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#1
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#2
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Hi and welcome Welcome to CWE! You've found a wonderful place to be! Mr B (aka Bernard) has built an awesome home for all of us to hang out in. RobinN's a wonderful source of all sorts of information, and Buckeye makes a wonderful cup of coffee. He should be by with it soon. Just don't ask TeeTee or Speber to make you any steak......(inside joke)......they'll claim to be incapable.....BirdBomb is quite the jokester as is CQ..... I've included a couple of links that you should go check out to get some more information. And feel free to ask any and all questions that you have, and if you need to rant or rave, well, we have the Padded Room for that. http://www.coping-with-epilepsy.com/...lepsy+101.html Alternative Treatments/Therapies for Epilepsy? Welcome! ![]() |
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#3
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| Hi Susan - Welcome to CWE My daughter is 16 and has had seizures for the last 2 yrs. We are getting a handle on them lately though. It is so exciting. My daughter has a heterotopia and yet she is still gaining control. She has a brother with high functioning aspergers. Did you know that neurofeedback works for both seizures and ADHD? It is an amazing therapy. Glad you joined us. Put your feet up and read a bit, jump in when you feel like it.
__________________ Robin Neurofeedback - Rebecca's Story Feedback Matters- blog Knowledge is power and knowledge shared is power multiplied. -- Bob Noyce |
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#4
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#5
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| Hi Susan! Welcome to CWE. |
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#6
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| Hello Susan! Welcome to CWE. I am sure you will like it here. You will meet alot of wonderful people. Take care and Enjoy!
__________________ "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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#7
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| Hi Susan, My daughter is fifteen. Two years ago, for the first time, she had two major seizures. I also found out from her that she had had several other ones when she was much younger, but that they were smaller ones, and that she simply had not thought about mentioning them to me. Well I took her to the doctors and eventually to the best neurologist in my area (people come from all over the world to see him). They ran some overnight test, which confirmed that she was having grand mal seizures. They prescribed some medicine for her. These had several side effects; mostly negative. Yes her seizures were reduced but her mood had drastically changed. She was sad and crying all the time. We went back to the doctors and they prescribed something else which made her lethargic. She would tell me that she felt as though her brain was in a fog. But the worst thing is that, if she skipped the pills just one day she would have a seizure. I felt that that made her a slave to those pills for the rest of her life. That was not OK with me. At that point, I decided to take things in my own hand and I went on the Internet to get more information. I found many sites with various suggestions, but none seem solid or based on measurable evidence. Than I found a site were the bloggers were discussing the use of Epson salt (sorry I don't remember the address). I also found a discussion on B6 and grape juice. I liked what I read about these three things and I decided to try them. That was six month ago and my daughter has not once had a seizure. Not only that, but she feels great; she has a great energy level, she's not brooding, she is fully active in sports again, and the best thing is that if she forgets (as all good fifteen year olds will) to take the medicine for a few days, she does not have seizures. My daughter takes half a teaspoon of Epson salt every morning. She drinks three cups of grape juice a day, sometimes only two. And she took 100mg of B6 a day. As taking too much B6 is not recommended, I stopped the B6 about two months ago. I will probably start it up again in three months, at half the dose. But now she continues to take her Epson salt and grape juice. This recipe works great for her; look into it. Last edited by adeline; 07-20-2008 at 06:18 AM. |
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#9
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| Hi Susan I joined the group recently myself, everyone is so friendly and helpful, I am sure you will find the support you need here, just like I have. I have been an uncontrolled Epileptic for about 20 years, I was diagnosed at the age of 10, unlike your son I had no support from my parents, they ignored the fact that I had E and offered me no help or advice, I always think it is brilliant when I see parents on this forum seeking ways in which they can help their children. Take care Kim |
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#10
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#11
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similar birth
I was on phenobarb, and Zarontin, Now I am diet controlled. |
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#12
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| Hi, Susan. Welcome to CWE. I'm pretty new here and have found this forum to be a blessing. I was diagnosed with epilepsy when I was 20 (and 9 months pregnant). I have complex partial seizures (I just seem to space out, sometimes lose track of what I was saying, etc). If I can't stop them, the progress to a generalized tonic-clonic seizure. Looking back, I probably had the complex-partials for years, though they weren't severe, and I didn't know what they were. My son was O2 deprived at birth, due to all the meds they pumped into me. So far he hasn't shown any signs of E Anyway, I think it's great when a parent takes a proactive step in their child's care! You'll find lots of support and information here.![]() Morgan |
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#13
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| Hi Susan, welcome to the forum.
__________________ 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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#14
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Susan!Another Texan onboard in CWE! Welcome! Make yourself a home here! |
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#15
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