NeuroTalk Support Groups - More whine - anyone got some cheese?

Quote:

Originally Posted by Tabbico (Post 462213)

Hey Polar,

Maybe we could take that cheese and have a yard sale and raise us some money.....

I didn't think anyone could have a bigger med bill than me, but you win!:eek:

I'm trying to avoide the big med bill, which is why I'm going thru all the financial aid carp..This is not a contest I want to win, believe me!:eek:

Quote:

Originally Posted by azoyizes (Post 462233)

Polar, I'm so sorry you're going through such difficulty trying to afford Copaxone. :hug: Have you contacted the Copaxone people? Explain to them that you can't afford the co-pay anymore, it's possible they have a patient's assistance fund.

Don't give up. Also, contact NMSS and explain the problem. Maybe they can come up with something.

It makes me sick every time I hear the cost of the DMD's. It's unbelievable!

I already tanked on Copaxone. My co-pay for that was only $25 a month, but if it doesn't work it doesn't work..What I'm working on funding for is Tysabri. It's newer, more expensive, and involves the medical procedure of infusion, so the sky's the limit on what they can charge..Fortunately, I have an MS Coordinator at my neuro's office that truely enjoys B*slapping drug company reps. They've been moving much faster on getting this coordinated. Ya gotta love her!
You're right on the ridiculous high price of of DMD's..Or any drugs for that matter. What good does all this stuff do when nobody can afford to use it? Oh, well...Maybe someday the world will make sense..:rolleyes: