It appears you have not yet registered with our community. To register please click here...


 Home Message Boards Health Guide Join for Free User Blogs Board Index
Search
 
Forgot your username or password?
Closed Thread
 
Thread Tools Display Modes
Old 03-10-2008, 07:35 PM   #6
LATW
Member
(female)
 
Join Date: Feb 2008
Location: Bremen, Indiana, USA
Posts: 59
Re: Avonex funding

I called Avonex and got my answer. You CAN have a 401K, IRA, savings, other resources. They just look at the WHOLE financial situation. We are a family of 7 and they said we do qualify based on our income.

So, I can rest easier! I feel like I have been left trying to connect the dots and I am pretty frustrated.

I thought I would get help all the way through the process of setting up the Avonex treatment. They are "helping" but we don't seem to be getting anywhere. But then I have not had my diagnosis a month yet...maybe I am expecting too much.

LA
__________________
LA
Optic Neuritis twice this year. Diagnosed with MS 2-13-2008
Started Avonex 2-2008
LATW is offline
 
Sponsors Lightbulb
 
   
Old 03-10-2008, 07:37 PM   #7
MSNik
Senior Veteran
(female)
 
Join Date: Sep 2006
Posts: 4,952
Re: Avonex funding

well, thats good. Not great, but better. I dont know why you ever would have thought it was 300$ a month, thats a very high amount. There is one thing you should also check into....in the USA, most injectables, are sent thru the mail- and most companies will not send you 90 days at a time...in fact, some pharmacies will NOT ship more than 30 day supply at once. I know mine, wont. I can only get one box of syringes...keep in mind, Avonex is only once a week...mine is three times a week...copaxone is daily....so I dont know for sure what insurance you have or what pharmacy they use- but FIRST make sure they are SHIPPING this to you, the cost to have it shipped is about 1/5 of what it costs to pick it up at a pharmacy...and second, verify that they will send you 3 months at once.
good luck to you.
N
__________________
RRMS- dx 06
Rebif since 06
"Every New Beginning Comes From Some Other Beginning's End"
MSNik is online now
 
Old 03-10-2008, 07:41 PM   #8
MSNik
Senior Veteran
(female)
 
Join Date: Sep 2006
Posts: 4,952
Re: Avonex funding

hi again. Just read your newest post, which you were typing, when I was responding to the other one. Again, without knowing your insurance, or your benefits, I cant say what to expect...but defintaely look into the two things I said..where it is coming from, being sure that it is by mail- and also finding out if they will ship you 3 months at a time. I KNOW Avonex, straight from the manufacturer didnt used to ship more than one month at a time, but I do not know if that has changed...I also think that their "help" is only for one year..after that, you are on your own....thats how it used to be. Again, it might have changed...all drug companies offer help for those who qualify, and if you have that large a family and little income, you should qualify.

also, isnt your doctor setting this all up for you? Your Neuro should be faxing in a script to your insurance company and they should be talking to you about the choices you have in getting the drug...follow up on that before you do anything.....

again, good luck.
__________________
RRMS- dx 06
Rebif since 06
"Every New Beginning Comes From Some Other Beginning's End"
MSNik is online now
 
Old 03-10-2008, 08:16 PM   #9
LATW
Member
(female)
 
Join Date: Feb 2008
Location: Bremen, Indiana, USA
Posts: 59
Re: Avonex funding

I checked with my insurance company and I can get my Avonex from the pharmacy or through mail order for either a 30 day or 90 day supply. The co-pay is the same in each case.

The $300.00 a month is the amount the lady at Avonex gave me. That is why I decided to call my insurance company myself. I think there is a break down in communication for some reason. Other than that I have no idea what is going on. Our out of pocket for scripts per month is $150.00. Which is pretty good considering what it could be!

I called Avonex back to let them know what our insurance rep told me. I also wrote everything down including names and dates. So now I feel like I have the dots connected!

LA

Quote:
Originally Posted by MSNik View Post
well, thats good. Not great, but better. I dont know why you ever would have thought it was 300$ a month, thats a very high amount. There is one thing you should also check into....in the USA, most injectables, are sent thru the mail- and most companies will not send you 90 days at a time...in fact, some pharmacies will NOT ship more than 30 day supply at once. I know mine, wont. I can only get one box of syringes...keep in mind, Avonex is only once a week...mine is three times a week...copaxone is daily....so I dont know for sure what insurance you have or what pharmacy they use- but FIRST make sure they are SHIPPING this to you, the cost to have it shipped is about 1/5 of what it costs to pick it up at a pharmacy...and second, verify that they will send you 3 months at once.
good luck to you.
N
__________________
LA
Optic Neuritis twice this year. Diagnosed with MS 2-13-2008
Started Avonex 2-2008
LATW is offline
 
Old 03-10-2008, 08:19 PM   #10
LATW
Member
(female)
 
Join Date: Feb 2008
Location: Bremen, Indiana, USA
Posts: 59
Re: Avonex funding

My doctor did get things started and we were sailing along until the insurance issue came up. I am not too sure my Avonex rep is following up. She was supposed to see if I need a PA for my Avonex. That was last week and I never heard back from her.

From what I can find in my insurance information I do NOT need a PA. But I am going to call the insurance company tomorrow to make sure.

On the bright side of this Avonex is going to continue sending me my medication free of charge until this all gets worked out!


LA


Quote:
Originally Posted by MSNik View Post
hi again. Just read your newest post, which you were typing, when I was responding to the other one. Again, without knowing your insurance, or your benefits, I cant say what to expect...but defintaely look into the two things I said..where it is coming from, being sure that it is by mail- and also finding out if they will ship you 3 months at a time. I KNOW Avonex, straight from the manufacturer didnt used to ship more than one month at a time, but I do not know if that has changed...I also think that their "help" is only for one year..after that, you are on your own....thats how it used to be. Again, it might have changed...all drug companies offer help for those who qualify, and if you have that large a family and little income, you should qualify.

also, isnt your doctor setting this all up for you? Your Neuro should be faxing in a script to your insurance company and they should be talking to you about the choices you have in getting the drug...follow up on that before you do anything.....

again, good luck.
__________________
LA
Optic Neuritis twice this year. Diagnosed with MS 2-13-2008
Started Avonex 2-2008
LATW is offline
 
Closed Thread

Bookmarks

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is Off
HTML code is Off


Similar Threads
Thread Thread Starter Board Replies Last Post
I need some help or wisdom, Please! april1848 Multiple Sclerosis 11 01-21-2008 03:35 PM
Injections ? tspetz72 Multiple Sclerosis 8 02-27-2006 09:37 AM
I dont think I can take this.... paigeH Multiple Sclerosis 18 10-17-2004 03:27 PM










All times are GMT -4. The time now is 08:20 PM.


Site owned and operated by HealthBoards.com (TM)
Copyright and Terms of Use © 1998-2010 HealthBoards.com (TM) All rights reserved.
Do not copy or redistribute in any form!