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Tuesday, September 3, 2013
September 3rd, 2013
This was Ella exactly 1 year ago. Hard to believe this is her today:
Head full of red curls and she always says"Mom, I LIKE my hair CrAzY!". Still, I KNOW we are the lucky ones. Ella completed treatment. The anniversary of her diagnosis came and went this year and I didn't give it a second thought. Other parents, are not that lucky. I see them in the halls as we go for Ella's monthly check ups. I see it in their eyes. The tired smiles that are exchanged in the halls between patient rooms, with a glimmer of hope in each. I don't want any child to have to go through what my girl did. So, this year, we walk. CureSearch is the organization that designed and researched the treatments that are currently being used for Childhood Cancer.
I encourage you to walk with us if your local, or think about skipping your morning coffee and donating. Every dollar helps. This year I am on the committee for the Chicago walk and I will be the photographer again, so I will post photos. Here is the link to Ella's page if your interested. Feel free to share with your friends! We walk this Saturday. Thank you to everyone that has donated and can walk with us! We are truly blessed for your support!
CureSearch~Ella
Blessings~Katie and Ella!
Wednesday, August 14, 2013
Update
So, I believe this is the first time EVER, but I cancelled Ella's clinic appointment and re-scheduled it for almost 2 weeks later. Ella attended a local Theater camp and I didn't want her to miss a day. In the back of my mind, I kept waiting for the doctor to call me and yell at me for changing it, but they never did! Then, they went to grandma and Grandpa's for a few days of spoiling and attention that I am so grateful they get! Seeing how much they love their grandparents often reminds me of how much I love mine, and often wish they were still here to talk to. I took this shot at a rest stop on the drive up to Wisconsin.
I also love how much these two love each other!
So, clinic went well. Ella's counts are looking good. She is looking good and we continue to pray and monitor every little ache and pain she has. For the most part, she is just such a happy kid! This past weekend, we held a Kid Olympics in our backyard with a bunch of neighborhood kids and friends.
It was a big hit. We had 10 events and included a 3-legged race with the adults and a mom vs. dad tug of war. We ended the night with a movie in our backyard, popcorn, and lots of blinkie lights. I've said it before, and I'll say it again- I love our friends!
Enjoy the rest of your summer! We are!
Blessings~Katie
I also love how much these two love each other!
So, clinic went well. Ella's counts are looking good. She is looking good and we continue to pray and monitor every little ache and pain she has. For the most part, she is just such a happy kid! This past weekend, we held a Kid Olympics in our backyard with a bunch of neighborhood kids and friends.
It was a big hit. We had 10 events and included a 3-legged race with the adults and a mom vs. dad tug of war. We ended the night with a movie in our backyard, popcorn, and lots of blinkie lights. I've said it before, and I'll say it again- I love our friends!
Enjoy the rest of your summer! We are!
Blessings~Katie
Wednesday, July 3, 2013
Loss
It feels like a time of loss in my life. In the sign wave of life, I feel like there are different sections of ups and downs. This is a loss time for me. Today I had to say good-bye to my cat Cole. A 17 year companion for me.
I don't know if you are a cat person or a dog person, most people seem to choose a side, but Cole was as close to both as he could get. When he was younger, he would bring me the string he liked to play with and drop it at my feet. He knew the sound of my Jeep and he would always be waiting for me at the door when I got home. He also had this keen sense that I was sad and whenever the tears were falling, he would be by my side. But, he was still a cat at heart. Very independent and purred louder than an airplane! Losing another part of our family is so difficult. Death, is not my friend. It makes me feel uncomfortable and my heart feels a little bit emptier. I know that we should be a peace knowing that there is a better life than here, but it is hard. Faith, at times, can be a hard thing. I like to believe that both Kailee (our dog that passed in October 2012) and Cole are in God's Animal Kingdom. I hope that right now Kailee is trying to play with Cole and Cole is telling him to back off.
I don't know if you are a cat person or a dog person, most people seem to choose a side, but Cole was as close to both as he could get. When he was younger, he would bring me the string he liked to play with and drop it at my feet. He knew the sound of my Jeep and he would always be waiting for me at the door when I got home. He also had this keen sense that I was sad and whenever the tears were falling, he would be by my side. But, he was still a cat at heart. Very independent and purred louder than an airplane! Losing another part of our family is so difficult. Death, is not my friend. It makes me feel uncomfortable and my heart feels a little bit emptier. I know that we should be a peace knowing that there is a better life than here, but it is hard. Faith, at times, can be a hard thing. I like to believe that both Kailee (our dog that passed in October 2012) and Cole are in God's Animal Kingdom. I hope that right now Kailee is trying to play with Cole and Cole is telling him to back off.
Ella had clinic on Tuesday. It was a long clinic because things were not going well on the floor- which usually means kids are getting sicker or kids are not making it. When Ella's doctor came in she had a smile on her face, but I could tell that the smile on her heart had been wiped away. This is why, this is why WE NEED A CURE! Please, please consider walking with us, or supporting Ella in her fund raising efforts this year. Our team name is: Kiddos Kickin’ Cancer – RMCH. Ella's Personal Page is: Ella Grace- Cure Search. We have only raised $20,000 and we are trying to raise $300,000. Kids are not treated the same as adults. Every fundraiser I hear is for adult cancers. Even the Relay for Life- less than 5% of the funds raised go towards Childhood Cancers. CureSearch is the only local walk for the kids. Please consider this very family friendly walk, and maybe we can help there be less bad days on the children's floor of the hospital.
Thanks.
Blessings~Katie
7/11/2013:
I would just like to add that I think Relay for Life/American Cancer Society does a wonderful job. My family and friends walk this walk each year in support of Ella's Aunt Carrie and Ella. My comments were only to support Cure Search and Ella and not to minimize the Relay for Life/ACS. I have updated my link to show The Relay's most current data.
Thanks
7/11/2013:
I would just like to add that I think Relay for Life/American Cancer Society does a wonderful job. My family and friends walk this walk each year in support of Ella's Aunt Carrie and Ella. My comments were only to support Cure Search and Ella and not to minimize the Relay for Life/ACS. I have updated my link to show The Relay's most current data.
Thanks
Wednesday, June 12, 2013
The normal.
HI. Sorry for the delay in my now monthly posts!
Ella had clinic last Tuesday. It is a different feeling for me to go knowing that she is not having chemo. It was unusually quiet and we had some time to chat with the nurses and Ella's favorite volunteer- The Craft Lady. She had some extra bruises on her legs, so I was a little concerned, but all is well and they are just normal every day "I'm a kid that plays" bruises. Ella has been off of treatment for 8 months and her counts are officially back to NORMAL! No more looking at her count sheet to see red exclamation points or the words Low or High. Just nice black letters that say everything is in the normal range.
But, what is our normal range? Our new family "Normal" is different. I think we have spent so much time the past few years keeping ourselves "Normal" and "Busy", that now we really have to stop, take a deep breath and figure out what this new normal will look like. For me, I think I have been trying so hard to keep myself busy and therefore a little numb that I'm not sure what our normal is.
When Ella was diagnosed my doctor suggested a low dose anxiety/depression medication for me. Knowing what I was about to watch my child go through, his suggestion was made to help me cope. I also suffered with Postpartum Depression after I gave birth to both my kids, so I had a history. Anyway, I didn't want to do it because in my eyes, that made me weak. I needed to be strong and prove that I was strong. But, who am I trying to prove this to and why do I care? I realized that I am a little too concerned with what others might think about me. It is each persons decision, but I did take that prescription. I think it kept my emotions more even during the process, but I think it numbed me a little to the normal. Normal life does have highs and lows. It is not all middle ground. It is not all everything is fine. I will have times of great strength, like signing the paperwork to add Ella to the National Cancer Registry or giving her chemo as I brush the hair off her pillow that fell out overnight. But, I think in order to grow, we must also go through times of great weakness. I will fail as a mom and yell at my kids for not focusing in the morning before school, I will let down a friend and hurt their feelings, I will forget to appreciate my husband, I will eat Oreo's at 9pm even though I know It's so bad for me. Sometime the weakness makes us stronger, and sometimes it just confirms- hey, I'm human- I'm just normal.
So, I am trying to un-busy myself. I decided to pass on the trip to Haiti this year, lessen my outside commitments, and I am going to focus this summer on enjoying a normal life with my kids. Making some plans, but I don't want to be busy. I just want us to find a new normal.
Enjoy your summer everyone.
Blessings~Katie
Ella had clinic last Tuesday. It is a different feeling for me to go knowing that she is not having chemo. It was unusually quiet and we had some time to chat with the nurses and Ella's favorite volunteer- The Craft Lady. She had some extra bruises on her legs, so I was a little concerned, but all is well and they are just normal every day "I'm a kid that plays" bruises. Ella has been off of treatment for 8 months and her counts are officially back to NORMAL! No more looking at her count sheet to see red exclamation points or the words Low or High. Just nice black letters that say everything is in the normal range.
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Ella playing with her cousin Sara. |
But, what is our normal range? Our new family "Normal" is different. I think we have spent so much time the past few years keeping ourselves "Normal" and "Busy", that now we really have to stop, take a deep breath and figure out what this new normal will look like. For me, I think I have been trying so hard to keep myself busy and therefore a little numb that I'm not sure what our normal is.
When Ella was diagnosed my doctor suggested a low dose anxiety/depression medication for me. Knowing what I was about to watch my child go through, his suggestion was made to help me cope. I also suffered with Postpartum Depression after I gave birth to both my kids, so I had a history. Anyway, I didn't want to do it because in my eyes, that made me weak. I needed to be strong and prove that I was strong. But, who am I trying to prove this to and why do I care? I realized that I am a little too concerned with what others might think about me. It is each persons decision, but I did take that prescription. I think it kept my emotions more even during the process, but I think it numbed me a little to the normal. Normal life does have highs and lows. It is not all middle ground. It is not all everything is fine. I will have times of great strength, like signing the paperwork to add Ella to the National Cancer Registry or giving her chemo as I brush the hair off her pillow that fell out overnight. But, I think in order to grow, we must also go through times of great weakness. I will fail as a mom and yell at my kids for not focusing in the morning before school, I will let down a friend and hurt their feelings, I will forget to appreciate my husband, I will eat Oreo's at 9pm even though I know It's so bad for me. Sometime the weakness makes us stronger, and sometimes it just confirms- hey, I'm human- I'm just normal.
So, I am trying to un-busy myself. I decided to pass on the trip to Haiti this year, lessen my outside commitments, and I am going to focus this summer on enjoying a normal life with my kids. Making some plans, but I don't want to be busy. I just want us to find a new normal.
Enjoy your summer everyone.
![]() |
Ella and Sara- our two ginger girls. |
Blessings~Katie
Tuesday, May 21, 2013
Ella's Birthday
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Ella 7 years old |
To say birthdays are important in our home would be an understatement. We have learned through this journey to be grateful for every second that has been gifted to us, and this week Ella turned 7!
This is not to say that my kids don't get in trouble and no one raises their voices in this house, but it is to say that when I hear my children laughing and playing together like only siblings can, I stop and thank God for that moment and pray that is can last forever.
This year we went simple and had a few of Ella's girlfriends overnight. They were all very well behaved and had a blast. She has such an awesome group of girls that she just loves. I am so very thankful that she has these bonds. Even at school, when I dropped her off with her special birthday snack, she got teary eyed when I had to leave. Immediately 4 little girls came over, put their arms around her and comforted her. So very amazing. I do not remember having girlfriends like that in 1st grade.
So, Happy 7th Birthday to my amazing, strong, beautiful, encouraging and HEALTHY Ella. We love you so much.
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Josh took this one of us. |
Blessings~Katie
Friday, April 12, 2013
Clinic Visit for April
Ella was in a really great mood on Tuesday. She was being goofy for everyone- even the Doctor she had never met that did her initial vitals. We were in and out and it was an easy day at clinic. Her counts are looking better each time we go and she is moving in the right direction!
Aunt Carrie joined us for clinic, and right after we celebrated her 3 YEARS of Carrie being done with chemo!!!! I took our little Cancer Butt Kickers to The Cheesecake Factory for some lunch and we went to Build A Bear to get what is hopefully Ella's last bear for a while. She has around 50, and I seriously am out of room to put these!
In the past 2 weeks, our hospital alone has lost 3 kids to cancer. I can not even begin to tell you how much this saddens my heart. The grief that the parents, family, doctors, nurses, and everyone involved must be feeling just brings me to tears. The fact that Cancer has beaten not 1, but 3 more children just angers me. I feel like there is so much attention to adult cancers, but no one wants to hear about Childhood Cancers- it's just too painful. And that is true- It IS painful! So, help us kick it's butt! think about supporting Cure Search which helps to raise funds to cure and support children with cancer.
Thanks.
Blessings~Katie
Tuesday, April 2, 2013
Child Life
Hi All!
Ella is doing well. I just wanted to share an article that was published by Cure Search this week featuring Megan- Ella's Child Life Specialist. You may remember that Megan made sure Ella had a Christmas Tree in her hospital room when she was admitted on Christmas Eve, and when I could not go past the magic line when Ella had surgery, Megan jumped into the gurney and rode with her.
Ella and Megan
Ella is doing well. I just wanted to share an article that was published by Cure Search this week featuring Megan- Ella's Child Life Specialist. You may remember that Megan made sure Ella had a Christmas Tree in her hospital room when she was admitted on Christmas Eve, and when I could not go past the magic line when Ella had surgery, Megan jumped into the gurney and rode with her.
Ella and Megan
Cure Search is dedicated only to funding Childhood Cancers. It is a great organization and Steve and I have been their photographers the past two years. This year I am on the committee for the 2013 walk. It is in September and it is very family friendly. When our team registration is ready I will put up the link, but in the meantime, please think about walking with us or donating this year!
Thanks so much.
Blessings~Katie
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