Homepage - KLS Foundation

Kleine Levin Syndrome Foundation

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This site klsfoundation.org currently has a traffic classification of zero (the lower the superior). We have scanned twenty pages within the site klsfoundation.org and found twenty-seven websites referencing klsfoundation.org. We have found one contacts and directions for klsfoundation.org to help you contact them. We have found one mass media accounts possessed by this website. This site klsfoundation.org has been on the internet for one thousand two hundred and seventy-four weeks, four hours, twenty-six minutes, and forty-eight seconds.
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Online Since
Jan 2001

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KLSFOUNDATION.ORG HISTORY

This site klsfoundation.org was created on January 25, 2001. It is currently one thousand two hundred and seventy-four weeks, four hours, twenty-six minutes, and forty-eight seconds young.
REGISTERED
January
2001

DOMAIN AGE

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LINKS TO WEB SITE

Hypersomnia Foundation

You may be able to help provide researchers with vital dat.

Its Not Mental

Monday, October 8, 2012. Getting Started - Diet Changes.

The Real Sleeping Beauty! Kleine-Levin syndrome

The Real Sleeping Beauty! Wednesday, 12 October 2011. Definitely not the weather for hats! So here we are, 3 weeks in and still healthy! And I am starting to get my life back! I have started back at college and I am loving it! However, its not all good luck;. I started college on Tuesday 5th of September, and everything was going good. Being able to go back to college after a year! It was really windy though, definitely not the weather for hats! My life was getting back on track.

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

There is more about us and our aims here. It is easy to contact us by filling in the Contact Us. For KLS Support UK news and updates. The KLS Support UK Information leaflet.

Pammieroses Dream World

WHY DOES GOD ALLOW PAIN AND SUFFERING? HALEIGH. FUNNY AND UNIQUE PHOTOS - PAGE 2. FUNNY AND UNIQUE PHOTOS - PAGE 3. AMAZING PHOTOS - PAGE 2.

Kleine Levin Syndrome - KLS - Our Story

Help us raise funds for KLS Support UK and hopefully answers for our son and others. But this short video by Tomo News - does a great job. Our journey so far with Kleine Levin Syndrome.

Síndrome de Kleine-Levin Información en español sobre esta Enfermedad Poco Frecuente

Información en español sobre esta Enfermedad Poco Frecuente. Qué es el KLS? Creando conciencia sobre el KLS. Hola, bienvenido a SindromeKleineLevin. Este sitio resume y traduce información en español sobre esta rara enfermedad. El KLS es una enfermedad del sueño que altera la conciencia del paciente. Durante un episodio, un paciente con KLS funciona en un estado de sueño alterado, presentando períodos de sueño excesivo y cambios abruptos en sus rasgos de personalidad. No dudes en contactarnos! .

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CONTACTS

KLS Foundation

Lucinda Maier

PO Box 5382

San Jose, CA, 95150-5382

US

KLSFOUNDATION.ORG HOST

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Homepage - KLS Foundation

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Kleine Levin Syndrome Foundation

CONTENT

This site klsfoundation.org states the following, "Disability Rights of KLS Patients." We noticed that the website stated " Educational Rights for KLS Patients." It also stated " Grants Awarded by the KLS Foundation. KLSF Awards Grant to Dr. KLS Symposium, World Sleep Medicine Conf. June 23rd and 24th 2018 in San Francisco. Meet and hear from KLS researchers who will present on the latest theories and findings. One in a million people worldwide live with KLS."

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Customization of the products offered. Manufactured as per set industrial guidelines. Extensive range of qualitative products.

Klasa VI-3 26 Korriku

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