Bobbi, that was my point exactly when I wrote (in this thread, above):
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Many people with MS are starting up their own Webpages and/or message boards. I do feel strongly that our words, which some of us find difficult to think up and type, should be recognized as ours.
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I haven't had a reply from the Paul Jones Website yet but I did have one from the NMSS Website developer, who says that when quoting material on the NMSS Website, it is sufficient to give credit to the NMSS Website and give the page URL.