Lauri Ann Molloy

My beautiful sister Lauri Ann Molloy, lost a difficult battle with leiomyosarcoma today, September 2, 2010. Lauri was diagnosed June 2008 had surgery, radiation and gemtax. She was NED until April 2010. In four months this disease took my sister from us.

Lauri Ann Molloy was a Registered Physical Therapist and loved her career helping and touching others’ lives. She has a beautiful daughter, loving family and numerous wonderful friends that have been so supportive throughout especially the past four months.

Lauri loved life. She loved her dog Roxy and cats, Minnie and Kimberly. She loved nature and being out in nature. Lauri loved visiting her friends and working around her cute house. Lauri loved travelling when she was able.

We had Lauri for too short of a time, but hope that with research, studies and donations that her disease will have effective treatment and a cure. Thank you for honoring Lauri.

We love Lauri and miss her, and she will live in our hearts forever.

Love,

Janice, her sister and our entire family

If you would like to make a donation in honor of Lauri Ann Molloy, please fill in 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.

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About Leiomyosarcoma Support & Direct Research Foundation (LMSDR)

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.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 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.

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.

 

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Donation Total: $500