Which do you choose, Positive Thinking or... - Cure Parkinson's

Cure Parkinson's

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Which do you choose, Positive Thinking or Negative Thinking?

JohnPepper profile image
46 Replies

Are you aware of what is going on around you? Spend five minutes of your time and watch this video:

youtu.be/KpNZoowANNU

Let's change the way we deal with our Pd!

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JohnPepper profile image
JohnPepper
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46 Replies
Scott714 profile image
Scott714

I keep gerrymandering an error message

jeffreyn profile image
jeffreyn in reply to Scott714

Me too (i.e. error message).

moparkie715 profile image
moparkie715 in reply to jeffreyn

Same here. Error message

jeffmayer profile image
jeffmayer

Same here

Kia17 profile image
Kia17

Broken link

andrehypnotic profile image
andrehypnotic

Same?

Dap1948 profile image
Dap1948

Can you repost, John?

JohnPepper profile image
JohnPepper

My apologies to everybody. I cannot find the original email from which I took this website address.

Iam59 profile image
Iam59

Dr. Bruce Lipton on Epigenetics explains placebo and nocebo effects in a simple manner. I agree with him but would like to hear from him more on how to make our consciousness work for us to remain positive. I mean has he any method for us to follow?

Will search YouTube.

Thanks for sharing.

answerseeker profile image
answerseeker in reply to Iam59

Hi Iam59,

There are many scientifically validated simple ways to do this. Here are a few:

Heart Math is a simple practice of recalling a feeling of gratitude, compassion, love. hearthmath.com to have a profound effect on our physiology bringing all of our systems into harmony or coherence which feels great and puts our body in healing mode.

This can also be achieved through what is called Coherent Breathing which we naturally do in meditation, prayer or practices such as Qi Gong, Tai Chi and Yoga.

video.search.yahoo.com/sear...

Also if you google Vagus Nerve you will find, practices that tonify that wandering nerve like all of the above plus walking in nature, laughing, singing, gargling vigorously, and more also lighten our mood and result in our brain cells producing more dopamine to boot. Will see if I can come back with a link. When I did this before I lost everything I had written!

Iam59 profile image
Iam59 in reply to answerseeker

The promptness with which you shared what you thought would be helpful reveals your positive attitude.😊

answerseeker profile image
answerseeker in reply to Iam59

Here's a link which I believe I saw on a previous post on Vagus Nerve stimulation specifically for PD with examples of what can work. My husband and I have been singing more together. What a difference it makes in his posture!

outthinkingparkinsons.com/a...

JohnPepper profile image
JohnPepper in reply to answerseeker

Thanks. I will pass this on to others.

answerseeker profile image
answerseeker in reply to Iam59

heartmath.com/ is the link that works for Heart Math.

Iam59 profile image
Iam59 in reply to answerseeker

Thanks for the links. Will follow

JohnPepper profile image
JohnPepper in reply to Iam59

If you have read my book you will have seen that I now use my conscious brain to control some of my movements, particularly walking, because I shuffle if I don't concentrate on each step; my writing, because I try to write so fast that it is just a squiggle; and bringing food to my mouth, because it falls off the fork before it gets into my mouth.

I hope this helps you!

Iam59 profile image
Iam59 in reply to JohnPepper

Thanks for sharing the method you follow . I too shuffle , can't write at all, typing is difficult and the list goes on..

Planning to visit your blog and any links you might kindly share on using conscious brain, and on fast walking,

I have moved away from carbidopa/levadopa tablets and other drugs. Presently on mucus prurient. The change has freed me of side effects of the PD meds I used to have but tremor, shuffling etc persist. Exercise has improved my condition but I am searching for some method for a permanent relief and cure if possible.

It'll be nice if I could get links or anything you think could help me.

Thanks.

JohnPepper profile image
JohnPepper in reply to Iam59

Hi Iam59. If you contact me on my website - reverseparkinsons.net - it will cost you NOTHING! I will send you a whole lot of videos and some very interesting articles at no cost. This is all too much to place on this HU site

Iam59 profile image
Iam59 in reply to JohnPepper

Thanks for the invite to visit the website. I will.

JohnPepper profile image
JohnPepper in reply to Iam59

I look forward t o talking to you.

Iam59 profile image
Iam59 in reply to JohnPepper

I will. Having a bad PD day today

JohnPepper profile image
JohnPepper in reply to Iam59

Excuse me asking you this. Have you thought of doing fast walking?

Fredzu profile image
Fredzu in reply to JohnPepper

I lift weights for ten machines and recumbent for 60 minutes. I workout for 6 days per week.

I was doing this regimen for before it was diagnosed 3 years ago.

I was running before they made shoes for running.

I would like to run but symptoms like back pain and a knot in my thigh stop my gait. Most of my symptoms do not

keep me from use of the recumbent.

What is my next step, John? To maintain is not an option.

Best,

Fredzu

JerMan22 profile image
JerMan22 in reply to Fredzu

Fredzu, I know you didn't ask me, but here's something to consider. 9 months ago, I was in a similar situation as you are. My main exercise has always been walking ever since I was a kid with a paper route. My cardio health was very good until last year.

At 60, having had PD for over 10 years, I had severe lower back pain to the point that I could barely walk. In addition to the constant pain (both dull and sharp) I had little energy.

A friend that I'd told this to sent me this link to a video, and it's changed everything. Now I can fast-walk up 15% grades, jog when I want to, even sprint across a field. I get my heart up to 80-85% of my max. I fast-walk at least 3 miles a day. I don't want to oversell it, because I know that everyone is different, and this might not be for you. But I'm just passing it along the way my friend did. Good luck!

youtu.be/vG44nMXpTrQ

JohnPepper profile image
JohnPepper in reply to Fredzu

Hi Fredzu. I can only tell you of my experience and you can make of it what you want.

Up until the time I was diagnosed I had been going to the gym for 60 minutes a day, six days a week. After diagnosis, I assumed that being a movement disorder, the more I moved the better it would be. I then increased my gym to ninety minutes a day. I did 60 minutes on aerobic machines and 30 minutes on weight-bearing machines. The interesting result was that my symptoms got worse much quicker during the next two years.

I then stopped going to the gym and started the fast walking program, against my better judgement. My late wife persuaded me to do it. After only four months of fast walking, when I had got up to the one hour every second day limit, my performance had improved by nearly 20% from over 10.5 minutes per K to less than 9 minutes per K. You can imagine how good that made me feel.

In the gym my performance was measured but the settings or the weights on the various machines, while the walking was measured by the clock. I still have one of my log books somewhere.

You make of this whatever you want. It is all up to you!

Fredzu profile image
Fredzu in reply to JohnPepper

As mentioned, I never recover. I work hard with both the recumbent and weights, six days a week. It is boring unless I am at the gym. I don’t know what to do without the working out.

I will try. What will happen?

Fredzu

Iam59 profile image
Iam59 in reply to JohnPepper

Yes. I have. My tremor is bad since yesterday and I am unable to focus on anything. Typing is tough. Using left hand today. Will focus on everything else when I have readjusted my mucuna dosage.

Thanks .

JohnPepper profile image
JohnPepper in reply to Iam59

Hi Iam59. Don't give up until you have really tried everything. Don't try to do too much to begin with. I suggest walking as fast as you can for as little as 5 minutes, if you are able. Less if you are not. Then stick to whatever your started with, every second day and increase that time by no more than 5 minutes every second week.

You MUST give your muscles time to recover from serious exercise.

Iam59 profile image
Iam59

I was able to watch the video.

Thia51 profile image
Thia51

Thank you, John, excellent video!

enjoysalud profile image
enjoysalud

Excellent! I had no trouble accessing the youtube presentation. THANK YOU!!

Happy21a profile image
Happy21a

That’s the way forward😀. Thanks for posting,

Iam59 profile image
Iam59

In the next few days I am going to spend most of my time on HU trying to finish reading ALL your posts. I am sure I'll be benefited. I'm searching for ways to be in charge of my body controlling it by my mind and not through medications.

Iam59 profile image
Iam59

Will try walking a few days after my mucuna dosage is adjusted. Tremor making everything difficult.

Thanks

JohnPepper profile image
JohnPepper in reply to Iam59

Hi Iam59. I don't want to sound like a stuck record but it is important to do the walking properly, in order to get the desired result.

Start walking as FAST AS YOU CAN for a maximum of 10 minutes every SECOND DAY, for two weeks. The add 5 minutes onto the time every second week. Don't do more than 1 hour. I have tried walking longer and more often and in each case, I picked up injuries. The worst was a torn ligament.

Concentrate on each step, if you can, to walk safely.

Iam59 profile image
Iam59 in reply to JohnPepper

I tried and did 5 mins today. Am going to try again every 2nd day. I focussed on placing my feet properly on the floor and walked fast. But right hand tremor gets in the way.

After 5 mins I sort of jogged with my arms raised above my head...for another 2 mins. Felt good.

All this at home.

Your encouragement means a lot.

JohnPepper profile image
JohnPepper in reply to Iam59

Hi Iam59. Well done! I don't understand what you mean by "Got in the way". Do you mean you are conscious of the tremor? If so; try clenching the fists and swinging your arms across your chest at 45 degrees to your torso.

Iam59 profile image
Iam59 in reply to JohnPepper

Hi John

Walked fast for 5 mins every second day ..thats 3 days done.

feel good. Walk consciously placing feet on ground properly. Right arm gets a bit rigid when I try to control tremor.

Should I try to add 5 Mins from tomorrow? That ll be the beginning of 2nd week for me.

Thanks.

JohnPepper profile image
JohnPepper in reply to Iam59

You should walk at each time level for 2 weeks and then increase it by more than 5 minutes every second week!

Well done so far!

Iam59 profile image
Iam59 in reply to JohnPepper

Just saw your other post advising me to walk fast for 10 mins. Will spend this week to try reaching 10 minutes.

JohnPepper profile image
JohnPepper in reply to Iam59

Please be aware that you should only do the fast walking every 2ND DAY!!!!!. You have to give your muscles a chance to recover from strenuous exercise!

Good luck!

Iam59 profile image
Iam59 in reply to JohnPepper

Yes. I am doing fast walking every 2nd day. Aiming at 10 mins this week from 5 mins of last week.

Thanks

mayree_egoor profile image
mayree_egoor

How about both when needed ..... not every person can be and will be so positive all the time (Human natural tendency ) :D

JohnPepper profile image
JohnPepper in reply to mayree_egoor

I'm put to shame!

mayree_egoor profile image
mayree_egoor in reply to JohnPepper

:O I thought that's how it is and that is how it is suppose to be isn't it John ?

JohnPepper profile image
JohnPepper in reply to mayree_egoor

Yes!

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