Thanks, health insurance company. Because I take a specialty drug, I now must pay $150/month copay for my Copaxone, as opposed to the 2008 copay of $50/month. Bastards!
I knew this was coming in November and have adjusted the budget with GH accordingly, as well as counting this new expense in re-figuring my flexible spending account for 2009 health care reimbursements. When I received the lovely package outlining our new options for 2009, I really nearly started screaming at someone. There was a separate brochure, all pretty and shiny, outlining the drugs considered "specialty" drugs. Before this list, there was a paragraph explaining why these drugs are so expensive. And, I kid you not, the first sentence says something to the effect of, "injectible drugs that treat conditions like multiple sclerosis." I was feeling a bit persecuted. Bastards!
I contacted Shared Solutions and they sent the paperwork to enroll in their discount program. I was accepted, so they will pay $50 of my copay. So now, my copay for 2009 is only double what I paid in 2008. Bastards!
All bitching aside, I am grateful that I have the income to pay for Copaxone. But what about those who can't? I know there are other programs for which they may qualify, but how do they find out about them? Since I began my MS journey, so many people have told me that you must be proactive about your health care. It is so true!
To all my dear readers, may you have a very healthy and happy 2009!
21 hours ago