We're at the hospital for an MRI. The doctor moved up the date a bit so we can see how the tumor is responding to the current treatment protocol. Dr. Thomas was expecting that the Kaytruda would be working by this point; the "worse before it gets better" would be over, and each treatment would be causing improvement. Unfortunately, that isn't what we're seeing.
Instead, we're continuing to see decreasing function. The aphasia (difficulty speaking and finding words) seems to be a bit worse. Mom is also needing more help to move in and out of her wheelchair.
Although we are doing the scan today, we won't know anything about the results until we meet with the doctor on Tuesday. After that we'll have a bit more information and we'll know whether or not we are continuing with the Kaytruda. Although we are anxious about this MRI, we are looking forward to having more information so we can make the best decision about what to do next.
I can relate. Waiting for the MRI/CT-Scan results and listening to the doctor’s findings have always been the worst part of being at the hospital for me. My dad died of lung cancer, and I guess reading through your mom’s fight against cancer brought up memories. I am very sorry for your loss. May she finally find peace and rest.
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