An article highlighting LDN was published in a Sunday newspaper in Ireland over four years ago and fortunately for me it was brought to my attention. When I was diagnosed with MS a year earlier my neurologist had immediately put me on beta-interferon - my MS symptoms got progressively worse during that year and my positive outlook was slowly being eroded which was mostly down to beta-interferon. I was delighted to give LDN a go and haven't looked back since. I immediatlely felt the benefits and here I am four years later, feeling very good, in a positive frame of mind which is half the battle and still able to live my life to the full. I would recommend to anyone with MS to give it a go.

HELLO MY NAME IS IMELDA AND I HAVE MS. HOPEFULLY I SHALL BE STARTING LDN AS ANYONE WITH MS WOULD WALK ON HOT COALS IF IT COULD HELP ELEVATE THE SYMTOMS.OVER THE YEARS I HAVE BEEN ON DIFFERENT DRUGS BUT AT THE MOMENT I AM FEELING VERY DOWN AS THIS RELAPSE IS LASTING SO LONG. I AM GOING TO TRY SUPPLEMENTS AS WELL. NORMALLY I AM A VERY POSITIVE PERSON AS MY NEUROLOIGST MAINTAINS MY MIND IS KEEPING ME ON MY FEET, EVEN THOUGH IT IS GETTING A LOT MORE DIFFICULT. IS THERE ANYONE THERE WHO IS ON LDN OR SOMETHING ELSE PLEASE CONTACT ME

KIND REGARDS

IMELDA

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