I want to ask you to follow this dot with your eyes. Was that easy? Without you even having to give that much thought, your brain is telling your eye muscles where to move to keep your focus on that dot. 1/
For most you out there, your eye movement would have looked like this, maybe it took you a sec, but then you probably got it just fine. 2/
Now look at what "Jill"’s eye is doing as she’s trying to follow that motion.
At 7 years old, growing up just outside Lyme, CT, she had a swollen tick attached to the back of her head. 3/
That tick bite was shortly followed by debilitating leg pain and mental health struggles which then mostly resolved for many years. She was able to finish school and have a career. 4/
But since another mystery vector-borne illness 10 years ago, she’s had daily headaches, Migraines, Brain Fog, Joint and Muscle pain, Nausea, Positional Vertigo, and then this was all made dangerously worse by a bout of COVID several years ago... 5/
No wonder she’s having all these symptoms, headaches, brain fog, her eyes aren’t even looking at the same thing, and she’s got to do so much additional processing work in her brain to try to sort out what she’s seeing. That’s exhausting! 6/
Right now, we’re not just learning about Jill’s eyes. We’re also learning about her brain. What’s working as expected, and what’s not working as expected. Jill has been to endless Dr. visits, hospital visits, she’s tried everything. 7/
So many Drs. have tried to help her along the way, but they still don’t know what’s making her so sick, or how to help. They’re making their best guess, and she’s spent the last decade in a loop of trial and error. Jill isn’t alone. 8/
We’ve heard hundreds of variations of her story. And as peoples' health slips away from them, they lose their identity, their work, their savings, their relationships. 9/
This has to change! We’re failing these patients. How can people be this sick, but clinical tests fail to pick that up? How do we help you get better if we don’t understand what’s going happening? 10/
If clinicians don’t have access to the right tests, and we don’t know what’s going wrong, what do you need to measure to try to understand? MEASURE ABSOLUTELY EVERYTHING. Complex diseases need bleeding-edge tools! 11/
We built a clinical study at MIT called MAESTRO to try to understand what’s happening in complex chronic illness and we invited 240 people to explore the unknown with us and let us glimpse inside to their brain through their eye movements. 12/
Also through the electricity that their brain is generating. They also let us look at their blood flowing upwards towards their brain through their ear. We collected throat swabs, vaginal swabs, saliva, blood, urine, sweat... We measured the hydrostatic pressure of their skin 13/
Just one example is what we can see when we look with a microscope at their fingertips, just below their nails, where your smallest blood vessels come so close to the surface you can see your red blood cells delivering oxygen to the tissue. 14/
And you can see your immune cells zipping through as they survey the tissue for infection. But in our study participants we see really important things in their capillaries. We can see swelling, where red blood cells are squeezing past a traffic jam or the path is blocked 15/
We can even see the blood leaking out when the barriers of the blood vessel walls just can’t keep the blood inside. It's important that you keep things compartmentalized. Blood is supposed to stay in blood vessels and circulate around the body. 16/
When things don't stay compartmentalized in your body where they are supposed to be, that can lead to trouble. 17/
Someone once asked me if it would be fair to say our bodies are essentially like a bag of bugs, and I said no, but it would be fair to say that you have an inner tube, from your mouth and nose out to your anus that is like a twisty balloon of bugs. 18/
You need to be able to get oxygen and nutrients across the barriers of this tube, but you want to keep out microbes and toxins, and so this is a very special living barrier guarded by cells and mucus that are protecting you and keeping things where they are supposed to be. 19/
So what happens when your barriers aren't fully intact? 20/
If we turn our attention back to what we saw when we looked at Jill’s blood, we found microbes that should be living their merry life in the bug balloon, except they were in her blood, where they’re not supposed to be. 21/
We also found proteins that should be locked up in her brain, but they weren’t, we could find them in her blood. We saw that her barriers weren’t intact, and weren't able to keep things compartmentalized in a safe way. 22/
We’ve spent the last 4 years collecting over 1 million data points per participant. Data that has been missing from this puzzle of why some people can’t just bounce back after an infection. Now we’re trying to figure out how it all fits together. 23/
Why do so many people have shared symptoms? Seemingly unrelated parts of their body are falling apart? Like 15 different diseases that connect. I’ve started to think about the different levers that can drive disease as if they were dominoes, capable of toppling one another. 24/
For some it’s barriers, and for others it’s blood flow or inflammation or infection. And once you can see those top dominoes, you can begin to build a recovery journey that is actually personalized. 25/
How do we help you heal if we don’t UNDERSTAND what’s wrong?
Not “maybe this is all in your head.”
NOT YES/NO tests that lead to guessing and trial and error.
It's time to reframe how we ask these questions. 26/
Can we reframe the question from: Does Jill have Chronic Lyme Yes or NO?
To: what is making Jill so sick? What is preventing her body from being able to heal? 27/
For those of you thinking about somebody you love, or thinking about your own unresolved illness, I want you to know something.
WE CARE very much! We are working hard to understand what’s going on, and we think this is a solvable problem!!! 28/
We can build a future where we know how to look.
A future where we can finally say: We see what’s going happening. We know where to begin. And here is your personalized path forward.
We’re geared up.
Let’s make personalized recovery journeys a reality. 29/
"Jill" came to watch me tell this story about MAESTRO through her data. I'm sharing this very special moment captured here, with her permission, as she watched me give this talk.
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1/ I want to explain a bit about our MIT MAESTRO study. 🧵How can we help you get better if we don't know what's making you sick? If we don't currently have a way to identify what's going wrong, and we don't have the right tests, I think we need to MEASURE ABSOLUTELY EVERYTHING.
2/ Your body is screaming for help, but how do we figure out why that is? Even if you find a clinician who will take your subjective symptoms seriously, different root causes that can result in the same symptoms. Currently even our best clinicians are guessing. That's scary.
3/ We need to question our assumptions. We need objective measures that allow us to identify root causes so that we can treat those directly, intentionally. If we imagine these disease drivers as dominoes, we're looking for the measurements that show us your top dominoes.
Finally online - sharing our findings that #Lyme disease bacteria can live in female reproductive organs for over a year and increase risk for gynecological disease!!! We found this increased risk in mice and humans! 😱 (thread below) medrxiv.org/content/10.110…
Mice with Lyme got cysts & tissue damage in their uterus and ovaries. The older the mice, the worse the damage was. We then studied 100,000s of human health records. People with Lyme had much higher rates of endometriosis & other problems. 📊👩⚕️
Lyme disease isn't just skin and joints. It can cause serious, long-term damage to the female reproductive tract. This is important. Special imaging showed #Lyme causing bacteria glowing in mice uteruses. We tracked the infection for months.
The absolute best post of the day, and probably of the month, was from the other place, but I'll tell you all about it here.
This public atlas came online to relate disease to protein levels found in the blood from thousands of people across many diseases, searchable by sex. 1/
The paper about it (published yesterday), is incredible! They highlighted proteins that show up across tons of diseases (GDF15) vs proteins that are disease specific, as well as proteins that show tremendous #SexDifferences in their disease involvement. 2/ cell.com/cell/fulltext/…
So, what caught my eye and knocked me off my seat? I looked up the IgE high affinity receptor (FCeR1A). This protein facilitates really pesky allergy symptoms, and I'm convinced this is an unappreciated culprit in #IACI. And would you look at that?! In females it seems to be! 3/
1/I finally have a moment to tell you why I think there's something really huge here in @arthur_courtin's new study. Because there's this superfamily of temperature sensing proteins I'm low key obsessed with and I don't think we have given enough consideration in immune cells...
2/Your ability to feel the heat of 🌶️ capsaicin depends on a protein called TRPV1, a critical member of the TRP superfamily of proteins. TRPV1 and the other TRPs aren't just expressed on nociceptive and peripheral neurons, but also immune cells and control inflammation responses
3/ Some of you may recall that the TRP protein superfamily made the spotlight with the 2021 Nobel to David Julius and @ardemp
1/ The term "chronic EBV" used to elicit an🙄from many (most?) clinicians before this enormous study profiling over a million service people for decades found a causative association between Epstein Bar Virus (EBV) and Multiple Sclerosis (MS). science.org/doi/10.1126/sc…
2/ One must consider that most people are infected with EBV. For many, it would just have been one of many unremarkable "colds" without any directly associated lasting disease. Remarkably, the Bjornevik et al study found that EBV could take over a decade to trigger MS.
3/ EBV, like other Herpesviruses, integrate themselves into the DNA of infected cells and express just a few latency genes as they wait for the right opportunity to reactivate. (side note that JAK/STATs are important suppressors of EBV reactivation- inhibit these with caution!)
One of the craziest things I learned last week at #AAI2024 was that we have more free-floating extracellular mitochondria in our blood than white blood cells. This was not in any textbook that I ever read!
Wow! Thank you so much for all these interesting and thoughtful responses on all the different threads. I'm going to try to compile some of the most thought provoking ones into this thread to keep track. 2/