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 » why no supplements??

 - UBBFriend: Email this page to someone!    
Author Topic: why no supplements??
VLSer
Member
Member # 8189

Icon 1 posted      Profile for VLSer     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know there are several LLMDs who do not want patients on any vitamins/supplements- but Why? Where is the research to support this?

I am taking the following:
-1 multi-vitamin
-2 100mg. CoQ10
-1 500mg. Vitamin C
-1 Mg-Tab (the kind Dr. B of ILADS reccomends)

that's it- it seems harmless enough.

I go to see my new Dr. on Fri. and I know that he is going to want me off these, but why?

If you have any mainstream, prestigious literature on the benefits of any of these, I would love the sites.

thanks!
VLSer

Posts: 48 | From Vermont | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
AliG
Frequent Contributor (1K+ posts)
Member # 9734

Icon 1 posted      Profile for AliG     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi!

Certain vitamins/supplements can react with or interfere with the medications Rxd others can evoke a stronger Herx.

Mine doesn't want me taking anything unless he has specifically told me to do so. I know he has another patient using supplements, so I'm trusting that decisions for me are based on my specific state of unwellness.

I go back on 10/6 after having completed a course for Babs. I'll get to ask him the reason then.

Hopefully others might have a better explanation.

Good Luck with your LLMD!

[Smile]
Ali

I'm also curious as to how you know he'll want you off them?

--------------------
Note: I'm NOT a medical professional. The information I share is from my own personal research and experience. Please do not construe anything I share as medical advice, which should only be obtained from a licensed medical practitioner.

Posts: 4881 | From Middlesex County, NJ | Registered: Jul 2006  |  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 
If you follow Dr B's guidelines on this, you'll be fine. I don't see the logic in not taking supplements. Just my opinion.

This has been argued many times, so if you'd like to see those discussions, do a search here. Just type in "supplements."

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
lymie tony z
Frequent Contributor (1K+ posts)
Member # 5130

Icon 1 posted      Profile for lymie tony z     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't believe anyone has said supplements are not to be used in conjunction with abx therapies.

Some of my llmds have actually approved of supplementation.

Dr B guidlines are specific and I have used them in the past. With added benefits.

Calcium and vitC can interfere with some medications so ill advised to use.

Then again you don't have to talk it over with your doctor...just do them on your own...as long as you get an ok thru your pharmacist.

Ya gotta play some silly games with this disease.

zman

The 100 of vit C you're taking should actually be B50complex...as I recall from his guidelines.

--------------------
I am not a doctor...opinions expressed are from personal experiences only and should never be viewed as coming from a healthcare provider. zman

Posts: 2527 | From safety harbor florida(origin Cleve., Ohio | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
VLSer
Member
Member # 8189

Icon 1 posted      Profile for VLSer     Send New Private Message       Edit/Delete Post   Reply With Quote 
Oh, I am also taking a calcium supplement, acidophilus, and a weekly vitamin B shot.

My old llmd loved supplements but he is very far away. This new one follows Dr. D's (Boston llmd) protocol.

I am really tired of researching lyme. If I'm going to insist on any supplements, what should they be?

He would never agree to Dr. B's guidelines. And I have agreed to work with him by disclosing everything. I've tried being my own doctor and it isn't working.

But I am good at arguing...

Posts: 48 | From Vermont | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
lymie tony z
Frequent Contributor (1K+ posts)
Member # 5130

Icon 1 posted      Profile for lymie tony z     Send New Private Message       Edit/Delete Post   Reply With Quote 
Vermont lyme sufferer,

No one here can or should tell you what to do specifically.

We're not qualified to prescribe anything...

What we try to do here is relate what worked or did'nt work for ourselves or what we have heard about or read about.

If you're gonna be totally honest with Dr D...then you've made your decision...

I only told you what worked well for me....
We are all similar...but in some ways different...

so we have to hunt and hunt for what works with our strain of disease and our biological and psychological makeups.

Good luck............zman [Smile]

--------------------
I am not a doctor...opinions expressed are from personal experiences only and should never be viewed as coming from a healthcare provider. zman

Posts: 2527 | From safety harbor florida(origin Cleve., Ohio | Registered: Jan 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.