Brad @AutonomicBrad Twitter profile | Pikagi

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Brad

@AutonomicBrad

4,228

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275

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Bachelor of Biological Science Degree. #LongCovid #TeamAutoantibodies #Bc007 . Any tweet is my opinion and not medical advice. Check out my podcast on Spotify

https://t.co/B8AGu09FC7

Joined March 2022

Don't wanna be here? Send us removal request.

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@AutonomicBrad

Brad

2 years

Long Covid begins in the brain. We have a breached BBB that leads us to not be able to regulate our cerebral blood flow in response to gravity. This leads to Sympathetic overdrive which is a compensatory mechanism and this leads to a blunted baroreflex and preload failure. 2)

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@AutonomicBrad

Brad

3 months

Was prescribed Yoga and was told to lose weight and exercise after being diagnosed with Long Covid Dysautonomia. Was told “I am a know it all” and that I wasn’t trying hard enough. The doctor said a disability letter would not be written. I was treated like absolute garbage.

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@AutonomicBrad

Brad

2 years

I’m cured as long as I don’t exert, speak, breathe, play sports, exercise, eat, sleep, drink, poop, sit too long, stand too long, overthink, underthink, work, read, play games. It’s like I don’t even have long covid if I don’t do those things 💁🏻‍♂️

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@AutonomicBrad

Brad

1 year

ME/CFS is the greatest medical scandal in human history. This disease takes people at the beginning or prime of their lives and destroys everything in their life. This disease is worse than death itself. The patient gets gaslighted by medical professionals, family members and

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@AutonomicBrad

Brad

2 years

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@AutonomicBrad

Brad

2 years

I still don’t think a lot of people understand that the autonomic nervous system is the problem with the majority of people that haven’t recovered from lc. I don’t hear this term enough. Let’s all say it together. AUTONOMIC DYSFUNCTION 👏🏻👏🏻👏🏻👏🏻👍🏻It causes the disability.

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@AutonomicBrad

Brad

1 year

A long covid patient has to be their own Doctor, Researcher, Scientist, Lawyer and Advocate all while being in a dysfunctional body that looks healthy but has the energy levels of a bed bound senior in a nursing home. #LongCovid

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@AutonomicBrad

Brad

2 years

Long Covid/Pots/ME/Fibromyalgia/IBS/Gulf War Syndrome will all go down combined as the biggest medical scandal in World History. Reversible Conditions if a cure was found but the patients imprisoned by medical and governmental negligence, minimization and psychosomatization.

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@AutonomicBrad

Brad

3 months

Post Exertional Malaise = Endothelial Dysfunction via SNS Overcompensation which decreases blood flow and oxygen perfusion to tissues which creates a hypoxic environment, reduced aerobic metabolism/less energy, and lactic acid buildup which drives neuroinflammation.

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@AutonomicBrad

Brad

2 years

No thanks, NOT interested in your nutritional advice, supplements, antidepressants, yoga, CBT, Coping Mechanisms, Spirituality, etc. Time to get to the root of the problem #LongCovid

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@AutonomicBrad

Brad

2 years

Tests that long covid patients can get that is helpful: Tilt Table, Trans Cranial Doppler, Skin biopsy, QSART, Endothelial function test, Arterial blood gas, PET Scan, Autoantibody testing (GPCR, IgA, IgG, etc). Comment below if any others have shown anything or been helpful 👍🏻

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@AutonomicBrad

Brad

17 days

ME/CFS and now Long Covid are a Career Ender for the majority of patients. This isn’t negative, this is just FACTS. The disease is Biological and Physiological and NOT Psychological. #LongCovid #pwME #Pots #MillionsMissing

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@AutonomicBrad

Brad

2 years

Things we know about LC Dysautonomia so far: 1)Reduced Cerebral Blood Flow When Upright 2) Tachycardia and/or Blood Pressure Changes upon Standing. 3)Debilitating fatigue at certain times. 4) Non Cardiac Chest Pain 5) Alpha Synuclein deposits found in small fiber nerves for some.

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@AutonomicBrad

Brad

1 month

Autonomic Dysfunction is the reason that Long Covid patients are disabled. The key to solving this mystery is what has caused or is driving this dysfunction. Functional Brain Imaging and Studies are needed. Not enough people talking about the Autonomic Nervous System.

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@AutonomicBrad

Brad

6 months

Long Covid = No Life. No friends. No Doctor taking this seriously. No money. No health. No exercise. No exertion. No spouse. No dreams. No weekend fun. No goals. No career. No treatments. No hope. No future. Get use to the word NO. #LongCovid

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@AutonomicBrad

Brad

6 months

Good Representation of Blood Flow to the brain. Long Covid and ME/CFS patients have been found to have up to a 47% percent decrease in cerebral blood flow when upright on Trans Cranial Doppler Tests measuring flow in the Middle Cerebral Artery. #LongCovid #pwME #Pots

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@AutonomicBrad

Brad

2 years

You can’t “believe” your way out of long covid/pots/ME/ibs/fibro/sjorgens. It isn’t about the mind. These are real physical diseases based on immune dysregulation and autoimmune tendencies with autonomic dysfunction which is a disability.

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@AutonomicBrad

Brad

3 months

Doctor: Brad, have you tried getting proper sleep? Those symptoms will go away if you get good rest. Me: No doc, I’ve been laying around housebound for 3 years and never thought of that 🙄That is Genius… 🤦🏻‍♂️ #LongCovid #pwME #Pots

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@AutonomicBrad

Brad

1 year

Patient in BC 007 trial is exercising/wakeboarding again and had unexpected impressive results on a stress test. Still not totally cured but his quality of life has improved drastically. BC 007 Emergency Approval Immediately 🙏👍🏻👨🏻‍⚕️ #LongCovid #pwME #POTS

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@AutonomicBrad

Brad

3 months

@marizaga yoga is useless and an insult to those with a biological disease

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@AutonomicBrad

Brad

1 year

Try any field of medicine and you will see that any symptom that is related to autonomic dysfunction they absolutely cannot cure and have no answers for. ENT can’t do anything for tinnitus. GI can’t do anything for IBS. Neurology can’t do anything for dysautonomia/pots. 🕵🏻‍♂️Useless

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@AutonomicBrad

Brad

6 months

EDS is the hidden curse behind many cases of Long Covid/Pots/ME/Fibro. This curse in the connective tissue causes lifelong immune dysregulation which combined with the right trigger (virus/vaccine/trauma/stress) can cause dysautonomia and other functional co-morbid diseases.

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@AutonomicBrad

Brad

2 years

2) The body responds by either increasing heart rate significantly or an increase in blood pressure specifically diastolic BP in order to get blood back up to brain. The Gut barrier is also breached along with autonomic dysfunction of the GI tract along with microbiome changes.

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@AutonomicBrad

Brad

2 years

All LC/Pots/ME patients need BC 007 immediately. Emergency access should be granted. This is the only drug on the market that is known to completely inhibit GPCR autoantibodies which are part of the pathogenic mechanism of these diseases. The drug is already proven safe....

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@AutonomicBrad

Brad

2 years

3) The immune system is dysregulated causing production of a variety of autoantibodies including GPCR AAB. Sweat glands are affected. The body seems to be in a constant state of autonomic dysfunction which in turn causes continued immune dysregulation. 4)

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@AutonomicBrad

Brad

2 years

Dysautonomia typically begins with the body feeling extremely weird and a feeling of not being able to adjust to gravity followed by anxiety/panic attacks randomly. These patients symptoms are not caused directly from anxiety, but anxiety can occur indirectly. Tachycardia next.

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@AutonomicBrad

Brad

16 days

Researcher for ME/CFS Ron Davis said something is in the blood that makes cells very sick. GPCR Autoantibodies circulating the blood disrupts the autonomic nervous system’s function and causes a decrease in microcirculation blood flow. When you neutralize these, the flow IMPROVES

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@AutonomicBrad

Brad

2 years

5) Endothelial dysfunction has been identified in lc. This results in slow capillary refill. Raynauds phenomenon has also been found. The body seems to be in a state of hypoxia. This is just a list of things that have been found for our record. Please add to this list🩺👍

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@AutonomicBrad

Brad

8 months

Low oxygen consumption and uptake by cells during rest and exercise is most likely caused by impaired oxygen delivery due to endothelial dysfunction. The Autonomic system signals to the endothelium and regulates their functioning. This is universal in lc/Pots/ME.

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@AutonomicBrad

Brad

2 years

4) 28 dysfunctional metabolic pathways have been identified especially Aerobic metabolism pathways causing us to basically run off of the body's anaerobic metabolism which only produces a small amount of ATP compared to Aerobic. This will result in pronounced fatigue. 5)

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@AutonomicBrad

Brad

1 year

friends. The financial burden on these patients is insurmountable. Future Careers and High Earning Salaries have been stolen from this demonic plaque. Most patients especially the ones without spouses and family are forced to live a life of poverty.

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@AutonomicBrad

Brad

3 months

Just had 9 viles of blood drawn and blood was coming out extremely slow. I told the nurse this is exactly how slow the blood is moving in my body and this is the main contributing factor to the debilitating bone crushing fatigue from Long Covid. LC = Autonomic Blood Flow Problem

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@AutonomicBrad

Brad

2 years

Notice the drugs that work on the Autonomic nervous system whether directly or indirectly are the ones with best results or at least provide relief for lc/Pots/ME(BC 007, Guanfacine, Xanax/ativan). Why is that? Because Autonomic dysfunction is the driving force of these diseases.

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@AutonomicBrad

Brad

2 years

They need to stop with the deconditioning mess. I’ve been basically bedbound with chest pain for 3 weeks and lost 15 pounds. Having a good day today and walked about a mile and a half no problem. Don’t feel the least bit deconditioned. I feel that term just gaslights pts.

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@AutonomicBrad

Brad

2 years

Ehlers danlos hypermobility predisposition is also found in some lc patients. New research should be coming out changing the diagnostic standards for this condition.

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@AutonomicBrad

Brad

1 year

The governments failed disability system is also a huge burden on these patients. The punches just keep on coming from this nightmare. Families and Relationships can also be destroyed. This disease strips the entire identity of the patient.

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@AutonomicBrad

Brad

8 months

Long Covid stole everything from me. I am a talented person with big dreams. I still have them but the future remains uncertain. I have now turned my attention to advocate and help others with long covid and Pots/ME/CFS. I am determined to help us get effective treatment.

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@AutonomicBrad

Brad

2 years

MCAS symptoms found associated with autonomic dysfunction. Widespread pain and PEM have been found occasionally or after exertion in the majority of patients.

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@AutonomicBrad

Brad

1 year

ME/CFS is living in Hell on earth. There is NO way out. You can hear the patients crying and screaming for help but it never comes. The devil himself is scared of ME/CFS. You can call for family and friends but NO one can help you. There is no light at the end of the tunnel. 🔥

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@AutonomicBrad

Brad

1 year

Anesthesia warnings and recommendations for patients with ME/CFS and now Long Covid for anyone getting surgery or dental work. #LongCovid #pwME

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@AutonomicBrad

Brad

2 years

Thanks to all of my longhaul friends for the birthday wishes. I only had one person besides my parents and family to contact me on my birthday besides all of my longhaul fam. All of the friends and potential relationship partners have left me to rot. I will remember 💪🏻

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@AutonomicBrad

Brad

2 years

The “your body is healing crowd “ is inaccurate when dealing with dysautonomia. Your body is learning to work being dysfunctional now. My friend is on year 7 and she still gets the “let your body heal” talk. It is all a load of poo poo 🧐

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@AutonomicBrad

Brad

2 years

Nobody talks much about the reduced cerebral blood flow when upright. Some days when standing too long you can feel the blood fluctuations in the brain. This can also be seen with an ICU line in the hospital. People with pots/ME/long covid have this.

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@AutonomicBrad

Brad

5 months

I see many people on here with ME/CFS and Long Covid that are privileged and have some money or someone supporting them but let’s also remember those whom the disease left them with nothing and they are fighting to survive. This disease can make you a pauper. #LongCovid #pwME

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@AutonomicBrad

Brad

1 year

After 2 years, I still think BC 007 is the best drug for covid longhaulers and pots/ME patients. This infusion improves endothelial circulation and has direct effects on the autonomic nervous system. We need this drug to get an emergency approval quickly 👍🏻

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@AutonomicBrad

Brad

2 years

Cognitive dysfunction/Brain fog has been identified in lc and is linked to decrease in Cerebral blood flow along with inflammation/cytokine dysregulation in brain. Hypemetabolism has been identified in the brain using a PET Scan.

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@AutonomicBrad

Brad

2 years

Muscle Weakness/Fatigue/Spasms/Pain can occur and has been identified in lc patients. This is thought to be due to reduced blood flow and energy available to the muscles due to a faulty autonomic response. Pain/spasms can also be due to lactic acid buildup from lack of energy.

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@AutonomicBrad

Brad

2 years

Costochrondritis is also common in lc dysautonomia. This is caused by the immune system attacking the rib cartilage and associated tissues. This generally occurs out of the blue. I have seen some patients get this right off the bat and my case specifically started on month 15.

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@AutonomicBrad

Brad

2 years

Anxiety and depression is common in lc but is secondary to the cause. Wouldn’t you be depressed if you lose your job, career, some patients lose family, docs gaslight you, can’t go to the gym, etc...? The financial impact is overwhelming for some bc disability isn’t easy to get.

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@AutonomicBrad

Brad

2 years

For people that are genetically predisposed to immune dysregulation and don’t even know it, every vaccine/viral infection/trauma could significantly impact your chances of developing a lifelong disability. This is why hEDS research is important to discover who may be at risk.

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@AutonomicBrad

Brad

2 years

You can study T cells, monocytes, covid virus, bacteria, microbiome, ebv and whatever else you want but ALL roads lead back to the AUTONOMIC NERVOUS SYSTEM and it’s dysfunction. Why is it dysfunctioning? Let’s start with autoantibodies against GPCR and go from there👍🏻

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@AutonomicBrad

Brad

2 years

Tinnitus can occur on occasion or chronically with LC dysautonomia. It is thought to be due to decreased blood flow and hyperinflammation of the Cranial Nerve that controls functions of the ear.

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@AutonomicBrad

Brad

2 years

Dysautonomia has nothing to do with your mindset. It works independently of your thoughts. You could watch or read doom and gloom all day and night or be positive 24/7 and do very little. The psychological stigma must be removed completely from this condition.

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@AutonomicBrad

Brad

2 years

Long Covid hands and fingernail beds are a big clue. Raynauds, finger nails with lines, etc. The circulation seems restricted possibly vasoconstriction. I wonder if BC 007 or Immunoadsorption could put an end to this. #LongCovid

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@AutonomicBrad

Brad

1 year

They can no longer be who they really are or desire to be. The past is too painful and the future is gone so you are forced to live in an envelope during the present time only.

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@AutonomicBrad

Brad

2 years

Hypoxia is most likely what is driving the constant sympathetic activation in longcovid/pots/ME.

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@AutonomicBrad

Brad

5 months

ME/CFS is the worst possible outcome ever. You can’t overcome it through positive thinking, medication or diet changes. Your life is over once you get it until research finds the answers (which we have mostly bottom of the barrel researchers studying it here in the US).

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@AutonomicBrad

Brad

22 days

36 years ago they said “We have no treatment for ME/CFS but we are currently looking into an IVIG and LDN trial.” Sound familiar??? This was 36 years ago and not one thing has changed. We don’t trust the ones in charge or the researchers. #LongCovid #pwME #MillionsMissing

@RFH1955

Royal Free 1955

22 days

Thirty-six years ago today. #myalgicencephalomyelitis #mecfs #cfsme #myalgice

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@AutonomicBrad

Brad

27 days

If your joints including the neck snaps/pops/clicks/cracks/crackles, You have EHLERS DANLOS SYNDROME. You were made of the wrong material genetically. These patients are prone to Pots/ME/Fibro/Dysautonomia after a strong viral or vaccine trigger. #LongCovid #pwME #Pots #EDS

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@AutonomicBrad

Brad

2 years

Microclots have been identified in a number of lc patients. This seems to be a downstream effect from GPCR Autoantibodies binding to GPCR receptors and initiating clotting factors specific for amyloid fibrin microclots.

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@AutonomicBrad

Brad

2 years

Lunulae (moons on fingernails) range from significantly decreased to nonexistent in certain digits. Skin on the hands have a dry or dead visual look. Blood pooling in limbs and abdomen has been identified due to failed response to gravity.

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@AutonomicBrad

Brad

3 months

Was told by a good source that BC 007 is helping the Long Covid patients with the ME/CFS presentation of Symptoms specifically the High BP issues and improves microcirculation. Heard results from phase 2 will show the improvements. Will wait for official announcement from BC.

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@AutonomicBrad

Brad

2 years

In LC dysautonomia, the neck and the joints in the body will pop, snap, crack, etc. This is due to inflammation of connective tissue in the stated areas. The neck specifically will make grinding noises randomly.

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@AutonomicBrad

Brad

2 years

Sleep problems have been identified in lc. This can occur occasionally or chronically. The autonomic nervous system controls the sleep cycle and the deep sleep cycle and REM sleep has been affected.

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@AutonomicBrad

Brad

2 years

Small fiber neuropathy has been identified in some lc patients. Immune dysregulation producing TS-HDS and FGFR-3 autoantibodies seem to be the cause of this neuropathy. This causes vasoconstriction that allows blood to pool towards gravity.

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@AutonomicBrad

Brad

1 year

Long Covid = Autonomic Dysfunction. Fibromyalgia = Autonomic Dysfunction. IBS = Autonomic Dysfunction. Pots = Autonomic Dysfunction. ME/CFS = Autonomic Dysfunction. Migraines = Autonomic Dysfunction. The doctors: We don’t treat the Autonomic Nerves 🤷‍♂️

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@AutonomicBrad

Brad

7 months

The reason people with Long Covid and ME/CFS tend to generally feel better at night is because the Autonomic Nervous System is less active during the evening hours and that means less dysfunction and can lead to less symptoms. #LongCovid #pwME #MECFS #Pots

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@AutonomicBrad

Brad

10 months

Hands down the best proposed mechanism for ME/CFS on planet earth. Yay finally some smart people👏🏻Definitively what I have been saying all along but great to find scientists 👨🏻‍🔬 that are working on this proposed mechanism. Highly recommend reading the full article.

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@AutonomicBrad

Brad

2 years

I am tired of these people that say I took these 50 supplements and i am cured. How about you cram that and your yoga, salts, fluids, mental health studies up your you know where so we can get to the real science about what is going on like the cause of autonomic dysfunction.

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@AutonomicBrad

Brad

6 months

No longer trust or will be reading forbes. The media can’t be trusted. Fake News. #LongCovid

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@AutonomicBrad

Brad

1 year

For the people that said LC is not ME/CFS, umm might want to check this out🕵🏻‍♂️. How about the researchers gather all of the old research for Pots and ME, learn about it, and then focus on new findings? No need to take 10 years to just repeat old findings that we should have known

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@AutonomicBrad

Brad

2 years

Migraines are common on occasion in lc due to an increase in intracranial pressure because of the faulty autonomic regulation of cerebral blood flow. This increased pressure is sensed as pain especially in the frontal lobes but can occur anywhere on the cranium.

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@AutonomicBrad

Brad

2 years

Blurry vision is common because the autonomics are responsible for the eyes to zoom in/out correctly and the dysfunction causes blurriness. Eye floaters are also common. Visible vessels also can be seen to due increased pressure in the eyes. BC 007 reduces this pressure.

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@AutonomicBrad

Brad

1 year

Can you Imagine? Getting Covid or getting a vaccination for Covid and never returning to be a normal healthy person. Can you Imagine losing your career and never being able to return to work? Can you Imagine not being able to support your wife/gf and kids?

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@AutonomicBrad

Brad

2 years

People with LC that “snap, pop, crack, stiff” their joints, tissues, neck, back, and have symptoms of autonomic dysfunction then you are definitely genetically predisposed to Ehlers Danlos Hypermobility. These patients when exposed to a strong virus end up with dysautonomia.

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@AutonomicBrad

Brad

2 years

Shortness of breath occurs during intense exertion and occasionally at rest in lc dysautonomia. Patients feel like they are breathing through “a straw.” The autonomics in part control the opening and closing of the airways.

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Autonomic innervation of human airways: structure, function, and pathophysiology in asthma - PubMed

The human airways are innervated via efferent and afferent autonomic nerves, which regulate many aspects of airway function. It has been suggested that neural control of the airways may be abnormal...

pubmed.ncbi.nlm.nih.gov

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@AutonomicBrad

Brad

2 years

LC patriots have temperature dysregulation. This is due to autonomic dysfunction specifically at the level of the hypothalamus in the brain. The hypothalamus works like a “thermostat” and keeps the body temperature appropriate to the environment. LC pts get too cold or too hot.

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@AutonomicBrad

Brad

3 months

Long Covid and ME/CFS Patients have one of the lowest quality of life scores on planet earth. The government, medical system, insurance companies, researchers, physicians, churches and even patients own families and friends FAIL these patients. Where is God? #LongCovid #pwME

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@AutonomicBrad

Brad

2 years

These diagnoses are common in long covid: Pots, Hyperadrenergic Pots, Neurocardiogenic Syncope, ME/CFS, Fibromyalgia, IBS, Complex Regional Pain Syndrome, Dysautonomia and many others. What do they all have in common? A dysfunctional AUTONOMIC NERVOUS SYSTEM and AUTOANTIBODIES 🕵🏻‍♂️

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@AutonomicBrad

Brad

2 years

BC-007 may achieve its long lasting effect not only be normalizing blood flow in general but also by abolishing drivers of inflammation (including neuroinflammation) and adrenergic hyperstimulation as well as exerting effects on the immune system and regulatory CNS functions.

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@AutonomicBrad

Brad

1 year

Long Covid and ME/CFS = Too sick to live but not sick enough to die. #LongCovid #pwME

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@AutonomicBrad

Brad

2 months

Mindset does nothing for Long Covid or ME/CFS. Hate these type of posts on social media. Your thoughts do nothing against a biological and physiological disease. #LongCovid #pwME #POTS

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@AutonomicBrad

Brad

28 days

The name Long Covid is a scam because it pairs people with all different kinds of conditions together and gives everyone false data and false hope. I prefer Post Covid Pots, Post Covid ME/CFS, Etc. These have nothing to do with Acute Covid. Covid was the Trigger… #LongCovid

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@AutonomicBrad

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2 years

Bulging veins are common in lc. This is due to the increase in central veinous pressure. Vein walls are weaker than arteries so an increase in pressure with bulge the vein. The veins have to work harder to get blood back up to the heart due to the faulty autonomic response.

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@AutonomicBrad

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2 years

BC 007 should be released immediately to the longhaulers that want to try it. Waivers could be signed to prevent legal consequences but patients have a “right to try” here in the US. People that are in position and preventing this should be held criminally liable.

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@AutonomicBrad

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2 years

Vasomotor Denervation has also been found in lc/pots/ME. Vasomotor function mainly controls the constriction/dilation of small blood vessels and capillaries among other functions.

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@AutonomicBrad

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2 years

Viral Infections and Vaccines are BOTH known to trigger autonomic nervous system disorders. Doesn’t matter if you are provax, antivax, if you’re name is max or just filing your income tax. 👨🏻‍💼

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@AutonomicBrad

Brad

2 years

LC Patients have a hard time adjusting to new environments/surroundings occasionally. This can result in trembling, shakiness, confusion, derealization. This will also cause excess adrenaline release so heart can pound extremely hard in these circumstances. This is debilitating.

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@AutonomicBrad

Brad

2 years

All previous Pots/ME/Dysautonomia patients must be included in the advocacy for long covid because the majority of long covid are these same conditions. These symptoms are not new. I can make an argument they have been around forever. #LongCovid #POTS

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@AutonomicBrad

Brad

4 months

Denied disability for 3rd time after hearing with judge. I have nothing left. I am tired of having nothing and giving everything I have left to help others who are mostly better off at least financially. Going to step off twitter for a while.

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@AutonomicBrad

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2 years

LC patients will have changes in the saliva in their mouth. The faulty autonomic signaling is the culprit. Also, bacterial changes have also occurred in the mouth in lc patients. Changes in breath and teeth health may occur randomly.

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@AutonomicBrad

Brad

2 years

GPCR receptors control the function of the autonomic nervous system and the control centers are in hypothalamus and brainstem. Functional autoantibodies altering their functions would explain autonomic dysfunction in longhaul. Years of previous research for pots/ME confirm this.

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@AutonomicBrad

Brad

3 months

Almost 30 years ago, ME/CFS patients were treated the exact same way that long covid patients are today. Greatest Medical Scandal in the history of the world and still no treatment while other diseases with higher quality of life scores get billions. Despicable. #LongCovid #pwME

@RFH1955

Royal Free 1955

3 months

Today, twenty-seven years ago. A newly elected Labour government in the UK loses its first MP since its election win a few weeks earlier. #MyalgicEncephalomyelitis #myalgice #cfsme #mecfs . @GwynneMP @UKLabour .

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@AutonomicBrad

Brad

2 years

Doc: Brad, the problem is we don’t know much about the autonomic nervous system. Me: Why not start trying to learn about it and the reasons for it’s dysfunction. Doc: 😲😲😳

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@AutonomicBrad

Brad

2 years

Exercise Intolerance is almost universal in lc. We have a hard time getting oxygen and blood flow to our muscles and tissues. Lack of available aerobic energy causes lactic acid to build up quickly.

Tweet card media

Use of Cardiopulmonary Exercise Testing to Evaluate Long COVID-19 Symptoms in Adults: A Systematic...

The findings of this systematic review and meta-analysis study suggest that exercise capacity was reduced more than 3 months after SARS-CoV-2 infection among individuals with symptoms consistent with...

pubmed.ncbi.nlm.nih.gov

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@AutonomicBrad

Brad

1 year

My prediction: BC 007 will be the Top treatment for not only Long Covid but Pots, ME/CFS, and Fibromyalgia. The infusion could potentially be a huge breakthrough for people that have any underlying autonomic dysfunction and other invisible autoimmune diseases driven by GPCR AAB.

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@AutonomicBrad

Brad

2 years

Autonomic specialist experience summed up: 1-2 years for an appointment. Good listener, Diagnosis, Treat with Salt, fluids, pacing. That will be 350 bucks. Prognosis: Screwed for life

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@AutonomicBrad

Brad

28 days

BC 007 Results will be shared November 21st and 22nd. I heard we have good news 👍🏻 #LongCovid #pwME #Pots

@LongCovid1997

John

28 days

Berlin Cures plans to present their Phase 2 BC007 Long Covid trial data on November 21/22 at the Demistifying Long Covid Conference in Spain

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@AutonomicBrad

Brad

8 months

If you have Long Covid, POTS, ME/CFS, Fibromyalgia, Vaccine Injury or any other Chronic Disease then just know IT WAS NOT YOUR FAULT. NOTHING YOU COULD HAVE DONE. You were failed by the medical system and the government. These DISEASES are REAL caused by AUTOANTIBODIES.

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@AutonomicBrad

Brad

9 months

ME/CFS is too big of a burden for any human to carry. It is too big of an obstacle to overcome without effective treatment. The patients are stuck in an endless dysfunctional hell where any exertion destroys you. You have to turn into an emotionless mummy to survive.

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