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Anyone had a spouse go through chemo?
Posted on 6/25/26 at 12:24 pm
Posted on 6/25/26 at 12:24 pm
My wife starts next week. Trying to figure out when to expect the “bad” days that I need to take off work and be with her. Thankfully my coworkers are champs and will cover for me no matter what happens.
What is the normal course? How long does the misery from chemo last? Just trying to prepare. TIA.
What is the normal course? How long does the misery from chemo last? Just trying to prepare. TIA.
Posted on 6/25/26 at 12:26 pm to Slippy
My dad had it several times before having to get CAR-T. For him it was alot of weakness and tiredness plus stomach issues. They pumped him full of steroids to combat the nausea, but that much roids also come with their own shitty side effects.
Posted on 6/25/26 at 12:27 pm to Slippy
quote:
What is the normal course? How long does the misery from chemo last? Just trying to prepare. TIA.
I'm not the spouse, but I'm the patient, and I can tell you that people’s experiences can vary due to many factors such as the type of cancer, how advanced it is, the type of chemo prescribed, age, and how in shape you are in.
ETA:
quote:
My wife starts next week. Trying to figure out when to expect the “bad” days that I need to take off work and be with her.
In my experience, I tolerated the chemo with almost no side effects, but the steroids suck. When I was on them, I felt like I could conquer the world for the first day or two, but a couple days later, you start to crash. Then the next day, your head is full of fog. I had to get ambien prescribed because I was up all night.
This post was edited on 6/25/26 at 12:43 pm
Posted on 6/25/26 at 12:38 pm to Slippy
My mom did when we found she had stage 4 pancreatic cancer. It was so bad for her that she wanted it stopped.
Posted on 6/25/26 at 12:58 pm to Slippy
Yes, my husband had a very rare form of Non Hodgkins Lymphoma. His chemo was inpatient, 24 hours a day for 5 days every 21 days. Part of his regimen included steroids, and he never had huge problems with nausea. I think he actually gained weight after diagnosis. His worst days were 3 or 4 days after we got home from the hospital. He would become very, very weak. We set up the hall bedroom because it was actually closer to the bathroom than the master would have been. I wasn’t supposed to use the same bathroom for the a few days because the chemo was eliminated through urine and it’s toxic. It was so bad for a couple of days each round that he could only walk from the toilet to the foot of the bed, sit down to rest and then crawl to the other end. I wore a mask and tried to keep everything as sterile as possible. Then he would gradually regain his strength and was back to mowing the lawn in the last few days before the next round. When he bottomed out, one of the things that gave me peace was praying for him from head to toe. He was incredibly strong and healthy before cancer, rarely even took anything for a headache. Like others have stated, every regimen and patient can be completely different. You will meet some incredible people-oncology nurses are angels. If she’s having side effects, communicate that to your care team. Use MyChart and/or call them; you’ll quickly figure out which is quicker. Praying for y’all.
Posted on 6/25/26 at 12:59 pm to Slippy
Damn. Prayers for Mrs. Slippy. 
Posted on 6/25/26 at 1:13 pm to Slippy
quote:
Trying to figure out when to expect the “bad” days that I need to take off work and be with her.
They are unpredictable. It’s not necessarily immediately after the dose.
quote:
What is the normal course? How long does the misery from chemo last?
Depends on the cocktail and how she responds. Often it’s 3 weeks between doses. It can vary between a couple of bad days or it could be the entire time.
Even if she isn’t ill, high probability she will be exhausted with no appetite. You have to make sure she is eating well.
Posted on 6/25/26 at 1:19 pm to Slippy
For me the chemo was not as bad as expected. I was sick for 48 hrs after treatment. Usually just nausea and chills. I was tired after 2 or 3 days for a couple of days as well.
The radiation was awful. I had head and neck cancer and it tore me up. Put me in the hospital 2xs for a total of 18 days all during covid lockdown BS, had to get a feeding tube to survive for 8 months. Drank protein shakes for 8 months after and took 3 years to be able eat normally again. Still have muted saliva glands so it takes effort to swallow, i drink constantly when eating just to wash it down. I still cant taste anything sweet 5 years later. Food overall can sometimes taste normal and others the flavors are muted. Fun times. Prays for your wife.
Each person and each type of cancer create such variables that no 2 experiences are the same. Have patience with her and keep her busy (as she can be) to help with the mental fatigue.
I will forever believe my wife saved my life.
The radiation was awful. I had head and neck cancer and it tore me up. Put me in the hospital 2xs for a total of 18 days all during covid lockdown BS, had to get a feeding tube to survive for 8 months. Drank protein shakes for 8 months after and took 3 years to be able eat normally again. Still have muted saliva glands so it takes effort to swallow, i drink constantly when eating just to wash it down. I still cant taste anything sweet 5 years later. Food overall can sometimes taste normal and others the flavors are muted. Fun times. Prays for your wife.
Each person and each type of cancer create such variables that no 2 experiences are the same. Have patience with her and keep her busy (as she can be) to help with the mental fatigue.
I will forever believe my wife saved my life.
Posted on 6/25/26 at 1:19 pm to Slippy
i went through it and have had a number or family members as well
each person will react differently, and each Chemo regiment is different due to how they need to attack the cancer cells life cycle.
the drugs are designed to destroy/disrupt the cells grow and cell division cycle.
for me, i was told to expect to lose all my hair and have GI issues, as well as blood count issues, because the life cycle of my canrer was the same as hair, GI tract, and marrow.
i had to have a 1 week pause between cycle 1 and 2 due to mouth and throat ulcers (GI tract) , i needed nupagen shots (white count) and 2 trans fusions (red count) due to low blood levels, and all my hair fell out
and it still took me months after chemo before i could so any activity without rest since my red count was 7-8 when normal is 14. so my heart had to pump x2 the blood just to deliver the normal oxygen . actually took yeas (10+) to finally get back to 14
each person will react differently, and each Chemo regiment is different due to how they need to attack the cancer cells life cycle.
the drugs are designed to destroy/disrupt the cells grow and cell division cycle.
for me, i was told to expect to lose all my hair and have GI issues, as well as blood count issues, because the life cycle of my canrer was the same as hair, GI tract, and marrow.
i had to have a 1 week pause between cycle 1 and 2 due to mouth and throat ulcers (GI tract) , i needed nupagen shots (white count) and 2 trans fusions (red count) due to low blood levels, and all my hair fell out
and it still took me months after chemo before i could so any activity without rest since my red count was 7-8 when normal is 14. so my heart had to pump x2 the blood just to deliver the normal oxygen . actually took yeas (10+) to finally get back to 14
Posted on 6/25/26 at 1:21 pm to Slippy
quote:
Trying to figure out when to expect the “bad” days that I need to take off work and be with her.
A colleague of mine who had throat cancer at 72 years old went through three rounds of chemo and the removal of his larynx. He used one of those buzzer things to speak. When the chemo was over and he was cancer-free he told me once that if it wasn't for the good Lord and marijuana, he wouldn't have gotten through it.
Posted on 6/25/26 at 1:24 pm to Slippy
My daughter was diagnosed with Leukemia when she was 2. The steroids were absolutely terrible for her. There were days after treatment where she would just want to sleep. There were other days she was absolutely wired. She's 7 now and cancer free but that baby put up every bit of the fight to get there. It's definitely not an easy road but with faith and support for your wife you can get through it. As someone said Oncology nurses are literal angels. Prayers for you and your wife on this road ahead.
Posted on 6/25/26 at 1:29 pm to Slippy
I have been on chemo now for four months, along with an additional targeted therapy drug, with very few side effects. I am relatively young and strong. Otherwise healthy with no other co-morbidities. My cancer has responded well to the treatments.
Other than the days I have chemo, I have been able to go to work every day without feeling miserable.
I know that is definitely not everybody’s experience, but I will pray for you and your wife that she will have a good reaction to her chemo and that y’all will have minimal disruptions to your normal routines. A positive attitude goes a long way! My oncologist told me immediately after he got done explaining all the horrible possible side effects, that if you go in there expecting the chemo to make you sick, then it likely will.
Other than the days I have chemo, I have been able to go to work every day without feeling miserable.
I know that is definitely not everybody’s experience, but I will pray for you and your wife that she will have a good reaction to her chemo and that y’all will have minimal disruptions to your normal routines. A positive attitude goes a long way! My oncologist told me immediately after he got done explaining all the horrible possible side effects, that if you go in there expecting the chemo to make you sick, then it likely will.
Posted on 6/25/26 at 1:31 pm to Slippy
My wife tolerated her chemo treatments fairly well. She had tired days and some days she used Zofran to stave off any nausea. That’s all I got. Good luck and bless y’all! 
Posted on 6/25/26 at 1:36 pm to Slippy
I don’t have any insight to add, I just wanted to wish you and your spouse strength and as smooth of sailing as you can get.
Posted on 6/25/26 at 1:57 pm to Slippy
hate to hear that. My wife was diagnosed with stage 4 metastasized cancer in April of 2024. Scans showed liver was just completely covered with tumors, had some in her bones and lungs. Doctor told us she likely had a month or so. We started conventional chemo right away. She also had radiation because of the spots on her brain.. Here we are 2 years later and while she is not considered cancer free she is doing pretty good.
The original chemo via a port really did not make her that nauseous. They gave her nausea meds via the drip before. She also had some anti nausea meds to take as needed. She struggled with loss of appetite due to the chemo. Loss of energy, but mind you, she was still incredibly sick when we started this. She continued to lose weight for a while until we completed the 2 week course of chemo.
They did some detailed tests that revealed that the cancer started in her lungs. Non smoker. They said this was good news as they knew of a chemo pill that is designed to target the very cancer that she has and coudl pass through the Brain/blood barrier and treat teh tumors in the brain as well. Not many side effects from that.
I would advise you get a full regimen of anti nausea meds from your oncologist. Try to stay hydrated. One thing we did weekly is go in for IV fluids. That seemed to help a lot. There were certain things my wife still liked to eat and that is what we ate. Her skin became much more sensitive due to chemo. Simple bumps or scrapes looked a lot worse then they normally would.
We mostly dealt with some nausea, a lot of fatigue and the weight loss. She has gained back some of the weight, eats pretty well now and her quality of life is good. Her latest scans show zero cancer in Liver, no spots in her lungs or bones either. She did have a what they called a "mini-stroke" that showed up on her brain MRI, but no new cancer. She is literally a walking miracle.
I hate that you are having to go through this. its a grind for the patient and the caregiver. I will pray for strength for you both and that the doctors will have supernatural wisdom on how to treat it. We have had excellent care here and I'm very thankful for that. Stay strong and fight!!
The original chemo via a port really did not make her that nauseous. They gave her nausea meds via the drip before. She also had some anti nausea meds to take as needed. She struggled with loss of appetite due to the chemo. Loss of energy, but mind you, she was still incredibly sick when we started this. She continued to lose weight for a while until we completed the 2 week course of chemo.
They did some detailed tests that revealed that the cancer started in her lungs. Non smoker. They said this was good news as they knew of a chemo pill that is designed to target the very cancer that she has and coudl pass through the Brain/blood barrier and treat teh tumors in the brain as well. Not many side effects from that.
I would advise you get a full regimen of anti nausea meds from your oncologist. Try to stay hydrated. One thing we did weekly is go in for IV fluids. That seemed to help a lot. There were certain things my wife still liked to eat and that is what we ate. Her skin became much more sensitive due to chemo. Simple bumps or scrapes looked a lot worse then they normally would.
We mostly dealt with some nausea, a lot of fatigue and the weight loss. She has gained back some of the weight, eats pretty well now and her quality of life is good. Her latest scans show zero cancer in Liver, no spots in her lungs or bones either. She did have a what they called a "mini-stroke" that showed up on her brain MRI, but no new cancer. She is literally a walking miracle.
I hate that you are having to go through this. its a grind for the patient and the caregiver. I will pray for strength for you both and that the doctors will have supernatural wisdom on how to treat it. We have had excellent care here and I'm very thankful for that. Stay strong and fight!!
Posted on 6/25/26 at 1:57 pm to Slippy
My chemo for lung cancer wasn’t really bad at all. I only got sick once (and that might have been bad food), then my hair fell out towards the end. Cog fog, too. She needs to put the phone down and read books and relax.
And yep, faith and gummies help.
Don’t let her lose weight in chemo. She needs the body’s energy.
Radiation is different. I couldn’t fricking eat well for a couple of weeks.
Metastatic brain cancer happened and that treatment induces a lot of cog fog. I’m undergoing radiation for that.
And yep, faith and gummies help.
Don’t let her lose weight in chemo. She needs the body’s energy.
Radiation is different. I couldn’t fricking eat well for a couple of weeks.
Metastatic brain cancer happened and that treatment induces a lot of cog fog. I’m undergoing radiation for that.
Posted on 6/25/26 at 2:02 pm to Tiger in the Sticks
High grade b cell? Your entire post sounds like you're my sister in law 
Posted on 6/25/26 at 2:05 pm to Slippy
Ill also echo what a couple of said here already. I'm a huge fan of Gummies these days. They helped with the nausea and helped with her appetite as well. Its legal here. A lot of doctors wont prescribe it but I just go through the doper drive through. LOL
Posted on 6/25/26 at 2:08 pm to Slippy
My now spouse was just my girlfriend when I went through cancer twice. How bad the days are is dependent on what type of cancer and chemo involved. I had leukemia, so all of the chemo sucked. There wasn't an easy route. Some days I was too sick to even call and talk to her as we were long distance when dating. She always gave me my space and was very supportive during it all. Just be available and allow her to dictate the pace of things. It can be quite sad seeing a love one going through it, especially if they lose hair, weight, and really struggle.
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