I will see my neurologist at the MS Clinic tomorrow for the first time since I had my CCSVI treatment. I'm not sure how to handle the response I'm sure to receive. Have suggested to my atheist husband that when the neurologist belittles my dramatic results that I should say that if it is not the CCSVI it must be the power of prayer. He is sure the doctor won't buy that either.
I have been lessening the medication I take for the spascity in my legs with no return of symptoms. I'm sure the doctor will find some other reason, like remission after a two year relapse. I'm sure there will be a good story to tell tomorrow.
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