What Does $7,000 Look Like to You?
January 20, 2008 by kfabrizio
Here’s what $7,000 looks like to me and to others with M.S.

This isn’t my story. I didn’t write it. Someone much more powerful, much more educated about Big Pharma, the health care industry, and public policy wrote this story.
This picture and the story that goes with it impacted me.
It made my stomach turn.
It made me feel immense guilt for that one time I didn’t get the cap on the top of my AutoJect just right. I hit the button and then I lost all the medicine in one of my syringes. While it was a comical picture — liquid squirting on the shower curtain, the mirror and the floor, instead of into my tummy — I know what my meds cost and I felt guilty right then.
And then, I saw this picture and I was reminded of my wastefulness and felt even more guilt than before.
I was floored. Tearful. Nauseated. Grateful that I have insurance. Saddened for those who don’t. Furious at those in control. Eager to learn more; to be less ignorant. Empowered to spread the word.
Read the story. Then thank the author. She’s trying, day and night, to educate and through that education, to change public policy for those of us with M.S. (oh, and a few million other common folk around the country).
And then consider what $7,000 looks like in your world.
Yes, I also read this post on Brass & Ivory…I found it so moving, I linked it to my blog. Oddly, I only just discovered YOUR blog/this blog today! I hope you won’t mind me “linking” your blog to my side bar of “107 MS blogs”? I am constantly updating new MS bloggers to the list, which unfortunately is growing steadily. The links aren’t unfortunate, but the growing number among the diagnosed is.
Best to you,
Linda D.
Pre MS I was never sick, thus never considering the cost of medication. Now is a whole different story ~ Rebif is $2250 a month giving me a grand total of $27,000 for a year. Now add in all of the other medicines I take…it is ridiculous! Fortunately I only pay a co-pay each month but should something happen to my insurance I would have to stop taking the medicine.
I have joked that I have a house pulsating through my veins. Joking aside, this is a scary situation for many people. They must choose, do I eat, have heat or do I purchase my medicine in hopes of buying myself a few more years of normalcy?
Thanks Kim for sharing this story.
Linda, I’m glad you’ve stumbled upon the Sunshine! I’ve visited your blog before and I’d be honored to be added to your list of bloggers.
Brenda,
I’m right there with you. Hoping, praying, that I never have to choose between food, heat, or my meds.
http://www.youtube.com/watch?v=714ezqNvK2U
thought you could pass this along I had a friend make this for me. hope you enjoy it please feel free to use for your own ms walk team its for everyone
Thanks for sharing Super Dave!! I hope my readers take the time to watch your video. It was beautiful! (Now I know why they call you “Super”).
BrainCheese busted you! (We get bored in Seattle, rain and all) Oh, big Pharma really is filling their pockets. I am just sooo happy I can buy another vacation home for the CEO of Teva. Pills due soon, FDA fast track—KA CHING