New Long Covid Breakthrough! First step towards a treatment?? Dr Gill
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- Опубліковано 17 чер 2024
- New Long Covid Breakthrough! Inflammatory Markers Identified? Dr Gill
One of the major problems with long Covid, as we don't really know what is that is the underlying mechanisms behind the symptoms we're dealing with.
But a new paper for Dr Liew et al may have shed some light on this and allowed the identification of five different phenotypes of Long COvid
Here is the paper in question
www.nature.com/articles/s4159...
#DRGill #Longcovid #Covid
00:00 - Introduction
00:19 - Overview of the Study
01:05 - Importance of the Study and Its Future Impact
01:34 - Details of the Patient Group Studied
02:40 - Study Methodology
03:27 - Key Findings of the Study
04:05 - Why is Long COVID So Tough to Crack?
05:24 - Complement System Activation and Processes
09:07 - Complement System and Long COVID
10:04 - Future Treatment Directions
11:50 - Final Thoughts
13:31 - Closing Remarks
As someone who has been disabled by ME/CFS for more than a decade, this video just gave me a glimmer of hope that the condition might be understood and possibly even treatable in my lifetime.
I think I speak for many that we still feel so bad for Diana "The Physics Girl" here on UA-cam, for her Long-Covid simptoms (being bed-bound for years).
My heart goes to all people in a similar situation...
(may studies like this one bring some hope)
@@neox6439usually people who study physics are not scientifically illiterate anti-vax types
As a long covid sufferer I appreciate you providing us with some positive news - sounds like we are one step closer to a potential treatment. Please keep us informed of any further advancements. Cheers.
I want a CURE not a test
Post viral illness has been known about for decades to centuries.
Unfortunately we are so far behind research and treatment that we are starting at the beginning of diagnosis.
You can blame Drs for not treating the illness seriously or believing it.
Government for misspending taxes on rubbish for people who don't deserve help.
The pharmaceutical industry for not caring
And the rest of the population shouting louder at their supposed problems for help.
Berlin Cures seem to be the hope to look out for on their work of autoimmunity
A serious subject made easy to digest and visualize. Thank you! I can listen to Dr. Gill for hours.
Such a travesty what the professionals have done to us all. A real crime against humanity.
Amazing break down of the study, thank you so much. Excellent that you mentioned ME too as 80% of ME patients became ill after a virus or infection. I’ve thought for a long time it’s an autoimmune condition so I await more studies like this into LC with optimism
This was great, would love to see more like this.
Nearly 2 years of suffer. F This disease. Please, find a cure for that mess.
Change dieet
Unfortunately, insurance companies in the USA are starting to deny coverage of biologics for those of us who are symptomatic but without diagnostic tools to specify the mechanism that's going wrong.
Yes, real scientific and academic analysis on youtube! What a breath of fresh air!
My life will peak if I learn the cure for long covid via ASMR
Seriously, as a person on medical leave from long covid, please do more of these!
Thank you for the amazing content. You are so witty and soft spoken, I could listen to you forever!
I liked this format and would appreciate more please
Wow, thank you SO SO much for this, you explained it really well, and as a Long Covid sufferer myself, gave me a tiny bit of hope. You’re a legend, Dr Gill.
Please explain more papers!
Keep the long COVID/ CFS vids coming!
Thank you for putting together this video.
++ for more paper discussions!
Very informative doc. Would love to see more like this !
Great video!!! Thank you 🙏
Excellent video! Very good information.
Great job
Thank you very much Dr Gill and I would certainly appreciate more such videos.
Does this latest research suggest that Long COVID has now become another autoimmune disease?
With homocysteine being a marker for so many disease processes, i propose that MTHFR polymorphisms will make up the bulk of long-covid/vax sufferers. Also notable that even if you dont have a MTHFR polymorphism, you can mimick it with the modern/western diet .
Thanks for the interesting video. Does the same apply for those suffering with long term systemic illness similar to long covid but instead related to the medical intervention we all took? I am struggling with palpitations, exercise induced fatigue, brain fog/unpleasant sensations in my head, insomnia. I get a few good days but then get slammed back down. Trying HBOT at the moment and have previously tried so many other different things with no joy.
This is Pretty Good Information 👌
This was so interesting, the explanations made so much sense even to someone who has zero medical knowledge ahah 😂 I would love too more videos like this in the future 😌😌😌
First thing I thought of was hope for Physics Girl ❤
interesting it took the researchers such a long time to identify the blood as a related problem, though the acquired antiphospholipidsyndrome due to PostVac and PostCovid has been known since quite some years by now....
I now have been diagnosed with COPD and Asuma
Remnant Viral Reservoir. Thats my bet. Treatment will have to be similar to Hep C. Heat Therapy or some miraculous new anti-viral.
I had a research doctor in which I took a special blood test . I tested positive for high inflammation markers. The protocol included an AIDS drug and a steroid. The trouble here in the US , doctors can lose their licenses for prescribing off label drugs. After asking 5 doctors, I just gave up.
The AIDS medication is an immune modulator. By the way, I'm mostly bed bound and home bound by extreme fatigue.
Was that Dr. Bruce Patterson and his team? I had tons of bloodwork done by his lab and also took HIV drugs off label. The numbers in my bloodwork improved but my symptoms continued until I got Covid for the second time. I’ll do one or two half days of work and then have to sleep for several days, all damn day and night. So sick and tired of being sick and tired.
@lowandslow3939 Yes, that is the doctor I was referring to. I'm sorry the treatment didn't work for you. I have heard that it works for some people but not all. I know what it is like to try to chase a cure, and nothing is working. I hope someday research can find medications that can help us all. But to be honest, I'm not holding my breath on that one. I've been sick too long, like you.
@@Gina-dn6xm Thanks for the response. I also believe his protocol helps many, but not all. I’ve pretty much accepted that this is my life for the foreseeable future. It sucks and it’s better than being dead, but not by much.
@lowandslow3939 I totally agree. I think I will be dead before they find medication that either cures us or keeps us in remission. The cruel thing about this disease is you don't die and you don't get better; you are a living, breathing, mostly bedbound person . The days turn into months, the months to years, and nothing changes.
@@Gina-dn6xm Another horrible aspect is that family members don’t understand and constantly tell me what they think, or heard will cure it. I’ve tried everything you can think of. I’m writing most of them off, almost wishing that just one of them would get it too, and validate my claims. My own mother tells me that if I don’t follow her directives, then I just don’t want to get better. She has no medical education but watches podcasts. Thanks mom but Ivermectin won’t cure it.
I do wish a fix was possible
May be trigger is some IgM cryoglobuline ?
I got post infectious illness after I got a bacterial hospital acquired superbug infection in 2016 ..I have pots and who knows what else . have you heard of Berlin cures ?
I was a patient of Dr. Bruce Patterson and did a ton of bloodwork, consultations and meds, including off label HIV meds. My bloodwork numbers improved but my symptoms hit a plateau. After my second case of Covid, they worsened considerably. Are you familiar with his work? We knew more than a year ago that I have severe inflammation but not how to rein it in. I’m bed bound about 3-4 days per week. So tired of this.
I’ve done the same with his protocol. My LC is strongly mast cell with some heart rate issues and mild dysautonomia. I’ve had some recent luck managing symptoms with ivermectin (blocks prostaglandins and reduces inflammation) and mast cell stabilizers like oral sodium cromolyn. Everyone is different but that has been helping me a lot.
I’m still waiting to figure out how to rid of viral persistence if that’s the root of all this mess. Miraviroc wasn’t it for me.
I have had Long-Covid for over 4 years now, Dr Gill. The symptoms seem to be very much consistent with symptoms of Mast Cell Activation Syndrome, which is often hard to detect, diagnose and treat as well. Could there be a link between Long-Covid and MCAS in your view?
I’ve had a lot of luck managing symptoms with oral sodium cromolyn (liquid 100mg bottle; start slow) and ivermectin 15mg every 3 days. Took me from bed ridden to functioning and occasionally able to workout. I’ve had LC for 4 years now. Not a cure but as close as I’ve gotten. Ivermectin helps reduce some of the cytokines and blocking prostaglandins which triggers mast cells. Helped a lot with brain fog. I hope you get well.
Yes!
Change your dieet.
Fast
Than omad
Low histamine food
No sugar and processed food
Tulsi
Quercetine
Vit c d zink
B
Woodworm
Charcoal
Milk thistle
Kurkuma
After two days you will feel it.
Go outside or sit on a bad day in the sun.
Keep moving.
Smile.
Eat bad
Crash
Start over
...
Long covid isn't just one condition. It can be 2 or more. MCAS is one of the most common
I've been hearing a lot about how it could be viral persistence, this would imply it's not an autoimmune problem right?
I think there are several processes. Clotting issue, autoimmune responses, histamine reaction, gut dysbiosis and viral persistence / reactivation
The question is which are symptoms and which are causative
@@DrJamesGill thanks for the reply doc
I coded twice in the hospital fighting for my life in ICU, life support, trak,intabated, total kidney failure and dyalises. Now my kidneys are working at 40%. I have had 2 ANA blood test done my number is 42. I hurt, I had dropped feet and feet stopped working and my left arm and left side of my face and had swallow issues while in the hospital, I can move my left arm and I am finally walking, but have limitations in my feet and legs, my hands and fingers are still problematic
Could it be related to the medical intervention which was supposed to stop Covid (but didn't) . . .
I have lost of pain,I'm tired all the time, I am now medically disabled
Is there any chance of getting treatment or a way to help with my pain. I have anxiety and stress and depression. Have lots of painful inflammatory issues.
Change your dieet.
Fast
Than omad
Low histamine food
No sugar and processed food
Tulsi
Quercetine
Vit c d zink
B
Woodworm
Charcoal
Milk thistle
Kurkuma
After two days you will feel it.
Go outside or sit on a bad day in the sun.
Keep moving.
Smile.
Eat bad
Crash
Start over
...
Hey doctor. When we eat meat, the stomach digests the meat. But why, when we are hungry, does the stomach not digest itself when it is made of meat?
Is autoimmunity caused by wrong signals from the brain?
I had Covid19 July of 2020 and came home January 2021
High SARS COV2 replication will, theoretically,induce more inflammatory reaction.
Did we know at what tissue temperature did SARS COV2 better replicate ?
Why ?
Because in 2020 at TWiV 659 at min29 virologist Christian Drosten suggest that SARS COV2 better replicate at low tissue temperature (35 -34C)
ive had covid 3 times, i might now have it a 4th...
Two years long....so tired of this....
Oh dear. I’m sorry you’ve had it that long. I do honestly believe we’ll get better treatments. We’re trying to use as much information as possible for our patients
@@DrJamesGillI believe the key to understanding this illness is to compare those vaccinated to non-vaccinated, and the degree-symptoms of Covid long. Surely AI can help! The challenge is to get both sample groups to admit to ANY health changes.
Four years with diagnosed Long Covid, POTS, MCAS, Not vaxed. Could really use a cure so I can have a life.
@@buppianoChange your dieet.
Fast
Than omad
Low histamine food
No sugar and processed food
Tulsi
Quercetine
Vit c d zink
B
Woodworm
Charcoal
Milk thistle
Kurkuma
After two days you will feel it.
Go outside or sit on a bad day in the sun.
Keep moving.
Smile.
Eat bad
Crash
Start over
...
The voice quality is so bad it’s painful to listen to. Any way to improve?
I have long Covid19
I say that long COVID is the result of exposure to COVID or COVID vaccines during a condition that increases IL-4 and IL-10. Why? These increase IgG4. So an ongoing allergy increases IL-4. Hypoxia increases IL-10. So the cure may be a reduction of LI-4, IL-10, and IgG4.
I also suspect that BanLec may fix IgG4 by making it trigger liver complement cascades.
I have long baldness
Have you tried keeps
😂😂😂
@@shelley7209 yes
@@shelley7209 are you making fun of people with hair loss?
@@jamiew.2718 I’m happy you came to a site where people have lost their health, homes and way of life over baldness! Thanks for coming
All that just to say… no one still has a clue what’s going on.
What’s long covid?
The definition is Covid symptoms remaining 12 weeks after initial infection, and here is the crucial bit, not explained by other pathology.
In the long Covid clinic we spend a long time ruling out other things
A vague set of symptoms attributable to people who enjoyed furlough so much they couldn't face going back to their shi**y jobs and wa*ker bosses.... be interested to see the stats for "long covid" vs jabbed and unjabbed status though....
Long vaccine
How much Long Covid is actually the side effects of the medical intervention which was mandated to so many . . . ?
Peut-on dire que c'est de la faute des immigrés ? Je pose la question.
Sans doute 😂😂😂
strange, you don't have a "please contact the CDC for more information" placard on your video. very interesting 🤔
I’m not American and this was a British study, I don’t have any connection to the Cdc
...🤨
Ok my side it has a link to the NHS now. Perhaps just took time for the system to do it’s thing 😊