Memorial at Moab

On April 18 Bryan, Julie and Nathan

traveled to the crash site near the

Moab Airport. (We could see the airport

from the crash site.)

I (Julie) was very nervous about going to see the site.

However, it was an neat experience.

I'm glad I had the chance to be there for the Memorial.

Some high school kids from Cedar put it all together.

They did a fantastic job. They had to get special permission

from the BLM to have the marker placed there. It's one of

two that the BLM has ever allowed.

I think this is where the plane first hit the ground.

It's hard to see in the picture but this is the large
burned strip where the plane slid across the top of the hill.



Then it slid down this slop.
It stopped at the bottom of this hill,
where they placed the large rock
with the plaque on it.



Keith's wife and baby son
looking at daddy's picture.

The plaque

Camping At Zion RV

We don't usually camp at an RV park,

but we love this one.

It is the only 5 star RV Park.

It is just outside of Zion Nat'l Park.

Zion the Lion


Bryan sure can grill up a great meal.
(He usually isn't this fashion challenged,
it was chilly and he was desperate.
He's really showing off his Disney clothes.)




We felt a little out of place.
The host stuck us in between a
bunch of fancy coaches.
Ahhh.....someday.

More Pics

So glad I get to spend 8hrs a day

with this sweet little one

Steph's b-day

(Alex our pyro.)

Mesquite Days Parade

Go Stephanie

Stephanie earned her Y.W. Award

WELCOME HOME CASSIDY!!!

Cassidy is finally home and improving daily.

5K

On Saturday, I participated in my first official 5k. I had only prepared for about a week before so I walked most of it. My friend and I walk that far every morning. I hope to cut my time in half. I haven't done much exercising for several years. Now I'm up at 5am for walking, counting calories all day, and working out at the gym most evenings. I'm in a contest. I joined the contest at the last minute and they told me Nathan was too young to join. Then when it was too late to sign up I found out that he wasn't too young. I had just talked to the wrong person. So he's not official but they let him do all the training with me. It's nice to have something we can do together. Bryan is very supportive. I can't seem to get dinner ready soon enough so he gets left to finish cooking and serving. So far, he has liked all my new recipes. Now if I could just get him to walk with me. Our family goal is that all of us participate in the 5K in Kanosh this summer. We all have a lot of work to do. (Janeece you inspire me but not enough to post a picture. :) )

Princess Cassidy

Cassidy is out of ICU! YEAH!!!From the Carepage:1/24/2009 1:15 p.m.Cassidy is doing really well today. She has been able to eat some soft foods and had pancakes, pears, and apple juice for breakfast. She is smiling and watching TV. Her throat is sore, and her voice is very quiet, but she was able to whisper, "Hi Grandma, I love you, Bye Bye," to my mom this afternoon. She has a pink wand that she has been waving around for therapy. Earlier today she was waving it at everyone and saying "Frog", but when Dr. Filloux got there, she said "Prince". He was really flattered. We love Dr. Filloux! Her brain takes longer than usual to respond to things right now, which is to be expected. They are adding Phenobarbital to her anti-seizure medications so that they can slowly decrease the Dilantin (it can have undesirable side effects in children). Her EEG is looking good. :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-) :-)
1/25/2009 12:00 p.m.
Cassidy is still doing well, except for an increase in her potassium level and having her days and nights mixed up. They gave her Phenobarb late yesterday afternoon which knocked her out for a while. So she was awake (and so was her dad) a lot of the night. Dr. Filloux said the EEG is the best it has looked so far. Hurray!!!
1/26/2009 10:30 a.m.Cassidy is still doing well. We are so happy! They may take the EEG off today, and they might remove the catheter. I'm sure that will feel great. Cassidy does her physical therapy from her bed. She has not been out of bed yet. She gets really tired. Her voice is still only a whisper. She ate eggs and oatmeal for breakfast. Her potassium is still high, but they are watching that.
1/26/2009
Cassidy got the EEG off and all cleaned up this afternoon. I posted a picture. She is still a bit puffy, but she looks great!!!
Looking good Cassidy! You are such a little fighter and we are all still pulling for you.

Girl Time

On the evening of the 9th Brylie and I went to see "Bride Wars". We went with our friends, Bailee and her mom Janeece. We had a fun time. The movie is really cute and I loved it. I can't wait to buy it on DVD and watch it a bunch more times. Stephanie was sick and went to the doctor instead. We missed her.

Then the next morning, Brylie and I went to Las Vegas to see "High School Musical on Ice" This time we went with our friends, Oakley and her mom Jennifer. The show was wonderful. The cast was well put together. We all
enjoyed it. After the show
we went to lunch at T.G.I. Fridays. I hadn't been there in along time. The food was yummy-thanks Jen. Santa forgot to bring Steph a
ticket and felt bad all day.

Thanks Brylie for being my
daughter. I love spending time with you.
I love you.-Mom