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 » I feel i have hit a plateau....need advice to talk to dr.

 - UBBFriend: Email this page to someone!    
Author Topic: I feel i have hit a plateau....need advice to talk to dr.
pippy
LymeNet Contributor
Member # 6005

Icon 5 posted      Profile for pippy     Send New Private Message       Edit/Delete Post   Reply With Quote 
bbbbbbbbbbbbbbbbbthe lyme at the same time...

[This message has been edited by pippy (edited 21 July 2005).]


Posts: 446 | From California | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
treepatrol
Honored Contributor (10K+ posts)
Member # 4117

Icon 1 posted      Profile for treepatrol     Send New Private Message       Edit/Delete Post   Reply With Quote 
Switch one of abx's out for another and in a month switch out the one thats left to a new one.
Try orals.

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
Jewlbug
Member
Member # 4554

Icon 1 posted      Profile for Jewlbug     Send New Private Message       Edit/Delete Post   Reply With Quote 
I agree with Tree on switching the ABX. I have hit setbacks after success as well. I've noticed that about every 2 months, a particular regimen stops working. When this happens, my LLMD switches one of the ABX.

Somtimes I will notice success with the new ABX, and sometimes I don't. If I switch and don't notice improvement, then we swap it out for another ABX. It takes a lot of patience, but I always have hope that the next ABX choice may be the key to my cure.

My best,
Jewl


Posts: 79 | From Chicago, IL | Registered: Sep 2003  |  IP: Logged | Report this post to a Moderator
Monica
Frequent Contributor (1K+ posts)
Member # 224

Icon 1 posted      Profile for Monica     Send New Private Message       Edit/Delete Post   Reply With Quote 
I went from doxy, to zith, to biaxin with suprax.

Now I'm on ketek with cedax.

Sometimes it is necessary to switch around, but unfortunately I don't know anything about mepron.


Posts: 1757 | From Somerset County, NJ | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi pippy!

I talked to you about my recent rough time, thought I would let you know what I ended up doing. I stopped taking the Mepron, as there was just absolutely no evidence of any improvement.

I have just started taking Tinidazole with the Zithromax. This keeps both me and the LLMD happy. This combo is supposed to treat babesia, according to Dr. S in SF, and it also treats Lyme, including the cystic form, which may be part of your trouble.

Now, this may or may not be your answer. Tinidazole, like Flagyl, can increase depression. However, for me it has been worth it, because it also gives me measureable improvements. I take it pulsed, giving myself time off when the side effects get to be too much.

It DOES cause herxing, headaches, heart stuff, depression, but in the inbetween times I feel SO MUCH BETTER. This may not be the combo to do that for you, but something will. I've been miserable for six months, and am finally getting some relief.

As the other folks suggest, there are other orals to try, as well as the possibility of the IM and IV. On warning on the IM. My son has found that IM Biccilin LA is back ordered right now, and he is having to use the CR.

BTW, I saw What the &*%**% Do We Know? the other day.While it has some very interesting points, how seriously can you take a movie whose main speaker is a 35,000 year old chanelled entity called Ramtha? Some interesting ideas here, but no secrets on how to heal Lyme disease.

------------------
Sonoma County Lyme Support
[email protected]


Posts: 2142 | From California | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
Lymester
LymeNet Contributor
Member # 5848

Icon 1 posted      Profile for Lymester     Send New Private Message       Edit/Delete Post   Reply With Quote 
Pippy... yes I am at that point also. Plateaud on amoxi in Dec. On doxy since Jan and going to the doc next week to discuss implementing a change and/or combo of abx.

I really use the information and questions provided here to have the ammunition/education to bring to the docs attention.

I still have the tingling thumbs, EVERY A.M. It's such a minor thing in the scope, but I'm waiting for it to disappear. I've actually felt more vertigo the past week and I havent felt that in about a year.

I think I forgot about the vertigo because I had so much back and body pain.

I will get back to you after my appt. Let me know what happens.

Yes, it is frustrating and when you feel you've got to do something NOW, make the appointment. It's what I did last fall and I'm certain that I would be hospitalized right now if I hadnt.


Posts: 519 | From CT | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
pippy
LymeNet Contributor
Member # 6005

Icon 14 posted      Profile for pippy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks so much everyone!
I talked to the office and the assistant to my llmd will call me tomorrow about switching abx and trying new combo.

It's good to hear other stories to know this is not unusual in Lyme treatment. I feel funny about bugging my doctor but I got the courage to say something because of the support here.

One of the worst sx for me right now is depression. I dont know if its because i have been going backward or if its a reaction to disappointment (having gotten my hopes up with how well i was doing) kind of reality setting in, or mostly the lyme. the doc thinks it is the babesia....but i just do not want to take any chances...

we'll see what he says...i'll let you know how it goes!
Thanks!

PS. Do other people find that the depression that comes with Lyme is not easily treated with meds? that is what i am finding....no antidepressant meds can break through it. that is by far the worst part of the disease for me.

Thanks everyone!


Posts: 446 | From California | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
pippy
LymeNet Contributor
Member # 6005

Icon 7 posted      Profile for pippy     Send New Private Message       Edit/Delete Post   Reply With Quote 
thanks everyone
cave,
are you called "cave" because that is what you feel like crawling into sometimes?

I feel like that a lot...especailly when i have to interact with family and people who are "on the other side" like i live in a whole other world....i just don't want to have to explain myself or bother with putting on a happy face and looking good so they think everything is fine when its not...my mom said that i looked so good and everyone was happy to see me smile and look good...uuuuggghhh i know she means well! that is the hardest part...family gets sick of it and you find yourself losing support. it goes on and on....they can't relate so they just get more distant. i know i would not know how to help someone with this problem...

That is the worst part of this for me....may be a vicious cycle with the depression too....my family does not know how to help me. i can't say that i blame them...i get sick of my tired complaining a** also! ;-)

Thanks for being here...this is a life saver having you guys to lean on when the family is running out of patience (i can't say i blame them) I dont tell freinds about it (except lyme friends here) because that would really be a great way to chase them off!

pip


Posts: 446 | From California | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 6 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
As for the anti-deps. I've never taken any SSRI's thank goodness. I've done well on trazodone. It works great for getting a good night's sleep too. Then there's Xango.

------------------
oops!
Lymetutu


Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
first free
Member
Member # 7140

Icon 1 posted      Profile for first free     Send New Private Message       Edit/Delete Post   Reply With Quote 
Pippy~ Iwas taking an antidepressant and sleep med. when I was still very healthy and active. They worked well. I'm seeing the same Psych. and we both feel like since the lyme my body has become resistant to practically everything. It's very frustrating~but we'll keep trying. ~jackie

Posts: 61 | From Missouri | Registered: Apr 2005  |  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.