still the same

we have not had a big snow yet here in Montana, but I can feel it is on its way.  I still have a big difficulty walking, but nothing is getting worse.  I have a neuro. appointment in less than a month.  the hospital he is at now has a policy that he cannot refill my copaxone prescription without seeing him at least once a year, I don't mind seeing him at all.   NO CHANGES AT ALL 
I keep myself busy by writing my haikus on facebook, I live on there.  I do a few things to fight off boredom.  I did listen to an internet broadcast the other day about the affordable care act and ms, it was talking about getting signed up with it.  I will see about that and I hope to report back here about it.  all that really matters to me is my copaxone.  I am in incredible health otherwise and I owe so much of that to exercising.  that is the ONLY good thing that has come from ms(and I have met some good people, also)