PoNS Device/Balance Issues/Traumatic Brain Injury

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  • เผยแพร่เมื่อ 2 เม.ย. 2017
  • Michael Yochelson, MD, vice president of Medical Affairs, chief medical officer and a neurologist with MedStar NRH, appeared on WUSA9’s morning show Great Day Washington recently to discuss a new device called the Portable Neuromodulation Stimulator or PoNS™ device. The device is being used across the U.S. and Canada, including right here at MedStar National Rehabilitation Hospital in D.C., to test and see it’s effective with patients who have less severe traumatic brain injury. Talk show host Montel Williams, who suffers from Multiple Sclerosis, appeared in the segment with Dr. Yochelson as well and discussed how effective the device is in helping him with his ongoing balance issues. Those interested in signing up for the clinical trial, to see if you’re qualified, should go to: braininjurytrial.com/en/
    Credit: WUSA9 D.C./Great Day Washington

ความคิดเห็น • 28

  • @christinekenny1583
    @christinekenny1583 4 ปีที่แล้ว +1

    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. :(

    • @ZZ-ol6mp
      @ZZ-ol6mp 3 ปีที่แล้ว

      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.☹

  • @jasonstockman97
    @jasonstockman97 7 ปีที่แล้ว +2

    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 :(

  • @Italy47mp
    @Italy47mp 6 ปีที่แล้ว

    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.

  • @christinejames8044
    @christinejames8044 6 ปีที่แล้ว +1

    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!

  • @Louie200Seven
    @Louie200Seven 3 ปีที่แล้ว

    Would the PoNs help with reversing Sensorineural Hearing Loss?

  • @BabyGangsterIsMe
    @BabyGangsterIsMe 5 ปีที่แล้ว

    US should approve it so people can use it.. FDA just rejected them couple days ago... :( VERY SAD for all patients out there

    • @tommyboy1986
      @tommyboy1986 5 ปีที่แล้ว

      Why?

    • @ZZ-ol6mp
      @ZZ-ol6mp 3 ปีที่แล้ว

      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.

    • @sehrishbalouch7068
      @sehrishbalouch7068 ปีที่แล้ว

      It’s approved by the FDA for MS patients now!

  • @imandecor
    @imandecor 7 ปีที่แล้ว

    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.

  • @jasonstockman97
    @jasonstockman97 7 ปีที่แล้ว

    I HAVE GOTTEN NO CARE LIKE YOU SPEAK OF AN NO ONE TO HELP ME

  • @luckycharmed96
    @luckycharmed96 7 ปีที่แล้ว

    sorry jay

  • @ButterflyVan
    @ButterflyVan 5 ปีที่แล้ว

    Have you done studies with people who have ALS??

  • @privateaccount8882
    @privateaccount8882 6 ปีที่แล้ว

    Can this help a Parkinson's disease?

  • @therealcrystalhughes
    @therealcrystalhughes 2 ปีที่แล้ว

    My daughter will be 5 months on the 5th of May can my daughter try this?

  • @jasonstockman97
    @jasonstockman97 7 ปีที่แล้ว +1

    I TRULY WOULD HAVE RATHER DIED

  • @ZZ-ol6mp
    @ZZ-ol6mp 4 ปีที่แล้ว +3

    This does not work for MS! Do not waste your money.

  • @jamesdodgers4315
    @jamesdodgers4315 5 ปีที่แล้ว

    HSDT is focused on making unfair money and that is it! Thanks God, BragarEagel will show their true colors!

  • @andreaant2723
    @andreaant2723 5 ปีที่แล้ว +2

    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.

    • @mikeb769
      @mikeb769 5 ปีที่แล้ว +2

      Andrea Ant bullshit it works and has been approved in Canada. I think you need to do more research before say stupid shit.

    • @BabyGangsterIsMe
      @BabyGangsterIsMe 5 ปีที่แล้ว

      approved in Canada

    • @barbaraaltman3751
      @barbaraaltman3751 5 ปีที่แล้ว +1

      It is helping me with spasmodic dysphonia.

    • @ZZ-ol6mp
      @ZZ-ol6mp 4 ปีที่แล้ว

      You are correct, Andrea. Absolutely no benefit after 14 weeks of use. Huge waste of money and time.

  • @johnnoot5315
    @johnnoot5315 5 ปีที่แล้ว

    This #pons reminds me noisy #telemarketing #advertising of some chip and useless stuff. Hope it will never be on #TV!