2 years of POTS GONE in 1 month (Change this approach) PART 1/2
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- Опубликовано: 28 дек 2022
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About Dr Nathan Keiser:
Dr. Nathan Keiser DC, DACNB, FABBIR is a board certified chiropractic neurologist specializing in non-surgical, non-pharmaceutical treatment of dysautonomia, traumatic brain injury (concussion), and movement disorders.
Dr. Keiser was certified as a diplomate in chiropractic neurology by the American Board of Chiropractic Neurology (ACNB) in 2010
and has since served patients from across North America and around the globe in private practice.
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Website: www.drkeiser.com/
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Don’t waste your time watching this video. He doesn’t actually tell you what he did to help this patient who he claims to have miraculously healed.
Watch part 2
ty🖒
Thank you
Thanks
Hey, some aminos helped a lot since they improve blood flow and are not Rx drugs (you can take as much as you need) try L Citruline + L Arginine, that has helped my POTS so much! My BP is now normal, no more spikes or afib issues. I can now gradually increase my activity level(s) to deal with the deconditioning that lack of exercise causes, very few doctors mention activity levels since we usually flare, I'm an EDS patients so I was born with this nonsense but I do feel much more "normal" now. LDN is another option that seems to help some.
You didn’t tell us what kind of treatment worked on her!!
Because it's all bulshit. ;)
Watch part 2
Thank you doc for sharing these stories - they offer a lot of hope 👏
Glad to hear that. Thank you very much for watching and taking the time to write a comment
That is what pots is, in pots the blood vessles dilate causing the blood to pool in lower extremities. The reason for the tachycardia in pots is the heart is trying to compensate for the loss of blood flow to the brain, by pumping faster to try and get more blood to the brain.
@Selenamilitao Given you susceptibility to being fooled, I think you never had POTS and was never cured of POTS therefore. POTS is a real thing and not a money making machine for snake oil salesmen.
Varicose veins / venous insufficiency can play a part too yet doctors never mention our vein condition....do they? I've never been asked by any practitioner.
I’ve been struggling for 3yrs with PCS and was diagnosed with POTS last year. It’s rare to find information linking the 2 issues so, I’m excited to find your channel.
I just started looking into a Functional Neurologist this week and I’ll be showing her your video as I suspect this is some or maybe even all of my issue.
Thanks for your passion - I’m hoping it will help me and others out there searching for answers.
I’m sorry to hear you’ve been struggling, but happy to know you can open the door to some new possibilities. Keep me posted on how you’re doing!
@@dockeiser can men get pots. MY DOCTOR KEEPS RULING ME OUT. AS LONG AS I LAY DOWN HEART RATE 60 BUT WHEN I STAND ITS LIKE 115.
@@hova575 yes men can have POTS the problem is most doctors aren't taught about pots.
@hova575 I feel like they should have a slightly different criteria for men.
@@Batshite_crazyI've had it fybromyalgia nowadays
What were the things you did to help her improve her symptoms? I rewatched it but all I heard was “we did some things and then she improved” looking to help treat my own issues with POTS
Hey there John, if you watch the second video in the series, it goes through the treatment process for this case. Thanks for watching
@@dockeiser thank you for the reply!
@@dockeiser I watched both videos & am a loss for what the treatment was? Can you please reply what specific treatment protocol is?
@@nickolwilson2212
I think the treatment protocol is to book with him and give him money.
You just lost me as a further viewer by not telling us WHAT YOU DID FOR THIS 21 YEAR OLD GIRL TO HELP HER GET BACK TO NORMAL!!!!!!!!! 😮😮😮😮. IT IS **NOT** ON THE SECOND VIDEO!!!!!!!!!!!!!!!!!!! Waste of time. THANKS FOR NOTHING!!!!!
I have POTS and ive been doing the wim hof method and it has really helped me a year ago i could not walk 50 feet without fainting and had really bad brain fog but i started it 2 weeks ago i felt a urge to watch him i didnt know anything about his method before but it has helped me alot and i feel normal again I did his method and mediation if you have POTS i would give it a try it may not work for everyone but it worked for me
That’s really great that it has been effective for you. I would throw a line of caution to others to consider the mechanism of their pots. some people will have a much different response. I’m super happy for you and I hope you keep after it!!
This makes so much sense!
I have a ton of symptoms. One if the confusing things is I also break out in a sweat to the point of overheating. It happens everytime I try to push through and I nearly black out if I don't lay down.
I have the same symptoms, no Doctor has diagnosed me. Or the doctor is not medically qualified
Can you do a series of videos with exercises we can do at home for POTS?
This is exactly what I needed to find. I'm suffering badly from this right now
Total breath of fresh air!
So what actions were taken to improve the situation please?
Thank you doc, this speaks to a lot and carries an important message, so much is possible with the right approach. And, as always, i have a question: can a compromised blood flow to the brain not be a result of an injury, but of other factors such as for example chronic muscle tension, postural problems, long term stress/anxiety, etc. And if so, can they be treated with some kind of tailored (or standardised?) training plan? Or is there some kind of 'brain gym' neuro-training people could use as self care? If i can do something to look after blood flow to my brain, i surely want to do it! Thank you and happy new year!
Great question, I'll do my best to answer it here! The type of reduced cerebral blood flow we are discussing here is the chronic type. This results from some type of pathological response in the body. It may be relative to the neural control systems which govern the signaling of the process. It may also be from disease or inflammation within the blood vessel walls, or even secondary to another type of problem that may restrict cerebral blood flow like hyperventilation or hypovolemia. In these types of cases it is worthwhile to prioritize solving the underlying problem.
For people that are generally healthy, but interested in sustaining good circulation over time, the good news is that there are general healthful activities that can support healthy circulation.
Regular exercise across domains have positive influences on CBF ranging from sustained low level cardiovascular exercise like walking all the way to heavy resistance training. Each provides a different stimulus that challenges the vasculature in an advantageous way.
Swimming or immersion in water also provides a hydrostatic pressure change that "squeezes" blood toward the head.
Breathing techniques that favor accumulation of CO2 (slow nasal breathing), improve vasoreactivty which has a positive effect on cerebral circulation.
Challenging your brain cognitively, emotionally and with progressive complexity requires more synapses to be active in concert with each other. This coordination of neural activity produces a high level of neuronal activity which in healthy system provides a challenge to synchronize the neurovascular unit.
On the diet level it is easy to get in the weeds, but eating a healthy diet can maintain neuronal and cardiovascular health as well.
Suffice it to say we could cover a lot of ground just answering this one question, but hopefully this is a good place to start. You are right. @hubermanlab has done a wonderful job of taking some of what we have learned in these different domains and made it accessible for people interested in applications across a healthy lifespan. Take care
@@dockeiser wow, Dr Kaiser, first of all i'm actually totally amazed that you put in time and effort to provide such a comprehensive answer. Honestly. I'm so greatful there are people out there who actually care! Thank you.
And another thank you for covering so much ground in your response. I know it's not exhaustive but gives me a great overview and actually provides many clues for further explorations of more healtful life choices. And yes @hubermanlab is a treasury of knowledge, so so helpful. You guys really SHOULD do a podcast together, i can provide an endless list of questions!
And on questions, i always have more of them to ask, however only when it's not overusing your generosity. Please let me know when i start pushing the limits!
Here's to a happy and healthy new year full of good people and meaningful connections, best wishes dr Keiser!
Haha! I appreciate the questions and the opportunity to share. One day that podcast conversation will come and I hope we can answer all of your questions!
Please keep them coming and I look forward to trying to answer them. 😊
I've had some success with improving POTS and my chronic fatigue syndrome by making painfully slow changes over time. For example, I took my hardest task, showering. 3 years ago I could only shower once a week. So then I pushed for 2 showers a week. When that finally became easy I pushed for 3 showers. It has taken YEARS but I can now shower about every day again. (With cool water as hot water makes me pass out). I've done this with other daily life tasks too and it has helped.
Glad to hear about your perseverance 💪
Does taking showers would help reduce POTS symptoms?
@@yuzhang984no, it’s just such a daunting task to even take a shower
I am so sorry to hear that. My wife also developed POTS after Covid-19 and has to rest at home with nowhere to go, which makes her very depressed. Is there any treatment for it?@@USAneedsGOD
@@yuzhang984taking showers specifically does not help POTS but deconditioning does worsen pots so it is important to do what you can to move and get blood flowing as to try to prevent deconditioning
I SEE NO TREATMENT 😢.. It does NOT HELP 😢
How did you fix the blood flow. I have preload failure and diminished flow diagnosed via advanced CPET w/ right heart cath. I'm looking at trying mestinon. I'm advised this will help with blood flow.
Your first opening sentences of this story completely mimics my own. Hope I can find some new insight to things because I’m now 24 and still struggling
The I can't
I am going through this right now. Ever since I got a really bad cold last February and since then I have dealt with lightheadedness, fatigue, tension headaches, increased heart rate when standing and sometimes chest pain. I can’t work, can’t go out and had to move back in with my parents due to not being able to work 🥲 I’ve went to doctors and had a mri but everything comes back normal, I just want to be able to have a normal life again. I’ll be 24 next month and if I can’t celebrate it I am going to be more depressed than I am.
Just read your sad story, I hope you have found some help to improve your symptoms and that you were able to celebrate your birthday 🎉
@Selenamilitao that is very interesting, thanks for sharing your success. What herbs are you taking that has helped you?
Why do people make these videos and say NOTHING about what helps ???
This is an awesome story
Thanks Chris! Part 2 on the treatment is coming next
How did you test for the blood flow and the brain?
Hello Dr., Could a person have the opposite problem, blood flow problems to the brain when laying down?
What was causing the causing the drop in blood flow on the left side of her brain?
Hello doctor, this is typically what I had after the traumatic brain injury on 2014 till now but doctors just diagnosed with dysautonomia following head injury.
What should I do? Thanks
These 2 diagnoses are similar and can have a lot of overlap. If you have the opportunity to work with someone that can help you improve the function of your brain, that might be a good next step.
@dockeiser where ?? Am not at US or UK
Yeas I need this now
It's a great story for her, but it's one case...the title is click bait.
Thanks for watching. The video tells a story of a girl with POTS who suffered for 2 years, changed her approach and solved it in a month. If you watch part 2 I discussed the full treatment model.
@@dockeiser So what's the solution ? I'm too lazy to watch the whole video.
Also all symptoms of thiamine deficiency. I started taking benfotiamine supplement and it’s changed my whole life and ALL symptoms
What's your dosage, how many milligrams a day?
This was very helpful, but you didn’t say exactly what you did for her, what steps you took to actually help her to recover??
What exactly did she do in terms of treatment to help that part of her brain get blood flow ?
I see you found part 2 so you saw the treatment 😊
@@dockeiser yes! I spoke to soon!!
Sir could you do an online consultation?
My daughter got diagnosed last Thursday, Cardiologist but her on beta blockers, but she has developed pain in her extremities after taking her medication. she is severely exhausted, can't walk more than a couple of steps without getting winded. I have been on hyper mode since.
I was wondering how can I contact you , I have high hopes that maybe you can help me find the actual problem that I have. I have been diagnosed out of no where with pots but I think it might be something else
Pots suck! Thank you for putting this out doctor!
I feel I meet the classic symptoms of POTS, to go along with other seemingly-dysautonomic symptoms. How do i get my doctor and neurologist--who barely have 5minutes to spend with me--to look deeply into these issues and order these tests? All my neurologist does is a basic examination and orders an MRI with contrast (which came back within normal limits). Or where can I go to find a doctor who will? Also, this sounds like a neurology issue and not a cardiology issue?
Ask for a tilt table test
Please try taking vitamin B1 (not synthetic) it helps with these symptoms. Also Please take a look at "Dr Berg pots" video. I believe it will help greatly..
Hi do you treat pots and pls where you base ?
I read that chronic inflammation is the root of POTS... so I started using curcumin, and yeah, it helped me relieve the strongest symptoms... however... the condition has already caused TR in my heart.
DNRS - Dynamic Neural Retraining System / Nervous System regulation. It’s all from the limbic system / trauma responses from the brain.
How do you monitor blood flow in the brain?
Where is your clinic located?
How did you know the specific part of the brain that had low blood flow? This is really interesting!
So being a pots patient in Canada who do I ask to map my cbf and what is the test called? Because they just told me to eat salt and my life is stalled in pots purgatory has been sine I was born
DNRS program it helped me with my chemical sensitives. Somatic therapy good for nervous system regulation. Acupunture might help or certain vitamins like b12 or b vitamins.
What test is this? I believe I am having the same issue! I always have low CO2 levels in my blood work. I have not been able to leave my house as I can’t walk longer than 5-7 minutes and no doctors are listening to me or seeing the big picture. I keep getting sent to specialist after specialist!
What test do we need to ask for to find out the blood flow to our brain?
They can for office visit. They Check blood pressure sitting then stand check again. The Dr can do in office. There is a Table Tilt Test they will have to write order for it to be done. Hope you find out and feel better. It runs in families. My granddaughter who is 22 has it. I had trouble when young. Now in my 60's and I am really dealing with it along with heart problems.
Hope all goes well for you
I think i have dystonia (tongue curls on its own eveb on meds... had body jerks prior and panic attacks). Is thiz commo.n after concussion.
I got pots syndrome following vaccines! I believe that we have small fiber neuropathy or injury to vessels. I believe that we can’t assure that a person can recover without knowing underlying condition. Some pots types are permanent
I think is just body response.
Correct! I am a vax injured too
Where are your offices located?
Hey man i started getting dizzyness and fast heartrate when standing it all started after a viral infection but doctor said it wasnt covid or flu could that have caused it if yes what can i do
at 1:45-“Mom drug [drugged] her?” To get her there, or was this an ultra-quick illustration of the stuff dysautonomia patients deal with?
B1 Thiamine....
How exactly are you increasing blood flow though?
You can watch part 2 of this video to see the treatment rationale from this case and how we did it. Hopefully that helps!
Where you located
Do you know of anyone in Wisconsin who can help me track these things I am 41 and still have a lot to offer the world and my 4 daughters need me I have been left to fend for myself at this point????
I believe that’s true!!! I don’t know anyone off hand in Wisconsin. But there are colleagues in Chicago, Minnesota and I’m here in Michigan. So not too far! Keep pushing forward 🙏
Where at in Chicago????!!
but this literally tells us nothing. how do you monitor the blood flow the brain? what did she change to get better flow? what was her routine? my bp is 130/80. when i stand its 140/90-100. i just get told to do the chop proctol and beta blockers. what should i be telling my doctor to improve blood flow to my brain?
How do you detect POTS?
Tilt table test
I’ve suspected my issue is a blow flow problem
Iv had pots since I had a seizure of had it for year's it ruined my life since I was 14. 😭 I came here because I want to change that.
You do realize you don't have a breakthrough treatment for POTS right. What, you told her to consume more salt, wear compression garments, and exercise. Why was that so hard to mention in the video.
You should check out the second video and see it was none of those. 👍
@@dockeiser Sorry, jumped the gun. Thanks for uploading these videos. They're actually very useful.
@@eddie8489 I appreciate you saying that. I’m glad you gave it a chance and watched the whole thing. Thanks for keeping an open mind
...helpful as mud.
I don’t like to rely on getting it thru diet alone because I end up craving McDonald’s constantly and my waistline and gut suffers lol I prefer salt supplements
It doesn’t help at all
What’s was the treatment
Hey there, there is a part 2 to this video that is the treatment. Hope you enjoy it
um hello why did you tell my life story
You did not say anything
I'm furious now. My heart showed low volume and the cardiologist said" those are computer generated numbers they don't mean anything". On my ECHO. How insulting! And I've suffered for 10 YEARS ! 😠
I understand the frustration. Keep moving forward. it's the only option.
What is your heart rate during the day?
People are not stupid: everybody realises that you are only stating what was wrong with her, her symptoms etc - but you refuse in any of your videos to state exactly how You helped her…what you actually did etc.
That is why there is a part 2… bit of an overreaction there
Your vidoe doesn't help... unfortunately. Where is solution
My POTS was exacerbated by covid..
I got nothing of any value from this
Sorry, but this works for very few people.
Thanks for letting us know. That hasn’t been our experience
Then you’re dealing with actual POTS. Most have a 15-20 year history. Literally not a single person, including myself, has been helped by chiropractic.
Constantly zooming the camera in and out while you’re talking adds nothing to the video, and in fact, is visually distracting and unnecessary.
I can only laugh at something like this. It was not POTS, because POTS will come back. It's about hypermobility, connective tissue disorders and the inability to maintain a blood pressure also possibly because of a cortisol receptor problems. It's a fucking dysautonomia.
I have been able to do one month of all those things - even much longer - along my life. But I will still vomit upon showering, can't stand carbs or anything more than 1.5 dl in my stomach. Heat of more than 21 C will make me a complete invalid with no capacity of digestion (as in gastroparesis).
I am sure you really excited about your own innovations regarding this, and it is always great that people try. But please. One month of getting better? Seriously? That is your criteria for 'cure'?
Didn’t say what helped her.Useless.
Worst video ever WHAT DID YOU DO,ALL I HEAR WE DID THIS AND THIS WHAT MANNNNNNN
Hi there make sure you watch both parts to this video! We also have more recent videos that are much better presented!
SCAM VIDEO BY SCAM CHIROQUACKTOR