Five Days

In five days I will be done. 

Is it me, or does it seem like time goes a little faster when I skip a couple weeks in between these updates?  It must to some, because I’ve heard over and over from people I talk to…

“You’ve had how many treatments?  Already???”

Twenty-five of thirty, as of this past week.

A double amen to that.

A lot has happened in these two weeks.  Right after I posted my last update, when I was at the halfway point, the very next day, this:

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The hair decided to leave. It had had enough.

I knew I’d lose my hair.  Well, sort of.  Dr. Smith said, “It might thin.”  I think what I’ve learned is most medical professionals don’t like to go off the deep end with all the negative details.  Even when they know WE know the outcomes given the experiences of family, friends who’ve been here and dealing with all of it long before.  Still, they sort of ease you into it all.  I now understand I will lose it all eventually but because beyond the “it might thin,” statement, nothing more was ever said until I inquired when I got the “pumpkin” this past week.

“Um, so, I’ve lost about half, will this next chemo round take care of the rest?”

Dr. Smith nodded, slowly.  “Yes.”

About two to three weeks from now, the last hairs holding on for dear life will bail and I will officially “look” like I have cancer.  I told Blaine, “Well, I reckon if I’m gonna have it, I might as well look it.”  So what did I do?  I bought…headcovers!  Are you kidding me?  Have you SEEN what they have?  Ladies, check them out, you might even want some for yourself.

I’ve already talked about all the other side effects I was having and continue to have, so, no need to trot down that path again.  Let’s just say, eating remains a challenge, but every now and then, I get a random thought of something I think I can manage.  The latest was this:

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The Best Ever Vegetable Soup

This cup of absolutely delicious soup comes from Sherry’s Bakery.  You folks from Dunn reading this, know what I’m talking about.  I’ve had Blaine make several trips to get me a bowl, and wow, in that moment, I know it’s just what I needed and wanted.  But, lets face it, I can’t stand the sight of it at the moment.

I was also able to eat, of all things, this:

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Okra! Okay, it’s a southern thing.

I know.  I know.  A lot of you – even on GOOD days – can’t eat this vegetable, but I can and do, and did.  Boiled.  With salt.  And it was good.   Was being the operative word.

Even though times have been difficult, as you know around one week ago I was dreading the week of…the pump.  Yes, when I thought about it, I turned just about the color of that pot of okra.  Funny thing.  When I went to Duke Cancer Center on Macon Pond Road in Raleigh and got “Pumpkin” back, that was one of my best days in a long time.

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The Infusion area at Duke Cancer Center clinic. Little Dog is right out there, waiting on us in the truck.

 

What made it even more amazing was I’d had a pretty bad day on Sunday.  Severe abdominal cramping (from radiation) that was quite debilitating.

As far as the rest of the week?  Well, I made it.  I don’t ever want a repeat, I can assure you.  When I went back yesterday to get unhooked, it was without a doubt the best day and the worst day since I started.  The worst part was I’d been getting sick most of the week and the worst was Friday, and let me tell you what.  That’s all I had to say when I drifted through the doors of the Infusion Area, here at the the lovely Macon Pond Road Duke Cancer Clinic.

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“Do you need fluids?”

“Yes, and I’m feeling pretty sick.  I haven’t been able to eat much this week.”

“Well, Dr. Smith is still here, let me speak to him and we’ll get you fixed up, and fixed up they did.  One liter of fluid and THREE anti-nausea medications later…

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Angel Nurse accessing port. Hurry. Hurry.

Phew, within minutes, I was feeling much better.

By the time the nurses got me hooked up and the fluids were dripping in at top speed, the pumpkin?  Finished her cycle.  Woohoo!  I got to ring a bell in celebration of my last chemo treatment!  Giddy just about says it all.

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Oh yes. We’re very happy!

But…enough about me.

I continue to receive the most wonderful mail.  Even hearing the mail truck has become as exciting for me as it is for Little Dog.  The cards, letters, and not to forget all of the online connections via FB, Twitter, and emails have certainly been uplifting.

Then, this past Sunday, a dear friend dropped this off:

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Warm and snuggly!
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Don’t get too interested.

Thank you, thank you, thank you, Lisa Fitchett from the bottom of my heart for this beautiful, warm blanket you made.  It did the job with that little cool front we had, and with the chills the chemo seems to bring on, it was perfect timing.  As you can see, the Bundle also approves!

I also captured some pictures of the radiation treatment room and the lovely caring nurses so you can see where I’ve gone each day, leaving the house promptly at 10:00 a.m. for the 10:45 appointments.

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Two of the AWESOME nurses who’ve taken me through the radiation treatments. I’m sure there are wings under those blue smocks.
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The Machine. It’s amazing really. That beige part rotates around me, like it’s on an axle.
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The (very) hard table. Those blue things hanging at the back are “forms” used for different patients to position arms, legs or whatever properly. The angel nurses do their best to make you comfy. A special head rest…warm blankets. It’s as good as it can get, considering what’s going on!
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The view from the table. I’ve studied these rose paintings a lot. I found faces in some of the background areas. One has to while away the time somehow.

Now it’s time to face the last week.  My radiation treatments will be less broad, meaning they’re going to shrink the field where I’m receiving treatment.  A winding down of the process, I suppose.

My hope is strong, my attitude fierce, but most of all, I eagerly await the outcome of all I’ve been through.  My radiation oncologist said it can take up to a year for this kind of tumor to disappear, and this means a year of watchful waiting.  More tests, more scary moments before knowing the results, but with Blaine, my family, and all of YOU, we will anticipate the best outcome.

Of course!

 

 

 

 

 

 

 

Author: donnaeve

Donna Everhart is a USA Today bestselling author who writes stories of family hardship and troubled times in a bygone south. A native of North Carolina, she resides in her home state with her husband.

14 thoughts on “Five Days”

  1. It is unbelievable to think that treatment is almost done…it feels it was just yesterday that you shared with me what you were going through. Wishing, hoping, and praying for positive results, for quick healing, and for a future of love and peace. xo

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    1. It seems almost surreal to me too, Susan. This all started on June 26 with that “discovery” and now, here we are…we’ve gone through the summer and are well into fall…it doesn’t seem possible! Thank you for all your support…you’ve been so encouraging and always there for me! It is appreciated more than you know. ❤

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  2. MY writer-friend, many years from now as an old woman, when you look back on this time, I wonder how you will view this frightening passage.
    That we are able to go forward, stand outside and look back is what makes us, us. Suffering builds steel, I guess. Your writing about all of this polishes that metal mirror-sharp for all of us. I think about your strength and humor every day. That you continue to take us on your journey is a gift for all of us.
    Thanks babe, you are one amazing broad.

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    1. This…”when you look back on this time, I wonder how you will view this frightening passage.” I will probably look at it like it was another person. I don’t feel like me, you know? This is NOT me. This is not who I am. Not by my thoughts, actions, or feelings anyway.

      I feel like some other entity (TUMOR) invaded me, and I’m doing my best to kick it’s ass outta here. 🙂

      Thank you for your kind words…spoken like a true northerner. (broad – that made me laugh!)

      If this is a gift, and if I can impart anything to anyone, then it has been worth it all. Much love to you. xxoo

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  3. Wonderful, YAY and HURRAY for the last chemo treatment, Donna!!! And what a relief that only five days are left. Also, I’m so glad the nurses let you take their pictures. They are angels indeed! Your hair will grow again, and even the hat looks good on you because you are gorgeous.
    I love your friend’s blanket. ❤ The chamsa ended up leaving Tel Aviv on Tuesday. It takes about ten days to get to the States, but its energy, blessings and protection are already on their way.
    We will keep anticipating the best outcome together, and we will SUCCEED!!! More candles are lit for you, and more prayers are sent…I love you. ❤ ❤ ❤
    P.S. I also believe in the power of visualization. If you are ever interested in that, just let me know.

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    1. If I could still do cartwheels around the house, Lilac, I would! I was SO happy to have pumpkin kicked to the curb! And there was supposed to be six days left, but I questioned the nurses and what??? There was a foul-up in my schedule so it was off by a day.

      I love the blanket too, and it has even more meaning b/c she made it – and just like that chamsa (!!!) which I can. not. wait. to. get!!! I’m so excited!

      I lover you too, dear Lilac. I am interested in hearing about visualization. We should Skype soon! On a day I am feeling well! It would be good to see you and hear your voice. ❤ ❤ ❤

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      1. How wonderful pumpkin was off by a day!!! That’s amazing, Donna! I’m SO happy for you and with you…

        I wish I knew how to make chamsas, because then, I’d make one especially for you. I should have said, though, that it would take about ten business days to arrive. And it should be PERFECT. Exactly what you’ve wanted (or I’ll talk to them, and they’ll re-send it. Your happiness is EVERYTHING).

        And YAY for visualization and Skyping soon on a day you are feeling well! I’d absolutely LOVE to see you and hear your voice again. ❤ ❤ ❤

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      2. Actually I messed up. I had “pumpkin” for five days, it was the radiation that was off by an extra day – so I don’t have six days of radiation, I have five left. I re-read my sentence above and realized I gave you the wrong info! No matter – a day less of treatment is ALL that matters! And yes, I’m sure I will love the chamsa – and when it gets here I am putting it on immediately!

        Will look forward to the day we can plan our Skype visit! ❤ ❤ ❤

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    1. Awww, Beth! Gosh that made me almost teary-eyed. Thank you. I love what you said here, “I hope the remaining radiation is kind to you, and unkind to the tumor.” Indeed. I don’t feel like a hero, but like I told Carolynn above, if I can impart anything to anyone through this mess, it’s been worth it.

      My idea is to never let the cancer win. Fight it. And if it does, then I know I’ve done my best.

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  4. Oh my sweet friend, I am in awe of you…I hope that I can be as fierce as you when/if I have to be. Tom had downloaded your first book for me to read…looking forward to it, and hope that we can meet sometime soon..love/miss you & Blaine!

    Liked by 1 person

    1. Oh Lisa. Whoever knew this would be a part of my life??? Never us. Not back in those glory days at Smith Mtn. Lake. It’s those times I think of…and what Tony went through with stomach cancer.

      Thank you for reading my book. I hope you’ll like it. Maybe we can figure out how to meet half way somewhere – for dinner? That would be awesome. xxoo Give Tom a hug for me.

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