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הצטרף אלינו

נמצא בחיים שלך, אנחנו כאן כדי לעזור CdLS אם

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We invite you to be a part of our CdLS community.

Who should join the CdLS community?


- The parent whose child is diagnosed with the syndrome.
- An individual diagnosed with CdLS.
- The sibling who wants to know what to expect in the future.
- Those who want to learn more about CdLS and how they can help.

Exclusive services and activities for members

- Attendance at the annual Conference with significant discounts.

- Social worker support and follow-up via e-mail, and telephone.

- Attendance at an annual workshop for families according to the Family Support Plan.

- Contact a group of CdLS specialized professionals via mail.

- Control visits to those affected within the framework of the annual National Conference.

- Invitation for national and international research projects of CdLS research.

- Free subscription to the newsletter: with specialized information, national and international specialist interviews, etc

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