The tingling in my fingertips is really getting on my nerves today and as I am typing I feel like there are pads on my fingertips, I also found it took me ages to do up six buttons yesterday, I usually just were tee shirts so was very surprised about it.
Is this tingling likely to change or stop, also had an MRI on brain recently as I have been getting noises ( not heared the voices yet) in one ear, yesterday I kept had the TV or radio on all day so as not to hear the noises so loudly.
Hi, Sorry can’t help with the fingertips but know qhat you mean about the noises…I have numbness in left ear which spread to the left side of my head followed by a heavy pressure feeling. I heard noises, usually as I was dropping off to sleep. My g.p. gave me gapapentin which increased the noises and freaked me out so I stopped the gabapentin and just stayed with the amyiltriptylline (spelt that wrong!) Did NOT like the hearing noises…made me feel very weird. Hope you get some relief soon
My MS symptons started in two fingers on one hand and the ‘tingling’ has now spread to all fingers on both hands. It’s really frustrating, I agree. I can only wear cloths with buttons if my husband is around to dress me. He also has to help me with laces and anything that needs to be tied behind my back. My experience is that the tingling only gets worse, not better. Sorry!
I’ve had funny sensations in my fingers since Christmas 2011…not saying yours will last this ling. some days I have found doing my sons buttons up hard however other days been fine. They can vary day to day. I’m mid relapse at the moment so they are a lil worse. I have weirdly got used to them and do forget about them. They feel worse at night and i feel them less when my hands are cold. Sensations have been my main symptom since diagnosis…these have increased more in the last couple of years well until this relapse. Hopefully these new ones will be zapped by the steroids. Sorry I can’t help with the noise thing. Hope you get it sorted. Luv Lisa x
I also have tingling in both hands and have ever since dx 15 years ago, unfortunately mine has never gone away, some days more bearable than others. I find the heat makes them worse in that they throb and tingle at the same time.
One of my main symptoms is tingling in my hands. Someone referred to them as fizzy hands - I prefer champagne hands! Seriously, originally my condition was thought to be carpal tunnel problems - but after 2 operations the symptoms returned with a vengance. Needless to say I have had to slow my typing speed down and my writing/shorthand is dreadful. I work in admin and I’m finding that some days are worse than others.
I am getting used to the fizzyness, but it doesn’t seem to go away.
I was diagnosed this week with MS, but thankful that I know what is happening to me.
