The AADC Family Network will be hosting the fifth annual AADC Awareness Day Event on Wednesday, October 23, 2024!

Links to previous Awareness days:
2021 / 2022


About

About Us

The ALADD Foundation, Inc.  was established in 1998 and was the first foundation for AADC (Aromatic L Amino Acid Decarboxylase Deficiency).  The foundation was established for the charitable and educational purposes of providing research, medical assistance, support and awareness and to participate in all services and activities designed to carry out and find a CURE for AADC. 


The foundation funded the first mouse model to better understand the disease and to find new treatments.  We also funded the very first database which focused on collecting information on signs and symptoms as it relates to severity of illness. 


AADC

Our Mission Statement is simple:



"One day I will walk, one day I will talk,

TODAY I can smile."

The ALADD Foundation Board

Bruce Heger

President

Kelly Heger

Director

AADC
Location

While we are based in Massachusetts, we gladly assist families suffering from AADC all across the United States!

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