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apologies for going off-topic, but your reason for treating stuck out like a sore from for me.
your odds of giving your children HCV in the next few years ( until better drugs are available) are probably similar ( to use Dr. Dietrich's words in the expert forum) to getting hit by a meteor.
as someone with zero liver damage, and concerned about their children, you should seriously consider how the side effects of treatment will affect both you and your children.
Maybe it is a small chance but one Im not willing to take. We travel often and on very long trips plus I live in Myrtle Beach where if it rains there is 25 accidents in the first 10 minutes of rain. Dont get me wrong. I know what your saying and I appreciate the advice more than you know. Ive just thought this out long and hard and I have been very upfront and honest with the kids about everything. They know the sx and they know what this disease does. It was a family choice for me to go ahead and begin along with the doctors advice. Ive even taken the kids on appts with me.
they are strong and have been thru a diversity of obstacles in their lives. Also one of the closest drugs to coming out is one that is for people that have already been thru tx and have not reached SVR. Thats supposed to be early 2010. Either way I have to undergo tx. This one maybe a lot worse but at least it will be over with and with Gods grace I will reach SVR.
Thank you so much for your concern.
I'm assuming you quoted your doctor and correctly, but just to clarify, it's not "SVR" that happens within the first four weeks, what you're looking for is to become undetectable within the first for weeks. Regardless of how soon you become undetectable you will still need to treat for a minimum of 12 weeks with the usual protocol being 24 weeks.
Two things you must discuss with your doctor prior to treating are getting a week 4 sensitive viral load test ( you want it) and in making sure the doctor will intervene with helper drugs (like Procrit,epo) instead of reducing your dosage. The other thing -- I guess that's three things now ;) -- is you should make sure you are put on weight-based dose of ribavirin as opposed to a flat 800 mg dose
Yes it was undetectable and not SVR. This all is still new to me and I get confused sometimes. Sorry. I have had a viral load test and he did say another will be in 4 weeks of beginning the meds. I also asked him about the rescue drugs and he said "Oh H*** yeah" He is very outspoken and upfront and takes a lot of time with me on my visits. Thank God for you all on this board because I have learned so much. when I went for my last visit I had a whole page of questions and he gladly answered each and everyone to his fullest extent while not worrying about the time it took. He seems very capable and kinda nice on top of it. I only want the best care i can get because I love me lol.. i will ask him about the riba dose and make sure that is what it is.
Thank you for being so kind and spending so much time with me and helping me
Best of luck with your treatment,
pro
My meds cost $2,300 per four weeks. So that at least gives you a bench mark.
I'm really surprised that Walmart would handle something like this. These are speciality pharmaceuticals. For one, the interferon needs to be refrigerated and handled with great care. It's not something you can pick up anywhere. I could be mistaken, but it surprises me.
And the real question is when you looked up the price, were you comparing apples to apples? These are a number of different products with very similar sounding names. In fact, you should triple check that the pharmacy understands what your doctor as prescribed.
All that being said, I think you're right there is an injustice. Unless the terms of your insurance state that they can steer you to a pharmacy, it sounds pretty awful. Was an agent involved in selling you the insurance? These folks can often be helpful in working these things out.
Enjoy
If you're using Pegasys, call Pegassist. They will verify insurance coverage, co-pay, and find the best pharmacy for you.
http://www.pegassist.com/pub/hcp/default.asp
Co
My co-pay was in the $470.00 range per month (20%) for the first six months (I think) and then dropped to $20 per month. With the new year, I'm back at the higher co-pay.
Precision Rx works great, Anthem can be problematic. You have to stay on top of them.
One good reason you treat now is that on rare occasions a geno3 can be almost harder to treat than a geno1 - best sometimes to find out now that way you would still have time in the future to change and extend treatment.
Considering the great amount of expense that the drugs cosst - $60 isn't really all that bad. It doesn't make sense to me why you'd HAVE to use a more expensive company except..........I'm sure that they want to make as much money as you can.
Anyway I just wanted to say - make sure you ALWAYS refill your script a week or two BEFORE you run out.....just in case! A few times the pens have jammed up or broken or the meds just weren't at the pharmacy when I went to get them...all sorts of odd things. You want to make sure that you have at least one at home in the fridge for the following week just in case.........it will save you a lOT of grief later on (and of course if you do it that way it will never happen and you will be fine ;)
PS Yes it was undetectable and not SVR
Don't worry about saying SVR instead of UND - we all get what you mean and we were ALL new at one time and said the same incorrect verbiage and newbie mistakes. If you have a question just ask it.......the more you learn the better off you will be.
And don't forget get copies of ALL of your test results and learn how to read them! At first you can post them in here so people can explain them to you, in no time you'll understand it all you'll see.
NYgirl - A car wreck was just one instance I could think of. I want to do the treatment and get it overwith. I want this gone while the doc says its the best chance. I have no liver damage in fact he said if he didnt already know I had it he couldnt have told by looking at my biopsy so i just want to get it gone before taking a chance of liver damage.
thank you for the excellant advice on ordering my scripts. I had never even thought of that. Im sure I would be panicing and driving everyone insane if I was to run out lol..
I have been asking a few questions and my doc was really surprised all that I have learned. I learned it from all of you. I am so grateful for this board because without it I would have known nothing. The people at Be in Charge say I am ready and well prepared to start tx. That also is because of you all. I also have copies of all my test on the way. As soon as I get them i will post it.
Thank you all so much..
My out-of pocket expenses for the first year of treatment was several thousand dollars.
That's factoring in co-pays and deductibles for labs, radiology, specialists, etc.
Before you get too excited, do understand that your coverage could vary significantly.
However, even with good insurance, this can be a spendy proposition.
Here's wishing you the best of luck.
my suggestion is get on the phone with your insurance company's member services (ugh, i know) and find out from them what exactly your out of pocket expenses will be. you will probably have to pay your annual deductible (if rx applies to it) and then pay either the flat rate, or the coinsurance. again, member services will be able to tell you specifically how much. if they don't, keep bugging them until they do. ALWAYS get the name of whoever you speak to. and if you aren't satisfied with what they tell you, ask to speak to a supervisor, and get their name as well. even though they may have hundreds of people working there, they can track down the person giving you the info because they note your account with all inquiries. but always keep a record of who you uspeak to as well.
whenever you call any pharmacy, mail order included, they will quote you a price they'd charge you if you didn't have insurance coverage. your insurance company has contracted with pharmacies for set rates, so what the pharmacy will charge your plan will be a lot less than what is originally quoted. and i believe all mail order plans will only give you three months at a time. (take a glance at any of your EOBs, you'll be amazed at the difference between what a provider charges and what is contracted.)
personally, my plan will charge me a flat $200 for a three month supply thru our mailorder company, even though the coinsurance would be more. its because of the contract the provider has with my plan and because my plan has a cap. this is an incentive for members to use the mailorder because it saves the insurance company $. my plan also allows me the option of using a retail pharmacy like walgreens, walmart, etc, if I choose, but my out of pocket will be over $700 a month.
most people don't know or realize that it is the employer that drives what benefits are available to you. they are the ones that choose what is covered, plus the levels of coverage the insurance company offers employees, based on how much they paid out in claims the previous year. and how much they're willing to pay this year. so if your benefits blow, blame your employer, not the insurance company. mine are the worst i've ever heard of (richest plan has a $3k deductible a year, AND i work for the stinkin insurance company.)
Oh, and all pharmacies are regulated and have to meet federal mandates, so they are all capable of handling ALL medications, not just the basics. this includes walmart, sams clubs, supermarket pharmacies, the local mom & pop pharmacy around the corner as well as all major chains.
Hope this helps. and i wish u well on ur treatment!
xoxo
Thank you all for the great advice. Your helping me more than you know.