Tuesday, December 1, 2009

Thanksgiving & The Christmas Tree Lighting

Katelyn & busy bee, Kiera, on Thanksgiving!
We had a wonderful Thanksgiving at Todd's Uncle Paul & Aunt Kim's house. There was plenty to eat, drink, and much wonderful conversation to be had. It was nice to be surrounded by so much family this Thanksgiving. Everyone doted on all three of the little munchkins. They are all so much fun to be around. Kate was obsessed with the trampoline and convinced just about everyone to take her up to it at least once. I took Kate & Tayden up there at one point and Tayden was so adorable. She can't actually get her feet off the ground when she jumps, but she would squat down like she wanted to jump as high as she could imagine! It was so cute! Kate would come jump near her then Tayden would fall. It never phased her though, she loved every minute of it. It was nice to have the whole Devermann Family together. It doesn't happen often enough. Now, we can't wait until July! We will be having a family reunion out in Hemet, and hopefully, the whole nation's worth of Devermann's will be there!
We had a good time with a turkey taste test. Kim cooked two different turkeys; one was organic, farm raised, & fresh and another was your typical frozen, pumped full of all kinds of stuff, regular old turkey. Although it got a little confusing I believe just about everyone liked the frozen one! We didn't know which was which until after we all voted. It was pretty good!
Overall, we have had an incredible month! November was fun filled and amazing. We are excited about December and starting a whole new year in January!!!
Tomorrow, December 3, 2009, Katelyn will join NBC and Rady Children's Hospital at NBC's Christmas Tree Lighting! During the festivities Katelyn will get to interact with Micky & Minnie Mouse, we will experience the Tree Lighting, they will show an interview that we filmed with them last week, and there will be three Ice Skating performances. The show starts at 7:30 and will be featured, Live (I believe), on NBC at that time! Tune in to see our little Angel in this magical event!

I just posted a TON of photos on my facebook page! Go check it out!

Love & Prayers Always,
Krystal


Monday, November 23, 2009

Disneyland & Life

What an incredible weekend! As most of you know Katelyn is the 2009 Miricle Child for Rady Children's Hospital. There was some confusion between myself and the paper so Katelyn's story wasn't printed in the Union Tribune, but she had a wonderful opportunity offered to her in spite of our confusion. Every year Horton Plaza opens an Ice Rink around Christmastime. The rink opened last Friday, Nov 19th. As Katelyn is the Miricle Child of the year, they asked us to be present during their Christmas Tree lighting and sent us to Disneyland! Disney put us up at the Disney's Grand Californian Hotel & Spa, which is located just beside Disneyland, Thursday & Friday night. We spent Friday morning filming in both Disneyland & California Adventure, then we went back to the Hotel for a nap. After a decent nap we headed back to Disneyland for a fun filled day! We spent the morning riding rides and interacting in front of the camera. Disney wanted some footage of Katelyn to show at the Christmas Tree lighting. It was fun.



Katelyn is at such a fun age for Disneyland. She was mesmerized by the Princess' and characters. She got to meet Micky Mouse, which was wonderful. She especially loved Pixie Hollow and was able to meet two faeries, including her favorite, Tinkerbell! She just loved Tinkerbell, it was so cool. Todd and I just adored watching her light up at the sight and interaction with her fave character. She was also mesmerized by the parade! We watched it twice, once during the day and once at night when everything was all lit up. Kate couldn't keep her eyes off of everything. It was amazing. She recognized a lot of characters and was especially excited to see the Princess'. During the nighttime parade she asked me "Mommy, is this real?". I was in shock, I didn't really know what to tell her. It was really happening in front of her eyes, so I said "Yes, honey, it is real". I couldn't believe that she formed that question. She is so smart, it amazes me. We stayed late and watched Fantasmic and the fireworks. After it was all said and done as we were getting ready to exit the park I asked her what she thought of the show. She said it was kind of scary! Fantasmic is kind of scary! I thought it was a little scary too. It was an overall incredible experience. I can't wait to take the girls back. They will love it all over again!

Katelyn had a check up last week. Her blood is all clear and perfect. We are so very thankful for her health. We pray everyday for all the kids and families that have been touched by cancer. I pray that she continue on this healthy road, and that every other child does as well. She is no longer on any medications and is down to bi-monthly checkups! Amazing! Keep her in your prayers please :)

Kiera is great, healthy and growing like a champ. She is crawling and pulling herself up on everything. She loves to eat, especially to eat our food! She has three little teeth and more on the way. She and Kate are already the best of friends. Kate wants Kiera with her all the time. SHe doesn't even want alone time with Mommy or Daddy. She wants to bring Kiera everywhere. She is such a good big sister. Kiera loves Katelyn. She brings out so many laughs and so much fun. They play really well together already. Katelyn has even learned that if she wants what Kiera has, she has to give Kiera a different toy. It's incredible watching them interact together. They are the highlight of my life.

Please pray for my Uncle Thad. He has had hurrendous headaches these last few months. A CT Scan revealed that he may have a leak in his spinal fluid. He may have to undergo surgery to correct the problem. Please keep him and his family in your prayers.

Love,
Krystal

Wednesday, October 28, 2009

Reflecting


It's has been an incredible year. One year ago last Friday we checked into Children's Hospital for what proved to be a rocky journey. I can't even explain those first days in the hospital. It was so hard. My mind was filled with chaos. I was confused, sad, angry, frusterated, scared, and hurting for my baby. I don't think those feeling ever really left. I am happy now, and blessed to have healthy children. I remember the first days at the hospital, sharing a room with our little buddy, Iker, and finally being transferred to our own room. Poor Katelyn had such chubby little arms and feet, the nurses couldn't get an IV in, and when they finally did it would fall out within hours. She was poked over 30 times in the first few days we were there. The second night we were there I had to leave the room while the nurses held my baby down and poked her over and over until they finally got a vein. I sat outside the room and bawled my eyes out in the middle of the night until the screaming was over and I could go comfort Katelyn. It was traumatizing. The next morning she was scheduled for a central line. That was the end of the pokes, thank you Lord. I can't imagine those seven months if they included constant pokes. It would have been horrific! The first 9 days were endless. Everyday we waited to hear something, we waited for someone to tell us not what was wrong with Katelyn, but that it was all a big mistake and Kate was in perfect health. I think every parent goes through denial. I spent most of our hospital stay making the best of things but always, in the back of my head, I was waiting for someone to wake me up from the awful nightmare that wouldn't end.

On October 31st, 2008 we spent Katelyn's second Halloween trick or treating through the halls of Childrens Hospital. We trailed at the back because we wanted to go at Katelyn's pace and enjoy the excitement. Katelyn was dressed as an adorable little bumblebee and was the cutest thing you have ever seen! A few hours after we were done trick or treating Todd and I sent Katelyn on a walk with a nurse while we sat in our room with a handful of doctors, nurses, social workers, transplant specialists, etc. Dr. Schiff explained that it was very difficult to get a diagnosis because Katelyn's cancer was very rare. She is the 41st case to date, and only 20 children have had this form of leukemia over the last 20 years. Due to the minimal amount of research we were going to go with a general treatment for AML patients. Wow! I remember sitting there, unable to speak as I felt like my throat was closing in on itself. I couldn't see anyone's face, only their outlines because my eyes were consumed with a boatload of tears. It took everything I had to keep from bursting into hysteria as Katelyn's care team made their way to the door. Before the door was closed behind them, Todd had already wrapped me in his arms and we were both crying a river. I don't know how long it lasted, but it wouldn't be the last time we cried into eachothers embrace. On Halloween night our family came to the hospital and listened as I explained what Dr. Schiff had told us earlier that day. I must have cried all the tears I could cry at that point because I was able to explain everything I possibly could to our family while Todd could not say a word. I remember the devastation that took over the room that night. It was the most difficult day of my life. That was the first day of our battle against cancer.

Katelyn was so brave, and continues to prove it day in and day out. She has an innate ability to fight and win. Believe me, I see it every day. Not only did she prove strong and fearless, she won the battle and gained so much strength through her journey. Katelyn is an inspiration to me. In her short two years of life she has proven to be more than I could ever hope to be. She is a survivor, a fighter, a hero, and has been carried by Gods Angels through the most difficult trials. She has proven that no problem is too big to fight and win. She has taught me that nothing in this world matters more than family. Nothing matters more than my children. She has taught me that the most important thing I will ever do in my lifetime is love my children with my whole heart, and be there for them through everything.

I wasn't sure where this day, these reflections, and these thought would lead me. Here is what I do know. I am thankful that Katelyn has reclaimed her health. I am thankful that the four of us are here together. I am thankful that we have family and friends. I am thankful that we have love. I am thankful that we have God in our lives. I am thankful for the children and families that have befriended us along the way. I am thankful for the support that has been bestowed upon us this last year. I am thankful for my life. I am very thankful that this year is over.

Here is to life-long health, happiness, & love. Here is to Katelyn!

Here is to Nadia, to Zara, to Khuong, to Connor, to Iker, to Kylie, to Chase, to Brittany, to Abram, to Julian, to Joe, to D'Mario, to Sarah, to Juan, to Oscar, to Omar, to Lynn, to Haddie, to Heavenly, to Thalia, to Christian. Here's to all the children in Hem/Onc, fighting their battles. Here's to their health and healing.

Monday, October 19, 2009

October 20th's Union Tribune

Every Year the Union Tribune puts out a "Kids News Day" paper. I don't know much about it except that it will be out tomorrow: Tuesday, October 20th. A lot of people volunteer & sell the paper on street corners and in stores all day long. I remember buying these papers multiple times over the years. All proceeds go to Rady Children's Hospital in an effort to support their work and healing.

A few months ago Todd and I were approched about Katelyn being featured as a Miracle Child of the Year in this paper. I haven't spoken with Children's lately but I am assuming that Katelyn will still be featured. We are excited to see the story and hope that it touches everyone who reads it. I hope everyone who reads this will go out and buy the paper tomorrow! Whether or not Katelyn is featured in it, there is no greater cause than helping kids.

Please show your support tomorrow and pick up a Union Tribune: Kids News Day!

Love to all!
Krystal

Ps. I'm uploading pictures this week!

Tuesday, October 13, 2009

Winter is here!

It's been too long since I've experienced the seasons. I'm happy to be experiencing the weather changes again! Only a month ago we had the doors open at night and the fans on all day long to keep the house cool. Right now, I'm cozied up on the couch in front of a crackling fire & I couldn't be happier. My kids are cozied up in their beds with warm little toes & noses & that makes my heart feel nice & warm. These are the days that I love. I love to be surrounded by warmth & love.

Katelyn is growing to be very independent. She often spends the mornings full of energy and joy. She always starts the morning with cuddles & cuteness in Mommy & Daddy's bed. Kiera lights up when she is embraced by Kate. My mornings are always pleasant with my Angels in such happy spirits. Both Kate & Kiera spent the morning running around our little studio. Kiera in her walker & Kate playing with her abundance of toys. Kate is becoming very creative. She brings me tea & baked me some "sourdough cookies" this morning. She loves to use her little kitchen. Hopefully she will always enjoy cooking and will learn how to please the pallet like her father. He is a much more skilled cook than I am. I don't have the imagination to be able to throw things together & make a delicious meal. Todd does & I hope our girls get that from him.

Kiera ran around in her Winnie the Pooh walker all morning. She navigates it really well & can turn it around corners & push it through doorways. She spent a little time in her Rainforest Jumperoo & jumped like a mad baby! She is all smiles & giggles. She busts into hysterics at Katelyn & is very ticklish, just like the rest of us. She has cut two teeth in the last 10 days. She is a great teether! She fusses a little more and isn't sleeping as well as she usually does, but she is much happier than I imagine most babies to be when their teething. Kate was an easy teether as well, there were times when we didn't even know she was teething!

Kate & Kiera have been taking a bath together every night. Kiera sits up really well, so she just gets right in with Katelyn. It is absolutely adorable watching them play together in the tub. Kiera lunges for everything in sight, and has landed face first in the water! She's still not afraid though. Kiera splashes & splashes! She loves the water, it is adorable. Kate is obsessed with bubbles right now. She likes to give herself & Kiera bubble beards & hair. The other night she had a huge Santa beard & had her whole head covered in bubbles as well... Kiera thought she was hiliarious & was cracking up at her sister. This, in turn, made Kate, Todd & I bust in to laughter as well. Our girls have such wonderful personalities... I wonder where they get them?!

I'll be better with updating my blog now that we have internet at our house. Thank You to those who still follow our story.

Katelyn is doing wonderfully, health wise. Her last Hem/Onc appt was September 25th and all of her labs came back normal. She looks great. She's gaining weight & growing & her hair is coming in beautifully! I continue to pray for her each & every night. I thank God for putting his healing touch on her & keeping her strong through all the trials & treatments she has had to endure & I pray that he continue to hold her in his heavenly embrace & keep her healthy. Please do the same for her. She can always use prayers. Thank You!

I hope each of you can also pray for our friends listed below:

Trayci Ozuna - Breast Cancer
Tino Cauzza - Tumors
Khuong Lu - Leukemia
Kenny Smith - Tumor
Cassidy Mitchell - Cystic Fibrosis
Brittany Wnek - Tumor
Kate McRae - Tumor
Connor - Tumor

And also for the children that Katelyn spent so much time with at Children's. Some of these children are in remission and off treatment (like Katelyn) and some are still on treatment. They can each use all the prayers they can get! Thank You so much!

Nadia
Kylie
Zara
Lilly
Julia
Iker
Abram
Julian
Connor
Lainey
Oscar
Juan
Joe

Thank You for all the prayers! We love you all!

Friday, September 11, 2009

We're really enjoying Julian! I love living in the mountains again. I feel myself. It's nice. We're staying busy and enjoying life. The girls are growing and happy as can be. Kiera is eating foods now, and sitting up all by herself. She loves to take baths and splash in the pool. She is still as happy as they come. Katelyn is growing as well, and is as active as ever. I can hardly keep up! I'm trying to get her involved in more activities so she can socialize with other kids, and give me a little break! Hah! She is in a Movement/ Dance class in Ramona on Wednesdays and we went to storytime at the Julian Library on Thursday. At storytime I met some nice ladies who invited us to their play group on Tuesday's! I am excited to get out there and be active with the kids.

Todd has been working a lot. His job ends in a few weeks and he'll be off to find more work. We're waiting on the LVN boards to send us the right paperwork so he can get his test date. It's been a hassle getting in touch with them, but hopefully we will get the right forms asap. January is right around the corner. I can't believe we're nearing the end of 2009. I am planning to take a class or two in the Spring as well. I'd like to get back to school, finish my degree, and head into a career that will help support my family! Lots of new things coming our way!

I went to a yoga class this morning. It was a nice break for myself, and very relaxing. Grandma Robin took the girls to the coffee shop and the park. They're hanging out at her house while I steal away a few more minutes of alone time at the library. Alone time is few and far between in my life!

We will have internet set up at the house next week! Halleluiah! I'll be able to post pictures and keep better touch with society!

I read a friends caring bridge a few minutes ago and found it very interesting. Here is some information that she posted. Keep it all in mind and do what you can. Thanks to everyone!

September is Childhood Cancer Awareness Month!!

-Cancer is the #1 leading cause of death by disease in children under 15 in the U.S.
-12,500 children are diagnosed each year in the U.S.
-Currently, 30,000-40,000 kids are undergoing cancer treatment in the U.S.
-2/3 of kids who survive childhood cancers endure severe side effects from treatment such as cognitive deficits, organ failure, and secondary cancers just to name a few.
-Childhood cancer research is vastly underfunded
-There are 15 children diagnosed with cancer to every one child diagnosed with AIDS yet the U.S. invests $595,000for research for every pediatric AIDS patient and only $20,000 per pediatric cancer patient
-Right now somewhere in the U.S. 7 children with cancer are fighting for their lives who won't make it through the daySome ways to help…

From August 15th until October 15th, the company will donate 100% of the profits of all bottles of Oatmeal Raisin Shower Gel sold via their website,
www.philosophy. com, to Cookies for Kids' Cancer. If you're a Facebook fan, there's a special Cookies for Kids' Cancer button on the Philosophy Facebook page explaining the promotion including the bake sales they're planning at their retail stores. In the month of September, the company will donate $1 for every special Facebook virtual cookie application you send to friends. Just a click of a mouse and $1 is donated! The parenting magazine Cookie has a write up about the promotion with Philosophy which we hope will also spur traffic to the website. PLEASE encourage your friends, family, babysitters, friends of babysitters, to support this very special promotion. It's not often a company donates 100% of the profits to a cause. Also,that Chili's Restaurants is running nationwide campaign for St. Jude, and September 28th is the day they give 100% of their proceeds to St. Jude.

Monday, August 10, 2009

"We going to the Mesa Nande!"

We're all settled up in Mesa Grande! It has been beautiful weather. I forgot what it was like to see the stars so clearly at night, and hear all the noises of the night. It's wonderful to see all the creatures you don't see so much in the city, even in Ramona. We have a King snake that patrols the rocks around the house, lizards galore that let you get within inches of them, turkeys, cows, frogs, dogs... all kinds of good stuff. Katelyn loves the animals, she loves the country. She never gets tired of the cows. She's done exceptionally well with the drive as well. Sometimes she wants to watch a movie, but mostly she wants to look out the window. She can express herself incredibly well, I love to hear her speak to me. She's also thoroughly enjoying the pool, or "tool" as Katelyn would say. She is a little fish, obsessed with the water and quite the little swimmer. She can swim all by herself, she'll swim about 6' under water, to and from people or to the edge. She can climb out of the pool all by herself (elbow, elbow, tummy, knees) and she can crabwalk half the pool. She's also enjoying the slide! She prefers to go down on someones lap, but she will still take a ride all by herself. She is fearless in the water, just like in every other aspect of her life.

We went to cousin Tayden's first birthday party on Saturday. I can't believe that she is ONE! The time has flown. She is absolutely adorable and had a wonderful birthday celebration. The company was nice, and it was a beautiful day. There were babies galore! And, lots of girls. There were 3 or 4 little girls between two and three, so Kate had a great time with the kids. She swam most the time, and played hard. We had a great time. Yesterday we had breakfast at the Lovely Lake Henshaw Grille and spent the day basking in the sun by the pool. Kate was in and out of the water, having an excellent time. I started the first of the Twilight Saga. Then I finished it. I was in a trance and couldn't put the book down. Todd gave me a break... I called payback for golf. I forgot how much I enjoyed reading.

Kiera is getting so big. She is still the happiest little girl. She is made of pure joy, I know it. It's rare that she shows you anything but a smile. She talks up a storm and today I heard her first laugh! It was adorable! I look forward to many, many more!!! She goes to get some immunizations this week. I hate to see my girls get shots. I hate shots but I would take them all for those two if I could. She can't have any live, or partial live shots as it could comprimise Katelyn and her immune system. Kate can't get any immunizations for another 6-8 months. Then she has to start from scratch. When all the chemo wiped or her immune system so many times it included all of her previous vaccinations, so we have to start from day one. Breaks my heart.

Kate is doing wonderfully. Her last CBC came back clear as we suspect and pray for every day. She goes back in a few weeks for her 3rd checkup. October is only a few months away. I can't believe that ten months have come and gone. I thank the Lord everday for granting Katelyn health, and life. I continue to pray that she stay healthy and that the Lord hold her close to his heart, wrapped in his embrace, so that she never experience the pain and misfortune that she has already experienced. I pray that for both of my girls and all of the children I've come across that need the prayers themselves.

Special prayers are needed for Zara, Christian, Haley Simonds, Trayci Ozuna and many more. Zara is doing well. She recently experienced her first bacteria infection, which, from our experience is trying and very scary. Her counts are rising as the last chemo round is almost out of her system. She'll be coming home soon. She will be monitored frequently and as long as her blasts are under 5% she will not go to transplant. Christian went through transplant a few months ago and recently relapsed. He is undergoing more chemo and will start radiation soon. Unfortunatly his cancer has proved treatment resistant. Please pray for him and his family. Haley has had some complications with her kidney, they are not sure what to make of it yet, but we are hoping and praying for the best. Trayci is undergoing chemo after her masectomy. I know it has been incredibly difficult on her husband, my step-brother Peter, as well as their three children. Please keep each of these people and their family in your prayers.

Well, I need to get the kiddo's fed! Have a wonderful night. Thank You for checking up on us. As soon as I get internet in Mesa Grande I'll post some updated photos.

Love to All,
Krystal