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This Action Day we are  focused on raising awareness among policymakers about sickle cell trait and asking that parents of newborns are automatically informed of their babies' sickle cell trait status.

As part of Action Day, there will be a reception event with invited guests and dignitaries from 5PM -7PM. This event is free for the sickle cell and the larger community. However, you must register and be confirmed to attend.

Register here (direct link in our bio): bit.ly/actionday2024
Please don't forget to register for this incredible event. The information provided will benefit everyone, even those who don't live in Canada. It will be empowering to understand the landscape of the various types of innovative treatments now available.

Register here: https://bit.ly/InnovativeCures
Join February’s Peer Support Group! 

Living with Sickle Cell Disease comes with its unique challenges, especially when it comes to relationships and love. Whether you want to share your own experiences, learn from others, or simply lend a listening ear, all are welcome! Together, we can uplift and empower each other on this journey.
Come connect with others who understand firsthand the ups and downs of navigating relationships while managing Sickle Cell Disease.

🗓️ Date: Saturday, February 17th
🕒 Time: 11:00am-12:30pm EST
📍 Location: https://bit.ly/febpeersupport

Don't miss out on this opportunity for meaningful connections and valuable support. Mark your calendars and join us! 💬 #SickleCellDiseaseAwareness #PeerSupport #CommunitySupport #RelationshipsAndLove
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