I want some of those gloves! I am an 82 yr old woman with PD stage 1. I have cardiac reactions to most PD meds which limits my options. This offers so much hope. Thank you.
Thank you Dr. Tass for your ongoing dedication to get the updated model of this glove out to those who need it. I benefit from your prototype and remain hopeful for continued success. Peace and gratitude.
Thanks for putting this on. Been following the PD glove closely. Was paying particular close attention to the Q&A. Hoping and praying for the glove to become a reality and benefit everybody with PD in some way long term as we move closer towards a cure.
Very good and helpful video. I am glad I got the last question answered as I live in Spain and can now hope this device will be available and affordable..I am 6 yrs in, tremor dominant and still med free, 74 yrs old, would be a good test subject but too far away.. keep us informed please
This is updated version of the original presentation uploaded in July 2022. Unlike the old version which contained too much and complex technology details, this video detailed results of latest clinical trials which is more relevant for average patients. Thank you Dr. Mischel and your team for publishing this update.
I came across several similar introduction videos with almost same content. If this therapy really works so well with little or no side effects expected then Stanford team should work for obtaining approvals on fast track and publish time lines for making it available for the PD community world over. Another device called Cue1 invented by research team in South Korea using vibration therapy has already arrived in the UK and expected to reach other countries in few months. Thanks
Whether PARKINSON's Gloves are available for TRIALS in INDIA. I am PARKISON's patient since 2009, Now for the past one year , I have the RLS and high-intensity tremors in both legs and both hands. Are you working on Other body parts tremors also ?? please let me know . I have tremors viz; Head tremors, JAWS tremors make a loud noise of JAWS chattering. I have also tremors at the foot base, which makes me lose balance while walking and also makes, my ankles to fold side wise tending to brake the Ankle joints
If this worked it'd be valued at 10b+. The fact that no medical startup has money to do it fast indicates to me it doesn't actually work yet. If it worked it'd be easy to prove it to people connected to Sergey Brin or Andy Grove and throw 100m at it. Instead we're in year six or seven of a small lab iterating on it. It's not just us in the first world it would help. There are millions of PD patients with no access to meds at all who would benefit from a few hours a week of this. A clinic there could rent it out 24h a day.
Exactly....the Fact that the Michael J fox foundation and the Davis phinney foundation and the national institute of health nor any major PD organizations have not contributed or showed any interest in this treatment is the biggest proof that these vibrating gloves are a scam.
My neurologist, a very prominent Parkinson's movement disorder specialist, is very skeptical about these vibrating gloves. Way too much hype, results not replicable, and too many evasive answers. Also, in my opinion, being that these gloves are non-invasive and pretty much harmless, FDA approval should have occurred long ago if they really worked.
Yes!! You are so right any new idea should be dismissed and never researched no matter the evidence. Especially if it associated with Stanford Univ. or any top ranked university. And all ideas have already been tried and evaluated therefore no reason to look into any new treattments
Ridiculous. Has your neurologist read any of the studies or scientific reviews of this technology? As with many other breakthroughs, the medical establishment will push back hard because it threatens revenues and medicine is ruled by money. Not to mention the pharmaceutical giants that will lose money when this comes out. I’ve done a LOT of reading on this topic and the science definitely backs up the claims. I would agree there is a little extra hype but that’s the way the media works. Your neurologist sounds clueless and is defensive mode.
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I want some of those gloves! I am an 82 yr old woman with PD stage 1. I have cardiac reactions to most PD meds which limits my options. This offers so much hope. Thank you.
Thank you Dr. Tass for your ongoing dedication to get the updated model of this glove out to those who need it. I benefit from your prototype and remain hopeful for continued success. Peace and gratitude.
Thanks for putting this on. Been following the PD glove closely. Was paying particular close attention to the Q&A. Hoping and praying for the glove to become a reality and benefit everybody with PD in some way long term as we move closer towards a cure.
Very good and helpful video. I am glad I got the last question answered as I live in Spain and can now hope this device will be available and affordable..I am 6 yrs in, tremor dominant and still med free, 74 yrs old, would be a good test subject but too far away.. keep us informed please
Yòooooò
This is updated version of the original presentation uploaded in July 2022.
Unlike the old version which contained too much and complex technology details, this video detailed results of latest clinical trials which is more relevant for average patients.
Thank you Dr. Mischel and your team for publishing this update.
😊
Thank you for sharing this !!
There is always hope😊
Good to know the updates thank you for this information dr.Tass
I came across several similar introduction videos with almost same content. If this therapy really works so well with little or no side effects expected then Stanford team should work for obtaining approvals on fast track and publish time lines for making it available for the PD community world over. Another device called Cue1 invented by research team in South Korea using vibration therapy has already arrived in the UK and expected to reach other countries in few months.
Thanks
The company said, that after FDA approval it would hit market mid\end next year in the US.
Does stim on each hand 12:30 happen in sync like mirrored.
Can this glove be used by someone who has had DBS surgery or focused ultrasound for Parkinson's disease?
Dr. Tass also published on the benefits of Neurofeedback for Parkinson's, which has been quite beneficial. Can we hear more about this topic?
This is really something.
how can i get these gloves
Hola, I am in Spain too, near Valencia and on Sinemet. I am very keen to try the gloves and would like to be informed when they can be bought. 👍😃
Made our own glove system. It works. Others are doing the same
Hi Can you please give me details of how you made your pair of gloves? And where you got all the parts from? Thanks
Can you give me info on how to make them?
Whether PARKINSON's Gloves are available for TRIALS in INDIA. I am PARKISON's patient since 2009, Now for the past one year , I have the RLS and high-intensity tremors in both legs and both hands. Are you working on Other body parts tremors also ?? please let me know . I have tremors viz; Head tremors, JAWS tremors make a loud noise of JAWS chattering. I have also tremors at the foot base, which makes me lose balance while walking and also makes, my ankles to fold side wise tending to brake the Ankle joints
We see a reduction in tremors at hour 96 of a FAST
Does anybody know when these gloves will be for sale?
There are DIY videos
Best estimates are late 2024, 2025
i have asked the company they said best est mid/end 2025
If this worked it'd be valued at 10b+. The fact that no medical startup has money to do it fast indicates to me it doesn't actually work yet.
If it worked it'd be easy to prove it to people connected to Sergey Brin or Andy Grove and throw 100m at it. Instead we're in year six or seven of a small lab iterating on it.
It's not just us in the first world it would help. There are millions of PD patients with no access to meds at all who would benefit from a few hours a week of this. A clinic there could rent it out 24h a day.
Exactly....the Fact that the Michael J fox foundation and the Davis phinney foundation and the national institute of health nor any major PD organizations have not contributed or showed any interest in this treatment is the biggest proof that these vibrating gloves are a scam.
@@chinko1953 the mjf Foundation funded coordinated Reset study with Peter Tass
Too many cynics. I appreciate efforts to ameliorate symptoms.
Hi I have PD .Where can i get some gloves so that I can try them out? Thank you.
My neurologist, a very prominent Parkinson's movement disorder specialist, is very skeptical about these vibrating gloves. Way too much hype, results not replicable, and too many evasive answers. Also, in my opinion, being that these gloves are non-invasive and pretty much harmless, FDA approval should have occurred long ago if they really worked.
Yes!! You are so right any new idea should be dismissed and never researched no matter the evidence. Especially if it associated with Stanford Univ. or any top ranked university. And all ideas have already been tried and evaluated therefore no reason to look into any new treattments
Get a new prominent neurologist
Yes, Stanford University is well known for being full of hacks who don’t know as much as your “prominent mds” 🙄
Ridiculous. Has your neurologist read any of the studies or scientific reviews of this technology? As with many other breakthroughs, the medical establishment will push back hard because it threatens revenues and medicine is ruled by money. Not to mention the pharmaceutical giants that will lose money when this comes out. I’ve done a LOT of reading on this topic and the science definitely backs up the claims. I would agree there is a little extra hype but that’s the way the media works. Your neurologist sounds clueless and is defensive mode.
Any approx time for FDA approval?