Starting Chemo in December 2013
Comments
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Jodi- my #3 was a "surprise" and my MO told me that it was that last pregnancy that probably caused my lump to grow enough where I could feel it. So I too believe he saved my life. Such a great testimony and blessing.
Sitting in the chair getting my last AC!! Woo Hoo!! Will start Taxol on March 6th.
Wishing minimal SEs for everyone this week.
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RHGSR- yay!!! Taxol is not that big if a deal! I am on my way for #10 now.
Not looking forward to FAC starting March 12th! Everyone is celebrating finishing that and heading into taxol. I am dreading it now:(. Oh well! Still closer to the end. I'll finish chemo around May 15th. Countdown.
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yeah taxol #2/12 done, MO office was running an hour late so everything was late. CBC was all good, WBC 8.1, hg 10.5 one week post taxol. I had benedryl, decadron and kytril in premeds. Taxol over just 1 hour this time. Stayed awake. Sleep for 2 hours after got home. Getting ready to put meatloaf in oven. Hoping everything went well for the othe chemo gals today, esp happy for Hollie on her last AC. So happy I do not need any more neulasta, at least for now.
Looks like I will go to work on Monday, 3 days per week for now.
To help celebrate the end of chemo in May. I bought a ticket to the only Ringo Starr concert in PA. He will be appearing June 8th at our local Community Arts Center. I guess that dates me, I turn 60 next week and I definitely had a crush on the beetles back in the day.
Barbara
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good for you Hollie!
I'm feeling better every day. Having bone density test tomorrow...
((HUGS))
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Barbara that is an awesome way to celebrate! I realized today that we are halfway through our chemo time. 10 weeks down and 10 to go!
I had #2/12 taxol today also. I am running a low grade fever 99.4. And my throat is killing me when not medicated. I didn't see dr today but the nurse asked him and Dr isn't very concerned about it. I'm not sure if I should go out or stay home. What do you gals think? I am so tired of not being able to plan things cause I don't know how I will feel.
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blessedw2
Hope you are just getting a virus and the sore throat will pass. If it counts call your MO to make sure you do not have any yeast in the throat/esophagus.
I have to see the MO every time I have chemo. I go for a blood drawn through the port and they leave in the needle for the infusion later. By the time I see the MO an hour later the lab results are done. He always does a quick exam before ordering the chemo. I pay my $30 copay and go to infusion center across the hall.
Just realized the weekly taxol is costing $360 In copays. Hopefully it is a good investment in my future
Barbara
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blessedw2 - if it were me, I would stay home and rest. you can't know why the low fever, better to get back to normal quickly, before you enter your lower blood count days. As Barbara says, be checking your tongue/throat for thrush. Easier to get cleared up if you catch it early. I do hope it passes quickly for you.
Mary
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taxol #2 done here too. That Benadryl just wipes me out, didn't nap this time, but wish I could have. Been having night sweats lately. Wore my cold mitts for over an hour, hope it works.
I see my MO every other week, she does a complete check up and we go over how I feel. I do lab day before and keep the access needle in the port so when I go the next day it's all set, MO won't write orders for chemo until she sees labs, I also have a log in to see all my labs in my online chart...I'm a freak about too much paper, I love my paperless office, just use allot of space on my computer quickly. A bit bothersome to sleep with the needle port in, but it's taped well and covered tight, not anymore discomfort than these rocks on my chest....lots of chemo ladies today, hope everyone is doing well.
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blessedw2 - I got sore throats a few times after taxol. Here's hoping it is just that! It was a sinus drip since nose hairs are basically gone my allergies were acting up. But I took a Tylenol severe cold and it would get better. Don't take my word, but just hoping it could be something easy like that.
I should be asleep! I have blood work at 6:15 and report for port surgery at 7:00.
Barbara- love the celebration! I am waiting until next May when it will all be done, and my middle one will graduate kindergarten on her bday. The family will be heading to WDW. I can't wait. Now, just have to figure out how to save some money for that lol! Cancer is expensive!!
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Jodi where is WDW?
Yes cancer is expensive. I am really lucky my blue cross is covering every thing except the copays and $500deductible when I stay in our local system. . I am trying to set up a second opinion on the need or not for more extensive breast surgery. Tried Fox Chase in Phili but they do not accept my insurance so MO gave me the name of a BS they have referred to before at Memorial Sloane Kettering , in NYC. Since it will out of network insurance will only cover 60% or less. What ever the cost I need to be assured that what I had done is enough.
Barbara
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Good Morning all!
I'm 2 weeks out from my last AC, haven't posted in a while. I finally caught up on all you posts. I was wiped out from this last treatment, feeling tired still. I guess the low red blood cell count is to blame. My biggest challenge has been the big "C", all the meds really F with my system. I feel like I look the cancer patient part, minimal eyelashes left, dark circles under eyes AND I've put on a few lbs. even my flannel pants are snug grrrr. Trying to not be too hard on myself while I recover.
I'm glad to hear that Tax. Seems to be a bit more tolerable for you all.
I am pre-disposed to BC, but I live a healthy lifestyle & was doing ever 6 mos. Breast Oncology Dr. visit, mammo/MRI, it still got me. BC is an epidemic in this country. Environment, food supply, chemicals we put on our body?
I'm amazed at the amount of young women here with young children, I can't imagine the energy it takes everyday!
Dragonfly, I'm at Dana a Farber too, our dx are very similar.
I've also worked through treatment, wearing scarves & hats, I don't like my wig, itchy. If it was warmer I think I'd go bald.
Good luck everyone! Kathy, are you buried in snow up in ME? We are here, I'm all set with winter!
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Neskir....I hope you get your energy back soon. You'd think you'd feel better after 2 weeks. My last a/c wiped me out too. Taxol has been much better. Yes, we are buried in snow. It's really pretty, but I could handle some ugly brown and green right about now. I won't complain about mud season this year. What did you do to celebrate your last chemo? Oh, I meant to tell you all one of the side effects that seems to be going away with Taxol. My eyes don't water like they used to. I just realized this. The first Taxol they watered awful for about 4 days and haven't since. That's been nice. My throat has been sore and scratchy. Today and yesterday I feel like someone beat me up all over, but only when I touch my skin.
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Barbara, I hope your second opinion works out for you, it's hard to make so many decisions. I knew when they saw all the cysts. Fibromoas on my left I just wanted both gone, no cancer there but I didn't want to keep worrying about it and opted for radical on right and a nipple sparing masectomy on left. I have no regrets there, the implants are a pain, but I believe I will have great results once the permanent ones are in. My spared nipple looks great, and the sizing is now comparable to each other and to what I had before.
I see my genetic test report states there is likely no need for ovary removal, I had only my uterus removed years ago due to extensive bleeding, I worry now I should have taken ovaries since mine is hormone positive, my scans saw a cyst in Oct on one ovary but Mo said not to worry about this,,,,but I do. My decision to not do rads is based on mostly my own research and studies I've read. The RO says I'm on the borderline, and he of course says do it. My Main concern is heart and lymphodema, when he said 1 out of 3 get lymphodema that made me very wary. As well as the AC and heart palpations I had, I decided enough is enough for me.
Here's hoping we all can enjoy our weekend!
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I'm feeling a bit more "normal" each day, my husband & son are away this weekend so I'm catching up with friends. Lunch today, dinner out with the girls tomorrow ( early bird:)). Did I mention my weight?? Oh well, I'll start Monday.
Didn't do anything special, we we're suppose to go to St. John next month for our 20th anniversary but we put it off until next Dec., I want to have hair. I still have reconstruction to complete, I'm anxious to be finished with that.
My eyes are still watering like crazy! And, runny nose ugh!
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good afternoon ladies!
Thanks you for your replies. The event tonight is at UF honoring cancer survivors and families. It includes a reception and then free admission to the gymnastics meet. I thought it would be fun for my kids, 8 and 9 yrs old. My husband said he would still take them if I decide not to go. I'm still undecided. Ugh! What do you do for thrush?
I have a couple of questions for everyone
1. What is everyone doing to celebrate their last chemo?
2. I was pretty sick and immobilized with the AC. I also put on quite a few lbs. Now that I feel stable enough to move without fear of hurting myself, I have decided to work on getting my strength back and some weight off. I will be having some serious lung surgery after chemo and want to be as strong as possible for that. So far I have walked my block the last 2 days. What is everyone else doing to regain strength?
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neskir99
About the runny nose, my 8 year suggested I stuff mine with toilet paper.
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I've been going to physical therapy because I had my surgery first ( since every one was so certain I didn't have positive nodes and I ended up having them). It has been a tremendous help with the chemo not just for my physical (although I am still pretty weak) but for my mental too. Not sure if you can request physical therapy after chemo or not (or if insurance would pay) but it may be something to look into.
Holli
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hi ladies,
I am feeling better every day, also! I have been trying to walk (albiet slowly) 30 mins/day. Would love to lose my chemo weight and then some, but I know it will take some time. I guess when rads are done I will get more serious. I'm hoping to go to the YMCA Livestrong classes in a few months also.
neskir, glad you are feeling better! That vacation will be something to look forward to for sure! I am counting the days til my hair starts to grow back also.
Got my bone density test done today. One more thing to check off my list!
Have a great week-end ladies!
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crazy wabbit- WDW is Walt Didneyworld;)
Weight- ugh! I have gained 10 lbs!! No more! Then again, I say just get through chemo and then hit it!
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lol disneyworld!!! Typo;)
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no exercise plan as yet. This week it's been a struggle just to stand in line at the post office or walk up my stairs at home. Very weak and so easily exhausted, my legs feel like lead. I'm one week post my final TC. I think recovery is going to be a slow measured process.
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Disney World sounds great.
I am struggling with not gaining weight on the decadron, Wicked appetite stimulant. The day after chemo I feel like eating tons of junk food.
Maybe losing taste buds later in taxol will make it easier to lose weight. I still need to lose another 30 lbs.
Barbara
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I have two TC treatments to go. Have a total of six. I am holding up and SE have been minimal! Fatigue from day 3 to day 8.
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Just finished round four of Taxol, this one included my Perjeta and Herceptin. Four down, eight to go. That's 56 more days!!! My MO is concerned that I already have neuropathy so early in the Taxol. She wants to monitor it closely. If it stays status quo then she will keep me on Taxol. If it gets worse then she wants to switch me to Taxotere. She said Taxotere is less likely to cause neuropathy. My question is, if it does the same job as Taxol why don't I just switch to Taxotere now? Why risk the neuropathy getting worse? My hands fumble and my feet hurt!
Oh and three of my nails are loose at the tips from the Hand and Foot Syndrome I had with the AC......Sigh
Deb
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Deb: I found this website that may be useful to answer your questions regarding to taxol am taxotere. It said although weekly taxol has the same overall disease free survival as taxotere, weekly taxol group may live longer. Did you try to ice hands and feet? I just had my weekly taxol, 2nd dose today. My nail is changing color and the nurse told me it's still OK and they will just closely monitor me each time. If it gets too bad, they may let me rest for a week before continue again. 10 more to go! http://www.cancer.gov/clinicaltrials/results/summa...
I am feeling ok so far, just sleepy and tired, good appetite. I also work during the process, only taking off during chemo and doctor appointments. I spent a lot of time at my desk, so it was manageable. Working to me is a nice distraction for my mental health. :-) I try to go to gym three times a week- not that consistent. I found it helped build the strength. I was so bad the first time after starting chemo and can barely do 5 min in elliptical, but now I could do 30 min at low resistance. Some progress, still have more chemo weight to lose.
Take care, everybody! Hope you have a great weekend!
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Good morning Ladies!
Did round 3 of taxol yesterday, then took.a three hour nap from the Benadryl, that stuff knocks me out. Had one bout of diarrhea, so far so good. I'm staying on top of the bananas, apple sauce and rice this time. After the first round I had diarrhea for a week. Counts were up and I'm feeling tons better. I have always had crappy nails but for some reason they are growing and getting thicker, so my daughter did a gel paint on them, now I won't see if they turn colors. My MO says I'm the oddball with my reactions to this.
In August I rejoined my gym, have been a member on and off for 7 years, when the bc showed up I asked if they could put my membership on hold, instead he extended it an extra 6 months and encouraged me to start coming and at least walking. Think I'll start that this week. When I'm through with rads I'm going to treat myself to a trainer, get this 56 yo body looking hot and feeling amazing after this assault on it. And we are going to Savannah, who knows what else because it is time to celebrate life and survival and being a tough bitch!
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J4DC, Thanks for the article. That helps.
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Port in and round #10 down. Funny thing! The surgeon that did my port loves music. He had it playing the entire time. When Harry Connick came on, I said I love him from under the blue sheet covering face:). All Louisiana girls love Harry Connick Jr. He asked me of I knew this other singer and I said no. He tell the nurse to put it on number whatever and then...
He starts singing! Like loud and was good. Nightingale in Some park was the song. Then, after that he sang Teddy Bear from Elvis. The surgery was finished before that song was over. They take the sheet down and there is a flat screw tv with the words being highlighted! He was singing real karaoke! Hilarious! Talking about having a good time at work. Made my day. His name was Dr. Brown, so if anyone you know ever has to get a port at MD send them his way. He did a great job and entertained!
I haven't had the fingernail thing yet. Maybe that will come when I start FAC? The numbness hasn't hit me yet either. 2 more taxols to go!! Have a great weekend ladies.
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Hey chickies, day 5 out of my last taxol and I feel like someone chucked me down the stairs, several times, just pain all over and it sucks, doing my best to keep on truckin, I feel like if you stop you just stiffen up more.
I am experiencing some numbness in my fingertips and feet which is a nuisance, as for the fingernails and toenails I have been pounding the opi nail envy to them almost daily, be nice to hang onto those, I still have some eyebrows that were thick to begin with and some eyelashes, but who knows if they will stick around. oddly enough my hair still grows on my lower legs. I have also been experiencing occasional spotting and had a full period 2 cycles ago, that blew chunks royally.
DJJ how many treatments of Taxol are you doing. I only have 4 every 2 weeks. I am done on march 17th, 8 treatments in total then the rads.
so envious of you all and your trips to the gym, before all of this .I was doing boot camps and the gym, that went all to the birds when we discovered a 10cm hernia in my abdomen from previous bowel surgeries, had to quit it all and wait for surgery on that. good times. That's been all taken care of..
we are buried in snow here on the east coast in Canada and its getting rather depressing. On the brighter side the sun is out today. We normally go south in the winter for a week, but not this year. booooooo....means next year will be even bigger!!
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Kimmie, I'm done March 17 too
So excited already. I am having sharp shooting pains every where today. Knees, hips,head,eye,hands etc. I thought the pain would be gone today:/ Planning a trip to Aruba in August. I feel better just day dreaming about it. My husband and I spent our honeymoon there. We wanted to go back on our 5 year anniversary. Had kids, and never made it. It will be 18 years. When I first found out I had bc again, I was like, guess we should have made time to go to Aruba huh? Mike was like, Oh we're going. This year. As soon as your treatment is done. He will feel really bad if we never get there. He always said "Next year. we can't afford it this year." This has been a wake up call. You're not always guaranteed a next year. Happy week-end ladies.
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