Welcome to all the Newbies!

Welcome to the Coping With Epilepsy Forums

Welcome to the Coping With Epilepsy forums - a peer support community for folks dealing (directly or indirectly) with seizure disorders. You can visit the forum page to see the list of forum nodes (categories/rooms) for topics.

Please have a look around and if you like what you see, please consider registering an account and joining the discussions. When you register an account and log in, you may enjoy additional benefits including no ads, access to members only (ie. private) forum nodes and more. Registering an account is free - you have nothing to lose!

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Hi and WELCOME to everyone who is new to CWE! :e:

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. :agree:

Take care, and I look forward to getting to know you all! -Julie :)
 
Thanks for the wonderful welcome S4E :) This is a great community and I'm enjoying the information and support that I'm finding here!
 
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've had a lot going on recently...so I decided to do a "one-stop" welcome to everyone new/relatively new....

Hi Julie, I totally understand. We've had a lot going on at our house as well. It's really great to meet you. I hope you are having a nice weekend! :)Sarah
 
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!!
 
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......:pop::woot:
 
MY FIRM BELIEF that the only stupid question is the one that remains unasked. So please feel free to ask away. Knowledge IS power......:pop::woot:

:agree: 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. :e:

I look forward to getting to know you. Wishing your family a seizure-free day!
-Julie :)
 
Thank you for the welcome

It's good to go somewhere where people understand.

The world can be a lonely place when you have a problem like this.
 
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