CdLS Awareness

1000 Photo Mosaic · 1 February 2022
Welcome to this years Cdls Awareness Day, I’m Philips mum, Ginny
As well as being Philips mum
I am also a Trustee for the Foundation, which was formed over 35 years ago by
like minded families (including my dear late husband Steve) and professionals, in a quest to help and support our Cdls children and adults to reach their full potential
Philip has called Maranello
home for many years now and I have seen improvements in his behaviour, mainly due to staff thinking outside of the box re diet and activities in which he will engage in, music and dancing are his world and he has got some brilliant dance moves, he also has a delightful sense of humour and those beautiful brown eyes do sparkle
My only wish for Philip is that he continues to enjoy life on his terms, sadly the self injurious behaviours will always be there
The pandemic has meant that I
was unable to visit Philip, but with the support of staff and technology we have been able to keep in touch via WhatsApp and FaceTime, sometimes only briefly but I feel that it keeps the consistency going and helps with his anxiety issues
Thank you for supporting the
Foundation, my hope is that we will be able to continue the good work that we do for many years to come
Why are we raising awareness about CdLS?
Cornelia de Lange Syndrome is a rare genetic syndrome. There are four main
features in this syndrome. Children with CdLS are small at
birth and remain small compared
to children of the same age. They
are all slow learners but this
varies from mild to severe. Many
children have limb abnormalities
which range from extremely
small hands to complete absence
of forearms or digits. The most
striking feature of the syndrome is that all the children can
look alike, like brothers and sisters. People with CdLS can
often develop challenging behaviours.
What your awareness and donation support will do
The CdLS Foundation UK & Ireland is a family support
organisation which exists to ensure early and accurate
diagnosis of CdLS throughout the world, promoting research,
and enabling individuals, families, friends and professionals
make informed decisions and plan for the affected person’s
present and future.
All we are asking
Step 1. Grab a piece of paper and write #CdLSmosaic and #CdLSawareness on it
Step 2. Take a selfie with it
Step 3. Upload the photo to all of your social media using the #CdLSmosaic and #CdLSawareness
Step 4. Please donate
Step 5. Share the just giving page to your social media
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