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I'm a 30 year old mum to a beautiful 4 year old daughter. I was diagnosed with epilepsy aged 13 from the start I was advised if I wanted children I should plan for them, as I was told I had higher chances of them having conditions such as down syndrome and cleft lip. In 2019 myself and my boyfriend decided to plan having a child we decided because of all the planning tests extra scans tests during the pregnancy I only wanted 1. In 2021 I fell pregnant with my daughter (she had until her due date/hospital appointment until we gave up). Unfortunately it was the pandemic. We was treated well and yes I had to have extra tests, scans etc and all the way though baby was perfect. However during this time all the information I was given was US based (I live in the UK) which then scared me as how can I trust a system I know nothing about. So from then on I had to trust my gut, from the information I've been given over the years. Thankfully everything went well until I had to have this glucose test thing. I had an experience I've never had before I passed out during this test, again everything was fine. I didn't have a seizure at all throughout my pregnancy. Longest time ever. My labour was simple although I was told to possibly be prepared for a c-section but it wasn't needed. I don't remember much in all honesty. She's now 4, happy, healthy and an attitude to match the family. It's not as scary as you might think I think the best advice I was given was to plan, plan, plan. Then you can have all angles covered. So that's my advice to you

I was induced with this baby as my first had come early. However she took 33 hours to get out. Perfectly healthy and straight to the boob when born.

In both pregnancies my keppra needed to be increased several times during the pregnancies. Frisium was added when I had serious cluster of over 50 focal aware seizures. I was 19 weeks with my first and I had just got married, so quite a lot going on. My keppra was increased then also.