A standard MRI wouldn’t show these changes. Sadly, most insurance companies won’t cover these tests. However, there is a set of diagnostic criteria.. if you watch this whole seven part series. Then I would suggest you look for a doctor of Functional, or Osteopathic medicine to help you. I would ask them about trying Low Dose Naltrexone (LDN). which has a completely different effect on the brain, than the much higher dose, used to treat certain addictions. It is a drug that’s been around 40 yrs. I’m not a doctor. I have a background and education in molecular genetics, & a bit of background and education in pharmacy. I have severe ME/CFS. I’m taking the low dose naltrexone. I’ve only been on 6 weeks, but I am feeling definite improvements. Best of luck to you
That's discussed on numerous occasions in this series of 7 of 7 parts so maybe you missed it. I think they mentioned three different kinds of scans such as PET, some kind of spectroscopy - not sure what was meant by that if they were referring to SPECT scans or something else, plus fMRIs were mentioned. All of this information here I'm sure is impossible to assimilate in just one listen.
Thank you for your continuing research.
Such an amazing series!! So very much appreciated.
Very interesting. Wonderful research, thank you for what you are uncovering.
how are these changes viewed in our brains? i have all the symptoms and "normal" MRI.
A standard MRI wouldn’t show these changes. Sadly, most insurance companies won’t cover these tests. However, there is a set of diagnostic criteria.. if you watch this whole seven part series. Then I would suggest you look for a doctor of Functional, or Osteopathic medicine to help you. I would ask them about trying Low Dose Naltrexone (LDN). which has a completely different effect on the brain, than the much higher dose, used to treat certain addictions. It is a drug that’s been around 40 yrs.
I’m not a doctor. I have a background and education in molecular genetics, & a bit of background and education in pharmacy.
I have severe ME/CFS. I’m taking the low dose naltrexone. I’ve only been on 6 weeks, but I am feeling definite improvements.
Best of luck to you
That's discussed on numerous occasions in this series of 7 of 7 parts so maybe you missed it. I think they mentioned three different kinds of scans such as PET, some kind of spectroscopy - not sure what was meant by that if they were referring to SPECT scans or something else, plus fMRIs were mentioned. All of this information here I'm sure is impossible to assimilate in just one listen.
It’s crazy because the frontal cortex is where I feel the swelling and burning
Well, you can't actually feel things right in the brain but it certainly seems that way when you have a migraine.
These are great findings. How can this be treated?
Excellent information
Thank you❤️🩹