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SOD and Botox Kathleen

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I haven't posted in some time now and I will be the first to admit I'm

a " lurker " more than a " poster " most times. However I have been

reading in recent posts about Botox being an option for SOD and that

you may have some info about that.

I have more pain from SOD than I do from CP. I have been using

Nitroglycerine under the tongue when mine gets really spastic and the

pain becomes more than I can bear. Of course it works 90 percent of

the time and leaves me with a splitting headache EVERY time. I have

spasms daily, sometimes multiple times daily. Most often in the early

hours of the morning when I would rather be sleeping. Today is a good

example of the multiple spasms. Of course (as discussed recently

here) I am just before starting my period and everything associated

with SOD and CP becomes worse.

Please share any info you have on Botox. I would greatly appreciate

it.

Thanks

Zoie

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