Changes for page CdLS World Federation

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From version < 9.1 >
edited by Gerritjan Koekkoek
on 2018/01/11 19:05
To version < 11.1 >
edited by Gerritjan Koekkoek
on 2018/01/11 19:07
>
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3 3  All over the world people; Parents, Sisters, Brothers, Family, Doctors, Caretakers, Educators and others, get together in small groups. These small groups are about Cornelia de Lange Syndrome, that's what unites them. Many of these groups have united in the federation; CdLSWorld. This is what we are: a federation of support groups from all over the world!
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5 -== [[image:cdlsServices.serviceWhoWeAre@PanelL2.png||alt="Support..." style="float: left; margin-right: 0.5em;" width="40%"]]Support ==
5 +==[[image:cdlsServices.serviceWhoWeAre@PanelL2.png||alt="Support..." style="float: left; margin-right: 0.5em;" width="40%"]] Support ==
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7 7  You’re told a person you care for has CdLS. It is very rare, so it's hard to find the support you need. We can link you with nearby support groups.
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9 -== Meet ==
9 +==[[image:cdlsServices.serviceWhoWeAre@PanelL2.png]] Meet ==
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11 11  Globally, there are others in the same situation as you. If they connect to us we can help you find them. Maybe you want to meet someone nearby with similar experiences.