"THIS EVENT IS ONLINE ONLY. It will be held on Zoom, hosted by OMEGA. You will be sent a link to the meeting shortly before the start time to the email address you sign up with. This event is FREE. Any enquiries, please email enquire.omega@gmail.com. OMEGA is a support group for people with ME and those who wish to help them. We are delighted to have Dr Karl Morten with us for our Annual General Meeting. Dr Karl Morten will present his current research projects investigating the causes and biological mechanisms of ME/CFS from14:30 - 16:00 BST." Register and further details at https://www.eventbrite.co.uk/e/omeg...arch-into-me-from-oxford-tickets-162977745825
from @Ben H twitter thread: From the Morten Group at Oxford: "Our ME/CFS Raman diagnostic paper is just back from review. They like it! But we need to run a further set of expts with new blood samples. Really important we get the PhD funded in order to collect new bloods." "In this proposal we will explore this association in detail in ME/CFS, Chronic Lyme and Long Covid examining not only the gut but also the currently unexplored blood biome." "We propose that the blood biome and its association with a leaky gut could be a pivotal factor in a number of chronic conditions including #ME/cfs, #LymeDisease and #Long covid." "The tools to study rare L-form bacteria in our blood and tissues are now available and we will utilise new technologies at two research centres at The University of Oxford and Softcell Biological research" "This PhD project will recruit ME/CFS patients using the current Institute of Medicine (IOM) criteria with follow up clinical assessments in collaboration with experienced ME/CFS clinical researchers..." ..."Lyme patients (Dublin) and Long Covid patients (Oxford) will also be recruited." "The final part of the PHD will involve the characterisation of L-form bacteria derived from MECFS patients using Raman microscopy. This technique will look for unique L-form fingerprints which we can be used to identify L-forms present in blood cells from patients". https://twitter.com/user/status/1434190297945284610
What do people think of their current fundraising? https://www.wrh.ox.ac.uk/team/karl-morten Anyone put the time in to make an informed judgement?
I was wondering that as well. Also there website requires quite a few clicks to get through to the actual donation piece.
We have a thread on Karl Morten's fundraising here: https://www.s4me.info/threads/karl-...ign-understanding-the-causes-of-me-cfs.13991/
Ah sorry to hear that. I only joined the webinar for 15 mins today but noticed they were recording it, so I’ll watch more later. It looked interesting - something about, could mitochondria have a role beyond energy production? Could they be involved in pathogen response? He also discussed the microbiome and leaky gut.
Watching bit by bit I’ve reached the end of KM’s talk (it finishes at about 1 hour 10 minutes). I haven’t watched the Q&A. I need to watch again to really take in what he is saying, but found it very interesting. I’m sorry that I don’t have the capability to provide coherent notes on something so long.
he talks a fair bit about this research paper (see around 22.31 for slide) https://www.s4me.info/threads/effic...nal-membrane-systems-2021-ravera-et-al.21269/ eta: he then goes on to talk about Prustys work in germany. starts talking about the microbiome around 25.40
Interesting bit on antibiotics more on disbiosis and leaky gut. then talks about this research https://www.s4me.info/threads/plasm...expansion-and-me-cfs-2020-lipkin-et-al.16005/ around 42.00 last part is the research done by Soft Cell, and KMs groups FMT research.