Is there a July 2011 group?
Comments
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Dear worriednlost, I just tell myself take it a step at a time. Docs will give meds for all the side effects and hence, to follow docs' instructions to minimise SEs. For me, the first 2 days are ok, just weak so a lot of resting and sleeping. Days 3 and 4 were worst off, cant sleep, very weak and drained and no appetite. I just lazed around the entire time. All suffering will pass... I am Day 5 now and getting better and could even go out for a walk today. Hang in there for her! She can do it.
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Day 2, still, fingers crossed, I am ok. Up at 3 and serious night sweat/hot flashes, but otherwise ok.
Definately feel tired but if this keeeps up I may have to decide that I can work on the day after infusion. That would be a plus. It's a lovely day in Vermont, want to get out for a walk if I can. My nurse worried most about constipation issues with me, she recommended senna and then an organic tea called "Smooth Move" (apt title) by Yogi. Tastes like licorice and seems to do the trick. Doing TONS of fluids, think it is helping. We'll see what day 3 and 4 bring....... Here is to a SE free day to all of you!
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Day 2 for me and I feel just ok, but not quite right. I can't explain it other than to say I feel like I should stay close to home. So, I ended up calling off work today after all. I have to go in for my neulesta shot at 3:30 this afternoon. Other than that, I'm sticking around here and puttering around the house/taking it easy.
I woke up in the middle of the night with some acid reflux/heartburn, but that may have been related to eating dinner fairly late last night. I truly felt perfectly fine; we even went over and visited my boyfriend's parents and grandmother, whom they just moved in with them from NJ.
But I overslept this morning and I took it as a sign that I need to slow it down for a few days. I'll keep you all posted if I can. Being home today likely means I'll be popping in here more often, seeing what you all are up to.
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I have the same fear- I feel ok but not quite me- sticking to home a good idea. Hope it continues to be a good day for you, Valbee.
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misswim, everything about that tea you mentioned sounded promising... until you said it tasted like licorice. Blech!
Wonder if there are any other flavors, because I can foresee that being an issue for me as well. Then again, who knows?
Hope you have a good day today, too!
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Hi, anyone on TC having diarrhea? Its Day 5 for me and I have been running to toilet after meals and drinks. Stomach ache as well. Is this the norm?
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It's definitely one of the SEs, FrancesC, and that's one of the reasons I'm not straying far from home today. I kind of have a feeling as though diarrhea could strike any moment today.
However, my instructions say to call my doctor if it persists more than 24 hours. So, I would contact them ASAP to find out if there is something else you should be doing.
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Thanks Valbee, it all started this morning at 5 am. I will monitor and if I am not ok by 5 am tomorrow, will call onco. Day 5 has been ok except for this problem. Getting my energy back.
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Whew! Ok, Frances, I read your post wrong!
I thought you'd said it had been going on for five days and I was alarmed. Big sigh of relief!
Just make sure to keep hydrated in the meantime, and maybe try some items on the BRAT diet (bananas, rice, applesauce and toast). Glad to hear your getting your energy back. Hopefully, the diarrhea will ease up and be the last SE you have to deal with for a little while. Hang in there!
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Thanks Valbee - LOL - I was unclear in my post:) so fed up with running to the toilet and wondering what is happening to me today.
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Day 9 today after my first chemo (TC); So far I am feeling much better, came back to work yday and worked full day, and I am at work today as i type this now.
I have been noticing a few things - my days are good but at the end of the day i feel like my body get soo tired and i just want to nap. Yday after work i came back home and i was worn out!!! thank God my kids were out with hubby, so i snuck in 30mins nap before they came back:-) had a good night sleep. Another thing i notice is that my feet get tired easily. I work in the city and live in the suburbs so my commute is kinda long (25mins drive to the train station then take the train 20mins ride to the city then walk for abt 10mins to my work) I noticed that i dont walk as fast as i used to because my legs hurt:-( also i get palpitations every now and then. Has anyone else noticed this? Other than that I am doing good; I eat whatever i used to eat before and i dont ahve the constipation problem:-) My mouth feels weird, i use biotene toothpaste & mouthwash.
I am hoping to have a great and fun weekend with my family. Hope you have a blessed friday & weekend.
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worriednlost - I feel for you and your mom. It is scary. They told me the first time was the worst because you don't know how it will affect you and they have to warn you of every possible side effect. Be sure to have her follow Dr's orders as far as nausea meds go - don't wait until she feels bad. I wrote down a med schedule since there were some meds to take every 8 hours and some every 6 and some twice a day - confusing! At the first sign of any side effect, I took the meds that I had, whether it was gas or heartburn or whatever. Make sure there is plenty of time for her to rest and a variety of liquids around - she won't know what tastes good to her until she gets there. She's lucky to have you looking after her.
FrancesC - I've had some issues with diarrhea since about day 3 but nothing too bad. Just a couple of times a day with stomach cramps. Did they tell you to take OTC meds? Mine suggested immodium - 2 with first BM, one with each thereafter until it clears. I have not been very good about it since it has been a sporadic issue. Just be sure to not get dehydrated and to eat simple foods. Not high fiber, not dairy, not spicy or greasy.
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Got a question for those of you who are a few days in, especially those getting TC. Did you get the metallic taste and how long after the infusion did it set in? Just curious when to look out for it.
My sister is having a case of Aqua Delight sent to me. Should be here today, in fact, but so far I'm not noticing any weird taste. Too soon? Infusion was just yesterday.
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Valbee - my mouth feels weird, not sure if its metallic:-( but its just not the same, kinda dryish, blunt feeling.
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Valbee - not metallic exactly. I got that fuzzy tongue feeling about 3-4 days after. My whole tongue was white. After a couple of days, that went away and now it just feels like sandpaper. Very dry mouth feeling. The Biotene mouthwash is soothing, as is yogurt, ice cream, stuff like that. I am always drinking some kind of liquid. Food definitely does not taste the same. I am on day 9 and it is better, but not gone.
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Valbee and anyone with the reflux. I have had it many years, Zantac worked until I started chemo. Doc prescribed Dexilant....I LOVE it. Pepperoni pizza was my test and no problems.
I too was plagued with the diahrrea...after my 3rd chemo. Everything went thru me. Jumped on the BRAT and took 2 imodium every 4 hours (onc orders)...took 2 days but finally worked wonders for me. And how anyone can drink Pedialyte and say it tastes good is beyond me....I had to cut mine 50/50 with Crystal Lite.
Stay positive and keep smiling!
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hi all,
I am doing pretty good, day 17, I'm thinking it takes about 2 weeks to feel pretty normal for me. Dreading Wednesday when it starts all over again, but also looking forward to putting #2 under my belt!
Hope everyone feels better and has few SEs.
xoxoxo
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hi Jenn
I'm happy to share my experiences with you...and please do the same.
As for the metallic taste, I had that for at least the first week, I think just the last 4-5 days have my taste buds been back to normal. Regular water, which I normally drink TONS of, tasted like metal, I had to go with seltzer water and a tad of lemon or organic cold green or white tea, mango flavored, different flavors. Ginger Ale even tasted just like metal, it was yuck. Hot coffee tastes good, didn't seem to be so bad...
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Hi Everyone - I too had the "carpet mouth" that you are all describing. I'm on day 9, and it is fading but I do think the one thing that has helped and I wasn't doing until this week is rinsing your mouth out with 1 tps of baking soda and 1 tps of salt in warm water, 3 times a day. trust me you'll notice a difference in 48 hours.
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Yep, I've been doing baking soda washes at least 3x a day and had a dry kindof funky feel or film in my mouth, but it never got bad, never got thrush..one small blister in the roof of my mouth. I just make it habit now to do the banking soda and/or salt rinses after each brushing and sometimes in between.
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Snoopy73: I believe the heart palpitations was one of the symptoms that they told me to let them know about. They have me calling the nurses for most of the side effects, just to touch base and then they can screen my calls to let the doctor know if it is something more alarming. I would feel more comfortable just calling and checking in, rather than wondering. I know the AC treatment can really do a number on the heart muscle.
I have been hearing that an hour of walking or other exercise is the ideal for those of us on chemo. Kind of hard to imagine fitting that in with all the naps, doctor appointments, work and taking care of a family though. I would like to work more in, but I cannot imagine doing that much yet.
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Greetings ladies! It is day 5 since my #1 chemo. Sorry, haven't logged on much. I'm really glad I did now. It's been crazy. Today I've been dealing with diarrhea. All I want to eat is Cream of Rice. It is so comforting. At least I'm eating, I guess, and drinking. I am just getting so tired of getting up to go to the bathroom.
Everything tastes funky too. I have these lemon drops and they taste so wicked lousy. Yesterday eve. I was feeling kind of feverish. Uh oh, but my temp was just a few marks above normal. I took a prevacid last night for acid reflux, burppy tummy and heartburn. That is about the most consistent and annoying thing so far.
Hoping all your SE's are minor ones this weekend....try to do something fun
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Hi, ok so I went back to the clinic to have my labs redrawn and everything came out fine this time. So as of now everything is still set to go for chemo to start Monday. I am soooo not ready. I like coming on here and seeing what to expect. I am just not ready to go through any of it. I keep going along as if everything is ok and knowing all the dates and going from one procedure to the next. I know what I have to do but I am not sure if I just put it behind me at time or what. But reality sets in when I get places like going to get the port. I had a massive headache which was from stress and lack of food since you have to be npo.
Hopefully, I can have a good weekend and not worry and miraclously be ok with getting started on Monday morning. I know it's a dream but maybe at least the edge can be taken off some -
Hello All, I started my 1st AC treatment on Tuesday, July 12th and followed it with the neulesta shot on the 13th. I am vitamin D deficient so I am taking 1000 IU of Vit D3. Is anyone else doing this? I was told by my chemo nurse it was okay as long as it did not make me sick..so far so good. The first day I had a brief episode of sweat running down my back and then I had a little upset stomach that evening. I took all of the meds the Doc told me to and began my drinking regimen the day before chemo and am finally going back to normal amount of intake of water today. The day after my neulesta shot (Thursday) I had an awful feeling in my shoulders and my neck???? Is this the bone pain? I can not tell if it is bone pain or my muscles??
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I'm sure I am jinxing myself, but today (day 7) was great. I tire easy and surely do not want to over do it. But everything tastes good (and comes out good), no mouth sores, no aches/pains from the Neulasta shot and even felt the desire to show affection to my loved ones. I would be so lucky if I could feel like this until my next dose next Friday. After talking with the Onc nurse I decided to go ahead and go out on disability (maybe that's why I felt good today). She said with the AC dose dense, I am getting hit hard and don't have that extra week to feel good. However, my port area still aches.
I am sending my feel good vibes to all of you so you can have great days too.
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Hi Cathy_C - well done, you are doing well. Thanks for the feel good vibes. Today is my Day 6 and I am still weak. Just got a neupogen shot in the morning. Doc says the runs I have could be due to food poisoning! He has advised no salads, no raw food, no juicing until everything settles.
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Cathy, I am happy to hear that! I am on dose dense too. Day 5 I was tired and felt sort of old. Today, day 6, all is back to normal. I think the Neulasta shot made me tired.
Otherwise I am with you, no SEs.
I am on ETC dense all two weeks for a total of 9.
Sommer
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Just home from the hospital.WBC dropped, opportunitstic infection, mouth ulcers and fever. Am doing better but my mouth is on fire. Miracle wash only lasts about 10 minutes then I am chipmunk cheek Susan. They willl adjust chemo does next time- of course this worries me. Onc said my bone marrow could not process all that cell death...sounds so unencouraging. Have open studios today. I am not going to be able to talk to anyone. Spouse will paly me I guess. Seems I am feeling better with aches but now my mouth feels like I want to trade it in.
Hope everyone is doing well.
Can't wait until this starts again.......(:
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Luvmy2kids, I had my Neulesta shot yesterday afternoon and this morning I woke up with some soreness in my shoulders and neck and a little bit of tenderness around the incision itself. I'm not sure if it's the Neulesta either, because since I was still riding on energy from the steroids I took for three days, I did quite a bit around the house yesterday. But I suppose it is possible.
Did the onc recommend anything for you to take to combat it? I'm taking Claritin and Tylenol right now, but was told repeatedly that if I needed anything stronger to let them know. So far, so good. *crossing fingers*
I don't know what the vitamin deficiency can do to how you're feeling; I'm completely unfamiliar with that. Sending good vibes!
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Frances! Food poisoining?? ARGH! That's not even fair. I hope you're feeling better soon!
Today is day 2 after treatment. I woke up this morning, took my thyroid meds first day (I had hypothryoidism before all this) and felt a little achy, but not too bad. So, I opted to go for a walk. Like much of the US, it's supposed to heat up like crazy around here. I figured I'd go early while it was still cool. I went for about a half hour, and then took a Claritin and two Tylenol in case that achiness is from the Neulesta shot yesterday.
Appetite is ok. I did take a Compazine last night before dinner, because I wasn't sure if I even wanted to eat, but then I was really hungry (hello again, steroids). I felt really tired around 10:30 and went to bed shortly after. No acid reflux last night and I slept well.
I'm hoping I'm not jinxing myself. If I'm up to it in a few hours, I might have my sister take me to my uncle's house to go swimming. It just sounds good.
Continued good vibes to all of us! Again, I am so glad you are all here because it is so helpful to have an idea what to expect.
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