I think its time for you to go beyond your PCP and be referred to a neurologist - they can get your entire history and get a good neurological examination - they will also be able to follow and interpret the results of any testing like MRI
The widespread nature of the tingling in both arms and legs might suggest a problem in the cervical spinal cord, the sneeze worsening it or the electric shock like sensation would support this. One of the possible causes is MS among other things, your age, gender, and family history makes MS a bit more likely. HOwever this post cannot take the place of a complete opinion as I do not know your full story etc.
MS is a treatable condition so it should be identifies and looked for along with other possible causes, for example, Vitamin deficiency, sarcoid, syrinx, or growths. Usually to identify MS, and MRI of the brain and cervical spinal cord is done, and also a spinal tap for analysis of the cerebrospinal fluid, and visual evoked potentials (an electrical test of vision). All these can be done through your local neurologist.
Good luck
I'm glad I found this forum...gives me room to vent :o)
Good luck to you and I hope you find relief.
Good Luck to you all!
Rena
Good luck with your doctors visit and check back in and let us know how it went.
But before all this back problem started ( completely out of the blue,last Oct., 2004). I developed this numbness in my left upper thigh. Runs from my hip to just above my knee. Its basically permantly asleep. Went to a neurosurgeon who did a EMG, and said that it was from a sensory nerve, that could last the rest of my life or suddenly stop. Well its still asleep and drives me nuts,because, you know its there, but you can't feel it. I was told by a tech giving the EMG that this happens alot to the elderly, or in plain English, as you get older.
For a Doctor out there, especially Neuro, I've had two severe head traumas, including a brain aneurysym in '90!! Along with all the head traumas and now this back problem could this sensory nerve be connected to all the current problems???
Just wondering if Anyone would know what i could be suffering from?
I went to see my general doctor about a week after I experienced my first symptoms (the tingling and burning all over). The doctor did a physical examination and concluded I must have a viral infection. She told me to go home to rest and return in two weeks if I wasn't better. Then, two weeks later I was feeling worse. Same symptoms, but with a lot more intensity. So the doctor ordered a complete blood count. They also checked for thyroid disease, diabetes, lupus, and even certain types of cancers. The results were ALL normal. No signs of a bacterial infection either. The doctor then prescribed advil for my headache, and diagnosed me with "atypical migranes". I was furious because I knew that someone with an atypical migrane would not be experiencing all the systemic sensations I was experiencing. But I went home and took a dose of advil every 6 hours to see if that would help. It did NOTHING. The following week, I consulted with another general doctor and she referred me to a neurologist. The neurologist did conduction nerve tests, an MRI of the head and the neck. Results were again all normal. So the neuro ruled out MS and ordered more blood work. They tested me for Hepatitis B & C, HIV (and all poss. STDs), other types of cancer, more tests for lupus, arthritis, heart-related proteins, and a whole bunch of other things. EVERY single thing came back normal! Now, the doctors had no idea what to tell me. THe neuro prescribed some anti-anxiety medicine to treat restless leg syndrome ( but this would not explain all my other symptoms), I went home and took the med for 10 days anyway. The medicine didnot do anything to treat my symptoms, but it did give me some bad side-effects. So neuro took me off the med. and reffered me to a rheumatologist because he thought I may have an auto-immune disease. The rheumatologist saw me twice and did a WHOLE bunch of more blood tests. They ALL came back normal. Everyone was puzzled. Thankfully, none of the doctors blamed my mind (thought I was crazy) and kept searching for possible explanations. After seeing about 6 different doctors, my rheumatologist finally diagnosed me with fibromalgia, although he did tell me I was a rare case since I did not have those tender spots that people with fibro usually have. I'm afraid now the doctor just wanted to put a name to all of my symptoms, and that I really do not have fibromalgia. I keep reading books about it, and it just doesn't make sense to me that I have fibro. Like I said before, I am a very happy and positive kind of person, and though I know the doctors have not yet found a real explanation to all of my bizarre symptoms, I go about life with a positive attitude and try to enjoy and make the best of every single day. To all of you who are going through a similar situation, please do not dispair! It is very important that you keep searching for possible explanations. But if you do not find them, then try alternative routes. Do yoga, eat healthy, exercise, socialize, try acupuncture, homeopathic remedies, etc. The point is to feel like you are doing something for yourself (when traditional medicine has let you down). Good luck to all of you. I'd love to hear from anyone with similar symptoms. Thank you!
Thank you
GOSH I FEEL LIKE IM GOING CRAZY TOO, LAST NIGHT I WOKE UP WITH NUMBING AND TINGLY BURNING SENSATIONS IN MY RIGHT ARM AND HAND.
THIS IS NOT THE FIRST TIME THIS HAS HAPPENED. THEN TODAY I WAS GETTING THESE WEIRD ELECTRIC LIKE SHOCKS IN MY WHOLE BODY, IT WAS SOO WEIRD, I HAD THIS BEFORE BUT THAT WAS WHEN I WENT COLD TURKEY OFF MY MEDS BUT THIS TIME IM ON MY MEDS AND THIS IS HAPPENING SO I DONT KNOW WHAT THE HECK IS WRONG W/ ME.
AND THE PAST WEEK ALSO I'VE BEEN HAVING THIS WEIRD SWOOSHING NOISE IN MY RIGHT EAR AND I ONLY HEAR IT AT NIGHT WHEN ALL IS CALM LIKE NOW. I HAVENT WENT FOR ANY TESTING YET BUT IM GOING TO GO SEE MY DOC TO SEE WHATS WRONG W/ ME. PLEASE PRAY FOR ME.
I JUST KEEP WONDERING WHEN I HAVE THESE FEELINGS, AM I GOING TO PASS OUT OR DIE FROM THIS? JOHNA
I know exactly how you all feel. I too have been experiencing constant tingling and numbness in my hands/arms and feet/legs. I have been sick now for several months, had all sorts of blood work done and all that came back fine except for elevated white blood cells which were attributable to a viral infection. My biggest symptom was SEVERE fatigue, could not get out of bed for a week. After a complete examination by an ER doctor I was told I had 'post viral fatigue' and that slowly I should start getting better. I did for a week and now I have this tingling and numbness and the fatigue has returned. The whole time no one has even suggested a MRI and Im so scared that I could have MS.
But, my only symptom that makes me think MS is the numbness/tingling. I only have slight visual disturbances which manifest themselves as eye discomfort (not focussing issues)and sometimes when I go out grocery shopping my legs get heavy and I feel tired. However I have also been told that numbness/tingling is a side effect of post viral fatigue. Anyone else in a similar situation???
I hope all goes well Rena, and keep us posted on the outcome.
sorry to hear of your problems as well, i understand exactly where you are coming from. In the past 4 months I have been to 4 GP's, optomertrist, ER twice, a ENT specialist and my own GP about 5 times. Its interesting that some days I feel great and people tell me how well I look and then I have these days where it is a struggle just to get out of bed and no one understands, people think im lazy. I live with my parents and they are always worried about me, especially when I get home from work at 5.00 and then im in bed by 7pm. I keep thinking that the worse thing I ever did was google my symptoms, for several weeks I was CONVINCED 100% that I had a brain tumor and now I am convinced that i have MS. Its funny you seem to look at the symptoms and then say to yourself, "well two weeks ago I noticed that I had this, and this and this" and you convince yourself that you are sicker than you probably are. I have now convinced myself that i have urinary frequency and urgency (another symptom of MS) becuase I go to the toilet about every 2 hours during the day, but then I realise that I have done this my whole life!!!!
I guess my only worry is that having a tingling sensation in the extremeties is NOT normal and that it indicates something no matter how minor or major is wrong. But its funny because the whole time I have been writing this I have not had any tingling sensations, as soon as I thought about it I noticed that i do!! Strange.....
If you want to discuss any problems further I am more than happy to hear from people in a similar situation (in fact I want to, so i know that I am not abnormal) please email me at ***@****
I am going through the same thing! But mine has been going on for TEN YEARS. It all started in 1996 with slight tingling in my fingers, and some numbness in 2 fingertips. I was just out of college, starting my new job, etc, and didn't even know about MS. I blew it off, but when the tingling and numbness recurred over the years in my feet, toes, hands, and legs, I picked a nuero out of the yelow pages in 1999 (big mistake!). First he told me I had "female hysteria" (ya gotta love that), and then he called me THREE MONTHS LATER, at work nonetheless, and said "I reviewed your MRI again and actually think you have MS. We need to start you on medication right away." This was over the phone, at my job. He was a real winner.
I immediately sought a second opinion--and saw a specialist at the Cleveland Clinic's Mellen Center. He was wonderful--and also said "absolutely NOT MS." At that point, according to the Cleveland Clinic, I had a very normal MRI (brain and spine), borderline VEPs (108 and 112), and normal evoked potentials. They explained the VEPs as possibly caused by my astigmatism, and said they weren't delayed enough to be concerning.
Over the years, my sx continued to wax and wane: a small spot of numbness on the bottom of my foot would last a month, then disappear. My palm would burn for a few weeks. A small tingle in my face. I live in Seattle, where the MS Centers are excellent, and have been seeing the Director of an MS Center here since 2001. I have had 3 more MRIs of brain and spine, all clear. My VEPs remain mildly abnormal, though I have never had optic neuritis. This summer, I had what seems to be my first real exacerbation--it all started in August, and is STILL going on--lots of patchy numbness, tingling, in feet, legs, hands and face, mostly on the right side of my body-- and this time, fatigue that feels like 10 trucks hit me and then backed up to park on me. I repeated all tests (normal), including b12, lyme, thyroid, and now I have my first LP scheduled in a few weeks.
My neuro is evasive about answering me directly. She calls this "very possibly MS," but when I asked what this could be if NOT MS, she had no answer. With clear and stable MRIs of brain and spine over 10 years, I am somewhat reassured, yet my symptoms are classic MS and can be explained by nothing else. Grrrr. So frustrated, so hard to live with such uncertainty. I am female, 31, about to get married. I like my job, eat well, exercise, take supplements, and do everything I can to minimize stress in my life. I am doing acupuncture, yoga, gentle chiropractic work, and meditation. What else can I do???
Is anyone else in a similar situation? Sorry this post is so long--I am just tired of living with this "probably MS but we may not know until it gets really bad and shows up" condition.
I forgot to say that 2 months ago I also started getting these round red crusty patches on my skin. I've had 1 on my shin and 3 on my upper arm, and not at the same time. Each came out one at a time and lasted about 10 days.
Thanx,
Neen
I'm new here and I can't beleive there's others like me! I thought that I was going crazy! My Symptoms started 4 years ago.
I started having slight numbness in my arms and legs. I freaked and thought I was having a stroke so I went to the ER. All test came back ok. I felt like a jerk for going. As the years went by I still got my 2 or 3 migraines a year. This feeling would not go away. I just got worse. I have suffered from Vertigo since 1992 and would get attacks about 1 time a year lasting 1 day to a week. I also had hearing loss over the years. I started having severe back pain in 2002 and taking alot of pain meds. I decided in 2004 to have my back fused in July. Everything went great. My symptoms seem to be gone while I was on pain meds. By August I was off all meds except for Birth control. I got severe vertigo that lasted for 1 month. I also lost 80% of hearing in my right ear and 25% in my left. So I now at 40 were hearing aids in both ears. The numbness and tingle has spread to my face and seems to move around. I have felt so sick and tired for a year I can't stand it. I have had several MRI's in the past 3 years of my brain I glow! I went to my Neurolgist, he just scratched his head. All MRIs and test came back negative. Then I started having weird feeling in my eyes. Eye Dr. said things look good.
I went back to my Neuro, he sent me to the Cleveland Clinic.
Went through more test. All came back NEGATIVE! That was in March of this year, so I gave up and am coping with whatever this is. The Cleveland Clinc said it's probably stress. STRESS!
I have no stress. I have an easy life! Now what? I am so tired of feeling the Numbness, Tingles, Severe Fatigue, Tightness in my muscles, Sick feeling, Eyeballs feeling weird, Shoulders and neck hurting and tension headaches.I'm so glad I found you guys. Hopefully someone will give us an answer.
Thanx 4 listining,
Neen2
I am an older man age 69 and have been in good health up to now. A few weeks ago I started to have a tingling sensation in my right hand and right side of my neck and face. I also am starting to have headaches at times, although not severe. I do have a few tender spots on my lower right leg down by the ankle area. I am wondering if I should see a neurologist, an internist or a orthopod. Could this perhaps be MS? And if so just how bad is MS and can it be controlled? Anyone out there have any suggestions to offer up?
Dave in WV