This is available in Canada. In BC and in Montreal. I was so excited when it was approved here. I live in Montreal so I found the clinic and contacted them. Sooooooooo excited and hopeful I call them to ask about it. They tell me there are no guarantees but it should help. I'm thinking hey let's give it a go. So here I am feeling like I just might have a chance at feeling a little better and being able to walk properly. They tell me it is a 14 week program. Here is where my heart and any hope I had to walk was shattered. It costs $30,000.00 Just another example of the poor being pushed aside. MS stole my lively hood as well. So yah for the well off people. :(
Don't waste your money. It did nothing for me. I had no improvements after the 14 week program. I wish I had listened to others, but I just had big hopes of even small improvements. None.☹
It doesn't work. The clinical trials do not show significant improvements. In fact, I went through the program for 14 weeks. I had no improvements. I met many people from around the world and I didn't meet anyone who was getting any benefit.
i have 2 tbi's from 2 injurys everyone has left me im about to lose my home and ive been denied dissability 6 times I NEED HELP!!!!!!!!!!!!!!! 7-8 PILLS A DAY AINT DOIN IT :(
My MS was finally diagnosed by Spinal Tap in 2016. My primary doctor thought my symptoms was related to diabetics. Needless to say after my new Nuro doctor confirmed, I have a NEW medical team for MS. I have taken Copaxzane Injections, Trysabri IV's,and done the first doses of Ocrevus (next one August 17th) Does not seem to be helping, I WANT in this trial, I live in Boise Idaho.
I have vestibular nerve damage. My symptoms are 9:10 TBI. I am in Australia! I want to be part of the trial. I know they are doing work in Melbourne. Please help!
My MS was triggered by traumatic brain injury I believe. I would be willing to be a part of the trial but I live in Canada I don't know if it's open to people that live outside of the US.
This is available in Canada. In BC and in Montreal. I was so excited when it was approved here. I live in Montreal so I found the clinic and contacted them. Sooooooooo excited and hopeful I call them to ask about it. They tell me there are no guarantees but it should help. I'm thinking hey let's give it a go. So here I am feeling like I just might have a chance at feeling a little better and being able to walk properly. They tell me it is a 14 week program. Here is where my heart and any hope I had to walk was shattered. It costs $30,000.00
Just another example of the poor being pushed aside. MS stole my lively hood as well. So yah for the well off people. :(
Don't waste your money. It did nothing for me. I had no improvements after the 14 week program. I wish I had listened to others, but I just had big hopes of even small improvements. None.☹
US should approve it so people can use it.. FDA just rejected them couple days ago... :( VERY SAD for all patients out there
Why?
It doesn't work. The clinical trials do not show significant improvements. In fact, I went through the program for 14 weeks. I had no improvements. I met many people from around the world and I didn't meet anyone who was getting any benefit.
It’s approved by the FDA for MS patients now!
i have 2 tbi's from 2 injurys everyone has left me im about to lose my home and ive been denied dissability 6 times I NEED HELP!!!!!!!!!!!!!!! 7-8 PILLS A DAY AINT DOIN IT :(
My MS was finally diagnosed by Spinal Tap in 2016. My primary doctor thought my symptoms was related to diabetics. Needless to say after my new Nuro doctor confirmed, I have a NEW medical team for MS. I have taken Copaxzane Injections, Trysabri IV's,and done the first doses of Ocrevus (next one August 17th) Does not seem to be helping, I WANT in this trial, I live in Boise Idaho.
Would the PoNs help with reversing Sensorineural Hearing Loss?
I have vestibular nerve damage. My symptoms are 9:10 TBI. I am in Australia! I want to be part of the trial. I know they are doing work in Melbourne. Please help!
I HAVE GOTTEN NO CARE LIKE YOU SPEAK OF AN NO ONE TO HELP ME
My daughter will be 5 months on the 5th of May can my daughter try this?
My MS was triggered by traumatic brain injury I believe. I would be willing to be a part of the trial but I live in Canada I don't know if it's open to people that live outside of the US.
This does not work for MS! Do not waste your money.
Have you done studies with people who have ALS??
I TRULY WOULD HAVE RATHER DIED
Can this help a Parkinson's disease?
sorry jay
HSDT is focused on making unfair money and that is it! Thanks God, BragarEagel will show their true colors!
Trials have shown that in fact there is no effect. Stop cheating people. You are giving them hope but this device isn't able to help.
Andrea Ant bullshit it works and has been approved in Canada. I think you need to do more research before say stupid shit.
approved in Canada
It is helping me with spasmodic dysphonia.
You are correct, Andrea. Absolutely no benefit after 14 weeks of use. Huge waste of money and time.
This #pons reminds me noisy #telemarketing #advertising of some chip and useless stuff. Hope it will never be on #TV!