The current standard of care costs for pegylated interferon/ribavirin is roughly USD $20-25,000/year billed to insurance; meds only. It can become substantially more expensive if other drugs like Procrit or Neupogen are required as well.
I’m not sure we have a picture of cost structure for the PI drugs Telaprevir or Boceprevir yet; although industry analysts are projecting an additional $20,000 if memory serves.
If you have no Rx coverage, you might qualify for mfgr’s patient assistance:
Pegassist (Genentech Pegasys system): 888-941-3331
Commitment to Care (Merck PEG-Intron system): 866-363-6379, opt 1
"Also, as a side question, any information on getting treatment in Canada would be helpful".
The latest info from the medical community in Can. is that the new meds won"t be avail until 6 mo.or so from the release time in the U.S.
As far as how "Health Can". and the insurance companies assessing coverages especially as it is in regards to these new meds is still an unknown.
Does it make any substantial difference if one takes generic peginf/RIBA vs pegasys/copegasys?
I realize there will not be generics for new meds, so generics of SOC would be great if they are equally efficacy as trade?
Generic ribavirin has been available since 2006-ish; I’m personally unaware of peg-ifn generics.
If cost is an issue, have you approached the manufacturer’s patient assistance programs yet?
Another option for you could be to contact Henry Ford Hospital. They conduct trials from the downtown location and if you can get into one of those everything is free. I participated in a trial through Henry Ford and no longer have Hep C.
hey bill .....be sure to let us know how this all turns out :) oh yeah make sure to tell us the cost!
Bill...my last post was in response to someone who posted to you just before me ..then it disappeared.....never mind :)
yes the spammer I saw it too you aren't crazy Will!
IS IT My puter or all the post going up out of order??
Before I treated I called around to all the pharmacies in my area and compared prices. I was really surprised at the differences. So shop around.......and call those numbers Bill listed.
I'd be interested to hear what they have to say. We have little drug coverage and I could sure use some help paying for my daughter's tx.
If you get treatment in Canada and you aren't Canadian, you're paying for it. If you are a Canadian and you've been living outside of the U.S. for awhile, then apparently....though don't quote me....you have to be living in Canada for 3 months before getting your healthcare benefits back. That also depends from province to province. Why would you be looking to treat in Canada?
Nevermind...missed the dual citizenship comment. Got it. Above comment still applies mostly. There is probably various nuances to that, perhaps someone else has better information for you.
One of our old/former posters (went by the names Veggie, Veggie-Dip, PSP-N-Me) was an American who lived in northern Ontario (had moose in her backyard). Her hubby was a real Canadian (like a Mountie or some law enforcement). I think she managed to get treatment in that big Toronto place (where Dr. Jenny Heatcote) hangs out. But, I don't think tx was successful. I don't think it was a trial and I don't think she paid.
Knew I should have been a mountie..otherwise we all pay .unless covered by group insurance policys
Sometimes there are government programs fot those that have no insur. and are destitue..and at that there is only partial coverage.
FlGuy, if he was law enforcement, she was probably covered under his benefit package rather than any government funding for drugs. Drugs are not fully covered here as a given by any provincial government and how much they are covered differs according to what is covered by any existing insurance plans through work for example, then your income and it varies from province to province.
If you are destitute, you're likely to get full coverage for drugs if you have no insurance through any workplan and no means to pay for prescription drugs. Beyond that, if you have no group insurance or partial group insurance, then you are given a deductible to pay - similar to a co-pay I guess - based on income. It also differs from province to province.
I think it may have had more to do with the moose maybe than being a cop. But like i said if you have no coverage and are destitute there are plans avail.
There is one aspect of health insurance that is universal. It's universally confusing.
It's universally confusing. absolutely corect
Thank you all for the helpful information, the smiles .. and the laughs!! The morning is officially off to a good start!!
As for clinical trials at Henry Ford Hospital -- aren't all of the trials finished for the new drugs (Tela & Boce)? How would one go about getting into a trial -- just call the hospital and ask? I'm not real crazy about my GI doctor and staff there so I'm thinking I might get a second opinion from a Hepatologist ... suggestions appreciated. Thanks!
Dr Stuart Gordon at Henry Ford is excellent and a top Hepatologist. I made an appointment with him for a second opinion and then treated in one of the Boceprevir trials. There are other new drugs in the pipeline currently in trials that you could speak with him about at your appointment. In the meantime do a search at www.clinicaltrials.gov using "Hepatitis C and Michigan". See what comes up then you can start your homework prior to your appointment.
Best of luck!
Here is Dr Gordons phone number 1-313- 916-8899. Call and make an appointment and he will discuss the available trials with you. If there are not any that you like you can request to put on a waiting list until a trial opens up that you are interested in. That's what I did and was very happy with Dr. Stuart Gordon, you will love him.
Thanks for the info on clinical trials and Dr. Gordon. I'll call him today!