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

© 2024 Parkinsons Recovery

How to Stop Tremors in Stressful Situations

May 12, 2008 / / 0 Comments

Question:

I start getting tremors in my jaw and left arm every time I am in a difficult or new situation. It doesn’t make any difference if I have just taken my Sinemet medication or not. I need to know how to stop tremors in stressful situations.

Response

Stress has a huge impact on symptoms. The husband of one client was having serious health challenges himself. Her symptoms deteriorated rapidly during this period. When his health problems resolved, her symptoms immediately improved. The correlation between the stress and her symptoms was near perfect.

Stress clearly is the trigger for the symptoms.There are helpful responses you can initiate in new situations to relieve the stress. A solid connection with yourself and the earth helps relieve the stress. Regardless of the technique, they all invite a connection with yourself and to the earth.

My online course developed over 20 years of research documents ways that reveal the secrets for how to stop tremors in stressful situations. Highly effective ways that reduce anxieties provoked by stress are  covered in this course : Tame Tremors.

When we go into fear in a new situation – everyone does -our energy tends to dissipate and scatter. We feel unsafe, some of us more so than others. Our energy begins to bounce around our heads and not our feet. The key to reducing the stress is to shift the energy down to your feet so that you can feel the support of mother earth and feel safer.

When we are able to move out of feeling fear in the moment and shift into a place of feeling secure and safe, the stress is relieved and the symptoms do not flare up. It is really a moment to moment thing.

It helps to remember that the stress is created moment to moment. We control the symptoms when we control our reactions in the moment.

Robert Rodgers, Ph.D.
Parkinsons Recovery
Tame Tremors

© 2024 Parkinsons Recovery

 

Diagnosis of Parkinsons Disease

May 12, 2008 / / 2 Comments

Before three years, I was diagnosed Parkinson with rigidity in neck, shoulders and back, less arm swing slowness. I am wondering if my diagnosis of Parkinsons disease is correct. 

I consulted a number of neurologists who diagnosed as stiff person syndrome or drug induced parkinsonism or due to depression.

Currently, I have following symptoms

1. Rigidity in arms, shoulders, neck back and whole body.
2. Within last one month intensity of muscle spasm in right shoulder increased which spread over neck, back with increase in rigidity.
3. Heavy legs, difficult to walk; body is dragged while walking
4. Spasm in right shoulder and upper back as a result the head is slightly bend over right shoulder.
5. Rigidity in right shoulder, upper back and neck create pain and very uncomfortable spasm like sensations which aggravate as day progresses.
6. Some times uncomfortable sensations in legs.
7. Anxiety with depressed mood.
8. Low energy level.
9. Restricted painful neck movement.
10 .Slowness in hand writing; no much change in size of letters
11 .Less arm swing

Things which I can not do:

Can not walk normally
Can not stand for long 
Can not lift heavy luggage
Can not drive car
Can not concentrate
Do not like to read , mix with people
Can not sit for long

Family history :

I have not undergone any surgery so far.
Congenital fusion of C6 to D1 vertebra
My mother had breast cancer and has undergone by pass surgery.
No PD in family.

Summary of health:

Lipid profile Normal
Renal profile Normal
Blood sugar Normal
BP Normal
Ultrasound of KUB Normal
ESR High
MRI of cervical spine Presence of Arachnoid cyst at C7- D1 level;
size appox. 11x15x13 mm
Congenital fusion of C6 to D1 vertebra
MRI Brain Normal
Glutamic acid decarboxylase test IgG Antibody serum Positive
Neurophysiology report Chronic partial lower motor neuron type of degeneration in the anal sphincter muscle with normal tone preserved
Thyroid profile Normal
Vitamin B 12 High

Facts :
No tremor
Near to normal gait
All of a sudden muscle spasm increased in last month.
Balance near normal, never fallen
Hand eye coordination good
Can cut vegetables, button shirt and handle coins
Can ride scooter
Normal 6-7 hrs sleep
No urination at night.

Current medication
1. Lelodopa + Carnidopa 2 tab a
day
2.Premipexaxole 05 mg three times a day
3. Lioceutical glutathione
4.Co enzyme Q 10 100 mg/ day
5. Vitamin B complex

I feel continuous feelings of rigidity in neck, shoulders, back and whole body. My legs have become heavy.

Please let me know whether my diagnosis of PD is correct and what should be the line of action..I wanted to do brain scan and dopamine absorption test but they are not possible here.

I am not a medical doctor so I am not qualified or trained to diagnose
or treat disease or even speculate on whether your diagnosis is right or
wrong. Diagnosis of Parkinsons disease needs to reside in the hands of the
medical doctors. My perspective differs from the conventional approach of
diagnosis and treatment of disease. Let me explain myself.

Parkinson’s is what we call a garbage can diagnosis.
Because there is no definitive test for Parkinson’s
it is terribly difficult for even highly trained neurologists to
diagnose Parkinson’s. Some researchers
even speculate that one third of the people with Parkinson’s
are misdiagnosed. Sometimes a neurologist will even
tell a patient:

“I am not sure whether you have Parkinson’s or not.”

So, let’s say there is a two thirds chance your diagnosis is correct
and a one third chance it is wrong. What does it matter whether
the diagnosis is correct or wrong? With a “diagnose then treat”
approach the key question turns on “what is wrong with
me and how do I fix it?”

I want to be fixed as much as anyone, but I also
know there is something inherently wrong with this
mindset. If I hold onto the thought that something is wrong
with my body then that belief will eventually become true. I will
become sick. I will become my thoughts.

How do I know this is true? Easy. Just think about what happened
when you were first conceived. There was only one cell in the beginning.
How did that one cell become two cells? Answer: the consciousness
and thought forms of the first cell created the second cell. And so forth.
These thought forms work their way up the chain as cells multiply
and we are fully materialized in human form.

How about considering a different way to think and respond
to your symptoms? How about acknowledging that your body is
actually working perfectly, exactly the way it was designed
to function?

Pain is a gift that is given by the body. Receive
the gift with open arms. Your body is simply giving you
signals that it needs a little help in returning to a
state of balance and health.

After all, most of the cells in your body are functioning perfectly.
Why not focus your attention on giving your healthy cells the
support they need to become stronger? Bodies with healthy cells
grow other healthy cells. The good news is that the body can
always rejuvenate itself.

I believe the key is to listen to what your body is telling you.
Best in my opinion is not to worry about whether a diagnosis of
Parkinsons disease is correct or not. Doctors have to declare a
diagnosis before medications can be prescribed so they have to
start somewhere.

By the description of some of your symptoms it might be the case
that your body is very, very stressed and traumatized.

In our newsletter I regularly offer information about many
different ways you can consider to address the stress and trauma
that is trapped inside your body (if that, in fact, is the issue at hand).

All the best. May you find relief from your symptoms soon.

Robert Rodgers, Ph.D.
Founder 2004
Parkinsons Recovery

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