This Is MS Multiple Sclerosis Community: Knowledge & Support

http://www.businessweek.com/news/2010-0 ... roval.html

This news may not have much to do with CCSVI, which effects I`m still awaiting to come but I noticed the last sentence.

I would like to know if they included CCSVI as a possible reason.

It is interesting- especially as their annual report (Feb. 2010) was nothing byt optimistic about the continuation of Copaxone sales, particularly against the competition.

Hmmmm.....

The article talks about a possible copaxone generic being approved. There there is also the possibility of oral pills stealing some of the market share. But CCSVI could be in there as a secret factor as well. Interesting!

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"However, the truth in science ultimately emerges, although sometimes it takes a very long time," Arthur Silverstein, Autoimmunity: A History of the Early Struggle for Recognition

For the record:
Drugs for immune system modification in MS will change from regular injections (daily to weekly) to oral drugs or irregular infusions (monthly to annually) over the next few years. CCSVI will not decrease the total market size for MS drugs as companies will position their products in combination with CCSVI therapy.
This highly valuable market analysis for free, if anyone is listening.
Kind regards,
MarkW

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Mark Walker - Oxfordshire, England. Registered Pharmacist (UK). 10 years of study around MS.
Mark's CCSVI Report 7-Mar-11:
http://www.telegraph.co.uk/health/8359854/MS-experts-in-Britain-have-to-open-their-minds.html

For whatever it is worth... after 2 1/2 years of daily Copaxone injections, I just stopped cold turkey about 3 weeks ago. I just can't do it anymore. I tell myself the oral drugs are just around the corner and I will be able to start one of them soon. So I am no longer contributing to Teva's bottom line.

ozarkcanoer

Teva is being sued as well by the company that originally developed the molecule alleging that Copaxone is effective ONLY if taken once a week, or even once a month, that TEVA is pushing once a day only to boost their profits - if anyone's interested I can post the original link - tho I got slammed at another forum for doing that, so I'm hesitant to do so again.

But I've quit Copaxone cold turkey now, am going to start LDN & hopefully get liberated one day.

Selkie,

Please post the link -- I'm on Copaxone and considering reducing the frequency of my injections, so the lawsuit sounds intriguing....

Thanks!

yes but post it in the right forum, not the ccsvi one!

Yeah I wondered why it was in this forum. Can the thread be moved then I'll post the link. But you can also google it -

The problem with other threads is that not so many people are reading it. So I think it will be lost there.
CCSVI thread has/can become a place where thousands people come every day and one can get great advice in any area of MS. It`s almost like a MS Forum itself with many people and their experience. But it`s moderated to stay for CCSVI only. So it has both pros and cons...

As for MS Drugs, there are also many cases where people get their drugs paid from public health (like us) and are prescribed the drug even if they don`t take/want them. So the companies get their money anyway.

http://online.wsj.com/article/SB1000142 ... 20752.html
This article says sales are good. I don't think CCSVI will matter much to drug companies for a long time. Hopefully we get pharma interest in myelin repair...I would be happy to look at paying for fixed nerves.

i'm listening! thanks mark!

i'm passing this onto my buddies taking copaxone! pls post link