CQ:)
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I'm the same Valerie. Before my surgery when I had appts with my neurologist I would go through my seizure diary (a notebook) & type up any seizures I had since my last appt with the neurologist. I would also put on the document what meds I'm on & the dosages. I would then print it out to give to him.I keep a seizure diary and type out all the seizures that I've had between visits, what I did during them and how long they lasted. I've also got on it all the meds that I'm taking (epilepsy and others) and any other dr visits that I've gone to and what for. I just give it to the neuro at the start of the visit and he reads over it. He's never said that it's too much info and I see that he's got them all in the folder that he has for me.
I print out a copy for me too and put it in a folder that I have. It's easier to answer questions that he asks and he's asked questions about things that I've got on it too.
When I did see the neurologist I found it much easier to hand him the print out instead of trying to remember the seizures I'd had. He never minded & would read through the print out while I was in with him.
When my neurologist referred me to an epitiologist I typed up my whole seizure diary of all my seizures from 2002 - 2010 & my history of epilepsy as a baby.
It took me ages to type it all up & think it was about 12 pages long :roflmao:. When I met the epitiologist I handed him the printout of my entire epilepsy history. He was fine with the printout even if it was really long lmao.