Starting Chemo May 2018
Comments
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My PT popped a cord for me a few weeks ago, little pain, but it felt good and the I had more mobility after she did it. I hadn't had anymore.
Just finished 6 of 12!! Half way there! It put a smile on my face today, I'm just so ready to be done.
I had my son buzz cut my hair today when I got home. Before chemo I had a very short pixie cut, but it started looking patchy and every time I touched it I had a hand full of hair. So, we got the clippers and put the no 1 on it and toke it all off! It kinda felt liberating. There is something about the advise everyone said about being in control and I felt it today for some reason. I didn't get a wig, I am just going to wear hats and scarfs. I already scared myself going to the bathroom...I didn't recognize myself!
I also am having a hard time sleeping. I know tonight will be bad cause of steroids, but this week my feet has been tingly and some pain. It also seem to travel to my legs. So, between hot flashes and having to move my feet to stop the pain, I don't get much sleep. Anyone else going through the same thing? Any recommendations on how to help stop it?
Hope everyone has a great weekend...its supposed to be hot here.
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Saw66,- might be a SE, and benadryl helped me with pain and fatigue. Also I didn't take additional steroids when i got home. I only had steroids as a premedication before infusion. It might not work for everyone but that's how I handled all my infusions. Also prior to dx i already had prescription for xanax for anxiety. Which also helps me with sleep and less irritability. Hope u find something to take the edge off so u can rest.. hugs
Wl002- congrats thats amazing news!!
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Hello and congrats Saw!! You are exactly one week ahead of me. I did a 1” buzz after #4 and am wondering when it’ll be sparse enough to take it down even farther. I have a big out of town party today and thought I’d keep it this long for that but we’ll see. And yes it is still very weird when I catch a glimpse of myself in the mirror. It occurred to me my husband must be much more used to it than I am. I take a Compazine at night the first two nights, not because I’m nauseous but to help me sleep. I told my RN I feel like my body is getting used to the premeds—I don’t seem to be nearly as affected by the steroid as I was the first week. Check out the March/April threads for suggestions about the leg tingles—I really haven’t had that yet
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Thank you urdrago71 and Ingrep for the advise. I’ll let know if anything wirks
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Hello! I have finished 2 AC treatments and have tolerated it well so far, but now I have horrible acid reflux/heartburn. I've been treated for GERD for years but it's never felt like this. It even kinda hurts when I swallow, like something is stuck in my throat. Anyone else experience this?
Heather
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Heather , I had the acid reflex/heartburn after 2nd chemo. The only thing that worked was Prilosec, which I still take thru Taxol as sometimes I still get the heartburn.
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Thanks, Karla. I've been taking prescription prilosec for years and this acid is really breaking through it. I'll have to check with my dr this week! Thanks so much!
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Hello ladies. I was just checking in for my mom. She just finished her second infusion of AC last Monday. Her hair started falling out on Friday so she asked me to buzz it on Saturday morning. It was hard but she is starting to be more comfortable with it. She even took her great grand kids to the pool yesterday while rockin a super cute hat. She's been fighting that metallic taste in her mouth and says that probiotics and diet (she's diabetic) ginger ale somewhat helps. She mentioned that the inside of her mouth feels spoungy and a little raw. She's religious with her mouth rinse. Does anyone have any other suggestions for mouth discomfort that is working for you?
Thanks, Susan
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iwannaseeyou- When I had mouth sores I rinsed with baking soda and salt. It seems to do the trick.
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My neulesta on-body just got placed today and it kinda hurts now. Weird. It didn't the previous two times. It is a little higher than it was last time...who knows. I'm probably just more sensitive this time around since it's #3 of AC.
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Heatherautumn, how did your 3rd AC go? I will have it next Friday and am scared if it. Was it pretty much the same as the other 3, or the side effects are worse this time? I hope not..
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Not gonna lie, i was really apprehensive about going to #3. #1 I was like, BRING IT ON!!! #2 i was, Ok, here we go! I got this!
For #3 I'm bald and starting to feel a little more tired and looking like a cancer patient! So, i was apprehensive. It went just fine. Today I'm doing well. Felt a little crummy last night but hydrated, at mashed potatoes (comfort food!!!) and went to bed early. This morning some scrambled eggs and yogurt. A banana for lunch. No nausea so far. Seems like the other two so far. My tummy really hurt at the site of my injection (whatever anti-nausea shot they gave me - huge needle and medicine like syrup) and my nulesta thing was a little funky. I'm just chalking it up to being tired and less busy.
I'm good today. Trying to stay positive! Only one AC left!!! (Then 12 weeks of taxol....but have to stay one step at a time!)
You can do this!!!!
Heather
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Hi everyone- hope you all are having a peaceful weekend.
InnaB i have AC#3 this week and half of me is saying “bring it on!” While the other half is hiding under the covers.
Im noticing that most of the SEs have been the same for the first two rounds but that my overall fatigue is increasing. I even left work early a couple of times because I just felt like cooked spaghetti. Not sleepy but heavy and more than a bit blue. Trying to get out and walk even if its just for 10 minutes a day. Anybody else having a similar increase in fatigue
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I am primarily hiding under the covers. That is, when I am not walking or exercising. Now I understand why my oncologist insisted on disability. Taking care of my body has become a full time job. I walk at least 5 miles a day, do 30 min of elliptical/stepper and light weights on alternative days, and still do my post mastectomy arm moves at least 3-4 times a day. It’s very counterintuitive, but somehow this regimen helps with fatigue. It takes a lot of time, too. But it relaxes me somehow. Plotting my Taxol strategies. Freezing hands/feet, nail/toenail care, neuropathy scare. Just the usual day in a cancer patient’s life. AC #3 is this Coming Friday. Hopefully it will not bring any new SE’s.
In other news, my husband just took our 16 year old son for a week long pre-college program, and I was left at home because, you know, dorms, people, infection fears, etc... It sucks...
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Clare--just my $0.02 on fatigue. I learned this from rads two years ago and a recent check in with a NP confirmed that sometimes you need to listen to your body. I've only had a day or two so far that I feel the fatigue--which is not the same as being tired. I don't really get sleepy, but feel an overwhelming desire to get off my feet. It hit a few Thursdays ago, and I found that if I did just that--put my feet up for about half an hour--I felt much better and had energy again. I get the exercise helping and all, but I think when your body is telling you to lie down, maybe the best thing you can do is listen.
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I'm back among the living! I've been in the hospital for the last week, they never really did give me a diagnosis. One doc said I had pnumonia, another doctor told me they just tell you that when they can't figure out whats going on. ha! It started last friday night with a fever so I called my onc, and he said to get to the ER and by the time I got into a room I was so sick they had to sedate me. If I woke up even the tiniest bit I was throwing up, it was awful! After an entire week and every test under the sun, I still had no diagnosis and they sent me home.
Just in time for chemo tomorrow. *sigh* My husband doesn't want me to go, but they did my labs and doctor seems to think we're ok to go. Pray this one doesn't land me back in the hospital!
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Ugh BigPeaches--that sucks. Do you get steroids with your premeds? You might even get a little pop from them for a few days. Fingers crossed you get through this next one with minimal SEs.
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Big Peaches so so sorry you went through that! I’ll be holding a good thought for you as you do your next treatment tomorrow. Let us know how you’re doing
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Hi BigPeaches,
I'm sorry to read about your hospital stay. It sounds like a neutropenic fever. They often don't find the cause of those. My wife had that after her first round of TC and was hospitalized for three days. She ended up back in the hospital a week later with abscess on her surgical site. Her counts were still down and it went into sepsis, but thankfully, they got on top of it. Our oncologist consulted with our surgeon and they decided to postpone the second round for a week and let the drainage stop. It ended up being a two week wait and she was able to get the second round last Wednesday.
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Gosh Engine104 that's awful!
For those asking about mouth sores, swish with hot salt water, as hot and salty as you can stand, seems to be the only thing that works for me.
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Those mouth sores suck. I feel like i have strep throat! I've been using baking soda and water but may try salt. Maybe I'll slam a shot of gin. Maybe that'll make me feel better.
I'm much more nauseated this time (nearly 1 week after my 3rd AC) and my taste is gone. So weird.
I just keep thinking a few more days I'll be feeling a little better.
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Bigpeaches, I'm so sorry to hear that you were so ill!! I hope tomorrow's treatment is boring and uneventful for you.
Those darn mouth sores are a pain, but isn't this entire process? My mom swears that the probiotic she takes every day seems to help but it's still a struggle at times. She just finished her third of four AC today and has minimal taste for anything. She says everything tastes like baking soda. She mentioned that raw vinegar seems to be helpful but then it exaggeratesthe mouth sore pains.
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Heatherautumn-Not sure if anyone has mentioned it, but ask your MO about magic mouthwash. It's a lifesaver for the mouth sores.
I'm just coming out of round 3 of 6 and this is by far the hardest yet...I've had more nausea and fatigue and just taking longer to recover from it. Trying not to wallow but chemo is mentally exhausting. My family has decided to take our planned summer trip to the beach and I can't wait...11 days until I smell the ocean
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Thanks. That's all resolved, thankfully. She's had constipation issues with the second round which became impacted, so it was back to the ER. They got things moving, so to speak.
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Finish my 4 cycles of AC the last one left me real tired lost most of my hair and my nails have started turning black on my thumbs it wasn't too bad with the nausea pills it was doable. I see my doctor tomorrow and he told last week I would get a 2-3 week break and then start 12 weeks of Taxol . The chemo nurses were great always giving me tips to help me thru this.
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Congrats on getting to one of the finish lines, llupp!! From what I've read Taxol will be a <relative> walk in the park.
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Hi, guys. Something funny for your entertainment. My first experiment with English poetry:
Ode to my hair
My hair is gone. I have no hair.
It wasn't much, but it was there.
A modest mop right on the top
To keep me safe from heat and cold.
I didn't like it. It was flat,
It looked horrendous under a hat,
But it was mine. And now it's gone
To rest in peace while I go on.
I lost too much in this long fight
But I'll keep on with all my might,
I'll soldier on, I'll overcome,
And at the end I will become
A mix of someone old and new,
With a few parts borrowed and a little blue,
And a fledgling brand-new hair crop.
A light peach fuzz right on the top.
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Dear InnaB,
Loved it! Great job!
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Innab, I loved your poetry, "Ode to hair". Thanks for sharing
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Innab, I love it!!
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