This Is MS Multiple Sclerosis Knowledge & Support Community

Patientx- you are so right very iffy if any actually balanced the budget. Used it for war?

I just want to remind all that according to Zamboni's preliminary findings that having the CCSVI intervention improvement varies in time. Go to page 75 stating recovery can take 4days to 4 months and further down the page was a Z test stating lower limb recovery as much as 6 months. and also mostly ...

Can't wait to hear from you Mark...

I am going to type his phonecalls to me so I can get info out asap.

I just watched a documentary by film maker James Surlock called Maxed out: hard times, easy credit and and era of predator. It is worth finding and renting. what does that have to do w/ NHC? It stated the last 3 presidents of the US borrow/took billions of dollars from Soc Sec to balance the budget....

Turtle_fi wrote: I wish to thank you Ernst that you have been feeding us to Finland the important info from here, it has gotten me to follow up also TIMS (of course I'm checking also finnish site). You are doing excellent work! Ernst it sounds like you are doing a great job spreading the word in you...

VROOOOOM...VROOOOOM

Good atmosphere to fart...

i don't feel so alone as a ppms'r now . we are a small part of the ms world

ditto jamies post

marc - there was a discussion recently on ms look alike deseases CIPD and one involing the PNS. here is the link if you missed it. http://www.thisisms.com/ftopict-7757.html regardless, wishing your the best holly P.S. Do you pace in your wheel chair? I am noticing that i have started to do so especi...

Well there are bits and pieces all through out CCSVI threads... first you need to know what kind of insurance you have...It sums up to HMO vs PPO whether it is through work or SSDI. The PPO platform is more flexible regarding out of state out of network as opposed to HMO. Then there is the co-pay is...

Here is a start...

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Read the paragraphs below FIRST before you watch the video. This is an awesome dance, called the Thousand-Hand Guanyin, which is making its rounds across the net. Considering the tight coordination required, their accomplishment is nothing short of amazing, even if they were not all deaf. Yes, you r...

Hi hlm -

I have a burning sensation on my feet as if they were sunburned. This is part of my MS symptomology. i just put my feet up and try to rest them although they still burn at night in bed...I guess I am stuck w/it at this time

I know that they are available not just wishful thinking. I saw one that collapsed in two...very small seat. Small girth all together. I don't know what one would weigh or cost. I would start roaming the internet, brouse through online catalogs....

Good Luck and good travels

cool