For those wondering, here's what a "typical" infusion day looks like:
-IV placed, blood drawn
-Vitals taken by Medical Assistant
-Meet with Oncologist who does a physical exam and reviews lab work
-Get cleared for treatment
-Oncologist orders medications
-Wait for medications to be prepared
-Receive ~one hour of anti-nausea IV medications
-Chemo starts
-1.5 hours later go home
That's it. Honestly, just typing it makes me a little sick to my stomach, but perhaps that is because I am still a little sick to my stomach!
Anyhow, as I've mentioned before, the first week after chemo is the hardest and this time was no exception. It pretty much went exactly like last time. However, I was prepared with toast, applesauce, NadaMoo dairy free ice cream, and pumpkin protein cookies. The good news is that I seem to be rebounding from chemo #2 similarly to chemo #1. Sometimes the effects can be cumulative, so I'll take the same!
Being a numbers person, I have been closely tracking my blood counts. I even made a nifty chart with some of the more significant values.
The "ranges" on my chart are the ideal ranges that my Nutritionist and I are targeting. "Normal" ranges are a bit more lax.
Here's my interpretation:
-My white blood cells are a bit low, but still in the "normal" range. This is despite not getting a Neulasta shot to help support immunity.
-Oddly, my red blood cell count, hematocrit, hemoglobin, and platelets all increased after my first treatment. I am taking whey protein and chorella to help support my red blood cells, however I still find this odd. Regardless, I'll take the little boost!
-The one value that I find a bit concerning is my BUN (blood urea nitrogen), which is an indicator of kidney health. It is lower than what we are targeting, however it is still in the low "normal" range. Other kidney health indicators look good, however from what I understand this value can also drop if your body is using more protein than it is getting. I suspect this may be the case with me as chemo significantly increases your protein needs and I have been exercising routinely. I will continue to focus on improving my protein intake.
In other news, I met with my radiation oncologist today. I really like her. If everything stays on track, I will meet with her again on October 1st where I will get measured and molded in preparation for radiation. Even though I am going to get a crap load of radiation-boooo-they are extremely precise with their target areas. My doctors typically have a hard time surprising me as I usually go into my appointments very well researched, however today I was surprised to learn that they will create a mold around my body that I will lay in for each radiation session so that I am in the exact same position. Actual radiation will start the week of October 7th and will be daily for 5-6 weeks. I was so psyched to "get out of" radiation back at my original diagnosis in 2011, however I know that it is 100% indicated this time around, so my plan is to move forward optimistically and see where the chips (i.e. how it affects my reconstruction) fall!
Photos from the week can be found here and weekly exercise here.
Anyhow, as I've mentioned before, the first week after chemo is the hardest and this time was no exception. It pretty much went exactly like last time. However, I was prepared with toast, applesauce, NadaMoo dairy free ice cream, and pumpkin protein cookies. The good news is that I seem to be rebounding from chemo #2 similarly to chemo #1. Sometimes the effects can be cumulative, so I'll take the same!
Being a numbers person, I have been closely tracking my blood counts. I even made a nifty chart with some of the more significant values.
Blood Counts
|
Target Ranges
|
Chemo#1
|
Chemo#2
|
Chemo#3
|
Chemo#4
|
WBC
|
4-8
|
4.18
|
3.43
|
||
Lymphocytes
|
>1 in treatment
|
2.5
|
1.6
|
||
Neutrophils
|
>1 in treatment
|
2.5
|
1.6
|
||
Monocytes
|
<.56
|
.3
|
.4
|
||
Eosinophils
|
<.24
|
0
|
0
|
||
RBC count
|
3.9-4.5
|
3.94
|
4.18
|
||
Mean Corpuscle Volume
|
<98 in treatment
|
94.6
|
92.2
|
||
Platelets
|
150-300
|
168
|
276
|
||
Protein Status
|
|||||
Hemoglobin
|
13-14
|
12.9
|
13.6
|
||
Albumin
|
4-5
|
4.0
|
4.3
|
||
Total Protein
|
>6.6 in treatment
|
6.6
|
7.1
|
||
Electrolyte Balance
|
|||||
Sodium
|
140-144
|
140
|
138
|
||
Potassium
|
4-4.5
|
3.5
|
3.4
|
||
Chloride
|
100-106
|
108
|
104
|
||
Kidney Health
|
|||||
BUN
|
13-18
|
15
|
9
|
||
Creatinine
|
.7-1.1
|
.63
|
.72
|
||
Calcium
|
9.2-10.1
|
8.8
|
9.1
|
||
Oxidation
|
|||||
RBC Distribution Width
|
<13
|
13
|
13.2
|
The "ranges" on my chart are the ideal ranges that my Nutritionist and I are targeting. "Normal" ranges are a bit more lax.
Here's my interpretation:
-My white blood cells are a bit low, but still in the "normal" range. This is despite not getting a Neulasta shot to help support immunity.
-Oddly, my red blood cell count, hematocrit, hemoglobin, and platelets all increased after my first treatment. I am taking whey protein and chorella to help support my red blood cells, however I still find this odd. Regardless, I'll take the little boost!
-The one value that I find a bit concerning is my BUN (blood urea nitrogen), which is an indicator of kidney health. It is lower than what we are targeting, however it is still in the low "normal" range. Other kidney health indicators look good, however from what I understand this value can also drop if your body is using more protein than it is getting. I suspect this may be the case with me as chemo significantly increases your protein needs and I have been exercising routinely. I will continue to focus on improving my protein intake.
In other news, I met with my radiation oncologist today. I really like her. If everything stays on track, I will meet with her again on October 1st where I will get measured and molded in preparation for radiation. Even though I am going to get a crap load of radiation-boooo-they are extremely precise with their target areas. My doctors typically have a hard time surprising me as I usually go into my appointments very well researched, however today I was surprised to learn that they will create a mold around my body that I will lay in for each radiation session so that I am in the exact same position. Actual radiation will start the week of October 7th and will be daily for 5-6 weeks. I was so psyched to "get out of" radiation back at my original diagnosis in 2011, however I know that it is 100% indicated this time around, so my plan is to move forward optimistically and see where the chips (i.e. how it affects my reconstruction) fall!
Photos from the week can be found here and weekly exercise here.