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Sunday, May 27, 2018

Light at the end of Limbo

This is our life now. Doctor appointments so often that this seems like a fashion choice and Ken just plays on his phone. My sister is so amazing to check on me like every day and see how I am emotionally and physically, but for the most part, life has to go back to normal for everyone but me and Ken. We live this stupid cancer thing every day. Ugh. 
Radiation starts the day after tomorrow. Yay! 
His boss is being so cool. He said Ken can leave every day at 2:00 to take me to my appointments. I really just want to get these treatments done so that our lives can go back to normal too. 
We did have a little fun this week though. 

Last weekend was my niece Kylie's baby shower. It was so good to see my family, and Kylie is the cutest pregnant mom ever. 

New baby!!!! Ken's daughter Jenny had a sweet little baby boy named Cooper James and he is already known as CJ. He fell asleep on my chest! I had been so worried about that. 
I  planted flowers in pots for the porch. Last year, I was in the trailer in Richfield all summer, and Ken wasn't exactly the most dedicated flower hydrator. lol. 
It was the Scandinavian festival here in Ephraim. We always go over on Fridays and have lunch. It gets too crowded and crazy on Saturday, so the locals hit the booths on Friday. 

Wednesday, May 16, 2018

Limbo Land

I'm living in limbo land. I know I need radiation but no chemotherapy. YAY for the no chemo part. But I don't know exactly WHEN I'll start radiation. 
And I get feeling better each day, which is super nice. 
But once radiation starts, I will get feeling super yucky again. I will go every day Monday-Friday for 5 1/2 weeks. 28 rounds of radiation. If you google it, you only see the very worst pictures of radiation burns and permanent skin damage. But what choice do you have, really? I had a grade 1 tumor with a teeny tiny little bit of cancer in the sentinel node that was removed. So maybe that was all the cancer that I had. And maybe it wasn't. So radiation. I had a test called a Mammaprint which is supposed to tell you how mean your tumor was. If it was a mean tumor, that was growing rapidly and likely to have moved beyond the lymph nodes, I would have needed chemo. But my Mammaprint came back as "low risk" so I just do radiation. Sometime. When my temporary expanders are full enough for eventual reconstruction. The drains are out, but the doctor acted like it was too soon to take them out. I was getting less than 25 ccs of fluid out of each drain each day, and that is when they take them out. But she seemed hesitant to do it. She warned me that the temporary breasts may fill up with fluid and I would need to call the surgeon  immediately if that seemed to be happening so he can use an ultrasound and manually drain the breasts. So like every time I feel a tiny bit weird, I think my breasts are full of fluid because my drains came out too early, I'm going to get some massive infection and the incisions will open up like an earthquake. I definitely went back to work too soon. I went back two weeks after my double mastectomy, with the drains still in place. I had staff meeting, a really tough court case, and I was supposed to do a supervised visit with the mom of the really tough court case. Fortunately, Val came through and did the supervised visit for me, so I was able to go home after court. I've had a lot of doctor appointments, so I'm not back full-time, but that first day was rough. Today was great. I wasn't tired, I got a lot done. I've found that if I drink lots of water each day, walk as much as I can, and force myself to stop for breaks and lunch, I do pretty well. Pre-cancer, I worked 12 hour days and never stopped for lunch. I lived on caffeine. I never socialized with my colleagues. Now I sit with them in the breakroom and eat a healthy lunch. It's good for my psyche and my body. 
 The best part of having cancer is that you get to see how much people really love you. I've had so many visitors since all of this started. These pictures barely put a dent in it. I love my people so much <3 p="">



Saturday, May 05, 2018

The Real Face of Cancer

 I make a huge effort to be positive about this whole cancer thing. One, I believe it will aid my recovery immensely if I go at it with a hopeful, determined outlook. Two, my family needs me to be positive. They love me. They are worried enough without me acting scared that I'm going to die. 
 But he knows that some days are harder than others. Some days I am scared that I am going to die. 
 And EVERY day includes emptying these bloody drains (pun intended) with the occasional clot or clump of tissue. 
 My daughter and my sister get glimpses of how I really feel sometimes too. 
And #tinastribe just makes it all better on the days when it isn't super easy.