As much as we love our non-slip socks, we know there is more to do to make the world a less slippery place. We're committed to supporting research to treat or cure the conditions which make frequent falls a reality for so many people - starting with Pompe disease. We donate 10% of all profits to organizations which research treatment options or provide support to better the lives of those living with Pompe. Read a bit about some of these PHENOMENAL organizations below!
Muscular Dystrophy Association (MDA)
Founded in 1950, the MDA seeks to transform the lives of those affected by neuromuscular diseases. From funding research breakthroughs to empowering families for support, the MDA is an unparalleled advocate for individuals with Pompe, muscular dystrophy, and other neuromuscular diseases.
Duke Pompe Disease Clinical and Research Program
The talented team at Duke, are some of the world's most knowledgeable experts in Pompe disease and are at the forefront of clinical trials for treatments which improve the livelihood of those living with Pompe.
Acid Maltese Deficiency Association (AMDA)
The AMDA was formed to assist in funding research and to promote public awareness of Pompe disease. The AMDA has funded research projects in several countries around the world and hosts an international Pompe patient and scientific conference.
United Pompe Foundation
Living with a rare disease can be expensive. The United Pompe Foundation was formed to assist patients and/or their families with medical costs and other expenses that these patients and families face and may not be able to cover, or fully cover, through their insurance.