For M_Rita More on ECF Chemo
JimboC
Member Posts: 264
M_Rita, since your post was at the bottom of a long older post, I wanted to start you at the top. Here's the link to the original post in case anyone is lost: http://csn.cancer.org/node/215824
Like Paul said, staying ahead of and managing side effects are key. I actually would take my first Zofran on the way to my chemo so that it would have time to get in my system. I knew for the next four days or so I was going to be taking one about every four hours. After a few days, I would test it by delaying my zofran to see if I was still getting sick. If so, I'd pop one down and wait a day or so for another test. I also received Aloxi as one of my premeds which was a tremendous help with the nausea. I just experienced the nausea from the big chemo day, not the 5FU.
Hydration is another key tip. I would drink Poweraid Zero about 64 ounces a day plus water. This chemo is tough on the kidneys so hydration helps keep you flushed out.
My job was incredibly accommodating with working around my treatment. I could have continued working the entire time as far as they were concerned. The had no problem with my taking time as needed. I wish everyone were as fortunate as I in that respect. Two days a week should be very doable if you have as mild a experience as I did. I talked to my boss, who is also one of my close friends, about dropping down my schedule. He was fine with it but I was the one who couldn't do it. I'm either on or off, it's tough for me to cut back a little.
As for the food-borne illnesses, E Coli is making it's rounds in Europe. With a compromised immune system, it could be deadly. Locally, in the past year, we've had Hepatitis A outbreaks tied back to an infected worker at a local restaurant. This was before I started chemo but that was in the back of my mind once I started. If someone has a cold or bronchitis and coughs on the food, it could be picked up. I was a closet germaphobe before I started and I feel it was helpful afterwards.
A little diligence will go a long way. I eat at home much much more than I ever did before. My wife would cook me anything I wanted. I tried early on eating out some. I grabbed a sandwich once at Chick Fil A and it had a hair in it. Since I didn't have any hair, I knew it wasn't mine. Broke my heart. I even tried a coffee from Starbucks. Same result, had a hair in the little cap they insert into the drink hole. Still, no hair on my head. Again, broken hearted. It seemed like every time I would try there for a while, something would happen to ruin the experience. One of my daughter's friends was a manager at the local McDonalds. I told him about my experiences and how bad I wanted to have a Big Mac but was afraid to. He told me to come in and he would personally fix my food. I took him up on it several times. They were the best Big Macs I ever had.
I'll private message you my email and phone. Feel free to call, email or post here if you have any questions or want to talk.
Jimbo
Like Paul said, staying ahead of and managing side effects are key. I actually would take my first Zofran on the way to my chemo so that it would have time to get in my system. I knew for the next four days or so I was going to be taking one about every four hours. After a few days, I would test it by delaying my zofran to see if I was still getting sick. If so, I'd pop one down and wait a day or so for another test. I also received Aloxi as one of my premeds which was a tremendous help with the nausea. I just experienced the nausea from the big chemo day, not the 5FU.
Hydration is another key tip. I would drink Poweraid Zero about 64 ounces a day plus water. This chemo is tough on the kidneys so hydration helps keep you flushed out.
My job was incredibly accommodating with working around my treatment. I could have continued working the entire time as far as they were concerned. The had no problem with my taking time as needed. I wish everyone were as fortunate as I in that respect. Two days a week should be very doable if you have as mild a experience as I did. I talked to my boss, who is also one of my close friends, about dropping down my schedule. He was fine with it but I was the one who couldn't do it. I'm either on or off, it's tough for me to cut back a little.
As for the food-borne illnesses, E Coli is making it's rounds in Europe. With a compromised immune system, it could be deadly. Locally, in the past year, we've had Hepatitis A outbreaks tied back to an infected worker at a local restaurant. This was before I started chemo but that was in the back of my mind once I started. If someone has a cold or bronchitis and coughs on the food, it could be picked up. I was a closet germaphobe before I started and I feel it was helpful afterwards.
A little diligence will go a long way. I eat at home much much more than I ever did before. My wife would cook me anything I wanted. I tried early on eating out some. I grabbed a sandwich once at Chick Fil A and it had a hair in it. Since I didn't have any hair, I knew it wasn't mine. Broke my heart. I even tried a coffee from Starbucks. Same result, had a hair in the little cap they insert into the drink hole. Still, no hair on my head. Again, broken hearted. It seemed like every time I would try there for a while, something would happen to ruin the experience. One of my daughter's friends was a manager at the local McDonalds. I told him about my experiences and how bad I wanted to have a Big Mac but was afraid to. He told me to come in and he would personally fix my food. I took him up on it several times. They were the best Big Macs I ever had.
I'll private message you my email and phone. Feel free to call, email or post here if you have any questions or want to talk.
Jimbo
0
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