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#1
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#2
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| hi louise, welcome to the forum! this is a great place to find lots of information when your new to epilepsy and support and understanding when the need is there. |
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#3
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| Thanks for your reply CeiliClare (Do i detect a wee bit of Irish there? )I've had a little look around and *gasp* even replied to some threads. It's great that theres forums like this out there, as i didn't really have anyone to talk to about it. At least because of the work i do, there's always trained people around in case i do have a grand mal at work! |
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#4
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| i'm new also, my son was recently diagnosed. the people here seem really nice and super eager to help! i'm a member of cafemom and tried some epilepsy groups and just like every other group on that site no one was helpful, lol. |
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#5
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| Hey there Kristy. I think i read the thread about your son. Parents will always worry, especially with something like this. My mum and dad were so worried (I'm 23!), but also really annoyed at me for refusing help in the ambulance when they picked me up one night. They gave me a good telling off and practically dragged me to the doc's when i would much rather stick my head in the sand. Anyhoo my point is that i really value my parents help and support, and i think your son will too. |