Cynthia Lynne Haney, my beloved wife, was taken from me abruptly by Leiomyosarcoma on May 4, 2016. It was only about a month from the onset of symptoms, and a mere 15 days from diagnosis, until her death at Casey House of Montgomery Hospice. Her disease had progressed so surreptitiously and manifested so aggressively that there was nothing that could be done to save her life.
Cynthia was best known for being a bright, vivacious spirit, whose laughter, love, and wit charmed all those who met her. She was a loyal and loving friend, a talented writer, pianist, singer, and artist. She is sorely missed by her many friends and family.
Walter S. Knauff
If you would like to make a donation in honor of Cynthia Lynne Haney go to the the boxes to the right.
Please note: your online receipt will not have the honoree’s name – however your name with the honoree will be listed in the THANK YOU DONORS page for the family to see.
About Leiomyosarcoma Support & Direct Research Foundation (LMSDR)
This fund was created out of love for Cynthia 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 website 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 which Cynthia Lynne Haney supported. We are proud to have Patient Registry to collect data, and ran successful blood collections for study. We have brought patients and loved ones together from all over 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 making a donation and 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.