The following is an edited version of my original posting on ThisisMS and updated with progress.
My MS diagnosis came more than 5 years ago prompted by numbness and tingling in my right leg which eventually lead on to weakening of my leg and arm on my right side. I hate the idea of long term medication and given the ineffectiveness of conventional MS treatments sought to explore the alternatives.
I have been particularly drawn to the postings regarding CCSVI as I underwent the procedure in September last year with very disappointing results (no noticeable improvement after a very brief lift lasting only a couple of days) and since then I had been looking out for other avenues towards halting my steady decline and possibly improving my symptoms.
By a stroke of good fortune my Internet searches came upon a very interesting article from the London Evening Standard published in 2009 describing the work being carried out by Dr Amir in Putney, London who has had great success treating MS patients through correction of their jaw and Atlas vertebra alignment. The article gave an email contact for Dr Amir so I thought what have I to lose? So sent a brief email outlining my symptoms and to my surprise he answered (around midnight the same night!). This lead on to more communication including an extensive questionnaire which went right back to the start of my medical history, something I felt very reassured by as no one else I have dealt with regarding my condition has been so thorough.
On my first visit Dr Amir quickly established that my jaw and Atlas are misaligned. He was able to give a demonstration of how my symptoms could be improved by deliberately misaligning my bottom jaw to a position he identified then holding my bite in this position whilst carrying out simple tasks - the improvements were instantaneous!
I had in my mind that because the correction takes months to complete that I wouldn't necessarily feel any significant change in my symptoms for a while but how wrong I was - as my travel to the London clinic requires all modes of transport and a lot of walking I used to really struggle on the way down but on leaving the clinic my balance and right side would feel noticeably better.
I have continued to visit him regularly over the past 7 months with a steady improvement in my symptoms although as he explained at the start the road is a winding path and there have been times when I have not been at my best feeling very low and questioning if the treatment was working or indeed worth continuing. However during these lows a visit and change to my appliance or brace would usually result in me finding my way again and progress has followed.
Before my symptoms started to take hold and all my energy went I used to enjoy an active outdoor life. I can now say 7 months in to treatment I have enough energy back to have started cycling and light hill walking again although nothing like the level I used to but the fact that I feel I want to is a huge improvement. I still find my right side weakening quickly but hopefully with time that will improve and I can continue to get stronger.
For me I feel that I have been given hope and a very clear path to follow towards halting and reversing my MS symptoms. The hypothesis Dr Amir gives (already well documented) makes complete sense and ties in with a lot of my own experiences of what aggravates my condition. I also feel very fortunate to have received the help of Dr Amir and avoided the hopeless trap so many others with an MS diagnosis fall into.
These are the graphs of my progress:
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