ANDI ORANSKY: I take medication one time a day. I used to take medication three times a day, but I hated taking it and remembering each second.
ANNOUNCER: Treatment still requires adjustment.
ANDI ORANSKY: It makes me think slower and work slower, but I can do the work like any other person.
FERN ORANSKY: Even if there is side effects, I'm used to it, and that's just her at this point, and I don't even know what she would be like without medication.
ANNOUNCER: For Andi, monotherapy works, but that may not always be the case.
TREVOR RESNICK, MD: Adjunctive therapy implies that what you're doing is you're adding on a second drug. So instead of the patient being on one drug, the will be on two drugs. And sometimes we need to do that.
ANNOUNCER: Now Andi's limitations are few.
TREVOR RESNICK, MD: Common sense would tell you that you don't them to go mountain climbing, you don't want them to go deep sea diving and you don't want them to go bungee jumping. Now can they play football? Absolutely. Can they play tennis? Can they go bicycling? Yes.
MICHAEL DUCHOWNY, MD: I stress to all the families that the children should be treated no differently.
ANNOUNCER: Research on epilepsy continues. Stem cell and genetic therapy hold future promise for this difficult disease, but for now Andi Oransky is right where she wants to be.
ANDI ORANSKY: A lot of my friends know the condition of what I have, meaning epilepsy. And none of them care. All of them treat me the same as everyone else.