Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's disease) and LDN

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Hi all,

I am new to this group and this is my first posting. Thanks to all

of you for the invaluable information provided in this forum and for

insight into your personal experiences with LDN.

My mom has jsut started on 3 mgs LDN. She was diagnosed with ALS

June 7/04 and the condition has progressed at a very rapid rate. We

learned about LDN through mom's doctor who practices both alternative

and conventional medicine. He has been very helpful, however, he does

not currently have any other ALS patients taking LDN and therefore

does not have much to offer us in terms of his observations.

I guess what I'd really like is to hear from any other PALS who take

(or have taken) LDN. Also, mom had a bad day today, probably one of

her worst so far, and I'm really hoping it has nothing to do with her

first does of LDN last night. Any thoughts on this?

Thanks again,

Marina