Saturday, December 4, 2010

Calissa turned 1!

Today my baby is 1, I don't know where the past year has gone! She lights up the room when she comes in. She has a smile that makes me just want to squeeze and kiss her. Just today I had been gone for a couple of hours and when I came in the house I walked past her and didn't see her and just as I passed by her she says "HI". It was so cute. She is a momma's girl, but loves to cuddle with her daddy too.



She had the best time with the chocolate cake (like you can't see that from the picture). We would just laugh at her and she would just get sillier and sillier. It was worth the mess for all the giggles we heard.


She loved the presents and let Jett know it if he got to close to her stuff.

Happy Birthday Baby Girl! We love you and the special part of our family that you are! Our lives are so much brighter with you in it.

Wednesday, November 24, 2010

Family Photos!

We finally got a family photo with all six of us here are some picutres of all of us!








I really liked this one of "MY BOYS" the one of the girls did not turn out so well :(





It was hard to get all four together to smile and look at the camera at the same time but there were some good ones anyway!

Tuesday, November 16, 2010

Family Time!



Our first trip the dunes in near Yuma in quite sometime. The last time we were there Jett and Calissa were both sick the whole weekend. We had a good weekend except the never ending wind. We did get some riding in and the kids absolutely loved it. Jeff loved the new RZR in the dunes where I decided the big dunes were a bit too much for me and my stomach to handle.



The kids decided to try to make it to the top of this 75 foot tall sand hill. They made it up more than one time. Even Jett had to give it a try. Total over the weekend they went up and down the hill six or seven times at least. I tried and made it maybe half way and my legs didn't have anything left (I blame it on the diet) :)!



Yes they made it all the way up!












It really is an amazing place there is sand all around big hills, small hills.........








And plenty of room for the kids to play!!!

Monday, November 1, 2010

Why I Love Sycamore!

SPOOKY RUN 2010!!




We have always liked Sycamore and the kids love it too! Saturday morning was the 2nd annual Spooky Run. It was a 5K and a 1K run for everyone of all ages. Caelin and Jace ran the 5K and Caelin finished in 39 minutes and 22 seconds and Jace finished 39 minutes and 10 seconds. They had a fabulous time and were tired at the end but I was so impressed with how well they did. Jeff, Jett, Calissa and I used the RAZR and volunteered to keep an eye on the runners and we enjoyed that. I love these great fundraisers the school does. Way to go PTA!

Halloween 2010

This year for Halloween we did things a little different. Because it was on Sunday we decided to go out on Saturday so we went to Thatcher a Mormon community that we figured would be ready on Saturday. Trym and Emily and there family was there, Mitch and Mandy (Emily's sister) and there family was there, and then Rocki and Brett and there girls, and Teonna and Luke and there kids. In all we had 16 kids dressed up that night. My dad was in awe of all the kids and costumes running around. We first to the kids to a Trunk or Treat and we were a little late so the kids thought they needed more candy so we went to Quail Ridge a community huge on the holidays and there were people everywhere. We had enough of that after just a few houses and went to a MUCH quieter neighborhood where two of my Aunts live. Although there were many dark houses the kids enjoyed the houses we did get and finally towards the end were tired after a long day of playing and then trick or treating.

Costumes this year were easy! We used costumes we already had.


Jace was "Darth Vader"


Caelin was "Ruby the Pirate Beauty"


Jett was "Stitch"


All three of them!

Then we had friends and cousins


Thanks Mom and Dad for having all of us! It was a great time!

Friday, October 1, 2010

A Month to Forget!!

So our month of September started off with Calissa and her ordeal and has ended with another child (Jace) and a visit to the ER. He started with some diareah and vomiting on September 15th, (only 5 days after returning home from hospital with Calissa). He had no fever and no other symptoms. By day 6 I was concerned and got him in to the Pediatrician (Dr. Valdes). He had lost about 7 pounds in the six days since his symptoms had started. They did urine test and blood tests and sent me home with the utensils for a stool sample. The stool sample took me two days to get and by that time he was dehydrated and couldn't keep anything down. We made another trip to University Medical Center only this time was the ER. After waiting in the waiting room for 3 hours they finally got us back and Jace was BAD off. His poor legs were aching and he was in tears. As a mother I have discovered this month there is nothing worse than watching my babies suffer like they have. They got an IV started right away, gave him anti-nausea medicine, and Tylenol and with in just a few minutes he was looking really good. His color was back and he was smiling again. After almost 9 hours in the ER we were able to come home, only to get home to a broken hot water heater, (yes you read that right, I know what else could possibly go wrong). We took COLD showers that night and Jeff moved the trailer in front of the house the next morning. Here we are on day 7 without the hot water heater and are still waiting for the parts. The place we ordered from messed up and it didn't get shipped out when it was supposed to so we have to wait until Monday. Luckily we have the trailer and haven't had cold showers for the past week. On Monday the 27th we took Jace back to the pediatrician for a check up after the ER visit and his symptoms were still there. The lab results on the stool sample was pending, the Dr. was baffled to say the least and was worried about Jace. She was leaving on vacation the next day and wanted to get a CT scan of his stomach to see if they could find what was causing it. Late Monday night the pediatrician called and I assumed it was to get the CT scan scheduled, instead it was to inform me that Jace had a parasite called GIARDIA. They started medication right away and on day four of the five day treatment his appetite is back and the symptoms are gone. In the middle of the craziness Jeff spent five days in Toulouse France for a business trip, (what fabulous timing). The bright spot of the month I have to say is the week I got to spend with my sister Sherra. She convinced Jeff that she would take care of me and the kids while he was gone, we all knew he really needed to be in these meetings. And yes I was a mess, and sad to say I still am. Sherra was here to keep me busy keep me company and just help with the kids, something I needed much worse than I thought. I can't remember the last time I was able to spend time like that with her and have the one on one time. It was really good for me. Thank you Sherra for being here with me it would have been a really tough week with out you. Although September is over and the kids are back to normal I for one am not. All I can say is that I would rather it be me than my babies.

Wednesday, September 22, 2010

Paraflu........Who Knew?!?!?

This will be lengthy I know, but none the less I want this to be documented for me and for her to read someday.

September 3, 2010 we were spending a long weekend in the White Mountains with family to celebrate my parents’ 45th wedding anniversary. In the early morning hours I heard my baby Calissa moaning in her sleep as I get up to check on her everything seemed fine. I thought maybe she was cold since it was a bit chilly at night (even with the heat on in the trailer). I covered her up and crawled back in bed. It wasn’t more than a half hour later that I heard her again so I got her up and put her in bed with us. I could hear a little bit of a wheeze when she was breathing, and could feel a slight fever. When morning came she was still the same, a slight fever and could hear the wheeze. After breakfast a group of the family wanted to go on a ride and of course I wanted to go, but I just wasn’t sure I wanted to leave my baby girl, so I stayed behind. I was sitting right beside her in the trailer and she was getting worse and I didn’t know what to do. Jeff had been gone at least an hour and of course I was scared. I took Calissa over by my parents and wanted my dad to give her a blessing but he said to wait for Jeff. As the minutes ticked by it felt like hours and I was ready to take her to the ER by myself. My sister had offered to drive me as well. Then another sister suggested I try Jace’s nebulizer to help her breathe better. They had their little boy in the ER with similar problems and they treated him with breathing treatments and sent him home. I decided it couldn’t hurt. It didn’t help her at all and as the minutes ticked by her breathing was more and more labored. When Jeff got back all I said is we have to go NOW! My dad and Jeff gave her a blessing and we left for the 45 minute drive to the nearest ER at the same hospital where I was born, White Mountain Regional Medical Center. We made it in about 30 minutes and never saw a cop on the road. We walked in the door and before Jeff had the paperwork filled out there were two nurses there and rushed us back; it was 3:00 p.m. They gave her a shot of steroids and started her on a breathing treatment. She had severe retraction going on in her little body. She was slowly improving and after a couple of hours the Dr. came in and said that we could probably leave in the next couple of hours. Then he found out we were camping and thought it might be a good idea to just keep her overnight and observe her. Within the next hour her breathing began to get worse and we could hear the wheeze. They checked us in the hospital and I sent Jeff back to camp to take care of the other three kids, (in my mind thinking this will all be over in the morning). She had two fabulous nurses and I wish I could remember their names. She wasn’t eating well and they were worried about dehydration so they tried to get an IV in her. They failed time and time again. They tried in her arms, hands and feet, but no luck. They finally gave up. They gave her another treatment and she got settled in her bed and was finally resting. In the middle of the night she woke up and as I was changing her I noticed her breathing getting bad again so I called the nurses and they came in and gave another treatment. I settled her back down and within an hour she was due for another treatment. They treated her and did some tests to see what it may be causing her so much trouble. It was about 5:30 in the morning when the Dr. came in and told me that they couldn’t treat her there anymore and we needed to get her to Phoenix Children’s hospital. Of course I said well we live in Tucson can we take her there and of course he said yes I will call the Dr.’s at University Medical Center and let them know what is happening. It was just after 6:00 a.m. on September 4, 2010 (Calissa’s 9 month birthday), Jeff had said he would call about 8:00 a.m. and check in since where he was at there was no cell phone service. I started to panic because I thought we could be gone by 8:00 and he wouldn’t know what was happening. One of the nurses in the ER the night before lived in the little town of Luna where we were camped and one of the other nurses offered to call her to see if she could go and let Jeff know he needed to call. He remembers that knock on the trailer door that scared him, he thought she had taken a turn for the worse and hadn’t made it through the night, and when he got the news it was a mad dash to get the trailer loaded and get on the road back home. When we left White Mountain Regional Medical Center they had diagnosed her with having RSV, Influenza A and B. Any one of those for a baby can be bad, but all three was terrifying. The Dr. there told me that the Dr.’s at UMC did not believe that she had all three, but the test there showed that she did. When the flight crew showed up to transport us they tried to get an IV in her as well. They tried what is known as an IO IV (a drill is used to go directly to the bone and get the vein there); they tried both legs and still failed. That I could not watch. I was by her side day in and day out through the ordeal but I couldn’t watch that. They flew Calissa and I (some of the staff there was surprised that I was being flown with her, not a usual occurrence) in a helicopter operated by Native Air from Springerville Airport to University Medical Center in Tucson. When we got there she was admitted into the Pediatric Intensive Care Unit a bit of a shock to me. We were all checked in by 10:00 a.m. and I sent Jeff a text to let him know. At approximately 2 p.m. (only four hours after arriving) my baby girl coded in my arms. The nurse (Whitney) was just outside watching and saw the look on Calissa’s face as she struggled for air, and was at my side in seconds. She tried to move her neck just right to get air through but Calissa had nothing left. She was blue and stiff and I really thought she was gone and I spoke to her not to leave me. Within seconds I am sure (felt like an hour to me) her bed was surrounded by nurses and as I listened to what was happening, “there’s no pulse, she is still not breathing”, I sank in the chair in corner and cried and then prayed that my baby would be ok, but at the same time I knew that if the Lord was ready for her to come home to him it wouldn’t matter how hard I prayed. They had her stable and breathing on her own within a couple of minutes (once again it felt like forever). Then Whitney told me to come be by her she needed to know I was there. Another great example of the nursing staff at UMC. Whitney told me later that if she had an IV they would have intabated her and if she had coded again they would have taken drastic measures to get an IV, like putting in a central line. They called a couple of nurses from the NICU to come and try to get an IV in her and after 3 failed attempts on the fourth try they got a very temporary one, but they all knew it wouldn’t last long. When Whitney went off her shift at 7:00 p.m. I was sad to see her go to say the least after all she had saved my baby in a calm collected way. The night nurse was Suz and she was great also. She is the one that finally got an IV in her that would hold. Calissa was poked at least 20 times trying to get an IV in, twice in each arm (four) twice in each hand (four more) 4 in each foot (eight more) 2 in her lower legs, the IO version (plus 2) one in her jugular, and the final one in her foot that finally held up, I believe that makes twenty. She was black and blue in all those areas and it was heart breaking to watch them try time and time again and get nothing. Suz used the temporary IV and pushed as much fluid as possible through it and covered her in warm blankets and finally after over 24 hours of being in the hospital Suz got an IV in her that would stay.
Calissa would be doing great and the Dr.’s and nurses would decide to try and space out her breathing treatments and it never failed she would take a turn for the worse and they would be giving her treatments every hour or two. It wasn’t until she was almost ready to be released from the ICU that she was able to go the four hours without the breathing treatments.
Whitney had told me that she couldn’t figure out why she was admitted to the PICU. They say they will take babies anywhere but for her to be in the PICU was not something that was normal at all. However after she had coded they were in no rush to let her out of the PICU. In fact one of the Dr.’s (Heather, I think her name was) told me that she didn’t trust Calissa because every time they thought she was on the mend and doing well she would take a turn for the worse. We had good nurses through the whole ordeal but none quite measured up to Whitney and Suz (that may be obvious since theirs are the only names I can remember). And Dr. Heather was so good about keeping us informed on what they were doing and was planned for Calissa. She also kept tabs on her labs that took days to get back because of the holiday weekend.
September 5th and 6th ; were both days of ups and downs with Calissa and my days started to all run together and on the 7th was the first time she had big improvement and continually got better.
September 7 an update I sent to the family; “Just want you all to know Calissa made good progress today. Decreased meds and is breathing better. She still has a ways to go but is improving.”
September 8 update; “So I know everyone is waiting on results but all we know so far is she was positive for paraflu (a common cause of croup). However the results on RSV and Influenza are still pending. We are officially out of the ICU and may get to go home as early as tomorrow but we aren’t holding our breath on that one but it should be soon.”
September 9 update; “Her only diagnosis was paraflu (croup), she has to go see an Ear, Nose, and Throat Dr and they will use a scope to check things out (like abnormalities) in 2 – 3 weeks. The RSV and Influenza all came back negative. She is doing well and breathing on her own without treatments for over 24 hours. The Dr. wants her to stay one more night for observation just because of the severity of her ordeal.
September 10, 11:35 a.m. “On our way home 3 ½ hours shy of one very long week”.
We are home and have not had any problems since. We are a bit concerned and cautious as I would guess anyone would be. It is frightening to know that a croup virus could do so much damage to our baby girl. “Paraflu….Who Knew”!!