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 » Medical Questions » other med to replace Malaron?

 - UBBFriend: Email this page to someone!    
Author Topic: other med to replace Malaron?
got1bite
Junior Member
Member # 11955

Icon 1 posted      Profile for got1bite     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does anyone know of a medicen to treat co-infections, [confused] besides the expensive malaron and mepron? Malarone works for me, i'v been on it for two months with good results for the first time in a year and a half of treatment. We are now tapped out and can't afford either med. Any idea would be a great help. Thanks, Shonna.
Posts: 8 | From butte valley ca | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
trueblue
Frequent Contributor (1K+ posts)
Member # 7348

Icon 1 posted      Profile for trueblue     Send New Private Message       Edit/Delete Post   Reply With Quote 
Shonna,
If you have no insurance and/or meet the income requirements, etc.. You might be able to get Mepron from Bridges to Access. It's worth giving a call to see if it's a possibility.

http://www.bridgestoaccess.com/enrollment/eligibility_criteria.html

contact info: http://www.bridgestoaccess.com/contact/contact.html


If you could qualify I believe Mepron is umlimited. I think they charge $10 per refill. Malarone they only allow, once a year, 16-30 tablets. It saved me some but not lots.


I hope it helps.

--------------------
more light, more love
more truth and more innovation

Posts: 3783 | From somewhere other than here | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Have you tried larium?

Also ask about free and needy meds programs for Mepron and malarone.

IP: Logged | Report this post to a Moderator
AmyJ
Member
Member # 6192

Icon 1 posted      Profile for AmyJ     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can you share how much malarone you were on.... I was taking 100mg a day (not for my lyme)... but man I felt good while on it... trying to decide if that was the reason, and if so... if I should try to find a supply. [Smile]
Posts: 22 | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
got1bite
Junior Member
Member # 11955

Icon 1 posted      Profile for got1bite     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the help. Yes i do have b/s HMO. Insurance won't cover Mepron or Malarone due to a negative lab test. I have one of the two dozen pick any one.... My LLD said i definnatley have a Babesia infection. I did receive several benefits from the malaron. The first month i took one pill a day...no changes but mild herxing. The second month i was taking three a day. Thats when night sweats and other side effects got better or even dissapeered. None of my other orals, rocefin and mepron did anything but made me herx/hurt more. I would choose to continue the malarone, but $ is the downfal, or lack of. Thanks for the info, anyother ideas? Shonna.
Posts: 8 | From butte valley ca | Registered: May 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 
Artemisinin.... www.organic-pharmacy.com I took it with zithromax.

I took clindamycin/quinine for the babs as well.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  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.