The Link Between ME/CFS and Long COVID

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  • Опубликовано: 29 ноя 2024

Комментарии • 31

  • @NSU_INIM
    @NSU_INIM  5 месяцев назад +2

    Sign up for the COVID-UPP Study:
    redcap.nova.edu/redcap/surveys/?s=RMEDJ7LKCX&_gl=1*1h830h7*_gcl_au*MTM2NDA0MTQyOS4xNzE1MDA0ODAy

    • @NSU_INIM
      @NSU_INIM  5 месяцев назад +1

      Donate to ME/CFS Research:
      givecampus.com/b3yrwb

  • @ChristineHampson-mo6uq
    @ChristineHampson-mo6uq 5 месяцев назад +3

    I am just so grateful to have become a recent patient of INIM and am just starting my journey to hopefully a better life. Local doctors dismissed my low immune numbers after several years of me telling them something is wrong with me suffering from PEM after minor activity. I was able to avoid covid until late 2022 but after that my symptoms worsened to the point where I could hardly get out bed for a year. I was lost until I finally saw doctors under Nancy’s group and now have some hope. So grateful for the institute’s work and everyone working on solving ME/CFS/long covid. They developed treatment for HIV, it’s time for us now.

  • @Gina-dn6xm
    @Gina-dn6xm 5 месяцев назад +4

    ME/ CFS can come about with different viruses and bacteria infections, not just covid.
    I was diagnosed with ME/ CFS with a late diagnosis of lyme-disease. I had a positive test after 2 years of symptoms.

    • @yeci8079
      @yeci8079 2 месяца назад +2

      Lyme disease and co infection for example

  • @moladhdodhia164
    @moladhdodhia164 2 месяца назад

    Is there any studies in Chicago or Indiana ?

  • @ceeemm1901
    @ceeemm1901 4 месяца назад +2

    Have you teased out the stats between people with vaxxed long covid sufferers and non-vaxxed long covid sufferers?

  • @magdalenafernandezsaravia6409
    @magdalenafernandezsaravia6409 5 месяцев назад

    What does ME/CSF stand for?

    • @SarahNelsonWA
      @SarahNelsonWA 4 месяца назад

      Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

    • @ceeemm1901
      @ceeemm1901 4 месяца назад

      I just Googled it. Took me a few weeks.It's- Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

    • @dansmith9724
      @dansmith9724 3 месяца назад +1

      ME is inflammation of the brain and spinal cord.

  • @justinf1343
    @justinf1343 4 месяца назад

    I am a lifelong athlete who has had covid 3 times, and I have developed terrible PEM. I am contemplating trying a 3-5 day water fast as I just don’t know how to get rid of it.

    • @PurposefulPorpoise
      @PurposefulPorpoise 4 месяца назад

      Get ur vit D checked. Covid depletes D with every infection. They are finding that around 80ng/ml is optimal for health, as opposed to the standard 30 ng/ml.

    • @tanyawieczorek6603
      @tanyawieczorek6603 4 месяца назад

      Did you try it?

  • @yeci8079
    @yeci8079 2 месяца назад

    focus on the triggers ,.. the cause the hidden causes..

  • @lessons9745
    @lessons9745 4 месяца назад +1

    what does it matter what color you are or language you speak ? If you have ME/CFS there is little to no help anyway.(regardless if you're rich or poor ) and hardly anyone gets better.

    • @tanyawieczorek6603
      @tanyawieczorek6603 4 месяца назад

      Alot do get better..!

    • @lessons9745
      @lessons9745 4 месяца назад

      @@tanyawieczorek6603 actually the recovery rate from long covid is much better than the recovery rate from me /Cfs /pots .

    • @god_king7440
      @god_king7440 3 месяца назад

      ​@@tanyawieczorek6603do get better or recover 100% ? And for howlong ?

    • @decus9544
      @decus9544 3 месяца назад +1

      ​@@god_king7440 It got better for me, incrementally, over the course of about 20 years. At this point it's maybe 10% of what it used to be at its worst, and still improves every year. How does this happen? Will it happen for most people? I have no idea, but it can happen at least for some.

  • @rowaneisner6802
    @rowaneisner6802 5 месяцев назад +1

    Full of ads not relevant to non local people