ASAN February Newsletter
Dear friend,
No matter how short the month is, there’s plenty of work going on here at ASAN! From educating our community on contagious illnesses to urging the FDA to do better for people with disabilities to uplifting the next generation of advocates, check out what we’ve been up to this month.
The time to honor those we’ve lost is fast approaching. This Friday, March 1st, the disability community will gather virtually across the world to remember disabled victims of filicide – disabled people murdered by their family members or caregivers. Since 2012, ASAN and other disability rights organizations have come together to send a clear message that disability is not a justification for violence. Everyone is welcome at our Virtual Vigil, or you can find a local vigil here. Feel free to choose one local to you, or plan to join one whose time or platform works best for you.
There’s only a few days left to apply for the 2024 Autism Campus Inclusion (ACI) Leadership Academy! The ACI summer leadership training prepares autistic students to engage in disability advocacy on their college campuses. ACI participants learn about making student groups, understanding disability policy, and talking to people in power. After the Academy, students get help from ASAN to meet their advocacy goals at their college. This year’s program will be held virtually from July 15th through 24th, 2024.
Earlier this month, we held a webinar on COVID-19 and Mpox. There’s lots of information being shared about contagious illnesses, including COVID-19 and Mpox. It can be overwhelming to keep up as new information becomes available. This can make it hard to understand what choices we should make to keep ourselves and each other from getting sick. Our webinar talked about what Mpox and COVID-19 are, who is most impacted, how they spread, and how we can keep each other safer. If you missed it, check out the recording here!
We’re still urging the U.S. Food and Drug Administration (FDA) to release a proposed ban on the use of electric skin shock devices to treat a person’s self-injurious or aggressive behavior. It has now been eight years since the FDA released its first proposal to ban these devices and ten years since a panel of experts recommended that they be banned. Over the decade that has passed since, people with disabilities have continued to suffer from painful and dangerous electric shocks. Keep up with the fight to #StopTheShock, learn what you can do, and keep an eye out for when the time to send comments here!
ASAN also submitted comments to the IACC RFI on Co-Occurring Conditions, and we appreciate everyone who submitted their own comments too! Submitting public comments is an important way for self-advocates to make our needs and priorities known when it comes to public policy. The IACC makes recommendations about where federal funds for autism research should go and what subjects should be prioritized, and it’s important to make our voices heard!
ASAN was deeply troubled by reports made by The Washington Post this month that the CDC was planning to change its COVID-19 isolation guidelines. ASAN condemned the possible shortening of isolation guidelines and will continue to hold the federal government accountable for protecting the public from the ongoing risk of COVID-19.
There’s a lot of work to be done, and we’re grateful to do it by your side!
Sincerely,
The Team at ASAN
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ASAN Condemns Possible Shortening of COVID-19 Isolation Guidelines |