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  1. hotblack

    Brain fog, cognitive dysfunction

    Absolutely. I’ve also experienced both severe depression and severe ME/CFS and see them as starkly different experiences. I think that’s how I was looking at it too. Seeing family or knowing people with various conditions which affect them intellectually and irreversibly in what to me feels...
  2. hotblack

    Brain fog, cognitive dysfunction

    The use of unpleasant was me. I will often classify experiences vey broadly as pleasant or unpleasant. I suppose a third option would be neither.
  3. hotblack

    Brain fog, cognitive dysfunction

    Yeah I see that. And mention of the hypothalamus is an interesting one. Certainly what I’ve been experiencing over the last few weeks and usually do when bad is on top of fatigue all around thermoregulation, hear rate, sleep, appetite, I notice shivering control is in there too which makes me...
  4. hotblack

    Brain fog, cognitive dysfunction

    The intellectual, cognitive or whatever you want to call it impact can be huge. Far far more than making simple mistakes. It’s a significant symptom with associated impact and can be extremely unpleasant. Brain fog is a completely inadequate phrase to describe it at its worst. And it’s...
  5. hotblack

    Pathophysiology of sleep disturbances/unrefreshing sleep in pwME?

    I’d never heard of this. But weird muscle ‘tremor’ or ‘shakiness’ that gets worse when moving is something I get when particularly bad. Quite common for me in summer. I was lying there watching my muscles in my legs move in little waves just a couple of days ago. And discussing nuances and...
  6. hotblack

    Cellular immune function in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) (2019) Cliff, Nacul et al.

    Thinking about this paper and the presentation @wigglethemouse highlighted in the context of the expanded T cell populations and if how expanded they are correlates with severity. Haven’t got much further but would be interested in others thoughts.
  7. hotblack

    Suggest a name for Chris Ponting's ME GWAS project!

    Definitely deserving of badges and t shirts It shows how long these things have been in the making and how various people from the community have been involved and influenced over the years doesn’t it?
  8. hotblack

    Suggest a name for Chris Ponting's ME GWAS project!

    Found this old thread looking for something else. Finding the name suggestions of DecodeME and SequenceME which are now actual projects gave a little bit of a smile.
  9. hotblack

    Reaction time deficits in a 3D virtual reality test in patients with ME/CFS, 2025, Ladek et al

    When bad or in PEM I often have coordination or accuracy problems, just become clumsy, and I think others say similar, I guess this could be a response time thing?
  10. hotblack

    Does anyone else get a runny nose, sneezing, coughing etc during PEM?

    My brain went straight to UTI and I got very confused
  11. hotblack

    Does anyone else get a runny nose, sneezing, coughing etc during PEM?

    Sometimes. Runny nose, sometimes eyes, definite airway iffiness. Maybe more allergy like than ill like? Like I think you imply, there are different PEMs. Some more me are much more dry mouth/nose/etc. Or maybe different phases, balances of symptoms or severities or something. But yes, what you...
  12. hotblack

    Clinical trial examines whether Ambroxol can slow dementia in people with Parkinson's

    But also from the same paragraph in the paper I see what you mean though @Utsikt the wording may be a bit weird and almost feels contradictory in places. They seem to have confirmed it’s safe and well tolerated, but be more vague on the second part of it is a disease modifying treatment. Seems...
  13. hotblack

    United Kingdom: Action for ME's PRIME project - research infrastructure

    That’s the big question for me. Quite a few of us covered the barriers in this thread
  14. hotblack

    United Kingdom: Action for ME's PRIME project - research infrastructure

    Looks very positive. I wonder if there’s a way for S4ME to get involved?
  15. hotblack

    Noise cancelling headphones! Oh Joy! (and other ways to block sound)

    Well the return went smoothly, printed out a label, someone dropped them off for me at at a courier pickup at a nearby shop, refund in full a few days later. So worth buying direct from Bose as @JemPD says.
  16. hotblack

    Preprint Indistinguishable mitochondrial phenotypes after exposure of healthy myoblasts to myalgic encephalomyelitis or control serum, 2025, Ryback et al

    Thanks for all the great insight @DMissa and @chillier we’re lucky to have you all and this knowledge on this forum. And great question to prompt it @wigglethemouse Maybe one day some of us will recover enough to if not make great scientists then great lab technicians.
  17. hotblack

    News from PrecisionLife Ltd.

    Posting a link to this page from PrecisionLife given in the recent ME Genetics Centre of Excellence webinar. Not sure if there’s anything new but it brings together the various bits of info from the company. And has a report on the First Year Review of the LOCOME Project.
  18. hotblack

    Inhibition of Histone Deacetylation Induces Constitutive Derepression of the Beta Interferon Promoter [...] , 2001, Shestakova et al.

    Really interesting. Thanks for sharing and for the explanation. Theres a few of these posts I have on my ‘to listen to’ list.
  19. hotblack

    Update from the Windsor Castle Research Event (Action For ME)

    I wondered about that too. PrecisionLife seem particularly focused on that aspect already, but beyond that? Even if they don’t already have ideas about treatments it seems sensible to start talking about the pipelines. Given I’m struggling at the moment after a good spell I’m keener than ever...
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