Thanks for taking my question:
I'm a 26 y.o. healthy
femaleCondoms
Female condoms
Female sexual dysfunction. June 2003 my symptoms appeared as follows: Day 1 - pins and needles in left
handHand or foot spasms
Hand tremor and arm, Day 2- spread to left leg, Day 3 - spread to all
extremitiesExtremity arteriography and
faceFace pain. Symptoms lasted for about 8 days after which I was left with slight
weaknessWeakness feeling in left leg and left arm that presently comes and goes on a
dailyDaily combo
Daily multiple for men 50+
Daily multiple for women
Daily multiple for women 50+
Daily multiple vitamins
Daily vite
Daily-vite men's formula
Daily-vite weight control basis. Also left with an odd sensation on left side of face, mostly near my eye but can also spread to cheek and neck, and occasionally to same area on right side of face. I have no loss of feeling, nor does it tingle. Vision is normal. This sensation comes and goes but is usually felt at least once a day although can be present for more than 24 hrs.I have felt it almost every day since first pins and needles episode last June. Had episode of pins and needles again Nov. 2003, exactly the same as described above. MRI in Dec 2003 normal, 2 X CT also normal, blood work normal. Meds include nadolol for heart conditon. No fam. hx of MS.
Have history of anxiety including symptoms of lightheadedness and skakiness. Most recently have felt like my left ear is "plugged", like I need to pop it, hearing may be slightly comprimised. Some mild pain off and on.
Neurologist claims this can all be explained by nerve inflammation. If this is indeed the case why would I only feel it on one side of my body? I fear this is MS. Any input would be greatly appreciated. Thanks.
The burning on my skin is probably the worst of my complaints. I also have an eye disease called Pars Planitis that makes me worry about MS. It is linked to MS in about 7-8% of cases. More than makes me happy, that's for dang sure!!
Keep us posted on what's going on. I will do the same.
Sherry
Good luck.
jwick
I am 33 year old female who has same symptoms for the past 6 months. Until last week I was very patient with my doctor's "god knows what you have, you could suffer from panic attacks", but than I got so sick of all of that, so I changed him for good.
It all started on Nov. 5th 2003..I was doing my clinical at the hospital and suddenly I was so dizzy that I almost fell over my patient. Two days after that incident I ended up in the emergency room. "Of course" everything was fine. Labeled as a "stressed" I was sent home. Later on I began having a more strange symptoms, occuring together or appart: very dizzy, tired, numbness in parts of my body, very poor balance, pressure in right eye, muscle and joint pain, constipation, cramps, tremors, urinary trakt infections etc...I cryed at my doctors office just to get a chance for any kind of test. He ordered Holter Monitor (only he knows why?!) and CAT scan of the brain. Thank god this test were O.K. So at least I knew I did't have brain tumor and my heart was fine too. My hero doctor decided to write down dx: panic attack disorder. Fine! He put me on Zoloft, which I am still taking. Then my symptoms got worse. I thought maybe...Zoloft's side effects? Three weeks ago, I went to the bathroom, done..and after 1 minute or so I was all wet, I could not hold urine at all. The same feeling as when the pregnant women's water brakes. This hapened couple of times since then. I changed the doc. and first thing that the new doctor asked me was" Is there anyone in your family who has an MS?" He ordered MRI which I will have next week. And he also said that I should have seen neurologist months before. I realy hope that at least I will know something, something which will put me on the right path, so I can treat this condition. I am not saying that I think it is MS, but I know something is not right, because I am not the same healthy and strong person anymore.
I do apologize for my spelling, I learned Engl. 5 years ago.
Thank you for sharing your feelings and experience and good luck to all of you!
I just had my MRI done, and I was looking at the pictures...Cool, at least I know I have a brain! Just trying to make myself smile...
Does any one know (since I don't have a clue) what does it mean
T-Flair-MS and T-Grase-Ms on two of my pictures? Is "MS" computer interpretation of the funding (Multiple Sclerosis) or is that just some kind of MRI abriviation that has nothing to do with dx.
I will realy appriciate if I can get respond from anyone who has gone throug this already, and has some knowledge about it.
Thank you in advance.
Thank you in advance.
On Christmas day I woke up numb in my right arm and leg. Well.
I am a type I diabetic 42 years old and 34 years diabetic. I always write the weird things that happen to me off to diabetes.
After the holidays, i went to my family doctor and he sent me for a cat scan and the heart monitor thing and other tests and referred me to a nerologist. sp?
I had an MRI in early March ( what long waiting time? I live in Canada and the wait list is said to be months long. I was in in 6 weeks or so.) I was told that I had MS. Spot on my brain and my neck is light in colour in a spot. The doctor told me that I should not worry and there is treatment now. I do not know what type of ms I have or anything. I am trying to educate myself on the computer but I am very confused.
If ms affects the nerves, why do my joints ache? Is the tingling from the nerves? What about warm feeling I get in my leg? Is the weird feeling in my throat related? Sometime i feel like something is in my throat and can barely swallow.
I fell on my poarch 2 weeks before Christmas, do you think that was from ms. My symptoms don't go aways for very long. I don't have one day where my arms don't go to sleep. Is this MS or damage from Diabetes? See all the questions I have. I have to wait 3 weeks to see doctor. I went for tests on nerves at his office last week. Felt much like the lightning bolt pains( call it that for lack of what else to call it) i get in my arms almost daily.
Well thanks for listening to me rant.lol. Any comments.
Before the twitching started I noticed tingling/numbness in my feet/toes and this is still fairly constant. I hope this rules out ALS but I'm not sure.
Saw a neuro 7 months ago and had a full brain/spine MRI, nerve conduction tests in legs and lots of blood work. All came back negative but I'm still worried about MS and ALS. Sound familiar to anyone?
similar to some of you...I am wondering if this might be early signs of MS...
4 years ago I started to feel numbness and tingly feelings on my whole face..and down my back...went to dr...and did the blood work, mri was clear of brain..they didnt do a spine one...said that although no scar tissue that it doesnt rule that out completely...but said woman get stuff like this after having babies?? lol at that answer...so each year during summer mainly...especially the more humid it is...I get tingly numbness...over the years it has gotten not only face but arms...and hands...toes have for longer years gotten numb with exercise....anyhow....last year when it was occuring went to new dr..who ddnt send me to neurologist ..she just said after good blood work..that it is stress...I agree stress aggrivates it..but dont think stress causes it to occur..as I am stressed as much in winter as any other time and hardly get this in winter...
help....thanks, sarah