Natural Options that Reverse Symptoms

Category: Parkinsons Disease Information (Page 13 of 16)

Access 20 years of research focused on identifying natural approaches, therapies and treatments that offer the opportunity to celebrate relief from the symptoms associated with a diagnosis of Parkinsons disease.

Parkinson’s Disease New Treatment

Parkinson’s Disease New Treatment

Below is a play by play account of how one man who currently experiences the symptoms of Parkinson’s receives tremendous therapeutic advantage by intentionally making his “good side” worse. This Parkinson’s disease new treatment is counter-intuitive to be sure.

  1. Why in the world would anyone want to make their “good side” worse when they already have one “bad side”?
  2. Wouldn’t you then be straddled with two “bad sides” and not just “one bad” side?

The answer to both questions is “no“. Check out my previous post on “Neurological Diplomacy” to understand why.

This Parkinson’s disease new treatment costs absolutely nothing and insures you are in complete control.

  • No one is doing anything to you.
  • No therapists are required or necessary.
  • This Parkinson’s Disease new treatment is free. 

The example below applies the principle of Neurological Diplomacy to a trembling right arm and hand.  The account was emailed to me by an individual who prefers to remain anonymous.  What follows is the description he emailed to me which I have liberally edited.  He wanted to get this information out to others who experience symptoms of Parkinson’s disease because the approach has been so helpful to him personally.

First of all, I only do this after my cold morning shower when I am already moaning and trembling from the cold water. My body feels energized then too. Other times of the day I do not do this technique. Admittedly it looks weird for someone else to see, so I do this when no one else is watching me.  I’d be too self-conscious to do it in front of an audience. Also, I need high energy to do this technique.

After my cold shower (which is the time of the day when I have high energy)  I make my “good” left hand and arm and “good” left side shake and shudder like the dickens out of control. I literally act like a crazy man. I would not want anyone to see me doing this. They would think I was insane.

I do this maybe 10 to 20 seconds maximum. My thought process goes something like this:

“OK body if you want to see a tremble I will SHOW you a real tremble. You think that pathetic tremble on the right side is something?  Let me show you a real shudder and shake. “

I try to make the left side (my “good side) feel just like the right side. In this space –

  • I am out of control.
  • There is no way to fix this.
  • I am totally frustrated.
  • I am completely disabled and cannot function at all since both sides are trembling to beat the band.
  • Then, I stop, dry myself and dress.

Here is the good news. I have had less or no trembling on the right side (my “bad side”) as the months go by. The length of time with no trembling is increasing.

The outcome varies. Sometimes I get poor results. Usually I get some results. It might be seconds or minutes of no trembling on the right side, but it is usually longer. Sometimes, and increasingly so, all morning until later afternoon, I have little or zero trembling on my right (“bad”) side.

That is the dramatic version that I would never do in public… something that I have made a daily routine as a finish my morning shower. You certainly do not have to be nude to do this. Loose clothing works just as well.

I also practice a scaled down version during the day when I sometimes imitate the right side tremble on the left side with the intention of getting a frustrated feeling about it. My intention is to help my brain work on a correction.

Sometimes I do this “homeopathically” where one cannot even see what I am doing. Or, I create the conditions in my imagination. You do not even see my tremoring on my “good” side.

Admittedly, such efforts do not work as well as my morning shower routine. But each time I do it – bold and brazen or just in the imagination – I always feel currents and shudders along the spine that feel to me like I am “waking up.” Usually, I get seconds or minutes of less or no trembling in the right arm. Intuitively, using such intuition as I have, all this feels to me like the very best thing I am doing for my Parkinson’s symptoms.

Anonymous

Why not give this Parkinson’s Disease new treatment some serious attention? There is nothing to lose and everything to gain. Best of all, this Parkinson’s disease new treatment has no side effects. The only expectation is improvement on some level.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease 

 

Dehydration: A Consequence of Hot Weather

Dehydration causes serious neurological problems if you do not take action now. Why ask for more problems?

When I ask people who have been diagnosed with Parkinson’s disease the question “Do you drink enough water” the answer I hear most often is “no.” This is summer time in the western hemisphere. It is already sizzling hot in many places in the US and elsewhere.

Look out if the neural pathways dry out. The neurological system has to be “wet” and “juicy” to function. Toxins stick to the neurons like glue.

I just recorded a new YouTube video to inspire everyone to drink more water because of the problems in the body that are causes by dehydration. Listen right now to get inspired to hydrate your cells. Say “no” to dehydration today.

YouTube player

Find information about the Aquas Hydration Formulas here: https://www.aquas.us

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

 

Mobility Exercises

Many people believe that the solution to mobility challenges is found in finding the right medications or supplements or herbs to take, not with mobility exercises. After an exciting decade of research into the question of what helps people regain excellent mobility, I have drawn the conclusion that medications or supplements or herbs do not offer a long term solution. Something else – something you would have never guessed – does.

I have concluded that practicing the ability to perform more than one task at a time offers welcome benefits to anyone who currently experiences issues with maintaining good balance and also anyone who fears the prospect of falling when walking. Watch my video below to discover mobility exercises that are fun and simple to do.

For information about the Walk with Ease and Confidence program, visit:

http://www.parkinsonsdisease.me

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

Road to Recovery Success

I received the email below which certainly made my day. Reports like this encourage me to continue my research into the various causes of Parkinson’s symptoms and the therapies that help to reverse them.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

Robert:

I have read all your books. They are really great. I have had Parkinson’s for five years now and those books have been my crutch. I don’t take any medication and have done it all alternatively. I have used a lot of your ideas and your books are very motivational. I have reversed a lot of my Parkinson’s symptoms. But there is still a few more to do. I don’t listen to your radio show as the time zone is very different. I’m really honored to be in touch with you. Your books are a lifeline to me.

I also wanted to add that your books gave me hope when NONE was around, the only hope friends and family believed in was the medication!!! I just wanted to let you know the great contribution you have made to our/my world. Your books really helped me when I was right right down . I had family and friends but in reality I was alone but I kept rereading your books and taking   small steps. I just kept trying until finally I felt I was on the road to recovery and that’s where I am now. Thank you from the bottom of my heart. I will recover from Parkinson’s, It’ just finding what needs tweaking for me/you being the car mechanic
😊Catherina

Thank you again.

Gait Disturbance

Gait Disturbance and the Critical Role of New Neural Pathways

I have concluded that after a decade of research, most people believe the way to correct gait disturbances is to keep close watch over the medications and supplements they take. Problems surface when medications (or supplements) no longer work. It is certainly logical to conclude that the problem centers on an issue with the type or dose of medicines.

I disagree with this conclusion.  Even when the underlying causes of a gait disturbance has been addressed and healed (such as clearing out toxins, releasing traumas and eliminating infections) a person is likely to continue to experience gait disturbances. But why is the so?

The body has slipped into some bad habits. The safe and effortless way to move has to be re-remembered. In this video, I highlight a brief clip that demonstrates what one rehabilitation clinic is doing to help the body “re-remember” how to move the right (and upright) way.

Discover the strategies, therapies and programs that will help you Walk with Ease and Confidence.  Register for a membership by clicking below.

sign up 2

For more information about Walk with Ease and Confidence memberships visit:

http://www.parkinsonsdisease.me 

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

Ataxia Gait

No doubt many factors contribute to ataxia gait disturbances, but one plays a central role. Such disturbances (which is a fancy way of saying a person is having difficulty walking) are more prevalent and problematic when a person is multi-tasking. When walking alone and totally focused on the task of walking, ataxia gait difficulties are minor. In contrast, when walking and talking with a friend at the very same time, ataxia gait disturbances can become problematic.

OK. So that is the problem. What can you do about an ataxia gait when you walk? An eloquent solution is to practice multi-tasking with totally fun and engaging exercises that coordinate the intricate interactions between the mind and body. For a suggestion of just such an exercise, watch my short video below.

Discover other strategies, therapies and programs that will convert an ataxia gait problem to rock solid walking in the Parkinsons Recovery online course Rock Solid Walking.

Robert Rodgers PhD
Founder 2004
https://www.Parkinsonsrecovery.com

Parkinsons Shuffle

In a recent Parkinsons Recovery Radio show, Bill Hubert made an interesting observation. People with mobility problems often walk with one long step followed up by a short step. That is to say, the right step is consistently longer than the left (or vice versa). This is described by some observers as a Parkinsons Shuffle. Shuffles can eventually lead to falls.

So much for describing what is a common problem with an abnormality of gait for a surprising number of people. What in the world can be done about this problem?

In this video, Bill Hubert from Bal-A-Vis-X describes a simple therapy that corrects the Parkinsons Shuffle.

What is Bal-A-Vis-X? This is is an exciting program designed and created by Bill Hubert from Wichita, Kansas. I believe his ideas and approach can have a profound influence on the ability of persons who experience Parkinson’s symptoms to find compelling relief.

Do you have difficulty with walking or freezing?

I believe his program offers promise that mobility can be significantly improved.

  • Do you use a walker?

I believe his technology and approach can make you entirely independent again.

  • Do you fall occasionally or often?

I believe his program offers the possibility of reducing if not preventing falls altogether. 

  • Are you currently bound to a wheel chair or fear you will be in the near future?

I believe his program can help you become independently mobile. 

Discover the strategies, therapies and programs that convert problematic mobility to one that is rock solid in the Parkinsons Recovery Rock Solid Walking Online Course.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery

Abnormal Gait

Many persons who have issues walking with ease and confidence engage a battle with stuck muscles. They are determined to make their muscles stop behaving badly! When a war is declared on the delicate tissues of body gait issues become even more problematic. Muscles tighten up. The body becomes as rock solid as the Rocky Mountains.

In the following video, I explain why attempting to “force” the body to move “normally” backfires every time,

Robert Rodgers PhD
www.parkinsonsdisease.me

Road to Recovery

Michael’s Journey on the Road to Recovery

Michael sent me this update on his journey down the road to recovery and gave me permission to post it here along with his email. ”

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

“Hi!

I haven’t written in a long time, so I’m going to jump right in.michael day

Crucial context

It is my experience and my belief from research that the human body-mind is innately curative. As long as there is ample energy (prana, chi) present,
and as long as the body-mind is effectively nurtured and supported in natural, compassionate, and non invasive ways; homeostasis is achieved/reclaimed if… that is ultimately what is meant to occur.

At this point, I can no longer see Parkinson’s strictly as a disease.

For a certain percentage of the global population, the body-mind reaches a critical mass of chronic illness and for these people their breakdown manifests what we call the symptoms of Parkinson’s. What confounds the medical community is that these symptoms display slightly or greatly differently in each person. This is because the critical mass of chronic illness
is never going to be the same in each person.
Unless drugs or surgery are chosen as a response to the symptoms of Parkinson’s…those of us who are dealing with this situation are basically on our own.

 

Five years of rigorous research has revealed a number of natural treatments
that a (usually) small number of people had used to successfully eliminate the symptoms of Parkinson’s. After much due diligence…I felt intuitionally led to try a number of these approaches. So far, each of my attempts to eliminate the symptoms of Parkinson’s have failed. Why…?
I suspect now that the critical mass of chronic illness in my body was too different from the critical mass of chronic illness in the bodies of those who had achieved success and/or…the scope of the particular treatments I was led to choose was not broad or deep enough to respond to enough of my particular array of imbalances to make a difference.
Some of the blogs created by people who have cleared the symptoms of Parkinson’s by natural means often have a statement at the end of their blog entries: DON’T EVER STOP RESEARCHING AND EXPERIMENTING! As long as I am able…I won’t!

 

After reflecting on all the approaches I have tried, a few things became clear.
Each time I decided on an approach, usually after much reading, meditating and prayer, emailing, phone, Skype video interviews, etc… the chosen direction always seemed comprehensive at that time. However, each time I failed, the experience always taught me where my vision had actually been shortsighted. Being careful at these times… to not fall into disappointment, impatience, depression, or self pity…what I learned from each failure
was always what partly led me to the next possibility which was always revealed to be more comprehensive.

 

Where I am now

 

 1. I have just started with a new team: A recently retired neurologist who is also an Ayurvedic physician. A medical doctor who is also an Ayurvedic physician and homeopath and runs an Ayurvedic hospital in India.
I am in an 8 month program utilizing diet, cutting edge nutraceuticals,
very strong herbs, and homeopathics. Both practitioners have much experience with clearing the symptoms of Parkinson’s. The program will concentrate a lot on the brain/gut connection.

 

One of the only real longings I have at this point is to return to India.
I would like to live at an Ayurvedic medical hospital/community for 6 months to a year so that I could undergo 5,000 year old profound restorative treatments. I have been to India twice and it has always felt like my true home and also a place of great healing on many levels for me.

 

2. After 10 months of saving, we can finally purchase a cutting edge machine that produces concentrated molecular hydrogen. Molecular hydrogen produces a hormone called ghrelin in the gut. Clinical trials have shown that increasing ghrelin in the gut has induced remarkable sustainable recovery in many people dealing with the symptoms of Parkinson’s.

 

3. Twice a day, I directly treat my brain by pulsing very strong electromagnets.

 

4. Radiance Healing

Radiance Healing flows into the mind, body and soul on a fundamental level, providing positive effects in all these areas. This energy pours divine light to the soul and gradually dissolves accumulated negative qualities. Over the course of receiving the energy for one year, the energy permeates into one’s system profoundly on the body, mind and soul levels.

 

Healing Effects

Fatigue & Stress Reduction; Improvement of Migraine, Shoulder & Back Pains, Anxiety, Irritability, and High Blood Pressure; Relief from Climacteric Distress; Recovery from Pre & Post Delivery; Recovery from Surgery; Over All Health Improvement & Health Maintenance; Disease Prevention; Relief Allergic Rhinitis & Other Allergic Symptoms; Improving Various Chronic Symptoms; Boost Vitality & Spirit of People with Chronic Fatigue; Raising the Spiritual Conscious Mind.

Currently Researching 

Endobiogeny

 

Current Physical Condition 

It’s been 2 years now since I have been able to leave the condo and take a walk. Thank god 20 minutes on the Chi Machine provides cell aspiration equal to a 1.5 mile brisk walk. I am currently unable to eat, shower, or use the toilet without assistance. Sleeping more than 30-45 minutes at a stretch is rare due to tremor. I have hardly been able to talk for the last 2 years.

 

Typing is almost impossible…this email took a week to complete.
Mentally/emotionally/spiritually:

 

I feel strong…quiet…still totally in love with existence…I feel an ever deepening faith in the infinite mystery of Life. I feel deeply grateful to have been given this life…I am deeply committed to recovering completely if that is meant to be…I spend most nights surrendering totally to the shaking that never stops…the relentlessness of the tremor is beautifully shattering the ego and is taking me me deeper and deeper into the heart…While this journey often scared me shitless last year,I no longer feel fearful of wherever this process is taking me.”

 

Michael Day
mday1008@gmail.com

Theracycle 200 for sale.

Elisabeth is interested in selling her used Theracycle. See her offer below.

Robert Rodgers PhDs
Road to Recovery from Parkinsons Disease

“It’s heavy so hopefully somebody in the San Francisco Bay area  would be interested. There is presently a THERACYCLE 100 on e-bay for $2,700. I would not charged that much. The cycle is in very good condition and we never had any problems with it. If you are interested email me at: elisabethstromberg@sbcglobal.net.”

Thank you again,
Elisabeth

 

Psoriasis

Robert-

I can add to what I wrote you last week that an inclined bed therapy benefit is that it is also slowly but definitely clearing up a stubborn case of Psoriasis I have had for months and months on the back of my legs. Varicose veins in my feet also seem to be improving. Arthur Fletcher talks about both of these conditions as potentially benefiting from Inclined Bed Therapy and that has absolutely happened in my case.

Psoriasis is interesting to me in connection with PD because, like Parkinson’s, the cause(s) are basically mysterious/unknown and the treatment options offered by conventional medicine are often ineffective and have harmful side effects. I wonder if anyone has looked to see if there is any correlation between the two diseases? I had no history of Psoriasis until Parkinson’s symptoms emerged. Maybe just a coincidence?

-Bill

Inclined Bed Therapy for Parkinsons

Now here is a natural, free therapy that may well be worth giving your serious attention. As you can see from the feedback from Bill below. he found it to be useful.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease 

Hi Robert-

For me Inclined Bed Therapy really shows great promise. I have inclined the bed I sleep in for about a week now and have already seen definite improvement in some areas:

  • Deeper, more restful sleep.
  •  Fewer trips to bathroom at night to pee.
  • Reduced lower leg swelling (edema)–this was an early PD symptom for me although I didn’t know it at the time.

I will send you a more complete report in a couple of weeks when more time has passed and I have more experience with this change.

Thank you so much for bringing this idea to my attention.

Bill

Invitation to Join a Support Group for Parkinsons Disease that Focuses on Recovery

The 2016 Parkinsons Recovery Support Group

My new support group has a few slots open. You can join an amazing group of individuals from across the globe who are dedicated to exploring ways that help to reverse symptoms of Parkinson’s. Sign-ups include the bonus of free lifetime access to my new Jump Start to Recovery Course.

Sign Me Up to Participate

I hear countless reports from those of you who have been deeply depressed after attending a Parkinson’s support group. If you have set the intention to reverse your symptoms, it is depressing to connect with others who are convinced their condition is destined to “deteriorate” over time. You know this is not true, but no one else in the support group seems to agree with you.

The 2016 Parkinsons Recovery Support Group will convene for the first time next week and continue meeting once a month throughout the year. The persons who have enrolled in the 2016 support group live in countries across the globe.

We will connect by phone or computer each month at either of two designated times each month. For each of our 12 sessions I will report any new discoveries that have helped people get well. I will then connect with each of you individually. Lastly, I will open up the discussion for everyone to talk with one another. All sessions will be recorded for access at a later time.

Here is the greatest deal ever. When you join the 2016 Parkinsons Recovery support group, you will have the opportunity to enroll in my new online Jump Start to Recovery Course for free. I love the platform I am using to support the course because it offers access not just for a year but for a lifetime. How cool is that?

Some of you may already be registered for the course. Great. If you are not currently enrolled in the Jump Start to Recovery course, I will send you a link to register for free after you enroll in the 2016 Parkinsons Recovery support group.

Since you are located in very different time zones, I have scheduled two times each month for the support group to connect: The last Monday of each month at 12:00 noon pacific time USA and the last Tuesday of each month at 8 PM Pacific time USA. This way, everyone will have an opportunity to meet together for the live, in person programs. Sessions will convene starting this month and continue throughout 2016.

Interested? Registration for the 2016 Parkinsons Recovery support group is a mere $10 a month or $120 for the entire year (which includes free enrollment in the Jump Start to Recovery online course) Click on the link below to enroll.

Sign me up to participate in the 2016 Parkinsons Recovery Support Group

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

Coconut Oil

My name is Wally I’m 23 year old from Australia. My father has been diagnosed with Parkinson’s disease. For the past 6 years we have tried multiple medications; even had surgery where they put a pump to his stomach connected to a needle witch injects him with the medication. Nothing has worked and he is getting worse. I just watched your video about the coconut oil and will get him onto it. Should I just rub his whole body with it head to toe? And make my mum cook food with it?

Thanks a lot

Wally

Hi Wally:

It is exciting to discover there are so many simple therapies that can make a huge difference to people who currently experience the symptoms of Parkinson’s Disease. For the full scoop on how you can use coconut oil, I recommend that you listen to the recording of my  interview below with Dr. Bruce Fife, ND, who – in my opinion – is the “go to” doctor when it comes to any and all questions about the use of coconut oil (whether applying it to the skin or eating it).

I personally love putting coconut oil all over my body after showers and using it for cooking . Food tastes so delicious when coconut oil is used.

May your father see improvements in his health with each passing day.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease
Parkinsons Recovery

 

Invitation to Participate in a Parkinson’s Disease CAM Study

CAM Study

Interested in helping yourself as well as millions of others afflicted with symptoms of Parkinson’s disease? Here is how. Participate in Dr. Laurie Mischley’s CAM study which is designed to identify common traits among those who maintain their health despite Parkinson’s disease. When you join in the study you will help shed the first useful research findings for Parkinson’s Disease after a century of learning little to nothing. You can participate in her online CAM study here:
Participation is one of the best decisions you can make for yourself and others in 2016!

I Have a Parkinson’s Challenge

I Have a Parkinson’s Challenge

By Dwight E. Roth 

When referring to my own Parkinson’s I prefer not to use the word disease.  I do not feel Dwight Rothat dis-ease with my health.   If my symptoms become severe maybe I will use the word, disease.  For the present I prefer to say I have Parkinson’s Challenge (PC) – a summons, a call to learn about the nature of Parkinson’s for others and myself.

People with Parkinson’s (PWP) typically become depressed when diagnosed as having PD by a neurologist.  Many neurologists are not very helpful   — they tend to say upon diagnosis, “Here is a prescription.  See you in three months.”   This is tragic because there are a wide variety of services that benefit PWP.  Most people are not aware of this. When depressed it is hard to look for these resources. Somewhere I read that about forty percent of PWP do not seek any service/treatment after being diagnosed.

When I was diagnosed in January of 2013 I was not depressed but I was frustrated by made my doctor because he gave me only a pharmaceutical prescription.   I wanted more for myself and I wanted to be an advocate for others PWP.   I quickly searched for another neurologist and found one in Wichita, KS.     A few months ago she moved to another state and I found someone to take her place.

  My new neurologist is holistic in her approach to PD and paid close attention  in our first meeting when I said I practice reflexology on my hands and feet (I was trained as a reflexologist by the  International Institute of Reflexology  http://reflexology-usa.net/).   Likewise she was interested in my taking lessons to help my balance through BAL/A/V/X http://www.bal-a-vis-x.com/.    The latter since its beginning thirty years ago has been for youth with special needs.  The creator / director of this program, an older adult himself, a long time professional educator (and in my view mystic/shaman) is beginning to see how  BAL/A/V/X might help in balance problems for people late life. I think that reflexology and Bal/A/V/X are helpful to me –at little cost and no side effects.                                                                                                  

    In my Parkinson Challenge in Wichita I have been served well by physical and occupational therapists.  Of all treatment for my PC these workers have been the most important.  They have taught me the necessity of specific exercises for Parkinson’s – especially use of a treadmill helpful for stamina, stretching, stride/gait, balance, etc. 

One of my occupational therapists (WWSD) seeing my interest in dance suggested I attend the Dance for PD program in Brooklyn, N.Y.  I did so and it was a great experience.  Positive outcomes for PWP who dance in a structured class include: improved motor control, decreased rigidity, increased balance, reduced risk of falling, and improved self-concept. 

Most physical exercise rearranges the neurological pathways.  For me, dance is the best way to do this.  Thus it was that in 2014 I teamed with a professional dancer, Danika Bielek, director of the Bethel College Academy of Performing Arts to create Rhythm Connections – a dance program for people with mobility challenges http://www.thekansan.com/article/20150905/NEWS/150909620.  We have led workshops in five PD support groups in central Kansas.  Additionally, we had our first class at the Academy this fall.  Eight individuals participated in this class that met for ten weeks, one hour weekly.  Danika meets each Saturday at the Kidron–Bethel Retirement Community for one hour.  We have received excellent feedback regarding our work. 

I did not ask for Parkinson’s.  Now, that I have it, as said above, I see it as a Challenge – a call. This summons is to learn as much as I can about PD to help others and myself, especially to create new neurological pathways. https://images.search.yahoo.com/yhs/search;_ylt=A0LEVvqAOHRWUHUAmQwnnIlQ?p=neeurological+pathways&fr=yhs-mozilla-002&fr2=piv-web&hspart=mozilla&hsimp=yhs-002.  Creation of these pathways, help counter the neurodegenerative that is basic to PD.   I want to help PWP to see that they have a responsibility to slow the breakdown of their system of nerves and muscles. 

In my PC I am learning so much about the amazing human brain.  I am meeting wonderful, exciting people – professional health care workers and PWP. 

I realize that my Parkinson’s symptoms could drastically worsen.  In that case I hope I can take the view suggested by Wendy Lustbader regarding the meaning of frailty. She said according to a Sufi idea two curtains separate the individual from the sacred – security and health. If  developed advanced PD after tried all forms of appropriate health care technology and found that I was frail, I hope would exp.erience the sacred in its mystery, wonder, and love.  And, maybe a bit of holy foolery to make others and myself laugh for if  can laugh at something problematic, chances are you have conquered it.

I am becoming interested in teaching ways to improve balance and how to fall to lessen broken bones, especially hips.  Hopefully, I will do so through instructions from Danika and the BAL/A/V/X program. 

 My Parkinson Challenge is expanding.  It is exciting.  It is as if I am receiving a first rate graduate school education where I simultaneously professor and student – somewhere past the borders of academia as we know it.   The PC summons is fascinating.    Sunnum bonum –Mysterium magnum

Sources

http://www.parkinsonsdisease-guidebook.com/

Wendy Lustbader, (1999).  “Thoughts on the Meaning of Frailty”,  Journal of the American Society on Aging.  Winter, pp. 21-24.

Parkinsons Symptoms Relief

Experience Relief from Parkinson’s Symptoms

What is virtually guaranteed to experience relief from Parkinson’s symptoms? Answer: Reduce stress. When stress sizzles, symptoms are bound to flare up. The strong correlation between stress and Parkinson’s symptoms is scary.

What can you do today to experience a reversal of your Parkinson’s symptoms? The answer is clear: Reduce your stress level. How in the world do you accomplish such a formidable agenda?

I have asked countless individuals who currently experience Parkinson’s symptoms about what stresses them out. The most frequent response has been: Dealing with difficult people stresses them out the most.

I took this insight to heart and developed a new online Udemy course: How to Deal with Difficult People. Content of the course provides practical ways to reduce the stress that is fueled by dealing with the difficult people in your life.

Check out my new course! Here is a link that includes a 50% discount on the course tuition.

https://www.udemy.com/how-to-deal-with-difficult-people/?couponCode=how-to-reduce-stress

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

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