January 2012 chemo
Comments
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So far I have not had pain with my Taxol infusions. I get #5 this Thursday. #3 the vein was slow but last week everything went swimmingly.
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Nancy~#6 was hard, since it was such a suprise when the pain happened, and my husband felt so helpless. I brought a Chemo buddy for #7 and gave him the week off (He's installing a new bathroom in my Dad's house down in Brick NJ) he's ready for this week and insists on taking me this Thursday. If figure I'll take the pain medication before Pre meds so I'm hopefully ready/numb to some of the pain. I wish I could fall alseep in the chair, but that seemed to stop for me on the 4th Taxol.
Kitchen~The Head Nurse thought that the original PIC nurse choose small a vein and offered to perform the remaining 5 PIC's finding a larger veins, since I now have this problem. My SE happens to a few people. Glad yours infusion went well, hoping they all do for you. The Head Nurse said that they should be less painful, but the areas she has in mind, will not allow my arm to move for hours.
Here's to a swimmingly good session for me too!
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Barb - thanks for your thoughts on losing my Mini at 20 years old. It has been hard - I just got her ashes back this week. I miss her sweet little spirit.
I have a port, so I can't comment on the vein pain, but I can say that DD taxol has been the worst. A/C seemed like a piece of cake compared. I get DD taxol #3 tomorrow and am dreading it. I end up with aches/bone pain and high fever for about 4-5 days, now dealing with neuropathy too. Both my toes and fingers have been tingling this week and my left hand actually hurt yesterday. I am so scared of lasting neuropathy as my hands are my livlihood.
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barb - I had all 12 weekly infusions through IV (which I kinda hate) but I was really not wanting a port! Some weeks it was a challenge (one hurt like hell). The best seemed to be in the crook of my arm but you do need to keep your arm pretty stil(they would give me a pillow for it). I noticed the IV was a lot easier if I drank a TON of fluids that day.
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Tina~I too have the Bone/Joint pain & some tendon pain...especially in my neck. I asked the covering Doc why my thighs felt like a I was hit with a baseball bat...what exactley is going on in there? He said that it is inflamation/swelling and both my Knees swelling was (of course) not unheard of. My finger/hands are my livelyhood as well. My fingers HUM, tingle and are very sensitive to the touch and temperatures 24 hours a day now, but there is a small relief with the Lyrica. The covering Doctor told me it will take a few months after the Taxol stops and maybe upto a year for the Neuropathy to go away. Do you have Numbness?? I don't so far, but I have finger pain off and on with no Rhyme or reason (scarey) and my nails are now lifting off, which really freaks me out. This will be done soon...repeat as necessry
I have three new kittens that were born under my shed...my husband is sooo pissed..I am soooo pleased
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Diane~Thanx, that is where the head nurse wants to go this week and I had done the crook of the right arm during the AC and one in the early Taxol...very painful too move and I needed that pillow too...but never the Ice fire wripping through my vein up my arm. It is better with the 100 of the Saline, as the 200 Saline was a bit too much, gonna have to mix it up the Saline amounts. Wish they could numb the vein a little before sending in the Taxol. I am drinking a lot of water, fluff up those veins, the carppy part is that I can't move that arm till the session is done...no bathroom trips. Oh and the MRI nurse who put in the contrast, screwed up the right crook for weeks, the Chemo nurses were pissed pretty pissed off, said they used too big of a needle.
Barb
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CatWhisperer - sorry you're having trouble with the Taxol. I thought AC was so much worse. I was soooo queazy for 5 days and didn't feel like eating at all. I'm doing ok on the Taxol, although I get some bone pain. Not sure if this time around it's from the Taxol or the Neulasta shot I needed - which I didn't need with #1 & 2. My feet are getting a little tingly too.
Anyone on Taxol having the bottoms of their feet peel? It's making me crazy. I put tons of lotion on them, but big sections of dead skin are peeling away. It's pretty disgusting. Fortunately, they're not bleeding!
As much as I bitch about my port, I couldn't imagaine doing this without it. I have 1 more tx to go. DH said to me this morning (as I was whining about my port), "you know, you can't have your treatment on Thurs and get your port out Friday." Why the hell not!!!???!??! LOL
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Barb - yes, I am having tingling/numbness in my fingers and toes. The last two days I've had the finger pain in my left hand too. What scares me is that my sister's neuropathy has never completely gone away - she has it permanently. Yea on the 3 new kitties !
I have one Siamese foster kitten looking for a home (my avitar), and 2 new long hair black kittens that lost their mom on the road. They are only about 14 days old.
Char - I'm the opposite. I don't feel like eating anything on the taxol and am nauseous a lot, in addition to all the other SE's I'm having. I have 3 different anti-nauseau meds. I am getting Neulasta shots both with A/C and taxol, but taking Claritin, so I know the bone pain/aching is from the taxol because I didn't get this with the A/C. I am not having peeling skin on my feet though. I'm glad that yours isn't bleeding and hope it stops soon.
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Barb- My nurse said that many of the DD people she treats end up switching to weekly because of the bad SE's. I have neuropathy on the pads of my feet but that started before Taxol. I also have a tender mouth and nose but no sores, thank G-d may it continue. I do get fluey feeling and mild headaches but they go away with Tylenol. I have no stamina but am getting used to working with my body. I will have short bursts of energy and then crash for a rest. But I think it is better than AC. On AC I had days where I had no taste and no appetite and not even a little burst of energy. I am getting used to the Taxol fatigue and see that I can work around it and get the necessary chores and errands done. I don't know how one works full time though.
DianeNMilRe: Port vs veins. I also really don't want a port. My two episodes in the hospital of low WC killed some of my veins. Here they have one guy...I call him "The Vampire" who does all the veni punctures. He is a magician. He always finds a vein right away. If I can get past the next 8 weeks I'll be home free. I'm sure I can manage one vein puncture every 3 weeks for the Herceptin as that goes in real easy. I've been told I have quite good veins for an old gal.!
BTW for TAxol #4 and all future ones they give no pre meds. So far so good.
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Thanks Jan
as for every one just calmimg peacefull thoughts and hugs and mwah
Love
Bela
Might not be here for few days after wednesday
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This is the night before my final DD Taxol (#4). I simply can't wait to walk out of that infusion room tomorrow afternoon. I still have herceptin every three weeks for a year, so I'll be saying "see ya later" to the nurses instead of goodbye. I'll be looking forward to those goodbyes next April. For now I look forward but also dread the upcoming steroid buzz and pending aches and pains, fatigue, etc. I suppose I'll be scheduling with the RO soon as well. Depending on when I start radiation, it looks like no vacation until after July 4th holiday. I'll look forward to that vacation. I feel like I'm rushing my life along when I typically savor every moment.
I hope for a feel good week for everyone!
Angie -
Having had debilitating bone/muscle/joint pain with DD Taxol tx 1 and 2, I thought of just stopping tx early. I just didnt think my body could take any more of this stuff. Because of all the SE my ONC wanted to switch me to weekly Taxol (no mention of Abraxane), which I declined. No way I'll extend this!!! -I cant stand to look at my bold head and chemo-acne, lash-and almost browless face in the mirror any longer, therefore I decided to toughen it out, no matter what.- Had dd Taxol tx3 last Wednesday and so far the SE have been very tolerable. I am very happy about that, of course, but i dont understand it... How SE are so unpredictable from tx to tx?!- In any case, just one more tx to go now - cant wait!!!
I am IN AWE of all of you ladies working through this!!!! I don't know how you do it!!! -
Cat,
I am so sorry for the loss of your kitty. Hope you find comfort in the fact that she had a long and happy life and that you were in each other's lives!
Laura,
Sending you a big hug and much strength!!!
Janet,
Congrats!!! You did it!!! How awesome does it feel to be done with this (cr*ppy) part of treatment?!
Bela,
Sending you lots of positive thoughts and well wishes for your surgery Wednesday, and for a easy recovery!!!
Jenn,
Happy to hear about your positive US results. One less thing to worry about -yay!!!! - I was wondering if you ever had your breasts checked, as a result of the pain you were experiencing a little while ago? - I have had similar pain (in both breasts, oddly enough), also nowhere near the surgery site/scar tissue, as well as what I would describe as several big lumps. My onc dismissed it, saying it is a SE of sorts, brought on by inflammation. -
SleeplessInSeattle- Hang in there. You're almost done. I have one more Taxol left, too - the day after yours! My 1st was rough, 2nd was not as bad, and 3rd has been good....no real SEs to speak of - other than the bottoms of my feet peeling!
I had to take my 15 y/o kitty to vet today. He's not doing well - he's in renal failure, dehydrated, and barely eating. I had to learn how to give him IV fluids. It was bizarre, since I get hooked up to an IV every other week. I don't think poor Milo is going to make it much longer. (He's my avatar.)
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Today was my 12th -- and last! -- weekly Taxol treatment! Yes, I'm dreading the upcoming DD AC which starts next Monday, but I'm so glad to be done with Taxol. The last few weeks have been rough on it, and I expect no less this week. So, I have 4 DD AC's, then surgery/reconstruction, then Herceptin for 9 months after that. Seems like I have so far to go...
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KristinFro - congratulations on finishing Taxol! LOOK HOW FAR YOU HAVE COME!!
You can do the rest, one day at a time!!!
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Thanks, Denise! And yep, that's exactly what I'm doing -- taking it all one day at a time!
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Char - giving fluids is easy once you do it a few times and it will really make Milo feel better and extend his life. Unlike IV, it doesn't go into a vein - you just poke the needle under the skin and most tolerate it very well. Also, you should look at feeding a low-phosorous food which will help the kidneys. I was giving Mini fluids 1-2 times per day for over a year up until the day she passed. The vet said she would have been dead a long time ago without my dialy nursing. I also gave her potassium supplement each day because it is lost in urine, especially when they pee alot. You should look at the website www.felinecrf.org. It has tons of info from giving fluids, to recognizing crf symptoms and all the different treatments of crf. Good luck with Milo. He is a handsome boy - I love B&W kitties. My sweet Mini was B&W too.
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Sleepless: I did have a breast ultrasound to follow-up the pain and lumpiness - nothing showed up except breast tissue and fat. I'm on a trial of Denosumab and have since found that lumpiness and pain in the breasts is listed as an SE... Guess it's likely I'm on the active drug...
Jenn -
Just about like clockwork, the pain and exhaustion started again today around 5:00 pm. Tried desperately to leave the office early so I could be home before it hit, but no such luck. Made it home okay, long enough to take a couple of Vicodin and hop into bed. Not looking forward to the next couple of days, but at least now I know what's coming and can plan for it, so it's not so scary. Three Taxols down, only three more to go! Best part is I finished my final papers for the semester, so I don't have any homework to worry about for at least another three weeks, so I can focus on just trying to feel better for now.
Today, two students stopped by my desk and shared their BC survival stories, and it was so inspiring. Every time I meet another woman (I have yet to meet, at least in person, a man with BC) I feel empowered and alive. Their joy is so infectious and delightful, and it helps me feel so not alone, even when I'm having an awful day. Both went through AC and Taxotere (neither could tolerate Taxol). They both said that they experienced alot of pain and that no one told them ahead of time it would happen (sounds so familiar!)
So - because apparently I'm not crazy enough as it is, I have signed up to run (walk, probably) the Komen race on May 20 - 4 days before my final Taxol. I am not necessarily a fan of SGK but my DH had planned this - along with a couple of his running friends - long before the whole PP incident. So, we have a team, and I decided the other day that perhaps I need to run/walk as my reward for facing my final Taxol! Wish me luck - I may crawl across the finish line, but I'm going to do everything I can to make it!!
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NancyHB- wow....props to you for running/walking in that race. There's no way I could even attempt it! My family wants to do it next year. Hope you get some rest and can take it easy today.
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krostinfro, glad you are done,
nanacy hope u feel better
hugs to all
bela
surgery tomoorow so wont be back for few days
good luck to all
Bela
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Sleeplessinseatle _ thanks
Bela
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Hello All:
Cat Whisperer: yes my feet have been peeling....huge...crazy..never seems to end. My feet look like they have been brought up from the depths of the Atlantic.
NCBeachGal: Congrats on FINISHING Taxol.
Tomorrow is my last DD Abraxane (Taxol) and because I am TNBC, thats it. Now its back to a life that was put on hold October 2011. After 1pm tomorrow, when that needle comes out of my arm, I have decided I am no longer a breast cancer patient. I have given this disease my breasts, six+ months of my life, my tears and fears. But I am 24 hours away from the end of treatment. Its the beginning of a new life.
Thank you all for your support.
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Denjak-you are one day behind me on diagnosis and chemo. I have 1. 1/2 hours left on my last taxol! Good luck and congrats to you.
I hope for a feel good week for everyone. -
Denjak - what a wonderful and postive attitude to have!!! Stay strong and healthy and enjoy the beautiful summer-like weather.
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Bela: Thinking about you as you prepare for your surgery tomorrow. Hope to hear from you again soon, and that all goes well. *hugs*
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Denjak and ncbeachgal (and anyone I may have missed): congrats on finishing chemo! Honestly, we should get marathoners' medals for making it through.
Nancy - I hope your discomfort is short lived this round.
Tomorrow is my penultimate treatment. Two weeks later I'll get my last dd Taxol and hopefully dance out the door. I never dance, so that shows how ecstatic I'll be to finish. I asked my surgeon if I could postpone my surgery from four weeks to six weeks post chemo. In early June I have a number of book related events scheduled that I'd really like to make. Having chemo when your book is published takes some if the fun out of the event, so I want to do what I can.
Just found out my company (I'm a real estate agent) is giving me something called the Spirit Award. Apparently all I had to do to win it was get diagnosed with cancer:)
Annie -
Congratulations NCBeachgal, KristinFro, and Denjak!! I hope your last treatments are good to you with only better things to come!!
Good luck Bela with you surgery. Let us know how it all went when you are feeling better.
Annie, Congratulations on your award!!
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Congrats to all finishing up. I'm soooooo jealous.... I've still got another 7 weeks of Taxol/Herceptin...
Just read my emails and got one from my gynae to let me know that my ca125 marker test has come back normal. This means that the cyst on my right ovary is not likely to be cancerous. Still have to go back in 2 months for a follow-up ultrasound to keep an eye on it - but good news for now!!!!!!!! My gynae wants to whip out those pesky ovaries but I still have a few months to make that decision.
Jenn
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