2019-09-06 Quick Update

Quick Update that I am still alive. Having gone through a period of bad and good days, with the bad having be in the majority, I had little time to do my daily blogging. Most time was spent either having to catch up with work that was to be done during the bad days, or having treatment days and new specially doctor’s appointments in an effort to figure out some new symptoms (side effects) treatment. Starting tomorrow, Dianne will be able to administer Hydration for me each day thanks to Sutter Health Home Care Services. This will be a great time saver.

More on that as I hope to resume my daily Living with Cancer blogging.

2019-08-29/09-01 Living with Cancer Day 904/905/906/907

I am sorry for not having blogged the last three days, but things are a bit hectic with doctor appointments and hydration, which takes between 3 and 4 hours for 2 Liters. The bad news, they still don’t know what causes the sudden fever and increase in some small sores on my lower legs and arms. Both are identified as possible side effects. On the bright side for the last week and a half, I have had no night sweating, however, I do have it every so often during the day lasting for an hour or two.

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2019-08-22/23/24 Living with Cancer Day 897/898/899

Quick note to let you know that I am OK. The reason for not having posted for the last three days was that we were very busy. On the positive side, my pain and discomfort levels were low enough for me to be more active than ever. Added to that, that my test results were also very good, including the antibiotic treatment numbers got were they are to be between 2 and 5, which with 3.7 is perfect, instead of 8.2. All this together gave me the energy for the last three days to be a bit more active.

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2019-08-21 Living with Cancer Day 896

Date: 2019 August 21, at 06:35:04 PDT, Weather: 63 °F Clear
Title: GETTING UP

I got up a bit earlier to be ready for my Chemo treatment to day. After doing my upstairs routine I went downstairs. I did have some light sweating, something that had disappeared since coming back from the hospital. I had bagel with cream cheese for breakfast. After that I took my regular morning medication before resting for a bit.

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2019-08-15/16/17 Living with Cancer Day 890/891/892

Let me start by saying I am back home. I got back from a 3-day stay at John Muir Hospital in Concord. I had a 102.4 F fever the night before my chemo treatment and my CBC numbers just before starting the infusion were too low, so they send me to the ER.

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2019-08-13/14 Living with Cancer Day 888/889

You may have noticed that I did not publish yesterday. The reason being, starting around lunchtime I was to fatigue to do anything as I constantly dosed of. This morning, after night with constant stomach cramps, Dianne took me to the cancer center for my chemo treatment. Drawing blood for a CBC to determine my premeds, it was found that I was at the limit of going ahead, but because of my stomach issues during the night and a high fever, I was told that I need to check in at John Muir’s ER because I have neutropenic fever, which the CC is not setup for.

That is where I am now. I am very fatigue and even typing this short note has taken some time as I dozed of two times writing it.

I will try to get back to my regular reporting after they find out what is causing this, or I am no longer dozing off for long periods.

2019-08-12 Living with Cancer Day 887

Date:   2019 August 12, at 06:37:31 PDT
Weather:    61 °F Clear

Getting up
Time to get up and ready for the day. Current status is, light stomach cramps, dizziness and ringing in the ears. After my morning routine I rested a bit before going downstairs.

Date:   2019 August 12, at 07:14:24 PDT
Weather:    64 °F Sunny

Now Downstairs
I went downstairs and had a light breakfast with tea because of my stomach aches. After that I rested and got ready for our walk.

Date:   2019 August 12, at 08:01:05 PDT
Weather:    72 °F Sunny

Out walking
The walk with Dean started of ok, however after 2/3 of our walk my left shoulder started to be painful. The pain forced me to stop and rest for the last 1/3 of the way. In addition to the shoulder pain my stomach started to act up. The good news I made it home.

Date:   2019 August 12, at 08:38:05 PDT
Weather:    73 °F Sunny

Back home from walking
Getting home Dean setup the Oxygen Compressor for me. It did help me with my breathing which was a bit shallow because of the pain. He watched me to make sure I was Ok before leaving. I had retired to my recliner and before I knew it was dozing off.

After about an hour later I was able to move around and get something to drink and eat. Not having much energy I just caught up with some TV shows I had recorded. Soon lunchtime did arrive.

Date:   2019 August 12, at 13:49:40 PDT
Weather:    91 °F Sunny

Lunch Time
Dean was so nice to get me a small salad from Wendys. In the meantime I was trying to get ESPN3 up on Apple TV. I was able to get it on my iPhone and Laptop but on ATV it tells me I have no account. I therefore watched Bayern vs Energie Cottbus on my laptop. However, not giving up with ATV I decided to logout and then back in, which suddenly allow me to have access to the game on ESPN3.

After the game was over I switched to regular TV watching some other shows I had recorded until I had to get ready for my doctor appointment.

Date:   2019 August 12, at 14:39:16 PDT
Weather:    93 °F Sunny

Time for Follow-Up Appointment
Dianne picked me up for my follow-up appointment with my oncology doctor. In summary the new cancer treatment seems to be very effective. The issue of fatigue is due to the fungus treatment, especially the antibiotics and its dosage.

Moving forward, my current antibiotic will be changed to one that does not have the skin issues as a side effect, a new trough ad fungus draw are scheduled for 1st week in September.

Before leaving, I went for a CBC and Myeloma blood draw. Since the result of the CBC draw sowed that the platelet count was low, 46, the doctor suspended taking the cancer pill (Pomalyst) for now.

Date:   2019 August 12, at 17:15:28 PDT
Weather:    95 °F Sunny

Dinner Time
Getting back home from the doctor appointment I rested since I was totally exhausted. Dinner time was not far away, therefore I watched some more recorded TV shows.

Once dinner was served, I just could not get my appetite up to eat much. Some of it is link to my lack of energy, the other that I still have stomach cramps.

Date:   2019 August 12, at 18:34:57 PDT
Weather:    93°F Sunny

Calling it a Day
As mention before, I am just unable to concentrate on anything. It took some doing to finished today’s blog. On the positive side, using the Day One application did help since I enter the events as they happen, leaving at the end of the day just the dinner and calling a day events to be entered.

Having finished dinner, we spend the rest of the evening watching TV before calling it a day.

2019-08-09 Living with Cancer Day 884

Today’s posting continues using the layout created by the application Day One which capture my activities. Let me know what you think.

Date:   2019 August 09, at 06:35:17 PDT
Weather:    64 °F Sunny
Location:   Antioch, CA, United States

TGIF – Plans for today
Got up a bit early for an appointment at the Cancer Center for some hydration before the weekend. Having our weekly lunch with some of my Premenos friends that I worked with from 1990 to 2000.

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2019-08-06 Living with Cancer Day 881

Today was another *so-so day, no real issues getting up and going downstairs for breakfast. I did start sweating a bit once I got downstairs. I had my normal Shoulder/Neck pain and by the time I started my morning walk, my lower back pain started. Interesting enough it did not bother me during the morning walk. For most of the day my pain location with higher levels were the lower back, hip, and shoulder/neck. Close to dinner time my stomach acted up a bit and I started to have a light headache as well. In addition, my energy level was at a low level, I did drink some energy drinks, which did bring up the energy a bit. Since I will have a full chemo day tomorrow, I will also get hydration, which will bring up my energy level.

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2019-07-31 Living with Cancer Day 875

Today was the 6th Chemo day on the new Emplicti – elotuzumab (ELO) Treatment plan. There are 3 more weekly treatments left before switching to once a month. Getting to the appointment was normal with a bit less energy thanks to the lack of sleep returning late last night from the Hospital. Two hours into the treatment, one hour after pre-treatment, my left leg started to experience strong spams. Lucky for me it lasted only about 45 minutes, not like hours one and a half years ago. In addition to the premeds and the chemo medication, I got 2 liter of hydration.

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