Drug prices have forced me to ration my multiple sclerosis meds.
Even though there are more and more multiple sclerosis drugs being developed and market competition is increasing, prices keep going up.
Drug company greed took five years of my life from me.
The price hike of clomipramine has completely derailed my life for almost half a decade.
An extremely expensive diagnosis.
No one should have to skip meals and ration the medicine that keeps them alive simply due to high prices.
I pay $600 on prescriptions each month.
This year, I watched as my copay for a one-month supply of Levemir, a long-acting insulin, skyrocketed from $20 to $180.
I worry about my daughter’s future.
I have spent the last few years switching jobs to try to find one that gives us insurance coverage that will help us to afford my daughter’s insulin and medical supplies.
I thought I was prepared.
No one should be forced to make the decision between whether to eat or whether to buy their medicine; whether to pay rent or buy their medicine.
$800 per month just on insulin.
We need changes that place patients’ needs first so that we can afford our prescription drugs.
A price tag of tens of thousands of dollars.
My kids don’t see the judgment calls I have to make about whether to pay a bill or copays for insulin.
