Prof Doug Kell CBE #FBPE #FBPA🔶🇪🇺

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Prof Doug Kell CBE #FBPE #FBPA🔶🇪🇺 banner
Prof Doug Kell CBE #FBPE #FBPA🔶🇪🇺

Prof Doug Kell CBE #FBPE #FBPA🔶🇪🇺

@dbkell

I tweet in a personal capacity. ENTJ. CBE. Against brexit/Govt lies. #FBPE https://t.co/Z2XFPIxkfi https://t.co/F5o0wIMw1H. Nothing I say is medical advice

European Union Katılım Mart 2009
10.2K Takip Edilen13.7K Takipçiler
Janiesaysyay
Janiesaysyay@janiesaysyay·
Thank you 💋💋💋💋💋 @xai @ElonMusk @Nikatabier @NicoVerderosa @dchaplot @dustinvtran for over a year I have argued with Grok giving it the papers showing the SARS2 spike protein all by itself, SUI GENERIS, with or without the virus, causes amyloid fibrin #microclots. Today it successfully recalled the data!! This is a beautifully written research paper by the great @ResiaPretorius & @dbkell showing that 2021 finding. #TeamClots #TinyBubbles For more gorgeous and accurate science like this to train Grok on see: dbkgroup.org/publications/
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RexesRule ⚓USN ⚓😺 🦝@CatsRule2023

Referring to Dr. McCairn's work, here's a recent response from Grok. Not bad! Grok, explain amyloid aggregates and their treatment. Amyloid aggregates in the context of Long COVID and vaccine injury refer to abnormal, misfolded protein structures—often involving fibrin(ogen)—that form resistant "microclots" or fibrils. These are amyloid-like and differ from typical blood clots because they are highly stable, resistant to the body's natural fibrinolytic (clot-breaking) processes, and can obstruct microcirculation, trap inflammatory molecules, and contribute to symptoms like fatigue, brain fog, neurological issues, chest pain, and post-exertional malaise. Research has linked these to the SARS-CoV-2 spike protein (from infection or mRNA vaccines), which can promote amyloid fibril formation, impair normal fibrin clotting, and lead to persistent microvascular problems. Dr. Kevin McCairn has investigated these aggregates in affected patients through advanced lab work, microscopy, and other diagnostics. Diagnostic Approach (as Described by Dr. McCairn): Diagnosis starts with testing to confirm the presence of amyloidogenic aggregates, elevated cytokines, or related markers: 🔹Blood sample analysis via labs like Synaptek (associated with Edogawa Hospital in Tokyo). 🔹Techniques include: amyloid monitoring, cytokine panels (e.g., Luminex Magpix), RT-QuIC, advanced microscopy, SEM/EDX, Raman spectroscopy, and UV analysis. 🔹Patients can send samples following specific protocols for evaluation of COVID- or vaccine-related injuries. This helps determine if amyloid pathology is a factor and guides treatment. Treatment Approach: Dr. McCairn's protocol combines double filtration plasmapheresis (DFPP) with stem cell growth factors (SGF). It aims to: 🔹Mechanically remove the problematic aggregates and related factors from the blood. 🔹Inhibit reformation of amyloid structures and support recovery. Key elements: Double Filtration Plasmapheresis (DFPP): A form of apheresis performed in a closed circuit. Blood is drawn, plasma is separated and filtered through specialized columns to remove amyloid fibrin(ogen) aggregates, autoantibodies, cytokines, and other large molecules, then the cleaned components are returned. Dr. McCairn emphasizes: 🔹Optimal venous access (e.g., jugular vein route for faster flow and better targeting of CNS/brain outflow, versus brachial). 🔹Specific filters that avoid discarding plasma unnecessarily or using donor plasma (which he critiques for potential risks). 🔹This differs from standard plasmapheresis or other apheresis methods like H.E.L.P. (Heparin-induced Extracorporeal LDL/fibrinogen Precipitation), which some patients try in Germany or elsewhere. Dr. McCairn says his method outperforms H.E.L.P as based on observed results. Stem Cell Growth Factors (SGF): Daily large-dose administration. These are peptides secreted by stem cells (e.g., from dental pulp sources). In lab (in vitro) tests described by McCairn, SGF inhibits amyloidogenic cascades and protein misfolding. Clinically, it appears to synergize with filtration by preventing re-accumulation of aggregates. Reported Outcomes: 🔹Rapid symptom improvement in some patients, measurable by reduced amyloid aggregates and normalized cytokine panels. 🔹No relapses noted so far in his cohort. 🔹Examples include patients with severe CNS damage regaining ability to leave the house and drive after years of disability. Synergistic effect: Filtration removes existing burden; SGF prevents reformation; targeted route enhances CNS benefits. Dr. McCairn describes his treatment as currently one of the most efficacious options for Long COVID/vaccine injury cases involving this pathology, though he notes individual variation and the need for broader validation/scaling (e.g., FDA approvals for wider use). Treatment is currently centered in Japan (e.g., Edogawa Hospital/Synaptek), so patients may need to travel.

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Sally can't wander right now
Sally can't wander right now@WanderingSally·
Australia just opened $23m in MRFF Long Covid Research Grants. $200k-$3m grants Stream 1 - $4m 2- $4m 3- $5m 4- $10m Grant docs w more recognition of LC mechanisms, complexity & heterogeneity. 🙏 grants focus on actual disease mechanisms this time! grants.gov.au/Go/Show?GoUuid…
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Karen Strine
Karen Strine@KarenStrine3·
@SalvMattera @ChristosArgyrop @dbkell I’ve edited 2x b/c this is so complex. The only thing that LC should be “ coupled” with is Covid. That in itself is a problem b/c few test to know to prevent more LC. Have you researched any nonprofits for grants to raise awareness?
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Salvatore Mattera
Salvatore Mattera@SalvMattera·
The philosopher of science, Karl Popper, has been one of the biggest influences on my thinking. You might not know who he is, but I guarantee his ideas have impacted your life in some way. When it comes to COVID, two of his concepts seem especially relevant: 1. Falsifiability - it was Popper who wrote that in order for something to be considered science, it must be falsifiable. Unfortunately, most "Long COVID science" doesn't meet this bar. I'm not talking about alternative medicine, but the actual studies masquerading as science. Take, for example, the recent fluvoxamine trial, which claimed to test the hypothesis that the SSRI could benefit people with Long COVID by reducing inflammation in the nervous system. But the study was designed in such a way that nothing relevant was measured - regardless of the result, the study was never capable of falsifying the hypothesis it supposedly set out to test. Or, take the lumbrokinase trial they're currently recruiting for. It supposedly tests the microclot hypothesis, yet the study doesn't measure anything having to do with microclots. No matter what happens, the microclot hypothesis cannot be disproven by the study. If the drug works, it could be placebo effect. If it doesn't work, maybe it was the wrong dose, the wrong group of patients or the wrong duration. Nothing will be falsified, and so nothing will change. A recent vagus nerve stimulation trial stimulated a nerve for 4 weeks and measured whether patients felt less tired. They never verified the nerve was actually being stimulated. No heart rate variability was checked. No inflammatory markers of any kind were measured. How can you falsify "vagus nerve stimulation helps Long COVID" if you never confirmed the vagus nerve was even stimulated in the first place? The answer is you can't. Popper would reject all of these studies. Not because the hypotheses are wrong (they may be right), but because the trials, as currently designed, aren't science. They're theater. 2. Now, here's where Popper's other idea comes in, and it connects directly to the political environment around Long COVID that determines which trials get funded: his notion of "Historicism" - the idea that history moves in a predictable pattern. Most people subscribe to some form of historicism, even if they can't articulate it. Liberals, for example, often think that, over the arc of time, history bends towards justice. But the truth is that it doesn't. You don't have to study history for very long to see that this idea is pure nonsense. History is unpredictable. It moves in both directions: Iranian women had more rights in 1975 than they do today. Afghan girls attended school for twenty years until they couldn't. Weimar Germany was the most progressive democracy in Europe before it produced the Nazis. Roe was settled law for fifty years until it wasn't. So when someone tells you "awareness is growing" and "research is progressing" and "eventually we'll find treatments" you should ask: who specifically is making that happen, by when, and what happens if they fail? Unless they can tell you that, then this is just historicism. The idea of historicism also applies more generally to people's attitudes towards the pandemic, and what the future has in store for us all. Early on, we saw pandemic deniers practice a form of historicism - "Pandemics come and go. Humanity survives. This is just another flu." In other words, history moves in a pattern. The pattern is everything, and it is inevitable. But I've seen other versions of this, as well. Take Iwasaki's "Lingering Shadow of Epidemics" paper, which documents how post-viral illnesses have followed every major pandemic for the last 100+ years. On the surface this seems helpful. But think about what the framing actually does. It recasts COVID and Long COVID from an urgent emergency that must be solved to just the latest permutation in a long, historical pattern. When it's a historical pattern, no one is responsible because this was always going to happen. But if Popper was still alive, he would say this is nonsense. We don't know the future. History doesn't repeat in predictable ways. One pandemic is never exactly like the last. Post-polio syndrome disabled people decades after they thought they had successfully recovered from their polio infection. Nobody saw it coming during the acute polio era. We still don't really understand it. EBV sits in your body for 20 years before it triggers MS in some people. The latency period spans a full generation. Think about what we've done with COVID. We have infected billions of people, multiple times, with a neurotropic virus that crosses the blood-brain barrier, causes vascular damage, and persists in tissue. We have six years of data. Anyone who tells you they know what this looks like 20 years from now is lying to you. There is no "shadow" of this pandemic - this pandemic is still ongoing. 20 years from now, maybe nothing will happen. Or maybe large numbers of people will develop serious neurological diseases. We have no idea, and we're not even trying to stop it. The future is open. People are making choices right now about funding, research priorities, and accountability that will determine whether millions of people get treatments or get abandoned. Those choices are, and have been made, by specific people with names. Not by history, patterns, or "lingering shadows." Stop telling me this "isn't new". Instead, tell me who is going to fix it, by when, and what happens to them if they don't.
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Salvatore Mattera
Salvatore Mattera@SalvMattera·
ME/CFS "coheres" with POTS which "coheres" with MCAS which "coheres" with EDS. The whole diagnostic framework is built on coherence: everything fits together, everything supports everything else, it's a beautifully coherent system. And it produces zero treatments and millions of sick people
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BBC Radio 4 Today
BBC Radio 4 Today@BBCr4today·
“We're finding problems in milder and milder forms.” Dr Suzanne O’Sullivan, author of 'The Age of Diagnosis', says we are over-detecting diseases in some people that may never have been harmful. Listen to Radical with @amolrajan on @BBCSounds
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Prof Doug Kell CBE #FBPE #FBPA🔶🇪🇺 retweetledi
RS Archer
RS Archer@archer_rs·
It's very telling that any post critical of Brexit almost instantly receives a large number of bot replies attempting to discredit it. Someone is very invested in pretending Brexit is anything other than a complete disaster and that EU Rejoin is inevitable.
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Dr Rae Duncan
Dr Rae Duncan@Sunny_Rae1·
@BBCr4today @amolrajan @BBCSounds Please stop platforming this woman. Why don’t you speak to those doctors and scientists with *actual” expertise in long COVID, POTS, ADHD, autism & the other non-psychosomtic conditions this woman doesn’t have the first clue about and then you might realise the level of damage 1/
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Emmanuel Pernot-Leplay
Emmanuel Pernot-Leplay@PernotLeplay·
🇬🇧NHS staff are boycotting Palantir. But the UK gov keeps signing new Palantir contracts while promising tech sovereignty. The UK paid Palantir £330 million in 2023 to build the NHS Federated Data Platform. But NHS staff are refusing to use it because of important concerns: > Palantir's close relationship with the US government > Its recent work with ICE on Trump's deportation operations > Privacy concerns over who ultimately controls NHS patient data Growing NHS staff resistance against Palantir Clinical and non-clinical workers are deliberately slowing their work pace when forced to log in. One official called Palantir "ethically bankrupt." (see article below) Even the British Medical Association has called on doctors to stop using it entirely. 🇬🇧 UK government contradictions on tech sovereignty But the UK government, which previously committed to greater tech sovereignty, just signed a new data contract with Palantir through the Ministry of Defence. And the Financial Conduct Authority quietly added a 3 months Palantir trial contract last week. My takeaway from that story is that NHS employees are more committed to tech sovereignty and privacy than their government. That's sad, but there's hope in it!
Emmanuel Pernot-Leplay tweet mediaEmmanuel Pernot-Leplay tweet media
The Register@TheRegister

NHS staff resist using Palantir software go.theregister.com/feed/www.there…

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James Tate
James Tate@JamesTate121·
Walk the Walk MAGA!
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