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Showing posts from January, 2023

A New Regimen

Last weekend Sid finished his last dose of Oxillaplaton. Good riddance! Thanks for your help, but we're glad to see you go.  His scans gave us great news! The cancer is still contained to the original areas and they are all shrinking! In the words of Dr. Nevela, "Your prayers are working." This coming weekend Sid will start his new regimen. It will be a combo of chemo pills and a target/immuno therapy IV infusion. The infusions are every 3 weeks now instead of every 2. The side effects are supposed to be fairly mild overall. We are so grateful for that! Sid will continue to get scans and tests regularly and adjustments will be made as necessary.  We don't have a timeline to report since it's all individually based. We know that Sid is getting the best care possible, and that's good enough for me.  Thank you for your prayers. Each time I hear my kids pray for their dad it just.... It hits home in a wonderful, meaningful way. Every single time. I hope they are l

Next steps

I know many of you who read these posts have diligently checked for updates over the past while. I know you worry. Thank you, for loving us that much. There hasn't been anything "new" so I didn't feel it necessary to write anything. The last treatment was hard and heavy, but that's fairly normal that each new treatment has left his body feeling the effects more severely. This Friday will be treatment #8 for Sid. As I said before, the last one was noticably more difficult than any other. So - as you can imagine - no one is really eager for this next one.  It's redeeming quality, however, is that this one is somewhat of a milestone. We were told that this one would be the last chemo that included the Oxaliplatin. This is the drug that has caused the neuropathy and cold sensitivity. With it being January in northern Utah I'm sure it comes as no surprise that Sid will be glad to be rid of it. That's really the only "sure thing" we know right now.