MS in Washington State

[michellejday]

Hello, I got diagnosed with ms 2 years ago. Last thing I had on what could of been wrong with me :/ So now, type 1 diabetic, ms and thyroid problems. Now because I still am able to work, I can not receive assistant with my insurance. So they are telling me that my ms medication has a $1,200 co pay (cause I am now paying for insurance). I have tried everything I can for help with this..nothing. What can I do??

[Raingrrl]

Hi michellejday ! Welcome! There is a broad spectrum of people dealing with MS here. We are a wide range of ages and experiences so you are sure to find people that can empathize with your experience.

If you haven’t contacted the pharmaceutical company that manufactures your ms medication, try that. Do an online search to get the number to call. Most of them have programs to help pay for the drugs. That’s how I afford the drug I’m on now and the one I was on previously.

[Diva1976 in reply to Raingrrl]

Yes a lot of the manufactures will assist to make sure you have your medicine. When I was on AUBAGIO for instance, AUBAGIO provided it for months until my insurance would cover. Your neurologist assistants will usually work to get your medicine covered.

[Peruzzot]

Welcome to the group. Search the MSAA and national MS Society websites to see if they have any links to help with medication copays. Here I was complaining about my copay nearly doubling to $50 from $35 per month. $1200 is beyond ridiculous!

[greaterexp]

Welcome to a great family here. I hope you'll get plenty of great ideas for how to help with the copay. It's frustrating to deal with insurance companies, doctor offices, and pharmaceutical companies. I think we've all been there.

[tnolan2006]

Those high deductible insurance plans are discouraging. There is an option, a generic version of a new MS drug that is affordable. The MS drug is Mavenclad, generic version is cladribine (off-label). Look into it, I did. Really good drug.

[Jazzihorsecat]

💛💐very warm welcome michelle.--Jazzy🌹💜

[hairbrain4]

Welcome. Sorry, you are having problems with your co-pay. Most of us have been there & experienced the same problem. Like others have said, contact the drug company and also check to see what NMSS (National Multiple Sclerosis Society) to see if they can give you any other resources for your state. Just don't give up, help is out there.

[mrsmike9]

Mine is over $5,000 a month. I have copay assistance. What medicine are you on?

[IFwczs]

Most drug manufacturers offer financial assistance if you have commercial insurance. Call them up and inquire.