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 » Eye and brain pressure.

 - UBBFriend: Email this page to someone!    
Author Topic: Eye and brain pressure.
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bad head day with head/eye pressure sensations.
Back of eyes hurts.
Is this a common herx with minocycline?

I went back to full dose for a few days but today is approaching unbearable.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
minimonkey
LymeNet Contributor
Member # 8693

Icon 1 posted      Profile for minimonkey     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, that was my most severe doxy/mino herx symptom, and I gather that's pretty common. Generally mino is a little less brutal than doxy, but both cross the blood brain barrier.

My docs have both recommended pulsing off the drug when it starts approaching unbearable, because that kind of encephalitis can be pretty dangerous.

--------------------
"Looks like freedom but it feels like death..
It's something in between, I guess"

Leonard Cohen, from the song "Closing Time"

Posts: 822 | From California | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yeah, pulse off today.

Yesterday felt like I was hit in the head with a 2x4.


I hope this means the mino is killing those little *******s though.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just thinking out loud:

Wondering if I need pulse high doses of mino instead of doing constant low dose.

Maybe low dose doesn't penetrate the CNS as well?

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
On my second pulse at full dose, but have yet to experience the same head symptoms.
Maybe in a day or two it will hit.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, it sounds like a herx.

VV, do you have the Parkinson head-bob/twitching?

This increased in me with increased brain pressure while taking mino.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:

VV, do you have the Parkinson head-bob/twitching?
[/QB]

No, I don't. My twitching in order of frequency:
toes (mostly right side)
thigh/buttocks (mostly right side)
fingers (only lasts for 20 seconds at a time)

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Twitching usually gets worse with other symptoms (often cognitive + weakness).
Posts: 922 | From Philadelphia | Registered: Sep 2012  |  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.