Has anyone tried using a hyperbaric chamber? If it used for helping stroke victims or wound healing, do you think it would help get rid of CPN?
I'm writing for my friend Anne, who has been on the protocol for about 4 months. She is taking doxy everyday, azithromycin 3 times a week and pulsing with metro every 3 weeks for 5 days. About 1-2 months into the protocol she was excited because she started noticing different things happening (she was diagnosed with MS and is bedridden) like tingling sensations, more upper body strenght, and different pain sensations. Now it seems as though she is getting worse because she is weaker and and just doesn't feel well. She sees her doctor once a month and he is willing to prescribe the antibiotics as long as there is continual improvement. Her appointment is next week and it is frustrating because she has seemed to decline.
I'm writing this for my friend Anne who has been dealing with MS for the past 20 years. She is bedridden but has a positive attitude. She ued to be on copaxane but decided to take herself off all MS medication because it wasn't doing anything. For the past 8 years or so she has only been on supplements and an MS diet. Although she didn't improve, her symptoms stayed stable. She always wondered if she had something else because a lot of her symptoms were not typical with MS. So when I went to Florida, I was talking to my husband's cousin and son. They told me about a friend who raises goats (I think it's Rica) and how she has cpn. After a lot of frustration my friend found a doctor who confirmed that she has cpn.