Chemo May 2013
Comments
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Hi everyone - while I don't start my chemo until 5/15 and I don't think I am too nervous, anxious yes, I wondered if anyone had any stress symptoms! Such as weakness or slight muscle spasms in the arms and or legs. I worry that my cancer is spreading, even though it's out although found in one lymph node, I just wonder if it's all in my head!!! Thanks for anyone's comments and support!!!
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Dennie I was anxious before chemo but didn't have any physical symptoms of it. I do know each ache or pain I feel makes me wonder if it is spreading. I had clear PET scan and still worry. Intellectually I know it's not true emotionally I am still adjusting to my new reality.
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I have the same fear of any ache or pain I feel.....before cancer I might have said it was an irrational fear, but I don't think it's irrational now. It's just another emotional challenge we have to conquer, or we won't be able to live our lives. Hang in there everyone!
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Ladies I need your opinions. I have appt Thursday after chemo to have hair shaved and wig styled. This will give me weekend to adjust to wig before work on Monday. DH thinks I should wait for it to fall out. I feel like this will put me in control. I cannot wear hat to work and just not feeling the scarf thing yet although that could change with time. What are your plans?
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Ipc- a bunch of people told me to get a short pixie cut because it hurts to get your head shaved as its very sensitive. I have not done either yet bc they say with CMF the hair may just thin. I did order a wig though and if it starts falling out will definitely do the pixie instead of shaving. Good luck!
Jsrose -
I don't know what to do either with the hair thing. I don't think I could stand it to just pull it out in the shower, but shaving seems so drastic too....
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I did the shorter pixie cut, it was an adjustment (from my shoulder length permed hair to straight and short!).
Hubby keeps asking what is the plan when it starts to fallout.
I don't know if I would trust HIM with the clippers. I have used them on my boys over the years, not on myself though!
I have my mother coming to visit for a doctors appointment (she is 2 hours away)...she has not been asking about my treatment or anything related to my condition. She should be arriving just about the time mynhair should be leaving!
She has some mental issues and I lost my dad a year ago, then she broke her back...I think life in general is a challenge for her, she doesn't need MY added crap! Anyhow, I was hoping to get rid of my hair the weekend she is supposed to be coming and make a big deal of it for the kids sake..."look at mommy laugh at herself"...so much for getting that figured out.
I'm thinking the kids will want it done at home for the privacy. I was thinking of going to the barber. I guess I will have to cross that bridge when I get there.
I have a wig I am NOT in love with, but might fool Mom. I also picked up a cool pink/white wig to wear to parties, because I do NOT want my picture taken in some ugly wig I don't like. I want to look back and see the humor I made of this situation.
Pat -
I had my husband buzz my hair to a number 2. I haven't "shaved" it though. I think it was about day 14 after my first treatment. My hair was coming out in clumps and my scalp was hurting. You will feel so much better when you do it.
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The place I got my wig told me not to shave it all off because my scalp may get sensitive. I have cut it shorter but thinking of going even shorter before day 14 as that seems to be the magic number
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I have decided to just love my hair, as long as, I can. I plan to collect it in a bag as it falls out, because I think it will come back grey (I am 49) and that way when I am allowed to dye it later on, I will have all I need to get a good match. I applaud all of you who can cut it short or buzz cut, but this is one of the areas I am not that strong. I couldn't wait for by breasts to go, but I love being a natural redhead and I want to enjoy it, as long as, possible.
I fooled around with the scarves I bought last night, not too bad.......not great either. I found a pink baseball cap in my closet, so I may try that, too. We were watching the original "Father of the Bride" the other night and in the first scenes with Elizabeth Taylor she was wearing a scarf and just letting her bangs show. So....apparently....it was a style at one time.
I really think the eyebrows are giving me the most fits, I am hoping my friend can give me lesson on how to draw those in. I am keeping a good/bad list in my head and trying so hard to focus on the good. Sometimes it is much harder than others.
Suzan
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Worrywart - I have not been prescribed the Neulasta shot day after chemo either. Just like you it concerns me about just waiting to see if my counts plummett after first infusion.
My first treatment is this Wednesday and I'm certainly getting nervous. My port placement was painful and is still very tender. Feel like a vampire got ahold of my neck! I am also stressing about my hair and having a hard time deciding what to do. I haven't bought a wig yet and still don't know whether I want one. It gets really hot here in Oklahoma in the summer so maybe bald won't be so bad. I just worry that no one will recognize me or that I will look awful. And the eyebrows! That's an even worse thought. So many things to stress about. I'm sorry that all of you are going through this too but it is good to know that I have all of you to share things with. Good luck to all the one's starting chemo this coming week.
Shelly
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Ladies thanks for all your input. I think I will stick with Thursday. My hair is long enough to donate to locks of love and wii get it short enough to get wig fitted properly. Am really quite anxious about going to work in wig even though everyone will be expecting it. Friend will help with eyebrows when necessary. Funny how important eyebrows seem all of a sudden when in the past I haven't touched them - no plucking no waxing nothing! Thanks again all
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Okie - From the input I'm reading some people do fine without the neulasta, it seems to be day 9 and 10 you worry the most about your white blood count dropping. I am on day 5 right now, will post how things go for me. I am certainly praying for the best for all of us.
Hope tomorrow everyone has a Happy Mothers Day!!!! Enjoy the day!!!
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Happy Mothers Day everyone! Even if you have no kids, we mother ourselves....so take a bow and be kind to yourself today.
I'm on day 3 after first treatment and all is well, Few SE's, a little indigestion, red face from the steroids, slight chemo brain (my kids cracked up listening to me try and order take out - couldnt get the words to come out right!). The real test will be tomorrow after I stop taking the steroids and other pre-meds. Hoping for the best though....so far it hasn't been that bad.
My new favorite chant is ATIVAN!. what a great night sleep I get with it...wake up feeling good.
Hope everyone had a restful and easy weekend. Heres to better days
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Hey Ladies - happy Mothers Day.
I had a rough day/night yesterday
I had a DJ gig in the afternoon and I woke up not feeling well. Gig was from 12-4:30 and my back was hurting, so was my port. And I was wearing a bra with a foam insert to try to even me up and that started to hurt too. By about 3:30 I was just plain miserable and I still had a good hour, plus load out, to go. My husband had to work also so I had to coordinate the kids all morning til I left. By the time I got home around 6pm I was in all kinds of pain and discomfort and then my stomach got upset. I ended up in bed at 9pm with an oxycodiene in me and around midnight I took a unisom just to get to sleep. It was pretty miserable. It's hard enough to have cancer and children to take care of, and then to work full time all week, but adding gigs on the weekend I think just tipped me over the edge. And I think I'm nervous about starting chemo tomorrow - I told my DH that I just don't want to feel any worse than I already do...
Anyway - new day today I guess. Husband is at work again so I'm just celebrating mothers day with my coffee and my computer! Going to try to tackle shoe shopping this afternoon. We have to be at the hospital at 8:45am tomorrow.
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Happy Mother's Day Everyone!,
IPC -I think I am going to wait until Thurday to do the buzz cut as well. Its so hard to let go of the outward appearance of not being a cancer patient for me. Somewhere deep inside I am hoping it will not fall out on day 14, maybe will get a few more days.......As someone else said though....I am really hoping my eyebrows dont go. My MO said that is a really common sentiment among patients..More worried about eyebrows and lashes than hair on the head. All I have to say is that if my hair goes it better not be my legg and armpit hair that stays!!! That just would not be cool. The only positives of losing hair is not to have to shave my legs for a few month!!!!
Annie- Ativan is my best friend these days as well!!!!!! I am a type A and cant sleep without it.
Ukkate- Good luck tomorrow with your first chemo. It really is not as bad as you are picturing in your head. My BP was so high when I went in that my MO gave me IV Ativan in the premed mix. It really helped. I slept like a baby the first night! I will be think of you tomorrow..Sending a big hug your way..take care of yourself today,its all about you today as you are a mom and deserve a break.
Hugs to everyone! We can do this hair thing girls, its just one more wonderful hoop we must jump through to get better!
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Hi everyone,
I have finished my 4 AC treatment and now have two left of 4 taxol treatments. What I wanted to ask is does anyone else get anxiety with the taxol? I am already medicated for OCD and anxiety but recently I just have this anxious feeling in my chest and arms and I feel close to tears some times. Does anyone know if this is a side effect of taxol? Thanks.
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Happy mother's day everyone. I'm also three days out from first chemo. Felt better the first day after chemo than today, but not feeling too bad. Took a zofran even though it's so constipating. Taking everything else to counter that, I don't like to take more meds than I have to but agree with Annie and Gully that Ativan is necessary to sleep. Half a pill seems to do it for me. Good luck tomorrow ukkate. The nurses are really nice and will take good care of you. I dozed through much of the infusion time. I'm looking forward to removing port bandages. And making some lentil soup but that never seems to happen. Afraid I'm going to feel depressed when dh goes to work and kids go back to school tomorrow.
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Happy Mother's Day ladies!
Gully so funny I am waiting for leg and underarm hair to go. Just my luck it wont!
Kate tomorrow will be fine. I really think the anticipation was so much worse than reality. Will someone stay with you? Do you have emla cream to numb port? I took xanax before I went not sure if I will need it or not next time.
Deb 3rd day was the worst for me. Very tired and lethargic. It has been all uphill since then. I have had difficult time bring home while family went to work and school. All my friends work so that made it all the harder. Tomorrow I go back to work. What a relief!
Valuing has been my sleep aid of choice. Prescribed for te spasms it does the trick for me! -
All this talk about not sleeping is worrying me. I told the nurse during my chemo training that not sleeping is NOT happening. I will be sure to bring it up again when I start on the 28th. I still have plenty of Valium and pain meds left over from surgery. Hopefully, that will do.
My mom mentioned something about Emla, I asked the chemo nurse and she said they don't see too many patients that need it. Is it just for when they put the chemo needle in? Or is it because the port is so tender and uncomfortable? This whole chemo thing is starting to freak me out, it is the biggest unknown and I am a planner not a "well, let's just see...." kind of person.
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Valium is sleep aid of choice just noticed autocorrect in previous post. I put emla on port prior to each chemo or lab draw. It numbs the area for the needle.
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I took a shower the next morning after my port was put in. They told my husband that I could tape Saran-wrap around the bandage and it worked. Took a shower every morning and never got it wet. Had my first treatment on Wednesday. Took 5 hours. I too was nervous about them accessing my port for the first time but it was only a slight prick. Not bad. I was fine all day on Wednesday. Even went out to eat and shopping after my treatment. Got up Thursday and felt great. Worked in the yard planting flowers. Got the shot for the white blood count in my stomach on Thursday night. Got up Friday morning and felt like I had the flu. Was very nauseous, headache, body ache and no energy. I told my family that I could not do this. Got up Saturday and felt a whole lot better and today I feel great. Today is the first day that I have had an appetite and been able to eat since Wednesday. Went to Church and walked a mile. I CAN DO IT! One treatment down and 15 to go!!
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Hello Ladies! I have been reading other discussions on this site since my diagnosis in Feb., but I also started chemo on May 2nd & was pleased to read of others taking the same journey. ( not pleased that you are on the journey, just that I will have company on the way.)
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I am on Day 10 today and expecting my hair to begin falling out later this week. I've kept it in the same shoulder length style so far, but I have an appt with my stylist on Friday. I asked her to shave it, but she says she does a very close "scissors over comb" cut that other clients have found more comfortable. I'll let you know how it goes.
It sounds like quite a few of us will be facing the hair loss this week. I just keep reminding myself that this is one of the trade offs for being well again.
If you are able to take in a "Look Good...Feel Better" class, it is very helpful and they give a bag of very nice skin & makeup products & show you how to create eyebrows. -
To everyone starting today I wish you the best! Remember to start claritin today if you will be getting neulasta!
Off to work today. I cant wait.
Lisa -
Ukkate - good luck today! I'm sorry to hear that you had such a hard time on Saturday - what a whirlwind!
I picked up most of my prescriptions yesterday from the pharmacy - oh boy. Funny side note - when I went to the pharmacy to drop them off, I handed over the whole gamut of scripts. The pharmacist handed back the "cranial prosthesis" script saying, "I'm sorry, we can't help you with this one". HA!
Did anyone end up getting generic brands for their prescriptions? I made sure that I got the Emend, but they gave me generic for everything else. I hope these generics work just as well - sometimes they aren't as great, and I don't want to risk that! As for all the Ativan takers, can you get up at a normal time for work, or is it a super-sleep pill that may make me oversleep? Thanks for your input.
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I'm here now The port poke was fine. I started to get really anxious when the pharmacist started taking about the taxo side effects that he decided to give me Ativan. So now I'm getting pre meds and waiting to start the "good stuff".
Still having so much back pain. I need to try to get a massage -
Ukkate-Ativan is the good stuff! Sleep like a baby and no fuzzy head in the AM. Just dont take it in the daytime when working they will think you are drunk LOL
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I start chemo on May 24th, very nervous. Nice to read how others here have handled things. Good luck to us all!
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Good luck today Ukate - and everyone with infusions this week! I start on Wed 5/15. I was delayed a week because I have a stubborn surgical drain.....it'll be in FIVE weeks and counting tomorrow. I am so sick of that thing, but my body still needs it. However this week the MO gave the go ahead to start so at least I'm moving forward again. I hate waiting for something that I so desperately want to get behind me.
Now, I'm making my shopping list in earnest, and all my pre-chemo questions. I'm using
all the suggestions from all of you who have gone before me.....the April Chemo group is a great resource as well - and another bunch of great sisters.
I'm off to get my port now. Hopefully that won't be too bad. -Amy
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