Hi G.R., thanks for helping us keep people informed.
Julie, volunteer webmaster
Epilepsy Foundation of Idaho
http://www.epilepsyidaho.org
> I mentioned on an earlier post about First Aid link on an older post I
> did (which I can't find at the moment). So here's the First aid
[quoted text clipped - 15 lines]
> The FIRST AID Page I like is
> http://www.epilepsyidaho.org/safety/safety3.htm . G./
> I printed the 2 FIrst AId ones when I was first diagnosed to show
> to family etc. and they had it posted for if they ever needed it.
[quoted text clipped - 4 lines]
> The FIRST AID Page I like is
> http://www.epilepsyidaho.org/safety/safety3.htm . G./
Hi Gordon, hi Julie.
After reading your 2 First Aid sites, I was wishing my parents had read it
when I was younger, then my mother may have stopped trying to stuff my
meds down my throat every time I had a seizure, and my father wouldn't
have thought I was possessed in some way!
I was also reading in my "Epilepsy Review", an acclaimed magazine
here in the UK written by specialists in neurology and neurosurgery for
people with Epilepsy and their carers, that there are special helmets
for toddlers aged about 1-3 with epilepsy, called "Thudgaurd" which is
suppose to stop youngsters knocking their heads badly, when they still
haven't mastered the art of walking.
The pic' in the Review, showed that they were cute little pink and blue
helmets, with "Mickey Mouse" type ears on the top. I couldn't find a pic',
or article about them on the web, as they're pretty new, but I did find a
few personal experiences about them, which I thought you might like to
look at if you ever wanted to write a small first aid article for
toddlers, or very worried parents.
http://www.babyblogger.co.uk/index.cfm?fig=comment&bid=81
All the best
Sofie

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