In Memory of Libbie Sanders 1948 - 2009

Wife, Mother, Friend, the true spirit of Christmas

When you say Libbie, you think also of Cole. They were an incredible team!

At the time we met Libbie and Cole, Libbie’s legs were already extremely deformed and in serious condition from her lymphedema. It was actually Cole who found, on the Internet, the diagnoses for her condition/disease. Over the years, we watched Libbie “battle” her health with determination.

Libbie and Cole became active members of the Lighthouse Lymphedema Network, servicing on the board of directors, hosting monthly meetings, summer luncheons, sponsoring the LLN website and simply always being there for us.

Libbie and Cole ran their business out of their home, but when Libbie would go outside, she used her scooter. The very last time we saw Libbie was March 11, 2009, at the State Capitol where the Lymphedema Legislative Committee was hosting an education and awareness forum. The story goes that Cole was in bed with a severe lung infection. He always took Libbie to “everything”, but this day, he said, “Libbie, I simply am too ill to go out”. Libbie asked if she found a way to go, would this be ok? Cole had no idea what Libbie was planning. Libbie arrived at the State Capitol with Bubba, a long time friend and helper for the family. She came wheeling in on her scooter with Bubba in toe pulling a suitcase full of cookies and fruit. They had traveled from Decatur to downtown Atlanta via MARTA. We were all so excited to see her and could not believe how she had gotten to the Capitol. This was our Libbie, always wanting to help and always there for all of us. March 11th was a Wednesday and Libbie died on Sunday, March 15th.

Libbie, our angel, your courage, determination, spirit, and love of family and others is your legacy. We miss you dear friend. God has our angel!

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About Us

The Lighthouse Lymphedema Network is a 501 (C) (3) organization of individuals who are lymphedema patients, or who have an interest in lymphedema.

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