This Is MS Multiple Sclerosis Community: Knowledge & Support

That's a bit optimistic! I don't mean the results of studies, I mean the length of the line..

I was pleased to read that post all the same, I mean my response didn't really reflect that.. :)

And my first post re CCSVI.

That is why I do not believe you have ms (my opinion only) - you are very closed minded. Not even curious.

In the legal profession one always reads between space.

I am with you leooreo

I used to do the MS150 and ask family/friends/neighbors to help out too. They do give back BUT ITS FROM THE MONEY THAT WE RAISE FOR THEM. Obviously there are people that feel they need the MS Society and those people should give to them. Those of us that have put 2+2 together need to put our money behind the best bet (CCSVI).

And anyone with an open mind that wants a history on the Vascular theory behind MS just need to go up to the STICKY POSTS and look for the POST RESEARCH HERE thread. Read through it and it becomes painfully obvious we should have been where we are now 30 years ago.

I went to Dr Franz Shellings website, downloaded his book of info and sent him an email thanking him for everything he has and continues to do.

To my surprise I got an email back answering my question as to why he wasn't able to get this out years ago. Basically he was held out by money mills on the auto immune theory side od things. I suggest that if you have the time go there and thank him for all he has done.

Thanks BadCopy,

I did not know about Schelling's free e-book. Here is the link where to download it:

http://www.ms-info.net/ms_040504.pdf

Rox

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Diagnosed with Transverse Myelitis in December 2008. Inflammatory demyelination of the spinal cord (c3-c5). No MS, but still CCSVI.

Printing it out now- should be good reading on the plane. To Albany. This Thursday. To get Liberated.

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Three veins angioplastied.  One renewed life.  

Thats right! I forgot you are on your way there. Have a great trip BooBear!!

Thanks, BadCopy!!! Just three more days.

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Three veins angioplastied.  One renewed life.  

If symptoms get better over time (heal) as the body miraculously does, why on Earth would we need respite care, wheelchairs, and someone on the other side of the phone trying to comfort our being crippled?

I think the MS Society understands that and if you saw the video on you tube, Dr. John Murray was so nervous his fingers were rattling all over the table answering questions from media - GOT TO SEE IT TO BELIEVE IT.

Sorry Leohero. I am from now on taking the high road and not responding to such silly posts. I believe that most people who come to this forum see the things that are posted here and have a good laugh and from now on I will do the same!

Scorpion - for someone who claims you have ms - your behavior is completely inconsistent with one's wanting to FIND A WAY OUT!!!!!!!!!!!

Rules of the Board
http://www.thisisms.com/ftopicp-4760.html#4760
Mon Dec 06, 2004 4:57 am
Personal attacks, which can consist of slightly veiled innuendo or sarcastic comments aimed at the poster as opposed to the content of the post, are not tolerated at This is MS. We of course reserve the right to ban or suspend any member who violates this rule.

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my approach: no meds so far - just balanced whole foods (partial 'paleo', much less outright elimination), science, supplements, & bloodwork
my regimen - www.thisisms.com/ftopict-2489.html
www.whfoods.com, www.nutritiondata.com

You have a point SCORP. It seems you hear all about how people are excited prior to their procedure but then after they have it you never hear from them again? Whats up with that? It seems to me the results have much to be desired...I for one had the procedure almost 7 months ago and continue to decline...