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

Leading long COVID researcher, Akiko Iwasaki, PhD, sterling professor of immunobiology at Yale University, joins to provide an update on the latest long COVID studies and clinical trials-and what their findings mean for physicians and patients. Dr. Iwasaki discusses what we know now about the causes of long COVID, the ongoing challenges with diagnosing it and the timeline for potential treatments. American Medical Association CXO Todd Unger hosts.
🎞️ Watch Dr. Iwasaki's previous episode here: • Long COVID: New resear...
🔬 Distinguishing features of long COVID identified through immune profiling published in Nature: www.nature.com/articles/s4158...
📰 Scientists Offer a New Explanation for Long Covid New York Times article: www.nytimes.com/2023/10/16/he...
🩺 The AMA is your powerful ally in patient care. Join now: bit.ly/AMAJoinRenew
00:00 AMA Update for Nov. 30, 2023
01:04 Understanding long COVID (Post-COVID conditions)
01:32 What is long COVID?
04:46 Causes of long COVID (autoimmunity, hyper coagulation, inflammation, reactivation of herpes virus)
02:18 Long COVID studies (post-acute infection syndrome)
02:45 Chronic fatigue syndrome and what triggers myalgic encephalomyelitis ME/CFS
02:57 Long COVID definition
03:56 New long COVID research
04:32 Cortisol and long COVID: Does COVID affect your cortisol levels?
04:46 Latent herpes virus and reactivation of Epstein-Barr
05:48 Serotonin and long COVID symptoms (SARS-CoV-2)
07:02 COVID antiviral medication
07:36 Long COVID clinical trials
08:00 Long COVID test: Are there diagnostic tests for long Covid?
08:19 Long COVID diagnosis
09:05 Long COVID treatment and therapeutics
09:52 Does Paxlovid reduce long term COVID?
10:13 What is the best treatment for long Covid?
11:09 Monoclonal antibody treatment for COVID
12:11 Is long covid permanent?
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#fightingfordocs #medicine #futureofhealthcare #physicianadvocacy #healthcare #medical #science #publichealth #medicalresearch #covid #coronavirus #longCOVID #longhaulCOVID #COVIDresearch #COVIDtreatments #Paxlovid #monoclonalantibodies #AmericanMedicalAssociation

[@darvell29scott5]

My prayers 🙏 to everyone who is suffering from it.

[@Portia620]

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

[@Imtired_AF]

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

[@oleeotv]

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

[@chriswerge]

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

[@mikebyrd546]

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]

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]

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 🥺❤️✨

[@VeganCheeseburger]

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]

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]

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!

[@boogiebegs]

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...

[@user-ju1gf3qp4n]

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!!!

[@swyllie30]

They still have no answers.

[@maryscarpa229]

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

[@rigoelliot115]

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

[@KATEB33ful]

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

[@monag.769]

Thank you so much for your effort🙏🏼

[@vespahandle]

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

[@katrinaluzier7321]

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

[@user-ii4hq5gd6c]

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,

[@katrinaluzier7321]

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.

[@roseogrady8785]

Thank You..

[@Portia620]

Thanks to scientist for their hard work. ❤🙏

[@brobinson8614]

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

[@marcobagut]

Dr Iwasaki ❤️

[@SZ-ed2gt]

Thank you 👍🏼

[@ryanlp5628]

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

[@TheMusicmaker25]

What is this?

[@kapaul1584]

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?

[@rhognaldmcdognalds1806]

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]

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

[@debrabass2556]

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.

[@TrevorVanDerLinden]

A colegue died of long covid last month.

[@Mau365PP]

Treatments!!!!

[@cb77153]

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

[@lorim8899]

Thank you 🙏

[@wejmluva]

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.

[@romygime5822]

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

[@Galatians-vr8xd]

❤❤❤

[@Prince-ut2xv]

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

[@lowandslow3939]

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

[@DCGreenZone]

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

[@Seagoatsunday]

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

[@maryr7593]

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

[@BasicBeachCommunity1]

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

[@MrHarumakiSensei]

Has anyone ever had Long Influenza?

[@ex8280]

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

[@uk7769]

zero answers

[@michaelshoemaker8440]

More bs

[@annalangham3950]

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

[@joycemckinney211]

Don't trust them or cdc

[@TimMurphy41]

Zero practical advice. 👎

[@cordyone]

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

[@freeandhappy]

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