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 » Huge Back Slide - Chronic Lymie

 - UBBFriend: Email this page to someone!    
Author Topic: Huge Back Slide - Chronic Lymie
Visual Afterimage Man
LymeNet Contributor
Member # 10435

Icon 1 posted      Profile for Visual Afterimage Man     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hey guys....

I got some dissapointing news the other day. I have been feeling pretty poor lately. Almost as if I hadn't done any treatment at all.

Doc called and said that my CD57 is now a 44. Last October it was at 155. He doesn't know why the big back slide.

Also, I am vitimin D deficient. He started me on Vitimin D, (5,000 IU per day) and said to get back on Flagyl.

I was making pretty good progress as I tailed off Flagyl back in November and moved to a 30 day run of Levoquin to address any bart issues I am having.

Since I complain of major vision issues, he suspected Bart could be whats keeping me from moving over the hump and on to healthy freedom.

I'm wondering if the month and a half of time I took off of Lyme meds caused me to have a big backslide. My understanding is that Levoquin isn't very effective for Lyme.

So now I'm ramping back up to 1,500 mg of Flagyl per day. [Frown]

I'm also on 5000 IU of vitamin D.

I feel sooooo poorly. I'm actually not feeling any worse on the flagyl than before I started the flagyl. Maybe thats soon to come? I'm only on day 4 since restarting flagyl.

Any advice?

I'm really considering going to see a psych. I'm so discouraged and fatigued. I'm having one of those moments of (am I going to live the rest of my life feeling like this).

When should one start yelling for IV abx? I've been on orals since Nov 2006.

Thanks for any replies.

--------------------
26 months of treatment. And counting.......

Posts: 298 | From Northeast Kansas | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
sfcharm
LymeNet Contributor
Member # 9392

Icon 1 posted      Profile for sfcharm   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sorry to hear you're doing so poorly. It's the nature of this disease. I thought I'd share with you about my IV Rocephin experience.

I'm 19 months treating lyme and just finished six full months on Rocephin. I'm hoping to go one year on IV Rocephin. I did a year of orals and would say I got back to 70% of where I was prelyme.

I was told up front that I'd never be cured but that we were working towards managing the lyme. Do you do any excercise? I honestly feel that besides the antibiotics it's the next necessary part of getting well. It usually is an indicator to me how my day will go.

You should probably have a discussion with your Dr. about going the IV route. I don't regret it and everyday I"m on it I'm feeling better.

Barb

Posts: 281 | From san francisco | Registered: Jun 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.