PONS available in Canada

[canpark]

The Pons device is available now for treatment in Surrey ( Vancouver) and Montreal. I have had my assessments done and will be one of the worlds first to get this PONS treatment starting on Monday Mar.11th. Hoping for the best. Approved by Health Canada in DEC. For more info go to Neuro site or [e-mail]

regards,

Canapack

[Hidden]

Is this it?

balanceanddizziness.org/hea...

How will this be used exactly in relation to PD?

Art

[enjoysalud in reply to Hidden]

Norman Doidge, MD, THE BRAINS WAY OF HEALING, 2015, addressed the PONS in chapter 7.

PONS = Portable Neuromodulation Stimulator.

If you do not own the book it's worth buying...NEUROPLASTICITY.

Unlike DBS, it's non-invasive and has been experimented on by the military. When my son was DX with PD, I kept waiting for the PONS to be released.

Chapter 2 covers John Pepper.

[PEB69]

That's great news, I have read the book by Norman Doidge where this device is used and quite frankly both of his books are an eye opener and a delight to read, knowing that there are (and have been for many decades) amazing medical professionals that have explored and created these ways of healing the brain. If ever these devices become available to purchase or used in clinics worldwide we will be first in line. Best wishes and luck to you.

[canpark in reply to PEB69]

The processs is with a trained Physiotherapy and twenty minutes at a time with the PoNs device in your mouth. I will dicribe the process as I go along.

Hopefully I will get results like the people in the book!

They have applied to the us and e.u so downunder should not be that far behind, exciting times ahead for all of the sufferers!

I am so lucky to be here in Canada for this treatment.

[enjoysalud in reply to canpark]

I agree, and I am looking forward to you sharing with us the process as you experience it in your treatment.

If you notice improvements and you find the PONS is up for sale to private consumers, please let us know.

Good luck!

Los Angeles, CA, USA

[Hidden]

Please see this press release from the company making the PONS device. They are seeking licensing in the US for the machine to treat balance issues arising from traumatic brain injury. They caution about any future uses for which licensing might be granted. heliusmedical.com/index.php...

[jayb12]

This Pons Devise Did not work for me made my symptoms worse. I met just a few others with PD using the Pons who had the same as my results. Also met many people with MS and they also had very little if any improvements. Only heard of 1 person out of 50ish who had good improvements but did not verify or meet this person only heard of them from the company so not buying it sorry. It is Severely Overpriced.

[vwolff]

You're experience is very interesting and potentially valuable to me. I have used the PoNS Technology, but I used my own version it. The Patent Is available online, I use that as a guide for engineering and assembly of a Neuro modulation stimulator. I have had marginal success in treating my PD using my Device. I use it mostly for meditation, stationary cycling and treadmill walking. As you can imagine this was no small task. I have invested much time and money out of my own pocket to develop a suitable device. I would greatly appreciate knowing more about your experience. What improvements did you notice? Thank you very much.

[canpark in reply to vwolff]

Hi there,

I used the pons device with great success while I had it for 14 weeks

Of my treatments. You cannot buy it yet. I am going to probably use it again but I want to see what my new schedule and the effects of the B1 hdt. And the magnesium L threonate and the mucuna powder with matcha tea. Has on me.

My improvements have been better stamina. No stooped posture and now I go to pd gym classes twice a week and kickboxing three times a week. Great fun!😁😁

[Parkie- in reply to canpark]

Hello Canpark

Where were you able to get this treatment?

You mentioned Montréal, where is it available exactly in Montreal?

Thank you

[canpark in reply to Parkie-]

Hi Parkir,

Go to helius pons web site for all that info. I know that the Montreal clinic has Been working with pep for st least 7 yrs.

[Parkie- in reply to canpark]

Thank you for your reply.

How much did the 14 week programme cost you?

[canpark in reply to canpark]

Thiis is the tough part. It is $ 30,000 for the 14 weeks of treatments. I included 2 weeks of intensive pjhysio at clinic. 2 xc 1 1/3 hr : morning and afternoon, assessment s before during and after. I know of s guy from Australia who took it and is doing another 14 weeks for $ 3400. He has gotten ride of his curved spine problem and posture is better.

[canpark in reply to Parkie-]

Pwp not pep .i don’t have trmors and my kickboxing is better than regular boxing because of the balance factor. I use 9 round kickboxing’s, they arrr rvery wherr.

[vwolff in reply to canpark]

Thank you for your reply. I go to boxing also, I'm headed to rock steady boxing 3 times a week.

May I ask one more question please? Did you go into the therapy with a tremor and did the tremor subside any?

[canpark in reply to vwolff]

I don’t have tremors. Thank god