Only now reading up about this do you think its rubbish guys?? Id give anything ago even if theres a lil bit of a hope snyone got his contact details?? Xx
Well, you could try his website (hint: google it).
One thing is that he is not trying to sell you a “cure”, rather he describes what happened to his wife, and you can read a full account covering more than 10 years.
You could also look it up on the Barts MS blog, and see what is there.
Geoff
Thank you geoff I have googled it but was asking your guys opinion also cant find any contact details Will try the bars ms blog . Thanks anyway xx
l did speak to his wife - about two years ago. She got quite a lot of flack ,from some folk on here, when she posted about how her husband had helped her treat her MS. He is based in Bedford. And at the time was willing to help anyone with MS - and was not taking any fee for this -only the cost of the anti-biotics he was prescribing. l think medical red tape restraints prevented him from taking his ideas any further. But do google him - as it is so important that we all keep an open mind. Nobody yet has come up with anything that will find a cure. And we are the only ones who understand what MS is all about.
Thank you spacejacket without hope and dreams theres not much in life, we all need some in our lifes with a sprinkle of happiness dust lol xx
In September 2012 I decided to give the Wheldon antibiotic protocol a go. I read about it on Cpn.org website and got in touch with Sarah Longlands, David Wheldon’s wife who has MS after she posted on this site. My understanding was that you need to give the protocol at least a year before making a judgment on whether it was working or not. I live in Spain and have a sympathetic GP who prescribed the drugs for which I pay (they’re not too expensive). By the way there are 3 different antibiotics involved. Metronidazole is only taken for a few days once a month after the other 2 are well tolerated. I have SPMS and seemed to be deteriorating quite rapidly. In September 2012 I was walking with a walker and could maybe manage 100m. Main symptoms were difficulty walking, numbness, bladder problems, spasms in legs ranging from mild to very painful, muscle stiffness and very bad balance. NAC is also taken on this protocol and neither this not the other antibiotics had a bad effect on me. So what was the outcome? Well, after 12 months my MS was quite a lot worse. I can probably walk about 20m with my walker but it’s really tough going. The numbness is much much worse, as is muscle stiffness. The other symptoms are about the same. The Cpn community seem like a supportive bunch. I can’t say that there appear to be that many positive stories although some people with MS have reported a good outcome. This account is just a factual record of my experience and neither an endorsement or a discouragement. When you have SPMS and the medical community have pretty much given up on you anything seems worth a go providing you feel it is not actually harmful - a personal decision. Hope this is helpful to anyone who may read it and feel feel to message me with questions. Best wishes, Karen