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#1
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hi im a new girl from iraqhello everybody, im from Iraq. i was diagnosed with epilepsy 4 years ago since then im taking tegretol. you know its difficult for someone with this disease to live in this country cause people think that you are kind of crazy. i recently found this website, its good to know people that have the same problem cause im not comfortable about talking with my friends about it. sometimes like the last 3 days im very depressed, i dont know weather it has something to do with my disease or its just because im watching too much tv and see these famous people. im really about to get crazy. |
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#2
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| Hey, welcome! I'm new here too and already I feel more more comfortable here about my epilepsy with complete strangers over the internet, than I do with my friends. You will find some very good advice here! Hang in there |
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#3
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| Welcome to CWE Board. If you ever have a question or something to say just post it and I am sure someone will respond. You will feel comfortable here talking about your Epilepsy. Everyone here knows what it is like. Nice meeting you. Take care
__________________ "Do what makes you Happy, Be with who makes you Smile, Laugh as much as you Breath & Love as Long as you Live." |
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#4
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Welcome to CWE![]() Come and visit our site often. We are a growing dinner party of people who can usually relate to each others problems. Even the most unique situations always seem to find a match here. Please feel free to post any questions you may have and don't hesitate to vent your frustrations. We are very non-judgemental and try to support all. Epilepsy and depression seem to go hand and hand for many different reasons. Sometimes it is due to medication and other times simply due to the fact that we can't live a normal life. When you are more comfortable with the site, I am sure many of us would like to hear more about you and where you live. But you can share that when you want (or never if you wish). ![]() |
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#5
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Hi thereJessica, it's nice to meet ya! I see Buckeye's already been here with his YUMMY coffee! ![]() This is probably the BEST site to be....Mr B has made us an AWESOME home here, so feel free to check out all the nooks and crannies......the Library, the Padded Room, Speber's Auditorium, the Kitchen......and more. Kick up your feet and stay awhile, why don't you? I'm sure you're going to find quite a few friends here. And guess what? We do understand how you feel, too.......really, we do. Take care, Meetz ![]() |
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#6
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| Welcome to CWE Jessica. I'm glad you found us! -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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#7
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| Jessica - Welcome to CWE It is still hard for me to discuss this disorder with many people because they just don't want to understand. Most are just self absorbed. I hope that you find CWE a safe spot to visit occasionally.
__________________ Robin Neurofeedback - Rebecca's Story Feedback Matters- blog Knowledge is power and knowledge shared is power multiplied. -- Bob Noyce |
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#8
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#9
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| Welcome to CWE ![]() It's a top place Mr. B. has made here - loads of info, and friendly support. It's a great place to talk, especially if you can't with friends...got to remember it can be hard for them too...the one's who are worth it will stick around and will come to support. We all need time to adjust and cope. Hope you find what you need here, I'm sure you will |
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#10
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| Hi Jessica! Welcome to CWE. As you can see, a nice group of people. So feel free to ask questions, vent, or just chime in.
__________________ "Watch your words, for they become actions. Watch your actions, for they become habits. Watch your habits, for they become character. Watch your character, for it will become your destiny." Epilepsy 101 |
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#11
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| Hi Jessica I also find it really hard to talk about my epilepsy, I cannot stand people to judge me because of it, a person has to really earn my trust for me to let the big E out of the bag and if they stick around then you've found yourself an understanding ear, if they run away, then they were not a true friend to begin with. I have had absence seizures for 20 years, but despite trying several meds they remain uncontrolled and happen daily, I am currently taking Lamictal. The Crazy Monkey
__________________ "Be What You Are" - Stiff Little Fingers Lyrics |
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#12
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| thank u very much you guys for this warm welcome ![]() |
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#13
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| welcome to CWE ! ![]() Feel free to vent , ask any questions you want, joke, whatever. C u in the forums !
__________________ Dr. Arvind Ramaswamy |
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#14
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| I Jessica, This is a really great place to be. You'll find support from everybody and find out stuff you didn't know that's so helpful. Welcome! Jan |
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#15
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#16
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| Aloha Jessica, and welcome to our home. Here you will find all things that nourish the body and the soul of those who live with or love someone with seizures. It will keep you warm, and fill you with acceptance and information. You will emerge a better patient and a better advocate for your own health. You will also find validation for many things that a doctor never asks or we might not volunteer so as not to appear 'nuts'. Enjoy this group and know that you are among many here. ![]() |
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#17
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| We're so glad you found us, Jessica! You will be accepted and supported here so stick around! |
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#18
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WelcomeI can say that in the very short time I have been here the support has been so wonderful. We have been living with E with our daughter for 17 months, and for all that time I did not have CWE. Thankfully my best friends Laura sent me here.......everyone here is comforting and wonderful. The resources are beyond imagination. ~Ryn |
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#19
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| Hi, I'm a new girl!! | Yorkie | The Foyer | 16 | 09-19-2008 03:06 AM |
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| New Girl In Town!!! | epiphanyd | The Foyer | 11 | 11-10-2007 07:42 PM |