Hi Guys
been told by docs regarding my MS that my speech is slurred
i dont see it at all nor my mum. I’m fine !! i believe anyway
anyone else speech due to MS affected?
Mine is not at all but 2 Neurologists have said it in their notes!
Does anyone struggle with their speech at all? I always tend o stumble across my words and end up choking a lot of the time.. and it always seems to happen when I'm talking to people I don't really know, its getting embarrassing... :/
Hi,
I was just wondering if anyone has had their speech affected by there ms? I’m currently going through a phase where my speech is quite slow and stuttered and I was wondering if that was common with the condition??
I really hate the way my speech is affected. It makes me feel stupid & thick @ totally inadequate. It's such a struggle to get my words & sentences out. It worries me that if I have this already after only 11 months & still undiagnosed how the heck I am gonna cope with god knows what els...
Hey hey! For The last couple of months, I feel like my speech has been horrific. when I talk it comes out mumble jumble, I get stuck on words ending up stuttering, and lastly my words don’t ever seem so sound close to English 😂. Answering simple questions, I seem to take a lot longer to think and ...
Got my first appointment 1st April. As had some issues around swallowing and coughing. Just wondered if anyone else has had this appointment and what to expect like do they put anything down your throat 🤣😂.
Thanks.
I have noticed over the past year that my speech is somewhat labored, and I find myself struggling to find words where and feeling as if I have a mouth full of marbles. Anyone else have their speech impacted?
It’s been 32 days since my last flare up off my speech from the day it started and have now got the same problems again, I was fine in the morning but my voice changed at work today. I’m on my period and have had a lack of sleep and poorly. I’m so worried that I not going to get the right help becau...