We ended up speaking to a friend who is in the neuro industry and she said that we definitely shouldn't be waiting until march. She is still so young that it could be affecting her developing brain so we ended up going to emergency and were seen by a paed who referred us to the neurologist at the children's hospital. We have an EEG appointment on Thursday. The doc in emergency confirmed it was epilepsy but can't say it's absence seizures only until they get the brain activity analysed. I'm very nervous but fingers crossed it will be easy to address. The frequency and severity of them have gotten worse this week so I'm glad we decided to take action now rather than wait.
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