Julie Marie Feest, 60 of Carmel was born into eternal life, September 19, 2015, after a lengthy and courageous battle with cancer.
Julie Marie Feest was born September 3, 1955 in Racine Wisconsin, to Leonard and Mary Jensen. She earned her B.S. in Pharmacy from the University of Wisconsin and her Pharm. D. from Butler University.
Julie was a Pharmacist for St. Vincent Hospital, Indianapolis and was an active parishioner at St. Elizabeth Ann Seton Catholic Church.
Julie is survived by her loving husband, Wayne Feest; father, Leonard Jensen; children, Christie (husband Brian) Moore, William (wife Shauna) Feest, Erin (husband Taylor) Smith and Adam Feest; brother, Jeffrey (wife Chris) Jensen, and grandchildren, Cole, Brielle, Dryden, Brooks, Savannah, and Dominique. She was preceded in death by her mother, Mary.
Visitation will be from 4 p.m. to 7 p.m. on Tuesday, September 22 in St. Elizabeth Ann Seton Catholic Church. The Mass of Christian Burial will be at 10:30 a.m. on Wednesday, September 23 in St. Elizabeth Ann Seton Catholic Church, 10655 Haverstick Rd. Carmel, IN 46033. Burial will follow at Our Lady of Peace Cemetery.
In lieu of flowers, memorial gifts are encouraged to the LeioMyoSarcoma Direct Research Foundation.
If you would like to make a donation in memory of Julie Marie Feest, please click here. (When donating through PayPal, you can use the Designation Box to specify a Fund.)
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.
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.
(When donating through PayPal, you can use the Designation Box to specify a Fund.)