I had dysautonomia/POTS/tachycardia after a covid infection early in 2020. It took at least two years for my autonomic nervous system to recover to anywhere near stability. I drank water, I took electrolytes, I did breathwork, I cut out a,b,c etc. But the reality - the body will adjust in its own timeframe. Dysregulation post-covid is so common as to be the norm.
I still have long covid after almost two years. I am just now learning to walk again and yet my nervous system is shot. I can't use my hands, open bottles, etc. The soles of my feet are always on fire. This is a monster of an illness and I agree with you. 3 times I have had to go to emergency for tachycardia. After two years I'm still in the process of 'healing' YES the body will adjust in it's own time. For anyone dealing with or suffering from long covid, may you heal fully, give yourSelf time. My brain is working hard to try to keep up...I wish someone would talk about covid brain fog.
not a "vaccine"..please! It's no 'injury,' either..it's the plan. I got this from the illness, march 2020, zero medical help for severe case...as planned, also. But yes.
That’s EXTREMELY rare (as with any vaccine) and it’s usually a LOCAL injury (the nurse injected in a bursa, in between the muscles of your arm, and that injures it, which takes a long time to heal). Vaccines are the reason we live for so long. We got very lucky that the mRna vaccines were already developed and they’re highly adaptable and we were able to make them as quickly (bc they’re adaptable, not bc they weren’t thoroughly researched) as we did. We avoided HUNDREDS OF MILLIONS of deaths bc of that.
Appreciable as for the phisiology, but does not INVESTIGATE THE ROOT CAUSES. That would be really interesting, but I'm afraid, much more compelling. Next time?
@@JBrandiTV I wonder if that can be the cause or a part of the syndrome. For sure most health problems seem to origin in the gut, so let's investigate that. Pesticides, environment toxins voluntarily o not assumed...
I've been looking into this kind of stuff for some of the issues my wife has, though she was diagnosed with fibromyalgia. I haven't seen anywhere explicitly say it but I'm wondering if Fibromyalgia is another form of dysautonomia, anyone have any thoughts on this? The symptom overlap for dysautonomia, Fibro, and even menopause is something I find interesting, along with the possibility that psoriasis may be linked to dysautonomia. Just something to think about.
Hi. I was also initially diagnosed with fibromyalgia but recently I was told it’s POTs. And it seems POTs and Chronic Fatigue Syndrome are related. And anything with the menstruation cycle including menopause may make it worse. I go through the same thing.
I had the virus and shortly after, went into post menopause. I have this weird fatigue, dizziness, digestive issues, brain fog and more. Was it the virus? Is it the menopause? I have also researched HP axis dysregulation that is common after the virus. Definitely nervous system related.
Estrogen dominance is something you can have most of your life, or not, but all women get it for a few years at least when they go through menopauee, since progesterone drops much faster. Eventually estrogen should also drop, but it might not. Fibromyalgia is one outcome of estrogen dominance, and pain levels increase at times when estrogen goes up, while testosterone and progesterone are protective and anti-inflammatory. I find it interesting that estrogen is eliminated in the same pathway as adrenaline in the body (COMT). When either estrogen or adrenaline are high, it will congest the pathway so the other will build up in the body as well. If there is chronic stress, including from chronic illness, the body will favour making cortisol over progesterone, leading to estrogen dominance even if estrogen isn't high. To end the cycle, the gut microbiome and the nervous system have to be addressed. Often seeing a functional neurologist and doing the therapy can permanently heal the nervous system. Then everything in the body works as it should, including the digestive system.
@@koalamama2are you a specialist, or became such from experience? What you say makes complete and absolute sense. Wish there were medical doctors who knew this and were able to address it. Do you know anyone of the kind?🙏
Discuss this tough sleep-disturbing issue with your Primary Doctor or a Cardiologist and ask for a treadmill stress test~Plus, let them know the frequent heart racing is disturbing your ability to get good rest during the night☆☆...Taking an Atenenol pill before bed is a lifesaver for me as this can also be an electrical issue occurring in the heart!! I have been on this safe medication for several years and feel so much better. Some days, I may need one earlier, such as late afternoon or early evening or my heart starts hitting over 110-120bpm:( Be firmly persistent in getting help to feel better and wishing you all the best on this health journey♡~Blessings from HOT Arizona, Holly:)
I’ve heard of people after having Long Covid getting POTS, But Never From the vaccine itself, so I would guess that if your son Actually Has POTS it’s from Something Else
I tend to go for half a gallon a day when doing well hydrating. The army says no more than one quart an hour, no more than 12 quarts a day. So that is a huge gap which should tell us that it is ok to chug water a few times a day. For optimal hydration, sip on a quart container and try to consume over a 2 to 3 hr period. We used to slam a quart a half hr after dinner at Ft Jackson in August. Yes, you spend the next 2 hrs going pee, but not more than 3 or 4 times. That can he easily fit in during commercial breaks.
Me too....nurse,worked the plandemic, but got this (plus more) after the severe Infection march 2020... not injection. I would never EVER sign up for or allow anyone to possibly ruin my health.....especially when they left me for literally DEAD. I miraculously survived but was also left to thrive. I spent the last 4 years doing literally hundreds of things, with positivity, faith, hope, fortitude....trauma therapy, A. Acupuncture, massage, HBOT, iodine, blood cleansing, etc...stay at it, but do not take 1 more shot if you did. Same spikes - poison. Ivermectiom is also helpful. Check your thyroid CASCADE.....also iodine,
@@jac1161I never had a single shot but post-plandemic in 2021 my anti-depressants suddenly stopped working for my anxiety. Ever since I have been on a horrible roller coaster of tests, doctors, etc etc. Now my body is rejecting so many medications.... I have gone both medical and the holistic route on trying to get my nervous system back in order but I struggle daily. I have my first acunpuncture session in two weeks and hope that this regiment will relieve some of my daily symptoms. Your comment captured my attention because I feel we are experiencing similar reactions.
WOW WOW WOW….. I can’t believe I am seeing you!!!!😁 I would LOVE to talk to you to tell you about what I found out about another reason why my hips dislocate but I didn’t know how to get in touch with you….. you look AMAZING and it’s SO WONDERFUL to see you 😊🤗 You have SO many patients that you might not remember me…… I was your patient when you were in Maryland. My last name has changed from Pinizzotto to Herford. I hope you see this and can tell me how to get in touch with you. Nina Herford
same, plus stroke that did't get help during my sevre covaids, mold illness, lyme, arsenic poising, type I diabetes no fault of my own ...but getting better since I got WAY out the system (scary swamp). See doctors or better, nurse practicers outside the system...you'll get to roots amd heal stuff. I cam't heal the diabetes\, heart hole, etc..but will take whatever I can :) Prayers, love. Gotta help yourself...be patient & perseverant
Getting POTS after Covid has explained 25 years of pain and other odd symptoms. Found out I have EDS at 49 years old! But, luckily my kids now have a diagnosis! They are super bendy and always in pain like I was. Maybe they will be able to get help that I never got!
