This Is MS Multiple Sclerosis Knowledge & Support Community

Frank, I have had MRIonce a year since before I began taking LDN. The MRIs taken after beginning LDN show no active lesions. I am including a copy of my LDN experiences for you. It was written in December of 2006. I continue to do well, and I am planning to attend the LDN Conference at Vanderbilt Un...

Are you on LDN? Yes How long? 2 Years and one month How many mg's? When do you take it? What kind of MS do you have (rrms, spms, ppms)? SPMS Positive changes since/while taking LDN? I have gone from being completely wheelchair- bound and on oxygen 24/7 to walking unassisted and oxygen free. Negative...

Robbie, I wish I had answers for you on that, because I have experienced those drugs, too. I have to worry about what the long term effects of all of those drugs will be, too. I am including, here, a simple explanation of how LDN works for PWMS. Again, I am sorry it has not helped you. Bill LDN- A S...

Thanks. I am sorry that it hasn't helped you, but then, none of the other treatments helped me. That is why I push for research of as many options as possible. The more that can be properly approved, the more chances each person with MS has of finding one that works for them. Bill

My MS Experience My name is William (Bill) Roberts; I am 57 years old, was diagnosed with RRMS in 1998, and upgraded to Secondary Progressive in 2002. My chief symptoms are (were) extreme mixed sleep apnea, COPD, inability to walk, total deafness in my left ear, and inability to concentrate for any ...

Dr. Emily Riser
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