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MEET BETHANY (Click on Our CF Story to learn more about CF)

Bethany is now 10 and in the 5th grade. Bethany is like any other young girl her age. She can run, play on the playground, ride her 4-wheeler, sled ride in the winter months, bowl, play softball. She enjoys fighting with her siblings. To look at her, you'd say she's in great health!
Unfortunately, Bethany has a disease called Cystic Fibrosis* (CF), a genetic, life-threatening condition which involves glands throughout the body. In CF, thick mucus in the lungs obstructs airways and allows bacterial infection and inflammatio n to occur.
Much of Bethany's day consists of medical treatments (some 35 pills and procedures) including pancreatic enzymes and many breathing treatments. She must take a handful of pancreatic enzymes with everything she eats in order to digest her food and grow properly. Thankfully, God has placed it on her heart to be diligent with her treatments and she does very well in managing her condition.
Bethany is very active and enjoys playing on her playground that "Make-A-Wish" Foundation built for her 4 years ago. Bethany is also very interested in arts and crafts. She has plenty of time to make beautiful pictures while doing her breathing and vest treatments every day.
MEET EMILY
Emily is 9, and she is still our princess. She is in 4th grade. She has many friends and would love to spend her evenings and weekends on the phone. She loves to play dress up, bowl, softball, and playing with her 3 dogs and 2 rabbits and on the backyard playground. She loves her music and has many dolls to play with. Emily, too, has cystic fibrosis. Sometimes she needs a bit more prodding to d o her treatments than Bethany. Although she is only 8 years old, she understands how important they are. Emily is also very active, which helps to keep her healthy.
I do have to say that Emily's favorite thing in life is when her pappy takes the girls on shopping trips. I don't know of a store that is not on Emily's list of favorites! She & Bethany are best friends! And Emiliy has a great sense of humor. Also, she recently recorded a song with Bethany, "He's Still Working on Me", on our latest cd..."Help Me Remember".
Visit www.myspace.com/yanceybrownministries to learn more about Bethany & Emily's battle with cystic fibrosis (CF). For more information about CF or to make a donation to help us find a cure visit www.cff.org. Please be sure to let us know if you do so we can recognize your help in our effort to make CF stand for "CURE FOUND"!!
MEET MCKENZY
McKenzy is 5 years old and her specialty is hovering over her lil brother, cleaning the house, ensuring the girls take their meds (lil mommy!), etc.
She can still change her clothes more times in one day than the rest of us do in a week. McKenzy has become a little mother to her younger brother. She scolds him often and lets Mom know when he is not behaving! And she is the "visiting home nurse" when it comes to the older girls' medicines and treatment s.
McKenzy has a real love for animals. She likes to takes care of our 3 dogs and 2 rabbits by feeding them and making sure somebody brushes them. Recently, one of our dogs gave birth to 7 puppies! She's right there in the middle of all the action being a "lil mommy". In the fall of 2009, a cat with her 4 kittens took up residence under the house. McKenzy did not want to part with them but she did. They found a new home at a friend's house that takes in strays. She can visit them there if she wants. A while back, a goat crossed the river and ended up at our house. She wanted to keep it, too, but we convinced her it needed to go back to its own home.
MEET RILEY (OUR VERY OWN RY-GUY)
Riley is now 3 and he just simply enjoys life. This little guy has no idea what's in store for him having three older sisters. He smiles all the time (hence we call him "Smiley Riley") and enjoys creating havoc and making messes!! He love to help Bethany & Emi ly get ready to do their CF treatments by finding their nebulizers that he has scattered around the house. He eagerly goes and gets their meds and will even huff, puff and cough with them to show his support in the CF effort!!
Riley loves to be outside. It is very hard to get him to come back inside. He rides his little bike on the porch, the sidewalk, the driveway or wanders around the yard just ignoring his mom's calls to, “Get into this house right now mister!". He likes to sing "He's Still Working on Me" (as recorded recently by Bethany & Emily on our newest cd).
*Cystic Fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:
-- clogs the lungs and leads to life-threatening lung infections; and
-- obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.
In the 1950s, few children with cystic fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Many people with the disease can now expect to live into their 30s, 40s and beyond.
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