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About this cause:Molly's Fund frequently posts information and support on Facebook, and it was one of the best resources I found after diagnosis. I am 2 years post-diagnosis at this point, and I am still learning new things every day and then educating my friends and family so they can better support me. Molly's Fund helps explain things in ways that I can't, and it helps me feel like I'm not alone and not insane with some of the crazy things that happen to my body and mind daily. I would like to support them financially so they can continue to grow as a company, and hopefully eventually expand to other areas of the country since they are only located in Portland, Oregon at this point. Please help me support them and their constant stream of information so that others can benefit from the wonderful articles they post, and so that others who are recently diagnosed (or even not recently) don't feel alone. Thank you for your time and support, and especially for your understanding with this cruel, mysterious disease.