Category: Parkinsons Disease Information (Page 14 of 15)

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.

Best Things in Life are Free

The Best Things in Life are Free!!

Good evening Robert,

So I’ve been reading these great books written by a guy named, Robert Rodgers, PhD…have you heard of him?

I was reading about energy healing, amongst a myriad of protocols and treatments suggested. I proceeded to type in a google search: energy healing in Hollywood for free. Long story short…there is a spiritual community that is literally 5 minutes from where I live, and every Tuesday night, they welcome people for 1/2 hr hands on energy healing…cost: zero.

They train these healers and it’s all very legit. So I called, made an appointment and Tuesday night I went. Sat erect in a chair with my hands on my legs. My right hand tremor was very apparent. 10 minutes in, my 4 fingers stopped shaking…my thumb continued. Then, at 15 minutes…my entire hand stopped shaking for the duration of the session, and it didn’t come back till I was outside. Amazing!

The best news is that they suggested me coming every Tuesday night indefinitely!!
Robert, it’s true…

The best things in life are free!!

Blessings, Marsha

Trauma

I’m very sorry I was unable to get to the seminar due to financial difficulty, however, I listened to your radio show on Trauma and believe that it played a major part in my PD

I’m having a little challenge in your website with connecting to the online course. I have purchased 3 of your books, but would like to further my efforts into getting the trauma under control. Is there an access to instructions on your site with a program I can do. Finances have been stretched with medical bills and supplements that its difficult for me to join a therapy program that is expensive. I was going to do Qigong or boxing at a facility but the cost would break me, so I’m doing some on you tube. If you have any suggestions I would appreciate it. I have to beat this……

Trish

Hi Trish:

I have created a 50% discount coupon for the online Jump Start to Recovery course which covers the same topics we just finished working with at the Alderbrook Jump Start program that concluded yesterday. There is an extended section in the course that identifies ways to release trauma. Many of the  methods I suggest are free to do.

I decided to put the content up onto an online course because Udemy (the company that maintains the course) offers a lifetime access. It is the best deal in town to be sure. If you are having problems signing up for the online course,  keep in mind that you first have to sign up with Udemy by entering your email and creating a password. The second step is to register for the course. You can get started by clicking on the link for the course that includes the discount: Jump Start to Recovery Online Course.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

 

Affirmations

Affirmations

Below is an email I received from songwriter Marsha Malamet with a link to an amazing YouTube video which plays one of her songs sung by Barbra Striesand. Take five minutes out of your busy day to listen and watch this video. It worked healing miracles for me.

Robert Rodgers PhD
Parkinsons Recovery

Robert,

I was so pleased that you wrote about Louise Hay. She has been a hero of mine for years. Someone created a video with my song as the soundtrack using her affirmations.This song sung by Barbra Streisand, is one of a few I have written with a spiritual theme to them, that were recorded.
Enjoy!
Marsha Malamet

 

Early Parkinsonism

Below is an email I have permission to post from Larry who is having a quite fascinating journey on his own journey down the road to recovery.

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

Hello, Robert.

In September 2014 a neurologist concluded that I exhibited symptoms of early Parkinsonism, which I understand could well be the initial stages of Parkinson’s Disease (PD). This followed a brain scan that discounted other explanations: tumour, aneurism, stroke. The diagnosis explained symptoms of slowly-increasing severity that I first became aware of some two years (?) earlier.

Those symptoms (mainly evident in my left hand) are declining finger dexterity – speed, strength, and proprioception, the effects of which are difficulty touch typing, tying laces, fastening buttons, using cutlery, etcetera and ad nauseam.

The neurologist concluded this no-hope-diagnosis with the cheerful thought that because I was at the time 74, I would likely die of some other ailment before the PD symptoms became debilitating, and should they worsen, there was always the promise relief by drugs.

Now, one year later, he has decided that because my symptoms have not worsened in the slightest that I don’t have PD after all! In fact, I am remarkably fit for my age. (I played ice hockey last winter and tennis this summer.) As for my “symptoms”, well, he has no explanation.”

Larry

Cause of Parkinsons Disease

Cause of Parkinsons Disease is Multifaceted

After only a few minutes of research, you will encounter one explanation that is offered as the cause of Parkinson;s disease – a deficiency of dopamine. Yes, this clearly can be a factor, but only one among many other factors. Where do you start with a recovery program once the symptoms have emerged?
Most people choose at the beginning to suppress their Parkinson’s symptoms.  I discuss during the radio show the many logical reasons why the is the first choice for most people.
In the program today I recommend pursing another strategy. Why not determine the cause of Parkinson s disease first and then design a treatment program that addresses the cause?
My research over the past decade has revealed many surprising conditions that cause the Parkinsons Recoverysymptoms which include (but are certainly not limited to) toxins, infections, trauma, stress and thoughts that we rattle around our heads that are not conducing to recovery. I discuss all of these issues and more during the radio show today.
I also announce an exciting new Jump Start to Recovery program that will convene at Alderbrook in Washington state November 1st – 3rd. Check out the program details.
Robert Rodgers PhD

Jumpy Hands

Hello Robert: This is all mew to us. My 62 year old fiance has insulin dependent diabetes and severe neuropathy in his feet from the diabetes and he has started having jumpy hands, fingers, legs, and other areas of jumpiness in his body such as his eyes twitching and shoulders jumping and some twitching of muscles. He takes morphine for severe chronic arthritis pain in his low back and tailbone. He takes reglin for diabetic slow stomach emptying. He also takes oxycontin for breakthrough pain. His balance issues was caused form the diabeteic neuropathy which he had way before the jumpey problems started. He did not have the jumpy problems until about 6 months ago and it is progressively getting worse a little at a time but is not severe yet. It is not constant but he does jump and twitch in his sleep too as I have noticed this when he is asleep.

Do you think he has Parkinsons Disease? We are very concerned about this, but he does not I am writing to you as I am very concerned for him. Will Parkinsons take his life and does it cause Alzhemiers Disease which I know can eventually take a persons life. How advanced are the drugs for Parkinsons as far as slowing or stopping Parkinsons Disease? How much and for how long do these drugs slow the progression of Parkinsons Disease? Which drugs do you think are the best on the market to use for Parkinsons Disease. Are their any other disease that this could be besides Parkinsons. Any help you can give me is very much appreciated as I don’t want to loose him as he is my whole life. We both met after we had both gone through bad divorces and have only been together 11 yrs and I would like to spend many more years with him. By the way I am 60 and he is 62. Do you think if he had bariatric surgery for weight loss ( he is about 310lbs and 6 foot 2 inches tall) and we have read that gastric bypass surgery will put the diabetes in remisssion as long as he adheres to the eating program after the surgery for good. I am going to have the surgery and I think it will help him too. Any help or information you can give us is very much appreciated.

Sincerely

Andrea

Response to your jumpy hands question follows ,,,

You have ask a series of questions that involve diagnosing and treating conditions medically with medications and surgeries. I am not the resource who can answer these types of questions which should be addressed to a medical doctor.

From the perspective of a researcher, I have two observations to offer. First, I would recommend that you investigate the side effects of the medications he is taking. Some of his current issues may be due to side effects. Keep in mind there is no research that reports side effects when two medications are used in conjunction with one another, much less more than two medications. The medications themselves combine together to create unreported side effects. Making matters even more complicated, the effects of medications differ depending on the person. Some people can tolerate them. Others cannot.

My second observation to your jumpy hands question is to suggest you take a different perspective. All of your questions address the treatment of symptoms. If you want to be together for another 30 years, think about finding and treating what is causing the symptoms. When it comes to reversing the symptoms of diabetes, diet changes do the trick. Change what you eat every day and you will be dazzled at the result.

Best of luck to the two of you and may you be together for another 30 years.

Robert Rodgers PhD
What is wrong with Me? 
Seven Secrets to Healing

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Depression and Parkinsons

Hi Robert: First of all, let me congratulate you for your nice work. It helps me a lot. though, I have 2 questions I could not find any answer in your blog about depression and Parkinsons.

1. You mention your book relating a few people that have recovered. And you also mention you are a researcher. I wonder if you have some data (bigger than these 11 people) that have completely or almost completely recovered. And where to find these data.

There are actually two Pioneers of Recovery books: A first set and a second set. I used to be a quantitative researcher and did analyses of huge data sets. I decided that was only proving the obvious.

I have switched over the past decade to qualitative or case study research. You get to hear the full story from each person about how they reversed their symptoms. A relatively small number of people are willing to tell their stories, but I can assure you that I hear reports from many people who have been successful in their healing journey. I might add – what does it matter anyway? Isn’t the most important issue for you to find the cause and heal it?

2. Also, and most important, how to deal with the depression related to PD? where to find it in your blog?

On the blog: click on the category listed in the right column entitled “depression help.” The posts that related to depression will pop up.

thanks again for your comments about depression and Parkinsons.
Eneas

You are most welcome Eneas.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery 
Road to Recovery from Parkinsons Disease

 

Qigong and Parkinson’s

Qigong and Parkinson’s

I am committed to a wellness model…I especially am exploring qigong at least 2 hrs/day for the past 10 mo.

I would like to titrate off of my daily 5 to 6 Sinemets (25/100mg) as well as my 1 mg of Azilect. I have limited myself to 4 Sinemets/day the last three. So far, OK.

Also it seems to me that there are stores of dopamine in the body as I take mylast sinemet at 6:30, sleep from 11 pm ’til about 4 am. I do about 90 min of Qigong and feel the most normal. What’s perplexing is that I can feel so good after about ten hours of last sinemet???? Are you aware of why this occurs? …when the 1/2 life, I believe is abou 90 minutes.???? I am grateful for your sharing of what has worked for others.

Blessings, John

Hi John:

Congratulations on your incredible wellness program! Hooray I say!

The thinking about the medication in your question focuses on the effects of medications independent of any other interventions or therapies the person is doing. Your body naturally makes dopamine when you practice Qigong. This is why our ancestors practiced Qigong for thousands of years! It is a tried and true therapy to be sure. I suspect that you are able to take less medication because your body is able to manufacture more of it naturally.

My suggestion for you is to watch my discussion below on the causes of Parkinson’s disease symptoms. As a researcher I have concluded that the causes are many and multi-faceted. If the intent is to suppress symptoms, flooding the body with more dopamine is the standard, tried and true approach that works more often than not. If you are interested in healing from the inside out, the focus turns on a very different journey to discover and treat the causes.

Subscribe to the Parkinsons Recovery Newsletter: http://robert_12.subscribemenow.co

Robert Rodgers PhD
Road to Recovery from Parkinsons Disease

 

 

How to Reduce Medication Dosage

“how do I wean myself off medications with out a doctor?”

The question for how to reduce medication dosage was submitted through My Q&A system available on the main blog at www.parkinsonsrecovery.com. Your doctor prescribed the medications for you in the first place, so you will have to involve them in the process of weaning yourself off of them. The weaning process can take some time, so you will more than likely need your doctor to continue prescribing the medications even though you have made a conscious choice to reduce the dosage.

Many people find reducing the dose very difficult, especially when the reduction that is attempted is too aggressive. Serious side effects can result under such circumstances. The best practice is to reduce the dose gradually and slowly. Give your body plenty of time to adjust to the change.

I think it is always a wise move to involve a compounding pharmacist in helping reduce the dose. They can make medicines that have slightly less in them and monitor how your are doing with the reductions each time the prescription is filled.They will also correspond with your doctor to advise them of the status of your progress to reduce the dosage.

I think it is a smart move to take control of your own recovery plan. Hopefully, your doctor will be supportive of your decision. The people who succeed in their recovery have a full appreciation of the importance of taking full control over their recovery.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery®
Road to Recovery from Parkinsons Disease

 

Causes of Parkinsons Disease

There are many factors that can potentially be the causes of Parkinsons disease. Once you discover the root causes, you are in a position to focus attention on healing the problems that cause the symptoms.

The is a good probability that the causes are toxins or infections or trauma or entanglements in family systems (or some combination of these possibilities). What follows is an email I received from Chris who succeeded in identifying a Lyme infection as the cause of his symptoms. His story is a victory we can all celebrate. Chris is truly a pioneer of recovery.

Robert Rodgers PhD
Founder 2004
Parkinsons Recovery®
Road to Recovery from Parkinsons Disease

Robert,

I wanted to give you and update. I am now a little over a month in treatment of my Lyme disease. My tremors have decreased a great deal but have not stopped. However the tremors are the only symptoms that still exist. I am no longer stiff and arm swing has returned. Simple tests like tapping my fingers shows that my right side has the same speed as the left. This was not true before, the right side was significantly slower.

I FEEL BETTER.

Last week I stopped feeling tired after the Bicilin shots. We believe the spirilia die off has stopped, meaning we have decimated the bacteria that causes the Lyme.

I start Clear Mind Neurofeedback therapy next week to start rebuilding the lost neurons from the attack of the disease.

I am going to continue the bicilin shots for another three weeks along with vitamin IV’s once a week. I am also detoxing heavy metals.

The bottom line is that it will take some time and patience to recover fully but I am making strong headway.

Chris

Difference between Bioenergetic Testing and Standard Medical Tests

Click on the purple arrow to hear Naturopathic doctor  Ivy Faber, ND, answer my question to her on the Parkinsons Recovery Radio show:

What is the Difference between Bioenergetic Testing and a Standard Medical Test?

what is the difference between bioenergetic testing and a standard medical test

Jumpstart

“I have just listened to “Jumpstart”. May I first encourage you to run that “2015 Jumpstart for Australia”; I’ll be the first to sign up.

More important still, I believe you touched on the dominant reason people do not have faith in their ability to recover and take control of their well being.

It is that first, damning “trauma” that accompanies every diagnosis of any form of Parkinson-ism; the inevitable statement in one form or another;

“It is degenerative and incurable, you won’t die of it but you will die with it”

I was diagnosed 5 years ago and have had definite success “following my instinct” in a number of ways; including visiting Dr Walton-Hadlock in Santa Cruz, “medical” QiGong, acupuncture and, not-so-simple-with-tremors, meditation.

It is my certain experience that each advance is reversed by the perpetual “echo” of that statement that I have now heard from three eminent neurologists and read in almost every book and website …”degenerative and incurable”.

You probably know there is a hospital in Putney, UK, that was established in the 19th century to treat neurological diseases. It was called “The Hospital for Incurables” until 1995 when enlightenment struck. The detrimental and counter-productiveness of that name was acknowledged and the name was changed.

Imagine being admitted under the archway emblazoned with with the original name – your “inevitable” fate.

Yet 20 years later no such enlightenment has struck amongst “Parkinson’s Specialists”, the very professionals whose hospital was re-named in recognition of the self-fulfilling damnation of the categorization “Incurable”.

I write in hope that you, a man of influence in the realms of this horrible, life denying disease, be inspired to arouse your multitude of followers, the “patient advocate and support organizations and those medical professionals aware of the values of “alternative” cures and self-motivation, in a campaign to cease and revoke the terms “degenerative and incurable”.

It is 20 years since UK’s “Hospital for Incurables” was renamed “Hospital for Neurological Dis-abilities” . Surely time to bring enlightenment to the neurological establishment by a campaign presenting the facts and recognizing the dreadful harm and hopelessness these terms impose on their patients.

In gratitude for your work.”

Sincerely,

Ian

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