Tuesday, June 29, 2010

Just a little bit of everyrthing update

Good morning everyone... Last night a CF friend on face booked informed many of us that there was a person faking that her daughter had CF and had even stole some pictures from this friend. How could some one do that.. Come on I don't wish CF up on any one. It just really upsets me and come on especially after the Jones Family loosing their son Conner. This person needs help and if she really does have a daughter I feel so sorry for daughter.

On another note Courtney has been having a good summer she will now go in her grandma and poppop's pool and ours with out her water wings, she now jumps of the ladder in to the water. Courtney just seems to keep amazing me on things. There are days that she fights me with treatment and I can't blame here who would want to come in side for a hour to do treatment so we have been trying to get it done before she can go outside and play and then she does her last one when it's time to come in for the night. The warm weather has kinda messed with her eating she seems not to be too hungry so we just keep fruit in the fridge for her to eat..

DeziRae is no longer in a booster seat so Courtney thinks she doesn't have to be in one .. Both girls will start soccer at the end of July. I am real curious to see how she does with that. I would like her to have a sport to play since it's good for her I just have a feeling come middle school she will want to be a cheer leader nothing wrong with that... Both girls have decided to add hip hop dance in with there tap and ballet so lets see how we all are going to handle Saturday soccer games and hip hop.

Courtney used to be on Nexium until the wonderful insurance company wanted to be a butt and make her have to try Omeprazole generic for Prilosec and honestly I think she has had more tummy problems with that med so I will talk to her dr and see.

The Catron Family

Friday, June 25, 2010

A Hero in my eyes

Late last night 7 year old Conner Reed Jones earned his angel wings. Conner is a hero in my eyes. Every picture that Sarah and Brad posted of Conner rather it be when he was in club med or home or any where he always had a smile on his face. I didn't know the Jones family only through face book and http://notsobrightandshiny.blogspot.com but the more I read the more they came like family to me. All my CF friends are my family to me my CF family. My heart is breaking I have shed so many tears today but I know Conner man is breathing easy and is up in heaven playing and running around. All I ask is that you keep this family in your thoughts and prayers as they go through all of this.

It's not fair he was only 7 yrs old. Why did god want him back already? That I don't think we will ever know. All I can think was it was to teach all of us something.


Tuesday, June 8, 2010


Well, it's going to be a busy week with Courtney and DeziRae having dance recital but well worth it. Today Courtney had pictures and oh my goodness she looked so cute. I am not liking my little baby with make up on though. I am hoping to have more pictures of her up by Sunday. She has been doing good. Sorry not much to report on the home front.

Wednesday, June 2, 2010

Courtney and the Dentist

Well the girls had a dentist apt today. My oldest DeziRae goes in there like a champ Courtney on the other hand doesn't so much.

She just started laying in the chair and let them clean her teeth with out freaking out took about 2 years so 4 visits. Today they wanted to try and get x-rays since she has never had them done well needless to say is that sat in the chair but wouldn't let them do x-rays she wouldn't opened her mouth. Later she told me it was because it would hurt. I told her it wouldn't . Times this like I HATE CF it has made her brave and strong but other times so freaked out thanks to throat cultures. I keep telling my self baby steps she did fine with blood draws at clinic so maybe in 6 months she will let them get x-rays of her teeth.