Honestly, a person would receive more benefits from going to a massage therapy session with someone who also does reiki & crystal healing... Why? Not necessarily because the crystals are actually healing but because they just had a full on massage that relaxed the muscles and mind. Add in topping off that massage with crystal healing and placebo effect of the crystals healing when in reality it's the actual massage. It's always helpful to clear a mind and relax a body, release tension, toxin release from the massage, flush out the toxins post massage by drinking water post massage, etc... I personally do not think it's the actual crystals that are healing.
I have been using Taopatch for just over 6 months. My balance has improved and my foot drop has lessened. This has reduced my limping and reduced my lower back pain (probably brought on by the limping). I am no scientist or doctor, so I cannot tell you if the science is real or not. All I can tell you is that it works for me. Funnily enough my neurologist, GP, family and friends all tell me that if something works then I should continue using it. I feel sorry for many who have commented in such a negative way. I truly hope they find something that helps them.
Aloha, I suffer from MS and was Dxed in 1995. I use the generic Copaxane injections since 97 with LDN 5.5 mgs since 2017. I’m working disabled Rr/MS. I started the taopatch starter kit 9 months ago and have had some surprising results. First and foremost the bulging disc in my neck which has need a problem since having a car accident in 2016 is not longer bulging. I had plenty nerve burns to resolve pain but they last only 1-3 months when they’ve worked and none of them stop the hump in my spine. We’ll after a month of wearing a these it’s been gone now for 8 months. Secondly they help me relax a little I’m very high strung from the MS lesions and I’m more relaxed wearing these. Finally foot drop on my left foot has improved by 80%
Just received this today and you have to watch a video before you use. If it doesn't work for you there is a 90 day money back guarantee. I'd say that's plenty of time seeing as how it's suppose to work within 4 hours. We'll see.🤷🏼♀️ I have RRMS and am willing to try since I won't be losing anything but a chance to gain instead. I'll keep you updated.
I am confident that every neurologist would suggest this to his or her patients if it was truly effective. Thank you for bringing attention to the flawed studies involving this product.
Dr's are there to push drugs. They listen to your complaint and prescribe some man made drug. So when something new comes along that is not a drug it automatically is snake oil. Try them for yourself and see. $300 vs drugs being thousands.
Really. How many times a patient will tell their MD of a major change in their health and the doctor shows little to no real active interest as to why.
Oh- crazy you posted this!! I just listened to a podcast and the guest (who has ms) mentioned that he uses the Tao patches and recommended them. I looked them up and couldn't find a price it just said contact the seller for prices. Made me wary. Thanks for posting a review- it's appreciated. We all want help with our insane symptoms that we suffer with daily.
I'm trying it and have noticed an improvement. I have relapsing remitting MS but I also have changed my diet alongside the Taopatch. My experience so far is improved walking and balance. It's too early to tell for sure, but will keep going with it for now 😀
It's a year later that I have come across this site. Just curious,, after a year why are your thoughts on these patches? Are you currently still using them? I hope you still have this email address lol I'd like to know your results. Thank you !
@@AJ-qe1ou hello 👋 I am still using the Taopatch start patches. I have been able to get back to the gym and made much progress with them 😊. I am going to get some more in the new year. I've not had a relapse now in 2 years but have made other changes alongside it too, stress reduction and diet changes
Dr. Beaber - I love your channel, started following you in mid 2021. Against my better judgement I purchased the TaoPatch Pro in 2021, although using credit card points so it was a tad less painful :) I have Lyme, EBV and maybe MS and have abnormal gait, etc. I tried the patch on two separate occasions without improvement. I’m scheduled to see you next week - new patient. I’ll bring the patches for some office frisbee.
Hi, yes I was an early adopter, shelling out $$ for just the starter set, then another set of the more 'advanced' patches. Didn't help me at all, only lightened my bank account. The placebo effect is a powerful thing, even I fell for it. There was no significant improvement. Thank you so much for this video. MS is a prime condition for these pseudo cures.
Got mine today (got the Pro) and will keep the group posted on how i go... it sounds a tad "black magic" and I dont believe it will work (im trying not let the placebo affect get me lol) - i have consistent, persisting disability and it will be interesting if i can walk better, have less nerve pain, see if i can keep my balance etc. I have also a baseline with regular physio for the past two months and will now continue my physio with the Tao Patch and see if there is a difference... for me success would be even a 5% change is symptoms so lets see...
Hello, I'd love to hear an update when you have one. My husband saw an ad for these patches today, I have PPMS and I am sceptical about giving it a try. So I'm doing a little online research and trying to find some unbiased reviews. Would appreciate to hear your opinion, kind regards - Mary.
Currently at the stage of wearing them 24hrs a day. Dx with RRMS and stage 5.5. I have noticed a difference with my balance and walking with all other parameters the same in diet/exercise/sleep. Hopefully that will continue or will begin my Ampyra script.
I am responding to my earlier comment… The patch does not work. It has been nothing but a scam. I have not received a single relief in symptoms. The company banks on the fact you’re going to lose one of the patches and have it fall off in order to void the guarantee. And trust me you’re going to lose one of the patches, it is an expensive waste of money does not work. Don’t fall for desperation.
Its like a solution that was out when I was first dx'ed 23 yrs ago. Big fuss for awhile and it eventually lost popularity....diet is something all MSers should work on.I think good food are vital to being at our best...Really!
Hello dr Beaver, i live in France and I have a sister with MS who lives in Morocco. Is there a way to take an appointment with you and come to see you for a consultation. I have Ms too in my MRI. I have no symptoms only tiredness sometimes. My sister has been using a wheelchair for more than a year. She is badly taken care of in Morocco. I appreciate so much all the information you bring. It is amazing how you care and take it personally. We love you. God bless you.
I have tried these. They seemed to help with my posture. I do have a slight bulge in my disc between C6/7. I don't know if putting the disc there helped because of that. It just seemed that I started standing up straighter without thinking about it. Normally it takes a lot of effort for me to stand up straight. I did have to stop wearing them though because I got what appeared to be burns underneath them. It didn't seem to matter what I did, I would get the burns. Since they never say what the nano particles are or what the discs are made of, it made me a little nervous. Too bad because I did feel more centered when wearing them.
Dear doctor, i follow your videos every week and would like to thank you from your eforts. I have one question (not i case of this video), but what do you know about Lion's mane and eracines A? Can it helps for the NGF? Thank you :)
Unfortunately, Italy has a very extensive record of this type of scams. I'm Italian myself, and I'm sorry this keeps happening. Stay away from this type of "weird and miraculous" products.
Mi dispiace che un italiano (?) si esprima così nei riguardi del suo paese. Di prodotti che vantano capacità miracolose è pieno il mondo, e l'Italia probabilmente è tra i paesi più seri in campo medico.
What about vitamins D and sunlight? Living at 7K elevation and already have had skin cancers. Recommendations? Never heard of Tao patch. Wary of these things as MS has had amalgams, bee stings and more. Need cure and repair too. Old enough to know better. Thank you.
I have tried it for 6 days so far & no change. I did have a few questions & sent them an e-mail & left a voicemail it’s been 3 days & still no word back from Taopatch.
This is because anywhere outside Italy, they don`t require professionals to take courses on their application! In Italy, we are seeing miracles! No one can apply them unless they are medical professionals and have done the courses before applying them to patients. In fact, in Italy, is prohibited for a patient to apply the device themselves.
I plan to publish a video on this next week going over the article in detail. I do think the Harvard study provides the strongest evidence yet that EBV is part of the causal pathway of MS.
Have you read the book fiber fueled on amazon? It’s actually pre biotics that drive probiotics, so there really is no point in taking them unless you are trying to top up slightly. You’d get much more from eating diversity of plants.
Snake Oil when you dig into the studies. I can't smell horse, I can't smell camel, I think I can smell bull? Shameful feeding on people's desperation. I did far more digging a while ago. As ever, the more you dig into the various references and follow them in a forensic investigatory manner a dead-end is reached. Have you followed it as far as the French references? If 'Alternative Medicine' worked it would just be called medicine.
Brandon, You can start by looking at where they were published. utterly discredited predatory Open Access Gold institution for 3 papers. Claiming it is based in NY but actually in Pakistan. Nothing wrong with Pakistan but deceptive. The same umbrella publishing group took a supposed paper by an American Physicist who had had it written by a computer program and listed the lead author as Marj Simpson. As long as the fee demanded was paid, the paper was published without question. An Impact Factor (IF) for a journal is considered v high at 10 (NEJM) and very average at three. Several of the journals were in the 1.5-1.7 range. I couldn't be arsed to check the rest. The lead 'study' cited in their whitepaper is nothing to do with humans, human biology, any type of human disease, and was conducted on plants. NOTHING remotely to do with MS. Then read the language in the abstract. If that isn't a steaming pile of bull designed to try and baffle people with pseudo-scientific sounding words then I don't know what is. When a dish is disgusting, looking at the recipe is insufficient. Looking at the people/methodology to concoct such a recipe is where you need to go. The French Institute? It is not an educational institute as the name implies to a non-Francophile. It is merely an aggregation service. In and f itself it carries no weight. Can you discern any consistency n the referencing system - you will have been told whether it was Harvard, Chicago, APA etc - used to write the hilariously and somewhat grandiosely titled whitepaper? If you have time, and I took a bit of mine, to dig into the cited authors of some of the so-called evidence base you'll be further enlightened as to the complete lack of bona fides of some of them. The fact is that when the idea is BS then attempts to reverse-engineer a supposed credibility base just entail stacking layers of BS upon layers of BS. Products like these are egregiously exploitative of the hopes, fears, and desperation that affects all MS patients at various points. I am not immune to the terror 0f these emotions at times. The utter uncertainty is awful. The idea that you can pay to avoid that is very tempting and the cynicism and utterly immoral act of pretending that, for a large (but hey worthwhile) sum of money the terrors can be fixed disgusts me. Preying on the weak is bullying by any other name. I think I am clear how I feel. The sad fact is that it requires some experience and a healthy level of scepticism to get under the PR gloss. The easy mantra is that 'If it sounds too good to be true, it usually is.' If you need to pay to unlock the secret sauce then there is the ultimate giveaway. Br, Dom @theMSguide.com he
I’m assuming to get noticeable effect you’d need to buy the most expensive it’s the same with buying cbd the strength that you need to receive the effects is expensive and people buy the weaker option price wise and then get upset because they don’t feel a differnce all I’m saying if you going to try this out of curiosity you would need to get the middle to most expensive option to see effects!
Nice video, not sure how the device could work given the spectrum (EM) emitted by the device is already present in nature bombarding the user and a relatively small percentage of the body is affected by the device, so any additional increase would minimal. Btw will you be reviewing devices utilizing electrostimulation?
@@kevineeverhart7869 I've looked at PONs and spoke to the inventors, and I'm convinced this has a much better chance of improving gait than a Taopatch does. These devices are very expensive to test and get into the market. Canada has the only clinic right now.
I’ve tried the light wave patches which are something similar. I think they’re pain patch works really well for your knees it’s called ice wave. I’ve tried their X 39 product which is about $100 it provides some balance improvements (but the product does make my skin look nice) thank you Dr. B
It's a scam so don't waste your money.. If it would have worked moist probably it would have gone viral and the inventor receive a Nobel Prize in medicine.. Both didn't happen!
Don't feel sorry for people. I haven't tried it myself but I know a few people it has worked for. I know a couple of people it didn't work for, but these people said they couldn't drink 2.5 litres of water which I believe is required. Drugs don't work for everyone either.
Dr Brandon Beaber is so smart, thoughful and caring neurologist that it makes me want to have MS when I watch these videos! Just kidding. I have Sjogrens/neuropathy/POTS, and follow this channel regularly in a lack of research on Sjogrens.
@@DrBrandonBeaber there is definitely not :D no channel, no research, and huge unawareness by neuorologists about how often it's neurological. I had 15-20 years only neuro symptoms before developing dryness!
I could tell in the first ten seconds that this was going to turn out to be snake oil. Sure, wearing a sticker is going to treat a neurological condition. Thanks for pointing out the issues with this product.
@@mandograssable Getting your money back doesn't mean it's not a scam you buffoon. It's total nonsense and doesn't work, you are selling bullshit, that's the scam
![[LIVE] : ONE ลุมพินี 79 | คู่เอก "ก้องชัย vs อาเมียร์"](http://i.ytimg.com/vi/WfPSA1A0NHc/mqdefault.jpg)
Excellent video! I've had a few patients try this out - all regret buying this product.
My own mom wasted her money on this
I haven't had any patient's try it, but a few people asked me about it. I figured it was worth researching.
Exactly! It’s BS
Honestly, a person would receive more benefits from going to a massage therapy session with someone who also does reiki & crystal healing... Why? Not necessarily because the crystals are actually healing but because they just had a full on massage that relaxed the muscles and mind. Add in topping off that massage with crystal healing and placebo effect of the crystals healing when in reality it's the actual massage. It's always helpful to clear a mind and relax a body, release tension, toxin release from the massage, flush out the toxins post massage by drinking water post massage, etc... I personally do not think it's the actual crystals that are healing.
Why exactly do they regret these?
I have been using Taopatch for just over 6 months. My balance has improved and my foot drop has lessened. This has reduced my limping and reduced my lower back pain (probably brought on by the limping). I am no scientist or doctor, so I cannot tell you if the science is real or not. All I can tell you is that it works for me. Funnily enough my neurologist, GP, family and friends all tell me that if something works then I should continue using it. I feel sorry for many who have commented in such a negative way. I truly hope they find something that helps them.
Thanks for sharing Michael
Aloha, I suffer from MS and was Dxed in 1995. I use the generic Copaxane injections since 97 with LDN 5.5 mgs since 2017. I’m working disabled Rr/MS. I started the taopatch starter kit 9 months ago and have had some surprising results. First and foremost the bulging disc in my neck which has need a problem since having a car accident in 2016 is not longer bulging. I had plenty nerve burns to resolve pain but they last only 1-3 months when they’ve worked and none of them stop the hump in my spine. We’ll after a month of wearing a these it’s been gone now for 8 months. Secondly they help me relax a little I’m very high strung from the MS lesions and I’m more relaxed wearing these. Finally foot drop on my left foot has improved by 80%
Just received this today and you have to watch a video before you use. If it doesn't work for you there is a 90 day money back guarantee. I'd say that's plenty of time seeing as how it's suppose to work within 4 hours. We'll see.🤷🏼♀️ I have RRMS and am willing to try since I won't be losing anything but a chance to gain instead. I'll keep you updated.
Can you share your input how is it now. I just received it it was recommended by a friend who has implemented since using it ( ms as well).
Can you share your experiance ?
Can you share your experiance ?
Can you share your experiance ?
I am confident that every neurologist would suggest this to his or her patients if it was truly effective. Thank you for bringing attention to the flawed studies involving this product.
Dr's are there to push drugs. They listen to your complaint and prescribe some man made drug. So when something new comes along that is not a drug it automatically is snake oil. Try them for yourself and see. $300 vs drugs being thousands.
Really. How many times a patient will tell their MD of a major change in their health and the doctor shows little to no real active interest as to why.
Oh- crazy you posted this!! I just listened to a podcast and the guest (who has ms) mentioned that he uses the Tao patches and recommended them.
I looked them up and couldn't find a price it just said contact the seller for prices. Made me wary.
Thanks for posting a review- it's appreciated. We all want help with our insane symptoms that we suffer with daily.
Because only trained osteopaths can properly put them on you and give you a therapy
I'm trying it and have noticed an improvement. I have relapsing remitting MS but I also have changed my diet alongside the Taopatch. My experience so far is improved walking and balance. It's too early to tell for sure, but will keep going with it for now 😀
Thanks for sharing your experience.
It's a year later that I have come across this site. Just curious,, after a year why are your thoughts on these patches? Are you currently still using them? I hope you still have this email address lol I'd like to know your results. Thank you !
@@AJ-qe1ou hello 👋 I am still using the Taopatch start patches. I have been able to get back to the gym and made much progress with them 😊. I am going to get some more in the new year. I've not had a relapse now in 2 years but have made other changes alongside it too, stress reduction and diet changes
@@ell86fabulous36 hey, still experiencing progress? anything else you can share with us?
Dr. Beaber - I love your channel, started following you in mid 2021. Against my better judgement I purchased the TaoPatch Pro in 2021, although using credit card points so it was a tad less painful :) I have Lyme, EBV and maybe MS and have abnormal gait, etc. I tried the patch on two separate occasions without improvement. I’m scheduled to see you next week - new patient. I’ll bring the patches for some office frisbee.
Hi, yes I was an early adopter, shelling out $$ for just the starter set, then another set of the more 'advanced' patches. Didn't help me at all, only lightened my bank account. The placebo effect is a powerful thing, even I fell for it. There was no significant improvement. Thank you so much for this video. MS is a prime condition for these pseudo cures.
Didn't you opt for the 90 day full money back guarantee??
Got mine today (got the Pro) and will keep the group posted on how i go... it sounds a tad "black magic" and I dont believe it will work (im trying not let the placebo affect get me lol) - i have consistent, persisting disability and it will be interesting if i can walk better, have less nerve pain, see if i can keep my balance etc. I have also a baseline with regular physio for the past two months and will now continue my physio with the Tao Patch and see if there is a difference... for me success would be even a 5% change is symptoms so lets see...
Hello, I'd love to hear an update when you have one.
My husband saw an ad for these patches today, I have PPMS and I am sceptical about giving it a try.
So I'm doing a little online research and trying to find some unbiased reviews.
Would appreciate to hear your opinion, kind regards - Mary.
Update?
Any update ? 7 months after
Thank you for posting this.
no problem.
I would love a review of FES devices like the Myocycle. Is it worth the expense to maybe stop muscles from atrophying?
Currently at the stage of wearing them 24hrs a day. Dx with RRMS and stage 5.5. I have noticed a difference with my balance and walking with all other parameters the same in diet/exercise/sleep. Hopefully that will continue or will begin my Ampyra script.
hey, are you still experiencing improvement? any other effects you noticed?
I am responding to my earlier comment… The patch does not work. It has been nothing but a scam. I have not received a single relief in symptoms. The company banks on the fact you’re going to lose one of the patches and have it fall off in order to void the guarantee. And trust me you’re going to lose one of the patches, it is an expensive waste of money does not work. Don’t fall for desperation.
Its like a solution that was out when I was first dx'ed 23 yrs ago. Big fuss for awhile and it eventually lost popularity....diet is something all MSers should work on.I think good food are vital to being at our best...Really!
Please begin Coimbra protocol.
I am doing since 8 years ago and all MS sympthoms improoved.
Hello dr Beaver, i live in France and I have a sister with MS who lives in Morocco. Is there a way to take an appointment with you and come to see you for a consultation. I have Ms too in my MRI. I have no symptoms only tiredness sometimes. My sister has been using a wheelchair for more than a year. She is badly taken care of in Morocco. I appreciate so much all the information you bring. It is amazing how you care and take it personally. We love you. God bless you.
I have tried these. They seemed to help with my posture. I do have a slight bulge in my disc between C6/7. I don't know if putting the disc there helped because of that. It just seemed that I started standing up straighter without thinking about it. Normally it takes a lot of effort for me to stand up straight. I did have to stop wearing them though because I got what appeared to be burns underneath them. It didn't seem to matter what I did, I would get the burns. Since they never say what the nano particles are or what the discs are made of, it made me a little nervous. Too bad because I did feel more centered when wearing them.
Djokovic has been using it during his major matches.
Dear doctor, i follow your videos every week and would like to thank you from your eforts.
I have one question (not i case of this video), but what do you know about Lion's mane and eracines A?
Can it helps for the NGF?
Thank you :)
I would also love to hear your thoughts on lion’s mane and other mushroom supplements.
Unfortunately, Italy has a very extensive record of this type of scams. I'm Italian myself, and I'm sorry this keeps happening. Stay away from this type of "weird and miraculous" products.
Out of curiosity, are there certain alternative medical practices which are popular in Italy?
@@DrBrandonBeaber not that I know specifically!
@@DrBrandonBeaberI believe ozone therapy is bigger in Italy than most countries around the world. Still probably not widespread.
Mi dispiace che un italiano (?) si esprima così nei riguardi del suo paese. Di prodotti che vantano capacità miracolose è pieno il mondo, e l'Italia probabilmente è tra i paesi più seri in campo medico.
Io li uso e funzionano. Non è uno scam
Thank you Dr. Brandon ❣️
Placebo effect is very strong - Novak djokovic
This is how I ended up here. I noticed the patch when he changed his shirt and wondered what it was.
What about vitamins D and sunlight? Living at 7K elevation and already have had skin cancers. Recommendations?
Never heard of Tao patch. Wary of these things as MS has had amalgams, bee stings and more. Need cure and repair too. Old enough to know better. Thank you.
My video on vitamin D and MS: th-cam.com/video/W9dAPqjhAwM/w-d-xo.html My video on sunlight and MS: th-cam.com/video/f0DqKB_L6-o/w-d-xo.html
I have tried it for 6 days so far & no change. I did have a few questions & sent them an e-mail & left a voicemail it’s been 3 days & still no word back from Taopatch.
This is because anywhere outside Italy, they don`t require professionals to take courses on their application! In Italy, we are seeing miracles! No one can apply them unless they are medical professionals and have done the courses before applying them to patients. In fact, in Italy, is prohibited for a patient to apply the device themselves.
Dr B, what do you think of the new EBV study? My take is both the authors and the media are make claims way beyond the actual findings.
I plan to publish a video on this next week going over the article in detail. I do think the Harvard study provides the strongest evidence yet that EBV is part of the causal pathway of MS.
@@DrBrandonBeaber awesome! Or maybe the same genetic predisposition is involved in the prevalence of both conditions
Would love a video specifically about supplements for fatigue like Carnitine, coq10, Fisetin
I call BS!!! TaoPatch preys on the vulnerability of MS’rs dying for relief! Excellent video and DEFINITELY SHARING
I use them and they work
Love your videos, do you have any video on the effect of probiotics on MS in particular VSL3?
Have you read the book fiber fueled on amazon? It’s actually pre biotics that drive probiotics, so there really is no point in taking them unless you are trying to top up slightly. You’d get much more from eating diversity of plants.
Thanks for doing this! I considered buying it
Snake Oil when you dig into the studies. I can't smell horse, I can't smell camel, I think I can smell bull? Shameful feeding on people's desperation. I did far more digging a while ago. As ever, the more you dig into the various references and follow them in a forensic investigatory manner a dead-end is reached. Have you followed it as far as the French references?
If 'Alternative Medicine' worked it would just be called medicine.
I couldn't find anything on Tao Patch on MS except these 3 studies, but if you have a link, I'll check it out.
@@DrBrandonBeaber I went all forensic on this 2y ago Was a real rabbit hole. Let me dig about a bit.
Brandon,
You can start by looking at where they were published. utterly discredited predatory Open Access Gold institution for 3 papers. Claiming it is based in NY but actually in Pakistan. Nothing wrong with Pakistan but deceptive. The same umbrella publishing group took a supposed paper by an American Physicist who had had it written by a computer program and listed the lead author as Marj Simpson. As long as the fee demanded was paid, the paper was published without question.
An Impact Factor (IF) for a journal is considered v high at 10 (NEJM) and very average at three. Several of the journals were in the 1.5-1.7 range. I couldn't be arsed to check the rest.
The lead 'study' cited in their whitepaper is nothing to do with humans, human biology, any type of human disease, and was conducted on plants. NOTHING remotely to do with MS. Then read the language in the abstract. If that isn't a steaming pile of bull designed to try and baffle people with pseudo-scientific sounding words then I don't know what is.
When a dish is disgusting, looking at the recipe is insufficient. Looking at the people/methodology to concoct such a recipe is where you need to go.
The French Institute? It is not an educational institute as the name implies to a non-Francophile. It is merely an aggregation service. In and f itself it carries no weight.
Can you discern any consistency n the referencing system - you will have been told whether it was Harvard, Chicago, APA etc - used to write the hilariously and somewhat grandiosely titled whitepaper?
If you have time, and I took a bit of mine, to dig into the cited authors of some of the so-called evidence base you'll be further enlightened as to the complete lack of bona fides of some of them.
The fact is that when the idea is BS then attempts to reverse-engineer a supposed credibility base just entail stacking layers of BS upon layers of BS.
Products like these are egregiously exploitative of the hopes, fears, and desperation that affects all MS patients at various points. I am not immune to the terror 0f these emotions at times. The utter uncertainty is awful. The idea that you can pay to avoid that is very tempting and the cynicism and utterly immoral act of pretending that, for a large (but hey worthwhile) sum of money the terrors can be fixed disgusts me. Preying on the weak is bullying by any other name.
I think I am clear how I feel. The sad fact is that it requires some experience and a healthy level of scepticism to get under the PR gloss.
The easy mantra is that 'If it sounds too good to be true, it usually is.' If you need to pay to unlock the secret sauce then there is the ultimate giveaway.
Br,
Dom
@theMSguide.com
he
Hi, Is there any comparison between Taopatch and bracelets such as Power Energy?
I’m assuming to get noticeable effect you’d need to buy the most expensive it’s the same with buying cbd the strength that you need to receive the effects is expensive and people buy the weaker option price wise and then get upset because they don’t feel a differnce all I’m saying if you going to try this out of curiosity you would need to get the middle to most expensive option to see effects!
I don’t know how these people sleep at night making money off of somebody else’s misery.
I used this product - it had absolutely no effect on my MS symptoms -
Thanks for sharing
Nice video, not sure how the device could work given the spectrum (EM) emitted by the device is already present in nature bombarding the user and a relatively small percentage of the body is affected by the device, so any additional increase would minimal. Btw will you be reviewing devices utilizing electrostimulation?
Do you mean like Walk Aide and Bioness? This is a good idea. I will make a note of it.
I heard something called PONS mentioned this week.
@@DrBrandonBeaber I was thinking more about NeuFit ... but neuroplasticity in general (Journal Articles) would be of interest.
@@kevineeverhart7869 I've looked at PONs and spoke to the inventors, and I'm convinced this has a much better chance of improving gait than a Taopatch does. These devices are very expensive to test and get into the market. Canada has the only clinic right now.
What about relapsing remitting Ms that has progressed to secondary MS I wonder?
I’ve tried the light wave patches which are something similar. I think they’re pain patch works really well for your knees it’s called ice wave. I’ve tried their X 39 product which is about $100 it provides some balance improvements (but the product does make my skin look nice) thank you Dr. B
What are they? And where do you get them from?
I was tempted to buy the Taopatch but I had reservations.
If you do try it, post your experiences here. I would be interested to know. Caveat emptor though.
It's a scam so don't waste your money.. If it would have worked moist probably it would have gone viral and the inventor receive a Nobel Prize in medicine.. Both didn't happen!
Dottore cosa pensa delle onde d'urto radiali?
Looking for a neurologist, where are you located?
Cosa consigli per i pazienti con sclerosi multipla che hanno problemi a camminare, gambe pesanti e soprattutto la destra rigida. Grazie
Terapia con tao patch pro
Vai da osteopata specializzato a riguardo
Txs! Does it have any side effects besides high cost? I ll try anything that doesn't have side effects, wether benefits r placebo effect or not 😀
You better try uvb light
@@arr2820 I ll look into it. Txs!
Umm. Absolutely scamtastic! I feel sorry for anyone who got taken by this. :(
Don't feel sorry for people. I haven't tried it myself but I know a few people it has worked for. I know a couple of people it didn't work for, but these people said they couldn't drink 2.5 litres of water which I believe is required. Drugs don't work for everyone either.
Can you do video on UvB light therapy for MS?
I do have a video on sunlight and MS: th-cam.com/video/f0DqKB_L6-o/w-d-xo.html
Dr Brandon Beaber is so smart, thoughful and caring neurologist that it makes me want to have MS when I watch these videos!
Just kidding.
I have Sjogrens/neuropathy/POTS, and follow this channel regularly in a lack of research on Sjogrens.
Thanks. I'm sure there is a sjogren syndrome channel somewhere out there.
@@DrBrandonBeaber there is definitely not :D no channel, no research, and huge unawareness by neuorologists about how often it's neurological. I had 15-20 years only neuro symptoms before developing dryness!
I would definitely give this a try. My most miraculous supplement is CBD oil.
I use CBD oil. It somewhat helps with anxiety and barely with muscle spasms.
Cosa consiglia dottore per migliorare equilibrio ,rigidità alle gambe?Grazie
It's a piece of plastic, an Italian judge has already expressed his opinion.
I could tell in the first ten seconds that this was going to turn out to be snake oil. Sure, wearing a sticker is going to treat a neurological condition. Thanks for pointing out the issues with this product.
Fascinating the world's most successful tennis player swears by it. Or is he only testing it?
i don't know it's work or not but novak hard to keep balance in wimbledon final and fall down multiple times which i had never seen before
@@hynguyen3213 true ;)
I think this is proven to do one thing. Separate money from your wallet. Nice of them to do research proving the placebo effect is alive and well.
😆
You think. They work tho
It's a scam, simple
Nothing with a 90-day money-back guarantee is a scam. Nothing to lose.
@@mandograssable That's literally the worst excuse i've ever heard for a scam
@@devidia If you get your money back what did you lose?
@@mandograssable Getting your money back doesn't mean it's not a scam you buffoon. It's total nonsense and doesn't work, you are selling bullshit, that's the scam
I use them. They work. It’s not a scam. You have to place them correctly tho and only a trained professional can do that.