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#1
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#2
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#3
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| thanks for the support. it is hard to deal with but your right, I agree wth what your saying: I am actually come to the reality of Me having epilepsy does not affect my dreams and goals in life. Im trying hard to fulfill my goals all the while treating my little problem. Thanks again. *Rose |
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#4
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| Welcome to the forums, Rose. My name is Jon. Its good to have you here. |
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#5
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| Hi Rose, welcome to the forum. ![]() If you are newly diagnosed (or about to be diagnosed) with epilepsy, I'd recommend reading the epilepsy 101 thread.
__________________ 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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#6
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| Hi Rose! Just a quick note to say hello and welcome to the forum! |
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#7
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| Welcome Rose Make yourself at home. CWE is one of the most interesting and helpful sites I know of.
__________________ |
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#8
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| thanks for making me feel so wecome, i took the time to read the epilepsy 101, it actually gave me better perspective on how to view myself as a person with epileptic seizures. Thanksa again you guys *Rose |
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#9
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![]() Welcome Rose. You hit the bullseye. "You are a person with epilepsy" Please don't forget that. Each of us is so much more than an epileptic (I don't like that term). I look forward to supporting you and helping you find answers, however I also look forward to learning a little bit about you. We all bring something new to the table and you never know when your experiences may help someone else. The central staff here is very helpful, but sometimes it is the 'newbies' that can offer a little more insight just because of their history with E or a certain medication. Welcome again. I serve the coffee and hot chocolate around here. |
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#10
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| Hi Rose WELCOME Glad that you decided to join CWE. |
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#11
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