Hi Everyone,

I thought you might find of interest this statement that appeared today in an
LDN-related group:

"I live in Japan and my wife has multiple myeloma. She has been taking LDN now
for four months. It is the only treatment that has worked for her. LDN is
unknown in Japan. I had to go out of the country to get some for her. If the US
FDA approves low dose naltrexone, other countries will follow. My mother died of
MS three years ago. I wish I had known about LDN then."

In 1999, one of my half-brothers died of multiple myeloma. He left a wife and
four kids. I, too, wish I had known back then about LDN.

For information about LDN in the treatment of cancer, visit

http://tinyurl.com/ldn-for-cancer

For information about LDN in the treatment of MS, visit

http://tinyurl.com/intro-to-ldn

With best wishes,

Dudley Delany, R.N., M.A., D.C.

http://profiles.yahoo.com/dudley_delany



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