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 » Vitamin C IVs?

 - UBBFriend: Email this page to someone!    
Author Topic: Vitamin C IVs?
Curiouser
LymeNet Contributor
Member # 14128

Icon 5 posted      Profile for Curiouser     Send New Private Message       Edit/Delete Post   Reply With Quote 
Saw my holistic doc today and was talking with her about lyme.

While she's not treating me for lyme (which is a whole 'nother story), she suggested I do IV vitamin C treatments.

She also didn't go into much detail about what they were for or why she thought it'd be a good idea (it was a rushed appt).

Admittedly, I'm a tad skeptical and don't really know anything about this.

I already take 3000mg daily of vit C, plus whatever I get through food.

Would someone be so kind as to point me in the right direction on this?

What are Vit C IV's supposed to do?

How are they supposed to help with lyme?

Drawbacks/side effects?

Are they effective?

Thanks!

--------------------
If you don't know where you are going, any road will take you there. - Lewis Carroll

Posts: 356 | From Body-PA, Mind-elsewhere | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ask your LLMD. [Smile] He'll have an opinion on them.

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

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Curiouser
LymeNet Contributor
Member # 14128

Icon 1 posted      Profile for Curiouser     Send New Private Message       Edit/Delete Post   Reply With Quote 
Oh, definitely going to talk to my LLMD before even considering doing them. I see him in 2 weeks.

Just thought in the meantime, folks who have tried them, know something about them, etc. could share the benefit of their experience. [Smile]

--------------------
If you don't know where you are going, any road will take you there. - Lewis Carroll

Posts: 356 | From Body-PA, Mind-elsewhere | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
roro
LymeNet Contributor
Member # 13383

Icon 1 posted      Profile for roro     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did them back b4 I knew I had lyme. It did help me feel better temporarily, but I dont know if it did anything for infection
Posts: 615 | From maryland | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
Curiouser
LymeNet Contributor
Member # 14128

Icon 1 posted      Profile for Curiouser     Send New Private Message       Edit/Delete Post   Reply With Quote 
Roro,
Thanks for your reply [Smile]

What reason did your health practitioner have you doing them? What were they supposed to do for you?

--------------------
If you don't know where you are going, any road will take you there. - Lewis Carroll

Posts: 356 | From Body-PA, Mind-elsewhere | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
mojo
Frequent Contributor (1K+ posts)
Member # 9309

Icon 1 posted      Profile for mojo     Send New Private Message       Edit/Delete Post   Reply With Quote 
My Dr. does these and I had one yesterday. They boost your immune system.

My Dr's contain Vitamins and minerals, not just Vit C.

Posts: 1761 | From USA | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
ByronSBell 2007
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
it's a good antioxidant but it wont get you well, I get them every week for immune support but they wont ever get me well
IP: Logged | Report this post to a Moderator
Lisianthus
LymeNet Contributor
Member # 6631

Icon 1 posted      Profile for Lisianthus   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have vitamin C IV's every month, about 30,000mg at a time. You can take more Vitamin C in if it doesn't go through your digestive tract.

In the beginning I was against them, when I really didn't much about them. But the more I read I thought I would try them. The first one I had I thought I was going to die! I herxed so bad, headache and pain everywhere. But the more I did the better I felt.

It does bring up your immune system and I believe it does help to fight lyme along with abx. I don't think I would be doing as well as I am today if I hadn't done some immune system building and chelation. This is my opinion.

Here is some info on Vitamin C:

High Dose Vitamin C

Vitamin C info

More on Vitamin C

Hope this helps,
Lisi

--------------------
yahoo 360 http://360.yahoo.com/my_profile-UqSNGiA9crUMRW.lFNGN5Jk-?cq=1

Posts: 986 | From Michigan | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Blackstone
LymeNet Contributor
Member # 9453

Icon 1 posted      Profile for Blackstone     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had Vitamin C (75-100g infusion) and Hydrogen Peroxide IVs towards the earlier stages of my treatment.

Vitamin C is toxic at high doses - thankfully, more toxic to organisms than it is to us. It creates a hostile environment for many bacteria. I had to get a Picc line for these infusions because they were very painful - Vit C is caustic, and irritates the venous walls. After getting a Picc, it was completely painless as the central line took the medicine into larger and "higher flow" veins.

Posts: 691 | From East coast, USA | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 13 posted            Edit/Delete Post   Reply With Quote 
IV Vit C does nothing to treat Lyme.

That is classic for what holistic doctors have to offer, and it's how they make their money.

Oral Vit C is fine, and in normal doses.
I did IV Vit C and also Hydrogen Peroxide and it did nothing but cost me thousands of dollars and burned my veins. IV C just makes expensive urine. Believe me I used to be all for this approach before I knew I had Lyme disease. Back when i thought I had CFS and viruses I used tons of Vit C IV's and a whole arsenal of alternative and nutritional approaches. Nothing worked and I got sicker and sicker until i found my LLMD and did IV antibiotics!

IP: Logged | Report this post to a Moderator
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
There are thoughts that high doses of IV Vitamin C can actually help eradicate infections. One of my doctors has recommended I try it, but I haven't chosen that path.

There is actually an NIH funded study looking at high dose Vitamin C in conjunction with chemotherapy for certain cancers.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
If Vitamin C could cure Lyme and treat bacterial infections we would not need antibiotics anymore.
Sure C is essential to our bodies and immune system, but it is not a magic cure. It can damage Lyme patients, mess with your insulin and screw up your adrenal function. Be careful folks!

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.