I recovered. The highlights: Fluoride sits in your pineal gland, slowing down melatonin production. If you stop sleeping, you'll never recover. I went on the raw food diet. My PH went up to 6.6. (my lowest was 4.5 yikes! At 8 oclock, all our lights are turned off. From 10-12 oclock, your liver does magnificent work. If you have any questions, please ask. I wish someone could have told me all this, instead of experimenting over and over. Also feel free to look at my blog about my experience.
There have been other studies showing biological evidence (e.g., cells not using oxygen though people with CFS taking in the same amount of oxygen as healthy people), but these have not been easily translatable to doctor office tests. It drives me crazy that with all the research showing that something is wrong (what they don't know) people still would insist that ME/CFS is psychological.
Agreeing with Thea Schlosser, the vid is a disappointment in that the lady is clearly unfamiliar with the subject. The disease is NOT a "vague" condition. It is in fact closely defined. There are about 5,000 published peer-reviewed papers about all the physical signs and tests, but these are ignored by the present psyche camp. For clinical diagnosis we have the Canadian Clinical Criteria.
We DO have an accurate name in use for over 55 years. It's M.E., short for Myalgic Encephalomyelitis .
It's about TIME they checked the spinal fluid! When Sophie Mirza died (horribly) of this in the UK, on autopsy there were definitive changes in the brain & spinal cord that pointed to something that causes a change in the central nervous system. For medical science to have avoided this type of research with that evidence being many years old is indefensible! It shows that there are too many lazy doctors out there who prefer blaming patients to solving medical puzzles.
Pretty as she is, this lady is not an ME/cfs expert.
If she was, then she would know that it is not "vague" at all.
The signs of illness are very real and measurable, if only the medical profession will do the tests or make them clinically available. The tests exist, they're just not being used adequately. That's one of the main reasons why there is still any "mystery" surrounding the illness.
I recovered. The highlights: Fluoride sits in your pineal gland, slowing down melatonin production. If you stop sleeping, you'll never recover. I went on the raw food diet. My PH went up to 6.6. (my lowest was 4.5 yikes! At 8 oclock, all our lights are turned off. From 10-12 oclock, your liver does magnificent work. If you have any questions, please ask. I wish someone could have told me all this, instead of experimenting over and over. Also feel free to look at my blog about my experience.
PamelaViktoria 10 months ago
There have been other studies showing biological evidence (e.g., cells not using oxygen though people with CFS taking in the same amount of oxygen as healthy people), but these have not been easily translatable to doctor office tests. It drives me crazy that with all the research showing that something is wrong (what they don't know) people still would insist that ME/CFS is psychological.
Claironess 1 year ago
So ME/CFS doesn't have signs? Probably because they never bother to test!
octrosie20 1 year ago
Agreeing with Thea Schlosser, the vid is a disappointment in that the lady is clearly unfamiliar with the subject. The disease is NOT a "vague" condition. It is in fact closely defined. There are about 5,000 published peer-reviewed papers about all the physical signs and tests, but these are ignored by the present psyche camp. For clinical diagnosis we have the Canadian Clinical Criteria.
We DO have an accurate name in use for over 55 years. It's M.E., short for Myalgic Encephalomyelitis .
wingfingers1 1 year ago
What a huge disapointment .
Wy does mental illness has to be a part of the report?
Ithe crippling desease had a proper name ,the report would be so diffrant.
Since 1970 Ihave this cfids-fibromyalgia ,AND WE DO NOT HAVE A PROPER NAME .
GIVE ME A BRAKE.
Thea S Schlosser
Author -survivor
cfidsmedia 1 year ago
It's about TIME they checked the spinal fluid! When Sophie Mirza died (horribly) of this in the UK, on autopsy there were definitive changes in the brain & spinal cord that pointed to something that causes a change in the central nervous system. For medical science to have avoided this type of research with that evidence being many years old is indefensible! It shows that there are too many lazy doctors out there who prefer blaming patients to solving medical puzzles.
1nerdse 1 year ago 2
Pretty as she is, this lady is not an ME/cfs expert.
If she was, then she would know that it is not "vague" at all.
The signs of illness are very real and measurable, if only the medical profession will do the tests or make them clinically available. The tests exist, they're just not being used adequately. That's one of the main reasons why there is still any "mystery" surrounding the illness.
thegodofpleasure 1 year ago 5
She sexy ;-D
victorcintron1970 1 year ago