Tom Goodwin, 67, of Chalkville/Pell City, Alabama, passed away at his home on Thursday, November 21, 2013, from leiomyosarcoma, a rare and aggressive cancer. Tom Goodwin is survived by his wife, Sandy Goodwin and is predeceased by his wife, Linda Bain Goodwin. Tom is survived by his daughter, Kelly (BJ) Nease and four grandchildren, Nicole Kennedy, Kelsey Kennedy, Danny Nease and Bradley (Ashley) Nease. Tom is also survived by his two step-daughters Carla Maul (Steve Conkerton) and Christy (David) Nason and three grandchildren Ashlee Azziz, Rylee Maul and Conner Nason. Tom is predeceased by his parents, Ivan (Ibo) and Delia Mae Goodwin and his Aunt Violet Bragan.
Tom was born in Chalkville, Alabama, where he was a member of Taylor’s Memorial United Methodist Church, the Chalkville Civitan Club and worked with the Local Girl Scouts. Tom served in the US Air Force from 1967 to 1971. Tom retired from Bell South in 1993. Tom and Sandy relocated to Logan Martin Lake in 2000 and are active members at Arbor Baptist. Tom was active with the Tannehill Woodcarvers and was one of the founders of the Logan Martin Woodcarvers. He received several first place ribbons in woodcarving competitions.
Tom will be greatly missed but remembered for living by the Golden Rule, treating all with respect, loving the Lord and his family.
If you would like to make a donation to LMSdr in memory of Tom Goodwin, 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.)