Family
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To all my friends living in Washington
There will be a fundraiser this Saturday from 9-3 on Commerce for Ronan. The New Hope Car Cruise is supporting The Ronan Thompson Foundation this year. My parents will be there and we could use all the support we can get, even if it’s just to give my mom a hug. A huge thanks to…
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Sweet baby Ro
I have nobody to compare Ronan to, really. But is this how every child with stage 4 cancer acts?? Running around all day long. Eating like a horse. Laughing and acting like he is the happiest child on the planet. Having adult conversations with me and saying things like,”I love my brothers so much!” He…
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LOVE
We had a busy day today and I am exhausted. What was supposed to be a quick little visit to the clinic, turned out to be a 4 hour ordeal. We had to wait over at the hospital forever to get Ronan’s EKJ (heart test) and his chest x-ray. This is standard protocol before they…
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A Lego kind of weekend
What’s different now? Everything. Nothing is the same and it’s like living in a foreign country, stumbling around in the dark, or starting completely over with your life. We are all adjusting to this new life. It’s not fun and I try to just take it day by day, but it’s hard not to worry…
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The little seal wants to play
We had a great Saturday. GREAT. Ronan woke up at 5:30 this morning and was ready to go. We played and let Woody sleep in. We made breakfast, watched cartoons, built Legos… he was full of energy. The only thing he was a little upset about was the fact that Liam and Quinn were not…
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Magic Medicine Day 5, Round 2
You know what I am thankful for today? That Ronan ONLY has cancer. I am thankful that Ronan is not in a wheelchair because he has arthritis so badly that he can’t walk like the girl I met today named Cynthia. Cynthia is in high school and was of the happiest girls I’ve ever met. She…
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Magic Medicine Day 4, Round 2
Another day at the clinic. I had an eye appointment this morning, so Mimi and Papa took Ronan to his appointment and I was able to do a few normal things. I swear though, I’ve got to figure out how to hold it together in public better. I break down in the most random places.…
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Magic Medicine Day 3, Round 2
We are sitting here in outpatient waiting for Ronan’s chemo to finish. Day 3 has been pretty good. Ronan is never happy about having to come here. This morning he tried to unhook himself then seeing that he couldn’t, he grabbed the machine he is hooked up to and wheeled it away while yelling back…
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Magic Medicine, Day 2 Round 2
Today went really well. We spent the day with Mimi in outpatient getting Ronan’s chemo treatment. He slept a lot of the day which he really needed to do. Wish mommy could have done the same; I’m beat tonight. Ronan got really sick to his stomach last night so I was up most of the…
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Diamondbacks baseball game for Ronan
DIAMONDBACKS FOR RONAN! Support The Ronan Thompson Foundation and Neuroblastoma by buying tickets to the September 25th 5:10 pm Diamondbacks game! A portion of every ticket sold goes directly to The Ronan Thompson Foundation. Pass this on! Click HERE to buy tickets – $20, $34 or $40 seats. Use code name Ronan A HUGE thank…
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