Jason H Maley, MD, MS
@JHMaley
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Dad, husband, He/Him | Director, BIDMC Critical Illness and COVID-19 Survivorship | #LongCOVID | Asst Prof @HarvardMed | @BIDMC_HDS, @MIT | @PennIMResidents
Boston, MA
Joined May 2013
Have begun posting about #longcovid on @tell_health, an app dedicated to connecting the public and medical community, eliminating medical misinformation, and allowing verified medical and scientific content experts to post.
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Independent replication of some reduction (~25-30%) of #LongCovid with Paxlovid treatment versus controls, among non-hospitalized, vaccinated people with acute Covid https://t.co/52pBWBYpBt
@rushin311 @SarjuGanatraMD and colleagues @LaheyMedicine @LaheyHospital
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My book co-authored with @AnupamBJena "RANDOM ACTS OF MEDICINE: The Hidden Forces that Sway Doctors, Impact Patients, and Shape Our Health" comes out this July from @doubledaybooks @penguinrandom! Available now for pre-order! https://t.co/Wxfbtf9Vbs
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Members of @ATS are not expressing ‘interest in location of the conference’. They REJECT the notion that their medical society would put commitment to inclusion at question for notion of ‘No margin, no mission” read our paper https://t.co/Z9B1SMnYKt & thread 👇🏼 #ATSWalkTheWalk
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1/n In the wake of our call to action, the ATS Executive Committee has emailed @atscommunity members defending the decision to hold professional meetings in states without access to the full spectrum of reproductive care and to life-saving emergency care…
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Finally OUT! A call to all medical societies to move all meetings from states with abortion bans. Read #OPenAccess paper here https://t.co/DxPKmWHLvF and 🧵 below! 👇🏼
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Thrilled to share this Comment in @TheLancetInfDis that I coauthored with the amazing @PutrinoLab on “Why we need a deeper understanding of the pathophysiology of long COVID”. Sharing an accessible document here. Thank you for reading and sharing 🙏🏼 https://t.co/PpJ2XXjyzK
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Excellent segment that also includes someone who got #longcovid from her second infection, despite recovering fully from her first one:
Spoke to PBS @NewsHour with @PutrinoLab & other patients on how millions with #LongCovid are stuck in an agonizing purgatory — it’s year 4 of the pandemic & we still have no treatments, no disability support, & **still** no public warning about this common outcome.
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Multi-organ impairment and long COVID: a 1-year prospective, longitudinal cohort study https://t.co/qK8IqgvzDR
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Why is cognitive impairment is huge problem? Because it impacts functioning. Our patients "run" red lights, leave the stove on overnight, forget words during presentations, pay bills twice. What have you noticed? #longcovid @CIBScenter @WesElyMD
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Our review of #LongCovid research is out! This was a HUGE labor of love over 10 months from @julialmv @LisaAMcCorkell @EricTopol & me! It includes 200+ references focusing on biomedical findings in Long Covid. I hope it educates & inspires new research! https://t.co/1PI42j6CXt
Our comprehensive review of #LongCovid has just been published https://t.co/EgO7gtFvoe Phenomenal work by @ahandvanish @LisaAMcCorkell @juliamv
@NatureRevMicro
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We're starting a new support group for #LongCovid survivors, utilizing acceptance and commitment therapy #ACT. We have spots left @CIBScenter. No cost! Using Zoom. Contact us if interested - we want to support you. @WesElyMD
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Physicians from world-renowned hospitals and research institutions are joining Tell Health because only verified doctors can post, helping curb the spread of medical #misinformation. #MedTwitter
tell.health
We doctors are an opinionated bunch. Most of us are very comfortable writing in medical journals. Some of us are ok with writing in local and national newspapers. A few of us are at ease on TV and...
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ME/CFS was America's hidden health crisis long before the pandemic. Now, COVID long haulers are experiencing its debilitating effects. That's why I'm pushing for $27 million to study the intersection of COVID and ME/CFS, and for medical education on the diagnosis and treatment.
Patients with myalgic encephalomyelitis, or chronic fatigue syndrome (ME/CFS); their caregivers; and the few doctors who treat them have spent years fighting for medical legitimacy. The coronavirus pandemic has now forced the issue, writes @edyong209:
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Finding patterns in the chaos of #LongCovid... We surveyed 5,652 people with Long Covid (most never hospitalized with acute disease) and allowed them to chart their symptoms over time. ---> Onset of symptom clusters happened in a predictable fashion. https://t.co/LhNSwI85BX
nature.com
Scientific Reports - A distinct symptom pattern emerges for COVID-19 long-haul: a nationwide study
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The latest from our team in @NatureMedicine The long-term neurologic consequences of #COVID19 A thread 🧵 https://t.co/jmQMBvHAQn by @evanjxu @Biostayan @zalaly
nature.com
Nature Medicine - Individuals with COVID-19 are at an increased risk for an array of neurologic disorders at 12 months, even in those who were not hospitalized during the acute phase of the infection.
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Join us on 9/23 1-2 pm ET for "Long COVID: The search for answers." A conversation with Admiral Rachel Levine, @HHS_ASH, and @JHMaley of @BIDMC_HDS. Moderated by @CarolHills of @TheWorld. #HarvardChanStudio Register: https://t.co/ibGFMk5vjo
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Excellent, succinct review of myalgic encephalomyelitis (ME/CFS) and its overlapping features with #LongCovid
@ScienceMagazine
https://t.co/CipzsAdv2r
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How does reinfection impact #LongCovid? Excellent early data from @long_covid and team shows reinfection makes Long Covid symptoms worse in many people, both children and adults. 1/
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