Aleva Stores is a leading fully integrated global e-commerce and consumer brand retailer. Aleva sells across fifteen (and growing) online stores (our “Aleva Stores”) and top online marketplaces globally including Amazon, Walmart, Google, and eBay. Distributing products in the medical compression, health & wellness, outdoor, personal care, and children’s toys categories, Aleva also holds national partnerships with many well-known consumer brands.
Aleva’s unique “all in one” model of e-commerce, Amazon, and marketing expertise combined with large-scale B2C distribution has led to tremendous growth over the past two decades and multiple acknowledgments as an Inc. 5000 fastest growing company.
Aleva Stores is a family of brands unified by a central principle: providing exceptional service and top-quality products to everyone we serve. Through creativity, innovation, and collaboration, we will meet the unique needs of our customers, clients and partners.
In addition to our commitment to our customers and employees, we believe it’s important to give back through volunteering and charitable donations.
Aleva Stores is a proud sponsor of the Make-A-Wish® Michigan Foundation. 99% of doctors say wishes help relieve families from traumatic stress, with 87% of alumni stating their wish was a turning point in their treatment. As of today, 11,000 Michigan wises have come true because of the network of supporters.
House brand Stego makes a Charity Series sock, with 25% of the purchase price going to Make-A-Wish® Michigan. Additionally, house medical brand VenActive offers a One Pair Purchased, One Pair Donated program.
Health, Education and Welfare (HEW) is a volunteer operated nonprofit based in Wisconsin founded by a breast cancer survivor who later developed lymphedema. HEW’s goal is to educate, encourage and empower those with lymphedema. Their Compression Garment Fund is Wisconsin’s first and only financial aid program helping Lymphedema survivors obtain their medically needed compression garments.
Ninjas Fighting Lymphedema is a nonprofit that was established by lymphedema patient and spokesperson, Amy Rivera to build the lymphedema community and give them a voice. NFLF helps patients, schools, hospitals, nonprofits and communities to better respond to the lymphedema epidemic. They educate, advocate and empower individuals and organizations to take an active role in creating awareness and spreading hope.