The latest long COVID research on symptoms, testing and treatments with Akiko Iwasaki, PhD

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  • Опубліковано 26 вер 2024

КОМЕНТАРІ • 58

  • @darvell29scott5
    @darvell29scott5 9 місяців тому +78

    My prayers 🙏 to everyone who is suffering from it.

    • @Portia620
      @Portia620 8 місяців тому +8

      Me too. I agree with her as we need a clinic dedicated to patients. 😢

  • @oleeotv
    @oleeotv 7 місяців тому +12

    So grateful for Doctor Akiko Iwasaki! Thank you for being a leader and a researcher.

  • @boogiebegs
    @boogiebegs 10 місяців тому +35

    another informative AMA update on LC with Dr Akiko Iwasaki - thank you both 🙏... please keep up the great work, we in the LC community are greatly appreciative...

  • @Imtired_AF
    @Imtired_AF 9 місяців тому +60

    Im at three years with dibilitating long covid , dizziness, brain fog shortness of breath, and alot more symptoms i appreciate how fast they are working

  • @VeganCheeseburger
    @VeganCheeseburger 9 місяців тому +51

    Look, she seems sincere and clearly trying to help, but saying there's been "a lot of progress" is pure B.S. There's still no reliable diagnostics nor treatments. Millions of Americans suffer from Long Covid, many of them so debilitated they can't work. This current Dec 2023/Jan 2024 wave/surge is going to create several million more LC cases. We need more urgency for clinical trials.

    • @glanee5487
      @glanee5487 9 місяців тому +1

      The truth about Vaccine injury is being suppressed so unfortunately, people are not getting the help they really need. There are many treatments that only people who are willing to face the truth have access to.

    • @cordyone
      @cordyone 8 місяців тому +11

      Correct, its shamefull how LC has been so neglected. People have been suffering for years now, the misery is unfathomable. Doctors donnt even know the simple stuff, like trying antihistamines and niacin, and calming mast cells. Its not good enough!

  • @maryscarpa229
    @maryscarpa229 6 місяців тому +9

    Maybe you could let every doctor and healthcare worker in this country aware and knowledgeable about this LC so they can at least be have compassion and empathy for all of who suffer from this There are so many doctors that are denying if even exist

  • @mikebyrd546
    @mikebyrd546 9 місяців тому +37

    i had long covid and caught covid again back to back. I almost died 3 weeks in hospital. I have a hard time just getting to bathroom now. My life has changed. It is horrible. Fatigue I mean severe fatigue is just one of the symptoms.

    • @jewelleryaddict
      @jewelleryaddict 9 місяців тому +12

      As a chronic fatigue syndrome patient of 20 yrs. I surely hope you are given help more then we received. at least they believe you and don't just make fun of you like they did us. This is serious and you deserve better. We were not treated fair mostly because we were mostly female. Wishing you good health.

    • @WildandFree4
      @WildandFree4 8 місяців тому +11

      I've had it for 20months. I have 3 children and very little support. I have never been so depressed.. I wish us all well soon 🥺❤️✨

  • @RichardMcMenamin
    @RichardMcMenamin 9 місяців тому +11

    Fourteen months. Totally active. Exercise six days a week. Now constant headaches, mail aide and pain after any exercise or activity. Thanks to these great researchers for their amazing work!!!

  • @Wds__99
    @Wds__99 9 місяців тому +31

    They still have no answers.

  • @monag.769
    @monag.769 4 місяці тому +3

    Thank you so much for your effort🙏🏼

  • @user-ii4hq5gd6c
    @user-ii4hq5gd6c 5 місяців тому +3

    Mine presented as severe Mast Cell Activation Syndrome
    1 WEEK INTO COVID INFECTION. Also have extreme fatigue and brain fog and my astma is 10 times worse. Please do more research for us,

  • @KATEB33ful
    @KATEB33ful 9 місяців тому +32

    It is long due for ME and Lyme. 40 years of time lost.

  • @chriswerge
    @chriswerge 3 місяці тому +7

    As a long hauler of more than two years, I greatly appreciate the content ✨

  • @katrinaluzier7321
    @katrinaluzier7321 5 місяців тому +3

    I have been sick and have severe pain. Most of my life I have lupus fireman alja epilepsy. When I got COVID 2 different times it made it 10 times worse. When you look at medical papers for me from 20 years ago that I filled out. It sounded exactly like I had COVID.
    I don't have a doctor anymore after years of over medication. Miss diagnosis, I can't get SSI I'm homeless staying in an RV that's broken. Now, now I'm at the Cracker Barrel. It was supposed to be temporarily in a motorhome until I found a place but I just can't get a freaking doctor and SSI is just running around sucks so bad I don't know what to do.

  • @rigoelliot115
    @rigoelliot115 9 місяців тому +14

    A new disease takes years to decipher and to study. It’s rough when it’s you and patience is limited.

  • @Seagoatsunday
    @Seagoatsunday 4 місяці тому +4

    Vertigo and panic attacks tinnitis ..its the worst! Its brain damage! yeah ill take prayers and LC research!

  • @roseogrady8785
    @roseogrady8785 4 місяці тому +1

    Thank You..

  • @Portia620
    @Portia620 8 місяців тому +3

    Thanks to scientist for their hard work. ❤🙏

  • @maryr7593
    @maryr7593 4 місяці тому +4

    I wish more drs knew and understand mast cell activation syndrome.

  • @SZ-ed2gt
    @SZ-ed2gt 9 місяців тому +6

    Thank you 👍🏼

  • @marcobagut
    @marcobagut 10 місяців тому +11

    Dr Iwasaki ❤️

  • @vespahandle
    @vespahandle 9 місяців тому +11

    what are the approved antiiflammatory meds? i wish they would have mentioned those by name. any one know what they were referring to here?

  • @ryanlp5628
    @ryanlp5628 9 місяців тому +20

    Triple anti-coagulation therapy helped me immensely. Why is this not discussed more???

    • @TheMusicmaker25
      @TheMusicmaker25 9 місяців тому

      What is this?

    • @kapaul1584
      @kapaul1584 8 місяців тому

      Good question, I wonder the same. About 3 months into it and I have had some improvement but still have substantial PEM, hoping that will continue to improve with the therapy. How long did it take for you to see improvement?

    • @Oldmaninthestream
      @Oldmaninthestream 8 місяців тому

      Possibly because it is not a good option for some people. Personally I'd take it if it's curative but comes with a 15% minor to major bleeding increase. "According to the 2020 ACC Expert Consensus Pathway for Anticoagulant and Antiplatelet Therapy, TT is not recommended for most patients."

    • @ex8280
      @ex8280 8 місяців тому +1

      That sounds like a temporary solution, as it doesn't eliminate the spike protein, it just prevent them from congregating in groups.

    • @debrabass2556
      @debrabass2556 8 місяців тому +1

      Where did you find such treatment and how did you know what kind of a doctor to go to with your symptoms? I would appreciate it so much if you could tell me.

  • @katrinaluzier7321
    @katrinaluzier7321 5 місяців тому +1

    This weeks especially hard because now it's starting to get hot. And I have such a high intolerance for hot or cold smells. Sites vibrations over over stimulated

  • @lorim8899
    @lorim8899 10 місяців тому +9

    Thank you 🙏

  • @TrevorVanDerLinden
    @TrevorVanDerLinden 7 місяців тому +4

    A colegue died of long covid last month.

  • @romygime5822
    @romygime5822 9 місяців тому +8

    still long way yet Here in Australia is cero treatments only give paxlovid if have covid positive

  • @Prince-ut2xv
    @Prince-ut2xv 9 місяців тому +15

    AMA..that's all you need to know.

  • @lowandslow3939
    @lowandslow3939 5 місяців тому +1

    No solutions. “Treatments” are all over the place. I’ve tried SO many. Still sick and pretty pissed.

  • @brobinson8614
    @brobinson8614 9 місяців тому +2

    I'm about to start lambda Interferon, Hopefully it helps for the severe ME/CFS I have

  • @Mau365PP
    @Mau365PP 6 місяців тому

    Treatments!!!!

  • @DCGreenZone
    @DCGreenZone 9 місяців тому +5

    There are at least 3 potentially effective treatements for LC on the NIH.

  • @cb77153
    @cb77153 5 місяців тому

    How do you know what triggered it? My doctors don’t seem to know that. I’m curious.

  • @wejmluva
    @wejmluva 6 місяців тому

    I've had long covid since 2022. My only symptom is insomnia. I used to sleep 7 and a half hours, now I sleep only 6 hours, plus I sometimes wake up in the middle of the night. Maybe it doesn't seem so terrible to some, but it happens every night. I'm getting desperate. I hope someone can help me.

  • @Galatians-vr8xd
    @Galatians-vr8xd 9 місяців тому +1

    ❤❤❤

  • @strunz5787
    @strunz5787 2 місяці тому

    without a single mrna-jab you might have very long covid

  • @MrHarumakiSensei
    @MrHarumakiSensei 9 місяців тому +2

    Has anyone ever had Long Influenza?

  • @annalangham3950
    @annalangham3950 9 місяців тому +9

    Can you speak in laymans terms
    I did not understand anything you said

  • @BasicBeachCommunity1
    @BasicBeachCommunity1 4 місяці тому

    My wife is soooooooo delusional. She has LONG COVE and is paranoid. She is trying to take my kids. INSANE.... AND SHE HAS 10 SYMPTOMS AT LEAST

  • @joycemckinney211
    @joycemckinney211 8 місяців тому +10

    Don't trust them or cdc

  • @uk7769
    @uk7769 6 місяців тому

    zero answers

  • @TimMurphy41
    @TimMurphy41 7 місяців тому +7

    Zero practical advice. 👎

  • @michaelshoemaker8440
    @michaelshoemaker8440 9 місяців тому +9

    More bs

  • @freeandhappy
    @freeandhappy 8 місяців тому +18

    maybe instead of studying this nonsense - maybe look at all the mysterious sudden deaths since the jab

  • @cordyone
    @cordyone 8 місяців тому +11

    Four year, and this is all you have? Pathetic.

  • @ex8280
    @ex8280 8 місяців тому +2

    Scary stuff, I hope every head the warning and get their vaccinations. No covid means NO long covid.