I started experiencing twitching in my
legsLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints, feet and arms about 7 months ago. I have had twitching in other
musclesDeep anterior muscles
Eye muscles
Lower leg muscles
Muscle aches
Muscle atrophy
Muscle biopsy
Muscle cramps
Muscle function loss
Muscle twitching
Rotator cuff muscles
Superficial anterior muscles too, butt, abdomen,
handsHand or foot spasms
Hand tremor,
faceFace pain, but mainly
legsLeg lengthening/shortening
Leg pain
Leg pain (osgood-schlatter)
Shin splints. I saw a neuro who did a full evaluation, and said everything was normal, and therfore would not order an EMG. The twitching only occurs when my
musclesDeep anterior muscles
Eye muscles
Lower leg muscles
Muscle aches
Muscle atrophy
Muscle biopsy
Muscle cramps
Muscle function loss
Muscle twitching
Rotator cuff muscles
Superficial anterior muscles are relaxed, as in I never notice it when I am walking or anything, only when I sit still. I have not noticed any
weaknessWeakness, and the neuro said no atrophy or
reflexBabinski's reflex
Infantile reflexes
Moro reflex
Urge incontinence change. I had my
reflexesBabinski's reflex
Infantile reflexes
Moro reflex
Urge incontinence checked again today by a PA, I work with, she said they were normal. I have noticed that my right bicept is significantly larger than my left, although I have not noticed
weaknessWeakness in my left. The twitching seems to
waxWax blockage
Wax blockage in the ear and wane, as in it is much worse on some days, and other days I barely notice it at all. How long does it usually take for someone to start noticing
weaknessWeakness if a neurodegenerative disease is present. My
fearFears and phobias is
ALSAls - resources
Amyotrophic lateral sclerosis
Animal bites
Bell's palsy
Cerebral palsy
Cerebral palsy - resources
Genital sores - female
Genital sores - male
Indigestion
Marine animal stings or bites
Parkinson’s disease, do you think I should push for an EMG, or should I rest assured that the neruo exam is enough. Oh I am a 25 year old cacausian
femaleCondoms
Female condoms
Female sexual dysfunction. Thanks
Shamrock
Here is someone who is living far away from your home
(Netherlands) and i can tell you that i have the same
problem as you,a lot of muscule twitches over my
whole body when i am sitting,when i am standing
sometimes a little twitch.this also depends on
the day. (sometimes nothing)
But i must tell you that i was suspected for ms because
i had a negative lp,but know i have something that has
the name to be postviral in my spine (back) and when i am
sitting i god strange feelings in my legs too.But to make
a long story short,i had a long conversation whit my ms
specialist and one of the things he told me.stress,stress
stress,what it can do ! (It can give you L’hermitte)
Don’t worry to much i do not think this is necessary.
If you don’t have muscle twitches and you think all day i would
like to have them,”you will get them!”
And to answer your question: I have them for 20 months
and i do not have weakness.
Good luck,alphie.
This is new to me. I have been experiencing twitiching all over my body for about 10 months now. I am a nurse and have of course been totally freaked out about possible MS and/or ALS.
I have been to a neurologist had an MRI of which was negative for MS. I don't think I have had "weakness" as such. Although I now have read on some websites in reference to ALS weakness more described as "fatigue" in the arms or legs. Of which I have noticed such way back in the past once in a blue moon where if I went up a flight of stairs it felt like the blood would kinda go out of my legs and they would feel extremely tired like they were going to give out but never did. I have that same sensation still and it seems more often then I used too but wonder if I just don't notice it more since I've had the twitching. It happens more so when I am carrying something heavy up stairs etc.
Has anyone experienced this?? My neurologist says if any of my symptoms get worse we can do a LP. I also find that I trip more. Of course all my friends say they do the same thing. I have also had an emg of which was negative also.
SCARy.