Kaelyn's Kure: Kaelyn's Puppy!

Monday, April 11, 2011

Kaelyn's Puppy!

As most of you already know, we'll be adding a new family member to our household in about 8 weeks!

Kaelyn's new puppy was born last week on April 6 in a litter of 7 pups total. We plan to get a female and have 4 to choose from since we're 1st in line to pick from the girls! We couldn't be more excited and the timing of the new puppy couldn't be more perfect! We'll be able to pick her up right around Kaelyn's birthday! It will be exciting to see the 2 of them together, especially since Kaelyn already has a love for dogs!

These pups are the breed of Braque Francais aka French Pointer. Below is a pic of the new litter which we will get to pick Kaelyn's puppy from. So far we like the one on the far right with the all brown head (as long as it's a girl of course!). :-)

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Today, nearly half of the cystic fibrosis population in the US are adults. This is due to:

Better antibiotics and airway clearance treatments. Right now, 40% of the cystic fibrosis population in the US are adults. The current median age of survival in the US is 36.5 years. CF used to be a disease of childhood, as patients with it lived only a few months in the early 1900's. By the 1950's, they were living long enough to go to elementary school and by the 1980's, the average lifespan was 19. Huge leaps in care and antibiotics have led to this improvement. May it continue!

True or False: I don't have to worry about having a child with cystic fibrosis, as no one in my family has it?

False. A person with cystic fibrosis has inherited the defective gene from both their father and their mother, for two copies. If you have inherited one copy of the defective gene, you are a carrier. 1 in 31 Caucasian Americans are estimated to be carriers. It also affects other races to a lesser extent. For more information on this disease, see www.cff.org. And please, help us fight CF!

We were completely shocked when we learned that Kaelyn had been diagnosed with CF just 13 days after birth. Just as the question states, we had no family history of CF on either side of our families. We have a 1 and 4 chance of having another child with CF, there is no guarantee another child of ours will have the same diagnosis.