New Research Finds Brain Inflammation Plays Significant Role in Pathophysiology of ME/CFS Patients

Posted , 8 users are following.

I signed up for this webinar with Dr. Jarred Younger held on Dec. 13 and posted the info for others who might have wanted to participate, but the mods wouldn't even post my discussion, for whatever reason. However, all is not lost — the host for the webinar, Solve ME/CFS Initiative, reposted the entire webinar on YouTube. I forwarded the link to my Neurologist and his associates to give them a better understanding of the science, current research and symptoms.

I won't post the link, as I know the mods will remove it — I still don't understand why they do that. If you go to YouTube and enter: ME/CFS Involves Brain Inflammation: Results from a Ramsay Pilot Study you will be able to view it. I highly, HIGHLY recommend watching it, and sending it to your Doctors to help them understand more clearly the scope of the disease.

Dr. Younger gives a presentation of his new research findings that indicate brain inflammation plays a significant role in the pathophysiology of ME/CFS. With pilot funding from SMCI’s Ramsay Award Program, Dr. Younger used a non-invasive imaging technique to measure temperature and other brain chemistry indicators in individuals with ME/CFS and control subjects. The results showed distinctly elevated brain temperature, indicative of inflammation, in patients. The involvement of brain inflammation in the development and progression of ME/CFS has long been an area of interest, but there has been a lack of direct evidence to support the connection. This seminal study further validates that neuroinflammation is occurring in ME/CFS patients and has the potential to point the way to an objective marker and effective medical treatments.

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  • Posted

    Thank you so much. I will watch this this evening.

    Sarah

    • Posted

      Be sure and let us know your thoughts after watching.

    • Posted

      That was really interesting to watch Dono and sounds promising. Thank you for letting us know about it.

      Sarah

    • Posted

      My husband watched it with me and found it interesting that Dr Younger mentioned how ME/CFS was like having the flu because that's how I've described it to him......."I've feel like I've got flu but without the snot"

  • Posted

    Thanks!!! Going straight there!

    • Posted

      Let me know what you think after watching. I'm very interested in others opinions on this matter.

    • Posted

      Amazing! Exciting! I'm very encouraged with these findings. I am so very tired of trying to describe this 'thing' when my tests all show that I'm 'healthy'. Thanks again for sharing. I look forward to seeing this move forward.

    • Posted

      I completely agree! I have passed this along to many friends, family and my doctors. I'm really looking forward to my doctors thoughts on this research.

  • Posted

    thanks for re-posting the info

    • Posted

      You're welcome! If you, like me, are tired of trying to explain the disease to your doctor, family or friends, send them this link and they may get a better idea. My mom just had knee replacement surgery, and her rehab specialists are real interested in learning more about it

    • Posted

      Thankyou, it's good to spread education about cfs/me.

      Beverley

    • Posted

      That it is, and I try and post everything new that is beneficial.

  • Posted

    Very interesting research findings,I dont know why the moderator will not allow you to post the link if it is of interest to people with ME/CFS , carers and other researchers.

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