Whoa! I know what you are thinking – two posts in one week, what is going on over there? Truth be told, I had mostly finished the last post, but delayed posting it and needed to get this next one out before tomorrow as this is an evolving situation. I don’t fancy my story as anything as riveting as Loki or Wandavision episodes, but there is a bit of suspense being inserted into the story in the last couple of weeks with the plan changing week to week depending on blood results. As I mentioned in the last post, I had gone out on a limb by scheduling some time away. After my first deviation from the planned chemo, all I could do was wait to have it rechecked the following week. Our plan was to get that taken care of in the morning, get packed up and then head out for our next holiday destination – Anstruther. This would mean someone would drive me to chemo the following day and then need to pick me up in the afternoon, but we were really only a 1/2 hour further away than if we were driving from home. I packed all my medications and even an extra blanket and hot water bottle, in preparation for the chills and fever that had been developing as part of the after effects of my new chemo regimen. Well we were only about 15 minutes drive from home when my phone rang through my bluetooth in the van. I could see it was a ‘01382-‘ number and knew what it would be before even answering the call – no chemo yet again. The nurse sounded very apologetic while telling me that my counts were yet a bit lower than the week prior – Argh! yet another delay! Well, I guess I didn’t need to worry about the chills/fever or losing out on my Friday of ‘holiday’ sitting getting my infusion after all.
Although this really felt like a setback, it was truly a blessing to be able to enjoy time away not feeling exhausted and unwell. I was able to hike a bit of the coastal path, walk with the kids to the park, and even walk from Anstruther to Pittenweem one morning, bringing back yummy hot chocolate treats for everyone (except dad) from the Cocoa Tree. For all of this I am incredibly grateful.
Making the most of it –
Mom and Dad are now on the short end of their time here. True to the usual, Mom is trying to shoehorn all the ‘last visits’ into the time left. We are glad they have been able to get across to visit after so long away and that they put up with all the extra hassle inserted in this particular trip with COVID testing on both ends and having to add an extra leg to the journey. Tomorrow will involve checking back in on my blood tests, last visit to the Balgay cemetery, then packing and final goodbyes before getting them on the road to Edinburgh, ready for an early am departure Friday back to the US.
Lots of moving parts –
So, there is a lot going on in the next 48 + hours. I cannot imagine my chemo would be called off 3 weeks in a row, but I know now it is a possibility. Prayers for an acceptable White Blood Cell count MUCH appreciated. The plan going forward will be for my chemo to be at a lower dose. Not gonna lie here, I would much prefer the highest possible dose even if it means feeling worse, but this is what has to happen to keep going in hopes of keeping the WBC count at an acceptable level to continue. So, what is needed is the perfect balance of enough chemo to continue killing cancer, but not too much to keep me from getting the chemo.
And the results are . . .
I started this post on Wednesday and was waiting for a few pictures to add to post it. Today is Thursday and I had my blood drawn. Even earlier than I would have expected, I saw a 01382 number calling my phone. Well, the WBC count over all is improved, but my Neutrophils are still too low. Chemo has not yet been called off, but I will have my blood checked again in the morning. They only need to show improvement and I will be able to go ahead with chemo – keep the prayers coming!
Thinking of you Ashley and prayers for good news in the morning x
Praying the blood draw in the morning indicates [enough] improvement. Also, praying your body responds well to further treatment and that the path ahead will be more predictable.
I’m so thankful you got your holiday without side effects.
Praying for the Neutrophils to rise by morning and the treatments to move forward. The holiday looks beautiful! I hope your parents have a smooth journey home. How lovely they could visit despite the extra hassles of international travel at present.
So inspiring to hear in the previous post how much peace you are experiencing and strength of faith ❤️
🙏🙏🙏
Praying for a higher count tomorrow and leaving you in the hands of our Lord Jesus Christ. We love you beyond words and we are so grateful that we were able to be with you and the family. Thank you for all the fun times and the care and love you, Matt and the family have shown us. See you next time♥️
We will be praying for those results! Love you and your sweet family.
Prayers, cuz!! I know getting through the chemo is a milestone you’re ready to meet. Love you.
Ashley you a Trooper in the most inspirational sense of the word. We think of Troopers as those who will do anything to get the job done. I think the word has a military history and refers to soldiers in battle who would face any obstacle to complete their mission. Some think of Troopers as the Highway Patrol or police officer, those strong unemotional folks who can handle any situation. The kind of people you want at your side in tough times. You are a Trooper.
And the rest of us, we’re trying to be Troopers for you.
I have absolutely no idea where that last month went, but you are a blessing, not just to your Mom and I, but also to the rest of your family and a widening circle of folks needing encouragement.
Re: The “chocolate” you brought back from Pittenweem on your walk. You did bring me something, an Americano that was much appreciated. And then there’s this from your youngest: (Borrowed from my Instagram post of the day)
“This is hot chocolate, but I’m pretending it’s cawfee.” She speaks with a pronounced and delightful Scottish accent.😎