AGS Advocacy Association

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Watch the Replay, AGS @ the 2023 ULF Family Conference

The AGSAA hosted a session about AGS at the 2023 ULF Family Conference. With a focus on advocating for individuals with AGS (Aicardi-Goutières Syndrome), this session provide attendees with knowledge about the latest advancements in research, treatment options, and support services available. Whether you're a parent, caregiver, healthcare professional, or an individual living with AGS, this session should provide valuable insights.