Got Neuropathy, But Not Diabetic? - The Nerve Doctors
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- Опубліковано 15 бер 2022
- Nuphoria.com
Got Neuropathy but not diabetic? Talk to one of our leading neuropathy specialists, Dr. Coppola or Dr. Monteiro, today. Visit www.HealmyNerves.com or call 844 400-0101 Monday - Friday 8 am - 5 pm
Resources Promised in Video:
List of Meds Know to Cause Neuropathy PDF: bit.ly/Meds-Causing-Neuropathy
Ketogenic Diet for Beginners Book on Amazon: amzn.to/3LEFIYR
Most people believe the only cause of peripheral neuropathy is diabetes, but nothing could be further from the truth. Did you know that diabetes is not even the leading cause of peripheral nerve damage?
In this video you'll learn what some of the biggest culprits are that lead to nerve damage and peripheral neuropathy and I’ll make it crystal clear for you to understand. Watch this video and get the answers you've been looking for.
Talk to one of our leading neuropathy specialists, Dr. Coppola or Dr. Monteiro, today and get the help you need. Call 844 400-0101 Monday - Friday 8 am - 5 pm or for more information, visit us at: www.NerveDoctor.info
Send Messages to: info@nervedoctors.com
NUPHORIA Products: www.HealmyNerves.com
Doctor & Neuropathy Information: www.NerveDoctor.info
Dr. Coppola’s Bio: www.healmynerves.com/pages/doc...
Dr. Monteiro’s Bio: healmynerves.com/pages/doctor...
#NEUROPATHY
#NERVETREATMENT
#THENERVEDOCTORS
San Antonio Neuropathy Center
Dr. Monteiro and Dr. Coppola are the founders of the San Antonio Neuropathy Center where they’ve been helping people recover from neuropathy for over 18 years. Their services have been sought after from people throughout the United States and Internationally. Their unique approach is drug-free, non-surgical and helps relieve neuropathy symptoms while restoring function and repairing damaged nerves.
NUPHORIA cm
Dr. Coppola and Dr Monteiro also developed a neuropathy product line called NUPHORIA cm designed specifically to help their patients recover faster from neuropathy. Once available only to their patients within their clinic, NUHORIA cm is now available to the public at:
www.HealmyNerves.com
Defeat Neuropathy Now … In Spite of Your Doctor
Dr. Monteiro and Dr. Coppola are the co-authors of the book Defeat Neuropathy Now … In Spite of Your Doctor and the e-book "The Great Neuropathy Hoax". These books give the reader an “Eye-Opening” look into why medications and traditional therapies leave most neuropathy sufferers stuck in misery without hope. "Defeat Neuropathy Now...In Spite of Your Doctor" has been touted by neuropathy sufferers as a survival manual for anyone suffering with neuropathy - dispelling myths and outlining proven treatments based on the most current research on reversing neuropathy. Get your copy today at:
healmynerves.com/collections/...
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Disclaimer:
Dr. Coppola and Dr. Monteiro are both Doctors of Chiropractic. Dr. Coppola graduated in 1996 from Parker Chiropractic College and Dr. Monteiro graduated from National Chiropractic College in 1992. The use of “doctor” or “Dr.” solely refers to that degree.
This video is for educational and informational purposes only. It should not be used to self-diagnose and it is not a substitute for a medical exam, diagnosis, treatment or recommendation from your treating physician. It does not create a doctor-patient relationship between Dr. Coppola or Dr. Monteiro and you. You should not make any change in your health regimen or diet before first consulting a physician and obtaining a medical exam, diagnosis, and recommendation. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition. Nerves Can Heal
• Nerves Can Heal - Peri...
My trust in Neurologists as whole is very low. I went in to a Neurologist about a "dead spot" on my right knee, just below the knee cap. You could stick pins into it and I felt nothing. The Neurologist just shrugged. The size was about that of a silver dollar. About a year later I had been driving a long distance in my car. Got very uncomfortable, and pulled over to have my wife pick up the driving. Got out of the car, and my right leg collapsed. And I was in high pain. After the trip, we got home and the pain just did not stop. Went to the doctor and they gave me ct-scan and found that I had a protruding/herniated disc (L5-S1) causing sciatica pain. Stretching and pain medication was minimally effective. About a month of pain later I came down with Bronchitis and was basically in bed for 10 days. That cured the pain, but I was left with Neuropathy in both feet. It continued to very slowly get worse over the years. So, I went to a clinic (famous one) and told them the issue. They did an MRI and said I didn't have anything wrong with L5-S1. I don't have diabetes, haven't had any of the listed meds (at that time, but do now have a statin). No poisons. Not any of the listed thing this doctor mentioned. For me, frankly, I don't think Neurologist's have enough understanding or ability to actually figure things out in the nerve system. (At least that is my experience.)
She missed one of the major causes which is vitamin B-12 deficiency.
B-12 is required for production of the myelin sheath
I had surgery for a herniated disc in 2015, i'm now in the full flow of the sypmtoms of PN. I have started with vitamin supplements, a low carb diet etc, all by doing my own research while waiting for my health providers to see to me again. Thank you for these videos they are helping me keep sane!
So happy we can help. 💖
I've seen multiple doctors who want to perform surgery on my back. The only problem is this. None of them have said what the procedure is going to be. What they're planning on doing to me and my back. I find that pretty scary.
The one doctor who said "Don't have it done" is the surgeon who operated on my neck for four hours. So, I'm going with the back surgeon who said no don't do it. I'll do chiropractic, diet, and whatever. I don't need even more pain with bad back surgery.
Exactly
🎉
@@rodgerrodger1839 I have had four neurosurgeons Tell me that I am in operable. Severe stenosis in C4,5 and six. Mostly osteophyte overgrowth. One told me to seek alternative complimentary care. So with diet, movement, supplements, cbg, thc edibles, and kratom i have a handle on pain but weakness and coordination continue.
I have never tasted alcohol in my life, never smoke, no diabetes, never taken any of the listed drugs, in fact not on any drugs, but I have neuropathy. The only time I got relief was when I stopped sugar completely and cut down carbohydrates. I’m looking for answers
That's great! It has helped us too.
Try taking 3000mcg of B12 per day and you might just get rid of it! It really helps me!
That is correct! Studies have shown that the therapeutic dosage of B12 for nerve repair is 1000-3000mcg daily! Keep up the great work!
@@jamesmondok8635 thanks, I’m going to order the Andrew less man B12 today
R-LIPOIC ACID STABILIZED and ALA research 😊
I had burning and pain in my feet, especially at night. I'm now at week four of taking B1 and B complex after looking into thiamine deficiences (which feet pain including tingling and burning is a common symptom of thiamine (B1) deficiencies. My pain has significantly decreased by about 80% so far
Once I got actual treatment for my lower back and stopped spending so much time sitting, all of my symptoms went away. Turns out that I had developed a bunch of impinged nerves in my lower back and pelvis, causing numbness and tingling in my left heel and sciatica with zapping pain in my right leg and hip. Once I got my driving posture correct and started walking and stretching after a chiropractic visit, all was better.
How'd you get driving posture fix
@jonathandaviss5327 heh... I had to change an entire vehicle from a sedan to a minivan for starters. Sedans are not made for tall people over 6 feet. In a minivan I can sit without hunching over, straightened my posture and spine.
I’m going to my neurologist today. You helped me arm myself with information! Thank you
So glad I found and listened to your video. Yes,, I found it extremely helpful.... You gave me so much understanding. I am grateful. Thank you.
I have all different types of neuropathies plus diabetic neuropathy, l am in so much pain every day plus flu symptoms and brain fog caused by a messed up spine being 75 years old now Doctors are not doing much about all my issues and l continue on with a hope and Prayer with no quality of life , l have severe carpal tunnel in both hands but l continue to crochet that draws some of the attention on my pain away plus 😊the stress of the life l have been given , thank you though dear sweet lady for giving all of us these very important and informative videos Gods Blessings to you and yours 🙏❤️🙏💜🙏🙏🙏🇺🇸
Thank you for your video. It helps greatly to know the causes and what we need to do to avoid damage to our nerves!
Thank you for your detailed information.
Fantastic information. Thank you SO much!
I'm so glad Your channel came up on my YT page everything makes so much more sence now. A few in the list you mentioned I have. I will be watching other videos you have.
Interesting to discover antibiotics are a culprit. I've recently acquired neuropathy in my right lower leg, and surprised because I don't fit into any of the other categories (have not yet confirmed I'm not diabetic, but it is improbable). I am a physically active 65 yr. old and have exercised all my life - lifting weights, swimming, and hiking. In the past year I discovered my neuropathy while hiking - muscle fatigue and pain in right lower leg and foot. 4 years ago I had a bacterial infection in my right lower leg that developed cellulitis. The doctor hit me with injections and several oral antibiotics, and I took them for a couple months. It killed the infection and I continued hiking shortly after with no noticeable effects. I had a minor suspicion there might be a connection to my previous infection, but I thought it would be a direct result of the infection itself, not the antibiotics. My only other suspicion of a cause is my computer habits - I spend a lot of time at my desk at home using the computer, but I have done that for years - since 1994 - and had a computer job 10-12 hours a day for 13 years, but suffered no ill affects then. Knowing the cause would be helpful in fighting the disease. If it was the antibiotics, then I would not have to have corrective back surgery, or bother trying to alter my computer habits or activities.
I fractured an ankle in 2015. That foot never returned to normal. I have numbness, tingling and sensitivity in some areas. Thank God the awful shocks no longer plague me! I don't take meds anymore. I just focus on life and try to ignore the discomfort.
This was an excellent article. Thank you for sharing this in such a wonderful manner!😸
Thank you!
Thank you so much 🙏🏻 your extensive knowledge, content and delivery has helped me so much. I've been prescribed 2 of the antibiotics you mentioned and since experienced legs and arms muscle weakness, burning foot, cramps and numbness. I'm hoping I can heal and fully recover 🙏🏻 so grateful for your video ❤
Excellent analysis
Don't drink alcohol I don't take any of those medications but I still have it
Can be a vitamin deficiency yoo
I don't have a vitamin deficiency either, but have it too.
Same here…I suspect that they pushed me too hard in physical therapy three days after scoliosis surgery (such as high kicks with 10-pound weights on my ankles)….😡….but the neurosurgeon insists he told them to do that😱
Me too!
Diet
I was prescribed an antibiotic for a urinary tract infection in that family even though i already had issues with peripheral neuropathy. I took one pill and immediately requested a different antibiotic, It made me feel so sick. Always research and advocate for your own health.
Thank you, Doctor!
Good video, to the point with some hard information.
George420 So glad it was helpful. Thanks for watching!
Crystal Clear! That's how you explain all things
Thanks so much, James
Eye opening video
Thanks doc 😇 for your content very informative. God bless 🙏🏻👍🏻
After surgery, too, so right!
Very very informative
You are excellent. Thank you!
I have neuropathy from having initially Cauda Equina from severely slipped discs in lumbar spine, then had several revision surgeries, have a Spinal cord stimulator, then to top things off I slipped the c5-c6 had acdf surgery had bone spurs removed, had moderate stenosis. Now have severe stenosis of the lumbar spine, which has really impacted my mobility, now need laminectomy.
Interesting info.
Keep spreading the good news and show love while you are telling the good news
I was previously on amlodipine besylate for many years for my heart. In 2010, I contracted a horrible case of near fatal MRSA infection following hip replacement surgery and I was put on Levaquin for 6 months and Vancomycin in the hospital. I now have peripheral neuropathy without diabetes
Same for me today I felt more been taking NAC & Natto- Serra.
Thank you for your video I think I developed these condition after chemotherapy.
Thank YOU
I had most of my pancreas removed several years ago. I'm not diabetic but my fasting blood sugar runs slightly higher than optimum 100-120. I developed neuropathy that was as bad as if I was very diabetic. Couldn't figure it out, saw several doctors and no answers. I found out about Thiamine deficiency causing nerve issues and started taking it a couple months ago. symptoms are getting better so I hope it continues.
Great video
was diagnosed in 1999 with idiopathic peripheral neuropathy
1) Chemotherapy - nope
2) statins - nope (although I now take a mild dosage and too much will increase neuropathy pain)
3) calcium channel blocker - nope
4) antibiotics - nope. No antibiotics.
5) alchohol - during the university days 1974-77, yes, but when I got married, I stopped drinking
6) autoimmune - polymialgia rheumatica - got it in 2012, 13 years after getting neuropathy
7) shingle,s HIV, MS - ruled out in 2012 by second diagnosis with a new neurologist
8) Barium - nope, contrast dyes: only since 2000 AFTER neuropathy diagnosis, because of lung embolisms/leg thrombosis.
9) injuries - ??? none immediatelyy before the initial diagnosis.
But then again, there's a reason that I was diagnosed with "idiopathic" neuropathy - because in 2012 (13 years after the first diagnosis) my present neurologist and then the Chief neurologist at the state hospital reconfirmed the diagnosis of idiopathic neuropathy, meaning in 3 days of testing, they ruled out any other causes.
I react very sensitively to the statins I take sonce my heart attack in 2018. My cardiologist, the cardiologists in the hospital and my daughter who is a GP all insisted, there was con connection between statins and neuropathy. I'd read the studies both for and against and both sides do not recognise the "work" of the other, even today. HOWEVER, both my neurologist and my GP both told me, that ALL of the known neuropathy patients had their statins histories. I now take Ezetimib/Rosuvstatin-Mepha 10 mg/10 mg M, W, F, So and that keeps the LDL value under control without enflaming my neuropathy pain.
I have a "cocktail" as my present neurologist calls it, of empirically tested substances I take without prescription, which on a good day reduce my neuropathy pain substantially. Main substances are: R-Lipoic Acid, Acetyl-L-Carnitine, N-Acetyl Cysteine, Omega 3 (fish oil), Borage Oil 300 mg (GLA = Gamma Linolenic Acid) and magnesium. Other empirically tested effective substances I've tried, which unfortunately either didn't work for me at all or only for a short time and then didn't any more: CBD Oil (without THC), cold pressed CBD oil, B12, Biotin, Vitamin D3. No topical applications have helped whatsoever.
Does THC still work? I have it from Celiac Disease. The pain has gotten really bad, and I can't take most medications because Pharma does not have to disclose Gluten.
Thanks for the education and medical info. You are a blessing...btw...You have beautiful hair and you wear it well :)
Chemotherapy in 2011-12 neuropathy has gotten worse in my feet over the years since the treatments. It wasn’t as bad after the first 6 months to a year after the treatment then got worse as each year has passed.
At the beginning of the video he said he would tell us in a few minutes which protein was the culprit, and that got me to watch THIS video. THEN, he said we have to watch another video to get the answer. I don't like getting duped, so I am out!
I now have nerve pain, hands arms feet, and legs, my blood sugars are normal.
Exlent information mam
Thank you for this video. I get a bolt of lighting type of jolt, from time to time, from my left foot to the left side of my head that lasts for 2 to 4 seconds about once a week or so. I never had that before I got Shingles of the left cranial nerve and suffered 5 weeks of total paralysis to the left side of my face, but now I get those lightning bolt jolts. Must be from the Shingles infection of the left cranial nerve.
I got peripheral neuropathy from listening to "doctors" on UA-cam.
One dr has a cure for PN, it was to increase your fat intake of certain types of fats. The fats help build the sheath around the nerves and then your symptoms are much better
Very informative! Thank you!!
Benjamin D'souza So glad it was helpful. Thanks for watching!
@@NerveDoctors please reply to tom notebaart and others. they are good questions!
Wow! I thank I have Peripheral Damage I have a lot of Pain , Thank you😇
I’m going to go check out my blood pressure medicine and see if any of them have caused Nuerapathy in my lower left leg
Got scary bad leg/arm nerve/brain symptoms after finding on scalp a tick carrying Borrelia sp, put on Doxycycline & then 3 months later Amoxicillin. Still dealing with constant weak, achy arms/legs, twitchy muscles, pins & needles progressing to having difficulty walking - 8 months since tick. Feels light wearing high heeled boots 2 sizes too small & trying to run a marathon in them. Now switching Amlodipine BP med that I have been on for 2 years to Lorsortan, taking mega B vitamins, & soon doing infrared light therapy 4× week & pool exercises....anything to stop this nightmare. Have to wait another 6 months to see referral neuromuscular Dr & rheumatologist because that's how booked up they are. Used to pray to get my old life back...now praying to stop symptoms from getting worse & putting me in a wheelchair or bedridden for the rest of my life.
Dear Doctor, which of the Vitamins can cause hot flushes? I am in Holland but could not buy your Neuropathy treatment. I take all the ingredients separate during the day. Thank you for your fantastic advice. Love it
You've got that so right about bariatic problems being a cause!!
Some of those you mention (of so called medicines, household chem...) were listed in a book as lowering Calcium APTase (puts calcium away after cell doesnt need it). Calcium connection by B Broady. So calcium is needed but only in amount needed. Have PN and wondered if a mineral inbalance, also note it gets worse after get up to urinate at night.
☀️I asked the lady dr in the ER to offer me a drug other than Cipro. She bullied me by saying she would not treat me if I would not take the drug she ordered. How unprofessional is that?
I wish I had not caved, but people are so vulnerable in a situation like that and some doctors take advantage. THANK YOU for the videos🙂
Huh the doctors meds are poison well I believe they are two tablets ruined my overall health they gave me but you are right they get very mad if you say this the side effects of some are terrible
Just say you are allergic if this ever happens again~Cipro makes my entire body feel like it is on fire, especially in the muscles, thus I absolutely REFUSE to ever take it again!!
Mary Gee,
You are so very welcome for the videos, and we are glad you enjoyed them!
I am a victim of Cipro. I took ONE SINGLE DOSE as prophylactic protection during a prostate biopsy (negative, I'm happy to say), but within a month, my right shoulder tendons melted down, rendering my right arm useless for all but the most basic movement (to this day). Then the tendons in my left hand started failing and my left thumb is almost useless. After that, I developed horrific neuropathy in my hands and feet, and while the finger pain subsiding after a couple of months, my feet are on fire, all the time, 2 years on.
Three doctors just shrugged it all off, but it doesn't even matter because there is nothing that can be done about it, as Cipro damage is permanent.
I'm sorry this happened to you. This also happened to my 27yr old daughter three yrs later she is still suffering...now on Medicaid and is applying for disability as she cant walk very far or stand also has SIBO and only weighs 102. NO Drs want to go there or recognize what happened with these antibiotics.😡
This is exactly what happened to me. I was prescribed Ciprofloxen and Levofloxacin for chronic UTI’s routinely multiple times for 3 decades and I had no idea of the dangers. I’m a nurse too 😕.
In 2005 I developed PN symptoms and I didn’t see a doctor until 2014. A Neurologist diagnosed me with RLS in 2014 along with Neurogenic Bladder and Urinary Retention for which I have to self catheterize after each voiding. I now believe this too was caused by Fluoroquinolones . Almost 2 years ago I was prescribed Levofloxacin again for another UTI and the next morning I thought I had had a stroke. I couldn’t walk and I had altered mental status but I had the presence of mind to reach into the pharmacy bag and read the voluminous pharmacy papers that came with the prescription. I immediately called my Urologist’s office to speak with the NP who prescribed it and she denied knowing anything about FDA BLACK BOX WARNINGS on these antibiotics. Apparently the majority of doctors don’t know or don’t care to research the drugs they are prescribing even though they are ultimately responsible for knowing what they’re prescribing. Instead they listen to Drug Reps peddling their poisons. Follow The Money Trail and it leads straight to The NIH, The FDA and Big Pharma.
I am not Diabetic and I do not consume alcohol regularly but I did have H1N1 in 2009 when it was a Pandemic and while in the hospital for that I also developed Hashimoto’s Thyroiditis! Soon thereafter I developed “Fibromyalgia” and everything spiraled out of control from there.
In 2017 I was a passenger in a devastating car crash with multiple injuries. I sustained a Tibial Plateau Fracture Type 6 and needed emergency surgery twice in the space of 4 days. The outcome was determined to be permanent damage and a severed Peroneal nerve was found 4 years later. I also have a number of Lumbar Sacral Spine conditions and I honestly don’t know how I survive from one day to the next.
Today I finally met with a Neuropathy Specialist and am hopeful that I can be relieved of at least some of the pain.
@@kimberlywallace6148 Holy moly, you've been dealt some crappy cards!
I hope the specialist can deal you a better hand.
(Sorry, I have no idea why I chose card-playing metaphors).
I wish you well.
@@imacmill Yes, that’s one way to put it! You know when you’re vibrating on a low energy level it opens up Pandora’s Box packed full of anxiety and depression.
When doctors “Gaslight” their patients we shut down but since I started standing up for myself and no longer believe that doctors are “All Knowing” I feel more in control of my health. The moment a doctor becomes condescending or angry about my questions I walk right out the door. Never again will I accept blatant disrespect and arrogance considering that nearly all of my health problems stemmed from prescription drugs and misdiagnoses.
Very informative video
I'm so glad the video was helpful! Thank you for watching!
Guillain-Barre Syndrome around 2 years ago went numb from the ground coming up stopped when it got to my rib cage my knees would just give out got to the point i was stuck on my parents couch been a long climb back my feet still mostly feel like they are wrapped in saran wrap its not painful for long thankfully and i can walk somewhat quite well now socks help so much.Its felt like i was only upper torso and rib cage down was a ghost for along time that i could control but not feel and not so trust and then those nerves started up.
I have Celiacs from being 38% Scandinavian. I take Natures Way Stinging Nettles capsules 2 in the morning and two maybe half hour before beer, pizza, wheat products. San Luis sourdough bread doesn't make me react. Great to have a bread not to worry about eating...
I always say I am allergic to fluoroquinolones. I was dozen levoquin many many times in the past for sinus infections and bronchitis. I developed severe pain and weakness in both wrists. I have severe PN now years later. However, I have very low B12 and D3 and this probably actually caused it.
The general practitioners are taught not to think about malabsorption of vitamins and minerals. I started taking D3, calcium and B12. All my problems with coordination, muscle spasms, and pain.
She didn't mention hereditary neuropathy. I developed foot neuropathy when 64 first starting out as partial numb feet which then started hurting 5-6 years later. My mom had numb feet which I only discovered in last 2 years of her life. But her neuropathy didn't cause pain. My dentist's mom has painful feet neuropathy at night, and her mother also had it.
I'm surprised you didn't include degenerative disc disease as a cause of PN. As the discs in my cervical spine degenerted, my spinal cord was compressed for a long period of time, leading to PN in on the entire left side of my body. Still, I appreciate what you are doing here and will definitely subscribe and explore your other videos!
Similar for me - I am in the midst of all kinds of tests. My entire right side is becoming weaker and my fingers no longer grip and I can barely lift my right arm. I have not taken any of those drugs. I have a lot of disc degeneration. I hope I can get this solved!
What about stenosis from spine? Injuries? Like corneated disc's thoracic hernia disk?
That's what caused my nerve damage to get worse! Failed spinal surgeries! Now taking Gabapentin and Cymnalta
Helps a little but not much! I also have PAD and Cardiovascular disease at age 60. My husband died at 42 from same thing😭
I don"t have perfect blood sugar-A1c(5.9) but I am very careful with my diet.I have Charcot Marie Tooth disease,Which I"m told is my main problem with neuropathy.
My husband had Hodgkin's lymphoma and was on ABVD successfully. But the day after each treatment, he got a Neulasta shot to boost his immune system. It was successful in that, thankfully and he even made it through flu season without incident. But we were warned, first by the nurses and then by other HL survivors, that it can bring on neuropathy. And yea, it has.
Thankfully, we live in NJ and he can take an edible 25mg THC gummy before bed. It makes a huge difference, if anyone is wondering.
It sounds like it is just dNgerous to live!
My son in law has CIDP from chemo, he also got AVN leading to bilateral hip and shoulder replacement surgery.
Getting ready to order my third mont of the nerve meds and second of the vitamins haven't noticed anything yet.
Excellent lecture. I love that you explain the why and how of the subject matter. I have a respiratory, oxygen, pharmaceutical background and I can tell you put an enormous amount of time researching this and then condensing into the time frame. You are spot on about the contrast dyes causing nerve damage and kidney damage and I commend you for bringing this truth to light that is hidden by the mainstream medical cartels that lie and tell people that contrast dye is safe when it's just the opposite. Thank you for an eyebrow raising subject. You and Sten Eckerg are the global masters at explanatory details which is what counts.
Thank you so very much from the bottom of my heart. You are correct, both Dr Coppola and I put an ENORMOUS amount of time into the research that we do because we want to make sure if people are depending upon us, we're giving them the most accurate information. Thank you for acknowledging that. It's truly appreciated. Blessings.
@@NerveDoctors you are welcome and thank you for bringing to light the dangers that are covered up and promoted by mainstream medical industry
It’s no mystery how I got it. Just completed my first course of chemo.
I like it. Thanks
Glad you like it. Thanks for watching.
Got PN from Ciprofloxcin (Cipro Toxicity) when administered the 'black box' label drug for a sepsis infection. Their excuse was it took too long for the blood test to identify the actual infecting bacteria. It took me three years to figure out my problem. The hospital neurologist said it was carpel tunnel (in both hands and then both feet?) . . . and no neurologist will even do a consult because then they will have to file an Adverse Reaction Report.
I'm so sorry.
Yes you are right after the booster terrible nerve pain began
Ive only had small doses of Cipro, and Lavaquin.
As for all the others, I'm clear.
I did sprain my ankle when first experiencing Morton's Neuroma. This sprain has never fully healed...
Keto diet is helping.
My mum has very bad neuropathy from an autoimmune condition called NMOSD. She is in a lot of pain from even skin contact with cloth
I think I got my PN from inhaling volatile organic compounds when I spray painted a lot of military vehicles back in 1982. I didn’t use a respirator or any personal protective equipment.
Don’t drink, don’t have diabetes or anything vascular issues. No kidney or liver issues, no HIV or malnutrition, no bariatric surgery, and still have this issue. It’s ANNOYING.
I have it due to Celiac Disease
Me too
Try vitamin B1 or benfitamine. I have thiamine transporter issues in my small intestine. Also try homemade yogurt and or kefir. Those help make thiamine in the gut.
Are you OBESE? Do you smoke? Are you always on your feet? On concrete?
Much of this tells me nothing unless I know whether the various causes of PN will last weeks, months, years, or forever. Without more context, this is not real helpful. (but still appreciated!)
Bingo, Lyme in 80’s without diagnosis. Only 7 years later while 8 months pregnant, landed in the hospital with pneumonia. They gave me IV Bioxin to save my life. Got rid of spirocete, saved baby and me, but nerve damage was already done. Many issues since.
This is the best video I’ve ever heard about this subject, so thanks a lot 🌹
You are so welcome. Thank you for the feedback.
I very much dislike these videos that ask people to "like and subscribe" at the very beginning of the video. That's like a retailer asking you to review a product, before you buy it.
If no one likes and subscribes, there would be no Nerve Doctor channel or UA-cam for that matter. It took 10 seconds for gosh sake!
@@Bob_AdkinsBut why would you subscribe before hearing what they have to say? The exhortation should be at the end when those who liked it are still watching. I agree with the comment above.
Review it and see what value you can glean for your situation. There is no one remedy that fixes all. Be prudent Ralph.
I have Peripheral nerve damage in my feet and lower legs. Dr said it’s idiopathic in my case as there is no known cause ,so he has me on Alpha Lipoic Acid but I didn’t get the R now I will order it! Thank you
I think mine was caused by being on my feet as a nurse in the hospital for 25 years.
Idiopathic means your doctor does not know the cause. Doesn't mean that there isn't a cause. We specializing in identifying and treating the underlying causes of peripheral neuropathy. Feel free to visit Nuphoria.com for more information.
@@NerveDoctorsi have imnm , would r ala help me ? Thanks
Thank s for the info
Gloria Montero So glad it was helpful. Thanks for watching!
@@NerveDoctors Good video!! Learned alot!! I have learned more from chiros than M.D.s......
This was wonderful
Thank you so much. Truly appreciate it!😊
that's what she said
I have it after many years of fibromyalgia. It was just diagnosed days ago. No diabetes...
Wow, this was an eye opener. I'm type 2 diabetic & have been experiencing PN for awhile. Supplements such as alpha lipoic acid & Benfotiamine have helped, but recently my condition has taken a turn for the worse. The pains are now shooting up both my legs and I'm in excruciating pain. I'm also gluten sensitive as well, and have been eating a ton of wheat products lately. I had no idea that one could develop peripheral neuropathy if you were celiac. 😢
You might find vids by Dr Ekberg helpful.
Quit sugar
Osteoarthritis of the spine, you forgot about that one!
It made all the difference to me , once I got off all gluten and dairy!
What about Flouride everyone is forced daily to ingest not to mention products loaded with it?
What about Quetiapine, 50mg.? Is that hurting me, too?! Mine is caused from my spine problems (Disk Degeneration in Lower Lumbar & Neck) Thanks for all this info. You are THE only person who is giving us HOPE... having major Neuropathy in both legs & feet, as well as my left arm and hand. I'll be following you, girl. I stopped taking my Cholesterol Rx as of today. Thanks again ~Houston Kat
I took statins for about two months and they made me want to kill people. My dr took me straight off them and put me on something else. Having googled the side effects it said can cause pain so I stopped taking it. Some of the pain went
Look at the lower back as well.
Treat alignnent there and inflammation .
Accupuncture helps .
Thanks
I had neuropathy from very low B12 levels, I can’t absorb B12 so I do injections! Thank you for being honest about some prescription drugs being routinely dispensed, to be fair, most of us don’t read the sheets that come with our medications or research them on our own.
But its cianocobalamin you're getting. So I try methylcobalamin sublingual high dose every day, and hope to be better from neuropathy in a few weeks/months🙏
same as you. i was very deficient in B12 but very high level of B1 for some reason.
I had that tested after I was diagnosed.
I'm had over 90 MIRs since 1990.
What about increasing or taking a NO progenitor? i.e. beet root powder, juicing beets, etc.
Interesting! I’m not diabetic but do take BP meds and just starting to get neuropathy.
Mine started I was diagnosed with Brain AVM,Chronic fatigue and migraine and dizzy and got a mini stroke and seizures started
I had a bit of neuropathy due to Type one diabetes but during chemotherapy for cancer, the neuropathy got Much worse and covered a much larger area. Talking to my haematologist about this, she said it was due to one particular chemical, the red stuff.
The dr said because I had lymphoma I did not need that particular drug and took it out of the line up. She never told me why it was ever part of the regime.
It is used in large amounts to women with b east cancer and they often have really bad neuropathy.
Undiagnosed B12 deficiency caused mine. Now I inject with B12 twice a week.
Does it make you break out with cold sores b12 shots
@@davidredford3111 It shouldn't do that. I inject B12 every three weeks and in many years it has never triggered such things.
@@davidredford3111 Hi David, It doesn't for me. The injections have helped me so much. I can walk again.
Are they going to move your dose out more and more over time?
Has the neuropathy decreased due to the injections? By how much? Is the numbness gone or is it slowly going away? Thanks for filling in the details.
I had a gazillion tests to try to find the cause of mine but it was diagnosed as idiopathic. They now think most idiopathic neuropathies are auto immune. They also know that those prone to immune disorders tend to get more of them . I also have allergies, eczema, asthma, a immunoglobulin A deficiency and MGUS (a precancerous condition that sometimes becomes multiple myeloma) . Immune disorders run in my family too. I think it’s a genetic weakness.
My neuropathy started after I had some chiropractic manipulations. Has any else had this happened to them and did you find any relief?