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LandauKleffnerSyndrome · Landau-Kleffner Syndrome
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Messages 20 - 51 of 1570   Oldest  |  < Older  |  Newer >  |  Newest
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20
Hi all.... I have written before, and I apologize for always asking so many questions and the same questions to boot!! I just never feel like I have all the...
Jennifer Gager
jenngager
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Nov 1, 2006
6:40 pm
21
Hi all, Just wondering if any of your children have been prescibed this drug? Did it assist with behaviour management and sleep problems? What were the side...
bptl4
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Nov 2, 2006
8:46 am
22
Hi Peta, CJ has recently been prescribed this for head banging behaviour when he becomes frustrated. He takes 0.25ml (tiny dose) at night. He was originally...
Lee
pandafreakk
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Nov 2, 2006
11:14 am
23
I don't see how 24 hours could be overkill. I haven't kept up with the posts too well here, but yours stuck out. I know my sister at one point had a 3-day...
Michelle
mianhi63
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Nov 4, 2006
10:00 am
24
We are going in for our second 5 day EEG at UCSF. I agree that you should push for at least an over night or more. Alany...
ajh1
bbmeridian
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Nov 4, 2006
6:01 pm
25
I agree. A one hour is not enough time. Especially on the chance that your child doesn't fall asleep or is only on the verge of sleep. We had to go through our...
Gina S.
donabug2001
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Nov 4, 2006
6:19 pm
26
Hello. My son, Will, was diagnosed with Autism in April. I still do research and read books. I cam across LKS. I am just wondering if Will could have that...
Beneal
benealhankam...
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Nov 8, 2006
5:41 pm
27
Hi Beneal, The first step in getting an LKS diagnosis is to get a sleep EEG done, preferably overnight. This will show up the spike and wave pattern that LKS...
Sam
samcambridge
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Nov 28, 2006
11:49 am
28
Hi everyone! Hope y'all had a good Thanksgiving! :) I was just wondering what kinda of experiences you've had with Lamictal? My LKS dd is currently on...
Andrea
andrea_hochs...
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Nov 29, 2006
7:00 pm
29
I have also posted this on 'Rare Epilepsy Groups'page, so please forgive me if I have caused your mail box to overflow! Hello Everyone, We received great news...
bptl4
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Feb 15, 2007
10:39 am
30
Hi Peta, Congratulations, that is fantastic news. We were in your exact position 2 years ago, and I posted all the same questions that you have! I admit I...
Sam
samcambridge
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Feb 15, 2007
11:27 am
31
Great News! Lee bptl4 <murray.peta.e@...> wrote: I have also posted this on 'Rare Epilepsy Groups'page, so please forgive me if I have caused...
Lee
pandafreakk
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Feb 15, 2007
11:56 am
32
Hi Sm, Thanks so much for your response. Taylor has beeen on steriods for 8 months and the neuros are talking about weaning her off slowly over the space of a...
Murray, Peta E
bptl4
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Feb 15, 2007
8:26 pm
33
Hi. I was looking for information on LKS and came across this group. A little bit about how I got here...My son was a normally developing little boy until just...
Kim Castaldi
rkcastaldi
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Feb 18, 2007
3:08 am
34
Hi Kim, Welcome to the group. You say that your son had a sleep deprived EEG, was he actually asleep during the EEG? Kids with LKS will have an abnormal...
Sam
samcambridge
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Feb 18, 2007
5:16 pm
35
Thanks for the e-mail. He was asleep but they gave him something for it and he woke very quickly after 20 minutes so he definitely wasn't in a deep sleep. We...
Kim Castaldi
rkcastaldi
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Feb 18, 2007
8:16 pm
37
Hi Kim, My son Tai was developing normally until about 18 months of age, when he developed some obsessive behaviour. We had just moved house and I was...
Sam
samcambridge
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Feb 19, 2007
6:17 pm
38
I want to thank everyone for all the great information. We just came back from Ft. Worth and my son's EEG was normal even overnight. So no LKS. Thanks...
Kim Castaldi
rkcastaldi
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Feb 22, 2007
10:34 pm
39
Hi Kim, I'm pleased that your son hasn't got LKS, but did they give you any idea of what could be causing his loss of language? It sounds so much like LKS,...
Sam
samcambridge
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Feb 24, 2007
5:43 pm
40
At this point they are saying PDD with possible migrane headaches which are causing his "spells". I agree that it sounded so much like LKS. That is why I am...
Kim Castaldi
rkcastaldi
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Feb 24, 2007
6:35 pm
41
Kim, I'm glad you are staying with the groups, please keep us updated on how things go. I hope you get a diagnosis soon for Vinnie. I know how hard it is when...
Sam
samcambridge
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Feb 26, 2007
6:17 pm
42
Is there a designated ribbon or anything that we can use for LKS Awareness? Missy- SAHM & Angel to Warrior Michael!! I am who I am because that's who I am, ...
Melissa F
zbetasmom
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Feb 26, 2007
11:20 pm
43
I am looking for anyone that would like to share some info on Landau Kleffner. As far as child's behavior, types of seizures <if any> and anything else you...
toadally_froggy
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Apr 7, 2007
2:39 am
44
Hello!! Let me know if I can help. My 8yr old son was diagnosed August 2005 with LKS. He is also on the autism spectrum and the behavior---OH MY!!! We have...
Melissa F
zbetasmom
Online Now Send Email
Apr 7, 2007
10:23 pm
45
Hi, My 6 year old son Tai was diagnosed 3 years ago with LKS after losing all language, receptive and expressive. He never had an outward seizure though. His...
Sam
samcambridge
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Apr 8, 2007
10:10 am
46
... seizure ... or ... Thank you for responding! Kerry has taken Lamictal, Depakote & Depakene, Carbitrol, Clonipin, Keppra, Topamax, along with a few others....
toadally_froggy
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Apr 9, 2007
12:17 am
48
Hi, Tai also used sign language for a long time to communicate. But, as his language has slowly returned, we never or rarely use it anymore. Have any of these...
Sam
samcambridge
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Apr 10, 2007
10:10 am
49
... Kerry is not on any med's right now. She has never had a clear EEG. I am looking for a new nuerologist now. I dont feel they are doing enough for her. Her...
toadally_froggy
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Apr 11, 2007
1:17 am
50
Sedona is on a extremely low dose of valium for her seizures (6mg 2xd). She did terrible on the meds and great off them so we have decided to stop most of her...
Gina S.
donabug2001
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Apr 11, 2007
4:13 am
51
Hi my son just turned three and five mos ago he had his first seizure. An EEG showed he has characteristics for LKS although his neurologist is hesitant to...
stacmonroe
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Apr 12, 2007
6:23 pm
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