One of my good high school friends (and fellow band nerd), a girl named Emily Dorris (now Emily Westbrook), was diagnosed with cystic fibrosis at the age of three. You never would have thought it. She was a tiny thing, but whatever she lacked in size she made up for in personality. Many times this girl had me bawling with laughter on the bus, and she had a belch that would put a 400-pound sumo wrestler to shame. She always has a witty or smart aleck comeback, and she was refreshingly down-to-earth, never cliquey or snobby, never judgmental.
Or whiny, for that matter. Marching band is hard work, broiling out under the sun and carrying equipment, making practice and staying long hours after school. Emily did all that and never ONCE complained or used her disease as an excuse to miss an event. (Unlike me--I was always looking for an excuse to take a break because I'm a good-for-nothing slacker.) Most of us had no idea Emily had CF. Her condition stated that she wouldn't live to age 18, and so far she's a decade beyond everyone's expectations. Nothing scares this little firecracker. She has the heart of a lion and the laugh of a demented clown. She's just one of those rare few awesome people you get to have in your life, and I'm pretty sure you're not allowed to have many.
CF is a progressive disease and lately her health has taken a turn for the worse. She's got pneumonia that refuses to get better, and she's in need of a double lung transplant. She's married and has a cute little kid that has no doubt inherited those awesome Funny Genes of hers, and her family needs both moral and financial support right now.
Visit Emily's medical blog for more info on her condition, and even if you can't make a Paypal donation (any amount will be greatly appreciated), please just keep her in your thoughts and prayers. She's a great person--I don't know why it's always the nice ones that end up with these horrible battles to fight--so please, help if you can.
Or whiny, for that matter. Marching band is hard work, broiling out under the sun and carrying equipment, making practice and staying long hours after school. Emily did all that and never ONCE complained or used her disease as an excuse to miss an event. (Unlike me--I was always looking for an excuse to take a break because I'm a good-for-nothing slacker.) Most of us had no idea Emily had CF. Her condition stated that she wouldn't live to age 18, and so far she's a decade beyond everyone's expectations. Nothing scares this little firecracker. She has the heart of a lion and the laugh of a demented clown. She's just one of those rare few awesome people you get to have in your life, and I'm pretty sure you're not allowed to have many.
CF is a progressive disease and lately her health has taken a turn for the worse. She's got pneumonia that refuses to get better, and she's in need of a double lung transplant. She's married and has a cute little kid that has no doubt inherited those awesome Funny Genes of hers, and her family needs both moral and financial support right now.
Visit Emily's medical blog for more info on her condition, and even if you can't make a Paypal donation (any amount will be greatly appreciated), please just keep her in your thoughts and prayers. She's a great person--I don't know why it's always the nice ones that end up with these horrible battles to fight--so please, help if you can.
Mood: hopeful
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