Dr. Jarred Younger - Neuroinflammation in ME/CFS

[@olivertruswell]

Thank you for all your hard work Dr Younger! These studies are truly amazing for someone who suffers because it validates our illness in a medical world that widely dismisses us, infantilises us, and it gives us hope for the future. Fantastic work :)

[@lorrainefletcher9087]

I agree, brought tears to my eyes, explains so much.

[@nxva8726]

My favourite researcher. JY is the man! Many, many thanks for this

[@lorrainefletcher9087]

Wish I lived in America, I googled Neuro inflammation as I feel mine, it brought tears to my eyes to see the link. This is what I have. Massive thank you 🙏🏽

[@Truerealism747]

Do you have fybromyalgia CFS in UK?

[@juanluisfernandez5985]

Lack of oxygen causes increased lactate production; lack of glucose causes increased ketone bodies, 6.04

[@KittenCasserole]

What a fantastic presentation with such fantastic research. I’m so grateful Jarred Younger and his team’s work. Thank you for uploading this video ❤️

[@julieontology7214]

I wish I could be in your larger study. I'm 75 minutes away, but I'm now in the severe category and cannot travel so far so frequently. When I called about being in your 1st study, I think I was disqualified because I was not willing to come off of NSAIDs. The pain is too constant and too severe. We are all hanging on this research. Is there a newsletter or other way to get information in a timely fashion? Are there any other medical professionals in the entire state of Alabama who know about ME and are willing to participate or treat patients? My PCP has been wonderful about letting me take any test I request, but she will not give me a diagnosis. As with many ME patients, all my tests have come out negative. But I have never had an MRS or a PET. Thank you a million times for your work. It is critically important. I'm 62 and hope that I don't die without an official diagnosis or any hope of treatment. People all over the world are hoping or official diagnosis and effective treatment.

[@s3r0t0n1n]

Thank you so much! I'm so happy that there is a step into solving this cursed puzzle. Wish you all the best!

[@69birdboy]

Nice work Dr Younger...i think this is right

[@juanweiheful]

Thanks great job, have cronic fatigue and it would be great to finally have some answers.

[@gaoshikui88]

What a legend.

[@danashannon8234]

Omg. I so want to have these tests & scans done. : ( I need to know what is happening. I really need validation. I am in KY and I have given up on doctors. They will not run anything besides basic tests... They refuse even a MRI .... Idk my story is so long....

[@johnathanabrams8434]

This was 4 years ago. We only have one year left till he comes up with this antiinflammatory and were good to go....

[@IchLiegFlach]

A very good researcher 😊

[@brobinson8614]

Yes he’s great! Which is rare for a psychologist. Jarred Younger is one of the few who bothered to listen to patients and realised ME/CFS is a biological disease.

[@gayatrimelkote6822]

Thanks for explaining it so clearly.

[@dominic2446]

18:58 primed/sensitized microglia and explosive synchronization are related? 23:17 the arrows should be white and thicker because they are easy to miss.

[@danashannon8234]

How come there is not some type of treatment. ?

[@nxva8726]

When is the new PET study coming out? Are T and B cells getting in the brain? Is the BBB breached?

[@danashannon8234]

I mean anything to help?? Herbs...cumin & black pepper.... How to stop the overactive glial activation and increased cytokines etc....any ideas

[@moxanation73]

I’ve noticed I feel a little better when I take zopiclone (a sleeping pill) but I can’t take it in the morning, obviously

[@dansmith9724]

I notice similar effects. I take my sleep meds at night and feel them kick in and for about half an hour the brain fog etc is gone or greatly reduced, then i fall asleep. I think any type of sedative or downer probably reduces neuroinflammation or atleast masks it. Even some anticonvulsant meds like lyrica etc seem to help??? Another thing i noticed a few years back when i had surgery on my knee, my brain felt great for about 2 days and i think being heavily sedated for surgery probably switched off my brain enough to calm down neuroinflammation.

[@Truerealism747]

You have sleep apnea highly linked

[@moxanation73]

@@Truerealism747 I was tested for it and it came back negative

[@mudslinger888]

What is the best way to send a narrative to you Dr. J? I want to share my personal observations, and some things I found to help.

[@justiceO8149]

Happy to hear your story here !

[@danashannon8234]

Leaky blood brain barrier?

[@danashannon8234]

We know we have neuroinflammation. I guess we need more physical proof.

[@maisiemostert2758]

Im Very very sick, have 40 symtems per day. Wet carpets, mold and my head explodes. I live in South Africa, Bilharzia, I choked-up, my nose leaks FLATWORMS. BILHARZIA! My head eyebrows are always hot, inflammed, feels like my heads in a vise. Without tramadol I dont sleep, joints burn till I throwup

[@danashannon8234]

Omg talking studies for another 5 years.... : (