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How do you pay for med?



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04/17/2008 21:05
2bpainfree
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Hi, Everyone. I have not been online much lately. I got really sick and missed work a lot. Then it took lots of meds to get me better again. I am sick again and just spent $100 on meds.

Now to the reason I say all this. I am behind on bills because of all the medications I have had to buy. I already spend a lot on my regular meds. All this made me wonder how everyone pays for there meds? I have insurance, but its still not enough.

How do you all handle the bills?? and Meds??

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04/17/2008 21:13
ALCSS2008
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I am having trouble right now. I bave two that are due and I do not have the co-pays. One is $20.00 and one is $40.00. I don't know how I will afford them this week. I may have to do without the one that costs twenty dollars. My co-pay on my meds is almost one of my husbands take home pays a month. I am hoping to get help with this. We are going to social services later this month. I need help. i am not too proud to try to do anything to help my family. I think maybe this my help me get into the court system for an appeal faster also. After they are helping me either way. My husband is getting another job, but that is hard to do when he already works 50 hours a week and hever knows when he is gettig home. Sorry to run on
ccc
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04/17/2008 21:20
Fletch2ya
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My Suboxone is 480 a month and my Provigil is 350 a month... Insurance does not cover any of it.....

VA cover some basic....med..very basic meds.....

other wise ..its up to me.........my insurance company says it is not part of my treatment protocal.....so they will not cover it....

WHAT treatment protocal....... No two doctors can even agree if fibro or RSD are real and if they are how to treat it.....



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04/17/2008 22:45
ALCSS2008
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It is time for these doctors to wake up. RSD and fibro are here to stay. Is it going to take someone rich and famous to get them to make the disease valid. I don't see how you do it. That is almost what my husband makes a month.
ccc
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04/17/2008 22:52
Matafleur
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So far, all that I've been precribed, have been paid for through Medicaid other than medications for my psoriatic arthritis, the psoriasis part. I go without those.

There are a few options for everyone:

WalMart, Target and some other stores offer $4 prescriptions depending on what the medication is.

http://www.walmart.com/catalog/catalog.gsp?cat=546834&fromPageCatId=5431

http://sites.target.com/images/pharmacy/ pharmacy_4dollar_program_list.pdf

There are a few free or discounted prescription drug programs:

http://www.needymeds.com/

https://www.pparx.org/Intro.php

Go to http://www.211.org/

Hopefully there is a listing for your state of all human services available. On the bottom right of the page, is a search option.

You can also try calling United Way. Your county social/human services offices. Your local hospital.

These last links can give you some other ideas.

http://www.editorsweb.org/money/prescription-drugs.htm

http://abcnews.go.com/gma/mellodyhobson/story?id=127643&page=1

Do a web search for 'how to save on prescription drugs'

Pass this info along and good luck!

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04/18/2008 00:34
Fletch2ya
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HI... We have tried all of these......... and a couple more.......

NOthing.....no one is willing to help...because I have medicare......

So now we are going through a canadian pharm... and that is the price I have to pay through them........I take 2 provigil a day and suppose to take 2 Suboxone a day..... The $480 for the Suboxone is half what the pharmacy here at home wants for it....

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04/18/2008 04:02
SuziWeaver
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I used to get all mine for free or for $20 for a 3 month supply. I went to http://www.rxassist.org/ . Sent in the forms to the drug companies for assistance.

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04/18/2008 04:26
auggie
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FYI: THE MAKERS Of THE DRUGS MIGHT HAVE A PATIENT HELP LINE. (It worked for me)

not sure if this helps all but i had found that the pharma companies will sometimes offer patient advocacy assistance. It worked for me.!!! i was amazed.

In 2004 i used a 75mg Fentanyl Patch. Some know this as "Duragesic". It was originally for cancer patients/apin. And my "good" docs that i had finally found were very clear that while i was in such extreme pain, they would manage the pain with an eye to treatment, to the future etc... and plan to bring the meds DOWN. Which they have.

At that time I was passing out in public or I would get such BOLTS of pain - electric bolts - that my KNEES WOULD BUCKLE.

Then in addition to the "patch" the docs prescribed a "Fentanyl" lollipop for immediate BREAK THRU PAIN emergency. Same drug/component that was in the patch that BS/BC paid for. The lollipops are alled "Actiq".

IT IS/WAS A NEWER CANCER PAIN DRUG at that time but i do NOT have cancer. So Blue Cross paid for the Ppatch but not the lollipop. ($1000 for a box/month). Makes NO sense. the SAME drug.

THE PHARMACEUTICAL website knew this was a good drug and knew it helped others NOT JUST cancer patients. They had forms and a 800# and they were very helpful in helping me get it covered!!!

It took about 3 months BUT we got re-imbursed! So maybe you could see if the manufacturers of the drugs can offer you advice? They are incentivized to have their drugs prescribed. Drugs like Nuerontin are origanally Epilepsy drugs BUT are widely used for other conditions because it "turns down" the central nervous system. So these companies know their drug will serve MORE THAN ONE PURPOSE.

try it or at least see if they have a link. I was surprised at how helpful they were!

Post edited by: auggie, at: 04/18/2008 06:33

".....Grant me the serenity to Accept the People I CANNOT change, the Courage to Change the ones I CAN, and the wisdom to know -- That's just ME!...."
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04/18/2008 04:41
redundant33
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I pay part of mine out of pocket (working on qualifying for Medicaid) and my Cymbalta is supplied to me through our community counseling center for free. I also see a counselor and a psychiatrist for free. I don't know what I would have done without them.

Popular posts by redundant33
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04/18/2008 05:55
hipmama42
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Medicaid pays for my meds right now. I have to reapply/re-qualify every three months, send in the paperwork to my caseworker and wait for verification in the mail. Every six months I have to have a face-to-face interview with my caseworker. My primary has to send my caseworker a document stating that I am unable to work, or else I would be forced to attend their job training/assistance programs in hopes of getting me off of medicaid. What, so I could get a minimum wage part-time job with no benefits? Makes no sense, but that is how the system works here in Ohio. And if my income is too great, like just barely over the federal poverty line, I will not qualify for my managed care Medicaid medical coverage. I would like to pick up a part time job and work maybe 15 hours or so a week, but I would make "too much" money and then would lose my medical insurance. My Rx drugs cost around $700 a month if I had to pay cash for them. The system makes it so that I have no incentive to work part time. Any small income I would get from that part-time job would be eaten up in medical bills and Rx. I had to get my last employer to pay me in cash and we called it "babysitting" money in case she was ever audited.

I didn't want to leave a paper trail in case my hours and income were checked out by Jobs and Family Services in which case I would lose my medical insurance for poor heads of families. They say you are allowed to work, but the amount you are allowed to earn and still keep the medical benefits is next to nothing. Soo....with my child support from the ex I could only work a few hours a week, like maybe 5 or 6? It was such a tricky numbers game and most of the time I was too sick and too much in a fog to deal with it. So now I am unemployed and having all of my meds and doctors paid for. It doesn't make sense, does it? The system is definitely broken. Oh, and my caseworker says that if I apply for disability, I will lose my medicaid from the moment my application is submitted.

I try not to think too far ahead and just take it six months at a time....and then worry about the next six months, and so on.

I guess a lot of you out there know what I am talking about.

You have to learn to work the system as best you can so you can survive and take care of your kids, and try not to stress too much because then you get sicker and sicker. I never would have believed that I would have become "used to" living like this. I was a professional with a good job and college degree, an IRA, great benefits, and all of that, but it is all long gone and in the past. Now, I am grateful for a pain-free day and feeling good enough to get out and enjoy the spring flowers.

When I didn't have medicaid or any medical ins. (I went for 5 years without any) I went without some of the meds,and I got samples from my doctors whenever possible. I wasn't ashamed of "begging" for these samples because I really needed them and would not have been able to afford them otherwise. Especially my expensive asthma inhalers!

My attitude is, "you don't ask,you don't get." The worst the doctor's office can do is say no, we don't have any samples of this drug. But sometimes, they had samples of something similar and would switch the Rx to that one (like with my asthma inhalers, there are so many didfferent brands!) so it doesn't hurt to be persistent. I would always ask for the cheapest effective antibiotic when I had a sinus infection, for instance. It worked just as well or better than the $100 dollar new ones.

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