Emma’s been taking her max dose of Keppra for over 2 weeks now. Since Sunday, she’s been having 30-40+ seizures a day. The most she’s ever had daily since they started in May. I feel awful for her. We need to get this figured out. I’m hoping after her neurologist checks her blood levels we can adjust back down to a lesser dose. We are also on track to start her Keto Diet next month. There are so many things that go into that as well and it’s a tedious process just to get admitted to the hospital. Trying to stay optimistic because we need this diet to work. I don’t want to introduce any new meds. I just don’t feel like it’s the best thing to do for Emma. I’m feeling very overwhelmed and stressed about everything. I wish Emma didn’t have to go through any of this. It’s so sad but she is amazing and is still progressing despite all of the seizures and setbacks. She’s truly inspirational. She is the reason I want to be the best mom I can be.