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 » Vitamins and antibiotics

 - UBBFriend: Email this page to someone!    
Author Topic: Vitamins and antibiotics
jhspn00
Junior Member
Member # 19733

Icon 1 posted      Profile for jhspn00     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello,
I have been trying to find some information on which vitamins are essential. I have not actually had a diagnosis of Lyme, and can't afford to go to a LLMD. I have convinced my doctor that there is a very good possibility of it being Lyme.


Although they only thing he did is give me a 30 day supply of Doxycycline. He wanted to do lab test, but after I was already on antibiotics. I am not sure lab would show anything, since it isn't a specialized lab. I can't really afford lab work either. The only reason I can get the doctors appointment done is I have free office visits. Thanks to my sister working there.

I started about 3 weeks ago taking several vitamins-
Vision Formula --daily
Calcium, Magnesium, and Zinc-twice a day
Super B-complex daily
Fish, Flaxseed and Borage Oil-twice a day
Glucosamine, Chondroitin- twice a day
Cranberry- daily

I have been on the doxy for almost 3 weeks now. I am not feeling any better at all.

I have the neck crunching, severe headaches, muscle aches, joint pain, severe fatigue, brain fog (some days), quite a bit of back pain, lots of hair loss(over the years).

I am just not sure why I am not feeling any better. Actually, in some ways I feel worse since starting the antibiotics and vitamins. I am starting to have heartburn, stomach pain(ulcer pain), can't eat much or I get that bloated feeling, lots of gas on my stomach.

Starting to feel really depressed cause I can't do anything. I cleaned my carpets yesterday, and it drained me. I tried to take my kids to the park yesterday evening, we were only there for 10 minutes. I was getting really light headed, and so tired I couldn't keep up with my daughter.

I thought vitamin supplements would help me feel better, but I feel worse.

Thanks for listening.

Posts: 7 | From kansas | Registered: Mar 2009  |  IP: Logged | Report this post to a Moderator
dmc
Frequent Contributor (1K+ posts)
Member # 5102

Icon 1 posted      Profile for dmc     Send New Private Message       Edit/Delete Post   Reply With Quote 
you don't say what dose of Doxy your taken.

I've heard Vit. Bs feed Lyme and if you scrollo down there's a discussion re: magnesium.

Posts: 2675 | From ct, usa | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
kgarrett
Member
Member # 17420

Icon 1 posted      Profile for kgarrett     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you have lyme - many people feel worse at first on antibiotics. Then they feel better - but every case seems to be unique.

Others have longer experience than I and can give better advice but, I would definitely put out the cash for at least a basic lyme panel at a specialized lab. I paid 260 - I think Fry might be cheaper. But, you need to plan now because the best way to be sure is to finish the 30 days of doxy and then have the blood drawn between 10-14 days after finishing the pills. Contact the lab to get the kit and your doctor will have to sign the slip.

I had like 7 tests at labcorp over 2 years and only one was positive so I know there are a lot of false negative tests.

I had stomach problems also with doxy and switched to ceftin.

Posts: 43 | From md | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
tcw
LymeNet Contributor
Member # 15698

Icon 1 posted      Profile for tcw     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would suggest that you either drop the cal-mag supplements or time them as far away from your doxy doses as possible. Calcium, magnesium, aluminum and other metals reduce the effective dose of doxy that gets into your body.

You should stay away from mineral supplements, antacids, Pepto Bismol or bismuth preparations and probably dairy foods also for 2 hours around your doxy dose if you want full absorption.

Posts: 263 | From Capital Region, NY, USA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
asummers
LymeNet Contributor
Member # 18068

Icon 1 posted      Profile for asummers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Check out Dr. B's Guidelines. He has a list of supplements that Lyme patients should be taking.
PM me if you would like the link.

Posts: 379 | From Sydney, Australia | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-

Here's the link asummers mentions:


http://www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf

Dr. Burrascano'sTreatment Guidelines (2008)


Within that are four pages for supplement suggestions:


http://www.lymepa.org/Nutritional_Supplements.pdf

Nutritional Supplements in Disseminated Lyme Disease

J.J. Burrascano, Jr., MD (2008)


========================


This book, by an ILADS member LLMD, holds great information about treatments options and support measures (supplements, diet, etc.):


http://tinyurl.com/6lq3pb (through Amazon)


THE LYME DISEASE SOLUTION (2008)

- by Kenneth B. Singleton , MD; James A. Duke. Ph.D. (Foreword)

You can read more about it here and see customer reviews.

Web site: www.lymedoctor.com


-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Hoosiers51
Frequent Contributor (1K+ posts)
Member # 15759

Icon 1 posted      Profile for Hoosiers51     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am of the opinion that Vit C is the most important Vitamin to supplement, and the others might not be as important if you aren't deficient in them.

If you have low energy, Vit B might be helpful.

One supplement that might help with the headaches is Wobenzym. They sell it on http://www.vitacost.com . I think the small bottle is only 26 dollars, so you can at least try it for a few weeks. You would know pretty soon if it was helping.

If you are really affected by Lyme though, the Wobenzym could produce a "herx" response, so be aware of that.

With Wobenzym, you would need 6 pills twice daily on an empty stomach. The only reason you would have to worry is if you have a bleeding disorder, or problems with your blood not clotting.

The other supplement you should be on is probiotics. Get a good brand from a health food store, preferably ones that require refrigeration. Take a 2-4 pills 2-3 hours after each antibiotic dose (so probably twice a day). This will prevent that gassy feeling in your stomach, I hope.

If money is really tight, I would drop a couple of the supplements from above that you don't think are helping you, and try those two things I mentioned. The probiotics are a must while on antibiotics.

If the doxy doesn't help you much, and it's not a herx (read up on Herxheimer reaction)....then consider switching to minocycline, but increase the dosage slowly on that one. That one may cause serious herxing if you have Lyme, but that is sort of what we have to go through (to an extent) to get better.

Good luck!

Posts: 4590 | From Midwest | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Hoosiers51
Frequent Contributor (1K+ posts)
Member # 15759

Icon 1 posted      Profile for Hoosiers51     Send New Private Message       Edit/Delete Post   Reply With Quote 
ps--the oils are a good thing because they reduce inflammation, but I would be sure it's a high quality brand that says "free of contaminants" on the bottle. Health food store would be a good place to ask about contaminant-free fish oil if you are interested.

The Glucosamine/Condroitin can be good for arthritis....my parents both use it for that. They even used to give it to our dog with arthritis and it made his last years more comfortable. He used to not be able to stand up, but then with the Glucosamine/Condrotin...he could.

If it isn't helping you after a few months though, it's not worth it. It normally takes quite a few weeks of cointinuous use to see if it will help though, so don't give up on that one too early.

Posts: 4590 | From Midwest | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
jhspn00
Junior Member
Member # 19733

Icon 1 posted      Profile for jhspn00     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you guys for your helpful information. I read the guidelines, but got confused on the supplements.

Hoosiers51- Thanks I will look into the Wobenzym and the Herx reaction. I read a little about it, but had alot going on and just skimmed it.

I don't know which of them is causing me to have severe heartburn, but I am going to stop all of the vitamins for a couple of days and restart one at a time so I know which one I can't tolerate.
I know when I was pregnant I couldn't take the prenatal vitamins because of the heartburn, but I blamed it on the pregnancy.

I think the hardest part of dealing with any of this is that my daughter rarely sleeps through the night. So I don't get a solid rest. I don't feel to bad today, and she did sleep last night.

I actually got 8 solid hours of sleep. That hasn't happened to me in a very long time. Usually my sleep is broke up into about 4 hours here and 1 hour there.


Thanks for the advice it is greatly appreciated.

Julie

Posts: 7 | From kansas | Registered: Mar 2009  |  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 
I was going to repeat the same thing TCW said. It's crucial to follow that advice.

--------------------
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
jhspn00
Junior Member
Member # 19733

Icon 1 posted      Profile for jhspn00     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just an update. I stopped all the vitamins and remained on the antibiotic. Oh and I forgot to tell someone above that asked.

I am on Doxy 100mg twice a day.

I don't have the heartburn I was having, and felt really good up until early afternoon yesterday. Then my neck started hurting again.

I can barely move my neck, and my headache came back full force. So starting tomorrow I am going to start adding back in vitamins one at a time.

I just can't afford LLMD or any of the testing. It just isn't possible. We have our own small home business, that pays our bills, puts food in our kids mouth, clothes on their back, and a roof over their head. We are lucky to get that done.

I am a nurse, but I hurt so bad that I haven't done it in quite some time.

Thank you for your help.
Julie

Posts: 7 | From kansas | Registered: Mar 2009  |  IP: Logged | Report this post to a Moderator
Cold Feet
LymeNet Contributor
Member # 9882

Icon 1 posted      Profile for Cold Feet   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Keebs, thanks for those links from Dr. B. I should have read them before but never did.

A few comments and questions for you folks:

- Has anyone tried the NT factor? If so, any positive results?

- He recommends SBOs from Researched Nutritionals?! This really surprised me...?

Thanks for any comments.

--------------------
My biofilm film: www.whyamistillsick.com
2004 Mycoplasma Pneumonia
2006 Positive after 2 years of hell
2006-08 Marshall Protocol. Killed many bug species
2009 - Beating candida, doing better
Lahey Clinic in Mass: what a racquet!

Posts: 830 | From Mass. | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
That is a low dose of doxy. It should be min. 300 mg daily ... or more! You can read about it in the Dr. B guidelines.

If you're really not going to be able to afford ongoing treatment, I'd look into what alternative treatment you will try. The one month of low-dose doxy won't cure it.

I liked the Buhner protocol. The book he wrote, Healing Lyme, is very good. His four core herbs are andrographis, resveratrol (Source Naturals brand), Samento, and Banderol. I had good results from these herbs, but they do not help much with coinfections.

I took NT Factor. I think it's a good product, but I don't know if you get enough results to justify the cost.

I really like the Triphala that has been discussed on the board recently.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  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.