This Is MS Multiple Sclerosis Community: Knowledge & Support

Well it's actually just over a year but anyhoo....it's been a great year, diagnosed 5 years ago, every year since then I've had at least one relapse a year and never had full recovery after but since meeting Dr Wheldon and starting the abx around late November last year I've had no relapses and better still I definitely have had some improvements.

Restless legs that kept me awake at night are no where near as bad. My energy levels are better, my balance is better.

I've tried various regimes since my diagnosis but this one is the one I have felt most positive about and I am definitely going to keep it going.

I'm quite a cautious person, hate jumping the gun, counting my chickens etc. and so I have been quiet about how well I think I've been doing, my wife, however, isn't so cautious and she regularly tells me how well she thinks the protocol is doing.

So, sorry if you haven't enjoyed the same success, but I'm so glad I met Dr Wheldon and started the abx.

Albhoy, What good Christmas news! (I'm glad I 'met' Dr. Wheldon, too, and for all the same reasons!)

Let us know how it goes for you every once in a while, please?

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The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

Hi Alan, long time no hear but I'm immensely glad that you are doing well and also that your wife thinks the same. Don't go overboard with the Hogmanay celebrations, though!

Sarah

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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.

Albhoy, so pleased to hear that you are making progress. Dr Wheldon looks after my daughter too and you both seem to have the same experience, some stability at last, some hope and beginning to see some improvements. Great news and I hope that 2008 continues in the same vein.

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Michele,  warrior4MS, mother and champion for Ella, the MSer. The solution is out there we just have to ask the right questions.