KLS Support UK

KLS Support UK was started in 2011 by three mothers of children suffering from Kleine-Levin Syndrome (KLS). They are an independent UK based group and, as well as having produced a leaflet on KLS, they aim to:

  • Provide support to UK families affected by Kleine-Levin Syndrome and help them make contact with each other for mutual support.
  • Raise awareness in the UK of Kleine-Levin Syndrome.
  • Support medical research with the aim of finding the cause, treatment and ultimately a cure for Kleine-Levin Syndrome.

Last updated on 11/03/2013

Document ID:
13900 (v0)

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