This channel has become one of my favorite and trusted sources on UA-cam for neuropathy information and support. Thank you for all you do to inform and help people with neuropathy. 🙂👍
Ive become a « cave dweller » five months ago after an angioplasty procedure which resulted in massive nerve pain. I already suffered from mild peripheral neuropathy which after the procedure worsened on a daily basis. I’m watching your videos and hopefully learn from them
Good morning, Jose. Well, kudos to you for realizing it because now you'll be able to make changes to your life to improve your health. Let me know if you have any questions or need any guidance. We're happy to help. Blessings.
After about my third ablation procedure, I started feeling a numbness in the last two fingers on my right hand. This translates into pain in my stomach when I eat. It's a pretty miserable feeling. I watched a good video last night on digestive problems and nerve pain and I need to watch it again to record all the recommendations she presented. All I have to do it find it again...
Be encouraged, with time you will get better... I had a procedure done after a massive blood clot that went from the centre of my lower back to my lower leg and I have already suffered from neuropathy from my knees down to my toes, no feelings only pain... however, I was able to curl my toes just a little bit but lost it after the procedure.... I am taking B-1 and other nerve healing supplements and I must say I can now curl my toes further than before and for the first time, I can hold them in a curled position... it does take time, but some healing is possible... don’t give up, be patient and I pray for your recovery 🙏🌹💕
Good morning doctor question pins and needles ever go away and when you have peripheral neuropathy what nerves repair first like the ones on feet’s , hands, back, neck etc thank you
I believe I suffer from attention deficit disorder. Trying to deal systematically with my peripheral neuropathy is proven quite difficult for me. Are there any please I can receive systematic training to treat my neuropathy on a daily basis so I can consistently comply with all the recommendations the nerve doctors make for healing. maybe some sort of a health retreat geared towards people who suffer from DPN Specifically?
Hi, what about small fiber neuropathy? Developed from a nerve surgery in my arm. Causing all sort of issues with my body . Non stop burning , can’t control temperature,waking up in the middle of the night sweating and burning . Pots , inflammation etc. any help for me ?
Flax seed oil and hemp oil - good or bad? They are put in a positive light, yet they are seed oils. Confused when they say seed oils are bad. I have neuropahy in feet. In retrospect, the ti gli g and temperature insensitivity started in my 30s and i didn't know what it was. I drank lots of oj back then... now on healthy keto, feet hurt. Thank you so much for all this valuable information!
I eat plant based, I noticed about two months ago I was getting pins and needles, burning, numbness in my feet, legs , and insomnia…i first thought it was from my new hip replacement, but then I noticed it happened after I had a little salt or something small from processed foods, like a once a week veggie burger.. I stopped all processed foods, started taking magnesium before bed, and the difference is amazing, I would say it has improved 80%…. Watch your diets, and walk in nature and getting sunshine…
@@hugmc if I had anything processed and salty let’s say like a potato chip my legs would give me neuropathy pain.. I do have salt , but not processed foods anymore
My most sincere congratulations: as an epistemologist and expert in science lobbyism, I really appreciate your careful analysis of the available evidence with a special attention to the impact of extra-scientific dimensions in the production of medical studies. I wish more doctors were aware of the enormous influence of big pharma on the biomedical ecosystem (from their funding of enormous research projects and sometimes entire university depts, to sponsoring of scientific journals and conferences, as well as the production of medical handbooks, educational programs, and strong interference with scientific soities and policy-making). Thanks! Bless you all (the cute big dog included : )
btw I came across your channel because I have been myself dealing with pudendal neuralgia causing severe constipation and numbness - this was caused by the strong sedentary life during the lockdowns which caused my tailbone to retrovert + fungi infection + plausibly spike neurotoxicity (not vaccinated, but got COVID twice and the symptoms appeared after the first infection and exacerbated after the second one). I have been searching for help, since doctors were only prescribing me laxatives, but I knew this could not be the entire story, since I had enormous difficulties in stay seated for a long time). I diagnosed myself by studying a lot and gradually got better through rehab exercises, vit. B etc.. - in sum, all the advices that you give (plus a lot of prayers () : ). Thank you again!
Hi Barbara. Wow, I have the greatest amount of respect for you as an epistemologist. We work extremely hard to check and cross check all of our data and that includes not just the studies but also who funded the studies. I'm sure you know, as well as we do, that whomever the funding comes through will greatly influence the outcome of the study. It's our motto that people do not need to hear our opinion, they need our objective expertise. There are far too many people (both professionals and non-professionals) who may be well-intended but are driven by their ego which distorts the information. Welcome to the human species...damn ego (lol). Anyway, thank you so much for recognizing and acknowledging the lengths that we go to. Truly appreciate it. BTW...our Big Girl (dog) is Brandy. We rescued her from the streets when she was about 9 months old and 35 pounds underweight and on the verge of death. She is the sweetest girl. She loves other dogs, people, children and all of her feline brothers and sisters. Blessings.
Hey Barbara. Ugh! Pudendal neuralgia is a beast. I'm so sorry you're dealing with this. Good for you for not getting the vaccine. It's amazing the amount of damage those spike proteins can cause because they're lab created and our body is still learning how to deal with them. It sounds like you're doing a great job getting a handle on this situation. If you hit a roadblock, you may want to consider adding in photobiomodulation. In your case, I would only do it if you're at an impass because it is costly. Also, don't forget to upregulate the mitochondria. Let me know if you need any guidance. Blessings.
@@NerveDoctors Indeed... I also put together a sort of metareview on the topic with other colleagues, which we handed over to politicians at all levels in Italy, in order to possibly avert compulsory vaccination, unfortunately in vain (I "had" to get Covid-19 in order to avoid the vaccine)...
Hi Hunter. Haven't heard from you in a while. Nice hearing from you. The brands that I like are: Pure Encapsulations - Benfomax Doctor's Best - Benfotiamine 300 Blessings.
@@kuldeepsingh-xl4zo I never found out what my problem was exactly. It’s been about a year and a half now and I only ever have intermittent symptoms in my hands and feet these days but it’s mild. I used to have it severely all over my body. What helped the most was just living my life and not letting the pain define me or control me. Cleaning up my diet and staying active has also been incredibly beneficial.
Hi there Doctors - Question why are the many , varied and sometimes weird symptoms of neuropathy so poorly documented? For example I have feelings that my feet are trussed up with invisible wire / very tight elastic bands or that something is stuck to the balls of my feet. Symptoms like this rarely get a mention - leaving the sufferers to feel like they are losing their marbles! I recently joined a PN forum - only to get a collective gasp of relief at talking about problems which I thought were unique! Doctors need to share this type of info more widely. I am writing to you because you hold out hope for sufferers who find themselves stumbling blindly through a maze of misinformation. Can you please help? Gill
Hi Joseph. The problem with tuna (whether it's canned or fresh) is that it's very high in mercury levels because of all of the pollution that has been dumped into our oceans for many, many decades. So, I would definitely stay away from Tuna.
Ever had any patients with femoral nerve neuropathy? When I started feeling my symptoms I was feeling it right in my hip flexor area on both sides and right above me knees caps into my lower thighs. I feel it mainly above the knees now and not so bad in the hip area but I do have my days. Almost a numb and weak type sensation. That along with my calves with twitching, feeling numb, tight etc. Meant to ask you this awhile back when we were talking about some things with me. Thanks in advance. Keep up the great content!
Hi Hove. Yes, we've treated cases of femoral neuropathy. It's important to make sure there's no nerve root compression, which is commonly the case, especially with spastic muscles, especially hip flexors. We've usually found with these cases if a person has had it for 6 months or less, they do well with the nerve support formula along with stretching (low back and hips) and physical therapy. If the condition has persisted longer, often they also need to incorporate IR treatment, as well. Thanks so much for your kind words and will do our best to keep the content coming. Blessings.
@@NerveDoctors thank you very much. You're responses and in-depth ones at that to everyone's comments is truly heart warming and much appreciated. I have never seen anything like it on UA-cam in 20 years. Doing gods work. From the bottom of my heart....Thanks again ❤️
Indigenous tribes vit d levels are about 70 so that’s prob what we should shoot for. The measured inactive vit D actually still binds to vit D receptors, just at much lower affinity. So levels matter. Study shows high levels correlate with more tooth problems
Water kefir may have quite a bit of processing. I haven't looked into this in great detail. However, if it were me, I would stick with regular Kefir (unsweetened...ie, no added sugars) or flavors.
Hi Rose. I put my patients on a few things to help with their pain: Phyto Ultracomfort and boswellia (both by Pure Encapsulations) and also Protease (by Transformation Enzymes). Natural supplements for pain relief aren't as potent as pain medications, which is why we have to use a few for nerve pain. On the upside, they don't have the dangerous side effects. Blessings.
I'd rather have the pain than take a pain killer that hurts kidneys. The pain tells me what to do maybe eat something different next time. But I don't really know how that works...
Hi Doc, I recently discovered your channel and I am already a big fan 😊❤ Do you recommend pqq for feeling heavy in legs especially going upstairs or poor circulation in general. I also have varicose vain problems?! Many Blessings !!! Star from Canada
Thank you so much for following us. Welcome to the family. Yes, I highly recommend PQQ. It's great for helping the mitochondria in your body regenerate. For varicose veins the best supplements will contain a combination of Pycnogenol, nattokinase and/or horse chestnut. For circulation I like formulas that contain Butcher's broom, Gotu Kola and/or Ginkgo leaf. Hope this helps. Blessings.
Good night Dr I am 52yrs from April 2020 till now crawling,biting all over me, late last year all that stop, and burning start , it’s too much to Tex , wish I could talk to u directly 🙏🏿 I’m DAS I’m on Gabapentin but not helping
Hi, Debbie Smith, After COVID, we saw the need to reach people globally. As a result, we went completely online to help our patients no matter where they live. If you would like to speak with a doctor, we recommend scheduling a consultation. To schedule a consultation, purchase our at-home kits, or any of our other products to facilitate nerve repair, you can visit our website at nuphoria.com. Simply choose the product or consultation you want, add it to the cart like you normally would, and make sure when you enter your shipping address you change the country selection from the US to the country you're ordering from. Otherwise, your order will default to the U.S. Let us know if we can be of further assistance.
Not sure I agree with sunscreen but this is good info. I would recommend staying far away from seed oils as ever since I’ve stopped consumption of them and switched to a healthy animal based diet, I can stay out in the sun for up to 10 times longer than I used to once a based tan is established.
Hi, new here! Does use of Gabapentin for neuropathy after brain surgery inhibit nerve regeneration? In a chair now and trying to learn to walk again... (can stand but spasticity and rigidity).
Hi Lulu. Gosh, I'm so incredibly sorry you're going through this recovery. Gabapentin has so many deleterious side effects. And, yes, it can slow nerve recovery. If you absolutely don't need it to control the pain, I would certainly have your doctor remove it.
@@NerveDoctors Thanks for your reply. They tried for almost 2 weeks in Physical Rehab but the pain was unbearable. I take as little as I can, which is said to be below average for my issues.
Hello Dr, is there any relationship between acetyl-l-carnitine and TMAO, and it’s impact on cardiovascular health? Can you please give me your take on this. Is l-arginine of use in NO production or is l-citrulline sufficient? If yes, at what dose? What’s your opinion on NAC? Thank you
Hi there, EOH. it’s always great hearing from you and you ask the best questions. First, let’s start with L-Arginine. Oral supplementation of L-Arginine will not increase nitric oxide (NO) levels because L-Arginine must pass through the liver for metabolism. The liver then breaks it down and leaves nothing for NO production. On the other hand, L-Citrulline bypasses the liver. It then gets converted to L-arginine which then converts to NO. So, L-Citrulline is always the AA of choice to increase NO levels. Next, let’s talk about Acetyl-L-Carnitine and TMAO levels. A report was released (by Big Pharma) to news affiliates that ran news stories stating that carnitine (found in red meat) may react with certain gut bacteria in certain individuals to promote a compound (TMAO) that could then cause heart disease. What they failed to disclose was that this so-called report was based on a sub-study of 10 people (are you kidding me?! 10?!). The results in the report were obscure and lacked concrete reproducible evidence. Now, the Mayo Clinic performed a meta-analysis study that looked at 3600 patients (not 10) taking L-Carnitine/Acetyl L Carnitine and found huge cardiovascular benefits. I’m going to include the link here which outlines what I’ve just discussed. It should help clarify a lot for you. bit.ly/3HjJZRm I know there were a couple of points I didn't answer. Please shoot them over to me again. This response is getting too long (lol). Blessings. p.s…Keep the questions coming! I love it!!
I can’t go workings because my spine don’t allow.😢I’m taking med for the diabetics and navy tabs for pain and I’m so much afraid of stuff I take. It’s absolutely against of u say and now I’m petrified. I can’t even walk a 1/3 . Really need so much help cause the docks here não quer less.😰😰😰😰
The worst thing you can do to slow down nerve recovery is to stop exercising, even if it’s uncomfortable. Unless you’re getting enough blood flow to your nerves, they’re not getting enough nutrients to heal. Exercise is the #1 thing you can do to live healthier and longer.
Hello. So we know that sleep is crucial for healing but what I haven't been able to find is a way to get a good night rest when the pain kick in every time after 4-5hrs of sleep and I probably need 10-12 with my cfs/me along with neuropathy. I wont be taking pain meds as I figured out (been 4-5 y on all kind of meds:pregabalin, amytriptilin, taita...) they do more damage. Is there a solution to this. Ive been trying all standard things like benfo, ala etc but nothing touches the pain.
Hi Marko. The first thing that is important to realize is that none of the critical ingredients are for pain relief. They support nerve repair and regeneration. For my patients, I place them on a combination of Boswellia, Turmeric and protease enzymes. This will not get rid of the pain completely but usually helps bring it down.
Good morning Doctor, 49 year old male and I’ve reduced my A1c from 12.5 in August 2022 to 5.5 as of yesterday. My question is, I was diagnosed with Treatment Induced Neuropathy (Insulin Neuritis) in January. I take R-ALA and Benfotiamine daily. The burning, cold and hypersensitivity has great reduced…yay. However, I’ve noticed for the last 5 days, a buzz/cat purring sensation on the bottom of my left foot. No pain, pins and needles or tingles…it’s a vibration. 20-25 seconds of buzz and 50 seconds of no buzz..all day for 5 days now. Neurologist and PCP seem to think it’s nerve innervation and healing. At my request, we did a comprehensive exam for muscle weakness etc..no issues. MS came to my mind but they both said no MS symptoms are present. Does this makes sense with peripheral nerves? It’s only my left foot.
Yes, it makes complete sense. First of all...congratulations on a job well done. Down to 5.5...THAT'S FANTASTIC! You should be very proud of yourself. That took significant lifestyle changes. You did great by taking the R-ALA and Benfotiamine but you need to add Methylcobalamin, Pyridoxal 5 Phosphate, folate and acetyl l carnitine to the mix. This should get you the rest of the way across the finish line and quiet those sensory nerves (that's what's causing the buzz-like sensation) Blessings.
hi I would like to know how did you reduce your A1C from 12.5 to 5.5? do you mind to share your secrets thank you in advance. Kudos to you for the wonderful work !
@@ThanhNguyen-ml8pz No bread, ice cream, pasta, soda, candy, and alcohol since August 2022. I eat fish steak, greens, Leto oatmeal (7 net carbs) and eggs.
Would you happen to have another recommendation on vitamin D3 together with the vitamin K supplement, the link you provide is broken 😟😟. Oh man.. I am already taking so many different kind of supplements including nuphoria gold and blue that this is getting kind of tedious.
Hi Yvonne, Our Nerve Defense formula ingredients are listed here: nuphoria.com/collections/our-products/products/nerve-defense-vital-nerve-protection?variant=47171923850 If you have any issues feel free to call our customer support line at (844)-400-0101
Go to the top row far right , click settings wheel, scroll halfway down ,click on speed and select 0.75 .That will give you an easier speed to listen to
I have learned so much from THE NERVE DOCTORS that a thank you is not enough. So may the Heavenly Father GOD Almighty Bless you both.
Thank you so much. Truly appreciate it!😊
This channel has become one of my favorite and trusted sources on UA-cam for neuropathy information and support. Thank you for all you do to inform and help people with neuropathy.
🙂👍
Excellent video. Thank you and God bless you.
Hello Dr. is a prostatectomy considered a neuropathy causing surgery?
Ive become a « cave dweller » five months ago after an angioplasty procedure which resulted in massive nerve pain. I already suffered from mild peripheral neuropathy which after the procedure worsened on a daily basis. I’m watching your videos and hopefully learn from them
Good morning, Jose. Well, kudos to you for realizing it because now you'll be able to make changes to your life to improve your health. Let me know if you have any questions or need any guidance. We're happy to help. Blessings.
After about my third ablation procedure, I started feeling a numbness in the last two fingers on my right hand. This translates into pain in my stomach when I eat. It's a pretty miserable feeling. I watched a good video last night on digestive problems and nerve pain and I need to watch it again to record all the recommendations she presented. All I have to do it find it again...
Be encouraged, with time you will get better... I had a procedure done after a massive blood clot that went from the centre of my lower back to my lower leg and I have already suffered from neuropathy from my knees down to my toes, no feelings only pain... however, I was able to curl my toes just a little bit but lost it after the procedure.... I am taking B-1 and other nerve healing supplements and I must say I can now curl my toes further than before and for the first time, I can hold them in a curled position... it does take time, but some healing is possible... don’t give up, be patient and I pray for your recovery 🙏🌹💕
The cat is awesome!
Thank you Doc 😊😊😊
Good morning doctor question pins and needles ever go away and when you have peripheral neuropathy what nerves repair first like the ones on feet’s , hands, back, neck etc thank you
I love this also can you do a video on nerves detox and how many days can we start with
That's a great suggestion
Good video !
Hey there, Tim. Happy New Year. Thank you so very much! Blessings.
Awesome stuff!!!
Glad you enjoyed it.
I believe I suffer from attention deficit disorder. Trying to deal systematically with my peripheral neuropathy is proven quite difficult for me. Are there any please I can receive systematic training to treat my neuropathy on a daily basis so I can consistently comply with all the recommendations the nerve doctors make for healing. maybe some sort of a health retreat geared towards people who suffer from DPN Specifically?
You are awesome. Thank you
Thank you so much. Truly appreciate it!😊
Does that re-routing of supplement nutrients, does that include magnesium malate capsules?
Yes it does, unfortunately. Blessings.
Vitamin d or vit d3? Whats the diiference?
Oh goodness, where were you 11 years ago when I injured my back and found out that I had degenerative disk disease, neuropathy, and fibromyalgia
Hi, what about small fiber neuropathy? Developed from a nerve surgery in my arm. Causing all sort of issues with my body . Non stop burning , can’t control temperature,waking up in the middle of the night sweating and burning . Pots , inflammation etc. any help for me ?
Flax seed oil and hemp oil - good or bad? They are put in a positive light, yet they are seed oils. Confused when they say seed oils are bad. I have neuropahy in feet. In retrospect, the ti gli g and temperature insensitivity started in my 30s and i didn't know what it was. I drank lots of oj back then... now on healthy keto, feet hurt. Thank you so much for all this valuable information!
I eat plant based, I noticed about two months ago I was getting pins and needles, burning, numbness in my feet, legs , and insomnia…i first thought it was from my new hip replacement, but then I noticed it happened after I had a little salt or something small from processed foods, like a once a week veggie burger.. I stopped all processed foods, started taking magnesium before bed, and the difference is amazing, I would say it has improved 80%….
Watch your diets, and walk in nature and getting sunshine…
But are bodies need salt how
@@hugmc if I had anything processed and salty let’s say like a potato chip my legs would give me neuropathy pain.. I do have salt
, but not processed foods anymore
Ok 👍
@@christined2495how are you now ? Is your neuropathy gone completely?
@@tr6151 I have no neuropathy anymore, the magnesium was a miracle for me
My most sincere congratulations: as an epistemologist and expert in science lobbyism, I really appreciate your careful analysis of the available evidence with a special attention to the impact of extra-scientific dimensions in the production of medical studies. I wish more doctors were aware of the enormous influence of big pharma on the biomedical ecosystem (from their funding of enormous research projects and sometimes entire university depts, to sponsoring of scientific journals and conferences, as well as the production of medical handbooks, educational programs, and strong interference with scientific soities and policy-making). Thanks! Bless you all (the cute big dog included : )
btw I came across your channel because I have been myself dealing with pudendal neuralgia causing severe constipation and numbness - this was caused by the strong sedentary life during the lockdowns which caused my tailbone to retrovert + fungi infection + plausibly spike neurotoxicity (not vaccinated, but got COVID twice and the symptoms appeared after the first infection and exacerbated after the second one). I have been searching for help, since doctors were only prescribing me laxatives, but I knew this could not be the entire story, since I had enormous difficulties in stay seated for a long time). I diagnosed myself by studying a lot and gradually got better through rehab exercises, vit. B etc.. - in sum, all the advices that you give (plus a lot of prayers () : ). Thank you again!
Hi Barbara. Wow, I have the greatest amount of respect for you as an epistemologist. We work extremely hard to check and cross check all of our data and that includes not just the studies but also who funded the studies. I'm sure you know, as well as we do, that whomever the funding comes through will greatly influence the outcome of the study. It's our motto that people do not need to hear our opinion, they need our objective expertise. There are far too many people (both professionals and non-professionals) who may be well-intended but are driven by their ego which distorts the information. Welcome to the human species...damn ego (lol). Anyway, thank you so much for recognizing and acknowledging the lengths that we go to. Truly appreciate it. BTW...our Big Girl (dog) is Brandy. We rescued her from the streets when she was about 9 months old and 35 pounds underweight and on the verge of death. She is the sweetest girl. She loves other dogs, people, children and all of her feline brothers and sisters. Blessings.
Hey Barbara. Ugh! Pudendal neuralgia is a beast. I'm so sorry you're dealing with this. Good for you for not getting the vaccine. It's amazing the amount of damage those spike proteins can cause because they're lab created and our body is still learning how to deal with them. It sounds like you're doing a great job getting a handle on this situation. If you hit a roadblock, you may want to consider adding in photobiomodulation. In your case, I would only do it if you're at an impass because it is costly. Also, don't forget to upregulate the mitochondria. Let me know if you need any guidance. Blessings.
@@NerveDoctors Indeed... I also put together a sort of metareview on the topic with other colleagues, which we handed over to politicians at all levels in Italy, in order to possibly avert compulsory vaccination, unfortunately in vain (I "had" to get Covid-19 in order to avoid the vaccine)...
@@NerveDoctors Although I don't drink alcohol, I ❤ Brandy : )
Is there a specific brand of just benfotiamine that you would recommend?
Hi Hunter. Haven't heard from you in a while. Nice hearing from you. The brands that I like are:
Pure Encapsulations - Benfomax
Doctor's Best - Benfotiamine 300
Blessings.
@@NerveDoctors thank you very much! I’ve recovered about 80-90% through diet and sober living so now I’m just giving my body some added support!
hunter kindly tell what was your problem, how long it was and how did u recover, and how much time it took, pls
@@kuldeepsingh-xl4zo I never found out what my problem was exactly. It’s been about a year and a half now and I only ever have intermittent symptoms in my hands and feet these days but it’s mild. I used to have it severely all over my body. What helped the most was just living my life and not letting the pain define me or control me. Cleaning up my diet and staying active has also been incredibly beneficial.
Hi there Doctors - Question why are the many , varied and sometimes weird symptoms of neuropathy so poorly documented? For example I have feelings that my feet are trussed up with invisible wire / very tight elastic bands or that something is stuck to the balls of my feet. Symptoms like this rarely get a mention - leaving the sufferers to feel like they are losing their marbles! I recently joined a PN forum - only to get a collective gasp of relief at talking about problems which I thought were unique! Doctors need to share this type of info more widely. I am writing to you because you hold out hope for sufferers who find themselves stumbling blindly through a maze of misinformation. Can you please help? Gill
Thank you
This really helps
Thank you doctor
Herma McIntyre You are so very welcome!
Can ur advices help stenosis, with people ,,who avoid surgery ??!!
Hi Ramu. For Stenosis, I have found the most effective treatment is Non-Surgical Spinal Decompression. Blessings.
What about canned tuna fish? Healthy or not?
Hi Joseph. The problem with tuna (whether it's canned or fresh) is that it's very high in mercury levels because of all of the pollution that has been dumped into our oceans for many, many decades. So, I would definitely stay away from Tuna.
Ever had any patients with femoral nerve neuropathy? When I started feeling my symptoms I was feeling it right in my hip flexor area on both sides and right above me knees caps into my lower thighs. I feel it mainly above the knees now and not so bad in the hip area but I do have my days. Almost a numb and weak type sensation. That along with my calves with twitching, feeling numb, tight etc. Meant to ask you this awhile back when we were talking about some things with me. Thanks in advance. Keep up the great content!
Hi Hove. Yes, we've treated cases of femoral neuropathy. It's important to make sure there's no nerve root compression, which is commonly the case, especially with spastic muscles, especially hip flexors. We've usually found with these cases if a person has had it for 6 months or less, they do well with the nerve support formula along with stretching (low back and hips) and physical therapy. If the condition has persisted longer, often they also need to incorporate IR treatment, as well. Thanks so much for your kind words and will do our best to keep the content coming. Blessings.
@@NerveDoctors thank you very much. You're responses and in-depth ones at that to everyone's comments is truly heart warming and much appreciated. I have never seen anything like it on UA-cam in 20 years. Doing gods work. From the bottom of my heart....Thanks again ❤️
@@NerveDoctors t dr te te red ze chhjb
Dag
Indigenous tribes vit d levels are about 70 so that’s prob what we should shoot for. The measured inactive vit D actually still binds to vit D receptors, just at much lower affinity. So levels matter. Study shows high levels correlate with more tooth problems
Very interesting
Great info thanks
Bern Blundell You are so very welcome!
Hi, for a person with facial nerve hypersensitivity, is it alright to drink water kefir daily? I drink about 500ml of it a day.
Water kefir may have quite a bit of processing. I haven't looked into this in great detail. However, if it were me, I would stick with regular Kefir (unsweetened...ie, no added sugars) or flavors.
What to take for pain i am taking 600 mg but it dose not take the pain a way so i take cayenne pepper
Hi Rose. I put my patients on a few things to help with their pain: Phyto Ultracomfort and boswellia (both by Pure Encapsulations) and also Protease (by Transformation Enzymes). Natural supplements for pain relief aren't as potent as pain medications, which is why we have to use a few for nerve pain. On the upside, they don't have the dangerous side effects. Blessings.
I'd rather have the pain than take a pain killer that hurts kidneys. The pain tells me what to do maybe eat something different next time. But I don't really know how that works...
Hi Doc, I recently discovered your channel and I am already a big fan 😊❤
Do you recommend pqq for feeling heavy in legs especially going upstairs or poor circulation in general. I also have varicose vain problems?! Many Blessings !!!
Star from Canada
Thank you so much for following us. Welcome to the family. Yes, I highly recommend PQQ. It's great for helping the mitochondria in your body regenerate. For varicose veins the best supplements will contain a combination of Pycnogenol, nattokinase and/or horse chestnut. For circulation I like formulas that contain Butcher's broom, Gotu Kola and/or Ginkgo leaf. Hope this helps. Blessings.
Good night Dr I am 52yrs from April 2020 till now crawling,biting all over me, late last year all that stop, and burning start , it’s too much to Tex , wish I could talk to u directly 🙏🏿 I’m DAS I’m on Gabapentin but not helping
Hi, Debbie Smith,
After COVID, we saw the need to reach people globally. As a result, we went completely online to help our patients no matter where they live.
If you would like to speak with a doctor, we recommend scheduling a consultation.
To schedule a consultation, purchase our at-home kits, or any of our other products to facilitate nerve repair, you can visit our website at nuphoria.com. Simply choose the product or consultation you want, add it to the cart like you normally would, and make sure when you enter your shipping address you change the country selection from the US to the country you're ordering from. Otherwise, your order will default to the U.S. Let us know if we can be of further assistance.
I don't find your "Links" . Where are they ??
Not sure I agree with sunscreen but this is good info. I would recommend staying far away from seed oils as ever since I’ve stopped consumption of them and switched to a healthy animal based diet, I can stay out in the sun for up to 10 times longer than I used to once a based tan is established.
Hi, new here! Does use of Gabapentin for neuropathy after brain surgery inhibit nerve regeneration? In a chair now and trying to learn to walk again... (can stand but spasticity and rigidity).
Hi Lulu. Gosh, I'm so incredibly sorry you're going through this recovery. Gabapentin has so many deleterious side effects. And, yes, it can slow nerve recovery. If you absolutely don't need it to control the pain, I would certainly have your doctor remove it.
@@NerveDoctors Thanks for your reply. They tried for almost 2 weeks in Physical Rehab but the pain was unbearable. I take as little as I can, which is said to be below average for my issues.
Hello Dr, is there any relationship between acetyl-l-carnitine and TMAO, and it’s impact on cardiovascular health? Can you please give me your take on this. Is l-arginine of use in NO production or is l-citrulline sufficient? If yes, at what dose? What’s your opinion on NAC? Thank you
Hi there, EOH. it’s always great hearing from you and you ask the best questions.
First, let’s start with L-Arginine. Oral supplementation of L-Arginine will not increase nitric oxide (NO) levels because L-Arginine must pass through the liver for metabolism. The liver then breaks it down and leaves nothing for NO production. On the other hand, L-Citrulline bypasses the liver. It then gets converted to L-arginine which then converts to NO. So, L-Citrulline is always the AA of choice to increase NO levels.
Next, let’s talk about Acetyl-L-Carnitine and TMAO levels. A report was released (by Big Pharma) to news affiliates that ran news stories stating that carnitine (found in red meat) may react with certain gut bacteria in certain individuals to promote a compound (TMAO) that could then cause heart disease. What they failed to disclose was that this so-called report was based on a sub-study of 10 people (are you kidding me?! 10?!). The results in the report were obscure and lacked concrete reproducible evidence. Now, the Mayo Clinic performed a meta-analysis study that looked at 3600 patients (not 10) taking L-Carnitine/Acetyl L Carnitine and found huge cardiovascular benefits.
I’m going to include the link here which outlines what I’ve just discussed. It should help clarify a lot for you. bit.ly/3HjJZRm
I know there were a couple of points I didn't answer. Please shoot them over to me again. This response is getting too long (lol).
Blessings.
p.s…Keep the questions coming! I love it!!
@@NerveDoctors Oh WOW! I keep learning a lot from you. Fascinating. Thank you again.
🙏👍
I can’t go workings because my spine don’t allow.😢I’m taking med for the diabetics and navy tabs for pain and I’m so much afraid of stuff I take. It’s absolutely against of u say and now I’m petrified. I can’t even walk a 1/3 . Really need so much help cause the docks here não quer less.😰😰😰😰
Does drinking kava also interfere with nerve healing?
The worst thing you can do to slow down nerve recovery is to stop exercising, even if it’s uncomfortable. Unless you’re getting enough blood flow to
your nerves, they’re not getting enough nutrients to heal. Exercise is the #1 thing you can do to live healthier and longer.
My Hip sockets Cartilage has been Dissolved now Bone on Bone. Don't want Surgery, cut in half and boned like a chicken. Will PRP offer Pain Relief?
Hello. So we know that sleep is crucial for healing but what I haven't been able to find is a way to get a good night rest when the pain kick in every time after 4-5hrs of sleep and I probably need 10-12 with my cfs/me along with neuropathy. I wont be taking pain meds as I figured out (been 4-5 y on all kind of meds:pregabalin, amytriptilin, taita...) they do more damage. Is there a solution to this. Ive been trying all standard things like benfo, ala etc but nothing touches the pain.
Hi Marko. The first thing that is important to realize is that none of the critical ingredients are for pain relief. They support nerve repair and regeneration. For my patients, I place them on a combination of Boswellia, Turmeric and protease enzymes. This will not get rid of the pain completely but usually helps bring it down.
Daylight come and mi waan go home. Jamaican.
Same
Good morning Doctor, 49 year old male and I’ve reduced my A1c from 12.5 in August 2022 to 5.5 as of yesterday. My question is, I was diagnosed with Treatment Induced Neuropathy (Insulin Neuritis) in January. I take R-ALA and Benfotiamine daily. The burning, cold and hypersensitivity has great reduced…yay. However, I’ve noticed for the last 5 days, a buzz/cat purring sensation on the bottom of my left foot. No pain, pins and needles or tingles…it’s a vibration. 20-25 seconds of buzz and 50 seconds of no buzz..all day for 5 days now. Neurologist and PCP seem to think it’s nerve innervation and healing. At my request, we did a comprehensive exam for muscle weakness etc..no issues. MS came to my mind but they both said no MS symptoms are present. Does this makes sense with peripheral nerves? It’s only my left foot.
Yes, it makes complete sense. First of all...congratulations on a job well done. Down to 5.5...THAT'S FANTASTIC! You should be very proud of yourself. That took significant lifestyle changes. You did great by taking the R-ALA and Benfotiamine but you need to add Methylcobalamin, Pyridoxal 5 Phosphate, folate and acetyl l carnitine to the mix. This should get you the rest of the way across the finish line and quiet those sensory nerves (that's what's causing the buzz-like sensation) Blessings.
@@NerveDoctors Thank you. Would love to get my number in high 4’s or low 5’s. Just weird it’s in one foot. But at least there’s no pain or numbness.
hi I would like to know how did you reduce your A1C from 12.5 to 5.5? do you mind to share your secrets thank you in advance. Kudos to you for the wonderful work !
@@ThanhNguyen-ml8pz No bread, ice cream, pasta, soda, candy, and alcohol since August 2022. I eat fish steak, greens, Leto oatmeal (7 net carbs) and eggs.
Would you happen to have another recommendation on vitamin D3 together with the vitamin K supplement, the link you provide is broken 😟😟.
Oh man.. I am already taking so many different kind of supplements including nuphoria gold and blue that this is getting kind of tedious.
Can marijuana or natural toddy help to recover?
They tell runners that you can't outrun a bad diet.
Why does it show different ingredients in the two nerve defense. One has a proprietary blend, the one I received does not have that.
Hi Yvonne,
Our Nerve Defense formula ingredients are listed here: nuphoria.com/collections/our-products/products/nerve-defense-vital-nerve-protection?variant=47171923850
If you have any issues feel free to call our customer support line at (844)-400-0101
Tax Dr I subscribe today your cool❤
Thank you so much. Truly appreciate it!😊
You talk far too fast for me to be able to follow you
Go to the top row far right , click settings wheel, scroll halfway down ,click on speed and select 0.75 .That will give you an easier speed to listen to