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bells palsy longterm effect on me
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I got diagnosed with bells palsy in july 2020. I say its a mild case, it started with a earache, it was the reason i went to the doctor and left finding out it was BP and didnt know i had vertigo, i just thought it was clumsiness. But did seem weird how often my clumsiness was at the moment before finding out i had BP. the 2 main factors i would say was stress and my braces treatment. My left eye can blink on its own now and my left side droppyness isn't nearly as bad as it was in the beginning. People dont notice it. I can still see the slight difference but its improved alot. I still have vertigo and ringing in my left ear. The ringing isnt as bad as it was in the beginning. When any noice would make the ringing louder. Now it can go unnoticeable unless i pay attention to it or its quiet. The left side of my head still feels somewhat numb. And i do have slight twitches that aren't really noticeable. i see alot people saying that twitches are normal in recovery which is a relief to say the least. But one thing i have noticed also is that i have had a hard time controlling my anger now. I get triggered easily and have a hard time getting out of that state of mind while being well aware of it. I wonder if anyone else has had a change in there anger after being diagnosed with bells palsy or is it just me

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3 years ago