ms symptoms pain hands

I've had MS for almost 11 years. For the past few years I've had problems with pain and spatiscity on my right side. About two months ago my neuro (after tests) told me I have Carpal Tunnel Syndrome as well as MS symptoms in my right hand. Three days ago tmy middle and my ring finger snapped down and were closed for five hours. All of a suddent they just unsnapped. It happened again and I am writing this with my left hand. Any ideas?

I have been keeping a timeline to give to my doctor, & have noticed some of my symptoms stick around all of the time while some don't. The awful fatigue stays all the time(sometimes slightly improves but is always present),these crazy muscle twitches are always here, & my right side seems to stay weak. I have also noticed that the spasms come & go as well as the headaches & eye pain. Some days my brain seems foggier than others.

Hi and welcome, MS doesn't generally cause any symptom to be symmetrical, or experienced in all peripherals (both hands and feet) and if you are experiencing hot, red hands and feet with or without actual swelling, whilst it's 'less likely' to be related to a neurological condition like MS......it's not normally something someone of your age would be experiencing.

The clear MRI of the brain makes MS less likely. I have read that ALS generally does not occur with sensory symptoms. I have had a full CBC, ANA work-up, tests for diabetes, vitamin deficiency, lyme's - all neg. My other symptoms are as follows. I usually don't have all of them at the same time. Several times I have had weeks or months with no symptoms at all.

sounds like ms to me too,Try to find a ms clinic in your area, i have suffered with ms for years and find the best results when you call a neurologist that has an ms clinic. god bless and good luck.

I don't have consistent leg pain, but I did have constant foot pain. They felt like something very heavy had just been dropped on them. Meds have helped completely relieve the pain.

I have many ms symptons but the only one which worsens in the heat is the tingling I get in both feet and hands. If you have ms are all your ms symptons supposed to worsen in the heat, or can it just be some??????????????

Look at Issacs disease I have that and its a copy of some MS symptoms. Ive set up a facebook with links. Look if you fancy, it is named Issacs disease.

I think I need to start this dmd and maybe get some sort of nerve test to see if the hand pain really is due to the MS. The sensation varies so much from an ache to a throbbing pain. Today is more like tiny shocks. Very odd but then so are most MS symptoms! I'm guessing nerve damage is what bothers me then as I've had a couple of definite flares and they're very different. I think if I was able to rest occasionally that would also help but hey ho, such is busy family life!

Bowel and bladder symptoms include frequency of micturition, urine leakage, eye symptoms like double vision uncontrollable rapid eye movements, facial pain, painful muscle spasms, tingling, burning in arms or legs, depression, dizziness, hearing loss, fatigue etc. You have many of these symptoms. The treatment is essentially limited to symptomatic therapy so the course of action would not change much whether MS has been diagnosed or not.

*Bladder issues (frequent urination, sometimes burns/stings) *Bowel issues (attacks of diarrhea, constipation, mucus (sometimes bloody), hard stools) *Heat makes things worse (showers, baths, moving around a lot/exercising makes me feel kind of sick, hot, and exhausted) *Electric shock sensations *Tingling/numbness in fingers, toes, right side of head and neck *Leg cramps *Muscle aches *Joint pain (not bad) *Eye floaters (sometimes see flashes of light especially when I move my head) *Eyes w

Hello, For the last 3 weeks I have had this tingling sensation in my right shoulder blade. No pain was involved just the tingling sensation. It finally went away this past week and it hasn't returned but now my back feels somewhat stiff. Still, it's not painful just an annoyance. Also, my hands feel weird. Not quite tingling but just odd. I don't know if it's anxiety or mild symptoms of MS but there is no actual pain or numbness.

Just curious if this sounds like MS or something else. No real other symptoms other than hands and feet tingle and also the brain fog almost pressure feeling. 40 year old male. I appreciate everyone taking time to read and reply. Have a nice week all.

I have had a few early symptoms of MS in the past 6 months or so and am still in the process of a diagnosis. I am curious if anyone else has had tingling in the hands that only lasted about 10 or 12 hours and then went away? It started in my right hand and moved up about halfway up my forearm. I don't know if this is relevant or not but would like to know if anyone else's tingling/numbness started this way. Thanks in advance!

Also, I have been told that MS is not hereditary but I had an aunt with MS. Has anyone else had someone else in their family with MS? My neurologist is planning on referring me to a university hospital to see a specialist. Just wondering what everyone's presenting symptoms were? Thanks for allowing me to join. And, thanks for any help.

Your clear MRI and entire list of symptoms is suggesting that its unlikely to be due to a neurological condition like MS, MS literally means many scars and the symptoms are caused by those brain and or spinal cord lesions (scars). RRMS doesn't typically 'present' with so many different types of issues, your symptoms are generally all over, in all peripherals, unrelated to MS etc and when there isn't any lesions, understandably conditions like MS become very unlikely.....

I have been diagnosed with chronic epstein barr and have numerous neurological symptoms as well. fatigue, pain, tingling in hands and feet, depression, confusion, tingling in hands and feet, muscle pain, dizziness, etc. what are some of your symptoms? sometimes it helps knowing you are not the only one... i recently had an mri showing one tiny lesion on my spine. i have to wait six months for another mri to rule out possible ms.

so now just under 2 yrs later after being completely free of these symptoms, I got a very bad head/chest cold lots of coughing up of phglem, stuffy nose, etc.. as these symptoms finally subsided, I started to have mild nausea, a pain when swallowing bruise type feeling one side of adams apple area, and that imbalance feeling, became pretty worried and also noticed that blurred vision on things close up, no eye pain or color symptoms, just blurry close up.

Of course now I have the numbness in the foot and am wondering if I am causing the other symptoms because I am anxious about it being MS. I know that just because your MRI is clear doesn't mean it isn't MS. So now I am very worried. Any opinions would help me. Does this sound like it could be MS or do you think maybe anxiety. Can MS come and go like my symptoms do? Does MS ever feel like you are hyper or jacked up on caffeine?

I was diagnosed with MS in August of this year and this finger pain was one of the earliest symptoms after I fainted in Feb (but had no idea that was anything serious) - I went to a rheumatologist for the finger pain and he couldn't find anything but did think I had carpal tunnel and the nerve test for that is what started me on the path to a MS diagnosis.

Ms symptoms pain hands

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