From MS Society twitter feed.

News today is that Fampyra has been recommended for use on the NHS in Wales

Let’s hope England, Scotland and Northern Island make the same decision too.

I pay for it, nearly £200/ month, without it I would fall and cost the NHS way more than the cost of the tablets. My neurologist agrees with me that it should be on the approved medications list.

Fingers crossed for all the Fampyra users!