It turns out that stimulating the vagus nerve reduces inflammation in the ENTIRE body without the nasty side effects of steroids. Now I'm on a quest trying to find out how to stimulate my own vagus nerve. While I would love to have the pacemaker type device implanted in my shoulder, it isn't available for use in CFS/ME yet.
Here is various information on the vagus nerve and vagus nerve stimulation.
BBC podcast (20mins long and explains the pacemaker style device)
http://bbc.in/1ycMkCm
The Gut Brain Axis (hint the vagus nerve is the info highway between the two)
Cort Johnson's article on The Search for Neuroinflammation in CFS/ME
http://www.cortjohnson.org/blog/2015/06/16/search-neuroinflammation-me-cfs-fibromyalgia/
Of course this would all go faster if someone would cough up a sizeable chunk of money for some research on actual CFS/ME patients. If it could get approved I would be first in line to give it a try.
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