Sunday, November 25, 2018

Chemotherapy - Day 10

Things are going fine, so far. Rather than wasting your time reading these posts, I decided to only add a 'chemo-post' if things start to go wrong...

Saturday, November 24, 2018

Chemotherapy - Day 9

Day 9 - 

Prescribed:

  • Procarbazine (Matulane) - 100mg (for chemo)
  • Doxycycline, 100 mg (for previous infection)
  • also Zofran - 8mg  (to prevent nausea)
6:30 AM - Again, I didn't take the zofran to prevent nausea. There seemed to be no issue, yesterday. If nausea kicks in, I can/will see if zofran works for me... As it is, I only need to take the procarbazine for chemo, today. I still have to avoid the tyramine foods.

8:30 AM - I'm supposed to give it one hour after the "P" before I eat, but I wasn't in a hurry - or, terribly hungry. I ended up cooking an omelet - just eggs and shredded cheese - and I'm not having any issues...

10:00 PM - No issues today. I just took the doxycycline and done for the day. I'm pleased with the way the day went.

Friday, November 23, 2018

Chemotherapy - Day 8

Day 8 -

Prescribed:

  • Procarbazine (Matulane) - 100mg (for chemo)
  • Vincristine - intravenous (for chemo)
  • Doxycycline, 100 mg (for previous infection)
  • also Zofran - 8mg  (to prevent nausea)


6:30 AM - While I now have Zofran on hand, I don't want to use more than I need. I'm giving today a test. If procarbazine - the "P" - doesn't cause me to get nauseous, I'm not going to take the Zofran. As such, I only took the prescribed 100 mg of "P," this morning. I'm drinking a lot of water with it.
Today also introduces the need to avoid the tyramine foods. This shouldn't be a major problem, for me. There are many things on the list that I don't like to eat, anyway. The problem is that aged cheese is on the list and I do like to eat a lot of cheddar and Swiss cheese - also, I'm not supposed to eat any beef jerky...

7:45 AM - Breakfast. Here comes the real test for nausea. It's one thing on an empty stomach but, now that I'm eating, we'll see...
At any rate, I'm sticking to the keto diet.

9:30 AM - just got blood drawn for testing the levels before the IV and waiting for the results.

10:15 AM - I just got the results through email! It's really scary that I have access to the results this fast through the internet! Everything looks normal except the BUN - that's a little high. Still waiting for the doctor to approve the "V" as a result of the blood test.

10:45 AM - Doctor meeting... Still waiting for "V" - this time, for the pharmacy to fulfill the prescription.

12:00 PM - Finally heading home. The IV shouldn't have taken so long. Literally, it was a 2 mg dose of the vincristine in 25 g of saline.

The rest of the day was uneventful. No negative reaction to procarbazine or vincristine - yet!


Friday, November 16, 2018

Chemotherapy Begins...

Not an exciting title to this post. Sorry...

Today, 11/16/18, I began the PCV chemotherapy and I decided to log my experience with it. I will be  updating the post as the day progresses and will continue to do so in my real-time.

Day 1 - prescribed:

Lomustine/CCNU, 210 mg (for chemo)
Doxycycline, 100 mg (for previous infection)

5:30 AM - The only thing scheduled for PCV today is one dose of the "C" - lomustine/CCNU (210 mg). Taken on an empty stomach. I was supposed to have a prescription for ondansetron (Zofran) (8 mg) to treat any nausea caused by the lomustine - taken 30 minutes before taking the "C" - but the prescription wasn't issued in time for me to pick it up, yet.
I'll brew some pau d'arco/taheebo tea for the day (my plan is to brew enough to fill one of my 64 oz. growlers for later use).

11:00 AM - So far, so good. No reaction to the "C" but the morning got away from me and I am just getting my breakfast! I was not intending an intermittent fast. I'm taking my multivitamin with my 'brunch.' We'll see how it goes.

5:30 PM - Just got back from the pharmacy to pick up the ondansetron prescription. Fortunately, I haven't needed it! Prepping/eating dinner. So far, I haven't experienced any nausea. With my dinner, I'm taking niacin (500 mg), potassium (200 mg), omega-3 (1500 mg), vitamin D3 (2000 IU), vitamin E (400 IU), and vitamin K2 (100 Mcg).

8:30 PM - Snack for dinner. Supplements: niacin (500 mg), potassium (200 mg), magnesium (160 mg), omega-3 (1500 mg)

10:30 PM - doxycycline

Tuesday, November 13, 2018

Good Times, Bad Times...

Thank you, Led Zeppelin  - "Good Times, Bad Times, you know I've had my share..."

That's been my share for the last couple of months - good and bad times. As I mentioned in the last post, here, I didn't start with the chemotherapy due to the spiked creatinine levels and potential kidney issues. Well... shortly after that, I ended up back in the hospital for a third surgery! The stitched seam from the second surgery had *popped* open and exposed my brain to the air. As a result of the surgery, I ended up back on vancomycin. This time, they only scheduled 1,250 mg twice a day instead of 1,500 mg three times a day. I didn't have the same negative reaction - Red Man Syndrome - this time!
Due to the possible source of the creatinine spike - muscle soreness - I didn't do ANY exercise during the recovery time... 6+ WEEKS of NO exercise! As usual with vancomycin, my appetite disappeared. This time, I tried to eat every day, but my intake was still only about 1,000-1,500 calories each day. On June 1st, I weighed in at 210 lbs., 24% body fat - fairly normal for me. As of today - Nov. 13th - I weighed in at 160 lbs. and 13.6% body fat! At one point, I was down to 156 lbs. - at 6'2" tall, that's not a terribly healthy weight!

...good times, bad times.

...excuse me for a minute - I need to answer the phone...

Well, while I'm sitting here and typing this post, I got that phone call... Apparently, I should expect a delivery for one of the three components for the PCV chemotherapy - specifically, the "C" - tomorrow morning. I haven't gotten any information regarding the second component - the "P" - as to when I should be receiving that but it will come from a different pharmacy than the "C." As far as the "V" is expected, that is actually an IV that I will have to spend at least an hour at the hospital for.
Once I start the cycle, I will take "C" on day 1. Then, nothing until day 8. On day 8, I start the day with the "P" on an empty stomach and, later, head to the hospital to get the IV of "V" that will take about an hour. I, then, stay on "P" everyday from day 8 through day 21. The last part of the cycle is a second IV of "V" on day 29 BUT, I then need a blood test every week until I restart the cycle. Oh, and an MRI.

...good times, bad times.

More on the "good times" side than the "bad times"...
Given that the doxycycline *apparently* didn't have much impact on the creatinine, I'm back to exercising!