January 2016 Chemo!
Comments
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Cathytoo
I'm sure you look adorable:) So was you hair not falling out at all 2 weeks after your first chemo?
Vicki
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On TC, I lost my hair during the first round on day 15. It came out in handfuls over a couple of days. I had cut my past chin length hair shorter, and so it was pretty easy for it to come out while I washed it in the shower. Interesting though, I never lost ALL of my hair. I have probably about 10% left and it's growing back now...and looks hysterical. I never shaved it bald because I didn't want any pain or discomfort. As I result, when I wake up in the morning I look like a troll doll after you shake it. If you plan to buy a wig, I suggest going in before you lose all of your hair.
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DFWFLYGIRL: With Taxol on Thursdays we always have our insomnia nights together, don't we? I'll have to post more often in the middle of the night
Colorado is amazing. It's so much better than I even could have hoped! Loving every minute.
Jill: I had taxotere along with carboplatin over the summer and that buzzy feeling is the worst. I found that there really was very little I could do to stop it...cued up a Harry Potter movie marathon for myself and blasted through those during a few bedridden days. It did help distract me! You have my sympathy!
Jen: I do need to get a humidifier. I feel like it's so bad I want one I can strap to my face! Haven't taken any pain killers but I'll keep that in mind if I need to.
buttaflydiva: yikes! Hope that can be resolved easily. My port decided to seal up yesterday so they had to inject a special medicine (not heparin) to dissolve a tissue film that was developing over the opening. The nurse was really nice and let me start the chemo through my arm so that I didn't lose two hours waiting for the medicine to activate.
JCS28: I am ordering Prevention as we speak, thank you!
LoveMyVizsla: bone pain is from Taxol. No Neulasta shots since I finished AC. The Neulasta did give me bone pain, too, but now it seems that Taxol does as well. My neutrophil levels are given by percent and right now I'm at 68.5% and normal range is 40-70%.
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thanks missbee, I have been watching a lot of Netflix. I don't even know how to explain the feeling, but it's good to know that somebody gets it. I keep trying to explain it to my friends and they don't understand what I mean when I say I feel like my whole body is buzzing. It just...is
I've been told neulasta can give bone pain, so can taxols , so the combination of the two also can. I did Neulasta with FEC and had no bone pain, my first taxatore I did, this one so far seems OK. I'm having the occasional achy twing, but nothing like the last cycle where every bone in my body hurt from the top of my head to the bottom of my feet
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Re: Mouth Sores
Hi ladies, I rarely post but always keep up with the group and am cheering you all on. For my mouth sores, got the magic mouthwash prescription like some of you. And, my MO wrote a prescription for folic acid, which eliminated them!
sideline note: My last chemo infusion was cancelled due to worsening SEs but hope I got enough to do the job
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Hey ladies!
@lovemyviszla my bone pain is from the Taxol itself. I'm not on neulasta now during Taxol but during AC I was and my bone pain was almost identical to the bone pain I feel from Taxol alone. Hope I made sense.
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Jen Thanks for the info on Aleve. My MO said to not take it daily if I didn't have to but my counts have dropped so will ask him about it next week:))
Buttaflydiva-a flipped port...that doesn't sound fun..glad they were able to do your treatment and hope it's an easy fix.
Lovemyvizsla- my bone pain is from Taxol and because I am on weekly..no Neulasta or Neupogen shots for me.
Jill. Good to hear your pain is not bad. Sorry to hear Taxotere is giving you a run:((
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I hate to hear about you guys having the mouth sores. I kept my mouth full of ice (I love eating ice anyway) during all my adriamycin injections and both my taxol injections and haven't had any mouth sores yet. The only thing is my tongue is really sensitive, anything the least bit spicy or acidic makes it burn.but I do think the ice does help
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!'M PEEING EVERY TWO HOURS AT NIGHT!
This is driving me crazy. Anyone else having this problem? Doesn't happen during the day
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Cathytoo-I am there with you...but am drinking a lot of fluids so thought that was part of it. Is it from something else in chemo?
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Cathy, I've had that happen each round of chemo on night four or five after infusion. My body retains fluid from the infusion which is what the roids are supposed to help, and then when it's ready to let it all go it seems to happen at night for me. I also read something about how the chemo drugs stretch the urethre or something but can't remember specifics. If I can muster some energy today I'll try to find it
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Jen...it's a real pain...not getting any sleep. If you can find the info, please post it. We should start a "middle of the night pee group"
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Hi everyone, I apologize that I have not been as active on the threads as I was before. I am so happy for everyone that has completed their chemo treatment. I will be having my 13th Taxol treatment on Monday, until I show no evidence disease. The great news is that I saw my oncologist yesterday and he went over my CT scan results of the chest, abdomen, and pelvis and I have significant shrinkage (close to 60% shrinkage). My lymph nodes, lung nodules, and breast mass have shrunk. I am beginning to see the light at the end of the tunnel. I am responding well to chemo. I cried tears of joy yesterday. Praise God!!
Sending you all best wishes and hugs.
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wonderful Geeper!!!!!
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Hi Jill, I've always admired your positive attitude. I am sorry to hear about your SE's. Keep kicking ass!! You are so close to being done.
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Geeper
So happy for your good news. 60% is a lot, praise be. Glad to hear from you on the board.
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Thank you Valstim! I just posted a response to the new IBC FB. I am so happy for you too!
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Geeper I am so happy for you!!!!!
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Jen, thank you!!! I am hoping all is well with you. I see that you finally have a plan in place, I am happy for you too! We've got this!
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Hi beautiful ladies,
Just had my last (woo hoo!) of 4 TC treatments the day before yesterday. To celebrate I blew bubbles and bought myself a new pink wig (see below). Today the steroids have worn off and I'm hitting that tired, buzzy, spacy, queasy part. But I know this passes and I have pretty much nothing but couch lounging, reading and computer surfing lined up for the whole weekend. I am going to be really glad to have this chemo phase behind me, and get my hair, energy and memory back....just in time to go through the next big step on my treatment path: BMX and reconstruction surgeries (no rads for me). I've got my BMX + expanders surgery scheduled for 4/26 and DIEP flap will be sometime in late June, assuming expansion goes as planned. Wow there's a lot of tough body image changes and rearrangements we deal with in this process, don't we? Guess I'll have to go stalk the surgery threads now.
RE: Neulasta and bone pain, I had Neulasta shots the first 2 TC infusions, and I only felt the bone pain was bad the first time (and Advil/Aleve and Claritin seemed to help). I had high enough numbers for infusion 3 that I passed on the Neulasta for that round and I have to say I had a much easier time bouncing back from the infusion. This last time my numbers were pretty high too so I think I'm going to pass again on the Neulasta (while of course making sure that I'm staying away from sick people and washing my hands a lot just to be safe...no need to court infection). Don't get me wrong, I think the Neulasta is a great idea as a prophylactic--no one likes the idea of landing in the hospital for a week with a neutropenic fever! I was ok with the relatively minimal risk in my particular case, but everyone has their own level of anxiety and risk tolerance. I wanted to see what it'd be like without it, and avoid more pain and side effects if I was able. So far so good.
Cathytoo et al: yes I'm peeing all the damn time at night too, but I'm also trying to drink 100oz a day of water and I often go too late at night with the water, so there's that. But it does seem to be worse when it's the days right after infusion.
Geeper: yay! Great news!
Phaila: 99.5% of my hair fell out between weeks 2 and 3 after the first infusion. The little bit that was left after I buzzed it the day after it all fell out has grown a bit longer but no new hair has come back. Starting to lose my eyebrows pretty seriously now too, which is a bummer because I was thinking I'd gotten away with keeping them. I heard they're slower to fall out than your head hair though, so I probably shouldn't be surprised. Oh well. At least I learned a little bit better how to draw them on in my Look Good Feel Better class.
Here's that pink wig:
Ok off for a nap now, and maybe I'll have enough oomph for a short walk later before the sun goes down...hang in there ladies and congrats to all who are finishing up their chemo rounds!
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sooooo adorable! And congratulations 👍👍👍😍💕💕
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Quixhobbit...CONGRATULATIONS
WHOO HOO NO MORE TC‼️
I did my 4th this past Monday. The couch and I are best friends. I have 2 more to go. Regarding your eyebrows, I still have most of mine. I've been trying pencils and bought one the other day that I love. IT super skinny brow power. Very natural. Don't know where you live, but Ulta carries the line.
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Great news Geeper!
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congrats quix! So cute!!
I haven't been to a lgfb class yet, so I went to Sephora and they gave me a free eyebrow lessons. I just washed one off to show (the "undone" one is still darker than natural here, I just gave it a quick wipe. Fully clean it's barely visible, what's left is completely blond):
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Quixhobbit: Congratulations, I am so happy for you! You have a radiant smile and I am in love with all the different wigs you wear. Best of wishes to you on your upcoming surgery.
LoveMyVizsla: Yeah...happy about the great news!
LovesToFly: My eyebrows are sparse and so are my eyelashes. Takes me forever now to put on my face. I color in my eyebrows, wear fake eyelashes, put on concealer and foundation to cover my acne from chemo, put on blush, highlighter, etc. This process takes like one hour and a half. My family and friends always comment on how good I look for having cancer. If they only knew that it takes a lot to look like I am glowing.
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geeper everybody compliments me too, they hav no idea the effort it takes. I can barely look in the mirror without my make up on. I do not, I have found that if I line my eyes it barely shows. I also get an eyeshadow listen it's up for him, so that is my eyeshadow looks nice Since there are no lashes to cover it. Since I don't have hair to style, it takes me about the same time to get ready.
Here's a picture With all but lipgloss, no lashes:
See how much see how stubblemuch I have?
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Loves to Fly, you have a talent with the makeup, too bad you, me and geeper don't live near each other, so I can get my eyebrows done. I went to the LGFG class, and she just told me to keep practicing. LOL.
I've still got a few left and pencil them in. I'm afraid when they go, I'll look weird with my kindergarten pencil talent.
Geeper, the effort no one knows Went to a wedding and everyone talked about how 'great' I looked. My daughter did my make up took her at least an hour.
I did feel 'back to usual' yesterday. I went landscape shopping, freshened up my garden, even went to an early dinner.
Tomorrow, back to my new normal #3 or 4 dose dense taxols. My side effects are getting worse each time.
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Jill ..beautiful and you do have a talent with makeup:))
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Quixhobit you inspire me. I got a purple wig to wear my last day of chemo 4/14. Yay.
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thank you ladies! I have always been into make up, so I try to use this crappy situation as a reason to learn some new skills!
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