This is topic tingly feet in forum Medical Questions at LymeNet Flash.


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Posted by janice victorov (Member # 22937) on :
 
hi all,
can't sleep due to tingly feet.

Any suggestions? Just started metanx. Janice
 
Posted by Remember to Smile (Member # 25481) on :
 
If we get the light from the computer screen out of our eyes and try to read a book in comfort, you may get sleepier than with your computer on.

I'll be taking my own advice shortly.
 
Posted by TF (Member # 14183) on :
 
Take sublingual B12. Good for any nerve-type symptoms like this.

Janice, your mailbox is full. Trying to reply to your pm.
 
Posted by hadlyme (Member # 6364) on :
 
ABX will help it go away in time. Other than that, I have given myself B12 shots and then take magnisium.
The lyme is playing with our nerve endings. I was able to get rid of the tingly feeling years ago on a strong 2 year regiment.

It's back now, and I'm back in treatment again too. Hoping I can someday get rid of it again!

Try not to get overly tired or stressed... it will make it more pronouced.
 
Posted by janice victorov (Member # 22937) on :
 
hsdlyme,
thanks. for some reason needed to hear that. I got rid of it six months ago when it was really pronounced.

Now its returned, not worse just there being annoying. [Smile]
 
Posted by LA (Member # 26353) on :
 
I can relate. I can't sleep because every time I lay down, I get these electric jolt feelings and then all my muscles tense up and jerk. It is like I have a 1 second long seizure while awake. I'll be just about asleep and I'll get one and it wakes me right back up. I find myself sitting up on the couch sleeping a lot.
 
Posted by Remember to Smile (Member # 25481) on :
 
LA, i've had that, too, just a few times in the past couple months. i often sleep on the couch, sitting up in the corner.

I've long felt i needed B12 shots! Will be asking my LLMD.
 
Posted by JS in OK (Member # 24526) on :
 
That's what I'm dealing with too. Buzzing, tingling in all over (head to toe). I'm on abx and taking B12 shots. It has improved some,but still very anoying. Also have electric shocks and never know what part of the body they will strike. Sometimes it makes me jump. My family just look and say "you got struck again!" I am looking forward to the day that it will GO AWAY!
 


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