Good Morning MMs;
I think Cancer compass was correct in letting this post, as yes some people are very fearful, but others will research. Once again the person here (in my town_) who is having it, had a zero protein count, so technically he did not show any MM cells at the time of harvest. Yes they try and kill off as many of the bad cells that can be done.
If you really feel comfortable with the original post, without any supportive website or newsletter, being commented on, how about I post this tomorrow:
"Dear MMS, did you see the latest website that Multiple Myeloma can be cured! Yes that's right! And with only six oral pills. Very similiar to a "Z-Pack" if you had a bad cold. Two the first day, and then one each day following. No side effects, no age restrictions, FDA approved. I can't wait to get mine. How about you?"
I do agree with you that people will search, and search, and search for this elusive webpage. When all that had to be done from the get go was post it with the comments. A fellow member here (PHOTOG) backs up all his posts with the website he received it from for all to do their own research. If people want to send messages like the original, do it privately.
Take care;
Kevin