(PART 1) Emergency Registries: A Misleading, Harmful & Non-Inclusive Fix

In this 2-part discussion, the broadly used term "registries" is narrowed to refer to registries for disabled people, sometimes referred to as” special needs” registries. These registries are used primarily by the government as disaster response and planning tools.

These registries typically consist of a database of individuals who voluntarily sign up and meet various eligibility requirements for receiving disaster response services based on a need.

The panel will take a deep look at clarifying the layers, cutting through the rhetoric, and examining the DIS, MIS, and flawed information regarding registries. The panel will also explore the hard work needed to build resource capacity and operationalize, embed and sustain viable assistance.

Panel: Moderator: Shaylin Sluzalis, Co-Executive Director, The Partnership for Inclusive Disaster Strategies; Alexandra Enders, Consultant; June Isaacson Kailes, Disability Policy Consultant; Marcie Roth, Executive Director, World Institute on Disability

Explore: The panelists will explore:
- Registries and disasters
- Harm they can cause
- Better options
- Evidence
- Tools
- Research needed

#Action#Administrative #Data #Deploy #DisabilityAssets #Capacity #Collaborative #Communication #Dangerous #Empower #FunctionalHarm #Impact #SpecialNeeds #Registry #Registries #Inaccurate #Tools #Capacity #Census #American #Community #Survey #AppropriateLevel #Research #Resources #Symbolic #Planning #Disaster, #Emergency #Outcome #Population #Specific #Undercount

Тэги:

#disabled_people #people_with_disabilities #others_with_access_and_functional_needs #special_needs #emergency_registries #government #disaster_response

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