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something specific?

Hi guys I’m thinking of joining speech and debate in college to help with my speech and stuttering more but idk if will actually help because with that I’ll probably start stressing about it? Or not?

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!

Is it the volume of my voice or my family needing hearing aids??? Anyone else I have thoughts? https://www.nationalmssociety.org/understanding-ms/what-is-ms/ms-symptoms/speech-problems#:~:text=Speech%20Therapy%20for%20People%20Living%20With%20Multiple%20Sclerosis&text=They%20can%20also%20teach%20...

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... :/

Lately I have been like choking on my words and then can’t think of what to say or what I’m trying to say. How do you guys help with that?

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...

I am a teacher but my speech is so slow. I haven’t seen a speech therapist. I am not stable and get shaky. Cannot run anymore but Dr says stable no new lesions.

* this post is for any one who’s COMPLETELY lost their ability to speak * How long did it take you to regain - I’m slowly coming back

Who has lost their ability to talk after a flare? Did you get it back? And how long.