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 » Malarone and dry eye

 - UBBFriend: Email this page to someone!    
Author Topic: Malarone and dry eye
Katcon
LymeNet Contributor
Member # 9812

Icon 1 posted      Profile for Katcon     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been on Malarone for a month now.

After the first 3 days had a horrible herx, and then got so much better.

Some things that have happen since Malarone are hair loss, dry eyes, and I have a rash near my left eye. Every time I take the Malarone within 15minutes the rash gets dry and sore.

On my third week of Malarone I experienced fatigue, and weak eyelids.

After my first herx, I did have 7 glorious days of high energy, and now it's all gone.

Katcon

Posts: 175 | From Pa | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
Vermont_Lymie
Frequent Contributor (1K+ posts)
Member # 9780

Icon 1 posted      Profile for Vermont_Lymie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Kat,

Everyone seems to have a different reaction -- it is truly variable.

Truth is, my eyes did not bother me until today. So I do not think it is the malarone. And no hair loss. Did you speak to your doctor about it?

Posts: 2557 | From home | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804

Icon 1 posted      Profile for AZURE WISH     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is malarone the only med you are on? I would call the pharmacist just to see what the side effects are of the meds u are on.

[ 28. April 2007, 10:53 PM: Message edited by: AZURE WISH ]

--------------------
multiple chemical sensitvity group:
http://www.lymefriends.com/group/multiplechemicalsensitivities

Group for artists. All media welcome:
http://www.lymefriends.com/group/creativecorner


http://groups.yahoo.com/group/Lyme_Artist

Posts: 3860 | From nj,usa | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
Geneal
Frequent Contributor (5K+ posts)
Member # 10375

Icon 1 posted      Profile for Geneal     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dear Katcon,

I had to drink lots of water while on malarone...

I often had to wet my contacts at the end of the day so I could get them off of my eyes.

I have had a couple of contacts tear and it took me a couple of hours to "fish" those torn

Pieces out of my eye!

I finished malarone about 3 weeks ago, but continue with dry eyes.

My hair is also starting to fall out....by the handfulls.

I think this may be more related to thyroid issues than meds

As I haven't seen this as a side effect to any meds I am on.

I would call my LLMD about the rash....

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Katcon
LymeNet Contributor
Member # 9812

Icon 1 posted      Profile for Katcon     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for you replys. I see my llmd this Monday.

I also take Cedax.

Kathy

Posts: 175 | From Pa | Registered: Aug 2006  |  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.