It’s a worry that they are narrowing drug choices down for the treatment of ms. If you need them it’s not good that they are abandoning some of the choices.
What if the drug doesn’t agree with you , what happens then ? Choice is always a good thing for this and many reasons. It might not affect people who are on the ones they are abandoning like copoxone but it will affect new people to ms and people who might need them in the future .
How do we make our voice heard. It’s not okay to affect our lives and limiting choice even more because of their cost cutting !
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