There is a big concern with Parkinson’s about dopamine…is it there? is it depleted? is it flowing? This concern about dopamine brings many people to a place of fear and doubt. When doing the Recipe, if symptoms seems a bit worse, fear creeps in and brings along its friend, doubt…is this really working for me? is my dopamine really there? Simple answers: Yes. Yes.
To assist all of you with the simple “Yes, Yes,” answers, I am going to remind you about a study in Denmark from three years ago that says that the brain cells are not dead and the dopamine is not depleted.
As you know, it is the position of Western Medicine that the substantia nigra, basal ganglia, in the brain are dying or already dead leading to a depletion of dopamine in the brain. They say they do not know the cause of this nor can they cure it, so they seek to treat symptoms of Parkinson’s with dopamine enhancement and dopamine replacement medications.
A study entitled, “Myth about Parkinson’s disease debunked,” found that “Scanning the brain of a patient suffering from Parkinson’s disease reveals that in spite of dopamine cell death, there are no signs of a lack of dopamine — even at a comparatively late stage in the process.”
For those of you who have been following this blog for a while or have spent any time with the Parkinson’s Recipe for Recovery®, you know I always have taken the position that the dopamine is not depleted, only blocked, and that the dopamine faucet is turned down low.
In the introduction to the Recipe, I say:
“I do not believe that the dopamine is depleted or gone. I believe that the body has been working in adrenaline mode and dopamine has taken a back seat, essentially, it has mostly closed the faucet and is not flowing at full capacity. It is why I believe the medications cause Dyskinesia – the body is being given artificial dopamine replacements that are not able to fully assimilate into the system and thus cause uncontrollable movement as opposed to controlled movement.
By listening to my body, talking to my body and examining my electrical impulses, I was able to re-open the dopamine faucet. The result was full recovery with 100% pre-Parkinson’s controlled movement.”
In the Affirmations/Meditations/Prayers section of the Recipe, I say:
“The medical profession says that with Parkinson’s, dopamine is depleted in one’s brain and the basal ganglia controlling movement are 60-80% dead. Having lived in a Parkinson’s body and thought with a Parkinson’s mind, and held my firm faith with a Parkinson’s soul, I can tell you they are incorrect. It is why after nearly 200 years, they are no closer to a cure than when they started. Parkinson’s is an electrical problem and they are trying to fix it with chemicals. The dopamine is there, but the flow is interrupted. Adrenaline has taken over, which ultimately leads to dopamine taking a back seat. Just like anything else, after years of operating in adrenaline mode, the dopamine just turns off the faucet.”
Three years ago, a study came out of the University of Copenhagen in Denmark. As you will see, it confirms the Recipe’s view of dopamine being blocked and refutes the Western Medicine view of depleted dopamine and dead brain cells.
In the section of the article entitled “A thorn in the side” the author points out that not only was there no lack of dopamine, but that the theory of “lack of dopamine” has not been established:
“A thorn in the side
Scanning the brain of a patient suffering from Parkinson’s disease reveals that in spite of dopamine cell death, there are no signs of a lack of dopamine — even at a comparatively late stage in the process.
‘The inability to establish a lack of dopamine until advanced cases of Parkinson’s disease has been a thorn in the side of researchers for many years. On the one hand, the symptoms indicate that the stop signal is over-activated, and patients are treated accordingly with a fair degree of success. On the other hand, data prove that they are not lacking dopamine,’ says Postdoc Jakob Kisbye Dreyer.”
Click here to read the entire article yourself.
A few things I would like to mention at this point.
1. This report comes as no surprise as I, and so many of you, are living proof that our dopamine is not depleted. However, it is very exciting that there is three-year-old scientific proof that we have been correct all along.
2. If you are taking medications, please keep taking them. If you stop taking them cold turkey, nothing good will come from that. Click here to read more.
3. To enhance the hope and faith of people with Parkinson’s around the world, I ask that you please send a link to this blog post to everybody who you know and encourage them to send it to others. It is important that people who are filled with fear that their dopamine is depleted and their prognosis is hopeless see this blog post and article. The reason I ask that you send a link to this post instead of just the article is that if people read the article only, it gives them hope but it does not tell them what they can do to recover. If you provide a link to this post, then they will come to the blog and site, see the Recipe, see this wonderful community made up of all of you, and they will realize that a road map to their recovery and other travelers on the path to recovery already exist and have existed for years. Imagine how that will enhance their faith and hope.
“I have the power to heal myself.” And I did.
“You have the power to heal yourself.” Marie did. Pratima did. Betty did. Helen did. Tony did. And you are.
“Together we have the power to heal the world.” And we are. Please send a link to this post to everybody who you know and encourage them to read the post and send it to others.
It is three years after this study was published, and nothing has surfaced to challenge its accuracy. When fear brings it’s friend doubt to the party, have your bouncers, Faith and Hope, show fear and doubt to the exit. They need not ruin your dopamine party.
You are worth it!!!
All my best,
NOTE: We have started a picture gallery. So far, we have over 30 pictures of people doing the Recipe or already fully recovered from Parkinson’s (plus some with their spouses or children). One thing you will see in this picture gallery is what I call the “New Faces of Parkinson’s;” people with big smiles filled with hope and faith about recovery. If you would like your picture included, please email it to me at
Click here to see the picture gallery. Also, the picture gallery is a permanent page on the website. On the computer view, it is under the blue picture at the top of each page, listed as “Picture Gallery.” On the mobile view, click the menu (near the top left of the mobile screen, there are three horizontal lines next to the “F” in Fighting). One of the menu choices says “Picture Gallery.”