Skip to main content

Lessening the Side Effects of Chemotherapy

I brought my list of side effects when I saw the doctor the week after my first infusion on September 22. That was very helpful as now we had a better idea of what my particular side effects looked like. For example, where some get diarrhea, I was constipated, so needed different treatment. It took a while to figure things out, but this is what worked for me - 


Chemo belly (bloated and gassy) - 

  • Every morning with my supplements - the maximum amount of stool softeners
  • With each meal - TUMS (I used Equate brand Antacid Chews) and Gas-X (I used Equate brand Gas Relief)

Heartburn / GERD - 

  • With lunch and after dinner / before bedtime - Acid Controller

Constipation - 

  • Every morning - MiraLax (I used Equate brand ClearLax) in 6-8 ounces of pineapple juice as it tastes better than putting it in water, and pineapple juice is also helpful for constipation
  • Drink as much water as my body could handle. This also helps flush the chemo drugs out of your system more quickly so you fell better.
  • Because water seemed to go straight through me, so the doctor suggested I drink electrolytes as well as water. One brand she suggested was Liquid IV. I drank two per day until I felt I could get by with only one and drink more water. The electrolytes contain a lot of sodium, so I did not want to drink more than I had to. 
  • Eat lots of fruits and vegetables.

Mouth sores - 

  • CHEW LOTS OF ICE DURING THE INFUSION!!! This is VERY helpful!
  • Use children’s toothpaste.
  • Over the counter mouth rinse for oncology patients
  • Mouth Rinse (mix all until dissolved; make a new batch daily)
    • 1/2 teaspoon table salt
    • 1/2 teaspoon baking soda
    • 1 pint (2 cups) warm water

Bone pain from the Neulasta injection - 

  • Claritin brand allergy medication - one pill in the morning and one in the afternoon; start the day before the injection and take for 3-5 days. I took them the five days to make sure. My doctor let me take another OTC allergy medication as well. If prescribed you should ask your doctor.

Sensitive scalp / hair loss - 

  • There is not much you can do about this unfortunately. Some use an ice cap to prevent some of the hair loss, but it seems it does not prevent it all, and the scalp will still hurt and be sensitive. The only thing that helped my painful scalp and neck was shaving off the hair. 
  • DO NOT shave your hair too close to the skin. Nicking the scalp can cause infections, plus you can get ingrown hair that can also cause infections. Infections can be very bad when you are going through chemo.

Nosebleed - 

  • Afrin (oxymetazoline) helps stop nosebleeds. Mine never got very bad, so I don’t know how well it works if there is major bleeding, but it helped mine.

Neuropathy (numbness or pain in your hands and feet) - 

  • Put ice on your feet and hands during the infusion. My infusion center provided the ice, but I understand not all facilities do so. You can purchase cold gloves and socks online if needed. You should ask before your first infusion if you need to bring your own so that you are prepared. The icing helped me.

Lightheadedness -

  • For me, this was usually due to not consuming enough protein, so I kept protein bars in the pantry and my purse as this was the easiest way to get the protein I needed. My favorite is Clif’s Builders Protein. It contains 20 grams protein, the most I found in any protein bar, and it tastes okay.

Consuming enough food / calories (Many foods don’t taste good or you just know they will not go down well.) -

  • I am fortunate that my husband made most meals and cleaned the kitchen, but I never knew what my body would be able to handle on any given day, so the week prior to the infusions I made a couple of different types of soup to make meals easier. 
    • I found a brilliant product that we still use. It is made to freeze one cup cubes. I freeze them and then move them to ziplock bags. We keep several different kinds of soup in our freezer that we can take out whenever we need.

Nausea - see the “Week After First Chemo Infusion” post.














































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...