Doc is almost ready to start the remicade. I went and checked with my ins and they said it's not covered. Have you experienced this?? Now what
Doc is almost ready to start the remicade. I went and checked with my ins and they said it's not covered. Have you experienced this?? Now what
i have tried all others . the doc says this is my last hope. Only One i have not tried is Humira.
Doc still unsure if i have UC or C.
Straight off the BCBS NC web site regarding coverage -
http://www.bcbsnc.com/assets/services/public/pdfs/medicalpolicy/infliximab.pdf
Not sure if PA has something similar - HOWEVER I did just find this -
https://www.bcnepa.com/Providers/FreedomBlue/9-2-13.pdf -
There should be something in your policy that specifies which drugs are and are not covered - if you don't have a copy of your policy I'd ask for one - you may be able to access it on line too....
Also - make sure they are looking under the MEDICAL BENEFIT - NOT the prescription drug benefit!
I know each policy is different even if the carriers are the same. We Have BCBSIL as well, under our contract it is covered under the medical benefit although though it took us a few weeks for that to be straightened out as they kept trying to say it was only covered under the prescription drug benefit.
I know each policy is different even if the carriers are the same. We Have BCBSIL as well, under our contract it is covered under the medical benefit although though it took us a few weeks for that to be straightened out as they kept trying to say it was only covered under the prescription drug benefit.
I know each policy is different even if the carriers are the same. We Have BCBSIL as well, under our contract it is covered under the medical benefit although though it took us a few weeks for that to be straightened out as they kept trying to say it was only covered under the prescription drug benefit.
Doc is almost ready to start the remicade. I went and checked with my ins and they said it's not covered. Have you experienced this?? Now what
This thread has been so interesting. It amazes me that so many of have BCBS and yet our meds are paid for in so many different ways
This just supports my thoughts when I first was diagnosed with this crap (yes, pun intended) over 30 years ago. We, as the patient, need to be our own advocate because no one else will, or can, be. Every one of us with our disease, insurance, personal life, etc is so different and everything affects each of us so differently. This is why I love this forum for the support we get from each other and ideas we can give each other. You never know, what suggestions you give could really help.
Thanks all, I've learned a lot from this thread.