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 » B12,Methylcobalamin, Injections better than Oral?

 - UBBFriend: Email this page to someone!    
Author Topic: B12,Methylcobalamin, Injections better than Oral?
Silverwolf
Frequent Contributor (1K+ posts)
Member # 9196

Icon 1 posted      Profile for Silverwolf     Send New Private Message       Edit/Delete Post   Reply With Quote 
With no LLMD at this time, no finances to speak of,and no insurance,I've been using -KAL- Oral B-12 chewable tabs-1000 mcgs.

Injections were mentioned to me in Gen. Sup.,can one get B12 methylcobalamin injections,and w/o a prescription?

Are they spendy? If they are I'll have to do the best I'm able w/the Oral B12s,and the Saventaro, I also use an Acidophilus mix.

The sudden surgery for TxC's eye,took our moneies for the vitamins etc. so we'll get more as soon as able.

Thot I'd check options,thanks for any tho'ts and ideas from all who post.

My brain is addled right now,so am hopefully being understandable..and more clear than mud?

Just dingy Silverwolfn'

--------------------
2006,May-August2006 Dx w/ Lyme/Bartonella/White Matter Lesion Disease on Brain.
[ Clinical Dx w/ two positives and several IND's on the tests from Igenex ], Prior Dx of CFIDS/CEBV 1992, and FMS '93-'94
Diabetes*2 Dx 10/'08

Posts: 3581 | From SE Idaho | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
lymebytes
Frequent Contributor (1K+ posts)
Member # 11830

Icon 1 posted      Profile for lymebytes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,
I do methylcobalamin injections and love them. They protect the nervous system and have been shown to cure bells palsy in trials, they help you regulate a sleep schedule and on and on.

Oral or even sublingual b12 vitamins are not as good because they don't absorb into the blood stream as well. According to my LLMD they are in and out via the urine within hours.

No better are cyancobalamine injections, as they are extremely weak, contain aluminum & the body must work to conver it to methylcobalamin. Here is info on the b12 shots. Burrascano recommends only methylcobalamin: http://tinyurl.com/2j3g6n

However, I don't know anything about these but they now make a b12 transdermal patch. I think it is worth checking into, here is one site and its description the patch & why orals aren't the best: http://www.b12patch.com/about-b12patch.html

Take care.

--------------------
www.truthaboutlymedisease.com

Posts: 2003 | From endemic area | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
TS96
LymeNet Contributor
Member # 14048

Icon 1 posted      Profile for TS96     Send New Private Message       Edit/Delete Post   Reply With Quote 
Another option if you cannot afford B12 injections is a product called "spray for life"
It's a nano particle sized b12 and is absorbed better than the sublinguals.(so I've heard)

It comes in a spray bottle, you can google the name to get info.

I plan on doing this in the future d/t cost of the methyl b12 just to see if it helps. My compounded Methyl inj were costing me over 80 bucks a month.

Just FYI

Maybe someone else has tried this and can comment?

--------------------
Bart Henslea 1976
Fibro/CFS/arthritis 2004
Lyme diagnosed 2007
3 1/2 years treatment with oral combos, Cowden, IV roc. BW herbs. Off all abx in 12/10. Feeling good.

Posts: 647 | From NY | Registered: Dec 2007  |  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 
If you can't afford the injections, you want to sublingual and not chewable. The sublingual go directly into the salivary glands and are absorbed better than chewable.

--------------------
"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
catalysT
LymeNet Contributor
Member # 10786

Icon 1 posted      Profile for catalysT     Send New Private Message       Edit/Delete Post   Reply With Quote 
Injections are definitely superior to oral or sublingual b12. However, if you can't get them for whatever reason. Your best bet is probably these jarrow 5mg sublingual b12's.

They are methylcobalamin and 5mg (5,000mcg). They also don't contain any sorbitol or any other stupid fillers that generally feed bacteria or yeast organisms.

You would probably want to take 2-3 at once, to try to reach the 10mg immediate dose that most people are taking intramuscularly. The high doses (10-25mg daily) are shown to cause nerve regeneration. I doubt that will happen significantly with lower doses, and also less so when not taken via injection.

Yes though, you do need a prescription for b12 injections. They are pretty affordable where I get them (http://www.mcguffpharmacy.com/) (about ~$20-25 a vile, with 30 10mg doses). Plus the cost of the needles (which was pretty cheap at local drugstore).

Methylcobalamin injections make a huge difference in how I feel from day to day. What I typed is just my opinion and I'm obviously not a doctor. Good luck!

--------------------
"You know, the worst, meanest, nastiest, ticks in the world are politicks," - Steve Nostrum

Posts: 242 | From South NJ | Registered: Dec 2006  |  IP: Logged | Report this post to a Moderator
LuLuFlorida
LymeNet Contributor
Member # 12066

Icon 10 posted      Profile for LuLuFlorida     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tried methyl B12 sublingual and they were not nearly as effective as the injections. Perscriptions are required for both kinds that I receive. The B12 I get is 50 per bottle. I have to say that B12 injections improved my nerve pain significantly and they also give me energy.

Hope this helps,
Lindsay

--------------------
"One day at a time"

Current:
-1.2 IM bicillin three times a week
-1.25 IV Vancomycin every day
-IV glutathione and IM B12
-Byron White since Jan. 2011
-ALA, Yasko protocal, Adapten-All, thyrosol, Pekano, phosphalipid exchange, probiotics, oregano...

Posts: 390 | From FLORIDA | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
treepatrol
Honored Contributor (10K+ posts)
Member # 4117

Icon 1 posted      Profile for treepatrol     Send New Private Message       Edit/Delete Post   Reply With Quote 
Silverwolf get the b12 shots you will see a difference. Your probaly like me intrinsic factor shot from abxs over the years .

--------------------
Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

Newbie Links

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
knshore
LymeNet Contributor
Member # 13451

Icon 1 posted      Profile for knshore     Send New Private Message       Edit/Delete Post   Reply With Quote 
I do methyl B12 shots and I really like them. I get mine from a compounding pharmacy and they're not that expensive.

I believe they're about $4 per shot. I do them 2x a week, so it's not that bad. But I don't have to "make" the shots...they come to me already filled and ready to go.

They're great! And, yes, you need a prescription.

Posts: 215 | From Student | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
Silverwolf
Frequent Contributor (1K+ posts)
Member # 9196

Icon 1 posted      Profile for Silverwolf     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for info' and comments <<<<< Lymer Friends >>>>>,

After we get TxC's post-op check-up on his eye surgery done on Friday[ 2-15-'08 ]. Perhaps we can start looking for an LLMD/ND again.

If we can find one that will take us w/ our extreme limited budget,I'll check on the B-12 injections.

The eye situation and our warning that we are about to lose our job [haven't resigned yet from the church mess],sorta took the wind out of our sails [Frown] .

Thanks for the helpful replies... I hate being so weary,especially now w/ TxC blind in rt.eye. For now.I'm managing w/ The B-12 Methylcobalamon chewables/sublinguals.

We found a place about 25 minutes from us, instead of over an hour that carries my B-12's from KAL.

Jus' Sleepy Silverwolfn'

--------------------
2006,May-August2006 Dx w/ Lyme/Bartonella/White Matter Lesion Disease on Brain.
[ Clinical Dx w/ two positives and several IND's on the tests from Igenex ], Prior Dx of CFIDS/CEBV 1992, and FMS '93-'94
Diabetes*2 Dx 10/'08

Posts: 3581 | From SE Idaho | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Methylcobalamin injections (prescription) combined with low-dose melatonin (store bought) helped my sleep considerably. I do them daily. They're kind of expensive at the dose I'm doing but most people do less than I do.
Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
From what I've read and learned on B-12... it's hard for the body to absorb the B-12 it needs. That's why it suppose to be better to do sublingual. Under the tongue slow absorbtion into your system.

If you can't do injections, at least try the sublingual B-12. Also due to body not being able to easily absorb B-12, might be why I found out after a few years that taking 500mcg was not nearly enough for me. Then I realized 1000 mcg was not enough for me within a few months.

When I started 3000 mcg a day or at least 5 days a week, I finally noticed more energy and a difference in me.

Everyone is different. Most everything we try from abx to supplements is different from person to person. Just because my LLMD rx'ed me flagyl 250mg a day, didn't mean I went there. It didn't take me but a few days to know that.

In fact within 2 weeks, I realized just taking one 250mg a day was not in my body's best interest. I then went to a sliver a day. Even had to pulse that sometimes.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  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.