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Originally Posted by spongebobgamma
That must of been really scary, I know my first thought would of been stroke also. How are you doing now?
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The day I realized what was going on, I scoured the Internet for information. I was particularly interested in what folks who actually had had Bell's palsy were saying. And most importantly, if this is curable.
I couldn't taste food. No matter what I ate or drank, everything had an extremely unappetizing flat, lead taste. My taste buds just gave out. I couldn't hold water in my mouth, especially when I gargled after brushing my teeth. It was exasperating.
When I went to see the doctor in a private clinic, I described to him what I had and he started to conduct a few tests to confirm the situation. He then concluded that I did have the symptoms of Bell's. He prescribed Prednizone, (a steroid) and sent me on my way. He also gave me a referral letter to get an EMG feedback from the hospital.
That night, I printed out a diagram of muscles which I got from the Net and asked my husband to help massage my face. Well, I need to start with some exercises to get my nerves healed other than wait for the drugs to cure me, right? This helps me learn to isolate muscle actions as well as coordinate multiple muscle movement. Regaining balanced, symmetrical movements is key to restoring the face as it was before. Also, I use my favourite Bel'Air aromatherapy Bois de Santal oil which helps to relieve tension and improves concentration of mind. PLUS, with lots and lots of prayers...
It woke me up to the fact that I'm not invincible to rare things, as much as every person would like to believe think that they are.