So, chemotherapy session number one came and went today. I spent three hours at Columbia Basin Hematology and Oncology Center where I had by my count 8 different substances fed into the port in my chest via IV. After the treatment, I felt pretty good and went to Walmart with my mom to pick up my anti-nausea prescription (Zofran), as well as a few other things.
When we went to pay for the prescription, we got a shock, as the Zofran was over $500 for twenty pills! I talked to the pharmacist, Kyle, about any alternatives, and he said that Zofran is usually reserved for where other nausea medicines haven’t worked, and use it as a last resort. He called Dr. Sierra’s office to confer with one of the chemotherapy nurses, Cynthia. She said that something weaker would be fine, and changed the prescription to Phenergan, which was only $6.
While at Walmart, I ran into a woman named Kathy who overheard me talking to the pharmacist about my chemotherapy. She went through chemotherapy for breast cancer a couple of years ago. In addition, she volunteers in the Wellness Center at Columbia Basin Oncology. We chatted a bit about what I should expect, and some of the things it is important to do. Probably the biggest thing I took from it was advice to not push my friends and family away. I’ve already caught myself doing that several times, and I need to make a conscious effort to not do that. To anybody I’ve already tried to push away (especially Dana and mom), I apologize profusely, and I will make it my #1 priority to be there for you guys, as I know this is tough on you too.
After grabbing a sandwich from Subway, I went home, took an anti-nausea pill, and went to sleep. Unfortunately, the phone would not stop ringing. Some well-wishers, which I certainly appreciate, but mostly telemarketers, which really annoyed me.
However, one of the phone calls was from Kyle the pharmacist. He said that Cynthia from the Cancer Center called him back, and I shouldn’t take the Phenergan, and he would exchange the prescription to Kytril. He said I should call Dr. Sierra’s office to confirm this was okay. Of course, I panicked, as I had already taken one of the pills. I called Cynthia, and she said that the Phenergan should be okay. I asked why she called them and told them to switch, and she said that she was concerned that the Phenergan wouldn’t be strong enough. She does have some drug rep samples back at the office of a stronger anti-nausea drug that I could pick up, though I can’t remember the name of the drug. My mom said she would head over to the office and pick them up for me. After all this, I went back to sleep.
After waking up from my nap, I sat down and played a little poker. I played some $50 NL on FullTilt, and though I certainly didn’t have my A-game, I was able to double my buyin in an hour. Unfortunately, my head started pounding, and I started getting nauseous, so I had to call it a night from the game. I decided to relax and watch some TV before heading to bed. My mind was racing over what tomorrow will bring.
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8 comments:
It's 5pm where I am, which means you are starting chemo in about an hour. Know that I'm thinking about you and praying for you!
Dana -
Have been thinking about you today. Hope your 1st infusion went well! Will continue to keep you in my prayers, along with TJ!
Judy
Dana:
Just wanted to let you know I been keeping up with your blog. Just wanted you to know that Leslie and I are thinking of you and keep you in our prayers.
Tom Livernash
From: staff@INVacations
To: Mr. Deeps
Welcome to Chemotherapy, Dana, from the staff and community at Involuntary Vacations.
We hope you enjoy your stay.
All your surprises with us are offered in vivid technicolor. Our friendly staff and probably overbearing community will be there for you. All the time.
Entertainment options include:
* Sports. All the games viewable through your personal network television.
* Mandatory Communication. With friends, staff, and family. Through phone, internet and in person, whenever we want.
* Consultations. Regularly scheduled doctor, nurse, and family meetings each week, day, and hour.
* The Sun. It goes up and down, east and west every day. On some of them you'll get to observe this in detail.
* Hobbies. Anything that can be done sitting or lying down... will only end up irreparably cluttering the area around you.
* Sleeping. You'll learn to love it. Or wish you had. Try it in exotic locations!
* The Bathroom. Where the complement of everything else in Entertainment happens. Some find peace here, usually hidden in the lock on the door. Turns out it was there all along.
I.V. Relaxation Time
For relaxation, we've scheduled you in for mandatory appointments twice a month at one of our luxurious I.V. Relaxation Time stations. These are currently outfitted with the latest in basic cable, internet facilities, and single person reclining seats. An attendant will be by regularly to supply you with refreshments.
Please ignore the microphone stand attached to your chest, and the potentially caustic bags attached to it. It does not function as an actual microphone, and karaoke is strongly discouraged.
Pay no heed if the alarm attached to your microphone stand goes off, an attendant will turn it off shortly. The noises from the next station over mean nothing. They did not just say what you think they said.
Personal note from the Management:
The staff informs me that our I.V. Relaxation Time stations are lacking internet support. Apparently when they said we'd have them by '07 they had meant 3007. Oops. I would highly recommend reading a book or magazine, and sudoku. Have fun with that.
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I\ /acations
NVoluntary
We hope you never come back. So do you.
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Hey, Dana,
The lack of internet connectivity at Kadlec is... most disappointing. I presume you've already tried wireless. Perhaps a coffee can antenna and some wardriving is in order?
Luck to you next weeks, sir,
TJ
Hi dana my name is Alechia Fludd my mom is friends with Wilma dixon. I had Hodkin's Lymphoma at fifteen, went through six months of chemotheraphy and 2 months of radiation, the biggest piece of advice I could give you is to stay prayerful, relax and most of all laugh as often as you can. Laughter soothes the soul, there will be days when you just don't feel like doing anything and may feel down, that's why I say laugh no matter what; some people may think your crazy, forget about them the laughter is for you and your sanity. I laughed many days and I'm sure my parents thought I was crazy, but I felt good. I had to laugh to keep from crying. I was diagnosed a month after my fifteenth b-day, my solphmore year in high school. Cancer and puberty were rough, but I made it, and so will you. I have been in remission for 11 years almost 12. I am a survivor; you have cancer but it doesn't have you! I,m praying for you, God Bless! If you have any questions here is my e-mail: Lelee1080@aol.com
Keep your head up!
Alechia
Dana, I will miss you and your smiles here at work, but wish you all the best in these next few days/months. I'm glad that yesterday went somewhat without a hitch. Who knew that you would have to finance for anti nausea meds. My thoughts and prayers are with you. talk to you soon. Looking forward to my steak dinner, lol.
Dana,
Just wanted to let you know I was thinking about you. I hope you know that we all love and miss you. Remember our conversation about the power of your mind to do incredible things.
Hey buddy, still keeping up with your blog. I'm glad you are doing well. Remember to keep your chin up. I miss you at work, there is no one to bug! The boys will never see the fun in having the salt container left on their desks... :) Hope you are back soon. Take care of yourself.
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