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Hat day raises funds for cystic fibrosis PDF Print E-mail

By Whitney Smith
Wallace High School

The Wallace National Honor Society recently held a “Hat Day” to raise money for the Cystic Fibrosis Foundation.
The way it was conducted was this: Students kindergarten through seniors and the staff at Wallace were able to wear a hat in school all day if they brought one dollar to donate to the Cystic Fibrosis Foundation.
It was a great way to raise money, and the students and faculty were all for it. We raised about one hundred and twenty-five dollars.
As the National Honor Society was gearing up for the event we learned a lot about Cystic Fibrosis or sometimes called 65 Roses®.
65 Roses® is what some children with CF call their disease because the words are much easier for them to pronounce.
Mary G. Weiss became a volunteer for the Cystic Fibrosis Foundation in 1965 after learning that her three little boys had CF. Her duty was to call every civic club, social and service organization seeking financial support for CF research. Mary’s four-year-old son, Richard, listened closely to his mother as she made each call.
After several calls, Richard came into the room and told his Mom, “I know what you are working for.” Mary was dumbstruck because Richard did not know what she was doing, nor did he know that he had Cystic Fibrosis.
With some trepidation, Mary posed the question, “What am I working for, Richard?” “You are working for 65 Roses,” he answered so sweetly. Mary was speechless. She went over to him and tenderly pressed his body to hers. He could not see the tears running down Mary’s cheeks as she stammered, “Yes Richard, I’m working for 65 Roses.”
Since 1965, the term “65 Roses” has been used by children of all ages to describe their disease. But, making it easier to say does not make CF any easier to live with.
The “65 Roses” story has captured the hearts and emotions of all who have heard it. The rose, appropriately the ancient symbol of love, has become a symbol of the Cystic Fibrosis Foundation.