LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » General Support » may i ask what your copay is??

 - UBBFriend: Email this page to someone!    
Author Topic: may i ask what your copay is??
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have three new prescriptions. The pharmacy just called and said my copy is 104. Holy crap....

Cholestyramin
Zoloft
And Levine

Whoa...didn't think they would be that expensive...

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maybe you can get them filled at Wal Mart??

Mine is cheaper than I'd like to announce here!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
That is Wal-Mart hon....and I have bc/b.s. and military....

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Grrrr, my insurance has changed the pharmacy benefit managing company, and my co-pays have more than doubled in some, to $75 per month per med---after they go through extensive

Preauthorization with the doctor and insurance to allow me to get it, and after the insurance company drags their feet so long on authorizing it that I had to complain to my state AG's office !!!

I hate this stuff!

Posts: 3792 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
surprise
Frequent Contributor (1K+ posts)
Member # 34987

Icon 1 posted      Profile for surprise     Send New Private Message       Edit/Delete Post   Reply With Quote 
It depends on the medication.
We have a $2,500 deductible to pay out the gate every year-

first 2 years daughter and I were in Lyme treatment, we would have that paid by February. No kidding.

And before that, we had Kaiser, and I paid tend of thousands of dollars for PANS treatments that Kaiser refused to acknowledge.

Not to mention what is deducted from my H's paycheck every 2 weeks.

This is top insurance from one of the largest American corporations.

Broken. System.
My personal retirement account from decades of full time work is gone.

Let's talk about grocery bills for decent healthy food next and really get ourselves good and depressed :-/

--------------------
Lyme positive PCR blood, and
positive Bartonella henselae Igenex, 2011.
low positive Fry biofilm test, 2012.
Update 7/16- After extensive treatments,
doing okay!

Posts: 2518 | From USA | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
stillsearching
Junior Member
Member # 42697

Icon 1 posted      Profile for stillsearching     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know from experience that the Cholestyamine is very expensive...I had to go from taking it 4 times a day to once to save some $$
Posts: 4 | From New England | Registered: Nov 2013  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.