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Well, this blog was/is about LDN and honestly we had hopes for this drug that was so highly rated by individuals looking for alternate cures for MS and other debilitating diseases - BUT Ed ultimately had to go back to the nuerologist who prescribed him Copaxone, which seems to be fine. We started this blog with the idea that Ed's experiences with LDN would be great, but knowing that we wanted to be truthful about his experiences on it.
LDN was not a miracle drug for Ed, but we will continue to document his experiences for those who are following and are interested in the things that we do try out.
Thanks all!
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Hello! Just discovered you all. Reading backwards you intrigued me with your comments about thyroid and MS. "Long ago" (Pre-MS) my wife Patti had her thyroid removed after a diagnosis of Graves Disease and daily Synthroid replaced the body's natural way. It could not have been more than a year or two that her diagnosis of "probable MS" first appeared, until 1989 when MS kicked down the door and became part of our life.
Caregivingly Yours, Patrick
http://caregivinglyyours.blogspot.com/
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