Category Archives:Meh

Jan. 04.

Next Up … The Common Cold

I am at the one week mark for taking the chemo and so far, I have been doing pretty well. Minimal side effects from the chemo … barring one possible exception. I have a head cold.

Last Thursday I saw my orthopedist because I had some fluid on the knee and my doctor wanted an X-ray. Unfortunately, the X-ray technician had an emergency which was far more important than my knee, so the orthopedist gave me a shot to help minimize the pain and sent me on my way with an appointment for tomorrow to have the X-ray. That night I started feeling a bit stuffy, but since our weather has been up and down like a yo-yo, I thought it might be that as well. But as I thought I might have picked up some sort of bug while in the waiting room, despite wearing two surgical masks for protection, I took preventive measures. Things started clearing and two days ago, I thought I had it licked.

Not the case. Yesterday, it fully bloomed and I have a head full of snot, a frog for a voice, and have sneezed more in the past two days that I usually do in six months. I called my oncologist to let her know the situation and have also talked with the pharmacist for my chemo meds. The oncologist told me to stop taking the medication today and tomorrow and to call her before taking on Friday. We’re trying to get me cleared up.

Why would she have me stop the chemo? Well, one of the side affects of this particular chemo is the potential for getting colds. So my already bad immune system is made a little worse by the medication I’m taking to help my bad immune system. Or it feels that way at any rate. I am sure this is just a little blip on my road to kicking cancer’s butt; however, we do have to take the right precautions and not allow the cold to get out of control.

I always feel a little silly calling a doctor because my head is stuffed up and I have a runny nose because colds happen and just have to run their course, right? Except in my case, now, we cannot allow the small things to get out of control. I don’t have any resources to fight off anything on my own. So what normally is something that makes me feel lousy, but I usually just power through, has me in bed and is keeping me there to give my body the best possible chance of fighting this thing off before any infection develops.

The picture at the top is how my head feels. All foggy and sluggish, and somewhat murky. Things will get better. But for now I must rest.

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Oct. 12.

Searching for the Rainbow

Lightning and Rainbow

Lightning and Rainbow

Yesterday I had my three month check up with the oncologist. I don’t mind admitting that the past three months have been difficult ones for me as I do NOT wait well. The BIG question for the visit was whether the blood values had started behaving themselves or whether they either maintained or became worse, which means the watchful waiting would change from watching to chemo. Based on the way I have been feeling and my increased fatigue levels, I knew the results would be worse, and my anticipation was that we would discuss when to do the bone marrow biopsy and when to start chemo again. For the first time, I have approached the blood-value checking without knowing what I hoped for.

Let me explain. Barring divine intervention, I knew I would not be walking in to find that my values had all returned to the normal range. With the way I have been feeling, even had God made that happen, I’d have probably dissolved into a puddle of tears because the truth is I don’t feel well — I’m not 100% and I know it. And if everything was normal then there was something seriously wrong. So what were the possible outcomes of the visit? The expected march forward toward chemo, which is not something to be greeted with glee … or to my mind, even worse, sentenced to waiting another three months because the values remained steady.

Soooo, the results were worse, and not just a little worse. The progression continues to be aggressive and the values jumped as much as they did between April and July. What did I feel on hearing the results? Validated. My energy levels have been extremely low and at least there is a cause I can point to … other than feeling like a slug. But here is where things went off course from expectation. Instead of hearing bone marrow biopsy and chemo, I heard come back in January. Ummm, my blood levels are as bad or worse than they were when I went through chemo in 2013, so I didn’t understand why we would continue to wait.

But here’s the thing, while my white blood cells and lymphocytes are clogging up my system, my platelets are fighting the good fight and refusing to be beaten back. They are still within normal range. And BECAUSE they are still hanging tough, the doctor wants to give them the opportunity to continue their fight … so we wait and check again in January. Did I see this as a positive? NO! Why not? Because my mind doesn’t deal well with feeling like I’m in limbo. I know I’m not well, so I want to move forward and FIX the problem. As unpleasant as moving forward can be sometimes, it is taking action, and I am GREAT at putting one foot in front of the other and powering through. No matter what.

My dear friend, Italia, helped me get back on track emotionally with a lesson in gratitude. I was seeing the storm and the lightning strike and feeling like things were just going to continue in limbo, and that I truly don’t want to spend the rest of my life like a hermit. I need time-based boundaries … because I can do ANYTHING for XXX amount of time, as long as I know. Doing things for ??? amount of time, I don’t do well. So I saw the storm and the lightning was the jolt that said, you don’t have any control here and you’re just going to have to wait. Italia tapped me on the shoulder and pointed at the rainbow — the positives in the situation like: not having to be in chemo through the holidays, giving the medication my doctor prescribed to help with the fatigue a chance to work so I felt better and more ready to face chemo, being able to continue working from home to help me stay as healthy as possible. She reminded me that God is in control and I was focused on my picture of what I wanted and not on the bigger picture He has for my life.

This is WHY we have friends. 😀 To help us look for the right things. Normally, I am always searching for the rainbow, the bright spot in the storm. But all I saw were the gathering clouds and the destruction caused by the lightning. Does seeing the rainbow make things easier? A little. I am still dragging tail and feel like some thief came in and stole all my spoons while I napped, but I have my little ball of hope back, and with that alone I can conquer the world.

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Feb. 19.

The Blahs Hit

The photo for today involves fog because right now I’m feeling a bit foggy. Today I was focused on the day job and got a lot accomplished. The problem is that when I was done with the day, I suddenly realized I wasn’t feeling all that great. Nauseous, tired, and completely unmotivated to work on anything—even this post. HA!

But then I realized one beautiful thing … I’ve been going through chemo for 4 months now, and tonight I’m more nauseous than I’ve been the entire time … and it’s manageable. I was able to have something to eat (nothing fancy, a helping of mashed potatoes) and I have not become one with the great porcelain bowl. And I’m starting to feel a tad better. Not great, but not as lousy as I was before.

I saw my doctor yesterday and she mildly chastised me for not sharing all my symptoms with her. (Ironically, yesterday I felt great.) And I told her my journey was so relatively light, I don’t really think of the negative symptoms as negative. Yes, after every chemo session I go through a few days of turning into a gas factory … I take the anti-nausea medications she prescribed and keep it in check. Yes, every treatment cycle means I’ll retain water like a camel and it takes a couple weeks to get back to normal. Yes, the injection to boost my white count gives me a headache and backaches, sometimes more severe than others, but these are known side effects, and none of it is beyond my ability to deal with. Yes, I get tired after the treatments, but I’m encouraged by how much better my energy is getting in between treatments.

So the bottom line is, I don’t talk about feeling poorly because I really haven’t had a bad time of it. I know many others who have had a much rougher time, so I feel blessed. But since I am not feeling the swiftest tonight, I am not working on things (other than this post) will probably watch a movie or read a little and get some rest. Oh, and I absolutely attribute my ability to stay well to keeping myself isolated most of the time, and being diligent about wearing a surgical mask when having to go out in public at any time.

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Feb. 13.

Cycle 4, Day 3 – Hydration

My Status: Two-thirds of the way through
Mood: Meditative

I’m going to start off with the MOST positive thing to come out of today … I am 66%, aka two-thirds, aka YAHOO, of the way done with my chemo treatments. Feels like I was only half way there just last month… oh, wait, I was. It doesn’t matter. Every little milestone along the chemotherapy highway needs to be celebrated and this is no different. Half way is great because the road ahead is no longer than the road behind, but when the road ahead is shorter than then one behind, it’s even better.

We had day two of the blood not feeding back through the port without a little heparin to unclog it. Hopefully, this is a 4th cycle issue only and doesn’t mean that the port needs to be cleared out or worse. It’s brand new still. But I do “heal” quickly, so it may be that I’m coagulating at the surface too quickly. We shall see what cycles 5 & 6 hold on the port front. For now, I’m not going to worry about it.

Today I sat beside a lady who was on her first bout of chemotherapy, and she had a bit of a rough start. She had an allergic reaction to her course of treatment almost as soon as they started the drip. They quickly got the situation under control, and gave her some water to flush her system before switching to the next drug she had to have. She was very concerned when they mentioned she might not be able to tolerate the drug they felt was best for her condition, but would try a different one. Understandable. Once again, I feel like my experience with chemo was there so I could help another through theirs. She was concerned that she was the only one experiencing pain and chills, so I shared my allergic reaction experience. And when they mentioned they might postpone treatment to allow for all of the reaction to pass, I was able to share my experience with having to wait a week when my liver functions were too high. She was able to take comfort in hearing that someone else had been down a similar road, and was able to calm down so the doctor and nurse could do their jobs a little easier, because she was willing to lie about her symptoms so the chemo wouldn’t be postponed.

On the way home, I shared the experience with Denny and he thought it ridiculous to get worked up over having to wait for the treatment. I mentioned to him, and it is truly the case, that the hardest bump in my chemo journey so far was being told to go home, that we’d try chemo the next week. His response, but it was only a week, and they made you wait so it wouldn’t hurt you. Yes, I understand that from a logical standpoint, and can now be philosophical about it, but at that moment, the emotion was something else entirely.

Caregivers: Please understand, there is not one of us who wants to be in that chair hooked up to a chemo drip. If we had our choice, we’d prefer to be perfectly healthy and living out our lives the way we had planned … without having to use drugs to kill off evil demons in our body. As a consequence, we want the treatments over and done with, so we can get back to the life we want to live. We also don’t hear the postponement statement with the logical part of our brain, we hear it through our emotions. When my treatment was postponed, I heard You’re too sick for chemo. What this woman heard today was not let’s give your body a chance to recuperate and we’ll try again … she heard chemo for you is not possible. And it rocks you to your core. Because as much as we don’t want to be in that chair, we want to be in the chair to get it over with—it’s what is going to give us our lives back. Please allow us to express the emotion of the moments from the bumps in the road without dismissing them from a logical standpoint.

PSA to Women with cellphones: Today, two 21-year-old women were diagnosed with stage 4 breast cancer … the common thread? They both carried their cellphones in their bra. I understand … it’s an easy place to tuck something to give you free hands, or when you’re not carrying a purse, a place to carry the cellphone so it’s not in your pocket. BUY A CASE—strap it on your hip, or carry a purse (something I rarely do). The ability to have both hands free and carry a cell phone by putting it in your bra is not worth the cost of your life. Please don’t do it.

The picture for this post is symbolic for me that the road ahead is shorter. We’re not to the peak yet, but it is in sight and hope is on the horizon.

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Jan. 17.

The Aftermath

My Status: Headache-y
Mood: Cranky

Today what my body has been through in the last week caught up with me. Tired, headache I can’t seem to get rid of, and I’m retaining water like a camel. So I took it slow and easy this morning. I had an appointment with the surgeon for the port recheck today at 11:30, so I geared my morning toward prepping for that. My only problem with the recheck was finding the doctor’s office.

Once again, I didn’t get a confirmation call… and if I had, things might have gone a lot smoother because I might have questioned them when they told me to go to an office I’d never heard of. Not even thinking twice about it, I hopped in the car and went to the office I know… to be told when I walked in the door that I was at the wrong location. The receptionist handed me a card with the address, a place MUCH closer to my house, and off I went. Good thing I was early for the appointment at the wrong place, eh? I arrived at the “new” location and couldn’t find the suite on the card, so popped into the Urgent Care facility on the ground floor and asked. The receptionist there looked at me like I had two heads. So I asked for the doctor… OHHHH despite having 101 as the suite number on the card, he was upstairs… they didn’t tell me what suite, but gave me lousy directions “just up the stairs”.

By this time, my temper was frayed. The headache I had been trying to outrun came on full force, and I was NOT a happy camper. This is one of those times where I know my anger was disproportionate to the situation, but I also couldn’t change things. (Don’t worry, I didn’t behead anyone… I just kept stating over and over that I was NOT happy.) Fortunately, everything is good with the port, and I don’t have to go back unless there is a problem with it. And the drive home was short after having driven half the county earlier.

Knowing I wasn’t fit for any interactions with people, when I got home, I took a nap, hoping the headache would go away. No such luck. Of course, I’m way behind on getting fluids into me because I haven’t figured out how to sleep and drink at the same time. Pushing the fluids will ultimately help the head situation. I did ice it, so the edge has been dimmed, but still suffering with it. I am now drinking tea, and will try a little food before nausea kicks in, but I do have to say today has not been one of my favorites. I really could have done without the extra driving and the headache can leave any time.

The picture shows how I feel… being beaten by the forces of nature at the moment.

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Dec. 17.

Cycle 2, Day 1 Chemo

My Status: Head-achy & slightly nauseous
Mood: Hanging in there

Today was long. Reeeeaaaallllly long. For a lot of reasons. Where do I start?

I’m going to start at the beginning of the day with the arrival of my in-laws half an hour early. Which I did anticipate them being a little early, just not half an hour. Okay, no problem, all I had to do was finish making my tea to take with for my chemo session—except my stress level is difficult to keep under control with them. They are the best-hearted people, and immediately insisted on being able to help once they knew I had to have chemo. I appreciate their willingness to drive me so much—I need someone to drive me. What I don’t need is my stress levels increasing, especially on a day when I was already a little stressed. I won’t go into the gritty details of the additional stress, suffice it to say I went from a slightly elevated stress level to through the roof. The reason my stress levels were elevated to begin with was that I didn’t know whether chemo would be a go today or not. Yesterday I went for my labs, but the test for the liver was done too late in the day to have the results same day and we wouldn’t know whether I’d even be able to have chemo until I arrived this morning.

We arrived early, and they took me back early, which ended up being a very good thing. Got the results. YAY!!! Chemotherapy was a go. I got myself settled, the pre-chemo cocktail all hooked in, and we were off. One the prep cocktail was done, we started the first chemo bag. I had brought movies, so was watching a movie and didn’t pay attention to when the bags were switched. But sometime between 10:30 and 10:45 I noticed labored breathing. I paused the movie and took a couple of deep breaths to see whether it would ease like it had the time before. My heart raced and it felt like something was pressing against my chest—hard. Not quite the elephant on the chest thing of a heart attack, but heavier than a two-year-old.

I knew this wasn’t right and it was getting worse quickly, so I told the chemo nurse I was having trouble breathing. She immediately turned off the drip and went for the doctor. They gave me a shot of something (not Benadryl—because I’m allergic to it) and the heaviness of the chest decreased, and after a few minutes the heart rate lessened. Apparently I was very flushed as well—even when I felt much more normal.

The decision was made to continue, but to give me chemo bag number 2 first, and then after I had gone through that one, we’d try chemo bag number 1 at a slower pace because I had handled it okay during Cycle 1. Normally Day 1 chemo of the cycle should last approximately 6 hours. We started this morning somewhere around 9:15 and it was after 6 PM by the time I was done. And THAT is a long time to be sitting in a chair with chemicals dripping into you.

The picture at the top of the post is because I feel as if I had a Christmas Angel sitting on my shoulder today. We were too close to making a hospital visit, and I am blessed to have a chemo nurse who reacted quickly and got things turned around as fast as she did. This also means I can count on the remainder of my Day 1 cycles being longer than the expected 6 hours. Hopefully not in the neighborhood of 9 hours, like today, but we will always need to start chemo bag 1 slowly and gradually increase to mitigate potential for the allergic reaction. Post chemo I have a blistering headache as a gift from the allergic reaction, I’m retaining water like a camel to the point where I can feel the swelling, and I have the after day 1 slight case of nausea. Tylenol has been taken for the headache, anti-nausea medication has been taken (and by the end of this post I’m feeling much better), and I have taken a sleeping pill to help counteract one of the prep cocktail drugs which causes me to not sleep well. I will have some tea and shortly (with any luck) sleep.

Oh, and the reason I need a driver? One of the drugs can cause confusion, as evidenced tonight when I reached into the back of the car we’ve had for 8 years and scrabbled around trying to find the door handle so I could put my things in the back seat. We only have two-door cars.

We’ll see what tomorrow brings.

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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.

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Nov. 25.

A Shot and a Draw

My Status: Tired
Mood: Fair to Middlin’

Today started off with an appointment to have a shot in my eye. Yes, you read that right. I had shot #3 in the right eye to help reduce a condition of macular edema. And the shot entails a vision test, then dilating the eye, followed by another eye test which uses bright lights and red lasers that play tag while you have to keep your eye on the center. Next a gel to numb the eye and an extremely bright light which is then muted slightly by a colored lens. Finally and apparatus is shoved into your eye to hold it open… and the doctor tells you to keep the other eye open.

HA! By this point, the left eye, having heard all the squeals and pleas for help from the right eye, is tightly closed, using turtle theory—if no one knows I’m here, they’ll pass by and leave me in peace. The shot doesn’t hurt, and in a weird, twisted way it’s kinda cool, but I am NOT a fan of the thing to hold the eye open. Also, the whole dilate one eye and not the other thing leaves me feeling unbalanced.

And I went directly from having the shot in my eye to having my blood drawn for my weekly labs. They need to keep a watch on the blood values to determine whether the chemo is doing what it is expected to do or not. And in my case … the jury is out. My doc isn’t in on Monday mornings—she sees patients Monday afternoons at the office where I go for the blood work, so she wasn’t there. The technician had a question about the blood values and asked the back up doc … you know, the one who forgot to date the sleeping pill prescription … to make a determination. Apparently my platelets are low, as in very low, and the question had to do with whether I was still in some sort of “window” where the low platelet values would be within the “norm” for my condition and length of time since chemo.

How do I know this??? Because Doogie (yes, he’s only behaved like an adolescent pretending to be a doctor, so Doogie it is) discussed the situation with the technician in the middle of the hall outside my open door. And though he said her repeatedly and not my name, I knew they were discussing my case because I was the only female patient in the office at the moment who had just had blood work done. He even stopped in the middle of the discussion to tell the technician a joke. Doogie had better hope that he never does have to see me because he is completely ill-prepared to handle a patient like me. He asked the technician twice to ensure that a copy of the report be left on my doc’s desk.

While I appreciate the fact that my report will have been reviewed by my doctor once she arrived to the office, let me share with you how it feels from the patient perspective. Like Doogie decided he was not competent to make a determination based on my chart, which I’m actually okay with, but if you’re that unsure, perhaps a phone call to confer??? Also it felt as if he was passing the buck, not willing to trust his own judgement in the case. Of course, I shouldn’t have known because it never should have been discussed in the hallway. I may need to chat with my doc the next time I see her and let her know, no matter what the results, I would like an accounting of the findings and what they mean. Brief is fine. But more than, “You’re fine. Ummmm, no need for an injection.” Especially since I wasn’t expecting an injection.

At a guess, I’d say that the results showed that the Neulasta wasn’t doing what they had expected, because the technician questioned whether I had the shot or not. The doc had double-checked that last Monday as well, so while my side effects from the shot have been minimal, it may need a kick in the pants this next time.

I always feel tired on the days when I have the shot in the eye. Partly because after all the poking, prodding, and bright lights, my eye is D—O—N—E! It honestly begs me to crawl in bed and just keep it closed so no one else can torture it. So I won’t be doing any writing tonight. It’s getting close to sign off time so I can relax for a bit and get some good sleep. BUT I was able to get a scene done yesterday that I’ve been trying to get on the page the right way for two weeks. So very stoked about that.

How am I feeling about the low platelet thing? I promised not to pull punches or to pretend things are great if I’m not feeling it, and I will keep my promise. I’m a bit ambivalent about the blood results today. Or lack thereof. I went in hoping to hear I’m doing great because I feel as if things are going well, but instead hear that I don’t need an injection I didn’t know they might do. And the don’t felt a little weak and uncertain. So glad I didn’t need the injection, but a little upside down on not doing a ninja impression on the cancer yet.

The picture for this post immediately grabbed me because I saw it and my first thought was Can’t see the forest for the trees. What is pictured above is the reflection of a larger piece showing a forest. I loved the upside down aspect of the reflection and the overall murkiness of it. It fits today perfectly.

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Nov. 19.

An Evening of Rest

My Status: Feeling Good
Mood: Cranky

Yesterday I thought I’d try an evening of rest. I’m back to work, albeit from home, knew I wouldn’t be writing, didn’t really want to do anything, so rest seemed like a good idea. Here’s the thing—I don’t rest well. I never have. Even when putting my feet up, kicking back and relaxing, my mind is usually working on something, in one way or another. Sooooo the rest thing … didn’t go all that well. So I tried going to bed early.

The sleep thing wasn’t happening either. *sigh* I’ll be tired, and as soon as my head hits the pillow … it’s not that my mind won’t turn off—my body won’t. Since having the chemo treatments, every time I hop in bed my stomach turns into a bubble factory. Literally. I am manufacturing so much gas, that if I could take what’s inside me, distill it, and convert it into fuel form, Denny and I would never buy another tank of gas. It’s ridiculous. And on top of that, my legs go into hyper-restless gear. It reaches the point where I want to give up and just stay up … forever.

But last night, after tossing and turning and keeping the dogs awake for two hours (or more), I had a brain wave. I haven’t been nauseous, but what if the same home remedies worked… a piece of toast, a few crackers to soak up whatever is burbling around inside me. And for the restless legs, a hot bath. Things like Gas-X were proving woefully inadequate against my bubble factory, so it was worth a try. What do you know? It worked.

In a very short time, I’m going to try the same thing (without the tossing and turning first) and see whether I was simply so exhausted anything would have worked, or whether this is a viable answer. I’ll let you know. Hopefully rest will come easily tonight… I need it.

Today has been a somewhat cranky day. I don’t have them very often, but today, it jumped me from the very start. What caused the crankiness? *shrugs* It could be the trouble getting to sleep. It could be simply what my body is going through and to be expected from time to time. Or it could be the increasingly unbearable silence in my head. My characters still aren’t speaking to me … not in the way they need to. I’m not writing—and this is bad. I need to write, but in order to do so, I need my characters to tell me what needs to go down on the page. Yes, I have an idea, but without them, it is only words, and has no meaning. No heart.

I did see the doc yesterday and all my blood work came back as being on track, and the doc is pleased with how I’m doing. So those are positive things.

If any of my fellow writers see my characters gallivanting about—tell them they are needed at home. Pronto!!

The picture at the top of the post is symbolic of my bubble factory. 🙂

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Nov. 14.

Chemo Cycle 1, Day 3 – Hydration

My Status: Tired
Mood: Meh Meh

I’m just going to jump in and say, I didn’t sleep well last night. Not because of any other unpleasant side effects (because I really haven’t had many), but I just couldn’t sleep. So I was tired today. I am STILL tired, and yet, not sure I will be able to sleep tonight. Also my right arm hurts because I had to have the chemo in the back of the hand, and I am retaining water like I’m a camel. Pretty soon I’ll have a visible hump. And the sleeplessness and water retention are both due to the steroid given during the chemo to make sure I don’t have an adverse reaction.

Yippy, Skippy—the thing to stop me from having a reaction is causing the issues. Lucky me. And I mean that in the most sarcastic and joking way. I know the steroid stopped me from having a respiratory reaction to the chemo, because on day 1, I did have a slight tightening in the chest at one point—enough to make me think about alerting the doctor, but then the wheeze loosened, and there was no need. The drugs were doing what they were supposed to.

So the side effects of sleeplessness and water retention we can deal with. The only reason I’m a bit miffed at the moment is that I mentioned the need for a sleep aid when I came in, and the doctor had to leave early, so the other doctor wound up writing the prescription … and forgot to DATE it. The pharmacy cannot fill a prescription with no date and will have to contact the doctor—who left early because of a meeting, and will not be available. I’m exhausted, but the night ahead could be a long one. When I crawl into bed, I’m going to pretend I’m floating in the boat in the picture above, on a nice sunny day—the perfect temperature, with a slight breeze as the water gently laps against the boat and rocks me to sleep. With luck (too bad I don’t have a slug of rum) I’ll sleep.

The bruise on my left arm, which now by the way looks as if someone has put an eggplant cutting on my arm, it’s so nice and purply-black. doesn’t hurt one whit. On my right arm, where there is minimal bruising, I hurt. It hurts to extend my fingers to pick things up and reaching down to pick things up from the floor—forget it. Pain shoots up my arm. I’m sure the pain is linked to the water retention. I have gained two pounds each day and have eaten less, so the doc wants me to flush my system with plain water because I am sensitive to the sodium in the drugs they’re giving me. Tonight, that plain water has been mixed with tea and milk to help me relax and hopefully sleep. 🙂

Speaking of bruises, during the night I rolled over and my left hand simply flopped on my right arm and sent sharp radiating pain throughout my arm … sure enough, this morning I see the beginning of a bruise. My hand barely touched the arm. I just hit it at the wrong point.

Small veins caused me to be there longer than the expected 3 hour appointment again tonight. Probably half an hour later than anticipated. But that I don’t really mind so far. Now I should stop complaining and tell everyone what went right today. My mom misread the treatment schedule and thought the appointment was for noon instead of 2 PM. This meant she was early to pick me up instead of late. YAY for small favors, and knocking one worry out of the way. And hubs was able to track down some arnica to put on my bruise. He had to go to multiple places, but persevered until he found some, so he gets the gold star for the day.

 

GoldStar

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