Since its creation in 2013, International Angelman Day has been the driving force in uniting AS families and patient organizations from all around the world around a common purpose – Angelman syndrome. The day is observed by over 50 charitable/support organizations based in over 40 countries around the world. These organizations are family-driven and all support people with Angelman syndrome, their families, caregivers, and service providers. They initiate and promote research for AS and create educational resources.
Check out IAD official website: https://angelmanday.infofo
Raise Angelman syndrome awareness worldwide.
Mobilize people to action & encourage fundraising for the AS organization in their country.
Promote research and educational resources in the organization’s own country.
Remember those people with Angelman syndrome who are no longer with us.
The official International Angelman Day website offers a wealth of downloadable graphics and templates in its resource section, tailored for effective Angelman syndrome advocacy. From customizable profile picture frames to eye-catching ‘Save the Date’ posts, the toolkit empowers families and advocates to share support effortlessly. Check out:
https://angelmanday.info/resources"International Angelman Syndrome Day is a date for visibility and awareness. Through the appeal of the GAMAS Initiative, the Brazilian Bar Association was lit in blue on February 15th, 2024 - joining dozens of buildings and monuments around the world illuminated to "shine light" on our cause.
But that wasn't all! Angelman families illuminated their own homes in blue. Neighbors lit up their homes in blue. Therapists and entire clinic teams dressed in blue. Friends dressed in blue and shared on social networks, promoting awareness of Angelman syndrome. Yohama Eshima, brazilian actress, recorded an awareness message at the request of the GAMAS Initiative, through a mutual friend.
But what is the purpose of all this? Visibility! And what does it serve? It serves to slightly alert a contingent of thousands of families living without a diagnosis. It serves to make people research what this Syndrome is. It serves to open a path of appropriate treatment for those who currently have none.
It also serves to bring acceptance. To make Angelman families feel seen, as rare families. It serves to receive each endorsement as a hug and an acceptance. And this matters. A lot. Very much so.
We would like to express here our eternal gratitude to each person and each institution that embraced the hundreds of thousands of people living with Angelman Syndrome around the world on February 15th, 2024."
Daniel, Co-founder GAMAS Initiative for Angelman Syndrome
The countdown to International Angelman Syndrome Day has begun, and we are launching a special CHALLENGE!
On this February 15th, dress in blue clothes 👕👖 and light up your space (home, store, office, business, headquarters, etc.) with blue light 💡🔵 to show your support for Ana and the Angelman community.
Join us in this symbolic gesture of unity and hope, and be YOU a vehicle for positive transformation in the world 🌎 for this rare neurogenetic condition.
Tag your posts with @gabi.gamas and share your photos 📷 using the hashtags #iadfeb15 #cureangelman #angelmansyndrome.
Invite your friends and family 👩🏽🤝👨🏻 to take part in this challenge! Share it on your social networks to expand our wave of awareness and solidarity. Together, we make a difference!
Our eternal gratitude.🙏🏻