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 » Anatomy of a recovery

 - UBBFriend: Email this page to someone!    
Author Topic: Anatomy of a recovery
blossom
Member
Member # 13260

Icon 1 posted      Profile for blossom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was wondering what people go through as they are about to recover - I'm not there yet but just curious.

Do most people feel 100% healthy at termination of abx treatment?

Do some feel some lingering symptoms, and then it tapers off after discontinuing abx?

Personally, if I begin approaching 8 or 9 months on abx with still a few residual symptoms, I will probably end abx and ramp up herbals (already doing some herbals now, 3 mo into abx treatment). I really don't want to be taking abx forever.

Any recovery experiences would be appreciated.

Posts: 29 | From NY | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
Geneal
Frequent Contributor (5K+ posts)
Member # 10375

Icon 1 posted      Profile for Geneal     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dear Blossom,

I am not there yet, but still heading towards remission.

I have been on antibiotics for over one year now.

I have addressed Lyme, Babesia (twice), bartonella and now CMV, EBV, etc.

It never fails to amaze me how well I can feel on some days and still how unwell on others.

I am going to keep going until I am symptom free for two to three months and

Then go on my LLMD's Remission Challenge of antibiotics for 2 whole months.

If I can go these last 3-4 months symptom free, then bye-bye antibiotics.

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
1981Z28
LymeNet Contributor
Member # 3484

Icon 1 posted      Profile for 1981Z28     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Blossom,

Been a while since I've visited this forum as I've been well now for approximately 4 years since my abx treatment of two years ended. Thought I'd pop in and see how others were doing and I ran into your post and felt compelled to answer as best I could, knowing that I might very well be corrected by others so the bottom line here is that I'm sharing my own experience here, others will be different.

As I recall, the longer one has been sick with Lyme, the longer it takes to recover but I think there is more to it than that such as what your health condition in general is, how much damage has been done, how much of that is irreversible, what strain of Lyme you have as well as the co-infections. How's your liver prior to treatment? Any candida issues? The list goes on and deeper from here but for the sake of argument, let's leave it at that.

The general rule of thumb is that treatment should continue until the patient gets at least two months back to back symptom free. I went longer for what I felt was my own extra insurance because I never want to go back to the days of wishing I was dead instead.

Ok, to answer your questions from my experience....roughly every six months I peeked out on the abx I was on and would have to swap it out while keeping the Tinidazole (1,000mg twice a day) going for the full two years. When I switched the Biaxin, Ceftin, Biaxin XL and then finally the Ketek, all 500 mg twice a day, I would go through a whole new herx session and each herx was always a little bit different but the deep aching always remained. Sometimes I'd have serious heart palpitations, sometimes I'd go downright stupid, who knew what would happen next but I'd just roll with the punches because everything I researched said this was a normal process. Every herx got easier and easier but for me other than the first few months of non-stop herxing when we added the Tinidazole where my brain was trying to leave my skull without coming through the ears or any other available orifice in my head, the only other really tough time was the Lyme rage. During that time I wanted to seriously mutilate my husband for turning the pages of his newspaper way too loudly....the nerve of him! He's lucky he's still alive, believe me!

Questions 2 - I felt about 95% fully recovered at the end of my abx therapy treatment. I still suffer minor nerve damage but in general I'm fully functional (except for being a blonde mentalpause victim).

Question 3 - The lingering symptoms after treatment can be hormonal related,candida, toxin related or possibly something completely different. Stay with the low carb diet, do what you can to detoxify yourself, exercise if you can, do all you reasonably can to boost your immunity system, sleep well and put yourself as #1....relax. Monitor your symptoms. Yes, it could be residual from Lyme but only time and your body will tell you if you listen.

I'm hoping my experience answers your questions somewhat and hope that others pitch in here as well.

Posts: 302 | From Kamloops, B.C., Canada | Registered: Dec 2002  |  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.