has anybody on here experienced partial deafness as part of the package of sensory symptoms ? , I’m just wondering cause I have been like it for a while now in the right ear , and it seems to get worse when my other sensory symptoms kick in (daily )
Yes , I had to go for hearing test eight months ago, I now have to wear an hearing aid in my left ear due to deafness . The audiologist said it was caused by nerve damage due to M S. Oh the joys of dreaded MS, part of its great plan for us to fall to pieces . Take care. Margaret .
Hi Margaret , thanks for the reply , I guess I’ll have to run it by the GP soon and see if they’ll refer me for hearing tests , I suppose if it ‘is’ MS causing it , it’ll just complete a bit more of my set of sensory losses
Oh yes; no-one knew except me, and a few others years later when we had a good raucous laugh at the situation. It wouldn’t inspire confidence in a professional orchestra if the conductor was faffing about desperately trying to find an ear trumpet!
Hi, I`ve had very little hearing in my right ear for years.
When i was told I had MS, I was sent for tests, but hearing aids didnt help at all.
I have to put up with it. It causes a lot of difficulty for me. I have to see people`s faces as they speak. When there is noise around me, it is horrendous to know where a sound is coming from.
I often feel left out of conversations, as Im always saying pardon, eh?`
Hearing loss is one of the possible symptoms of my ISP.
general noise is a real problem for me too , not just the hearing though , it seems to send the sensory symptoms into overdrive , I always thought it was just a concentration thing , but , when you’re missing bits of the conversation too , it just makes it worse !
I sometimes hate to think how I must appear to other folk , and then other times I guess I’ve just got used to not having my finger on the pulse as they say ? well not got used to it to be honest , just tried to get resigned to it
still b***** annoying though isn’t it ? , I’ve had MS about 8 to 9 years , and sometimes kid myself that it’s part of my life , but some far distant sub conscious niggle keeps reminding me that it’s not how I “ever” was at all !!
MS can go for hearing, but it’s rare. So much so that, if a person is suffering from a sudden worsening in hearing, MS is pretty low on the list of likely culprits, even when the person has MS. Or that’s what I was told when it happened to me!
Mine didn’t fluctuate - I was just suddenly deaf in one ear, pretty much, and that’s the way it stayed until I started IV steroids because I was relapsing all over the place as well as the hearing and it was getting beyond a joke, so I gave in and went for the steroids. The ear started working again on the night after the first infusion. Absolute magic. I have never had such a quick and complete response to steroids, ever.
So it can get better, like any other sort of relapse, with a bit of luck, and I hope you see an improvement soon.
Hi Alison , well I’m still hoping it’s either something else or a short term relapse , I’m in a bit of a relapse at the moment , though it’s hard to tell sometimes because my symptoms don’t seem to go much inbetween , but they definately get worse at will , it’s still a mystery at times to me as to what defines a relapse ,
They always say to me it’s if there’s new stuff , with ‘me’, it seems the multiple combinations of symptoms can vary , which sort of makes it ‘new’ in my book if you know what I mean ? , but sometimes I read what I write myself and get baffled ! x