KLS Support UK - Helping families affected by Kleine-Levin Syndrome


Please note that anyone who suffers from KLS or thinks they suffer from it should consult a doctor who is experienced with dealing with the condition. The information included on these pages is intended to be useful to patients and doctors but it is no substitute for skilled medical advice. The same caveat applies to any pages to which this site is linked.


Information (including personal data) submitted by individuals via our website will be collected, used and retained according to the principles laid down in this policy and in line with other policies of KLS Support UK. KLS Support UK reserves the right to amend this privacy statement and, if this is the case, will post notice of any changes on our website. By entering KLS Support UK's website you will be deemed to have accepted such changes.

Any information we obtain about you will not be used for commercial purposes.

KLS Support UK are not associated to any other UK websites and at present are only linked to the KLS Foundation of America. We do not endorse any other websites or individual. Any harm which may arise from reports made of the event by anyone outside KLS Support cannot be held attributable to KLS Support UK. KLS Support UK comprises of the Trustees.

Thank you to Morguefile for the use of some images.

Please make contact using KLS Support UK's Contact Us form. Thank you.