This Is MS Multiple Sclerosis Community: Knowledge & Support

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PostPosted: Wed Jun 29, 2011 8:06 am 
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Joined: Thu Jun 17, 2004 3:00 pm
Posts: 2012
Location: Bedfordshire UK
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!

Sarah

_________________
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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