http://klsfoundation.org/kleine/forums/ KLS Foundation Discussion Forum en Copyright 2008 2008-10-23T10:47:41-08:00 http://klsfoundation.org/kleine/forums/viewthread/72/ http://klsfoundation.org/kleine/forums/viewthread/72/#When:10:47:41Z <p>My daughter, Alanna, was featured in a British Documentary that aired in July 2008. We would like to offer a copy to any of you seeking more information on this illness. Many people have commented that it was helpful and informative. Many have used the documentary to show to teachers, friends, family, doctors, etc. to help them understand what a KLS sufferer goes through. If you would like a copy of the documentary, please contact Diane at rwong2323 at comcast dot net. Hope all is well. </p> 2008-10-23T10:47:41-08:00 http://klsfoundation.org/kleine/forums/viewthread/48/ http://klsfoundation.org/kleine/forums/viewthread/48/#When:08:07:20Z <p>Here is the url to Tanis’s KLS Forum.&nbsp; It is another great place to connect with others with KLS.</p> <p><a href="http://klssupport.proboards100.com/index.cgi?board=kls">http://klssupport.proboards100.com/index.cgi?board=kls</a> </p> 2008-05-16T08:07:20-08:00