March 2012 chemo
Comments
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Hair starting to fall out, one small clump, day after second chemo, 3/15. First chemo on 3/1, a Thursday...second chemo on Wednesday, 3/14. So official day# of first hair loss is Day 15. Today I brushed out another clump. Still presentable. No nausea, but a bit of acid reflux. I stuck with the compazine the first few days after my first chemo and this time I skipped..nope, I'm going on compazine preemptively from now on. (Dose Dense AC)
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Kam - hope the compazine works again for you. Yes, I have read take the anti nausea meds even if you feel ok!
Clumps no fun.
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OMG I just counted our list...there are 51 of us. I find that heartbreaking.
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Masserz, I noticed there were a lot too. When I went to my oncologist the amount of people in the waiting room for chemo was depressing to me.
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I hate it that we are all here but at the same time I couldn't be doing this without y'all. I had posted on boards at a couple different sites (including a popular pastel colored one) when I was diagnosed and there are no others that hold a candle to this one. (((hugs))) to all.
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onvacation....u r so right....about so many people in the waiting room...plus the ones that were in the treatmant cubicles. when i went to "chemo class" we had 15 people in class...then on the tour of the facility there were two large rooms filled with people.
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This is day 4 for me. Very achy, some bone pain. Only concern is low-grade fever. Anyone know if that is normal? Thanks
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Amy, sorry you are achy, hope that gets better. Is your temp over 101?
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It's been climbing. Right now 100.5. My onc orders are to take 2 extra-strength tylenol if it gets to 101, wait an hour, and if it goes back down to 100 just monitor it. I guess under 101 is considered ok. Still, I'm kind of concerned, mostly because I feel so crappy.
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Yes Amy. Normal, but make sure to let your doctor know if it gets above 100. Last time I went for labs, they said I had a low grade fever, and here I felt fine! So they can definitely sneak up on you!
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Amy, So sorry to hear about your fever. Watch it carefully. I hate having to be so paranoid about every little thing. But we do, so err on the side of caution.
To all: My current obsession is: am I allowed to eat fruit? I have been loving grapes, for instance, and washing them well, but then have read some things which say you are only safe to eat things cooked, or if raw, then you have to be able to peel it. Must get my fibre intake up, and I am do used to raw fruit and veg.
Any thoughts as always so very very welcome. -
Katycb: I asked this question yesterday during chemo and they said since my counts are low and I'm having to get neulasta now I should not eat any raw fruits or veges, I am so craving a salad. They said it's not worth taking a chance. So I agree. I don't want any setbacks! The nutritionist came and talked to me and said even frozen fruit was not safe. She did say if I wanted some carrots or crunchy broccoli I could peel carrots, drop in boiling water for about 45 secs and it would kill the bacteria/ germs and still remain crunchy, same with broccoli. She said even peeling thicker skin fruits after washing was still risky because it does come in contact with actual fruit when you cut through. It kind of sounds a little extreme but like I said I don't want to have any extra SE or setbacks! I want to get better ASAP!! On the flip side: I think if all your counts are normal you don't have to be so cautious.
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Thanks Msbelle. I will for sure try to stay in the safe side, and also ask when I'm in next.
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Katy I asked my MO about eating raw fruits and veggies because I do a lot of green juice etc, and he said yes that was fine. I think if you get an infection they don't want you to eat the raw stuff.
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Thx Kim!
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Just stopping in to say hi. Day 4, tired, brain seems in low gear. I was thinking about getting a wig, my Mom doesn't really know, she is a snow bird and by the time she comes back up here my hair will be gone. Thought it might be less of a shock for her if I had a wig. My question is whether you just order them online or do you need to get them fitted? Hope everyone is doing well. I agree with the looking forward to new hair and new boobs. Oh and the having been hit by a truck.
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On the wig, mine is adjustable. I am sure there are some that are more custom/sized but the one I got isnt. A wig shop could probably do any sizing for you and then you could order online from what they tell you. Hope you (and Amy) and all others with SE this evening feel better.
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I went to a wig shop. They were so nice and helpful and I tried on several to find the best fit and style! If you have one near you I would vote for that, but I have read lots of ladies order them on line and are happy with them.
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I think it really helped to go try wigs on so I could get an idea of what actually looked good on me. What I thought I wanted just made me look like one of the real housewives, so I'm glad I didn't order it online! Most wig dealers have strict return policies, so you can't really just take a chance. However, if you go try some things on, it will be much easier to find something similar online and sometimes you can find them cheaper that way.
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KatyCB...I think it would help if we could support each other with our exercise efforts. My doc said any exercise with weights or resistance has been proven beneficial during chemo. I think it's two fold...the normal benefits like energy etc., but also with bone and muscle loss. I'm not sure if the bone loss is just a concern for those of us on herceptin or all of us. I know I had to get a bone scan before starting chemo. I'm open to posting on this thread or starting a new one, depending on how everyone here feels. Please chime in everyone. With fifty-one (?) of us now want to make sure no one objects. Oh, we have to get Muscles in on this lol.
Welcome Muscles and all the other new Marchers!
Fifty some people for our March 2012 thread and it's only March 17. So unbelievable and sad.
I've been wondering if anyone chewed ice during their chemo and if anyone put anything cold on hands and feet. Chewing ice is supposed to help preserve taste and prevent or reduce mouth sores. I did chew ice, and never lost taste. I don't know if it was coincidental or if there is benefit to it. Also putting ice (frozen bags of veggies on/under hands and feet is supposed to help prevent neuropathy and can also preserve nails. I have read postings and heard stories from women at a support group at the hospital where there nails turned black and peeled back and eventually some of the women lost nails on hands and feet. I don't know which chemo they had though. I believe there is definitely something to this as I have heard some hospitals give cold mits out for hands and feet during treatment. Mine is not one of them. Just wondering if anyone else is doing this.
Msbelle...I would love to get some of these docs/nurses in the same room. I was told I could eat any vegetables as long as they were washed well. They did say it was important to wash all vegetables and not to think it was okay not to because you would be peeling skin and mentioned what you said about the knife cutting through could contaminate inside of vegetable but again just said that is why you have to wash the outside well. They did say that I should stay away from all salad bars and not order any salads out because I would have no way of knowing if the vegetables had been washed.
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To those of us who suffered from headaches, I just read on another thread that headaches are a side effect from Zofran. I was taking Zofran. The post said the side effect is listed on the Zofran label. I am guilty of not reading that pamphlet that came with it. I hope that was not the cause for me because I benefited from the zofran. I really had no nausea the first time. Tiny bit when I woke but nothing after the morning meds kicked in. May come down to picking headache or nausea. Life can be so cruel!
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Holy crow, I had no idea there might be restrictions on raw produce. I drink at least one veg/fruit smoothie daily. I'll have to ask my MO about that...
Regarding fevers, my mo warned that Tylenol can mask the true extent of a fever and that if I get a fever I shouldn't take it as it will make it hard to judge how high it truly is. I was told to call in if it's 100.5 or higher. It's frustrating how we all get different information.... -
Just finished 2nd chemo. counts dropped low. I will have to watch closely for shortness of breath, dizzy spells and extreme fatigue. I have always had a problem with blood counts even before BC.
Just another of those bad boy SE's stepping up.
Any advice on keeping up blood counts?
Sorry to hear about so many In our group. There is strength in numbers.
Bev
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Hi Bev...someone said peanut butter helps with counts. I hope you will not have to deal with those side effects as well. Do you have to go for more frequent blood work when counts are low?
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Day 20. Just a quick check-in. I hope everybody's doing okay.
So my period started on Thursday night. Was kind of hoping to skip them for a few months, but I'm glad that at least the heaviest and most painful time will be over before my next infusion.
Yesterday afternoon I started feeling like I was getting a cold - runny nose, scratchy throat. This morning it was obvious, I definitely do have a cold. I've had a sore throat, felt achy and fatigued, and had a bit of a cough this evening.
I slept the afternoon away, and this evening took some pain killers, cough syrup and ventolin. I'll head back to bed soon. I've also been monitoring my temperature, and have had a mild fever, highest temp measured = 37.2'C / 98.96'F.
Things seem to be under control now, but I'll keep monitoring myself overnight. Hopefully I will avoid a trip to the hospital. Fingers crossed.
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Brax: Count me in for discussing exercise. I started back exercising as soon as the fog lifted from first chemo & I do feel good. The topic might be a bit much in this thread unless everyone is interested.
Galena: My period started the day after my first chemo & it freaked me out. For some reason, I thought chemo would put me into immediate menopause. I thought something was wrong. I'm now curious to see when (not really if) it will stop. Sorry to hear about your cold. The last thing the Drs. want is for us to get sick. Hopefully, it doesn't delay your treatment.
I just started getting drenching night sweats again. I'm beginning to wonder if it is related to my starting to eat dairy and chicken again. I had went almost vegan when I was diagnosed and they tapered off. Anybody else experience anything like this?
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Hi Girls: Just checking in. Finished my chemo March/10, surgery June/10, radiation Nov/10. Arimidex for another 3 years.
Just wanted to let you know that I am feeling great, enjoying friends and family, and am always looking forward to tomorrow. You girls can do this - you are a very strong bunch of ladies. Before you know it, you will be on the other side of crappy chemo.
I send all of you the warmest of wishes, and hopes that this part of the experience passes quickly.
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Good morning ladies! I would love an exercise thread! I am going to do my best to do something everyday! I know it will make me feel better! It makes me feel better when I do it now, so it must be true! I had some weird dreams last night about chemo etc. Counting down to the start of my treatment. I am ready to get it started, deal with the side effects and live!
I'm not sure if this has happened to others, but I was talking to my cousin last night who has stage 4 lung cancer and she was telling me how bad I was going to feel and not want to eat etc etc etc, I told her I was going to do great, I was going to work out, work and eat right and feel decent. She poo pooed me and said well I guess you have a good attitude but not being realistic. Love her to death, but I don't need any negative talk right now! maybe I am just being sensitive! I am not under the impression this will be a cake walk, i am just trying to stay positive and believe I will get through this with minimal side effects. The mind is a powerful thing!
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I just saw a Zumba commercial and I have the DVD's so I think that would be a great workout to do through this! It is uplifting and you move! They have several different workouts that vary in length so you could do the shorter 20 min one if you weren't up to a longer one. Any one do Zumba now?
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Onvacation and everyone else, we definitely are better off being positive. I also have found that many people who have gone through or are going through chemo seem to be "experts" on the subject. I think all of us have found out that not all chemo drugs are the same, not all treatment regimens are the same, and most of all, not all of us are the same. I think if we eat our small meals, even when we're not hungry, take a short walk, even when we feel like crap, take our anti-nausea meds, even when we don't have nausea we will do the best that we can do. I'm on Day #12 and did all those things, and really believed it helped. I did stop taking the anti-nausea after the first week and did okay, but I think it's a good idea to take it at least during the first week after treatment.
In defense of your cousin though, her situation could be very different from ours. Stage 4 is pretty serious and they are probably loading her up in treatments. The drugs used could be really different than ours. it's unfortunate that she wanted to scare you when she should know that what she is going through is not necessarily what you will go through.
As someone who has gone through one treatment and heading in for a 2nd on Monday, I think you will do just fine. Yes, you'll feel lousy, especially that first week, but you have the right attitude about eating and exercise that will make all the difference in the world. Good luck.
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