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  • Hello, and thanks for joining me on my journey.

    This is Owen. He is a 3 1/2 year old boy who is loving, energetic and loves to have fun. He was diagnosed with Leukemia on November 18, 2012. This is his story.

Owen’s Leukemia – Days 251-252

Yesterday was supposed to be Owen’s first day of Long Term Maintenance.  He was ready.  He wore his scrubs, and doctor coat and was the hit of the floor.  All of the nurses had to come see how cute he was.  He did so good with them accessing his port and getting his blood.  The results came back… and the ANC was down to 560!  It was 1270 when we were in the Emergency Department the other night, and I guess I assumed it was going to stay up.  They think he must have had some kind of little virus and that is what knocked it down.  Due to it being down so low, they couldn’t begin this new phase of treatment.  It needs to be 750 or above.  So, we go back next week, have to fast, and try it again.

Today was Nana’s birthday, so they came down to spend the day.  The boys had so much fun!!  Owen loves helping out Pap Pap, and taking hikes.

KimAugust 2, 2013 - 3:39 am

I’m sure he was a BIG hit. What a cutie! Hopefully everything is good to go next week!

Owen’s Leukemia – Days 242-250

Sorry again for the delay in posting.  When we have such good days, it gets away from me.  Last week went very good.  We had a fun outing with a friend at Animal Treasures in New Castle last Thursday.  It is a zoo, but a lot smaller.  They also have a lot more interaction between the animals and the guests.  One thing I thought was really neat is you can buy food and put it in a bucket, and send it to the monkeys and they will get the food out and send it back for more.  And the male lion likes to put a show on every several minutes.  He comes to the front rock and stands and roars for a little, like he is talking to everyone.  So neat!

Saturday was another special day. I won tickets to a Superhero Cruise on the Gateway Clipper.  Jeff and I took Owen.  He dressed in his Spiderman outfit and got to meet some of the superheroes.  It was a lot of fun for him.  That night we noticed he was running a little bit of a fever.  We monitored it all day Sunday.  It was in between 99-100 which wasn’t too alarming.  Monday, he seemed fine, we went to the park in the morning, came home and it was up to 101.  I thought maybe it was just because we were out in the sun and he was running around.  After nap, it kept going between 101 and 100.5 and up.  We called the hospital after dinner and talked to the Oncology doctor on call and she wanted us to bring him in.  So, I took him down at 7:30 last night so they could run some blood work and give him some antibiotics.  His ANC was good (1270) so we were able to come home instead of staying there.

We go back tomorrow, and as long as his ANC is above 750, he will begin Long Term Maintenance.  Tomorrow is going to be a rough day.  His procedure isn’t until 1:30 pm and he has to fast before since they are doing sedation and giving him a lumbar puncture.  I am going to try to keep him out of the house and occupied so that he doesn’t think about food.

Best Buds

Joanne&Barry MurphySeptember 25, 2013 - 9:20 am

Hi,

Just returned from a trip and read Owen’s blog. So happy to hear he is doing so well. He will continue to be in our prayers. Love, Joanne&Barry

Owen’s Leukemia – Days 239-241

I am so thankful that the Doctor’s reduced Owen’s quantity of Methotrexate for this week.  They reduced it by 20% of what he had the time before.  It has made a world of difference.  No mouth sores, and he has been feeling great!

Saturday, we took the kids to see Monsters University.  Owen loved it, and it was Logan’s first movie, so he didn’t know what to expect.  He did relatively good.  I only had to take him out a few times.  Today, the boys got to see their cousins.  Cleaning out Nanny and Poppy’s old house, they found some duct tape.  Oh my, boys and duct tape… they came up with a lot of uses.  Here they are planning on what to do with it next.

Owen’s Leukemia – Days 236-238

Well, yesterday was the last day of treatment in the intense phase.  2 weeks and we start Long Term Maintenance, as long as his counts are good enough.  He had a good day yesterday.  He had a hearing test in the morning, which he aced, then his chemo in the afternoon.  While he was waiting to get his chemo, he got to visit with the therapy dog (Bubbles, the Chihuahua)  and her owner.  He LOVED it!  Usually the therapy dogs are big and he gets a little intimidated, but since Bubbles was nice and small, he didn’t want to leave her.

Here they are, hanging out, telling stories.  The volunteer was so good with Owen too.  He told her this story that went on for about 15 minutes, and she even recapped it back to him!  What a great listener!!

KendraJuly 18, 2013 - 10:58 pm

Awww…this is a great picture!

Beth HuffmanJuly 19, 2013 - 4:59 am

Owen’s story continues to amaze and inspire. Keep swimming, Renee!

Joanne & Barry MurphyAugust 10, 2013 - 8:35 pm

We couldn’t be happier for Owen. Hopefully, the worst is over. He will still remain in our prayers every day. xxxoo Joanne&Barry

Owen’s Leukemia – Days 231-235

Well, we made it through the weekend without ending up in the hospital.  Owen’s mouth sores are still there, but we have been managing the pain.  He hasn’t used too much pain medicine, and has gotten a lot better at swishing the mouthwash.

Saturday we did something really fun for the boys… took them to Idlewild!  Neither had been to an amusement park before, and they both loved the rides!!  Owen even got his face painted like Spiderman!  Although, with no nap, something happened when we got home, and a little breakdown occurred… hence the running paint.

Sunday was spent recovering from the busy day on Saturday.  We put the pool out and they kids were soaking it up!  Pretty much the same today, but Nana and Pap Pap came for a visit.

Pretty excited for Wednesday.  It marks the last day for Owen’s intense treatment.  After this phase he moves into Long Term Maintenance.  It will still consist of taking chemo drugs by mouth daily, and monthly visits to the hospital for chemo, but it will be a much needed relief for the constant weekly trips.  Long Term Maintenance will last for another 2 1/2 + years.  We still have a long road ahead, but it will be so nice to be out of the really rough stuff.

KimJuly 16, 2013 - 7:32 am

What a cute little Spiderman! Good luck tomorrow! What a relief to be through this phase!