1 Year on LDN Progress Report

[Guest guest]

Dear all, I started taking LDN last September for Primary Progressive MS. I had difficulty walking (20-30 mts max), frequency and urgency urinating, itchy feets and numbness. The initial effects were amazing and I was filled with hope. I felt my fatigue lift overnight, my feet returned to their normal colour and stopped itching and I stopped getting up to go to the toilet at night. Fatigue and the itching of my feet did come back but I rarely go to the toilet at night compared to twice a night previous to LDN. My walking is worse at times but sometimes it is better. In all honesty I don't know whether LDN is stopping my progression. I still feel it is too early to say. On bad days I feel it doesn't work. One thing I have noticed is that everytime I forgot to take it or dropped the bottle on the floor, loosing

all the liquid and therefore not having any for days I got ill (Flu. fever, colds and laryngitis). It seemed more than a coincidence as this happened 3 times. So I always intend to take LDN. I take 4.5 mg of LDN in a liquid solution. As I am Unsubscribing to this group if anyone wishes to comment contact me you can do this personally on sa_mcguinness@.... Best wishes everyone. McGuinness

All New – Tired of Vi@gr@! come-ons? Let our SpamGuard protect you.