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 » scared on factive

 - UBBFriend: Email this page to someone!    
Author Topic: scared on factive
laura_from_nh
Member
Member # 18885

Icon 1 posted      Profile for laura_from_nh     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just started on factive. i took my first pill 24 hours ago. Around three hours ago i started to feel really dizzy.

i am assuming this if from the factive as it's the only new thing i am taking. i feel pretty spacey, an even worse disconnection with myself, and like i'm being pulled to the left (for lack of a better description).

I'm on this for bartonella. i was on rifampin last month and didn't have any weird feelings like this. I have also taken rifampin in the past and felt no improvements on it.

could this be a good sign (wishful thinking) that the bartonella is being targeted. this feeling is very scary and i am working very hard not to let it turn into an anxiety attack.

thanks!

--------------------
Misdiagnosed and untreated from 1993-2008.
- iGenex positive western blot for LD: 9/08
- Clinical diagnosis for Babesia: 2/09
- Positive blood smear for Bartonella: 3/09

Started treatment: 1/09

Posts: 91 | From New Hampshire | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
feelfit
Frequent Contributor (1K+ posts)
Member # 12770

Icon 1 posted      Profile for feelfit     Send New Private Message       Edit/Delete Post   Reply With Quote 
hmmm, don't know. But I will say those of us with Bart are reporting feeling 'spacy' on the 'quin' drugs, which i believe that Factive is as well?

All of us but Hoosiers who have started this class of drug recently has had the same reaction...

to me that says 'yes we are on target'. If you can ride it through, the 'spaciness', it does get better as the days go on. Might also try dosing down for a few days until you adjust to the med.

Oh yes, forgot to mention, I also have a feeling of incoordination, or as you have described 'pulling to the left'....don't know if that is good or bad.

My doctor has told me to try and stick it out. If it becomes intolerable, STOP.

Just my experience. Tt your doctor if you are concerned....safe is always the best option.

Best,
feelfit

Posts: 3975 | From usa | Registered: Aug 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 
I did 2 5 day on and 5 day off pulses of Factive in November/December. I had BAD Bart herxes while on it: hyper, anxiety, very revved up, worse insomnia, etc. And, I got ligament problems in my thumbs (not good!) and double vision--freaked me out!!

BUT, many of my neuro sxs: horrible balance, feeling like I was on a boat all the time, bad brain fog totally vanished after the first day on it. And stayed that way!?! Unreal!

So, if you can hang in there, it may well be worth it. But, of course, check with your doctor. Everyone is different. It was like a miracle for me, except for the darned side-effects and herxes (herxes are time-limited, however).

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
laura_from_nh
Member
Member # 18885

Icon 1 posted      Profile for laura_from_nh     Send New Private Message       Edit/Delete Post   Reply With Quote 
thank you for the words of encouragement. this morning i'm feeling less freaked out. still have that "pulled to the left" feeling, but i can live with that if the end result is beating some of my most dreaded symptoms.

when you say brain fog, do you mean depersonalization? i know some people have different ideas of what brain fog is to them. i live with an incredible sense of depersonalization and would suffer any number of herxes/side effects if i knew in the end it would go away.

thanks for the responses!

p.s. i am on a five day pulse too. tonight will be my third night. i started at night because that is when i picked it up from the pharmacy. is that when you guys took it?

--------------------
Misdiagnosed and untreated from 1993-2008.
- iGenex positive western blot for LD: 9/08
- Clinical diagnosis for Babesia: 2/09
- Positive blood smear for Bartonella: 3/09

Started treatment: 1/09

Posts: 91 | From New Hampshire | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
sammy
Frequent Contributor (5K+ posts)
Member # 13952

Icon 1 posted      Profile for sammy     Send New Private Message       Edit/Delete Post   Reply With Quote 
I take Factive first thing in the morning. It has only made me feel better. No noticeable side effects.

Maybe it would be helpful to try taking it at another time with your next pulse? It's worth a try if you can feel better.

Posts: 5237 | From here | Registered: Nov 2007  |  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.