I have relapsing/remitting MS and was having attacks every 6 months; it took months for a relapse to recede, only to have another one start. In October 2003 I was told I had secondary progressive MS and there was nothing anyone could do to help me.
I decided to take matters into my own hands, and started LDN in December 2003. On my next check-up at the hospital in February 2004, I was told I didn't have secondary progressive MS, but was in fact still relapsing/remitting. LDN has helped me with fatigue, restless legs, bladder, bowel, burning legs, leg strength, tingling in feet, sleeping and 'fog in the head'. I now have a better quality of life and hope for the future.
I wanted everyone to hear about LDN as a treatment option. I'm not saying it would work for everyone, but it is worth looking into. The LDN Research Trust became a UK registered charity in 2004 and has gone from strength to strength.
