<br />
THE NEWSLETTER OF THE CORNELIA DE LANGE SYNDROME FOUNDATION, UK AND IRELAND<br />
R<br />
REACHING OUT<br />
August 2020<br />
HAPPY FAMILIES<br />
WHY IT'S GOOD TO TALK AT CONFERENCES – PAGE 8<br />
MASSIVE<br />
BOOST TO<br />
RESEARCH<br />
FUNDING<br />
PAGE 2<br />
2 news<br />
Get all the latest news, information, and research on our website: www.cdls.org.uk<br />
MISSION<br />
“The CdLS Foundation UK & Ireland is a<br />
family support organisation which exists to<br />
ensure early and accurate diagnosis of<br />
CdLS throughout the world, promoting<br />
research, and enabling individuals,<br />
families, friends and professionals make<br />
informed decisions and plan for the<br />
affected person's present and future.”<br />
The Foundation is a registered charity in<br />
England and Wales (no 1054033) and a<br />
member of the World Federation of CdLS<br />
Support Groups.<br />
CdLS Foundation UK & Ireland<br />
PO Box 8368<br />
R<a title="CdLS Reaching Out - August 2020 page 1" href="https://secure.viewer.zmags.com/publication/a057a3b9?page=1"> THE NEWSLETTER OF THE CORNELIA DE LANGE SYNDROME </a>
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