This Fund was established to raise awareness and direct funds toward specific LMS research.
This photo was taken of our Mom, Bernadette M. Hollis, in June 2005. One year later, in June 2006, she was diagnosed with leiomyosarcoma (LMS). Since then, she’s endured numerous surgeries and chemotherapeutic/hormonal treatments while continuing her law practice in upstate New York.
Despite Stage IV LMS, Bernadette continues to enjoy her profession at a full-time pace, and spends time away from law visiting with her children and their spouses, Amy (and Matt), Ellen, Alfred (and Kelly), Philip and her grandson, Daniel, going out with friends, painting (oils and watercolor), cooking/baking, and traveling around the world.
Read about the “Flip-Flops Fundraiser“.
If you’d like to make a donation to Leiomyosarcoma Support & Direct Research, please do it HERE. We will let the family know of donation – even if you don’t see it on your receipt.___________________________________________________________________________________
About Leiomyosarcoma Support & Direct Research Foundation (LMSDR)
This fund was created out of love, to help others win their battle with leiomyosarcoma by funding LMS specific research. Leiomyosarcoma Support & Direct Research Foundation (LMSDR) raises donations for Leiomyosarcoma research and patient support. We advocate directly with sarcoma researchers to study leiomyosarcoma. We offer the largest moderated support group online for leiomyosarcoma, where patients and loved ones get the latest LMS news and personal support. The LMSDR’s website offers local support groups, details of what we do, the research we have funded and many resources for the Leiomyosarcoma community. The LMSe Alerts is our monthly newsletter, offering more updated clinical trials, news and community events. The Leiomyosarcoma Lifeline is our new blog, featuring patient stories and our well-known Long Term Thriver stories.
We collaborate with researchers and other organization to reach our mission and vision of finding treatments that will work. We have created the Leiomyosarcoma Tissue Bank for researchers to study our disease, the Leiomyosarcoma Patient Registry to collect data, and ran successful blood collections for study. We have brought patients and loved ones together from all over the world for education and support at our Leiomyosarcoma patient conferences, in Denver, Colorado, San Francisco, California, New York City, New York, and Maui, Hawaii. Please stay in touch with our website for more upcoming events sponsored by Leiomyosarcoma Support & Direct Research Foundation.
Leiomyosarcoma Support & Direct Research is an all volunteer organization. We are proud to have the minimal amount of expenses as possible, to ensure your money goes directly to funding promising research for Leiomyosarcoma specifically. You can volunteer, put on fundraisers, promote LMS awareness and ask your employer for matched funds. Please consider helping us Work, not wish, for treatments that will work for us. We have been a 501(C) (3) since 2006 and a tax-free charity.