The Hughes Family: ALL better

Tuesday, March 23, 2010

ALL better

Thank you to everyone for my comments on Facebook about Ben. He’s doing much better. He woke up this morning completely back to normal, thank you Lord. We’ll try peanut butter again in a couple months. I’m slightly disappointed because pb has good fat and protein for little CFer’s but I’m just glad he’s okay.

Any hoo, I didn’t get a chance to post up some pics from our times in Carmel Valley this weekend.

On Saturday we had a BBQ with some friends at my parents home.

Ben and his future girlfriend, Abby.

Ben kept trying to give Abby “kisses”.

Ben and his Papa

Ben and his godmom

Wrestling with his Uncle Weston

No comments:

Post a Comment

I love hearing from you, thank you!

What is Cystic Fibrosis?

Cystic Fibrosis is a life threatening, inherited disease, that causes mucus to build up and clog some of the organs in the body. Majorly in the lungs and pancreas. When the mucus clogs the lungs it makes breathing very difficult. The thick mucus also causes bacteria/germs to get trapped in the airways, which causes inflammations and infections that damage the lungs. The mucus can also block the digestive tract and pancreas. It stops the enzymes from getting into the intestines. The body needs enzymes to break down food, which provides important nutrients to help us grow and stay healthy. People with cystic fibrosis often need to replace these enzymes with capsules they take with their meals and snacks to help digest the food and get the proper nutrition.

How do people get CF?

Cystic Fibrosis is a genetic disease. Which means people inherit it from their parents through genes (or DNA), which also determine a lot of other characteristics including height, hair color and eye color. Genes, found in the nucleus of all the body’s cells, control cell function by serving as the blueprint for the production of proteins. The defective gene that is responsible for causing cystic fibrosis is on chromosome 7. To have cystic fibrosis, a person must inherit two copies of the defective CF gene.one copy from each parent. If both parents are carriers of the CF gene (i.e., they each have one copy of the defective gene), their child will have a 25% chance of inheriting both defective copies and having cystic fibrosis, a 50% chance of inheriting one defective copy and being a carrier, and a 25% chance of not having CF or carrying the gene.

What is the life expectancy for people who have CF?

There is no way to accurately predict how long people with cystic fibrosis will live, as many different factors may affect a persons health. Severity of disease and time of diagnosis are two such factors. Many people have a mild case of CF, while others can have moderate or severe cases. In addition, some adults with cystic fibrosis have only recently begun to use new treatments, while an infant diagnosed at birth will have the advantages of starting specialized treatments that were not available even a decade ago. Improved treatment and management of Cystic Fibrosis now results in a much longer life expectancy. Since the 1960’s, average life expectancy has risen from 5 up to just over 37 years

People who think Ben is cool

Find me on Facebook

Followers from Facebook

Blog Archive

Search This Blog

Our visitors

You're number:

Blog Design By:

Order a Breathe Easy Mask here!

Get diapers sent to your home!

Tuesday, March 23, 2010

ALL better

No comments:

Post a Comment

Our Greatest Joy

Our Family

The Author

Ben's Current Med list

Thank you!

Popular Posts

Check out Josh's CF kids videos!

People we think are cool

What is Cystic Fibrosis?

How do people get CF?

What is the life expectancy for people who have CF?