I've read several blogs of CFS and Lyme patients who say they attribute some of their healing to the use of O2 via nasal canula I'm assuming.
I wouldn't even know where to begin- I doubt either my family doctor nor LLMD would agree to it. I wonder how these patients get their O2. I do deep breathing but would love to try something different.
Posted by Haley (Member # 22008) on :