Monday, July 01, 2013
Need to start taking these in an effort to try to help with the nerve pain in my face. Lots of fun feeling like your face is on fire :p My MS nurse says that it is Trigeminal neuralgia. I can't even pronounce that :p
Another invisible symptom to add to the list. Most of my symptoms, the average person can not see, which does of course cause the usual looks and whispers behind my back that I am perfectly fine. I am very vocal about the fact that not all disabilities are visual, there are so many that you cannot see but they still effect a person. I just wish more people realized this and didn't immediately jump to conclusion that a person is making everything up.