Old questions

A forum for the discussion of antibiotics as a potential therapy for MS

Postby SarahLonglands » Wed Jun 29, 2011 8:06 am

Daisy, one person with ppms who has improved amazingly is Rica, pen-name Katman, who writes here sometimes but can be found most days on http://www.CPn Help.org. Send her a private message at either place and ask.

I never got a big reaction from the NAC test, but I was well into the treatment before I took it, so I can't really be used as evidence.

David does still see patients with an MS diagnosis and quite a few are ppms people. Send him an email: you can find his address at the bottom of page number one of his MS pages: http://www.davidwheldon.co.uk/ms-treatment.html. Funnily enough, not everyone is rushing off to get ccsvi treatment!

An Itinerary in Light and Shadow Completed Dr Charles Stratton / Dr David Wheldon abx regime for aggressive secondary progressive MS in June 2007, after four years. Still improving with no relapses since starting. Can't run but can paint all day.
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