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  1. Mij

    Covid-19 vaccination experiences

    Early on Canadians were happy with free Tim Horton coffees and ice cream offered at the vax centres, until we saw what you guys were giving away in the US. Suddenly we're feeling worthy of more.
  2. Mij

    Covid-19 vaccination experiences

    The party is just getting started up here. I'm thinking I'll wait a little longer to get my vaccine . . . If the nurse calls to book my home visit, I might just be a little more reluctant.:whistle:
  3. Mij

    Covid-19 vaccination experiences

    In the US they are offering incentives like million dollar lotteries, sports event tickets, new guns etc to convince the anti-vaxxers to get vaccinated. Canada is starting to do the same except for the gun giveaways. Some doctors are saying that this is not going to motivate anti-vaxxers.
  4. Mij

    Nanoneedle technology licensed for early disease detection, biomarker discovery, and more

    https://otd.harvard.edu/news/nanoneedle-technology-licensed-for-early-disease-detection-biomarker-discov/
  5. Mij

    USA: Centers for Disease Control (CDC) - Post Covid Conditions: Interim Guidance, June 2021, updated June 2024

    https://www.cdc.gov/coronavirus/2019-ncov/hcp/clinical-care/post-covid-management.html
  6. Mij

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    The modern coinage is called 'ego-surfing'.
  7. Mij

    Covid-19 vaccination experiences

    @Ariel I understand and relate to your situation. My GP strongly advises I get the vaccine even though I've been sick from a possible Covid exposure early last year. I think 99% of GP's will advise that you get the vaccine. I have not been vaccinated yet and cancelled my MRI...
  8. Mij

    My PEM seems to have changed its character from last year

    My PEM has remained the same until I developed autonomic impairment years later.
  9. Mij

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    @borko2100 There is a subgroup that don't have autonomic dysfunction, I didn't until 10 years into the illness after I had a relapse from reactivation of EBV and HHV6 at the same time. I also didn't experience PEM until years later. It does appear that autonomic issues plays a role in...
  10. Mij

    Possible chronic viral infection in ME/CFS (& other illnesses inc Long covid). Discussion.

    The persistant viral theory gets recycled every 6-7 years.
  11. Mij

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    I can think of a whole new thread dedicated to naming his new cameo.
  12. Mij

    Are there any studies that include bedbound CFS patiënts playing tennis within 6 months?

    Hi @Arvo welcome to the forum! I've heard of several tennis players who contracted EBV/glandular fever and had to retire from their professional careers because of ongoing illness. Sweden's Robin Soderling comes to mind.
  13. Mij

    Removing energy with an exoskeleton reduces the metabolic cost of walking

    https://science.sciencemag.org/content/372/6545/957 “Removing energy from a person's legs during walking may sound counterintuitive, like applying the brake in a moving car,” says Michael Shepertycky, a recent PhD graduate and lead author of the study, “but our muscles naturally remove energy...
  14. Mij

    Perception of infection: disease-related social cues influence immunity in songbirds

    https://royalsocietypublishing.org/doi/10.1098/rsbl.2021.0125 For canaries, just seeing their feathered friends get sick may be enough to preemptively rev up their immune systems.
  15. Mij

    Over which physiological abnormalities in ME/CFS is there a scientific consensus about?

    All my lymphocytes (CD4, CD8 etc) are all below normal, only normal range counts are my NK cells. I've read that CD8 deficiencies also occurs in healthy blood relatives of patients with autoimmune diseases, suggesting it is genetically determined.
  16. Mij

    A proprietary herbal drug Young Yum Pill ameliorates chronic fatigue syndrome in mice, 2021, Yin et al

    This CFS mouse took those pills and now he's recovered! Watch 'til the end ;)
  17. Mij

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    We can change the language of calling it 'fatigue' and replace it with autonomic impairment? There are treatments available for this. Many of us would be a lot less disabled if this was properly diagnosed and treated.
  18. Mij

    Possible chronic viral infection in ME/CFS (& other illnesses inc Long covid). Discussion.

    I had all the PCR RNA/DNA testing under the sun done years ago when I felt very 'viral', everything came back 'normal'. I seem to recall the virologist telling me that it was high levels of interferons that were making me feel this way. I also know what active EBV and HHV6 feels like...
  19. Mij

    Covid-19 vaccines and vaccinations

    @Sarah94 I haven't been vaccinated yet, but I am concerned about the type of chairs we have to sit on to wait the 15 minutes. Something most people wouldn't even think about. Hoping I get a home visit soon so I can jump in my bed and relax after.
  20. Mij

    Warning Signals of Post-Exertional Malaise in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Retrospective Analysis of 197 Patients, 2021, Ghali

    Same, it's only from past experiences that I'm able to avoid PEM, and when it occurs there is no stopping it.
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