copaxone

[scout718]

What is the best way to get help paying for copaxone or is there a generic version that is less expensive? I was hoping to start taking it soon, but Im afraid I can't afford it. Also, has anyone taken the new oral version? Is it less expensive? I was advised not to use it but I certainly will if I can afford it. Plus, what are the other benefits of using copaxone othr than slowing down the formation of new lesions. Will I get my energy back? Will my concentration get better? Any info you kind folks have will help me very much.

[Lulu54]

Scout, there are assistance programs for all of the drugs and with persistance you can find those for  copaxone.  Don't take no for answers if you run into a wall .  Keep l;ooking until you find the help you deserve.

hugs,
L

[doublevision1]

What is the best way to get help paying for copaxone?
Try contacting Shared Solutions/Teva.  They may be able to offset the cost for uninsured/underinsured.


http://www.sharedsolutions.com/Getting-Started/StartingCOPAXONE/BenefitsAndInsurance.aspx


Is there a generic version that is less expensive?
No.


Also, has anyone taken oral version?
Some forum members here are/were subjects on drug trials for Gilenya.  I myself haven't.


Is it less expensive?
No.  Gilenya has been priced at $31K in Canada, almost double the cost of the injectible DMDs (around $18K in Canada)


Plus, what are the other benefits of using copaxone other than slowing down the formation of new lesions?
- reduces relapse rate by approx 30%
- delays clinical worsening


Will I get my energy back?
Not from being on a DMD, though medications like Provigil or Ritalin may help.  
Also, studies have show that MS patients who start an exercise program do see improvements in their energy levels.


Will my concentration get better?
Not from being on A DMD.
Check out this resource for some tips on managing cognitive symptoms:

http://www.mssociety.org.uk/about_ms/symptoms/memory_and_thinking/memory_hints.html