The PCMA’s Pull for Pompe is a family-friendly fundraiser to support Pompe Disease Research through the Acid Maltase Deficiency Association.
Pompe disease is one of a family of 49 rare genetic disorders known as Lysosomal Storage Diseases or LSDs. Pompe disease is also known as Acid Maltase Deficiency or Glycogen Storage Disease type II. Please visit the AMDA website to learn more.
All proceeds from the Pull for Pompe will go towards AMDA’s Pompe Disease Research Grant! However, it is possible to make a donation here throughout the year.
Check back here for details on the 2027 Pull For Pompe event and in the meantime enjoy some of the moments captured at ths years ev
The PCMA’s Pull for Pompe is a family-friendly fundraiser to support Pompe Disease Research through the Acid Maltase Deficiency Association.
Pompe disease is one of a family of 49 rare genetic disorders known as Lysosomal Storage Diseases or LSDs. Pompe disease is also known as Acid Maltase Deficiency or Glycogen Storage Disease type II. Please visit the AMDA website to learn more.
All proceeds from the Pull for Pompe will go towards AMDA’s 2026 Pompe Disease Research Grant!
