This is topic Any sublingual B12 (methylcobalamin) experiences? in forum Medical Questions at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/1/50383

Posted by BartonFink (Member # 10818) on :
 
Have you tried this product? I took my first tablet today and it made me feel very warm, calm and relaxed. The nerve pain decreased also. Any similar experiences?
 
Posted by iceskater (Member # 8655) on :
 
I have had a round of Im injections of B 12 and then went to sublingual B 12. My neuropathies are pretty intense so I am still waiting to see if I have any results. Sorry that I can't be more encouraging right now. Hopefully, it will work.
 
Posted by BartonFink (Member # 10818) on :
 
Yes lets hope so. How much are you taking?
 
Posted by bettyg (Member # 6147) on :
 
i took b12 SHOTS for the last 5 months; for last 2 months used stomach area to take my shots since my thighs had calcified. [Frown]

started out daily for 2 weeks; then every monday, wed., and friday; got 2 refills.

felt no different at all.

had my b12 blood lab done; was 1200; SUPER HIGH.
 
Posted by david1097 (Member # 3662) on :
 
Sublingual did nothign for me, Ihad to go with the IM shots. The IM shots DID make a big difference
 
Posted by erinbaba (Member # 10829) on :
 
Hi everyone, I just posted a separate topic "Do not take extra B vitamins." My Lyme doctor, Dr. D in Boston, who has been in the field for 25 years and actively pursuing research, says that B vitamins feed the Lyme bacteria. Be very careful!

[ 20. December 2006, 10:20 AM: Message edited by: erinbaba ]
 
Posted by Vermont_Lymie (Member # 9780) on :
 
I think this is one supplement that has really helped me a bit; with energy level and well being. I have been using sublingual B12 (methyl) for a few months now.
 


Powered by UBB.classic™ 6.7.3