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#1
01-17-2009, 08:37 AM
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Welcome to all the Newbies!  I try to drop into the foyer frequently and welcome people, but I've had a lot going on recently. Anyway! Welcome to our site. Well, technically Mr. B's site, held together with a team of great moderators! I hope you find all the support, answers, and laughs you need. Chime in with a question anytime or simply to support others with your understanding or information. Every member is important and has a place in our community.  Take care, and I look forward to getting to know you all! -Julie 
__________________ "I WILL NEVER GIVE UP ON MY DREAMS; I WILL JUST MODIFY MY PATH FOR REACHING THEM" -j (me) "Life is better left to chance. I could have missed the pain, but I'd have had to miss the dance." -Garth Brooks     |
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#2
01-17-2009, 08:40 AM
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| Thanks for the wonderful welcome S4E This is a great community and I'm enjoying the information and support that I'm finding here! |
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#3
01-17-2009, 09:27 AM
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| Hi Fruity, So glad to hear that you're enjoying the site! I usually try to welcome as many people as possible individually, but as I said, I've had a lot going on recently...so I decided to do a "one-stop" welcome to everyone new/relatively new. It's a pleasure to meet you and I look forward to getting to know you! -Julie
__________________ "I WILL NEVER GIVE UP ON MY DREAMS; I WILL JUST MODIFY MY PATH FOR REACHING THEM" -j (me) "Life is better left to chance. I could have missed the pain, but I'd have had to miss the dance." -Garth Brooks |
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#4
01-17-2009, 09:53 AM
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| Originally Posted by seizures4ever  :
__________________ New to CWE? I suggest reading the proactive prescription and epilepsy 101 threads. Also check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. More great stuff can be found in the list of the best forum threads. Would you like to help support this forum? |
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#5
01-17-2009, 10:36 AM
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| Originally Posted by seizures4ever :
Sarah |
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#6
01-17-2009, 11:15 AM
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| Hi, I've been on this forum for the first time today, and already I'm getting a good response on my thread. I also belong to the Guillain Barre Syndrome Forum in the UK and there I've learned that the best way to get first hand information is from the people dealing with the medical condition. My son unfortunately had to endure Meningitis, Guillain Barre Syndrome and now Photosensitive Epilepsy within 2 years - he is 7 now. Thank you to all you wonderful people. I know that being uninformed one sometimes asks silly questions, but I do believe that you guys will understand and be patient with me/us for the time being. Looking forward to lots of communication! From a lovely warm South Africa!! |
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#7
01-17-2009, 12:51 PM
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It is MY FIRM BELIEF that the only stupid question is the one that remains unasked. So please feel free to ask away. Knowledge IS power......   |
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#8
01-17-2009, 01:41 PM
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| Originally Posted by Meetz1064 :
with Meetz!Welcome Reinardt! I'm so sorry to hear that your family, most especially your little boy, is having so many health problems. Ask any questions you have...if we don't know the answer, we'll try to point you in the direction of someone who may. I look forward to getting to know you. Wishing your family a seizure-free day! -Julie
__________________ "I WILL NEVER GIVE UP ON MY DREAMS; I WILL JUST MODIFY MY PATH FOR REACHING THEM" -j (me) "Life is better left to chance. I could have missed the pain, but I'd have had to miss the dance." -Garth Brooks |
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