Відео

I’ve got all these symptoms and is awful shit

If you've really been around the block, you know any doctor mentioning "Irritable bowel syndrome" (worthless trashcan diagnosis) immediately discredits them. Why can't these guys identify a damn cause 99% of the time? it's such a common problem with them. GI doctors are the laziest, worst doctors. Zero critical thinking it's like they're some glorified Google bots. I've been through absolute hell and they've never helped...

Benzos are also mast cell stabilizers

If I am to take b1, should I be concerned with side effects or depletion of other nutrients with higher doses

Wow.. this is powerful now that! Understand what it is about

Eat lying on your stomach ????even with y hyper mobility I would still choke

Oh this was such a healing video! Thank you so very much for this❤

Also the other Dr has assaulted me in the examination room but no one has done anything about my complaint! Gets worse! The closer-called the police and medical insurance company!

Is there ANY LINK with premature birth and Gastroparesis?

9 mm herniation. Need surgery. If any life threatning?

dr recently said iron was a little low, said not much , no reasons why but determined to find something but never thinks about the actual conditions being involved with why. im also allergic to nuts and olive so im trying to work around foods with that in it. i tend react to lot of things , the only thing an allergist said was, 'your system is just touchy i guess just avoid stuff" no real reason or what is going on. or real advice or help. way most doctors in my entire town act with conditions. they don't even want to send me to a pots specialist.

I’m way too sick to train a dog. I’ve been in this room 99% of the time for eight years. I have an emotional support dog that has cancer and months to live. I can’t imagine not having another dog, but can barely get him to the door for potty time. I might have a little life if I had a service dog and a power chair, but I’m definitely too poor to buy them, and too sick to train a dog.

I’m hyper mobile, have full body neuropathy and dysautonomia on top of a thirty year old spinal cord injury. Much of my pain these days is burning, which isn’t easy to control with medication, but for decades I had severe back and leg pain below my injury. I’ve also suffered for years with trigeminal neuralgia. Besides head to toe burning, I have neuropathic itch. All my peripheral nerves, inside and out, are sick. I’m finally having a sleep study in a few weeks. For more than fifteen years, I’ve only slept for three of four hour hours, at most, usually interrupted. Now it’s two- I go to sleep about 10PM, and wake up at midnight. When I’m falling asleep, there’s a revving of the heart and a need to vocalize if I don’t want to move. This is usually repetitive. These are DEFINITELY waking me up. Oddly, I’m wide awake after sleeping two hours and can’t recall any wake up process, I’m just awake again. If I happen to manage five hours or more, which happens a few times a month, THEN I’m tired. 🤷🏼‍♀️

What if you have parasites in your intestines? I have told my nurse practitioner that I have intstal parasites and you should have seen the look i got 😳..ni have been fighting on my own until I got to the point my body is so weak.. now on top of that my doctor put me on diazepam.. now I'm having extreme intestinal distress.. along with all the other symptoms that come with.. extreme dehydration/ malnutrition malabsorption 😭

Love your presentation! Most informative and well spoken video I’ve seen on this topic. Hope you continue to post videos. I’m sure it’s helping so many people. THANK YOU!!!

I'm 21 and I remember having symtoms since I was 9, I was diagnosed 3 months ago and it makes so much sense. Somehow I treated myself (before having a diagnosis) by drinking gatorade, eating salt and sitting upside down

ANYONE who reads or watches this, have your doctor check your b12 and d3 levels!!! I’ve been suffering for years and it TOOK YEARS Before my doctor thought to check those levels!! I felt like my “ lights” were going out is the best way to explain it. I felt better almost immediately after starting these 2 supplements! I just hope my nerve damage isn’t permanent. It can take 6 months to a year of supplements to get the full benefit ….

please any info on .. enviromental .. eg .. electro 4G/ 5G sensitive.. heavy metals weather modification, .. micro plastics, .. nano particulates, ( I live west coast ireland, a exit corridor for euro aroplanes, an age 73 )

Some helpful info BUT no mention of animal based foods solution. So misguided. We must eat pastured meats and definitely pastured eggs. An egg, the perfect combination of protein and fat macronutrients, wasn’t even mentioned! Raw milk is replete with healthy pre- and pro-biotics. This was nutritional malpractice! Is this person a paid shill from the “fruit and veggies” industry?!

I have POTS. I was finally diagnosed after about 7 years. I suspected it and mentioned it to my doctors. I was brushed off until my symptoms became undeniable.

OMG, I have been struggling with these symptoms for years now. The heart doctor thinks it's a heart thing. The PCP thinks it's everything from stress to depression to rheumatoid arthritis. My gastro keeps testing me and scoping me and finding nothing wrong. I've been tested for low T, low Estrogen, polio, Lyme's. I've had 2 colonoscopies, 2 heart attacks and three stents which have not fixed these symptoms. My labs keep coming back normal (this is the most frustrating thing.) I feel like a have a small case of the flu every day of my freaking life. Not sick enough to stay home, but certainly sick enough to make life miserable. I have stopped enjoying anything. My inability to regulate my body temp is the worst symptom. I'll go from wrapped up in a blanket with thermal underwear on sitting on a heating pad to sweating and shucking off clothes and back again all while simply sitting watching TV. My recent heart catheter held promise for relieving this heaviness I feel in my arms and chest and weakness but it didn't get better. I have an appointment with an arthritis doctor in two weeks and hope to get some help. This is miserable.

It causes ms as well ???

Thank you for sharing this information. I am in constant investigation of myself and so far this is the condition that match in all symptoms. I also came across a video from Dr Lair Ribeiro, that alerts people about dysautonomia and he related this condition with low tocotrienol ( a form of vit E) this is found in a plant called urucun, native from tropical contries. I am now in process of testing it.

Dec 29 i am having bad nausea

❤ Thanks for sharing ❤

I totally agree with your findings thankyou for your intelligent research and therapy.

Have any studies been done on non-diabetic sugar fluctuations within range but large swings? Leading potentially to nerve damage involving the autonomic nervous system?

I notice that you did not mention low copper....but I have found that many people (like me) that have iron issues....have the root of that problem caused by copper deficiency....copper deficiency leads to iron transport issues and anemia / low oxygen / extreme fatigue etc....

My notes... Supplements to try: Vitamin d-3 Iron Thiamine B12 Vitamin C (helps with Pain) In general: More salt Less Gluten Smaller, Lower Carb Meals Increase Fruit and Vegetable Intake Cacao for less fatigue Beets and Nitrates help with Exercise tolerance Easy Recipe Ideas Avo Toast Jicama + Guacamole Cut veggies carrots celery cucumber Wraps Nuts + Seeds Apples and Nut Butter Greek Yogurt and Fruit Edamame Celery + Cottage Cheese Premade soups: Butternut Squash Soup Garlic and Potato Soup Creamy Tomato Soup Oat Milk Cumin Carrot Soup

So we're and how do you get a proper diagnosis from

Doesn’t Propranolol decrease melatonin? When is the best time to take it so sleep won’t be impacted?

EDIT: I’m sorry for my typos and bad grammar my phone is glitchy so much! Does anyone else have severe adrenal issues too?? I think adrenals are the extend nervous system kind of right? 🤔 and I Tourette syndrome, sleep apnea and asthma history! I have blood sugar issues but I had two normal a1cs over a year ago and I have been labeled a very extremely massive hypochondriac for 11 years but pretty much ever major claim ended up to come out to be true this year 😭 I’m getting a lot of ableism and gaslighting unfortunately from my family and I absolutely can’t take care of myself. I have extreme urinary excess and loss of bladder control and Brady and tachy almost an arrhythmia if not an arrhythmia. This is fun,lol but I’m grateful despite being told some pretty offensive things and being humiliated and shamed so much that I got diagnosed so quickly. I get my testing done February 2nd . Also the dr that originally diagnosed me , granted he’s very old for a dr and has been working professionally for about 45 years , always said I needed to see a psychiatrist and when I could not walk I forced myself to his office eventually after months in a wheelchair bc I was desperate and he got so frustrated and begged my mom to make me go to a psychiatric hopslital to be assested for a mental breakdown but I got assessed many times lol, it is baffling that a dr who knew of dysautonomia in 2020 didn’t think it could be that bad, plus adrenal issues that are bad too. Wonder if that’s common . What I’ve been through is extremely embarsssing and hurtful from many types of professionals and it has me tearing up thinking about it. And what I go through with people in gereral so often it’s tough. I probably don’t have POTS so idk what all is wrong with me I’m very upset I shut this out my head 247 and am constantly in a freeze state I was in a ginormous insane fight or flight earlier this year and I haven’t gotten therapy still unfortunately. I’m so depressed and I have no one to talk to . It seems everyone just hates that this happened to me and they resent me for it. I literally am in a survival mode so badly constantly and I can’t process or function cognitively either. Feel like I can never have children and prettt much confident I can’t but I wouldn’t anyways being so sick. I lost all contact with my family and they seem to hate me . They just don’t under stand and I just want someone to talk to and the er is the only time I can potentially get support nobody deserves to live worried about everything like that and consumed of any type of sickness. I will pray for our world everyday bc suffering seems inevitable for anyone almost now in all types of ways 🙏🏻

Word if you think it is a Snowman of that reference back to narrative learning of times takes for multiplication Often recommended for those with same memory issues dyslexia whatever label you want to put on that… yeah this is not going to equate to being able to do long math problems it’s a trick in a toolbox for a moment in time but it does not get the child to where they need to get to a level in their functioning to progress In a real applicable way to say algebra or any form of higher level math. Been there done that hit that wall

There is no sleep. There are no Drs

I can't tell you how grateful I am that I found this video.

Thank you for the information.

Thank you

What blows my mind is that you don't mention Myalgia encephalomyelitis tied to CFS & PEM?? The most common of the autonomic disorders, and now seen to be found in many Long COVID sufferers. Heck, you didnt even mention EDS. You might consider updating this video, & lose the music. Very agitating to lots of people with ME/ CFS. Btw, it can cause inflammation in the brain, spine, & peripheral nervous systems as well. It is a very serious disease affecting at least 70 million Americans. Might want to mention it since most doctors still dont know about it. Ive had it for well over a decade & have veen misdiagnosed multiple times, & untreated. As such, I’m now in the severe category. Know what you're talking about if your going to put out information on such a serious topic. Otherwise, you can send people down rabbit hole after rabbit hole, not knowing they’re missing the key piece of the puzzle.

Thank you for this. My general practitioner told me that the root of my issues was anxiety and that I just needed cognitive behavioral therapy. I pushed to see a neurologist out of my network and finally got the suggestions to take propranolol, nortryptaline and he was the one who recognized my hEDS along with my immunologist. Your information in this video helped me decide against Zolpidem (also prescribed by my GP) as I was worried about taking that living alone but also because of any residual impairment. I’m sincerely grateful for doctors who think outside the box to help us find a better quality of life. ❤

This is one of the single most annoying videos I have seen on UA-cam. The music is both maddeningly repetitious and distracting. The delays in the spoken content to wait for the drawings to happen make for content that is anything but easy to listen to.

I have neurogenic orthostatic hypotension which is NEVER discussed....as far as nutrition..I have migraine so foods are extremely limited..I have MCAS also..I realize pots is more popular..have no care team...waiting for an appt with a real doctor..the orthostatic director at the Cleveland clinic..sad part 6-7 month wait list 🥺😢💔..sodium triggers migraines by the way

No mention about cannibus ? Plus or minus ?

Hey folks, this is a nutritional deficiency in most cases… do research, don’t just take the drugs they give you, especially since they don’t cure this. EO NUTRITION, here on UA-cam, is a good place to start your education.

The main symptoms for me is exhaustion, heat and excercise intolerence, doing any form of physical activity IMMEDIATELY makes me feel exhausted hot and sweaty, cant leave the house on a hot day, as the sun makes me feel absolutely drained, and i feel like tearing all my clothes off just to cool down, its horrible.

Can I use bisoprolol for the night time adrenaline? I am currently taking it in the morning, but my sleep is always extremely shallow. Will shifting this betablocker at bedtime help with the sleep?

Why is there NEVER any info about NOH???? WHY IS POTS TARGETED? I'm suffering from nOH and other issues brought on by Dysautonomia has ruined my life and keeps me homebound..HELP???!!! PLEASE

Thanks. Now I can understand the relation between Dysautonomia and nutrition

Hi i have just had fundplication surgery for a giant hiatal hernia. Can this cause Gastroperesis?? As my doctor cannot diagnose me and i seem to have all the symtons of it. I have been out hospital 8 weeks now but symptons started 2 weeks ago. I feel depressed and fed up with it .😢. Any advice would be helpful please. Thanks

Its stupid because you can't work, but have to work to survive. So your at a job having constant heart palpitations, feinting ECT ECT to make ends meet but you can't work too much or you get denied.

as a mast cell patient (along with the rest :P) the discussion of gen 2 antihistamines being designed *not* to cross the BBB was just a huge epiphany. gonna have to try out some hydroxyzine. speaking of mast cells, anyone discovered a sleep monitor that doesn't induce skin irritation yet? because that has stopped me from using my garmin regularly (though i suspect it's less accurate anyway)