No images? Click here Join CLAPA’s Big Garden Party this summer! Bring your family, friends and community together by hosting a garden party in August to support our work, share your story, and help get everyone talking about cleft lip and palate. We've put together a digital fundraising pack to give you everything you need to plan your party, and we've got lots of CLAPA branded goodies to help you boost your event. In This Newsletter:
Events in August Coffee Club: 'Dealing with Diagnosis' We're pleased to announce that this month's CLAPA Coffee Club on Monday 9th August at 8pm will revisit our most popular topic: 'Dealing with Diagnosis'. Whether you've recently received a diagnosis of cleft lip and/or palate during the Covid-19 pandemic, or if you received a diagnosis years ago, this month's discussion will be a great chance to connect with other parents/carers and share your experiences with others who will understand. If you prefer, you are also very welcome to come along and listen to the discussion without taking part. As always, parents and carers of children of all ages are welcome to attend, as are close relatives. We hope you can join us! Family Fun Bake Off Join CLAPA volunteer, Nadine, on the 18th August at 4pm for some baking fun! There’ll be plenty of time to chat as we go through the recipe together, giving children the opportunity to meet other children born with a cleft. Family Fun Scavenger Hunt On Friday 27th August at 4pm join us on Zoom for a virtual scavenger hunt led by CLAPA volunteer, Nadine! You'll hunt around your house to see how many items you can find, while making new friends. Kiltwalk for CLAPA! Dust off your walking boots and get ready for the live Kiltwalk in Glasgow on the 26th September! By walking for CLAPA you'll save money on your registration fees, receive a free CLAPA t-shirt, and have full support from our team throughout your fundraising experience. Most importantly, you'll be playing a huge part in making sure others going through similar experiences to yours can benefit from our support services for years to come. Invite friends and family to join the fun, and contact fundraising@clapa.com to get your place today. CLAPA Voices The voice of the cleft community is the foundation of everything we do at CLAPA. From developing new services to shaping our messaging, we want people affected by cleft to be involved every step of the way. CLAPA Voices is your chance to be heard! SLUMBRS II Should babies with a cleft palate sleep on their back or on their side? This is the question the SLUMBRS II study aims to answer. Find out more with this Q & A on our Facebook page. Need to Talk? Wherever you are on your cleft journey and whatever you're going through, you're not alone. With CLAPA's Peer and Parent Support Service, you can chat to a trained volunteer about whatever's on your mind. Keeping Your Data SafeWe’ll use the information you’ve provided when signing up to send you the most relevant content, and you can update this data (and your preferences) at any time. Read our Privacy Policy to find out more about how we collect, store, and use your information. You can also get in touch at any time at info@clapa.com or call 020 7833 4883 if you have any questions or concerns. |