Giving Tuesday November 28, 2023
Help us continue to advocate for newborn screening for ALD & RUSP diseases!
How would you like to support?
As of November 2023 there are 12 states that are still NOT testing all of their babies for ALD.
- Advocated for federal funding so that ALD and other federally recommended conditions may be added to state newborn screening panels through the CDC's grant program. Two states are currently using the funding to add ALD to its panels, and three others are using funds to expand their panels to include other RUSP conditions.
- Provided assistance to EIGHT state newborn screening programs as they implemented ALD onto their panels and submitted two formal nominations to states requiring legislative rule making to add a new condition
- Hosted our first IN-PERSON ALD Standards of Care Conference since the COVID-19 pandemic
- Served as expert contributors to the Every Life Foundation's The Cost of Delayed Diagnosis in Rare Disease report
- Sent out 50+ care packages to families across the United States receiving an ALD diagnosis for their newborn baby
- Hosted TWO virtual town halls on the recently FDA approved gene therapy treatment for childhood cerebral ALD
- Completed our Psychological Impact of ALD online resource