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 » Am I doing the right thing?

 - UBBFriend: Email this page to someone!    
Author Topic: Am I doing the right thing?
ladycakes
LymeNet Contributor
Member # 12619

Icon 1 posted      Profile for ladycakes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I seem to frequently go back and forth over whether I'm making the right decisions about my healthcare.

I got sick in 1999, got diagnosed and started treating from 2006 to 2009. I was in remission for all of 2009, thanks to a combo of oral and IV meds, and a new doctor.

I relapsed, or got reinfected, or whatever causes people to get sick again in 2010. And it feels harder, this time.

I've done oral antibiotics, and I've done IV. Thanks to some allergies, we've exhausted my options on the IV, and I'm getting my line pulled today. This is my... 5th or 6th round of IV meds, I've lost count.

I feel like I make some progress, and then plateau, and then backslide. Rinse and repeat. I tried going off of antibiotics back in October, and while my fatigue and some other general symptoms actually improved, my pain got worse. So back on the antibiotics I went, and it's been up and down, but overall I'm improving.

So sometimes I think if I'm making progress, even if it's small, I should stick it out. Keep doing what we're doing, stay with this doctor. Sometimes I think after four years of treating, I should feel better than this.

I don't know, maybe it's just a need to vent. The first round of IV I did, I felt so dramatically better, but it seems like every round after that helps a little less. So I'm sad, and trying to not feel defeated about it.

I don't know what I'm doing.

Posts: 306 | From Brownsville, PA | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ladycakes, this illness is so tough. You're not alone.

"I don't know what I'm doing."

It sounds like you're doing the best you can. It's so anger inducing when you try to do the right thing and it just doesn't work.

I understand it's so frustrating when what worked the first time doesn't work the second time.

We're all survivors and I'm sorry the battle with the IV was lost, but you haven't lost the war! You're still here and your strength to deal with the next healing challenge will come back.

It's okay to feel defeated. Let yourself grieve, then pick yourself up again.

I'm not going to type my whole story, but just how my doc changed gears the last time I went. I hope it will be helpful/hopeful that not all options are exhausted.

I got my Lyme into remission the first time around with oral antibiotics.

I got reinfected last year and the orals have done very little this time around and I'm horribly allergic to many. (which is frustrating to both me and the docs). I can't do common combos.

I got the "you're a difficult patient" speech my last appointment.

I'm allergic to amoxicillin (full blown rash and neck swelling), but my doc just started me on bicillin LA shots, along with ketotifen to help with drug allergies.

So far (knock on wood) I'm tolerating it.

[ 02-06-2014, 06:47 PM: Message edited by: Judie ]

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ask around (here or anywhere) to make sure you are with one of the best LLMD's. If you are being treated in PA, there is huge discrepancy between the abilities of the LLMD's there.

Hoping and praying you get the help you need.

Have you been treated for all coinfections?

Moving this to Medical Questions for more help.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
ladycakes
LymeNet Contributor
Member # 12619

Icon 1 posted      Profile for ladycakes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
The guy I'm seeing now was recommended to me by this group, so I think he's good? I've never heard him say any of the duck code words that send folks running for the hills, at least.

I was terrified to go off of the IV so soon, but I'm actually doing well so far. He added another oral, since he's always had me on at least two meds at a time.

My bloodwork for coinfections came up with nothing, even though my lyme bloodwork came up very much positive. So he's treated those based on symptoms. As far as I know, he's specifically treated for bartonella, although some of the medicine combinations I've been on would have hit others.

I'm creeping up on about 90% functioning now, which is amazing. I feel like most of what I call my 'satellite' symptoms have either improved drastically or disappeared altogether. What I'm left with is some fatigue (always the hardest thing to kick), and pain.

I just can't seem to get that last little bit gone. And honestly, if my health would just hold steady here off of my antibiotics, I'd be fine with that. But once I go off of them, the pain increases and the other symptoms come back. I'm JUST sick enough that I have to keep taking all these pills.

Posts: 306 | From Brownsville, PA | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have you tried addressing candida/yeast in a big way? Nearly everyone is left with that after months or years of abx.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Tbrown2
LymeNet Contributor
Member # 42446

Icon 1 posted      Profile for Tbrown2   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lymetoo whats a non prescription way to treat yeast that wont interfere with abx besides diet. My LLMD doesnt think I have a yeast issues as Ive been examined and have no obvious symptom but I have always wanted to treat it because it cant hurt right?

--------------------
T. Brown

CDC Lyme Positive
Co infections? Who knows...
Bands 18+ 30+39+41+45+58+66+ IGG
23+39+41+IGM

Posts: 351 | From Boston MA | Registered: Oct 2013  |  IP: Logged | Report this post to a Moderator
desertwind
Frequent Contributor (1K+ posts)
Member # 25256

Icon 1 posted      Profile for desertwind     Send New Private Message       Edit/Delete Post   Reply With Quote 
I can throw some suggestions out to you till lymetoo chimes in.

For Candidas/Yeast natural route I like;
Byron White A-FNG
Oil of Oregano
Olive Leaf Extract
Pau D Arco
Carprylic Acid
CandiGone (has a nice combo)
ART
Black Walnut
Garlic

A lot of these hits parasites as well.

Posts: 1671 | From Tick Infested New Jersey | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
phyl6648
Frequent Contributor (1K+ posts)
Member # 28522

Icon 1 posted      Profile for phyl6648     Send New Private Message       Edit/Delete Post   Reply With Quote 
I feel the same way. I haven't had the treatment you have and have fallen short due to cost and not sure what to do. I just don't understand all this and feel so defeated.

No answers but sure can relate.

Posts: 1058 | From VA | Registered: Oct 2010  |  IP: Logged | Report this post to a Moderator
CherylSue
Frequent Contributor (1K+ posts)
Member # 13077

Icon 1 posted      Profile for CherylSue     Send New Private Message       Edit/Delete Post   Reply With Quote 
Keep treating, and do not give up. You may have to be on abx for sometime. A good llmd will now what abx to give when for
your case. One protocol does not fit all.

Posts: 1954 | From Illinois | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Re candida, do you crave sweets and bread? That's a pretty good sign that you have it.

If so, it's a good idea to go on a noncandida diet - ie, one that doesn't feed the yeast. I did a step-down diet - no sugar, but ate sweet fruit. After I got over the sugar craving, - took about 10 days or so, then I gave up the sweet fruit. The diet is mostly vegetables and lean meat, if you eat meat. You can google the diet.

Posts: 13116 | From San Francisco | Registered: May 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.