Starting T/C Chemo June 9th need feedback on side effects
hi ladies looking for personal side effects you had during your T/C Chemo treatment. I have 4 treatments over 12 weeks beginning 6/9.Please share your experience side effect no side effects etc. .Thank you and God bless💟
Comments
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Hey Marge..chemo for me was bad. I got very sick the first two treatments. I changed Oncologists after the second treatment. My new doctor gave me a different type of of drugs and I didn't get as sick. I had 4 treatments all together. On or about the 7th day after each treatment I could tell I was not feeling well and all I could eat and drink for about 4 days was lemonade and lima beans and rice. My hair fell out the 17th day after my first chemo. That didn't bother me at all. God bless you Marge on your journey.
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marge, I had the same TX plan as you are having. For me, the first two weren't bad, really. I lost my taste for almost everything....including water. I craved cheetos of all things! But, make sure you hydrate! I had the Neulasta shot the day after chemo, which gave me aches and pains, but I took Claritin and hot showers. I had thrush and yeast infections, fatigue, insomnia (from the sterioids), but all in all, they were minor SE's. Just seemed major at the time, maybe bc they came on top of each other. I got heartburn in the later TX's. The SE's are cumulative, so you will probably feel more tired at the end of TX than the beginning. I had my MO reduce my last dose bc I was having a slight allergic reaction. I tried to walk often and worked most of the time. I lost most of my hair by the end of TX. My SE's were very manageable and not near as bad as I thought they would be. No infections, nausea or fevers. Make sure you stay on top of the SE's, so your MO can get you something for relief. I hope that is helpful. We all react differently; I hope yours is easy peasy! Good luck! You can do this:)
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Marge, I too had 4 TC treatments. My experience was good even though I was very worried before starting. I had had bad experiences with seemingly 'harmless' drugs before, such as nexium and I used to suffer from weekly migraines. I was surprised that I had very little SEs with chemo. I had a splitting one day headache and swelling with the first infusion ( after 6 or 7 days) but in retrospect, I think the headache was associated with my periods. They stopped since the first infusion. The swelling might have been due to the steroids but MO had me take one benedryl for it and it resolved about an hour later. Didn't feel a thing with the 2nd infusion, I traveled and moved house on my 3rd and I did feel a little more tired on my 4th ( but could have been due to the move). I did experience weirdness in my taste buds after the last infusion but now 6 weeks later I had forgotten all about it. I did, however, discussed with MO about dropping most of my meds since I did not have many SEs. I think the meds itself can cause SEs. I did take claritin and that kept the achiness at bay.
I had no nausea, no chemo brain, only lost half my hair, 10% of my eyebrows and lashes, no stomach problems etc. The good part was that I no longer have my periods, no more migraines and my skin cleared up. I did gain about 10 lbs but have lost 6 already, keeping fingers crossed.
I believe everyone's experience is different and to just expect everything. I prepared for it by reading through the tips provided here on this forum and discussing with the MO about all my concerns. That way I feel I will be more in control and would know what to do when things happen. It also helped calm my fears knowing that there are options and treatments for the SEs.
Here's wishing you the best with your chemo.
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Hi Marge,
I had the same treatment. Really very few side effects. Some heartburn for a few hours after a treatment, bad taste in my mouth for about a week after. I also took Claritan after the Neulasta and had very minimal aches. Eyebrows just thinned a little but I think only I can tell. Held on to a little bit of hair until after the third treatment and then it all went. I never missed any work except for the treatment days. I tried to make sure I did the treadmill every day, and I think that helps. I am now six weeks post treatment and my hair seems to be coming in pretty good. I went on vacation three days after the last treatment and hosted my grandson's Christening party for 40 people two weeks later!
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That was the exact same chemo cocktail I did 5 years ago starting 7/11/11. I had relatively few side effects, continued going to the gym and work. Here are some good things to do:
take the nausea pill reguarly for the first 24-48 hours after chemo. Don't wait to get nauseous. The first 24 hours worked for me. I never got nauseous
drink 10 - 8 oz glasses of water each day for at least 7 days after chemo. I just started doing it every day, and still do
if prone to constipation, drink one glass of metamucil or similar fiber drink each day for 7 days after chemo
for 72 hours after chemo - rest. Let your body do what it needs to do. Sleep when you want to sleep. Be awake when you want to be awake.
take short walks every day or do some type of light exercise daily
eat/drink high protein foods. My favorite go-to was muscle milk, scrambled eggs, and peanut butter sandwiches
the tast buds going wacky was the worst side effect for me. The only thing that tasted good was sweets, and you have to be careful with those. I kept a bag of low calorie mints with me at all times. And I drank flavored water because regular water was yuk. Lemonade was good as well.
keep Benadryl and itch cream on hand in case you get hives. I only got them once.
use Nail Tek daily on finger and toe nails
Take Biotin and a probiotic daily
get a night cap for your bald head, if you tend to get cold easy.
Get a nice wig before losing her hair. I bought my wig to match my hair color and style almost exactly. No one whould have known I had lost my hair if I did not tell them.
I cut my hair very short before I began chemo, then shaved it when it started coming out in droves. You can expect to lose her hair 10-14 days after first chemo.
When I finished chemo I began using Ovation Hair Advanced Cell Treatment on my head. My hair has come back prettier and thicker than ever. I still use it 5 years later.
hook up with a group on this board who is going through chemo at the same time, with the same chemo cocktail. You will learn from each other as you go throught he process.
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My experience:
Nausea days 1-2 after treatment; I had to really stay on top of anti-nausea meds.
Hair loss about two weeks after first infusion. I'm 8 1/2 weeks post final chemo and the hair on my head is happily back with a vengeance. BUT I didn't begin losing brows and lashes until maybe two weeks ago, and have about half left.
Constipation--ugh.
Loss of taste for a week or so after infusions.
Fatigue on days 2-5 after infusion. Some days I could not stay awake. I worked throughout but missed time here and there.
Nails--no problems during, but now they feel soft.
Fevers--I ran fevers after infusions 2 and 3, possibly due to Neulasta. I took Cipro in case I had an infection but my oncologist didn't believe they were neutropenia because I had them right after infusion. In one case I think I just had a cold. But CALL if you run a fever--I think they'll tell you anything over 100.4 degrees warrants an immediate call to the doctor.
In general, the week after the infusion is the worst, and you steadily feel better. I would suggest you be careful to avoid driving long distances until you have an idea how the fatigue will affect you. I drove eight hours round trip out of town for work three days after my first infusion and I ended up having to break up the drive to sleep.
Good luck to you! My experience was not that bad.
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