**CASH DONATION** To the POMPE disease research charity!
*PROCEEDS FROM EVERY ORDER WILL BE DONATED TO POMPE DISEASE RESEARCH!
Harper Mae's story inspired this fundraiser. Pompe disease, a rare genetic condition, prevents the body from breaking down glycogen, leading to its accumulation in muscles—particularly the heart and skeletal system. This progressive disorder manifests as muscle weakness, respiratory challenges, and cardiac complications. Management combines enzyme replacement therapy with physical therapy and comprehensive supportive interventions. Diagnosed as a baby, Harper Mae undergoes consistent monitoring to detect disease progression and intervene proactively, maintaining her quality of life through vigilant medical oversight and treatment adherence.
*PROCEEDS FROM EVERY ORDER WILL BE DONATED TO POMPE DISEASE RESEARCH!