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Net profits are donated to scientific research and patient support organizations.

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Our goal is to connect science with youth culture to inspire future generations of science advocates. The more people who are behind science, the better we are at facing and overcoming challenges in our health, environment, and future.

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HOW WE DONATE

Our net profits are donated to organizations that we are involved with. Customers also have the option to choose any nonprofit organization including those not listed below to donate to with their purchase. 

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WHO WE DONATE

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NORD is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services.

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InvisiYouth Charity is an organization that helps teens and young adults around the world with various chronic illnesses and disabilities gain the right lifestyle programs, empowerment tools and fun resources to keep living life with any health struggles. With InvisiYouth, older youth are motivated in all the non-medical aspects of life with any illness, visible or invisible, and have access to resources and platforms so they can have joy, success, and thrive in their diverse lives.

Findacure is a UK charity that works to unite, empower and transform the rare disease community. We help rare disease patient groups professionalise their work so that they can advance their specific rare condition’s awareness, funding, research and treatment. We offer support and training services to help rare disease patient groups become more confident, so they can approach industry, pharma, medical professionals and other patient organisations with collaboration opportunities to move rare disease awareness and research forward as a united front. We want to see a world in which all rare diseases have treatments – made together with patients for patients – and are fierce advocates of drug repurposing as a viable option to reduce the time and cost associated with rare disease drug development!

The Ehlers-Danlos Society is a global community of individuals, caregivers, healthcare professionals, and supporters, dedicated to saving and improving the lives of those affected by the Ehlers-Danlos syndromes (EDS), hypermobility spectrum disorders (HSD), and related conditions. We are proudly working to provide global learning conferences, collaborative research and education initiatives, awareness campaigns, advocacy, community-building, and care for the EDS and HSD population: Giving HOPE to all those whose lives are affected by EDS and HSD.

Cure SMA leads the way to a world without spinal muscular atrophy (SMA), the number one genetic cause of death for infants. We fund and direct comprehensive research that drives breakthroughs in treatment and care, and we provide individuals with SMA and their families the support they need for today. A few programs that we’ve put into action for the SMA community include our Summits of Strength, virtual support series, and community support packages. Our Research, Clinical Care, Family Support and Advocacy teams actively work with key partners, including individuals with SMA, family advocates and pharmaceutical companies to advance early detection and treatment of SMA, fund new research and treatments, and provide families with the support, care, and equipment they need.

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