Guest guest Posted September 30, 2011 Report Share Posted September 30, 2011 We had another and she is a fine. We waited 5 years because we tried to find out what had gone wrong for Finlay, but no one could give us an answer. We had fetal MRI's, but PMG does not show until after 26 weeks, so they are really only a way to prepare you is things go wrong. In our case, the doctors were a bit out on the dates (not an exact science) and kept telling us that the baby's brain was underdeveloped. Not exactly what you want to hear when you already have a child with a migration disorder. As it is Rowan is a bright and healthy little girl. Annelies Mum to Gregor ,13; Finlay BPP, 10 and Rowan ,5 RE: seizures and medication Kat, Has the doctors considered Ketogenic diet? The neuro is going to have to recommend the vit b6 dose. Nisha takes 50 mg liquid. Since the B6 she is no longer has mouth sores, she seems more focused and no seizures but it may all be in my head. Diane Quote Link to comment Share on other sites More sharing options...
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