Multiple Sclerosis Community
source of decreased sensations/parathesias
About This Community:

Our Patient-to-Patient MS Forum is where you can communicate with other people who share your interest in Multiple Sclerosis. This forum is not monitored by medical professionals.

Font Size:
A
A
A
Background:
Blank
Blank
Blank
Blank Blank

source of decreased sensations/parathesias

I am trying to wrap my head around this.  Can anyone help?

I had areas of decreased sensation in parts of left> right hands and  left foot.  I have also had the fall asleep feeling to hands and feet and the "bee stings" randomly that I think that has gotten better since starting Savella.

I had EMG's of arms and legs that were normal.

So what I'm trying to understand (again), this isn't peripheral neuropathy right? since the EMG's were normal.  So the decreased sensations are from some where else?

Please enlighted me!
Thanks in advance,
Karen
Related Discussions
3 Comments Post a Comment
Blank
Avatar_f_tn
I'm really so far from knowledgeable here, so don't take what I say as gospel. It might be a starting point for research, though.

As best I understand it, small fiber neuropathy is a kind of peripheral neuropathy that is not detectable using EMG and similar tests. It affects the sensory nerves close to the skin, and is often found in hands and feet. Decreased sensation in the affected areas is common.

Apparently this is a rule-out diagnosis, so in that sense it's somewhat like MS.

Good luck with getting to the bottom of this.

ess
Blank
338416_tn?1260996698
Karen, are you diagnosed with MS?  Or still in limbo-land?

Paresthesia and loss of sensation are very common in MS.  One of my first symptoms was buzzing and numbness in my chin and lip.  Now quite a lot of my skin is numb to the touch, and there's a couple of places that have lost pain sensation as well.
Blank
620877_tn?1282767697
I too have a loss of sensation on the left side of my face.  Like most of my symptoms, it comes & goes.  I get tingles & buzzing at various times and various parts of my body too.  I should say that I am not diagnosed, but I am in the "probable MS" category at this time.  I have 1 lesion in the corpus callosum and numerous symptoms.

To test for small fiber neuropathy, they take a small sample from your hip & ankle and analyze (I am not sure how) to see if there is a problem with the nerves.  I had this test done in January - it is all a part of ruling out the MS mimics.

Good luck,
Chrisy
Blank
Post a Comment
To
Go
Blank
Multiple Sclerosis Tracker
Log symptoms & treatments
Start Tracking Now
MedHelp Health Answers
Top Neurology Answerers
338416_tn?1260996698
Blank
jensequitur
Fort Worth, TX
667078_tn?1316004535
Blank
HVAC
Durham, NC
1045086_tn?1332130022
Blank
twopack
northeast, OH
Avatar_f_tn
Blank
SarahL2491
AR
751951_tn?1299202836
Blank
PastorDan
Caledonia, OH
739070_tn?1338607002
Blank
rendean
GA
RSS Expert Activity
748543_tn?1371556709
Blank
Jaw like a Plane?
17 hrs ago by Hamidreza Nassery , DMD, FICOI, FAGDBlank
521840_tn?1348844371
Blank
When your child needs a Psychologis...
Jun 13 by Rebecca Resnik, PsyDBlank
1741471_tn?1369660473
Blank
NBA 2013 FINALS START TODAY- Train ... Blank
Jun 06 by Michael Gonzalez-WallaceBlank