Amy Reed
This fund is to honor and continue the heroic advocacy of Dr. Amy Reed and her devoted husband, Dr. Hooman Noorchashm. Together they challenged the gynecological establishment to ban the process of routine morcellation for uterine fibroids in which 1 in 350 women actually has leiomyosarcoma or another cancer. Their tenacious efforts to also find a cure for leiomyosarcoma will continue with this fund going directly to their nonprofit, Slay Sarcoma. She will not be forgotten by the leiomyosarcoma community of patients and loved ones.
Sharon Anderson
Executive Director, Leiomyosarcoma Support & Direct Research Foundation (LMSDR)
Sign the petition to end morcellation
If you’d like to make a donation to Leiomyosarcoma Support & Direct Research in honor of Amy Reed, please do it HERE.   We will let the family know of donation – even if you don’t see it on your receipt.

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About Leiomyosarcoma Support & Direct Research Foundation (LMSDR)

LMSDR

Leiomyosarcoma Support & Direct Research Foundation

This fund was created out of love for Amy Reed and 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 leiomyosaroma. We offer the largest moderated support group online for leiomysarcoma, 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.