My GP did not bother to send me anything 😞 all by myself doing research

Is there a study about white clots, that are different than clots from red bloodcells.

What is the maximum dose for the niacin?

Chronic debilitating fatigue, Vision loss and dizziness and EBV in IgM here after a virus years before Covid came along. Don't have ME as never had PEM but i can assure you the other things are debilitating enough. We don't get counted or listened to. Just bullied in to the 'you sound in denial of ME' brigade. Nope, I know my body after 7 years thank you and I'm not going to conflate data for people with actual ME. Helps noone. I have POTS. Acquired same week as flu and reactivated EBV. Yeah, spectrum illnesses.

Why didn't you tell us this before everyone took the safe and effective vaccine that was proven in 3 months when it takes 7 years to prove any vaccine why were there no side effects posted heart attacks ,clotting ,brain dysfunctions ,numbness etc. They didn't post possible side effects because they won't know what they are for 3 more yrs. Dont be a cow fallowing the one in front on the way to the barn think for yourself dont fall for anymore of this bullshit

Dizziness depression also

3 años con long covid y ningún doctor que he visitado me ha podido orientar, estoy cansada de que todo se resuma a ansiedad

Its in the jags.. JUST DONT DO IT.

Thanks for sharing this with you as a group 2 person. I just want to know what is the most effective way to treat? seems like for a group one person you can slightly begin exercising but for a group 2 person you say it is very hard to treats. how and what should we do? Thanks!

This is incredible info Gez! I'm currently stuck walking super slow and having to take deep breaths wile walking. I only do about 50-150 steps at a time to keep my heart rate from going too high. Only get in about 500-800 steps a day. It freaks me out being stuck inside as I'd have to climb up and down 4 flights of stairs to go outside. I was forced to go to the doctor across the street 3 weeks ago which destroyed me and I've yet to recover from. This is so tough to navigate...

Hiya Gaz, one of your followers since 2020/21. Hope you're well, or as well as can be. I think I ask you yearly, are you still on the medication or 'supplement stack' you once made? Also if we are taking H1/h2 life long, is there any evidence in damage to any vital organs for the extended use? Thank you again for all your work buddy!

I’ve been doing all that and no improvement. Basically all of you “experts” are pushing simple multivitamin supplements. I still have brain fog, chronic fatigue and muscle pain. I have to stop watching these videos. I’ve lost all hope and accept my post Covid symptoms and deal with them.

Very interesting explanation. Our LC son fits into group 1 & 2 with dysautonomia & delayed PEM

Autonomic small fiber neuropathy, get tested!

I've just "returned to your fold" after about a year, and am delighted to see that I barely recognized you! You look 20 years younger, your hair is lush, your eyes sparkle, your facial configuration has filled out, and your expressions are enlivened and vital. You present the best possible role model! I really needed this, and I thank you for all the work you've done and manifested!🙏

I have both. Its been hell working with both trying to get better. Thanks for the video.

4324 Kautzer Inlet

I strongly disagree, there is no evidence of REPLICATING/LIVING virus in the body.

I’ve been coming back every 6 months and hoping that you’ve finally recovered, Gez. I’ve been following since Sep 2020 as I have been going through a long term illness equally as torturous (protracted antidepressant withdrawal syndrome), that was originally mis-diagnosed as post-viral fatigue. Hopefully one day I’ll come back here and you’re better, and I am too. Keep fighting.

Thank you so much for this!! Been struggling with flare ups for the past 8 months and its really optimistic to see this data. I have hyper-mobility so thats interesting to hear the other research going on . Im deff more predisposed to stuff with a bunch of autoimmune issues :)

Look at red light and near infrared

Low dose naltrexone works with a spike protein detox

Often a sore and stiff neck is the result of getting rear ended. It appears this world has been rear ended as they defend the ones that caused. Good drivers are safe and effective apparently.

What about Cromolyn Sodium?

Quick nap.

Do you have any info on elevated IgG4 and what to do about it? Mine became high months after first covid infection and keeps increasing.

lets say I do the test and am feeling curently fine, will the test change if I do the test while having a flare up? if so how to time the test while having a flare up

Hyper mobility increases risk of long covid by 30% :-(

I have all of these symtoms from chemo over a year still bad

For the past few months, I have been experiencing fatigue, lightheadedness, tinnitus, and lately, heart arrhythmias, and palpitations. It got to the point where after working out I felt like I was having a heart attack, but with no pain just extremely hard to breathe and very rapid heart rate so I rushed to the hospital twice, and they could find no problems with my heart . I was sent to a cardiologist for observation over the course of a month and they also could find no heart problems so I was dumbfounded until I found out about POTS/long Covid, histamine intolerance. This is what I needed today. Thank you so much for doing your research. I realize this is from three years ago, but it is relevant to me today as I got Covid in December 2023 and I have all the symptoms of MCAS, histamine intolerance, Long Covid. Incidentally, Dr. Sanjay Gupta Has videos on this as well and he’s using a saline IV solution to help clear out histamines in people with POTS.

What is our take on this nowadays Gez? I fully recovered for a year and I 'd like to think this stack contributed to it. I'm back on the LC wagon and am severe and almost scared to take the wrong things at this point. Either way, I think we need a follow up with Ade!

There is one thing out there, that will set you back (alot further and for alot longer) than any vaccine. Covid reinfection. Just remember that.

Ty for this…been suffering with both most of my life.

I HAVE BOTH CHRONIC FATIGUE SYNDROME AND LONG COVID AND MURDEROUS PSYCHIATRISTS ARE TRYING TO KILL ME WITH ANTIPSYCHOTIC DRUGS !!!! S.O.S. !!!!

So helpful! Thank you

I’m sorry, you spew hogwash.

Thanks Gez, for your research and experiences with LC, you continue to help me and others. I’m currently in an energy crash, and seeking answers still...

OMG, you touched something in this video that I have been trying to explain to doctors to no avail unfortunately !!!!

You should watch: Diet is not where you start Josh Dodds For those who have POTS you must follow Dr. Yonit Arthur. She helped me tremendously. For those who have PEM: strength training and the moment there is an attack you sit still and tell yourself: it is safe. It can be one repeat at the beginning. The energy problem was solved for me by keto. Carnivore did more harm than help. Also do not take one specific vit B in mega doses it will destabilize metabolism pathway. Also you have to walk everyday, something happens to the brain during moving forward. Huberman talks about it In addition to this yoga nidra, breathing, earthing, sunset everyday. And the most difficult thing. You have to let in the idea that you have a traumatized nervous system and this is what causes problems. It was the most difficult part im my recovery.

I have been dealing with long covid for months and months as a young man. What seems to have helped is doing "all the right things". The frustrating thing is the benefit wasn't immediate. Unlike before covid, where if I ate right and got sunlight and the like I'd immediately feel better, I would do healthy habits and it would take weeks to really see results. Your body needs to heal, and because it's so disorganized it has a hard time healing. As of now I'm still not 100%, for example, my HPA axis is still clearly wonky. However, I'm going for runs, I'm lifting weights, and I'm not crashing just from doing daily activities like I was. A huge one for me was walking. I introduced it really slowly, and any time I felt like I was pushing it too far, I'd stop before I crashed. Mild walks went on for months, until I finally felt ready to try going for a light jog. I was so deconditioned that what used to be a warmup before covid felt like a full workout, but I didn't crash and slowly I got my cardiovascular fitness back on track. The important thing is to not "overtrain", even when it comes to non-athletic activities. Just as when an athlete exercises more than their body can recover and they slowly get worse, the same thing seems to happen with long covid. Our energy and tissue recovery systems are greatly weakened, and so you don't want to risk further damage by exceeding them.

Have you noticed niacin helping at all with any symptoms its very safe to try from what i gather.

What about from vax

A long-term Remdesivir study? Based on what trials and history? Remdesivir killed a lot of people in the hospital with the original Covid strain. Are pharm companies trying to recoup their losses? Do not be a guinea pig pls. Also, what is the difference in mutations of new Covid variations and/or strains, for the vaccinated and unvaccinated? What are the differences of those who get more specific, persistent, long Covid symptoms compared to those who get repeating Covid symptoms from new variations? Documenting blood immunity markers, timing and types of symptoms, frequency of symptoms in the vaxxed and unvaxxed, and specific spike changes associated with these data points, will tell a lot about where we are headed. Will our immunity degrade until we get sick and die? What can we do to stop the progression of spike changes in individual responses to original Covid mutations and spike changes from vaccinations? The body has an amazing ability to heal! Check out the Nutritarian Diet to optimize your body's ability to prevent and repair damage.

Just got covid again after 4 years. My long covid symptoms re-ignited, such as numbness in my hands and anxiety. My doctor put on Metformin which is one of the only meds I haven't tried yet. It comes with its own side effects, so its hard to tell what is the long covid or the meds. There is some research into Metrofrmin with Vit D for long covid. Have you heard of that med being used for LC? I'm hoping my long covid symptoms don't last as long as they did the first go around. I've already been on an antihistamines like Zyertec, which if I don't take it I have trouble sleeping. Doesn't help that a life situation is increasing my stress levels which makes my symptoms worst.

Well. This could be a mystery solved. I dont do well on herbal tincrures with alcohol. If I take 20 drops in water a day soon I am even more tired all the time. It might be MCAS. My alcohol tolerance is basically zero.

What's the name of the test for POTS?

Hi Gez, I'm trying to get in touch with you as we (Attomarker Ltd) are a start up leading on the subject of immunity profile research testing of Long Covid patients , with some interesting results . Gez , what is really cool is that we are based in Exeter Devon UK and it would be great to explain to you the science behind the test that is showing that 65% of patients we have tested here at Attomarker have a weakened antibody immune response across the spectrum of the variants of the virus. We just need a way of letting the poor people suffering that there is a bit of hope, we have also interviewed a local patient who was keen to help us communicate the value of the test , this can be found on our KZbin channel. Although we are just at the start of the understanding of this complicated condition with 256 estimated symptoms , we are working with private gp clinics across the world who are excited about the potential of the test. If you are open to finding out more please contact me directly [email protected] . Many thanks Gez . Mark

Rodriguez Eric Martin Angela Martinez Sarah

Terrible! I have this all...

Thanks. Quite interesting science around altering sulfide reducing bacteria composition in the gut with sodium thiosulfate (foto fixer...quite cheep :)) taken per os. Seems to be effective in the MCAS, histamine/antioxidant department. Worth looking into imho. Good luck.