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Progressive Symptom Reduction Strategies for Parkinson's Disease
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The Nervous System and Parkinson's Disease

February 19, 2025

I am re-posting this major article, originally published in September 2017, to bring it attention to newer readers who may have missed it before. This is the central thesis and main breakthrough we had in understanding Parkinson’s Disease.

INTRODUCTION: THE NERVOUS SYSTEMS

In my pursuit of pragmatic solutions to Parkinson's Disease, I found myself increasingly researching the nature of stress in humans, and inevitably drawn towards studying the Nervous System (NS).

I have already shared much of what I've learned, together with the practical applications to lessening Parkinson's symptoms, via this website, but here is a summary of my current understanding. We consist of many Nervous Systems in one body - we could say there are, at least, five of "me" in each of us. These include the Central (brain), Sympathetic (fight-or-flight), Para-sympathetic (relaxed), Enteric (gut instinct), and Somatic (free movement) Nervous Systems (and probably several others too). We may consider each one of these as a semi-autonomous "program", which becomes more or less active in response to bio-rhythms and our internal/external environments. As each program is excited or inhibited, this can profoundly affect how we think, feel, move, act and re-act.

For example, our decisions and actions in times of great stress can be diametrically opposed to those we might have taken if we were in completely relaxed frame of mind. Our gut and brains can also often be in disagreement, with many factors influencing which one we decide to trust in a specific circumstance. When we are well and our entire system is functioning as it was designed to do, these various Nervous Systems work together in harmony, keeping us safe and optimizing our survival. The right programs become more active when the right circumstances call on them, while others become more passive. A well balanced NS then results in a sense of a single integrated "self".

However, when we are chronically ill or our internal environments are disrupted, the different Nervous System programs may start to give contradictory signals and even compete for food & brain power. The external environment which our NS also perceives through our senses may itself be considered as a "diseased state" if its far removed from that which our bodies and brains are designed to survive and thrive in. Humans are unique in that we have been able to self-create new environments in which to live. Unfortunately, our modern societies tend to create discord and confusion in our Nervous Systems, precisely because we weren't designed to live our modern lives.

These internal and external imbalances can create circumstances in which some of the NS programs may become over-active or under-active for prolonged periods. These confused NS states can then lead to chronic illness, especially if the body receives contradictory signals from multiple "programs" at once, leading to a breakdown of self-identity. 

In this article I will cover how Parkinson's Disease can now be elegantly and simply explained from the perspective that one of our NS programs has become permanently inhibited, while another background process is inappropriately permanently switched on. I aim to show how all the major symptoms of PD simply come out in the wash of this explanation, and then begin to provide suggestions for pragmatic long term solutions to the condition based on these conclusions.

INTRODUCTION: THE POLYVAGAL THEORY

The different Nervous Systems can also have their own "sub-programs". For example, the Para-Sympathetic NS includes the Vagal Nerves and other Cranial Nerves. These sub-systems may themselves branch in multiple ways too, conveying different information and affecting different parts of the brain and body through their own instruction sets. The "Polyvagal Theory" of Dr Stephen Porges reveals how the Vagus Nerve has a multiplicity of branches (separate bunches of nerve fibers arising from different parts of the brain, which take different pathways through the body, with different roles). Application of this theory provides us the required framework of understanding, which for the first time, allows us to explain Parkinson's Disease completely and coherently. In this article, I would like to try to provide as clearly as possible the explanation, in order to help other people with PD ease their suffering.

Porges' original paper is very long and full of unfamiliar jargon, and the theory has evolved (become more complex) over time with the originator's own understanding, however our focus here is firmly on the pragmatic application of the theory to Parkinson's Disease, not on the intricacies of the theory itself. The aim is to:

  • break Porges' original work down in to a much more readily understandable form;

  • provide simple and elegant explanations for people with PD, which we can apply in real life;

  • avoid getting bogged down in technical details or exactitude;

  • cover only the original, basic version of the theory, as this is more than sufficient at this stage.

Key Points of the Polyvagal Nervous System

An Evolutionary Perspective

  1. The Vagus Nerve contains two main branches which contribute to the regulation of the internal organs, including the heart and lungs. The two branches originate from different regions of the brain. The Polyvagal Theory is based on a perspective that the different branches arose during the reptilian (earlier) and mammalian (later) stages of evolution of life on Earth. Porges' refers to these two branches with a myriad of different names, but henceforth, and to avoid confusion, I will consistently use the terms "Vegetative VN" and "Smart VN". The Vegetative VN deals with subconscious, reflexive functions, involuntary muscle flexing and glandular secretions, while the Smart VN is involved in more conscious, voluntary and social activities.

  2. While reptiles tend to freeze when threatened and don't communicate well with other members of the species, the development of the Smart VN in mammals and humans allowed us to actively pay attention after being startled, e.g. by listening to or observing the potential sources of threat, together with the ability to communicate information to others in a social grouping, via complex facial expressions and vocalizations.

  3. The differences between the reptilian and mammalian cardiac systems provides insight into why mammals needed to have more complex Vagal Systems: the metabolic output and energy requirements of mammals can be four to five times higher than that of reptiles, requiring a more complex system for safe regulation. Reptiles tend to be passive, sit-and-wait feeders, slow moving and spend a lot of their time still when they are not being threatened, while mammals tend to be very active in hunting/searching for food, in order to supply their higher metabolic demands.

  4. The response of reptiles when threatened is typically characterized by a freezing of gross motor activity and a further slowing down of heart beat: consider the familiar fear response in turtles withdrawing into their shell. In contrast, the initial response of mammals to threat is fight-or-flight, for which heart rate needs to rapidly quicken to prepare the body for action.

  5. The Vagal System is responsible for the change in heart rate in both cases. The Vegetative VN in reptiles is inhibited under non-threatening conditions, but becomes activated when danger is perceived, causing a freeze response and bringing the heart rate down even lower. In contrast, however, the Smart VN of mammals is most active in safe situations, keeping a break on their heart rate, preventing metabolic rates becoming too high. It is most active during sleep or complete relaxation. When higher metabolic demands are needed, such as under stress, the Smart VN is withdrawn temporarily, allowing the heart rate to accelerate.

  6. The reasons for this difference in the roles of the VN is evolutionary, because if mammals still adopted the reptilian strategy of freezing with the corresponding reductions in heart beat rate due to stress, the result would be catastrophic for the oxygen-hungry mammalian brain and heart. If prolonged, this strategy would rapidly produce heart attack, brain damage or even death.

  7. While the Smart VN usually provides the main regulatory cardiac signals in mammals, the Vegetative VN still remains and has a role in mammalian neuro-anatomy. Mammals still exhibit freezing behaviors and can "Play Dead" when they are very scared.

The Role of Other Cranial Nerve

  1. In humans, the Vagal NS is also inter-linked with other Cranial Nerves, including the trigeminal, facial, accessory and glossopharyngeal nerves. These nerves control muscles and sensation in the face, biting, chewing, the tongue, tilting and rotation of the head, shoulder movements, ear membranes, sucking in air, and muscles in the throat for vocalization and swallowing.

  2. The Smart VN systems in humans therefore integrates functions such as head rotation to orient the senses toward the source of stimulation, mastication to ingest food, salivation to initiate digestive processes, facial expression and creating noises for purposes of social communication.

  3. Furthermore, in evolutionary terms, the voluntary muscles supplied by these five Cranial Nerves evolved from regions in the body which were gills in early stages of life, and hence were, and remain, strongly associated with oxygen supply and chemically sensing oxygen and carbon dioxide levels in the body. They influence the rate of rhythmic movements such as heart beat, impacting on states of stress or relaxation, via the voluntary control of breathing, and are also responsible for voluntary control of the volume and tone of vocalizations (speech and making noises).

  4. Hence the overall Smart VN System is also strongly associated with movement, emotion, and communication, contributing to the unique social and survival behaviors observed in mammals.

Vagus Nerve BRANCH Competition and Contradiction

  1. The concept of competition between Sympathetic and Para-Sympathetic Nervous Systems is well known, as is the VN's ability to inhibit Sympathetic influences, allowing us to discharge from excited or stressed states.

  2. However, there may also be a different type of competition, in which the two Vagal branches convey contradictory information to the target organs. Both branches of the VN are capable of regulating heart beat rate, for example, via signals they send to specialized muscle tissue in the heart.

  3. This competition between the two branches readily explains many medical issues when the Smart VN becomes very weak (low Vagal Tone). Its regulation of the heart may then be easily inhibited, resulting in sudden loss of control. If there is a surge of Vegetative VN activity in response to this withdrawal of the Smart VN, the consequence is a rapid slowing of the heart rate, from which it might not be able to recover, and the heart and brain being starved of oxygen. Examples of this occurring include massive bradycardia in hypoxic babies and sudden death of athletes following exercise.

  4. Similarly, the breathing rate in people with a weak Smart VN system may be overly prone to the influences of the Vegetative VN, and sudden changes from Smart to Vegetative VN control can cause asthma attacks.

THE COMPLETE EXPLANATION FOR PARKINSON'S DISEASE

Notwithstanding the types of sudden onset PD caused by blows to the head or acute chemical poisoning, we now have a complete, simple and elegant framework of understanding of "Ideopathic" Parkinson's Disease, which is readily explained as follows.

By the time of diagnosis, the Smart Vagal Tone in People with Parkinson's Disease (PwP) has become critically low: the Smart VN and the associated Para-Sympathetic Cranial Nerves have become almost permanently inhibited. The potential causes of the weakening of the Smart VN System are manifold, and each of us will have our own cumulative history of why our Smart VN has malfunctioned. Known contributing factors include: viral infection of the Smart VN itself; chronic stress, leading to under-use and hence atrophy through loss of neurons and neural connections; genetic weaknesses; nutritional regimes which don't support the Smart VN, causing deficits in the neurotransmitters which it operates by (acetylcholine in particular); chronic pain due to physical trauma and injury that cause other parts of the NS to be permanently excited, and hence the Smart VN inhibited; emotional trauma and mental health issues which cause deep negative emotional states, also leading to prolonged inhibition of the Smart VN; broken circadian rhythm/poor sleep patterns resulting in the shortening of time periods in which the Smart VN is supposed to be at its most active.

With the weakening of the Smart VN and associated Cranial Nerves, go all their functions outlined previously, leading, precisely, to all the well known major non-motor symptoms of Parkinson's Disease. Facial expressiveness is lost and the face becomes a blank mask. Use of the larynx and muscles in the throat are lost, causing the problems with speech and vocalizations, swallowing, chewing and saliva control. The ability to rotate and tilt the head is lost and the neck becomes extremely stiff and painful. The ability to raise the arms is lost and shoulders become painful and frozen. The sense of balance provided by the ear is lost, causing falls. The ability to experience positive emotional states, and to read these in the faces of others, is lost and anti-socialness increases, leading to feelings of isolation.

The sensory roles of those Paras-Sympathetic nerves involved with Smart VN activity are also inhibited and hence atrophy too, causing the major sensory symptoms of PD: loss of senses of smell and taste; severe problems with vision and movement of the eyes; malfunction of the internal sense of oxygen and carbon dioxide levels in the body leading to very shallow breathing; an inability to heed what other people are saying; aversion to music and noise; aversion to physical touch.

With the withdrawal of the Smart VN, other programs of the NS become over-activated in order to fill the void. In diseases like Autism, it is the Sympathetic Nervous System which becomes ascendant, leading to pathological fight or flight behaviors. In PD, however, it is the Vegetative VN, in particular in its role of activating Freeze/Playing Dead behaviors, which becomes dominant, resulting in the almost permanent shut down of motor functions, as well as very shallow breathing and a low heart rate, leading to blood pressure and anoxia issues. Typically, some triggering event - a severe physical or emotional trauma resulting in a near death or out-of-body experience - has occurred in the past, through which the NS "learns" how to Play Dead. The "Freeze" program of the NS then becomes increasingly ingrained and dominant as the Smart VN weakens and withdrawals, such that Playing Dead becomes the default response to being startled (stressed).

As the Freeze response of the Vegetative VN becomes more easily excited, its other role in regulating rest and digest function is inhibited, resulting in the appearance of the gastric problems associated with PD (constipation, malabsorption, digestive enzyme deficits), together with imbalances in the gut microbiome.

The body may begin to exhibit tremor in an attempt to stimulate the Smart VN, trying to release itself from the Playing Dead mode (this is an observable and natural mechanism by which mammals can release themselves from severe trauma, especially after a life-threatening event). Unfortunately, the Smart VN is too weakened for it to ever become excited enough to take back control, so the body perpetually tremors without release. In rigidity dominant (no tremor) forms of PD, the Freeze is so deep that the NS does not even attempt to release itself.

Thus begins a series of very vicious circles. Inflammation and toxicity soar as the NS is never in relaxed state, causing both pain and negative emotions to rapidly increase. The system starts to increasingly become a source of self-startlement and self-stress, feeling threatened due to the internal inflammation, pain and negative thought processes about the future,  the fear and sense of falling, and an increasing perception that it is unsafe due to lack of social support/isolation. The pain and mental anguish cause further degradation in sleep. Digestive malabsorption causes further decrease in the nutritional support of the Smart VN. Past unhealed physical and emotional traumas recur and worsen due to the inflammation. This results in the Vegetative VN Freeze program rapidly becoming increasingly self-activated, while the Smart VN to continues to atrophy further.

Other parts of the NS then begin to atrophy too, due to prolonged under-use. Other programs weaken, and more unused neurons and neuronal connections are lost. For example, dopamine producing cells in the Substantia Nigra of the Central NS, responsible for initiating voluntary movements, become dormant as they are no longer being called upon. Awareness of the extremities (hands and feet) is also lost.

If these negative feedback cycles are not interrupted, these vicious circles lead to the apparently degenerative nature of Parkinson's Disease.

... AND HOW TO FIX IT

We have now explored a framework of understanding of PD based on the Polyvagal Nervous System, and seen how this provides, for the first time, a complete, coherent, simple and elegant explanation for Parkinson's Disease. This new understanding provides us the practical and pragmatic solutions to the condition.

Firstly, the bad news. Since we now know "Ideopathic" PD onset is due to a long term process of atrophication of the Smart Vagal System, usually over many years or even decades prior to diagnosis, we simply cannot expect any quick fixes. It will necessarily take significant time (probably also in years) to rebuild what has already been lost, but it should now be very clear that PwP can be pro-active to prevent further decay. We should definitely not sit and wait in the [according to our new understanding, false] hope that a chemical "cure" will one day be found.

Resolving Root Causes

To prevent further deterioration, we can take all possible steps to minimize those factors in our lives which are causing the inhibition our Smart VN and exciting our Vegetative VN to Freeze. So, first and foremost, we should attempt to identify and address all the root causes which caused our Smart VN to atrophy and the life-threatening traumas by which our Vegetative VN "learned" to Freeze/Play Dead. Indeed, if these underlying causes are not addressed, they will simply continue to feed the vicious circles of NS degradation, and thus even if a "cure" came tomorrow it would, at best, be a temporary fix only. Therefore, I believe we need to accept that our lifestyle choices matter, and face the somewhat hard truth that we cannot ever to return to our "old lives".

Steps we can take in this regard include:

  1. Identify and address all sources of Stress in our lives, putting in place appropriate Stress Management tools, and giving up as many of our responsibilities as we can;

  2. Make informed and appropriate anti-inflammatory nutritional choices; adjust our diet and take supporting supplements and probiotics accordingly;

  3. Identify and adopt appropriate treatment for all unresolved physical traumas, injuries and sources of pain, not just relying on pain killers nor leaving injuries to fester;

  4. Identify mental health issues and seek appropriate therapies, treatment and support; address unresolved emotional traumas, especially those connected with near death or out-of-body experiences;

  5. Fix broken circadian rhythm and sleep patterns; learn and practice relaxation techniques often;

  6. Ask to be tested for known viruses, infections and allergens associated with PD and for the appropriate treatments, therapies or management tools for any which are uncovered, including genetic and microbiome analyses.

REBUILDING THE NERVOUS SYSTEM AND REGENERATING NEURAL CONNECTIONS

Now for the very good news. Since we now understand that PD is principally a problem with the Nervous System, it is entirely possible that we can pro-actively prevent further degeneration, and even regain what we've already lost, because Vagal Tone can always be improved, neurons regenerated, neural pathways re-written, and senses retrained.

I would go much further than this, as in pursuing these solution strategies, I can honestly say I am now, in many ways, better than I ever was before PD. Indeed, when I am the "on" state, I can actually move in ways I never could before, I am much more flexible and fluid, and have increased ranges of motion. I also have much better awareness of my own body and extremities and balance sense (proprioception), much better understanding of what my body is telling me (interoception), much better eyesight, including peripherial vision and appreciation for color, much better listening skills, including a profoundly increased appreciation for the nuances in music, and so forth.

Below are just a few things we can all do to help ourselves.

  1. Start stimulating the Smart VN and Cranial Nerves on a daily basis, in order to re-strenthen Vagal Tone. I am collating simple and quick methods for doing this here: THE VAGUS NERVE AND PARKINSON'S DISEASE and THE CRANIAL NERVES AND PARKINSON'S DISEASE.

  2. Engage with movement therapies to regain range of motion. A major point which is often totally missed in "exercise for Parkinson's" is that this must be done mindfully - both the body and brain have to be simultaneously fully focused on the therapy. Watching the TV while on an exercise machine will not work! We have to really feel, and be present to the sensations in our bodies, in order to rebuild the NS. Therapies which involve rotating or tilting the head, moving the arms and legs across the body (breaking symmetry) and core rotation are the most important.

  3. Engage with sensory therapies, such as Neurological Music Therapy, aromatherapy, color and light therapy and eye exercises, in order to re-strengthen the Cranial Nerves through stimulation of their sensing functions.

  4. Use vibration therapies to mindfully stimulate the hands and feet, in order to rebuild awareness and sense of the extremities.

  5. Practice making facial expressions in front of a mirror, especially smiling - don't underestimate the importance of a "cheesy grin" , waggling the eyebrows and twitching the nose!

  6. Practice using the vocal chords, whistling and humming, and especially singing.

  7. Practice making eye contact with other people.

  8. Ensure plenty of long cuddling sessions with loved ones.

  9. Practice breathing exercises, in particular breathing awareness techniques - mindfully observing our own breathing, without judgement or effort.

  10. Eat mindfully, try to experience the taste as fully as possible, and chew each mouthful well.

Basically, try to practice and fully experience as many as possible of all the functions which the Smart Vagal System and Cranial Nerves are designed to do, as often as possible. As we've said, there are no quick fixes for this condition, but there are definitely things we can to do continually reverse the symptoms over time and, I believe, to recover our health over the long term.

In Brain Science, Diet & Supplements, Mental Health, Music, Therapies Tags Polyvagal Theory, Nervous System, Cranial Nerves, Vagus Nerve, Symptoms, Symptom Relief, Theory
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February 18, 2022

By Florencia Cerruti, person with Parkinson’s Disease and author of Rebirth at 50: in the end, it was not The End.

Very shortly after my diagnosis of Parkinson's disease at age forty seven, I asked a neurologist how long I should work. His answer was: "Until the last day that the disease allows it." His words echoed within me: what would happen that day? Would I be the one to decide or would it be my colleagues and bosses at work who would warn me before I had the chance to decide? What would the signal be? In any case, what would it be like to work until the last day the disorder would allow me to?

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February 18, 2022
Survival Instincts and Parkinson's Disease
February 3, 2022
Survival Instincts and Parkinson's Disease
February 3, 2022

To help shake off the gloom about this, I call our survival instincts our superpowers, because it is a more resourceful way to look at the body and the problems we might be experiencing. Try saying "thank you, body, for keeping me safe, but now it is time to bring me out of the safe survival state and back to the normal range of health and grow." This ought to give us a little more faith in the dispositions of our body.

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February 3, 2022
Feeling Trapped and Parkinson's Disease
December 13, 2021
Feeling Trapped and Parkinson's Disease
December 13, 2021

As a first step, we perhaps need to identify the places where we are stuck in our lives, those stressors which come with a sense of being trapped, the stressful things we can’t fight or flee from, and try to address these. This is because the tonic immobilization framework of PD predicts that it will be very hard to reduce symptoms in circumstances that our nervous system is constantly feeling trapped by a proximate threat. Examples include being in a toxic relationship, living in a house with neurotoxic mould infestations, workplace exposure a chemical agent, enduring a long and stressful daily commute to work.

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December 13, 2021
Motivation, Pleasure, Pain and Parkinson's Disease
November 4, 2021
Motivation, Pleasure, Pain and Parkinson's Disease
November 4, 2021

The activation of the habenula inhibits or deactivates the dopamine neurons in the substantia nigra and ventral tegmental area, and, conversely excites or activates them when it is deactivated. This has profound implications for PD, as this points to the possibility that it is not cell death which causes the issues in PD, but chronic activation of the habenula permanently switching off the cells in the substantia nigra from producing dopamine. This is a more hopeful hypothesis, as it means the cells are just dormant, not dead. If we can figure out how to deactivate the habenula, this could provide significant symptom reduction.

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November 4, 2021
Dopamine Cell Receptors and Parkinson's Disease
October 2, 2021
Dopamine Cell Receptors and Parkinson's Disease
October 2, 2021

Cell receptor population dynamics therefore may play a primary role in environmental interactions (nurture) and can profoundly affect biology (nature), and may be the mechanism through which history gets written into the body, such as affects of childhood trauma in later life. Cell receptor population dynamics also provide strong and significant neuroplasticity without the need for new neurons or new synaptic connections/wirings per se, by profoundly affecting the functions and sensitivities of the existing neurons themselves.

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October 2, 2021
Dopamine and Parkinson's Disease
August 15, 2021
Dopamine and Parkinson's Disease
August 15, 2021

The Huberman Lab podcast is a lecture series by Prof. Andrew Huberman, professor of neurobiology and ophthalmology at Stanford School of Medicine, on practical and free tools for optimizing health based on the very latest neuroscience and human biology research. This podcast contains vital, actionable, and need-to-know information for people with Parkinson’s Disease, in particular of the latest pragmatic research into dopamine biochemistry. Dopamine is the major neuromodulator which is most problematic in PD, and the target for the mainstay medical interventions. So here I’ve extracted from the podcast episodes the timestamps of everything Prof. Huberman has to teach us on the subject of how to optimize our dopamine biochemistry. The format is the episode title, in order of release, followed by the corresponding timestamp links and descriptions whenever dopamine is referred to.

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August 15, 2021
Visual Cues and Parkinson's Disease
July 26, 2021
Visual Cues and Parkinson's Disease
July 26, 2021

I learned about the connection between the eyes/vision and movement of the body in an online course run by my friend and "Wisdom Coach" Cheryl Townsley, where a tutorial showed how, looking up or down with the eyes (not via movement of the head) creates an immediate increase in the range of specific arm/shoulder motions. I could quickly check this was indeed true for myself. Indeed, the connection between eye and body movement is so important that professional athletes are being trained in these types of techniques, and are given specific eye exercises to improve sports performance!

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July 26, 2021

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Testimonials Carousel: What People Say
March 13, 2025
Coloring with Parkinson's
March 13, 2025

By D.M. via email

Works for me, I am coloring mandalas now and everyone tells me they are very beautiful. I find coloring helps my focus and my tremors. I fall asleep in my chair, if I start coloring I am wide awake and on the ball. I started by coloring adult swear word books, they were most amusing. Mandalas are complex sometime take four or five days to complete. By the way: I am 90 years old and have had Parkimson’s about three years.

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March 13, 2025
November 28, 2024
Very Encouraging and Refreshing
November 28, 2024

By Katrina B.

I thank Gary and Lilian for sharing their experiences, findings, and recommendations regarding Parkinson’s. I have a Parkinson’s diagnosis and also experienced the cold news of “no cure, progressively degenerative,” etc. I purchased and read Lilian’s book. Very encouraging and refreshing. I also bought a book Gary recommended called Music As Medicine (Daphne Bryan, author), which has helped me to walk without firing the dystonia in my left foot. That’s a huge win for me! I followed links in Gary’s material to videos on breathing techniques to release stress and reduce my adrenaline. That’s helped my tremoring remarkably. So… many thanks to Gary and Lilian. I will continue to follow and engage. Oh, and I have shared your names and resources with my occupational therapist, physical therapist, and speech therapist. They were very interested. I tried to share with my neurologist. He wasn’t interested. No surprise there.

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November 28, 2024
April 19, 2024
Stuck on Pause
April 19, 2024

By Dave F.

Hi Gary, I just found your Parkinson's online information a week ago or so. Your perspectives on a potential root cause of PD being related to trauma, stress, inhibited parasympathetic system, etc. seems synergistic with my path to address my PD. Although I do not call it PD anymore. I call it being "stuck on pause". I have a list of over 150 things I could be doing (does not include pharmaceuticals), and the therapy I am primarily focused on is based on the books "Recovery from Parkinson's" and " Stuck on Pause" by Janet Hadlock (available as pdf's on pdrecovery.org). While I address symptoms with 2 hrs of exercise daily, meditation, clean vegan diet, etc... my approach to recovery is getting unstuck. Unstuck from a norepinephrine/adrenaline based nervous system back to a parasympathetic/sympathetic balanced nervous system. Are you familiar with Hadlock's work? If so, what might be your perspective in relation to your findings? If not, I created a 2 page overview I can send if interested... or you can download the books for free.

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April 19, 2024
August 12, 2023
Photobiomodulation or Red Light Therapy
August 12, 2023

By S.S. via email

I have late onset vascular Parkinsonism-diagnosed age 83, and came across Dr Catherine Hamilton’s blog redlightsonthebrain.blog. The author is a retired general practitioner who is involved in research in Australia. I have been using transcranial and intranasal lights for 5 months and have experienced relief from symptoms that has greatly improved my quality of life and am surprised not to see many (1 only) references to the benefits of this therapy.

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August 12, 2023
July 7, 2022
Tremors Reduced
July 7, 2022

By Facebook Group Member

I have been having great success with the Hope Shortcut programme. I have both Lilian Sjøberg and Gary Sharpe courses. The material really resonates with me and this approach together with John Coleman Rethinking Parkinson’s is really helping. The tremor I have been experiencing is much reduced and often gone completely. I notice how it ramps up when I am stressed or self conscious. My mood and energy levels are much improved.

What hasn’t improved is the slowness and stiffness in my right hand and leg. It is probably not noticeable to others but I notice when using static bike and when folding washing etc. any thoughts on root causes of this slowness? Left hand side fine.

Thank you all for your work

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July 7, 2022
March 29, 2022
Accessible Knowledge
March 29, 2022

By S.A.

Thank you both for all the work you have done. Lilian Sjøberg for your knowledge and Gary for helping to make it accessible. My daughter who suffers from anxiety and panic attacks and myself with PD found it so enlightening. I can also see how when my father 93, who also has PD, gets stressed his cognition deteriorates dramatically

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March 29, 2022
October 19, 2021
Staying Positive
October 19, 2021

By Brad Maybury

Gary, I mainly want to thank you for this site and for your inspiring example. I was diagnosed with PD two months ago. On top of that, I'm in my sixth week of radiation therapy for Prostate Cancer with the accompanying hormone meds (fatigue). Your attitude and example are helping me to stay positive and feel that I can beat both of these! I've been doing the fast-walking per John Pepper, plus a bunch of other things. I'll get a mini-tramp soon. I already understood the trauma link, having discovered my own about six years ago, as well as being a fan of Gabor Mate (I see his book on your site). I had not made such a precise connection with PD until reading your story (thanks!). You are a huge inspiration and have already helped to improve my life!

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October 19, 2021
July 28, 2021
Suggestions for Exploration
July 28, 2021

By Frederick Lowe

Your understanding of the many important factors that contribute to Parkinson's and the many practical suggestions on how to address them runs parallel to my learning over the last 5+ years. You are a man after my own heart. Love the Polyvagal theory knowledge. I knew somewhat of the importance of improving vagal activity, but not to the depth you have shown. Thanks. Totally agree with knowing how the Cell Danger Response is involved with being stuck in the inflammatory and alarm state. And few others besides ourselves appreciate the amazing role the fascial system plays in this, from head to toe. This is besides nutrition, movement, social interaction, meditation, breathing, eye exercises, inflammation, etc, etc. Big thanks for mentioning the Eye Guide. That looks amazing. Hope it is available in the U.S. sometime soon.


Now suggestions of a couple of things: 1). More exploration on the ramifications of mitochondrial dysfunction, all the factors that affect that, and how it can be addressed (so far, all genetic abnormalities affect mitochondrial function). 2) Learn about Stephen Kaufman's Pain Neutralization Technique work on rapidly, effectively improving vagal function. I believe it works reflexively via its effect on the fascial system primarily, but also probably the nervous system.

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July 28, 2021
June 20, 2021
Educative Posts
June 20, 2021

By Milan Hoste

Dear Gary, I really enjoy and admire your educative posts. Thanks to you my lectures at University and my private coaching are better.

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June 20, 2021
March 24, 2021
Parallels with Trauma
March 24, 2021

By Dennis S.

I am 45 years old and I was diagnosed with Parkinson’s in 2015, at an age of 39. I always thought about chronical stress as a possible reason for Parkinson’s and recently I discovered the Polyvagal Theory. I guess similar to you, the parallels between Trauma and Parkinson’s seemed to be quite obvious to me. I had the experience that Somatic Experiencing can be helpful. Later someone recommended your website to me and I feel excited that you see it like I do. Thank you for that. it is always good to know that someone is sharing your point of view. I will read through your articles.

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March 24, 2021
February 4, 2021
Correcting Dysfunctional Sleep
February 4, 2021

By Jacob Kidney, Essential Movements Yoga for Parkinson’s/movement disorders (ET/Dystonia)

I really love reading everything that Gary Sharpe has to write about his experiences with Parkinson's. He is always spot on. I know this is true from my own experience as well. My symptoms are always worse when I don’t sleep well. I love what he says here about sleep being the foundation for symptom reduction and moving in a positive direction.

So what can we do to have better sleep? I would love to hear what everyone does to help them sleep better.

For me, doing some sort of intense exercise earlier in the day and followed by a few different deep relaxation techniques/routines in the evening have dramatically changed my sleep patterns.

My sleep patterns were always very inconsistent all throughout college. Between working full time and full time school I would often go for three or four days at a time with only sleeping three to five hours per night. This pattern persisted for more than four years. It resulted in my tremors and overall health getting worse.

It has taken me two years of persistence to correct these dysfunctional sleep patterns to the point where I can manage my symptoms much more effectively and have begun to move in a positive direction.

This has been done by doing intense exercise every day. This can include biking, running,, hiking, weightlifting, yoga, etc. you need to effectively use the adrenaline in your body or else it is going to exacerbate your symptoms.

Then in the evening I will try a number of different things to help my body wind down and prepare it for sleep. This could include deep breathing, meditation, Yin Yoga, Restorative Yoga, and Yoga Nidra. I always have an air mister defusing essential oils and gentle soothing music while falling asleep.

Also, scheduling daily free time to rest and take a nap if I need it has been invaluable. Especially, right after doing intense exercise.

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February 4, 2021
October 27, 2020
REM Sleep Behaviour Disorder
October 27, 2020

By Darrell L.

REM sleep behaviour disorder (RBD) and the onset of PD

I stumbled on your site while probing the internet for info relating to a sleep disorder known as REM sleep behaviour disorder (RBD). This has been a fixture in my life since I was a child...and has continued into my middle-aged years (I'm 37 now). At times it's been a mere curiosity as it doesn't noticeably disrupt my life to any great extent; however, in the resent years I've been sharing a bed with a partner who is somewhat less of a deep sleeper...so I've been hearing more about my night-time adventures. The curiosity took a bit of a turn when my reading suggested that RBD is a very common marker for the onset of PD. Statistics range from 80-90% of those who develop RBD receiving a PD diagnosis within 10 years. Interesting. From there, I started to investigate possible therapies/treatments. Currently, the sleep disorder could be considered ideopathic. Very little is known about the origins. Aside from lifestyle changes (diet, exercise, caffiene/alcohol intake, sleep hygiene, etc.), Clonazepam is recommended. There's an aversion to this treatment for obvious reasons. Melatonin is another potential option, as is, full spectrum CBD. Beyond these suggestions, there's not much else; however, Clonazepam is used to treat anxiety, so it got me thinking about the potential emotional links that may be embedded in the disorder. This got me thinking about Gabor Mate and his book, ''When the body says No.'' So, with PD and Gabor, I found you!

Such a wealth of information. I've only just scratched the surface, but feel a wellspring of gratitude that it's here. Just delving into the Polyvagal theory...and trying to put together some ideas for a course of action. I don't know that I'll develop PD, but so much of the material here rings true for me...so it's got me thinking about what I can do now.

I'm wondering if you've got any material on this link that exists (PD and RBD)...or if within your network you've encountered those who have story that's similar to mine.

Thank you so much for sharing your own journey. Such a helpful resource.

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October 27, 2020
August 11, 2020
Yoga Therapy
August 11, 2020

By Theresa Conroy, C-IAYT (certified yoga therapist by the International Association of Yoga Therapists).

Gary Sharpe's website provides something invaluable to my Yoga Therapy clients with PD: informed, personal experience. My clients are engaged and knowledgeable about their disease, but they crave real-life input on treatments and wellness. Gary does that with clarity, style and humor. That's why his site is one I often use as a resource for my students.

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August 11, 2020
November 27, 2019
Strategies of Recovery
November 27, 2019

By Babs Meade

Thank you Gary ! Your work is informing my work and life. As a healer-bodyworker, neuromuscular integrative movement therapist, Acupuncturist nerd, Esogetic Colorpuncture person with neuroimmune issues - addressing trauma awareness and recovery for people. Trauma-shock, shake, Reaction Patterns, Adaptations, Addiction. Sorting these out...sorting out strategies of recovery. Nourishment, laughter, music, art, emotions, Soul, Body, Spirit... thankyou Gary Sharpe for your excellent life’s work

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November 27, 2019
September 3, 2019
Applications of Polyvagal Theory
September 3, 2019

By Olivia Streater Lavizzari

I spent the day reading your blog and videos -- SO profoundly MOVED AND AMAZED by what you are doing! It is incredible and wonderful. I wondered if you have the new(ish) book Clinical Applications of Polyvagal Theory. In the chapter on strokes by Deb Dana there is some great stuff that I think could also be applicable to PD. A lot of which you already cover in your blog; things like frozen facial expression etc. Very glad I came across and shared with my professor, who is researching use of Flamenco and Tango in dance movement therapy PD interventions.

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September 3, 2019
May 24, 2019
Hope and Inspiration
May 24, 2019

By Rick Potvin

Your site was the very first thing I read the day I came home from the neurologist with my diagnosis of PD. It gave me so much hope and inspiration that I started the very same day on program of strenuous exercise, diet, etc. I actually picked up my guitar, my one true passion, and thought I can do this. Two years latter I'm still doing it thanks to your insight, research and sharing of knowledge.

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May 24, 2019
February 7, 2019
Headed in the Right Direction
February 7, 2019

By Cheryl Nicholson

I’ve been very inspired by these posts. I have a Parkinson’s client who was in a wheelchair and who would crawl to get places. He’s now able to get up and walk to the washroom on his own. He even went out and shoveled his driveway. We are using targeted nutrition, intentional movements, red light intranasal therapy and Natural Bioenergetics to improve his life. He still has days where he goes backwards, but overall things are headed in the right direction. Many thanks for reporting on your own progress and providing information that helps others!

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February 7, 2019
September 10, 2018
Husband Diagnosed
September 10, 2018

By Kay Pyke

Did a quick search this morning and found the website which has so much info that I’ve been looking for. My husband has just been diagnosed and I’m researching how to help him. This is so inspirational and I’ve forwarded it onto our neuro physio. Oddly enough she came today armed with hand exercises which is what led me to this website. I’m in tears. So happy to have found you.

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September 10, 2018
September 10, 2018
Making Changes
September 10, 2018

By Adam M.

Gary, I want to say a huge thank you for your website! It has been a big help. I’ve changed my diet to fit Dr. Mischley’s recommendations generated by her research. I also bought the smovey rings. Right now I’m doing a Feldenkrais style movement intensive which seems to be helping.

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September 10, 2018
June 21, 2018
Craniosacral Therapy
June 21, 2018

By Sue Watson, Sue Watson Craniosacral Therapy

Hi Gary,
I am so excited to come across such a refreshing approach/understanding of Parkinson's sisease. I am a craniosacral and physiotherapist doing a bit of digging for useful info about gut health and P.d. for a client when I came across your website. I don't know if you have had any experience of craniosacral therapy, but big into the effects of whole systems harmony, polyvagal theory and impact on neurophysiology/psychoneuroendocrinoimmunological etc.

I have recently taken a career break from the NHS to follow my passion for cranial work and develop how I integrate the understanding that comes from cranial teachings with movement based practice. Your findings sit so in harmony with my experience. I have to say that I haven't gone out of my way to look further into similar approaches to P.d. - from what I see on you website, you appear to be pioneering a way forward - is this all your own research, or can you point me to other sources too?

I have worked with a number of Parkinson's clients very effectively, but - as is often the case with 'complementary' approach, the challenge is in embracing quite a different way of thinking - and the medication/grip of disease/anxiety and stress are powerful and seductive hooks. The gentlemen I am looking into gut health for has found after a couple of our sessions, but not all the time, he is able to play piano after 9 years of his tremor being too disruptive. Our next work is with me carrying out cranial work while he is playing and exploring the sensory experience/interoceptive experience of doing so - then looking at ways he can find balance and access that 'place' for himself.

We (therapists) do a lot of work with trauma recovery, establishing resources with - building stronger neural pathways to grounded/balanced CNS states etc., as well as the benefits of the hands on work itself. Familiar with Gabor Mate/Lavine/Roschild etc, all sitting comfortably with how trauma affects movement and inhibition of such.

My experience as a physio in the community has involved lots of work with Parkinson's and increasingly I see the effects of stress and the social engagement system being critical to understanding and improving movement, and in the last 3 years have done much more work with body awareness during activity, whether it be gaining flexibility or strength or balance. The toughest part is engagement especially when the general physio community is not promoting the same message. As you're website implies, it requires such a commitment to your well-being. I totally admire your perseverance and have empathy for how challenging it must be for you at times.

Is your approach being embraced by the professionals researching the rehab/recovery work? I would be really interested to hear more. You may be interested in the work of Body Intelligence/biodynamic craniosacral therapy, Pain is Really Strange (FB and blog site) - although name implies about pain, it's that full mix of what you have been exploring yourself (Steve Haines, craniosacral therapist).

Kind regards, Sue Watson (Scotland)

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June 21, 2018
May 27, 2018
Music is Medicine
May 27, 2018

By Consuela Harper

Gary, I love your approach, and the way you describe and illustrate it so well in this article. Watching the music and dancing video was a true delight. I also read your post about digital music as medicine, and wanted to comment on that because I felt so moved by it. I love this post so much!!! I can relate fully. I've said for a long time that music is medicine for my body. And it's a delight to see the videos of the effects of your music medicine on your body and spirit! :)

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May 27, 2018
April 26, 2018
Social Isolation
April 26, 2018

By Marva Lee Weigelt

What a revolutionary week this has been for me to integrate new understanding, launched by Gary Sharpe’s post about how trauma and chronic dysregulation affects other people’s perceptions of us in social situations. I had a giant aha that helped me understand and have compassion for my own mysterious social isolation as a child and well into adulthood.

Integrating that with my increased awareness after taking a class a year and a half ago and staying in touch through groups like this, I am able to understand that honing my interoception skills allows me to recognize virtually instantly when I am in the presence of a dysregulated person. I’m sure I’ve always done this, but without the comprehension of what’s happening.

I am using this raised awareness to great advantage in my peer support practice, and also observing how I am assisting others with cor-egulation.

Then, last night, in a community ukulele group I lead, I could understand why I was reacting as I was to a young woman who is a beginning player. It is quite clear that the rest of the group is having a similar reaction to her. In fact, one player stayed afterwards to talk to me privately about how the awkward young woman made her feel unaccountably “nervous.” I was so happy to have the language and concepts to help her understand what I thought was happening at the nervous system level. Then she said, “I used to be that way myself,” and I knew I had a new ally in building compassion instead of following the natural, but heartbreaking impulse to avoid and exclude this young person."

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April 26, 2018
March 31, 2018
From Malta
March 31, 2018

By Mildred Atanasio

Hello Dr. Sharpe, I am very glad I came across your videos and messages on facebook! I just want to say a huge thanks as all your info is very useful. My mum was diagnosed last year. In Malta, even medication is limited. But anyway, I have lately also started helping out with managing the page Malta Parkinson's Disease Association, which tries to bring Maltese people with PD (and others) together. I find your articles (and especially your improvement) very admirable and much more helpful! Thank you once again.

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March 31, 2018
March 6, 2018
Impactful Discoveries
March 6, 2018

By Julie Brown Sheil

I really admire this man. Gary Sharpe is a Warrior in the fight against Parkinson’s Disease.

He has been tirelessly researching therapies and documenting their effects along the way so that others can witness how he is healing himself. He also shares them with the world so that others can benefit from them, too.

He has refused to let doctors convince him that there’s nothing that can be done to slow or reverse symptoms. He has refused to become a victim of, or defined by, his disease. The best part is, he’s winning. He’s improving his quality of life (and that of others).

I follow Gary because once I found out I had neurological disease from Post-Concussion Syndrome, I began researching ways to help myself. Even though I don’t have Parkinson’s, I do have a chronic disease and I have found all of Gary’s insights (listed below) to be true in my case as well. Doctors don’t know everything. Specialists only know their specialty. Doctors chase symptoms rather than chasing the cause of the symptoms. Patients who are intimately involved with their own healing do better. Patients who think outside the box can make some impactful discoveries, not only for themselves, but for others.

It’s a sad state of affairs that patients are left to navigate their own recovery and healing. But it can lead to some amazing discoveries.

Gary is the reason I started my Mind Matters Mondays posts. I want my journey to be able to help others, to make it a little less likely that someone will have to struggle to find answers or relief the way I have.

Thank you, Gary, for all that you do!

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March 6, 2018
March 6, 2018
Co-Regulation
March 6, 2018

By D. Hutton

I experience chronic pain on a daily basis due to chronic disease. Chronic pain is mentally and physically exhausting. Part of my self care is co- regulating my nervous system with my husband everyday. We sit quietly, calmly together and observe how our bodies feel, just breathing/existing. We are in physical contact, sitting on the couch. We practice observing how our thoughts, conversation and emotions affect our nervous systems. Sometimes I get very anxious if he shows empathy when I don't want it. Sometimes we just sit quietly. I actually resisted the co regulation aspect of the poly vagal theory, but you were so persistent with this information that I finally tried it out. Life is so much better now!! Thank you for your persistence, dedication, and information Gary Sharpe!

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March 6, 2018
February 6, 2018
Outstanding Information
February 6, 2018

By Brandon Knight

Outstanding information, you are very helpful as you explain what you are feeling in a clear way. Thanks for putting in the effort to make these. Disconnect between the brain and body feels about right to me and I will be making some devices for myself to test out. Just started with sinemet and I am 40 so far it has been a big help my right foot has been about like yours since I was 34. I am not even sure if I have Parkinson's maybe some other dopamine issue have dat scan scheduled seen multiple neurologist and they have not been able to pin it down they are going off medication response at this point thinking it might be a dopamine responsive dystonia. Any way just wanted to thank you for putting these together and explaining that the medication on its own will not be enough. The sinemet gave me to mobility to move with less pain so I can work out again as well as helped me think more clearly but I do believe that it is what you do with the room the medication buys you that will make the difference although I understand we are all different. Thank you again for posting these they do help.

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February 6, 2018
January 21, 2018
Slowing Down Progression
January 21, 2018

By Simon Clarke

I came across your website at a very opportune time - much of your research, information and experience corroborate my own. Many of the PD symptoms (before and after life hacks) you demonstrate in your videos bought a smile to my face, seeing someone else taking a proactive role and showing real progress. Thank you!

I was diagnosed with idiopathic PD at the age of 48. As you know- getting that diagnoses and prognosis ruined my day... and the rest of my life (or so I thought). I went through the various stage of grief and went on Meds with resignation to my fate.

However about 2 years after diagnoses, I had an epiphany (of sorts) and realised I no longer needed to be a victim as there must be some way of alleviating and/or slowing down progression. This led me to shiatsu, yoga, yin tuinna, mindfulness, meditation and to Zhineng QiGOng which I have been doing for the least 2.5 years with great success. During this time, I have searched the web relentlessly (PD trait!!) and come across some useful info..

However I think your website is one of the most comprehensive resources I have seen of all the information and practical, holistic guidance collated in one place. It’s a very useful place to start when looking for a way through PD that encourages the understanding and healing of the entire BodyMind system.

The last week I have been reading Norman Doige's book-the brains way of healing. Full of good information

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January 21, 2018
October 25, 2017
Exploring All the Potential Causes
October 25, 2017

By Ken Howard

May I also add my humble gratitude for all you are doing to help us tackle Parkinson’s. In a recent “Live Loud” session organised by the Cardiff branch of Parkinson’s UK, we were asked to nominate someone who has inspired us to fight against this pernicious disease. I nominate you, Gary! You have shown me that we should not give in and accept the inevitable, but should keep on fighting! Rule 1 in any battle is “know your enemy”. You have been tireless in exploring all the potential causes - physical, chemical and psychological, and sharing your findings with us. Secondly, you have amazed us with your enthusiastic approach to trying any potential treatment, no matter how obscure it may seem. I am trying out many of these, principally the exercise, diet and mindfulness related therapies. These have helped me significantly, and I’m particularly interested in your research into the Vagus nerve issues. Please keep up the good work - I shall keep on fighting with you!

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October 25, 2017
September 10, 2017
Can-Do Attitude
September 10, 2017

By Tina Gebhart:

Gary, I may have been researching before finding your page, but your consistent encouragement, posting of your supplement and exercise trials, and general can-do attitude have been super motivating for me. I would not have gone gangbusters on this fish oil and fasting thing if I had not seen your experimental models. I may not have built up the nerve to go against my first neurologist and then find a better, awesome one. Thank you a million times over. I consider you my big brother, as sappy as that may sound.

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September 10, 2017
August 28, 2017
Connecting the Dots
August 28, 2017

By Gregory Layer:

Gary, you are a gift to this world. Your effort to connect the dots of our daily life and daily choices to our long term health and how disease manifests in our bodies is making a huge difference in my life. I am inspired by your work but more importantly, I am inspired by the spirit with which you share your experience with others. Keep up the great work and know that you are loved and appreciated, just as you are!

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August 28, 2017

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