Hi everyone, we are in this fight against MS TOGETHER to support each other; together we stand divided we fall. Let us support each other!!!! MS is enough of a battle to deal with. Love you ALL!!!!!!

Yes, and, also people whom are new to trying to understanding their testing procedures and the terms and how to cope if dx is made are also reading and wanting to know more.

Can't this thread just be let go? It started on a high note and now... if I found myself faced at the point I was a couple of years ago: I'd be leaving here as fast as possible. No one wants to be ensnared in a firestorm while trying to find info. and support.

Who wrote what? I dunno. But the info that was initially shared was helpful in understanding. I'm sorry that it's gone, when no one has still offered info. about whom actually authored it. Maybe, as I mentioned, it is Public Domain, which actually means that attribution is not mandated.

If I were "new" to being sent for testing, I wouldn't have a part of what's going on here and likely find myself feeling alone.

Can everyone please move on?

Whooooooooooooo lives in a pineapple under the sea.....
oh, HI Bobbi. Pay no atttention to me. I never discuss MS.....SpongeBob SquarePants!!!

Kinda hard not to pay attention to you, or anyone whom makes time and takes the effort to post . For me, posting is an all out effort. So I just imagine it may be for others too.

Bobbi, that was my point exactly when I wrote (in this thread, above):

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.

Which is in the body of what still exists on this site. Now will folks stop debating and get on with the business of learning to stay healthy with MS and helping each other manage with viable information?

Here is a new source of information i just became aware of. The link is in the post.

New International “Atlas of MS” Launched
The Multiple Sclerosis International Federation (MSIF) has launched the Atlas of MS ( www.atlasofms.org), a searchable database of information on the epidemiology of multiple sclerosis – who gets MS – as well as treatment access and resources available to people with MS within a particular country, region, or worldwide.

http://www.atlasofms.org/welcome.aspx I hear the link posted has an error message. I just got in with this link.