Hi everyone!
Can you believe it?! CASS turns 30 years old this year! I’m sure many of you feel as thankful as I do for our original founding families who carved time and space out of their lives to advocate and provide service to our Canadian AS community.
I would also like to express my deepest gratitude to all of our directors, supporters, and volunteers who continue to work tirelessly to help us achieve our mission of improving the lives of individuals living with Angelman Syndrome and their families. Despite the challenges posed by the COVID-19 pandemic, we have made significant strides in raising awareness for AS and keeping Canadian families strong. Our organization has continued to offer a range of educational resources, including webinars and online forums, the CASS Family Fund, and the 2022 Kelowna conference to help families navigate the complexities of AS and find the resources they need to ensure their loved ones receive the best possible care.
As we move forward, we remain committed to keeping families strong. CASS is deeply impressed by the commitment and dedication of our AS community. It is inspiring to see the incredible work being done by so many.
I hope to see you and your beautiful families at one of our Angelman Strong Walks this spring. We have lots of exciting news and updates coming your way. Follow us on social media and visit our website to stay connected.
If there’s anything CASS can do for your or your family, please do not hesitate to reach out via my email below. Big love to you all,
Kelly Meissner
executive.director@anglemancanada.org