Newly diagnosed. Has anyone bought the Parkinson's Protocol and have any positive results/comments?
thank you,
Newly diagnosed. Has anyone bought the Parkinson's Protocol and have any positive results/comments?
thank you,
I wouldn't be surprised if the "protocol" which makes it sound more scientific and/or impressive has some tips regarding diet and exercise which are helpful, but not anything which couldn't be found on this forum for free.
I may have become somewhat jaded, but I really dislike it when people exploit our desperation and try to sell us their "protocol, " particularly when their credentials appear modest at best and/or they also claim to have remedies for other ailments like diabetes or cancer, etc.
Here's what I learned about Jodi Knapp, author of the Parkinson’s Protocol:
"Jodi Knapp, a health practitioner, is the author of the Parkinson’s Protocol. Jodi is an experienced author who has published many books, and one of her best-selling books on Amazon is about beating type-2 diabetes, and it received a 4 out of 5 ratings.
Besides writing books, Jodi is a neuropathy expert and a health researcher. Jodi believes nature has provided a cure for every disease, and for this reason, she likes researching natural solutions for different health conditions."
Maybe Jodi knows something which has escaped every one of us and every Parkinson’s researcher, doctor, or clinician in the entire world, but I doubt it...
Thank you 🙏
Jim is such a diplomat. "... nature provides a cure for every disease..." If anyone believes that, their problems are worse than their Parkinson's - considering nature doesn't do so well with, oh, let's just throw out a few; MS, PD, ALS, AD, Huntington's, MSA, PSP, Ataxia, and that's just from the neck up, then there is heart, lung, liver, kidney disease, cancer, covid, diabetes, etc.
.
Was just appreciating your entertaining replies in a previous discussion of the subject:
healthunlocked.com/cure-par...
Was also duly discussed and dismissed here as well:
By the way, I should also say welcome to this forum. I feel very fortunate to have found this forum within days of my diagnosis three years ago. At the time, I thought/worried about Parkinson’s disease every single moment of every single day. I have learned a lot from other members of this forum and have been greatly comforted by other members who are going through this experience with me. I hope you gain the same knowledge and comfort and eventually come to know that you can live a very happy and productive life. Parkinson’s Disease has really helped me focus on what matters most in life. I no longer sweat the small stuff. I no longer obsess about past regrets or possible future problems. I live for today...and today I am going to a St. Paul Saints baseball game with my son! Life is good. I was diagnosed three years ago and I feel better now than I did then. Again, welcome! You will be just fine for a long time. 😊
Go for it, man! I like your attitude! Enjoy the game, with your son! Enjoy life, while you can! During the ‘honeymoon’ stage ( First five years, after diagnosis ), I felt the same way! I went to all of my Grandson’s hockey games, and his team won several state and festival championships, so it was a time, of making great memories! Now, a few years later, I have some wonderful memories, to hang onto!! This is a very helpful forum, and I hope you find it as a great source, of information, and support, as I have, over the years!! Welcome!
@jimcaster, way to go with that attitude. Your son will thank you later in life 🙏👍
RKM
Thank you so much! Your words are very encouraging,
Hi Art , welcome to the group.
You may or not have noticed this :
"Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialing emergency services because of something that you have read on HealthUnlocked."
Parkinson's is different for different people , you may not experience what some other person does.
There is a very large library of old posts and information in "Search Health Unlocked " at the top right corner. It is rare that we get a new question that has not already been discussed and filed there. Feel free to ask any question you want though. I was thinking that we should number the various topics and it reminded me of an old joke.
A young man, call him Harry had joined a lodge and went into the bar to meet a friend. It was a very jovial place, a lot of laughing. Then a man stood up and called out "number 46 " and every one there started laughing and pounding the tables. Harry looked puzzled so his friend told him that there were many old jokes that everyone had heard over and over so they numbered them to reduce the time and effort to tell them.
Harry wanted to fit in so he asked if he could tell one and his friend agreed. Harry stood up and said "number 39" . There were smiles but no laughter. Harry embarrassed, asked his friend what happened to which his friend replied.
"Harry some people can tell a good joke and some people can 't.
good luck
Welcome to the forum. Since you have expressed an interest in nonprescription interventions, here are several that are worth your attention. And the information will not cost you anything
• High-dose thiamine, courtesy of Dr. Antonio Costantini highdosethiamine.org/
• Sulfurophane from broccoli seed, courtesy of our very own Albert Wright. Helps with nonmotor symptoms: patientresearcher.com/2021/...
• Mannitol parkinsonsnewstoday.com/202...
• Cinnamon, extensively researched by Prof. Kalipada Pahan, PhD. My report healthunlocked.com/cure-par...
• Ambroxol healthunlocked.com/cure-par...
Hi The broccoli seed looks worth trying. Do you use it and it what form. I have found powders with other healthy looking additions and ready made tea bags. What would you recommend? Much appreciated
I do not use it because I have only motor symptoms. If you choose to use this or any of the interventions you must read up and follow instructions provided at the respective link. Just because these are not prescription does not mean they can be used casually based on a few words from me or anyone else.
We are all different. Everything I have listed I believe it is worth a try if applicable to your particulars. Personally I am using only high-dose thiamine at this time, because of the specifics of my case.
I'm waiting for the Gwyneth Paltrow cure to drop.
I don't know anything about the Parkinson's Protocol, but if you are newly diagnosed and you want to do something to help your self get better then maybe you should also look at doing Fast Walking. I have reversed many of my Pd symptoms and have lived a normal life since 2002 without the need of any Pd medication.
How much fast walking?
You start for a maximum time of ten minutes every second day. You slowly build up to one hour every second day. Here is my storyyoutube.com/watch?v=_QVIdPo...