Skip to main content

Stomach Issues

Nausea

 

Nausea is something most people associate with chemo, and I did have some. I don’t know if mine was less severe, or if I was able to handle it better because I had done research and controlled it.

 

The first couple of days after an infusion I was not concerned about feeling sick, as they gave me a pre-med that included a heavy-duty anti-nausea medication. 

 

As soon as I knew I would go through chemotherapy I bought a ReliefBand from the internet. I had heard stories from some who had been nauseous from chemo, as well as those who have motion sickness. They all said ReliefBand helped keep the nausea away.

 

It is a strange thing - looks like a watch, and you put it on your wrist with the watch part on the inside of the wrist. It comes with a gel that helps conduct the electricity through your skin. The gel is not cheap, so when it is gone you can use aloe vera gel instead.

 

You rub a small amount of the gel on the inside of your wrist where you will put the watch part, then secure the band so it will stay. It has ten different settings depending on your need. I usually kept mine at 3. When you turn it on it starts ticking, the higher the number, the stronger the ticking becomes. You can feel the electrical surge move down the fingers to the tips. It’s a strange sensation, but it worked for me. I usually wore it the first week after each infusion, mostly at night.

 

Before I went to bed during the first week, after the pre-meds had worn off, I took a Compazine, an anti-nausea medication. It makes you drowsy, so it not only helped with the nausea, but aided my sleep. It’s safe to take even if you have sleep apnea according to the pharmacist. I took the sublingual Zofran during the day if I felt I needed it. I was fortunate and did not need the Zofran very often. That pill was helpful during MRIs, as the intravenous blue dye made me nauseous. 

 

Foods are a major factor in feeling nauseous. Many tell us what we should eat to stay healthy, but we are not always able to eat these foods. The medical professionals who helped me suggested I eat whatever my body would let me. For me this was a lot of toast, but we are all different.

 

Chemo Belly (bloated and gassy)

 

If you have ever been bloated and gassy you understand how frustrating and painful it can be. The four months of chemotherapy, as well as a couple of months afterwards, I wore nothing but large and soft sweatpants and sweatshirts. My regular clothing did not fit as my stomach was distended and her. TUMS and Gas-X helped but did not take care of all of it. I am glad I did not have to dress to look good. A blessing of not having to go to an office.

 

Constipation

 

Many women get diarrhea, but my digestive system tends to be sluggish to begin with, so it was no surprise when I had major constipation issues. It is painful, makes you look pregnant, and water goes straight through, so you need to urinate frequently. That is very frustrating, as drinking a lot of water helps your system function better. My friends became electrolytes to keep the water in my body. This is still an issue, so I continue to drink one Liquid IV each day. 

 

Heart Burn (GERD)

 

There are signs of heartburn that I did not know. I thought it was just a burning pain in your chest. It turns out that is just one of the symptoms. Other symptoms are a feeling that food is coming back into the mouth, an acidic or bitter taste at the back of the throat, pain after meals and / or when lying down. Some of these are also signs of a heart attack, so it is important to let your doctor know what you are experiencing. 

 

Acid controllers work well. I started with TUMS and Famotidine, but ended up with the stronger Omeprazole, and still take one each day. Heart burn has not only been a problem during the day, but also prevents me from sleeping, and the medication helps.

 

 

The best and easiest way to keep all these issues as minimal as possible is drinking as much water as your body can handle, not trying to eat foods that you feel you *should* eat even though just thinking about them makes you feel sick to your stomach, and moving, even if you are only able to go for short walks.


Comments

Popular posts from this blog

The Second Post-Treatment Checkup - still NED!

My last cancer treatment was December 17, 2024. It was a relief to be finished and not have to go to the cancer center every three weeks. Three months later, March 17, 2025, I had my first post-treatment appointment with the oncologist. At that point it had not been enough time for me to process everything yet, and my brain was not back to functioning completely (it is still not fully normal), so I was happy to see my wonderful doctor and have my blood drawn without having to stay for an infusion. The tests all looked good. Craig retired in February and we had been thinking about what to do. Our children are grown and have their own families. They all live a few hours from us. We love them enormously and love spending time with them, but felt we needed some time to ease into retirement. We had been talking about serving a mission for our church and thought this would be a perfect time. My oncologist gave her approval, so in the beginning of May we got off an airplane in Vientiane, Lao ...

The Long Tail of Chemo

Eleven weeks after my last infusion of Kadcyla my body still seems to think I am receiving treatments. Some of the side effects still occur about the same time they did when I was getting treatments. They are not as severe, and do not last as long, but they happen almost like clockwork. My energy level is pretty much back to how it was pre-cancer. Sleeping has never been one of my superpowers, but it got worse when I started getting the infusions. It is sometimes difficult to fall asleep, and sleeping beyond 6:30 in the morning is late for me. Even though I try hard, my body very rarely lets me nap.  The brain fog is almost gone. It feels terrific to be almost back to my normal self. Not having so much brain fog so nice, but it also means my obnoxious self comes out more frequently. Now Craig must deal with me not agreeing with him all the time again. On the good side, I am better able to control my temper. It is easier to keep myself from getting angry and frustrated. The migraine...

The Call

There are some things we think only happen to others - cancer is one of them. When I went in for my routine mammogram on Wednesday, July 19, 2023 I did not expect to be in treatment for years to come. I was not concerned when I received a phone call saying they needed to do an ultrasound on my right breast as there was a mass they wanted to look at more closely. This happened once before and it turned out to be a benign cyst. I have many fatty cysts (lipomas) and assumed this would be the same thing. July 26 I went in for the ultrasound. It was not until the technician brought in a doctor I got concerned. It turned out to be not a lump, but a spiculated mass. My understanding is that it is sort of shaped like seaweed, flat with offshoots. This was not your normal cyst. The doctor wanted me to get a biopsy. This was not the news I expected. The next day, Thursday, July 27, I went in for a needle biopsy. Craig, my husband took the afternoon off so he could take me there and home. Everyon...