Can I depend on the neuro to see and hear me?
I have been fighting with fatigue for my entire MS life, and the increased meds for pain have given me increased fatigue, so the neuro gives me more drugs to block the fatigue.
More off lable "speed" and sleeping pills to keep me knocked out at night instead of THINKING
Maybe the increased "speed" has started working.
The latest MRI has come back with no change since last year, but last year I had a NEW spot on my brian.
On the temporal lobe.. which he assures me is no biggie.
I am begging to differ...
Google shows many articles about memory and such in regard to these spots on the temporal lobe..
My memory and function is in the toilet
Time to find another doctor???
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