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 » When or If to try new LLMD

 - UBBFriend: Email this page to someone!    
Author Topic: When or If to try new LLMD
tmmort
Member
Member # 14013

Icon 1 posted      Profile for tmmort     Send New Private Message       Edit/Delete Post   Reply With Quote 
How many Lymies quit their LLMD for a different LLMD and gotten better?

My story is so long and confusing that I cannot even recap it......in a nut shell, I had been treating Lyme/Babs for about three years on orals only. Started to notice improvement at this point.

We moved out of state and I started to see the only Lyme knowledgable Dr. in new state who switched everything up on me, dropped some vital meds and added a cpn diagnosis. Said I couldn't possibly still have babesia with all the malarone I had taken. I do not believe this.....

Ended up almost not being able to walk and having the most intense pain I had experienced ever.......have started traveling back to 1st LLMD and am catching a vibe that this Dr. has taken me as far as possible...

I don't know if the vibe is accurate, however, I have been backsliding physically/neurologically ever since our move. I feel as bad as I ever did.

Since I now live in CO, I can go east or west for treatment and I am thinking about the Lyme Dr. in MO.

I'm also wondering why my first LLMD had me on orals for over three years, not I.V. I brought it up at our last visit and now says since I'm out of state, can't do I.V.

Can anyone give me some advice here on switching LLMD's? Has anyone had IV treatment ordering from a Dr. out of state?

Can I talk to or email with any patience of Dr. ? in MO?

I've been fighting this over 4 years now and I'm not quitting in my current state.

Any advise is greatly appreciated. I hope this makes sence..... [bonk]

Posts: 69 | From fort collins, co | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
viva
LymeNet Contributor
Member # 8183

Icon 1 posted      Profile for viva     Send New Private Message       Edit/Delete Post   Reply With Quote 
I sent you a PM.

Viva

Posts: 532 | From southeast US | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628

Icon 1 posted      Profile for METALLlC BLUE     Send New Private Message       Edit/Delete Post   Reply With Quote 
You're welcome to e-mail me about your experiences with the other LLMD's. I could use reports on what you experienced -- good or bad points, and I'll also give you information on specialists, including the doctor you're considering. I have a lot of recorded reports on him.

E-mail me: [email protected]

--------------------
I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.

E-mail: [email protected]

Posts: 4157 | From Western Massachusetts | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think that doctor switching is probably fairly common. Sometimes it takes a while to find someone who thinks in a similar way and who is open-minded when it comes to treatment options--hard vs. soft....

I started off with a couple of lightweight MDs because they were close to me and it was convenient but after a year of inadequate progress I'm LLMD shopping again...and I have a couple of the more noted docs lined up...

Hang in there...

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

Icon 1 posted      Profile for lpkayak     Send New Private Message       Edit/Delete Post   Reply With Quote 
i think you need to give them 2-3 yrs...as long as you know they are ilads and know what they are doing

often they will say i can't help any more but if you go to another they want to try different stuff

i know someone who stayed with one for 7 yrs and then went to a new one and got better fast

i still say get to the best early...

the research does not show that IV is any better than orals...and it is more dangerous

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
tmmort
Member
Member # 14013

Icon 1 posted      Profile for tmmort     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you for your replies.

Just gonna put this question out there, cuz it's on the tip top of my bean.

Is there such a thing as the most successfull LLMD with the long-time sickies? One's that have success where other LLMD's didn't?

I sure would like to hear about it if you have knowledge or experience with this.

Posts: 69 | From fort collins, co | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
quote:
Originally posted by tmmort:

Is there such a thing as the most successfull LLMD with the long-time sickies? One's that have success where other LLMD's didn't?

NOT to my knowledge, and i've been giving out names going on 3 years. we're each unique ... no 2 alike due to lyme and/or co-infections.

were we dx promptly?
dx late in life like me; 34.5 yrs. late or tutu's 40+ years, etc.

just my opinion from doing what i do on this board....

IP: Logged | Report this post to a Moderator
unsure445
LymeNet Contributor
Member # 15962

Icon 1 posted      Profile for unsure445     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maybe take some time off from meds and then re-test for everything.

I think you have to trust your doctor. On the other hand if you have reached a plateau you need to step treatment up to injections or an IV.

I know if I don't hear what I want to hear my instinct is to run.

Bottom line is that LLMD's that have been practicing a while have much more concrete information than anything you are going to read on-line or in a book.

Best of luck and I hope you get back on track. Onward and upward all the way!!!

--------------------
unsure445

Posts: 824 | From northeast | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

Icon 1 posted      Profile for lpkayak     Send New Private Message       Edit/Delete Post   Reply With Quote 
yes-i know 2...but i would have to talk to you more to give out names

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  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.