Search the web
Sign In
New User? Sign Up
LandauKleffnerSyndrome · Landau-Kleffner Syndrome
? Already a member? Sign in to Yahoo!

Yahoo! Groups Tips

Did you know...
Want your group to be featured on the Yahoo! Groups website? Add a group photo to Flickr.

Best of Y! Groups

   Check them out and nominate your group.
Having problems with message search? Fill out this form to ensure your group is one of the first to be migrated to the new message search system.

Messages

  Messages Help
Advanced
Thank you!!   Message List  
Reply | Forward Message #183 of 1721 |
Re: Adults w/LKS

Hi,
My son was diagnosed at age 3 and a half, he has just turned 7. We
tried the Prednisolone after his diagnosis, and this cleared his EEG.
As we reduced the dose, the spike wave activity returned and could
not be controlled again, even after upping the dose again.
What I am saying is that most children only get one chance with
Prednisolone. If it is reduced too quickly, it may not work again,
even if it had previously.
Tai was diagnosed in Paris by a Professor Dulac. His treatment of
choice is another steroid, Hydrocortisone. He also recommends that
the treatment should last no less than a year. Of course he is very
aware of the side effects, but he also knows how devastating this
illness is if it isn't treated. There is a much smaller chance of a
relapse if the treatment lasts for a year. Tai was on Hydrocortisone
for 2 and a half years, his EEG cleared again, and he has slowly
regained his language. We are so pleased with his progress.
I'm sorry I can't be of more help with the IVIG, I don't know much
about it.
Does your neurologist have much experience in treating LKS or other
related disorders? I think its very important that the neuro has
successfully treated it before.
If you would like my neuro's email address for advice, please let me
know, he is happy to respond to other parents.
Sam





Sun Sep 2, 2007 9:40 pm

samcambridge
Offline Offline
Send Email Send Email

Forward
Message #183 of 1721 |
Expand Messages Author Sort by Date

He was diagnosed at 4 and 1/2. At that time we did 3 months of ACTH. After that, we had to start Prednisone. He responded very well. Over the last three...
Sherry Jones
sjones0707
Offline Send Email
Sep 2, 2007
2:50 pm

Hi, My son was diagnosed at age 3 and a half, he has just turned 7. We tried the Prednisolone after his diagnosis, and this cleared his EEG. As we reduced the...
Sam
samcambridge
Offline Send Email
Sep 2, 2007
9:40 pm

Sam, I feel our neurologist is just playing a guessing game with meds for Kyra. First we tried Klonopin, she was on that for 5 mos, and continued to have...
Terry Street
groovy1202
Offline Send Email
Sep 2, 2007
10:26 pm

Terry - The prednisone was our miracle. My daughter, Hannah was on pred at age 7 (She is now 10)for about 9 months ( Iwanted it longer) it has worked for her...
Martha
mrth_ryn
Offline Send Email
Sep 6, 2007
12:59 am

Terry, My son has never been diagnosed with LKS, but what he has (developmental aphasia) is the closest thing to LKS that I can find ANY kind of...
Jennifer Gager
jenngager
Offline Send Email
Sep 6, 2007
4:08 pm

Terry, Since she is so young and having feeding problems anyway, you might want to look into the ketogenic diet. (It worked for my daughter for a year and a...
Lisa Matzenbach
peachannetoo
Offline Send Email
Sep 2, 2007
10:54 pm
 First  |  |  Next > Last 
Advanced

Copyright © 2009 Yahoo! Inc. All rights reserved.
Privacy Policy - Terms of Service - Guidelines - Help