2017 Finale Video

Sunday, October 21, 2012

Temporary Home

On Friday my wife's family were visiting together at her aunts house talking about her dad and remembering the good times we had together. It was raining outside and the afternoon coffee hit the spot as we sat on the big couch next to the fire place. It was a good place to be together after the small private funeral we had for my father in law that afternoon. The shock of his sudden passing still lingers, but the support we have from family, friends and the church keep our broken hearts together.

I find it ironic that during our vacation, in our home away from home, is where he was taken away to heaven. I have heard countless sermons from Pastor Bob in 13 years and I think his final sermon is one that I have heard before. He would say that our lives on earth are like visiting someones house for a family event. There are many people and things that make us feel comfortable during our short stay, but this is just a short visit in this temporary home. (note the snow at the end of the music video)

 
For our light and momentary troubles are achieving for us an eternal glory that far outweighs them all. So we fix our eyes not on what is seen, but on what is unseen, since what is seen is temporary, but what is unseen is eternal. 2 Corinthians 4:17-18
 

Monday, October 15, 2012

A Thousand Memories part 3: Gone Too Soon

Everyone's talking about the weather and the weather has been changing fast, but you would never have guessed what happened while we were in California at Disneyland. On the third day of our vacation for Lincoln's Make-a-Wish trip, we were expecting rain in the forecast, but in the middle of the night in the most magical place on earth, there would be snow flakes falling over our hotel room.

Before I tell the whole story I want to share the last few pictures that I was able to take during the unexpected final day of our vacation of a Thousand Memories.

Lincoln's trip to Lego Land
 


 
Green Hulk as Lincoln calls him
 
Beauty and the Beast
 
A special breakfast with lots of food and friends
 
 
 
 
 
A Princess kiss
 

A Thousand Memories...
...that will never fade.
 

 
Lincoln's wish was granted in Disneyland and a Thousand Memories were made that will last a lifetime, but one such memory will be of his Papa Bob who suddenly and unexpectedly passed away while on the trip with us. In the middle of the night, the snow in Heaven began to fall as the angels of God welcomed Pastor Bob Swope into his eternal home above. Bob always loved the snow because it reminded him as a child that God would never leave us or forsake us. He was our Heavenly Father and would always take care of us if we were good, bad, sick or in need. Today our family has suffered a great loss and as we have always asked you to Pray for Lincoln, please keep my beautiful wife Jenny and her mom Mary in your thoughts and prayers as well. This has truly been a life altering event for us all and we will miss Bob like a child who misses Disneyland after the very first visit feels like its gone too soon.

 

Sunday, October 14, 2012

A Thousand Memories part 2: Lincoln's Birthday

The first day on our vacation was spent at the California Adventure where Make-a-Wish would help make a special moment in Lincoln's 4 years last a lifetime.
After a day of travel it was time for Lincoln to see what he had been waiting all this time for.
 
Pluto was first to welcome Lincoln and Emma on their adventure

 
Lincoln said he was not afraid so he wanted to go on a scary ride first
 
There was still a lot more to see during the day before the big surprise that afternoon


 
Emma and daddy
 
Getting ready for the Big Moment
 
 
Meeting Buzz Light Year
 
 High Fives
 
 and Hugs
 
So many great memories on his 4th birthday with Buzz and Papa Bob
 
but more memories will be made...in part 3 coming soon
 
 
Happy Birthday Lincoln!

Take a look and LIKE Lincoln's page for more about his Make a Wish trip @ http://www.facebook.com/prayingforlincoln

A Thousand Memories Part 1

Its not every day that a limo drive up to your house to drive you away to the most magical place on earth, but for one special boy a thousand memories were just beginning to take place.
 
Lincoln and Emma could hardly sleep the night before
 
But early the next morning they were ready to go on Lincoln's Make a Wish trip to Disneyland

He was so excited about the seats he wanted to sleep on the way to the airport
 
At the airport
 
Everyone at the airport knew he was on a special trip
 
First time looking at a real airplane
 
Meeting the pilot who asked if this was his first time on a plane and then replied "Mine too!"
 
He kept the window closed most of the time
 
953 miles and 2 hours later we were ready for some fun and food
 
Red Robin was in walking distance from the hotel
 

The first day was perfect for traveling and getting ready for the next two days of fun a the parks. Time to get some rest, more pictures coming in part 2
 

 

Monday, October 8, 2012

Is Childhood Cancer Taboo?

I am enjoying every minute of my vacation so tonight I want to share something I read today. Please take this to heart because there needs to be change for our kids fighing cancer.


Is Childhood Cancer Taboo?

Before my son Cole was diagnosed with neuroblastoma cancer when he was 4 years old I remember how painful it was to watch a St. Jude Children's Research Hospital commercial. As soon as I saw those precious little children with their heads bald from chemotherapy or radiation treatments, their small bodies connected to IV tubes and meanacing looking monitors I would quickly change the channel. I just could not bear to watch children in such pain and suffering. Many have told me that they felt the same way. I would dutifully make a donation each year thinking that at least I was doing something to help children with cancer, but other than that I would block childhood cancer out of my mind. Maybe subconsciously believing that if I didn't think about it, it didn't exist, and if I didn't think about it, it surely would not happen to my children.
In June of 2010 it did happen to one of my children and I was forced to face the horror of childhood cancer that I had closed my eyes to for so long. Within days of Cole's diagnosis my family began to live one of those commercials. I watched my active, silly, beautiful little boy suffer through painful surgeries, I saw the fear in his eyes as he looked down at the broviac line surgeons implanted in his chest, monitors surrounded him, toxic chemo medications pumped into him, he was injected with numerous painful needles, the look on his face screamed, "what is happening to me, why are you letting them do this!" I felt so very helpless.

The absolute terror of what Cole, my family, and so many other children and families have been forced to endure is something no family, no parents want to think about. How many of you have changed the channel as I did because children with cancer was too painful to face? This past September I became angry about the lack of attention and discussion during "Childhood Cancer Awareness Month" I wondered why this was the case. Was it because as some have told me there is not enough profit for the pharmaceautical companies to promote and invest in childhood cancer research? Is it because those of us who are unwillingly thrown into the "childhood cancer community" have not yet learned how to organize our cause as well as those in the "breast cancer community" have? Is it because the approximately 10,000 children diagnosed with cancer and the 3000 children who die from it each year are not large enough numbers to warrant greater attention? Or is it because childhood cancer is taboo, too painful to think about or to discuss? One mother who lost her little boy to cancer about a year ago recently told me that she contacted many radio stations asking if she could go on their shows to talk about the need for greater childhood cancer awareness and funding, she never heard back from any of them. I was lucky enough to get on one of those shows a couple of weeks ago, before we went on air the show's host told me he wanted to try to "lighten things up a bit, try not to make it too depressing" Well there is nothing "light" about it, it is nothing but depressing! That is the challenge we face in striving for greater childhood cancer awareness, I'm afraid that companies are hesitant to air commercials about childhood cancer awareness and color their products with gold because it may depress people and be bad for business. Could that also be why the NFL does not honor our Heroes and Angels with gold in September? Could that also be why the White House and towns and communities do not illuminate their buildings and commons with gold lights in September? If that is the case we must destroy the taboo of childhood cancer. We can only do that by being persistant, by being vocal, by gathering as one loud voice for our children! We must not quit until we get the job done!

A year ago in October I was in our yard raking leaves with Cole, his twin brother Troy, and his big sister Tara. They had all asked me if they could help. After about 15 minutes Troy and Tara became bored and ran off to play in the leaf piles. Cole stayed with me working hard, soon it started to get late and cold and I was tired, I told Cole we could finish tomorrow. Cole insisted that he wanted to keep going until the job was done. He was weak from the cancer and toxic treatments that had tormentd him for more than a year but he kept going. He slowly raked piles of leaves into his little wagon pulled them to a neat pile beneath our porch and kept working until he was satisfied. He did not quit until the job was done.

I wear a chain around my neck with beads that were made from ground up fragments of Cole's leaf pile. It is a constant reminder of his strength and determination. And it is a motivation for me to never quit, to keep on working until the job of increasing Childhood Cancer Awareness is done! Please help me break the taboo of childhood cancer, let me know how you feel about this, share it with your friends and family, post this story on other Facebook pages, get the discussion of the need for greater awareness going and keep it going. If we do this we will see Gold next September, everywhere.
Sincerely,
Tony Stoddard (Cole's dad)

Please LIKE and SHARE http://www.facebook.com/yellowandgoldforcole