Sunday, January 21, 2018

Almost...

Almost done with chemo
Almost time to find out about next phase of treatment
Almost time for mom and Bill to go home
Almost time for my hair to start growing back
Almost a month break from treatment
Almost time to get back into the swing of things... work, church, 'normal' 
Almost cancer free...


It's hard to be in this place of almost, especially as I'm not feeling good from this last infusion of the carboplatin/taxol chemo cocktail I received on Tuesday. It's the last of the cocktail though, and now I just have 2 more taxol infusions, which don't take me down as hard typically. I was reminded this week that this last carbo cycle is the lowest I will go (in terms of feeling crummy and immune suppression), and even though the taxol will kind of keep my system 'down,' I will start building up from here. As soon as this carbo is out of my system, my hair will start growing back. As soon as I receive my last infusion (scheduled for Jan 29th), I don't see the oncologist again for another month. Almost done with this phase of treatment!

In the meantime, I see the radiologist at Stanford tomorrow to determine my needs for radiology. So, if you are praying with me through this, please pray that my case is not complicated and the dr will feel confident about referring me to a more local dr to receive treatment. I'm not sure yet what my procedure/schedule would be, but was told typical radiation is 5 days a week for 6 weeks... that is a LOT of time right there, thus the desire to have a good local option. There is a Stanford affliate radiologist in Turlock (about an hour and 15 mins away from home), and my oncologist was ready to send me straight there, but I insisted on meeting with the dr who sat on the Tumor Board and determined that radiation would be required for me before getting referred out. So, I get to meet with her tomorrow. My prayer is that the Dr. knows someone brilliant in Sonora who she is confident about referring me to, or that the Turlock dr is a really great option (it's easier in the system to stick with Stanford dr for the medical records and such). Almost time to learn about the next phase of treatment.

We are also preparing around here to send Mom and Bill back home... they have been here since Oct 15th--3 months!!! I can't even begin to describe the gratefulness I have for them. They have been such a support in so many ways, to try to list it all out would come up short. The plan is for them to roll out on Wednesday to start their trek back to Ohio... I am thankful that I am doing well enough that we all feel it is time for them to go, but man, we going to miss them. We have loved having them here--getting to attend all the kids programs, basketball games, awards assemblies, having them here for dinner every night and building puzzles and working on projects. It's going to be so quiet, and honestly probably a bit overwhelming for us how to figure out how to do this on our own again. Almost time to say goodbye still gives us a few days...

I am looking forward to the 'almost' of feeling like I can be 'normal' again--whatever normal means. What it means to me now is no nose bleeds every day, food tasting good again (especially bread!), no more numbing in my hands or feet (neuropathy--a typical side effect of this kind of chemo), being able to attend a friend's birthday party and Bible study, not having to drive down to the Bay Area weekly, being able to hug people, being able to go to church, not worrying about germs so much, being able to participate in our home remodel stuff, and being out of the chemo brain fog to see students at work again. The feeling of being productive is one I have missed. I know my 'productivity' now has to be internal--building my white blood cell counts, platelets, taking care to eat foods that have lots of protein and help my liver detox from all the meds, resting/sleeping... this is what keeps me moving forward in my treatment and allows my body to heal. Thankfully, with mom and Bill here, and Brian working as hard as he does, there has been a lot of activity around the house in terms of upkeep and forward progress, but I'm looking forward to getting my mind and hands back into it. Almost...

The last almost... cancer free... when I asked the doctor when I would get to hear those words and the response was "we will keep monitoring you," I had a bit of a melt down. Apparently my oncologist will not tell me I'm in remission or cancer free. I will get 'monitored' every 3 months after the active treatment phase is over. At each check-up, if they don't find cancer, then I'm free of cancer... for now. I can imagine this will be a bit of a nerve-racking experience each time I go for a check-up. This will be another way my faith and trust in God will have to have victory over my heart and mind. 

The song playing in my heart over and over with this is "Only King Forever"... especially the lyrics: We bring our expectations, Our hope is anchored in Your Name, The Name of Jesus, Oh, we trust the Name of Jesus... and the chorus: You are the only King forever, Almighty God we lift You higher, You are the only King forever, Forevermore, You are victorious!


So... living in the almost phase right now... lots to be thankful for and lots to look forward to, with some tears, miles and struggle in between. So blessed to have your prayers, love and support along this journey with me.

2 comments:

  1. Thank you Kirsten, for your openness and wisdom. We are lifting you up in prayer, dear friend. Prayers for no complications. Prayers for a really good local doctor. Prayers for the peace that surpasses all understanding each time you go for a checkup. Prayers for you to be cancer-free!

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  2. Almost done sweet friend. Thank you for all your updates. Love you!
    Also I have updated Kirstens meal train to help her through these last few weeks of chemo. If you'd like to check it out it is www.mealtrain/12v2v6

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