Starting Chemo in May 07
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Hi all,
Been a few days for me. I've been trying to transfer files from my old computer to my laptop and it didn't work. They were linked for 2 days and hadnt changed yet so I figured I'd unhook them and get online tonight. My neighbor is my computer guru so he will do the transfer this weekend.
I'm having a little bit of a hard time this week. With treatment 2 I ended up with thrush in my mouth and I got it again this time but I'm taking meds and yesterday I got a sore throat the was very painful. Called my onc's office and the nurse said strep is going around. I dont have a fever or anything other than a sore throat so I went to a primary doc tonight and he said it wasnt strep which is good. He gave me a script just in case it doesnt start feeling better in a couple of days. I'm using cloraseeptic losenges to numb it and they seem to be helping. My biggest problem is lack of sleep. Even taking bynadril (SP) I can't sleep at night.
I'll be finished with summer school on Friday which is good because I'm moving on Sunday. I'm trying to go through stuff and pack but I have no energy, and always an excuse LOL its hot, I'm tired, etc. My mom and I did clean out the boxes from the shed and moved them to my new house and I have cleaned out some of the cabinets in the kitchen. I have to go through everything with my 19 year old because he is staying at the trailer where we live now and will need some items. It's a very confusing thing to do especially while going through chemo. I don't recommend it to anyone, but sometimes you gotta do things you dont really want to do.
I'm hoping I have a good 4th, I have treatment on the 2nd and my daughter comes to visit for a month on the 3rd. Man am I gonna be busy. She is very supportive of whats going on but hasn't been here so hopefully she is patient with me. She's 15 and boy crazy. I can't waite to have her here.
OK I feel like I'm rambling. I need to try and get some sleep.
I'm so glad most of you are feeling better and send hugs to you and great big HUGS to all who are still having side effects.
{{{{HUGS}}}}}}
CindyKS -
Hi, everyone. I had my third dd A/C treatment a week ago and I have been so tired. Sounds like some others of you are having the same problem. It is so debilitating. I've never had so little energy in my life.
As a positive, I don't work outside the home and my daughter is 14yo, so I can nap as much as I want. Not that napping really helps that much.
Pat -
Hi Girls! It's been a week since A/C #3, and though the nausea, bloating is settling, the eye & nasal tears (duct problem) started up again today. That stopped the day before my recent treatment, and I was so glad and hoped it was over....shucks! Now the tears are streaming again.
It's interesting, the connection between infertility and bc. It took me 7 years, two losses (the first at 5 mos of preg), and pergonal, etc. to finally give birth. Of course, if I had it to do over again, I would not have changed anything (even though mine is 18, giving me a run for my money as well as giving me love). My sister also had infertility problems and bc. Fortunately, last week I got the news I was BRCA negative! But I wonder about hidden genes since my mom had ovarian C at age 70 and bc at 73.
On another topic, I ordered two sets of bangs, a monk hair piece, and a bathing cap. I so anticipated ditching the faky wig when these arrived; but when I put them all on, I felt so phony and freeky looking. So bummed and bald at the moment!
On a positive note, there are 2 sayings that have helped me in the past:
1. "That which doesn't kill you makes you stronger". Note all the strong women around that survived breast cancer. Living proof!
2. "This too shall pass". And PASS it will, and we will have many, many great days. And we will be like my sister who says she doesn't remember having side effects. Her hubby remembers them though.
Peace, comfort and strength to all!
Mar
P.S. As for the question about the stubbles, at first the hard stubbles hurt and hurt. Now I have soft stubbles...more like fuzz that does not hurt. I feel like a chicken....but not a spring chicken :-( -
Hey everyone!
I'm still waiting for my buffs to arrive...maybe that "free shipping" wasn't such a good deal afterall!!
My positives:
I played beach volleyball yesterday - even without my buffs!!!!! (and I played well - we won and are now in division 1) I also rode my bike to and from work and then to and from the sand courts. I was TIRED last night but it was that "good tired".
School is out for my kids in 2 more days! YEAH! I love summer and having them home - especially since I always cut my hours back at work during the summer!
I have my cousin's grade 12 grad tomorrow night - BIG deal in her life! My goodness grads have become what weddings used to be - but I'm all for celebrating so I'm excited too! Her older sister graduated from college in April so the three of us are taking a hot air balloon flight in 2 weeks...I'm excited for that too! Then on the 14th of July, we are all going hiking to the mountains (my daughter is coming too!) So much to look forward to!
Both of my children's soccer teams won their divisions and now go on to the city finals next week! Between the 2 kids, we will have 8 soccer games in 5 days beginning the day of my next treatment - I hope I will be up to all the spectating!
This weekend, we are going camping (it's a long weekend here as July 1st is Canada Day - same as your July 4th)
So, for a change, I am not whining but am happy with all my positives!
I'm still working on that avatar. I finally figured out how to make my photo smaller but then it was too small...you will get to see my smiling "Bill Murray" face soon - I promise! (I really don't see the resemblance but others do)
For those of you who are at your "bad time" of treatments (SE's) I send out healing hugs to you. For those of us feeling good - celebrate!
Have a wonderful day everyone!'
Mandy -
Hey girls,
Pat, glad to hear from you. Sorry you're so tired. I can relate. Just rest, girl, it's OK. At least while you're asleep you can feel better, maybe?
Mar, infertility is hard, isn't it? We have two gorgeous babes from Russia, and I'm so grateful. They're the BEST. Nobody else in my family has struggled with bc or infertility, though. I'd like to have that soft stubble you're talking about! I shave mine every few days now--it feels much better that way.
Mandy, good for you for playing volleyball, even without a buff!! Did you wear anything or go bald? I'm in awe of your ability to do so much during chemo. Wow, that is AWESOME.
I'm still dishragging it over here. Can't remember if I said I got the pump off yesterday. I couldn't take it any more--HAD to have a bath. So now I'm paying for it with more nausea, but I'm trying to just veg today and take compazine and ativan and get through. I'm not going to throw up or anything, I just feel gross. Still not hungry. Positives? my kids are at a friend's house and I'm sure they're having a blast today. I have AMAZING friends helping me with everything. My hubby has learned the art of not pointing out the positive to me but just holding my hand and telling me I'm doing a good job. I love him.
Love to all of you,
Amy -
I just got back from the cancer center...today I had my final A/C treatment. I know I'll feel like crap for the coming week so I'm not totally done, but at least the final infusion is done and now I get a few weeks to breathe and recover before starting radiation.
For today, I'm just going to enjoy the fact that I have no cancer left in my body (that we know of), and I'm all done with A/C!!!!!
Hugs to you all...
sarah -
HOORAY, SARAH!!!!! I'm rejoicing with you!! This time you know that when you start to feel better, you don't have to go back for MORE!! Awesome!!
Amy -
Good Sarah. I hope your side effects are minimal and enjoy your break before radiation!
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O no,,,,,,,,,,,for me..........Liz I am an oldie and I have been thru menopause already...........but I can relate to hot flashes and all,,,,,,cause I still get them. I would have thought after going thru menopause like 8 years ago,,,,,,,the hot flashes would have stopped,,,,,,,,,,guessssssssss nottttttttttttttttt. lol
They actually do seem to be less since I have been on chemo,,,,,,weird huh? Cause the dr said they would get worse. Anyone else out there with fluid retention, besides Liz?
Enjoy your week gals,,,,,,,Cindy
And good for you Sarah,,,,,,,we are jealous,,,,,,we want to be done tooooooooooooooo. Boo Hoo lol -
Amy, sorry for the dishrag-ness......
Sarah, congrats on your last a/c! Be extra nice to yourself this coming week. The last a/c was rough, rough, rough for me.
Cindy, lucky you that your hot flashes decreased! I have to say I didn't expect to have to deal with them before 50 or so, and it's umm...not fun.
My first taxol is tomorrow, and they're having me take 5 dexamethazone (steroid) tablets at 11 pm and ANOTHER 5 at 5 am. Did I mention that night time is when I usually sleep??? I fear there'll be no sleep tonight, so I actually brought a work project home, just so I'll have something to do for hours and hours and hours. Yikes! Wish me well -
Holy Crapola 5 Dexamethazones????? They don't call it dex-a-METH for nothing. Heck, even on one I find myself doing bizarre things like polishing 10 year old silver earrings just because. You might find yourself detailing the house with a toothbrush tonight! Good luck with the Taxol. I'll be anxiously awaiting your report as I follow you next week. I know my docs give lots of Benedryl with it, beyond that I have no idea.
Tomorrow is my last A/C and I keep crying thinking about having to do it AGAIN, even though it is my last one. I can feel myself getting more and more worn out each round and I hate to think of what the next 2 weeks hold. HOWEVER, Portland's fabulous Blues Fest starts 4th of July and I WILL be there, even if I have to rent a darn wheelchair. It's my favorite festival of the year and no stupid side effects can keep me home.
Anybody else have a rash on their legs? LOL - it's always something with me.
Hugs,
LeeAnne -
just found this fascinating website with a great philosophy of patient involvement and self-advocacy, addressing how to make decisions around breast cancer. It's basically what my SIL and I, both patient advocates by nature, did....but we had to fight really hard to do it (and in the end my health ins. broker switched my work from an HMO to a PPO):
See http://www.natlbcc.org/nbccf/info/ -
Congratulations SARAH wish I was with you on being done.
My sore throat is gone but now its itchy and my nose is running and I think I have a summer cold. Joy just what I need during chemo. Hopefully I feel better by Monday when I get treatment again.
I have my bloodwork tomorrow so am wondering what my WBC will be since I have the cold.
Mom is coming tomorrow to help me pack up my kitchen stuff. We have to sort through and decide what to leave for my son. He really wont need much but dont want him to have to go buy stuff. Will leave him a pie pan so he can make a pecan pie for Thanksgiving. LOL he's 19 but makes the best pecan pies.
Well I'm tired so am going to try and sleep.
Positives: My daughter is coming in 5 days and I'm really excited. I haven't seen her for almost 2 years.
Nite all,
CindyKS -
Hi everyone,
Amy - I hope your "dishrag days" are behind you and that you've turned that corner again! I am so glad to hear that you seem to be having a better round - at least no ER this time!! (yeah!!) By the way I played volleyball with a scarf under a ball cap the other night - it stayed on pretty well! Just don't have the nerve to go commando!
Sarah - Congrats on being all done with chemo! It's time to heal and CELEBRATE!!!
CindyKS - Man, you are one busy woman! I hope your move goes well - don't overdo it!
LeeAnne - Only one more A/C...I totally understand your apprehension about the Taxol - but others who've gone before you say the SE's are way easier than the A/C. And the Bluesfest? Good for you! Ours is in late August and I plan to be at ours too! Sounds like a great time!
Amanda - I echo LeeAnne when she says "Holy Crapola" re: the bazillion dexamthasones!!!! I didn't think Taxol gave one nausea?? At any rate - good luck with your next tx and thanks for the link to that website - most interesting!
Hope this evening finds you all feeling well and that you all have a good rest. I'm off to bed myself! Nite.
Mandy -
Hi. I will have to take 5 decadron the night before and 5 the morning of my first Taxol trestment, too. I have heard that it is to handle any possible reactions. Don't know for sure, though.
Pat -
Hey Pat - Yes, my onc. told me that the carrier substance for taxol can produce highly allergic reactions in people. He scared me into taking the steroids actually, saying that the people who have severe reactions and end up hospitalized or worse are the ones who may not have taken their steroids (which I took with a grain of salt, as I try to take things on time but can be a little forgetful/overwhlemed). So anyhoo, the point is that yes, it's not for nausea. Though that would be a welcome side bennie.
And I'm sure that they'll give me a heavy duty antihistamine and more steroids, all IV. Oh joy. Last time my face got all puffy fr the steroids.
Let me know how your taxol goes!
LeeAnne - way to go on the wheelchair determination! I hear the Blues Fest is wonderful. I don't do so well with crowds myself and am usually out of town, but it sounds like great fun.
Mandy - love your signature
Positives: A girlfriend that I went to France with as a teen is here and she's going to cook for me! Love that. -
Hey everyone. For the record, I'm not completely done with chemo yet. Since I had a new mass of IDC pop up while I was on chemo, they decided to do rads in between A/C and Taxol.
So once I finish rads, I'll be going back for Taxol weekly for 12 weeks, and Herceptin weekly for a year. But from everything I've heard, A/C is by far the worst chemo, so at least that's behind me.
Take care, everyone.
sarah -
Hey girls,
I almost hesitate to say this, but..... I THINK I might be starting to feel hungry. And I DIDN'T wake up nauseated this morning. WOW. This is huge. I'm not sure I feel as good as I did when I "turned the corner" last time, but getting there. Definitely a step in the right direction. Coffee still tastes AWFUL, whereas it tasted great right before my last treatment, so maybe that will come back at some point. For now I'm happy to enjoy jello and a few random items that look good.
I see my onc tomorrow for a cbc and to check in about how this tx went. I'll be curious to see what he thinks, and if there is ANYTHING at all we can do to make it even minutely better. I'm glad I didn't go to the ER this time--definite improvement--but getting to "the other side" has been grueling. I'm also curious if my red counts are down this time. Last time I got a shot for that, but this time not (and I don't really know why) and I definitely find myself feeling more lightheaded this time than I remember feeling last time. So we'll see what that all looks like.
Sarah, sorry you still have taxol to go. But that is GREAT that you're done with A/C.
Sorry, Amya, when is your taxol #1? Today? I apologize for being out of it on that!
All for now, girls,
Amy -
AAAHHHHHHH I have a head cold. It's driving me crazy. Went for bloodwork today so am wondering about my counts. Oncs office hasnt called me or anything yet. The sore throat is gone which is good but now my nose is getting sore from all the blowing. YUCK, I have too much to do to be sick.
Amy: I'm glad you are feeling better this time and no er is a big plus.
Everyone else just keep on hanging on. The light gets a little brighter at the end of the big Chemo tunnel each day, and even closer with each treatment.
Well need to go pack some more stuff in the kitchen.
Have a great evening all,
CindyKS -
Sarah - you had a NEW mass of IDC pop up while on chemo????? How did I miss that? and how did you find it?!!
Amy - eating is good! Hope that you feel like it soon
Cindy - Ahh...I hope you get through the cold soon!
re: my first taxol, wonderfully uneventful and boring. Yay!!
My lymphotocyte count is low (see http://labtestsonline.org/understanding/analytes/differential/faq.html)
"Lymphocytes are natural killers of infection and regulators of antibody production."
But from my googling it looks that's normal for taking steroids, especialy dexamethosone. And my WBC are normal, it just means that I have few T cells and B cells (that make up lymphocytes) running around to fight off infection, so I'm going to be a little more conscientious about hand washing, touching my hands to my face and nose etc. And hopefully when the steroids wear off the lymphocytes will increase.
Also, my RDW was slightly high, and MPVs were low, so:
# Red cell distribution width (RDW) is a calculation of the variation in the size of your RBCs. In some anemias, such as pernicious anemia, the amount of variation (anisocytosis) in RBC size (along with variation in shape poikilocytosis) causes an increase in the RDW.
Mean platelet volume (MPV) is a machine-calculated measurement of the average size of your platelets. New platelets are larger, and an increased MPV occurs when increased numbers of platelets are being produced. MPV gives your doctor information about platelet production in your bone marrow.
So, what I assume is that even though I still have enough red blood cells, white blood cells and platelets, the production process for all 3 in the bone marrow is decreasing, and not as many new ones are being made. Which is normal for chemo because chemo impacts the bone marrow. And my neulasta shot tomorrow will hopefully help with that.
It's funny, my doc tells me not to worry about these things, and it's not so much that I worry but that I like to have at least a very simple grasp of what's going on. -
CindyKS: I just got over a head cold too, but my blood counts never went down as far as I know. I have CBC every Wednesday. It definitely isn't fun being sick on top of chemo. I was afraid to go to the gym. ANd it seemed to take me twice as long to recover as normal.
HOpe you feel better soon.
AmyaM, I'll be curious to hear how you do on the taxol. I'll be on that after my last A/C in two weeks.
Hope everyone has a good evening. -
Hi all,
had my 4th and last A/C yesterday. Had problems with my port where they couldn't get a blood return, tried two needles and still did not work. said it was flushing but not giving a return. The they did an xray and said it was still in place. Has anyone else had problems like this with the port? so they drew blood from my arm and chemo in the port. Spent a few hours longer than usual but I am done. This morning I woke up very nauseus, I attempted to go to work but driving there I just decided to turn around, figured I wouldn't make it even half the day the way I felt anyway. Went home and slept until 11am, then got up and went to lunch with my daugher.
Had neulasta this afternoon, we'll see how tomorrow goes.
I will be starting Taxol in two weeks, my onc didn't say anything about taking steroids the night before?? Should I ask about that?
Well, 8:30 and I feel like going to bed already so I may just turn in.
Have a great weekend everyone. -
I have problems with my port sometimes not wanting to work for withdrawals. The nurse said it can be a positional problem. Like the tube is too close to the vessel wall so it's acting like a vacuum cleaner with the drapes. So they have me hold my arms up or twist around to get the tube in a better place for sucking. It always flushes fine for input. It's just the withdrawals that are tricky.
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OK, girls, TOTALLY OFFICIAL, TURNAROUND HAS TAKEN PLACE!!!!! WaHOOOOOO!!!!! My definition of turnaround is that I get HUNGRY, and start EATING!! Tonight I found myself making nachos, and hubby made me a cocktail with the special brandy he brought back from Brazil when he was there a couple of weeks ago. MAN, it feels good to eat!!
YAY,
Amy -
Good for you Amy. Enjoy!
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Amy, I'm happy to hear that you are feeling better.
Pat -
Heck, Mary, I had chemo this morning and they couldn't get a withdrawal from my port no matter how I twisted and turned. So they had to draw my blood from my arm.
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Hi All,
I haven't written in a week or so, but I've been reading to keep up-to-date with everyone. I think of you all often.
I got sick twice last week after my 2nd treatment--both were in the morning after coffee, but before food, so I decided to cut coffee out of my morning routine. I'm drinking Peppermint tea, which is a nice substitute.
I've felt pretty good this week--my third treatment is on Monday. My sister is coming to visit next Thursday to give me some TLC and to help me figure out if I can wear red and purple now that I'm wearing the red wig. I definitely need help in the fashion department!
My company had our office picnic last Friday and I wore a scarf pulled back into a ponytail-type thing under a matching baseball hat. That worked out well.
I've been bloated, too. Good news: I think the hair on my legs stopped growing!
Mar in NJ, I like "This Too Shall Pass"--I just try to keep putting one foot in front of the other and do what I have to do each day and eventually, we'll all be through this.
I had ten radiation treatments in five days before chemo via a MammoSite catheter--did anyone else do that?
TGIF,
Suzanne -
Hi all,
Been kind of busy, but wish I was more "in the loop" here. I finish on (or about) Sep 5th as well. I did ok on A/C. Have lots to tell but on the other hand only one thing to tell - my beautiful, wonderful, 16-yr-old son (who cut all his long hair to suppport me through chemo) has been diagnosed with a brain tumor. We don't think it is malignant but it is large and needs to come out. I have an appointment with a top neurosurgeon on July 18th for him and am getting other stuff lined up.
Meanwhile, we need as many prayers as possible. I don't even know what else to say at this point.
Sheree in Florida needs hugs and prayers -
Oh Sheree, I am SO sorry to hear the news about your son.
That is just awful - I am glad to hear that you think it is not malignant (thank goodness) but it must still be so scary. Why can life be so unfair? You, your son and family will definitely be in my thoughts and prayers!
Take care,
Mandy
Please keep us posted on how he (and you) are doing.
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