A quick background in me. I am a 37 year old male and I have been under the most stress of my life this past year. About a
littleLittle noses decongestant
Little tummys over a month ago I started to get these muscles twitches (actually feels like a bubble effect) in my thigh. It left my thigh and then was random through-out my body, from my
foreheadForehead lift
Forehead lift - series,
eyelidsEyelid bump
Eyelid lift
Eyelid twitch, calfs, triceps...so on. I also notice a tightness from time to time in my right
footAthlete's foot
Athlete's foot, tinea pedis
Clubfoot
Clubfoot deformity
Clubfoot repair
Clubfoot repair - series
Diabetes foot care
Diabetic blood circulation in foot
Diabetic foot care
Erythema toxicum on the foot
Foot pain arch. I feel none of this when I am sleeping, and when I wake up, it is like my mind is waiting for the twitching to start. I really fixate on this. I never had these experiences. I had a cousin who died of ALS this past year, and he was 36. He was 1 of 2 people on his
nuclearNuclear ventriculography sub to develope ALS. I am sure there is no connection with me, but what is going on. I do not feel tired nor do I feel that I have lost any strength, but could all of this be a sign of ALS. I also briefly experienced, in very small areas of my body, a slight prickly to electric feeling on my skin. Again, it is very
isolatedIsolated sleep paralysis when it happens. Most of my twitching happens when I am sitting or relax, or just standing without any movement. What does this sound like? Thanks for any help.
This is important, because if you don't find the source, whatever the chemical exposure you are having - can mean - that you are also at risk for the harm from the long term effects of this chemical.
A common chemical that could cause such is 2-butoxyethanol (aka ethylene glycol monobutyl ether). Fatigue is a long term effect plus the 'gulf war sydnrome' symptoms. But without the assorted symptoms I wouldn't suspect this one.
After 'chemo therapy' treatment a woman experienced odd 'twitching' So do you see what I'm saying?
Here is the list of other signs of such.
HEADACHE,
sore throat,
voice change or loss,
constant humph,
catarrh,
unexpected tiredness,
fatigue,
sore/watery/gritty eyes,
irritability,
anxiety,
depression,
loss of concentration,
short-term memory loss,
reactions to other chemicals,
dizziness,
blocked nose,
rhinitis,
mouth ulcers,
bad/metallic taste in mouth,
lip sores,
chest tightness,
shortness of breath,
chest pains,
asthma,
sinusitis,
nasal discharge,
nose bleeds,
ulceration of nasal mucosa,
itchy burning skin,
rashes,
dermatitis,
aching joints and muscles,
fibromyalgia,
uncontrollable twitching,
heart arrhythmia's,
palpitations,
abdominal pain,
nausea,
diarrhea,
tinnitus,
earache,
pins and needles,
numbness in fingers and toes,
Raynaud’s Syndrome, menstrual irregularities,
pain/difficulty urinating.
Other areas of concern may include liver damage, cancer, teeth and gum problems, reproductive effects and lack of interest in sex.
My $0.02
I'm a 4th year medical student about to finish and start an Ob/Gyn residency in July. I'm no neurologist, although I have studied some Neurology.
ALS is a very scary disease, and it is understandable to worry about it. However, the last comment posted about 12 years of twitching is definitely not ALS. I mean, I guess anything is possible, but ALS victims do not typically survive past 5 years (most famous exception: Stephen Hawking). But it is a motor neuron disease, which means it will affect muscle. The twitching in ALS is the result of denervation of muscle, which will lead to atrophy (weakening). It typically starts in the upper limb, and progression is asymmetric. If there is no associated muscle weakness, it seems HIGHLY unlikely to be ALS. BFS seems more likely if EMG test results come back.
Please go over to Harvard University's "Braintalk" site. There you will find dozens...even hundreds...of individuals with your exact symptoms. Most have had them for months or years and have been diagnosed with nothing, other than BFS. Post your story and you'll get tons of reassurance.
This site has recently been moved to a new server. Here is the URL
http://brain.hastypastry.net/forums/forumdisplay.php?f=191
It would be worthwhile to also go to the old forum and browse the archives. It can be accessed at:
http://neuro-mancer.mgh.harvard.edu/cgi-bin/Ultimate.cgi?action=intro&category=2&BypassCookie=true
and select "Neuromuscular"
Carling
seriously, are you prone to anxiet/depression?
Somatic complaints are common with depression, it just doesn't feel like it at the time..
or haven't taken any magnesium lately..or if im slightly dehydrated or in need of some potassium..