electrical shocks drooling

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rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 7/17/2010 2:25 PM (GMT -6)   
Does anybody ever get electric shocks down their legs? Usually just one leg?  Feels kinda like I'm pluggine in to an outle.  Also has anyone experienced drool?  thanks

Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 35853
   Posted 7/17/2010 3:37 PM (GMT -6)   
I get a lot of electrical shocks - in my legs, arms, back... but usually my legs.
For me it's usually just one area at a time, but I have had them in several places at one time.
Some get quite painful.
-Live simply- Love generously- Care deeply- Speak kindly. May we all find peace along the journey to find healing.
Trav


bucci
Veteran Member


Date Joined May 2006
Total Posts : 1477
   Posted 7/17/2010 10:52 PM (GMT -6)   
roses , are you on antibiotics? any meds? antidepresssants ..any psychiatric stuff? did you ever have seizures?

were you treated and got well and went OFF meds?
hep c , lyme
Dad has lyme


Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4399
   Posted 7/18/2010 2:28 AM (GMT -6)   
rosesinjanuary,

I drool a lot while sleeping, because I have an enormous amount of saliva. If I'm not careful, I can choke on it really easily.

My Dad also had too much saliva, not sure why he had this problem.
-Razzle
Chronic Lyme Disease, Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, etc.; G-Tube; TPN via PICC (trying again to wean off the TPN).
Meds:  IV Cipro, Heparin (to flush PICC line), Singulair, Claritin, Domperidone, Colloidal Silver, probiotics, digestive enzymes, Milk Thistle & other liver support herbs, Magnesium, homeopathy.


ineisa
Regular Member


Date Joined Dec 2009
Total Posts : 72
   Posted 7/18/2010 5:09 AM (GMT -6)   
For me one of my most common symptoms are those electric shocks, I get them every day in different parts of the body, can be a small muscle but also and much more often the bigger muscles. It only lasts a few minutes, and it can be one shock or 2 or 3 and then its stops.
Lyme is sooooo confusing!!! Am I going mad???

Post Edited (ineisa) : 7/18/2010 5:12:08 AM (GMT-6)


+Lyme
Veteran Member


Date Joined Apr 2009
Total Posts : 1304
   Posted 7/18/2010 9:46 AM (GMT -6)   
I don't know if this is the same as what you all are describing -- I guess it feels more like a shock than anything else, but I would not call it painful. Especially when awakening in the nite (maybe they woke me?) and upon waking in the morning, these have become very strong and shoot all the way down my legs and all the way down my arms. Used to only be my legs, now most of my body is involved.

Whatever that feeling is, I have had it before in the past, but much milder. I noticed that it sometimes used to happen at the beginning of a hot flash when I was in menopause (long past)

My daughter says she sometimes has 'nerve shock'. I looked that up and it does not quite explain what I feel.

This does happen a few times during the day, but is most prominent while in bed.

These shooting 'shocks' or whatever they are used to not bother me, they were so mild. They have gradually become stronger and stronger and I will still not describe them exactly as 'painful', but the sensation is becoming quite uncomfortable.

Going back to Roses' original post: yeah, I guess it does feel sort of like being plugged into an electrical outlet. And I think I only drool at nite.

What is this?
Bit 1972: Acute and chronic tonsillitis, UTI, miscarraige, appendicitis, hypoglycemia,  chronic neck pain w/ crushed vertibrae, chronic severe back pain, mitral valve prolapse, depression, resolution?
 
Bit Mother's Day 2007: Lyme, Babesia microti, hypothyroidism, EBV, HHV6, Parvovirus B19, low adrenals &misc other hormones, depression, anxiety, more of the above.


rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 7/18/2010 10:13 AM (GMT -6)   
What would I do w/o mi friends with no faces?
It is so comforting knowing u are here, I was treated by a lyme doc for years I did get better but never cured? I have no slpeen which I hope explains this so that all of u will indeed get well. drugs are prozac a beta blocker (blocks the feeling of mitral valve) and xanax when needed. at least mi brain is working this time the electrical shocks in mi left thigh have preceded the numbness in legs but because knees hurt i know legs are there. having a dinner guest from hubbys work i willhave to wash this sweaty greasy hair. whew. dog hair all over too. wish me luck as I wish u. if only there were a pill
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