Tag Archives: blood values

Dec. 30.

And So It Begins … Again

When I saw the oncologist last week we didn’t have the results from the CT Scan. I saw my regular physician this week and he had the results. And I’ll be candid … they aren’t good. The scan revealed what I already knew — that the nodule on my neck was not the only lymphoma mass that would be found. In fact, by the time I went to the doctor this week, a few more had made their presence known. I have a smattering in the neck area, one in the chest, and several in the abdomen. My doctor, who is a cautious physician, wants me to discuss prognosis with the oncologist. And being me, I asked what value it would have to know a number that is going to be inaccurate anyway?

My first acts to accomplish in 2017 is to get my affairs in order. Not because I believe I’m dying or that I won’t recover, but because it needs to be done and has been on my mind for some time and it is time to stop procrastinating. EVERYONE should have their affairs in order. You never know when that bus is going to run you over. Plain and simple. No one is guaranteed any specific time on this Earth. And now that I’ve said that, I have NO intention of going anywhere anytime soon. I have too much to accomplish with my life and I intend to do it.

My doctor was a little down with my results. My lab results are bad. My scan results are bad. But I was ready to dance a jig because the scan results had one result that made me very, very happy. I have been having near constant pain under my left rib cage for a few weeks, and eating certain foods made it extremely painful, which I have been finding out by trial and error. When with the oncologist, we discussed and we both felt it might be an enlargement of the spleen. Which is something you DON’T want. The scan results showed that my spleen was perfectly normal and the area where the pain is coming from is where there are some lymphoma lumps taking up space. We’re getting ready to blast those with chemo, so they will be going bye-bye, and I’ll just have small, soft meals in the meantime. But there was one little problem. I didn’t have the chemo meds yet and didn’t know when they would arrive. My doc got the oncologists office on the line and asked them to find out what was going on as he wanted me on the chemo immediately. There had been a slight mix-up and the meds had not been ordered, but they got it straightened out same day, and I received the shipment yesterday.

The chemo comes from a specialty pharmacy and so far I am incredibly impressed. They provide a mechanism to help you remember whether you have taken your medication or not as well as timer to put on the bottle cap that will alert you that it is time to take your next dose. And for me, this is fabulous. I don’t do pill dispensers well (it is such a hassle to fill them for me), so the little thing to flip it to show that you’ve taken it IS something I can do. Especially as it sticks directly on the bottle itself. And the timer??? Brilliant. Especially when I lose track of time so easily. Then after they arrived, the pharmacist called and went over how I am to take the medication, what to do, what not to do, and to let me know that they had trained staff available via phone 24/7 if I had any questions or couldn’t reach my doctor.

I will shortly be taking my second dose. So far, so good. A brief period of wooziness, but other than that feeling the same. The biggest thing for me to figure out was when to schedule the dose because I have to take on an empty stomach, so nothing 2 hours prior and 1 hour after (except water), and it has to be taken at the same time every day (hence the handy dandy timer). When I saw that it may cause dizziness, I decided to wait until after I had seen the knee doctor yesterday (yes, I managed to get some fluid on my knee that was giving me some trouble), so I felt after dinner would be good. That way, if I’m not feeling well, I can simply go to bed.

The picture at the top of the post fits the mood right now so perfectly. Yes, there is darkness, but the light is shining through. I am filled with hope and am so encouraged to be taking action to beat this cancer back down into submission. I am blessed in my friends and the number of people who care about me, I will never be able to say Thank You enough.

Tagged: , , , , , , , , , , , , ,

Apr. 12.

Change in Values

It has been awhile since I updated this blog … and for good reason — there hasn’t been anything to say. Two years ago, April 10th, I had my last chemo treatment. File that under “WOW, Time flies!!” Today, I had my quarterly blood-letting to check to see how things are going. In some respects, those two years have passed like I only blinked my eyes, but in others, I realize how much I have accomplished and how my life has changed … for the better. Throughout it all, my doctor has been thrilled with my blood values, as they have been smack dab in the middle of the normal range. That changed today.

Today my visit brought a bit of news. My lymphocyte count is no longer in the normal range; it has crossed the line into the “high” territory. At this juncture, the doctor is adopting a wait and see attitude because I have recently been sick, and that could be the cause of the elevated lymphocyte count. We discussed testing, but since the tests she would run at this time were negative when my system was 50% compromised, we decided against doing any tests. And I swear, any more radiation tests and I’ll start glowing like a Christmas bulb.

What does wait and see mean? I put renewed focus on my health — eating the right foods, exercising more, and making sure I get enough rest — and in July we look at my blood values again. From there … who knows? I am not going to speculate. In fact, I’m going to keep on moving forward with my life, focused on the wonderful things I’m involved with, and figure this is a blip on the radar caused by the recent bout of bronchitis.

I liked this picture of clouds because even though they’re dark and night is falling, they are still lit by the sun and their radiance is beautiful.

Tagged: , , , , ,

Dec. 10.

False Start

Christmas ball by fotoman228

Christmas ball by fotoman228

My Status: Tired and Congested
Mood: Disappointed

Yesterday was Chemo Eve, or so I thought. I went yesterday for my labs, the machine they use to assess the blood values was not working correctly, so they told me they’d call with the results. In the afternoon, I did receive a call from the doctor’s office—to confirm my chemo appointment. I mentioned that I had not yet heard my results and wanted to make sure everything was okay. The gal was on the phone and I was told someone would call. That call never came. And one presumes no news, is good news because they would have called if something wasn’t right … right?

I woke up early this morning, packed up all my stuff, and exited just as my driver pulled up. I was totally prepared. A bag of snacks and water, a thermos of tea, my blanket for if I get cold (and slippers because my feet do get cold), and my laptop along with some movies. A veritable pack-mule ready for her trek. We arrived timely and they took me back. I kicked back in my chair, changed into my slippers, had the first movie loaded and laptop all plugged in when the chemo nurse came back and told me they were sending me home.

Um, What??? Honestly, I thought she was joking because I had already set up all my stuff and was ready to roll. But apparently my liver enzymes were high. One of the chemo drugs I could have had, but the other—the one I have two days in a row—cannot be given when the liver levels are out of whack. So they sent me home to drink lots of fluids and we’ll try again next week.

Why are the liver enzymes high? My guess is the antiinflammatories I had to take to get the pain in my knee under control. And that I’ve had to take Tylenol for pain management. Not in doses which would normally elevate the liver functions, but since my body is definitely not handling things well these days, the liver decided it was going to whine along with the rest of the body.

By the time I got home, the day was half gone and I needed to rest. I’m not really sure how I’m supposed to drink more throughout the day… I already drink more than a gallon a day. Next thing you know my bladder will throw up picket lines and go on strike.

On one hand, I am disappointed we had to postpone the chemo until next week. I’m not a patient person, and I want to get on with things. But on the other hand, one thought that crossed my mind this morning as we were headed to my supposed chemo treatment—we’d had a lot of winds yesterday and I am congested and coughing, would that have made it more difficult to get through the chemo? Since the one drug is known for respiratory issues, my guess is yes. So maybe, just maybe, postponing things a week is a blessing in disguise.

Tagged: , , , , , , , , , , , , , ,

UA-19119025-1