LASIK Surgery Health Chat: Tuesday, December 15th 5:00-6:00 PM Eastern. Free live Q&A with Dr. Omar E Awad. Ask your question in advance!
Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
 | 

Possible MS Symptoms

by TheLadySkye, Nov 09, 2009 05:06PM
I'm not sure why I couldn't post to the MS forum, so I am hopeful that someone here would be able to help or at least provide some guidance.

I'm a 35 year old female with no neurological history.  My symptoms started about six months ago, and have been a pretty constant progression since.  The first thing I noticed was that when I was exercising, my hands would start to feel swollen and tingle and feel almost numb (like they were "asleep").  This would pass an hour or so after I stopped the exercise.  This same happened once during no exercise while out in the sun on a warm day.  The most extreme time occurred while out at a fair.  It was over 90 degrees - both hands/all fingers started tingling/numb and this lasted the entire 8 hours I was at the fair and did not pass until later that evening.  I was well-hydrated all times.

The next symptom to come was that my hands felt "sticky," especially when wet or damp.  They would feel almost like there was a tacky glue on them.  The feeling usually subsided once my hands were thoroughly dry.  No one else can seem to feel this effect.  My dermatologist did not do any tests, but claimed to have never heard of any skin-related issues that might cause "sticky skin."  My primary doctor thought it might be neurological and might only "seem" sticky when they actually aren't.

I began seeing a neurologist a couple months ago when I started experiencing a burning/stinging feeling in the tops of both feet.  This was coupled with the ongoing issues in my hands, which has progressed to an extremely painful burning/stinging as well.  My joints are not stiff or painful.  Peripheral neuropathy was the original thought since these extremely painful/disruptive symptoms seem to be relegated to both hands and feet.  I also have occasional bouts of dizziness/light-headedness, but this has always been attributed to sinus issues and never lasts long.

However, in the absence of a suitable cause, they are now broadening their initial ideas:

- My reflexes seem good and I have no numbness to be discerned during office examination
- An EMG showed no evidence of a pinched/compressed nerve, actual nerve damage, or carpal tunnel.  The EMG was only done on my right side, but I was told this was okay since my symptoms are uniform on both sides
- Thyroid, BUN, creatinine, sodium, potassium and ANA bloodwork came back fine.  The only thing slightly low was B12.  It was 300, so while I have been given a supplement, neither my primary doc nor neurologist seems to think this is the cause of my symptoms.
- Glucose is slightly elevated (94 - 125), though A1C results are not indicative of diabetes.

Both doctors seem to be at a loss, and I admit I'm starting to be concerned.  An MRI (without contrast) has been ordered (in a couple weeks) to rule out MS.  The neurologist told me he is not overly concerned because MS doesn't usually manifest this way (both hands, both feet, and mostly relegated to those areas), but at the same time, they don't seem to have any additional paths lined up to pursue.  Needless to say, I'm pretty frightened about that idea.  My doctors also don't seem inclined to pursue anything related to circulation.  I have no discoloration and no extreme temperature shifts, so my primary doc has pretty much ignored that element.

So my questions are these:
1). Has anyone with MS ever had theirs manifest in this way?
2). Will the MRI be a definitive indicator?
3). Do you know of anything else I can be considering to get a diagnosis related to my symptoms?
4). Are there any other tests/ideas I should run by my neurologist?
5). If I wanted to pursue the circulation possibility, what tests should I request, or what type of doctor would specialize in this?  My primary doc seems highly adverse to pursuing this area.

What am I forgetting?  It's horrid being in pain all the time.  My hands feel like they are constantly on fire with the burning and stinging, and it's pretty hard to function like that.  I've all but stopped exercising because the tingling/numbness is quite scary.  Any insight you could provide would be much appreciated.
Post Comment
To
Comment
Post Comment
Recent Activity
newway commented on Tramadol & Ultram...
30 mins ago
FinallyFred commented on Tramadol & Ultram...
31 mins ago
chasha33 uploaded new photos
49 mins ago
Head
57 mins ago by farsights
edsherman asc
forget_me_not commented on Tramadol & Ultram...
3 hrs ago
Skippys commented on Silly Songs With Larr...
4 hrs ago
cake698 commented on Tramadol & Ultram...
4 hrs ago
RSS Expert Activity
Simple tool to Assess your Risk for...
10 hrs ago by Lee Kirksey, MD
Premium IOLs have a disproportionat...
Dec 13 by John C Hagan III, MD, FACS
EyeNet Article about MedHelp.com Ey...
Dec 13 by John C Hagan III, MD, FACS
Community Members