craftygurl
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Just wanted to introduce myself. I live in Sanger, CA (teeeeny town in Central CA) and was diagnosed 3 yrs. ago with "generalized epilepsy, it's no big deal" (that was my neurologist who said that). After going round the bend with him, I switched about six months ago and finally got a descriptive diagnosis from an epileptologist of Juvenile Myoclonic Epilepsy. I also have t/cs that go along with the myoclonic jerks (lovely).
I am having a hard time right now, because after 3 yrs. of testing/changing meds, changing my diet, cutting out activities/stress/whatever and turning into a vampire vic from all of the blood tests, I have just been informed that my condition as it stands is about as good as I can expect it to get. Apparently meds/diet/exercise will not control my JME. It came as quite a blow, especially as I was also told that I really should not be working because of the stress. I'm pretty bummed and everyone that knows has been "poor thing"ing me to death, which I hate so I've stopped telling people.
Anyway, sorry for the drag. This looks like a good website (sorry, I've lurked while waiting to be approved ;P) and everyone looks really supportive and nice.
:dontknow:
I am having a hard time right now, because after 3 yrs. of testing/changing meds, changing my diet, cutting out activities/stress/whatever and turning into a vampire vic from all of the blood tests, I have just been informed that my condition as it stands is about as good as I can expect it to get. Apparently meds/diet/exercise will not control my JME. It came as quite a blow, especially as I was also told that I really should not be working because of the stress. I'm pretty bummed and everyone that knows has been "poor thing"ing me to death, which I hate so I've stopped telling people.
Anyway, sorry for the drag. This looks like a good website (sorry, I've lurked while waiting to be approved ;P) and everyone looks really supportive and nice.
:dontknow: