Julie Strack

640 posts

Julie Strack

Julie Strack

@juliestrack

Health writer and communicator. Patient with #LongCovid since March 2020.

New York Katılım Kasım 2008
281 Takip Edilen462 Takipçiler
Julie Strack retweetledi
Julie Sullivan
Julie Sullivan@CureLongCovid·
Medication categories for dysautonomia: Treatment depends on the subtype and the underlying physiology of the autonomic dysfunction. Here are the main groups: 1/
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Michael Stingl
Michael Stingl@neurostingl·
Hier wird wieder einmal ein Grund geliefert, warum Trainingstherapie bei ME/CFS kontraproduktiv ist, egal was Leute, die PEM nicht verstehen, behaupten. Es kommt zu einer messbar pathologischen Reaktion auf körperliche Aktivität.
ME/CFS Science@mecfsskeptic

1) This study from Cornell University tested more than 6000 proteins before and after two exercise tests. It found altered patterns in ME/CFS patients compared to controls, particularly in proteins involved in the immune system, signal transduction, and muscle contraction.

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Eric Feigl-Ding
Eric Feigl-Ding@DrEricDing·
Future vaccine…. Epstein-Barr Virus, which causes certain cancers, and very likely causes MS (multiple sclerosis), now implicated to also likely cause lupus. If we can develop an EBV vaccine someday, it could prevent so much suffering.
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PolyBio
PolyBio@polybioRF·
We’re excited that Dr. Akiko Iwasaki—a member of our long COVID consortium—gave such an excellent AMA talk on recent developments in #LongCovid. She refers to several RCTs underway, including the PolyBio-supported trial of Miraviroc & Truvada at @CoRESinai. youtu.be/ilIOh4cZiNI?si…
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Putrino Lab
Putrino Lab@PutrinoLab·
I know today is a frightening day for many with #LongCOVID, #MECFS, chronic #lyme and other infection-associated chronic conditions. Today, all I can offer is a small piece of advice and a small piece of reassurance. Advice: please take care of yourselves and practice some 1/
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Vlad Vexler
Vlad Vexler@VladVexler·
Severe ME is lying in darkness wondering how you can be so ill without being dead, while the world stymies medical research that will make you better. Severe ME patients are the most socially abandoned group I can think of in the Western world. Millions of them. #SevereMEday
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Hannah Davis
Hannah Davis@ahandvanish·
They need 1000 responses before they can start analyzing! It is a long survey but will have high impact - please fill it in if you haven’t already! They recently made some updates to make it easier. #longcovid
Brian Fog@useless_priest

Someone recently mentioned - on Reddit or here or both - that there should be a database for treatments people have tried and what the outcomes were. This is a project overseen by FDA / NCATS / CPATH. There over 300 submissions from Long COVID patients. cure.ncats.io/explore/cases/…

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Putrino Lab
Putrino Lab@PutrinoLab·
I’ve been fortunate enough to have some time to stand back and reflect on the state of the field of post-acute infection syndromes(PAIS)/infection associated chronic conditions (IACC) such as #LongCOVID, #MECFS and chronic #Lyme and I wanted to share some opinions. Before I 1/
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Dana Ludwig
Dana Ludwig@danaludwig·
Oops! Cat is out of the bag. Most of us have complained that Covid isolation of 24 hours is too short. Now someone actually collected data. The MEDIAN time for Covid recovery is 20 DAYS! MEDIAN excludes all the LC cases (worst 22.3%). 50%, not 95% recovered in 20 days.
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Diane O'Leary, PhD
Diane O'Leary, PhD@DianeOLeary·
For those convinced that female hysteria is a thing of the past - look. Outside of MH care, ppl think hysteria was rejected long ago as a grossly sexist physical threat to women w disease. Inside MH care, it's "Hey this great book from the 80s helps you treat hysterical women!"
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Billy Hanlon
Billy Hanlon@bhanlon15·
@juliestrack @MrkStdngr Hi @juliestrack! Wasn't sure where else to ask this so please permit sending here (it doesn't look like I can DM to you on here). As a health writer, I was wondering if okay if I sent a topic for your radar or for future consideration. Thanks
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🕸️Dr.T, PhD
🕸️Dr.T, PhD@chydorina·
The straw(s) that broke the camels back Chronic illness and post-viral syndromes do not come on overnight. It might 'seem' like it - indeed, many of us can remember the precipitating event but the reality is that we were laying the ground work for chronic illness before the 'event' happened. When we look at the distribution of who gets sick - some trends stand out. Middle-aged women (often in high stress roles -work or family), athletes (both male and female), high performers in general. Sure, kids can get sick and so can teens and young people but when you look at the health history you often see EVB (mono) and other infectious diseases pop up. There is often a history of allergy or asthma. In adults pre-existing lung pathology from infections and heart attacks can sometimes set the stage. I often say recovery is not just a matter of turning around and retracing the steps of illness and in many ways this is true. The processes of healing are not the same as the processes of pathology. BUT - when you open your viewfinder wider and consider your health history in general - from being born by caesarian or bottle fed as a baby (which can affect our immune systems) you can start to put together the clues for what primed your system to be vulnerable. This may not be true for everyone but for many of us a virus was the last straw - many previous hits had been layered on already that compromised resilience. Human bodies are marvels of being able to handle incredible abuse and still keep going - but there is always a tipping point beyond which function cannot be maintained. Dont try and go backwards to what you remember health to be like. For most of us we are remembering a time when we were functioning but already laying the groundwork for being vulnerable. Many of those straws can be removed in time. And even if the final trigger has no viable solutions yet (i.e. persistent pathogens) it does not mean symptom management and treatment will not help. Start low. Go slow. Be gentle. 1% and 5% improvements are a big deal.
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betsy ladyzhets 📊
betsy ladyzhets 📊@betsyladyzhets·
I just finished livetweeting the Senate #HELPLongCovid hearing, see the thread below. I'm also working on a recap article for @thesicktimes -- send me your thoughts/comments here or at betsy@thesicktimes.org!
The Sick Times@thesicktimes

Good morning! This is @betsyladyzhets, getting started with livetweeting today's hearing at the Senate HELP committee about #LongCovid. Follow along in this thread for updates throughout the event.

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The Sick Times
The Sick Times@thesicktimes·
📢 BREAKING: There will be a full U.S. Senate HELP Committee meeting on Long Covid, January 18th at 10am EST. Look for more details on the hearing and coverage from us. help.senate.gov/hearings/addre…
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Monica Verduzco-Gutierrez, MD
Monica Verduzco-Gutierrez, MD@MVGutierrezMD·
In a Facebook group of physicians, someone brought up the topic of #LongCOVID due to their own fatigue/PEM. MANY chimed in with similar. Reminded me I need to continue Long COVID education for colleagues. Also, one doc had never heard of POTS. Read the post & realized she had it
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