Nicholas is a 14 year old kid who loved to hike, swim competitively, and run track. On October 30th, 2012 his life was forever changed on this day, for it was the first time he had ever heard the word Osteosarcoma. Nicholas was diagnosed after a couple weeks of sports related, as well as normal rough and tumble boy injuries. For a couple weeks he complained about pain in his upper knee area. I told him that is didn't surprise me after watching he had his brothers flinging themselves up our stair case one day trying to see who could jump the highest. After a couple weeks of ibprophin and ice, one morning he woke up and the swelling was beyond what was considered "normal". In the pit of my stomach I knew this was cancer. Reluctantly I made the Dr's appt. where there was an x-ray given. By 5:00 that evening I was phoned at work and told that I needed to get him in for an MRI. This was the first time I had ever heard the word osteosarcoma. In that call, the two phrases long road and leg removal were used. I walked away from work that day knowing I wouldn't be back. I was VERY aware our lives were going to be changing very drastically in the next few months. My husband and I went home where we had a family meeting to break the news we had just been given to the boys. We cried together but decided we would go through this as positively as we could. We decided at that point we would live day by day, not worrying what the future may bring. The next day the MRI was schedule where the diagnosis of Osteosarcoma was confirmed, later finding that is had metastasized to his lungs.. Nicholas was placed on a 29 week chemo plan with leg salvage surgery taking place on February 13th, 2013. Nicholas was thrown into an unfamiliar world of doctors, nurses, testing, surgeries, chemo therapy, nausea, throwing up, mucositis, mouth sores, pleurisy so painful I can only compare it to child birth, maybe even worse, 20% weight loss, among several other odd effects that chemo causes. Nicholas was placed on a feeding tube after losing 20% of his body weight. Initially the feeding tube was presented as a threat if he wouldn't eat. In my mind I would always wonder what drug these people were on since there is no human that would want to eat with the condition he was in. The feeding tube was finally introduce, where I watched my son become the bravest person I have ever met. The feeding tube has been a huge blessing that I believe should be introduced in the beginning of EVERY treatment plan to aid patients as they struggle through these difficult times. We continue to stand behind Nicholas as he fights his battle, moving into the lung surgery phase of his treatment. We live day by day enjoying every minute we have together, nothing more nothing less. With the grace of God and a whole army of thought and prayer warriors behind us, we continue to fight this nasty battle.
Cards & well wishes can be sent to: Nick/Tracy Floyd, P.O. Box 7903, Surprise, AZ 85374 - for Nick's story & donation info. click about/see more
Donations can be made to Nicholas's Fund at any Chase Bank: Tracy Floyd FBO Nicholas Floyd Acct: 433016438; paypal - email@example.com
For gift cards - Places the Floyd's frequent for gas and groceries: Costco, Fry's, Sprouts and Target. Thanks for the offers to help!
Please help him.
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