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This Is MS Multiple Sclerosis Community: Knowledge & SupportWelcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones. |
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Joined: Mon Jun 06, 2011 3:00 pm Posts: 1 |
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| Topics | Author | Replies | Views | Last post | |
|---|---|---|---|---|---|
 | Copaxone and LDN | 3 | 3987 | Wed Jun 09, 2004 12:17 pm | |
| Is it the Copaxone? | 2 | 3233 | Sat Aug 28, 2004 5:15 pm | |
| Copaxone and SP | 0 | 2059 | Wed Sep 28, 2005 6:40 am | |
| Copaxone | 0 | 1975 | Wed Aug 02, 2006 1:26 am | |
| First MRI on Copaxone | 5 | 3703 | Fri Feb 02, 2007 8:34 pm | |
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I am a German postdoc and wondering whether to apply to a postdoc position in the Republic of Ireland. I have MS and have taken Copaxone for nearly 8 years; it seems to work very well and I have had only one acute episode since. So I wonder whether Copaxone is available in Ireland to everyone who needs it? I mean, considering the cost, are there people who are denied this drug? I also considered a position in England, but I know that NICE believes it is not cost efficient. Since it works so well for me, I don't want to be forced off it, though. I would appreciate any information / help you may have on this. Thank you so much!
Abacus