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More whine - anyone got some cheese?
I am so frustrated. I have been on Copaxone for 2 years, with my pathetic insurance paying only a 25% copay. I've maxed out my home equity, drained my savings, and now Teva has raised the price so my C. now costs $5014.43 for a 3 month supply!!!! I make too much to qualify for any aid (around $38,000 per year), but how can I manage over $20,000 of that for C????
In 2 years I have had no progression and no new lesions. I love C., but only have 5 syringes left with no funds to buy more. And what's REALLY frustrating is that I just saw that generic C. is now available in Canada. Maybe I'll go buy a lottery ticket. Heck, I've tried everything else. |
Sorry Tabbi, about the expense of C...surely if ever I am put on something I am wondering what my insurance would cover. that is sooo darn expensive.
sorry no help here, but wanted to say sorry and give you hugsss,sarah |
I am so sorry this is happening to you. :hug:
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i'm so sorry.
that is a terrible expense. have you tried contacting the chronic disease fund? they may be able to help. can your neuro offer any suggestions? they won't negotiate at all? the bums. |
That stinks, Polly. I am so sorry..:(
I hope you can find help..Good Luck..:hug: |
That just sucks. You cannot get assistance yet you cannot afford it. Just not right.
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I live near Wisconsin. Are you kidding? I could bring ALL the cheese :D..I'm going thru the financial thing for Ty myself.. When they told me the cost without insurance is around $10,000 a month, it took a while to pick my jaw up off the floor. Of course, they cut a deal with my insurance company, so it's ONLY $6700 a month. Much better..:confused:
I feel your pain! Pass some more whine.. |
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: |
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! |
Quote:
However, since I whined about this on another board, a guardian angel came my way in the person of someone having to go off C. who is sending me what they have left. This is the second time I have gotten help like this. I know we're not supposed to do this (per gov't. regulations and all :eek:) but heck, if it will keep me ambulatory, I don't care. This is for you, angel -> :hug: |
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