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 » Mino vs Doxy for neuro lyme

 - UBBFriend: Email this page to someone!    
Author Topic: Mino vs Doxy for neuro lyme
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
I cannot take minocycline. As much as my doctor wants me to, I just can't. The migraines were torture.

So, I was wondering if doxycycline is easier to take (I know everyone is different), and if it could also help with the severe brain fog that is my worst symptom.

Thanks so much,

brooke

Posts: 117 | From PA | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
seekhelp
Frequent Contributor (5K+ posts)
Member # 15067

Icon 1 posted      Profile for seekhelp     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD told me last week Mino is so much easier to tolerate than Doxy. He's treated thousands of patients.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well it's very difficult for me so maybe I'm in the minority? It hits me like a ton of bricks, even 25 mgs.
Posts: 117 | From PA | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
HaplyCarlessdave
Frequent Contributor (1K+ posts)
Member # 413

Icon 1 posted      Profile for HaplyCarlessdave   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Brooke, you are probably having the "Herxheimer reaction" This is fairly common, and could well indicate that the Minocycline is decimating the Lyme. But there are many factors. You may also have one or more "coinfections"- additional infections that the ticks were carrying.-- these can make a huge difference in how you respond to a treatment too. Doxy, and probably mino, too, are effective against the common (in some parts of the country, including coastal New Jersey, where I was bit..) coinfection, ehrlichiosis.
Doxy is kind of hard on the gut. For me, Yarrow and psyllium seed were helpful; I occasionally took some of both of these several times when I was having G.I. trouble, from doxy (and cefuroxime axefil, an ora cephalosporin).
DaveS

Posts: 4567 | From ithaca, NY, usa | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for your reply. I would rather have stomach problems than head problems. It makes me so out of it and I'm already out of it, if you know what I mean.

Also, is sun sensitivity really as bad as people say it is? Maybe that's what she's worried about.

brooke

Posts: 117 | From PA | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
The sun sensitivity is horrible. I got sun poisoning through the car window with sunscreen on ... I had to wear gloves to drive .... and it wasn't even summertime.

Sounds like you are having a cognitive herx with the mino ... the mino is known for helping with cognitive problems.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Brooke. My daughter had to start at 50mg of mino once a week and sloooooowwly work up to 200mg/daily.

But, I can tell you, that once it took hold, it worked the best for her neurolyme. She is taking college classes now.

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
The sun sensitivity does kind of scare me. Is it a common side effect or does it just affect some people?

kelmo, I might have to do the 25 mgs once a week too, if my doctor keeps insisting. It's just so hard to feel worse when you already feel horrible.

Thanks for the replies.

Posts: 117 | From PA | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
kreynolds
Frequent Contributor (1K+ posts)
Member # 15117

Icon 1 posted      Profile for kreynolds     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have taken IV Doxy and oral Doxy and am now on oral Mino.

I find that the Mino is hitting everything harder than the Doxy was.

It also breaks the BB barrier better than Doxy.

I know it stinks to feel so bad, but maybe like mentioned above, it's a Herx. Thats a good thing.

I am currently at 200mg a day and will be moving to 400mg a day next week.

Best Wishes!

--------------------
Diagnosed CDC + 6/2007

Quest: + IGG Bands 18,23,39,41,58,66 and 93.

Quest: + IGM Bands
23,39

Quest: + Bartonella (B.Henselea & B. Quintana),+ Babesia, and + Mycoplasma and Lyme-Induced Addisons Disease

+ Biofilm blood test 12/2010

Posts: 1185 | From New York | Registered: Apr 2008  |  IP: Logged | Report this post to a Moderator
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does doxy cause migraines like mino? That's another reason I'm worried. I had so many migraines the last time I took it. I think I spent more time in bed than anywhere else.

brooke

Posts: 117 | From PA | Registered: Aug 2008  |  IP: Logged | Report this post to a Moderator
btmb03
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Hi brooke, I had a ton of gut issues with doxy but no increase in headaches/migraines...was also on mino for an unrelated reason years ago and didn't notice any difference either.

Macrolides have been worse for me re: migraines/headaches and sometimes I can't distinguish that from a sinus HA either. Weird.

Good luck!

IP: Logged | Report this post to a Moderator
hope4sofia
LymeNet Contributor
Member # 20577

Icon 1 posted      Profile for hope4sofia     Send New Private Message       Edit/Delete Post   Reply With Quote 
I haven't taken mino but I can verify the sun sensitivity with doxy. I have chronically burned arms and nose regardless of wearing 85 sun screen, hats, and sleeves most of the time.

Other than that. I had headaches at first but, once I got through those, the side effects haven't been bad.

--------------------
Sofi

Posts: 150 | From Northern California | Registered: Jun 2009  |  IP: Logged | Report this post to a Moderator
brooke
LymeNet Contributor
Member # 16606

Icon 1 posted      Profile for brooke     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks to everyone who replied. I'm not sure what I'm going to do yet.

brooke

Posts: 117 | From PA | Registered: Aug 2008  |  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.