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Reply | Forward Message #11 of 1721 |
Hello everyone,

I am surfing the internet looking for support groups and info on LKS.
My daughter is 3 1/2 and was diagnosed with LKS in May 2006. Her
receptive and expressive language has all but disappeared. Her EEG
continues to get worse, instead of better - even though she is on a
cocktail of Epilim, Lamictal and Prednisolone. The steriods are
really playing havoc with her behaviour, so much so that we are now
seeing a child psychiatrist and we are also considering medication to
curb her aggression, sleep issues, hyperactivity etc.

I feel like we are travelling a very long and lonely road here and the
end is no where is sight.

I would love to hear from anyone with a kind word and sound advice.

Peta







Thu Sep 21, 2006 9:46 am

bptl4
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Message #11 of 1721 |
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Hello everyone, I am surfing the internet looking for support groups and info on LKS. My daughter is 3 1/2 and was diagnosed with LKS in May 2006. Her ...
bptl4
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Sep 21, 2006
9:52 am

Hi Peta, I'm Sam and I live in England. My 6 year old son Tai has LKS. Tai was diagnosed in April 2004, he was also 3 and a half. By the time he was diagnosed,...
Sam
samcambridge
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Sep 22, 2006
9:43 am

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

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

Hi Sam. Thanks so much for replying to my post. I am also a member of the LKS Australia yahoo group -however it is not a very 'active' group. Taylor was...
Murray, Peta E
bptl4
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Sep 22, 2006
10:58 am

Hi Peta, First of all, thank goodness you have a paed who is so on the ball. Most children take years to be correctly diagnosed. You have that in your favour,...
Sam
samcambridge
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Sep 23, 2006
1:09 pm

Hi Sam, Wow, I had no idea that the steriods were a 'longer term thing'. I was originally told 6 - 8 weeks! I find that the doctors here, although wonderful,...
Murray, Peta E
bptl4
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Sep 23, 2006
10:35 pm

Hi Peta, Thanks for your call recently - please try again, anytime from Mon 25th onwards; am home during the day this week. Am keen to find out more details...
Lee
pandafreakk
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Sep 23, 2006
11:15 pm

Hey Lee, Yep - will call when I have a quiet moment. Chat to you soon. Peta ... From: LandauKleffnerSyndrome@yahoogroups.com on behalf of Lee Sent: Sun...
Murray, Peta E
bptl4
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Sep 24, 2006
3:58 am

Hi Peta, Yes, a lot of neuros prefer the short term treatment, the only problem is if the activity returns afterwards. Sometimes it can't be controlled twice...
Sam
samcambridge
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Sep 25, 2006
10:57 am
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