LDN and ALS (Lou Gehrig's Disease)

[Guest guest]

Dear Group, Someone posted an e-mail with respect to LDN use for ALS - it was addressed to me specifically. Wouldn't you know, I have not been able to locate it since it was first viewed. I think it may have been dated sometime in the fall of 2007. I hadn't been keeping up with the posts.) I would appreciate hearing from you or another member who may know who was trying to contact me. I may have valuable information they want regarding our LDN/ALS experience. Thanks! Marina Dajka (caregiver; mom diagnosed with ALS June 2004)

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