Exactly what coolioness said. You may end up paying nothing.

My insurance does not cover my MS medication *OCREVUS I go through the actual drug company and qualify for a grant program with them and the majority of the cost is covered.

In the past, my neurologist office would provide me with copaxone samples that the drug rep would drop off. I did that for 2-3 years. And I also have had success contacting the manufacturer directly through a special phone number they each have for patient assistance program.

As long as you have a good relationship with your Doctor.
They should, may have access to better prices.
You won't know until you asked.

I guess I am lucky. My Neurologist office does a lot of trials.
That is how I have tried a number of MS drugs.
I am currrently Iam waiting for the newest drug my Neuro wants to put me on.

Check with the drug companies.
I Habra my meds paid for by the drug companies.
Always ask. T he worsecthat cam happen is yhey say NO. It won't be the last time you here no.
Good luck, Be Well!