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Mine has cleared - I had to tape up my eye at night and do some face exercises. Its a case of IMAGINING that part of your face moving - that way tiny muscles will actually be working even if nothing appears to be moving. I think it took about 3-4 weeks to get moving again.
I am now researching my nerve problems connected with overload excitary nerves (I got my Bells day after trying an electric toothbrush) avoid mobile phones as they are proved to excite the brains cortex and naturally will excite the nerves (yes that would be good to get moving but in this case it may be too much excitement)
Good Luck and don't worry it's not life threatening or disabling.
The Slug
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thank you.
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Please contact:
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My son is one year old and has BP but his eyes blink its just when he's crying you can tell that he has it. It happen over night I was so upset I didnt know what to do I cried and cried but he has seen the doc and the report was good news cuz it could have been worst so I thank the man up above just hold on and have a little faith
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My name is Sandra . I had Bell's palsy at the age of 12. It lasted for long time. I was eventually taken to an ENT where I received electric shock treatment to my face to stimulate the nerves. It cleared up lot after much treatment Im now 54 years old . Every now I then I still get that facial twitch or. slurred speech, and a slight crooked smile.
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I just thought I would share my story with BP. I was diagnosed at the age of 3 and was told I would most likely only have it the one time. I did not however, I got it again at age 6, at age 9, and once again at age 13 for a total of four battles with it. Mine came on so quick the first time my parents did not know what to do as I was fine one minute and when I turned around the next I had it. I do not however remember this as I was only 3. I also don't remember it from when I was 6 either. I do remember what it felt like coming on though both when I was 9 and 13. At first it felt like little needles were poking me in the face then my face felt funny and started jumping. Soon after that I stopped feeling just about everything on that side of my face and I stopped tasting things too. My eye would not close so I had to wear an eye patch as well. The physical pain however was not as bad as the pain of the other kids laugh at me and calling me names. I am now 18 and understand that having BP is not the worst and I could have been sicker as a kid or I could have had something worse. My cases have lasted from 3-4 months up to almost 9 months when I as 9. I have had it switch sides between cases as well. The best thing I know to do for it is rest and un-stress to relax. Also if your child has it the best thing to do is treat them like normal because just because they look different on the outside doesn't mean they are different on the inside. a
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