March 2010 Chemo Start
I have found great strength in having a topic for the month you are starting ... we are going through the same thing together and that support and help is priceless! If you are starting chemo in March 2010, please join in!
Jojov - start 3/1; 4 AC
Gemini2010 - 3/1; AC 4x; T 4x
EZH - Taxotere, Cytotaxin 4X, start 3/2
Staceyt - TC 4X, start 3/2
Frosty1 - [port 2/25] Taxotere, Carboplatin, Herceptin start 3/3, 6X every 3 weeks, then Herceptin for 1 year
Taty - start 3/3; TC 6x; Avastin 1 year
TiffanyGanell - start 3/3; AC x4; Taxol X12
AnneMarie_1970 - TCH 6X; start 3/5
Rohm - TCH every 3 weeks; start 3/8
Groundhog - Taxotere & Cytoxin x 6, every 3 weeks; start 3/9
Marigunn - start 3/8; AC + T
Sarikasd - 4 AC; 4 Taxol; start week of 3/8
baileyjm39 - 3/8; TCx4
karenm50 3/8; TCH
Julesgg - 3/9; TAC x6
knotes - 3/9; TH x12
momto3 - 3/9; TC x4
elle40 - 3/10 TC x4
Lesinindy - 3/11 TCH x6
MelB - 3/11; taxotere, carboplatin, herceptin 6x
charley 3/11; TC x6
chelseaB - 3/12 CT; AC start 4/2; then TH
jloverwhelmed - 3/12; AC/T; Taxol
JLLG - start 3/15; TC
PiscesMoon - start 3/15; TCH
GurleeGirl - start 3/15; TAC x6
Melanie36 - start 3/15; T
64karin - 3/15; AC
mbalcombe - 3/15; TAXC x6
Julia257 - 12 weeks Cytoxan & Andriamycin; start 3/16
mary1996 - 3/16; TC x4
SuzyE - 3/17; TCH x6
Alison34 - start 3/17; FECx3; Taxotere x3
Lovemygarden - start 3/17, Taxol + Herceptin, weekly for 12 weeks
lillyc - 3/17; Taxotere & Cytoxin x4; radiation
undecided - 3/17; taxotere & herceptin, add Zometa
NorthVanCheryl (FKA Surprised) - start 3/18, 4 cycles DC
Anna1973 - start 3/18; Taxotere & Cytoxin x4 then radiation
1vamom - 3/18; ACx4; Taxol x4
kell414240 - 3/18; 4x AC
Carolsue63 - start 3/19; 6X TCH
Hereandnow - start 3/19; FEC 3x; T 3x
lorrhaw - start 3/22
Barb-k - start 3/23; DC 4x
llm822 - 3/23 AC
Teemee - 3/24; 4x TC
Joj129 - 3/25; Taxotere/Cytoxin
Horsedoc - start 3/26; TC x4
dublin4 - 3/26; 4x DC
SGJ05 - 3/29; TCH x6
HMH - start 3/29; 4 AC; taxol; radiation
Thereishope - 3/30; TC x4
peverson - 3/30; DD/AC; taxol; radiation
farfromhome - start 3/30; AC x4; DD x4; surgery; radiation
momof3bugs - 3/31; 4DD/AC; 12 taxol; radiation
Terry731 - 3/31; Taxotere-Carboplatin-Herceptinx6; Herceptin 1 year; rads
SandieK9 - dose dense AC + T
Kayne - 4 adriamycin & cytoxin; 12 Taxol
Hunter11 - ACx4, THx12, HERx13, RADS
Yeshua4Me - Adriamycin-Cytoxan x4; Taxotere x4
LSF - Adriamycin-Cytoxin x4; Taxotere X4; Herceptin x4
Comments
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Hello -- I'm new to this forum, and starting chemo March 8 for triple neg BC after mastectomy 12/24/09. Will have AC + T, and then a clinical trial. Just want to get it over with. I'm a teacher and am planning on continuing to work through treatments, if possible.
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Right now I'm scheduled to start on March 17th but that may be changed to the 19th. Either way definitely that week of March.
PowerPort "installed" during my bilateral mastectomy on Feb 1st. Going for my first "flush" tomorrow (and am nervous about it because my oncologist won't use EMLA; see my thread about Port Discomfort) because it will be six weeks between the installation and the start of chemo.
I'll be getting Taxol + Herceptin weekly for 12 weeks, then for the rest of the year it'll be Herceptin alone every 3 weeks. Planned premeds will be Benadryl, Decadron, and Aloxi. Going on "house arrest" because I can't afford to get Neulasta shots (cancer + no health insurance, what a joy) on top of the cost of everything else. Fingers crossed that Genentech will agree to supply the Herceptin...
Going for my baseline MUGA scan on Wednesday, which I assume is the only other thing that could derail the chemo plan (an unacceptable baseline ejection fraction).
Also am planning to wear the frozen gloves and slippers during the Taxol treatments in hopes that it might avoid hands/feet damage. -
Hello - I'm schedule to start March 18, 4 cycles of DC. I had a total left mx Jan 11. Going back to work next week before chemo starts and will just take time off as I need it, if I need it.
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Just want to give you guys some encouragement from a March "alumna" -- I was a March 2008 chemo gal. I did 6*TAC. From one who has been there, I can honestly tell you that it's doable. It's not a walk in the park, but it is doable. I worked through treatments, taking treatment day and the next day off, then working part time for the next couple of days, then I was able to go back full time again. I bought a great wig, but ended up wearing it only a few times - I ended up wearing mostly baseball caps with dangly earrings. Everyone is different when it comes to what, if any, headcoverings you will use - some are like me with baseball caps or other hats, others wear their wig all the time, others get into pretty scarves, and some "go commando" and just go bald.
While losing your hair is no fun, on the good side it's really easy to get ready for work in the morning when all you have to do is towel off and don't have to spend time blow drying and styling your hair. Also, think of this - no shaving for months, yet your legs and pits stay silky smooth. Those nasty little chin hairs - gone! And you never have a bad hair day.
Please feel free to PM me with any questions you may have - lot of chemo "alums" gave me info and support while I was going through chemo, so I'm glad for any opportunity to "pay it forward." Rely on each other as well - I could not have gotten through my chemo without the frank and wonderful support from my fellow March 2008 ladies. I hope all of you will develop a strong and supportive community for each other as well.
It won't be easy, but you CAN do this. Going through chemo helped me realize that I was a lot stronger than I thought I was, and the strength I found has helped me in other parts of my life as I've moved beyond active treatment. I even found the strength to ask for help when I needed it - that was the hardest strength to develop of all. Good luck to the March ladies!
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NatsFan -- thank you for the encouraging words! I love the silky smooth skin part. I initially joined the February group until I found I had to wait until March to start, and they started a list of 'good' things that have come from chemo -- and getting ready in the morning was top of the list.
Surprised - we are surgery sisters! I too had a left simple MX on Jan 11. It is the pitts as I am now feeling great and will soon start the dreaded SEs of chemo.
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frosty1, thanks so much for adding me to the list. There's a small correction, though: After the 12 weeks of Taxol + Herceptin weekly, I will then be getting Herceptin every 3 weeks for the next 9 months... so won't be done (assuming all goes well) until March 2011.
*sigh* Wouldn't it be nice if it WERE only the 12 weeks?! But ah well, 'tis what it is! ;-) -
I'm not sure how to add my name to the March list....can you help me?
EZH: Taxotere and Cytoxin, 4 rounds, start 3/2
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I'm with you, lovemygarden -- I am in for 6X (mid-June is the last) and then continue Herceptin for a total of 12 months. Then on to more fun with Tamoxifen for 5 years. Yippee!
EZH -- I will add you to our illustrious list.
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frosty1- please add me to the March list, I start chemo 3/9 but not sure about tx regimen yet. Saw onc 2/23 and he gave me two options: AC+T or TC.
AC+T: Adriamycin & Cytoxan once every 3 weeks x 4 treatments THEN Taxol once a week x 12 treatments
OR
TC: Taxotere & Cytoxan once every 3 weeks x 6 treatments
Path found a 0.1 cm (1 mm) met in sentinel node, onc said either would work. We had a good discussion about the risks and side effects but he is not directive, just said he would be OK with the TC option, but the ultimate decision is mine.
AC+T has a 2% greater chance of permanent heart damage; TC has a 2% greater chance of ca reoccurrence.
After chemo will be tamox for a couple years then arimidex. I'm in peri-menopause now but he says chemo will put me into full menopause.
I have a few days to decide, will need an echo-cardiogram next week if I go with AC+T. Left a message with surgeon's office regarding a port. Boy oh boy the fun just never stops...
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Frosty1 , I also started in the Feb thread as I too was to start in Feb (tomorrow 2/25), but I am now scheduled for 3/2/10. I believe I am TCx4, with another surgery following the chemo. My first surgery was 12/4, did not have clear margins, re-excision on 01/25 with a close margin clearance, therefore just to make sure my surgeon along with my onc doctor feel I should have another "touch-up" around the margins to be sure. After all that, radiation and of course Tamoxifen. These boards are the greatest, great advise and encouragement, and everyone shoots from the hip and doesn't sugar coat anything.
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Welcome groundhog and staceyt! The February thread has some great info, especially for those of us jumping on the chemo train next week.
Groundhog: it is nice your onc is letting you make the decision, but sometimes I don't want that responsibility! My onc is partial to the TC route, which I'm happy with. I also get the opportunity to experience Herceptin, so I have my port surgery tomorrow.
Onward!
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Frosty - before your port install tomorrow, put a line around where your bra strap usually goes to make sure that they don't place the access point of the port there - you don't want your bra strap rubbing on it all the time once it heals. Chances are your onc will want to leave the port in for some time after you finish chemo, so you really don't want to be dealing with that issue. I had my port installed the day before my first chemo - it was a little sore but there was really no problem installing it that close to chemo. After your mx, the port install is nothing.
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Thanks, Frosty, I know what you mean about not really wanting to make the decision myself.
Saw my primary care physician today, he's been my doc for 20 years. Asked him if my heart is strong enough for the Adriamycin and he said yes BUT recommended against it due to family history of heart disease. So it's TC x 6 for me, which also means no port. Good luck in surgery tomorrow!
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Thanks for the heads up on the bra strap drawings ... when I met with my BC a couple of weeks ago, she indicated she puts it farther over. I told her about the drawings and she thought that was a good idea. Ugghh. Now to find something to wear to the interview on Friday that will cover my new hole.
Groundhog - I was glad my onc said TC as my family also has a history of heart issues. Made the decision easier.
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Morning Frosty1,Marigunn,lovemygarden.Surprised,natsfan,EZH and groundhog.
Thank you for welcoming me to March 2010 Chemo start. I finally updated my Diagnosis, there are some questions I need verification on. Natsfan - thanks for all the encouraging words. I was told that if you lose your hair it grows back curly, well I have a slight problem with that because I don't think my curls could get any curlier. I simply put a little gel in and go in the morning. Starting to get a little cabin fever, we are finally getting the snow that everyone else already got and I am ready for spring and have the sun out! Frosty1 - Hope all goes well with your port. My best to all and happy thoughts.
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I am so obsessed with Girl Scout cookies ... both DH and DD bought some this week and I haven't eaten any. But since I can't eat until after surgery today, that open box has been screaming my name all morning -- I drool every time I walk by. Dang. I am off to join the Collective (sorry ... Star Trek Next Generation -- Borg -- they had all these tubes and things coming out of their bodies that connected them to all the other Borg -- the Collective). Getting this port makes me feel like I should be hooked up to someone or something. But wait ... that's next week. Argghhh.
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Hello, March chemo team. I started the Feb 2010 thread and am just popping in to offer support. I am doing TC 6x. So far I've had 2 treatments (the second one was yesterday). Virtually no SE other than hair loss. I feel pretty good and am at work today.
We've shared some good info on the Feb thread so if you are interested feel free to visit. We are just a month ahead of you and don't hesitate to ask questions there, too.
You can do this! This forum has been wonderful for me - you've come to the right place.
frosty1 and staceyt, great to "see" you here! Good luck on your surgery, frosty1!
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Hello to everyone, fellow March chemo ladies and others that have kindly visited.
I have been doing a lot of following of the Feb. group, as I, too, was supposed to start in February. Did the pre-meds, drank oh-plenty of H20, was totally psychologically there and then, NO! The onc that was covering for my vacationing onc thought my reconstruction zone (t/e's fully, and I mean fully, expanded) looked "pinkish". Sent me away with Augmentin, 875mg, (nice on the stomach) and told me to re-try after being re-examined by the PS (who, was also on vacation that week, so had to wait for him to get back this week). Anyway, 7 days of antibiotics later, still pink. PS says its the "just" the stretching and now, I'm scheduled to re-attempt chemo on 3/2.
This waiting and anticipating is hard on the psyche...really just want to get started. I keep telling myself, mantra-like, that chemo is not the enemy, but the ally. Though dread looms large, we need to move through so that we can move on! Totally helps to read the Feb. thread, as those ladies. and all the others that have come before us here, are amazing.
Looking forward to getting to know you all and moving through this together.
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Hi all and greetings frosty1 our Borg Queen! (that means your SO gets to be Data *lol* another trekker here).
Made an appt for next Tues to get my haircut. I have long hair and am donating it to Locks of Love (LOL has a new meaning now). This may sound crazy but I am having a harder time with losing my hair to chemo than losing my breasts to a bmx.
Thanks faithfulc for the visit & info, I'm also doing TCx6 and planning to work as much as possible, glad to know your SE's are mild. This weekend I plan to spend reading through the chemo forum.
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Hello all. I am popping in from the March 2009 Warrior Princesses thread to wish you all the warmth and support I can as you set out on this journey. I did chemo from March-September (AC then Taxol) last year, then radiation. You'll get through this fine, I promise. We all did.
I felt such wonderful companionship from the other women on my thread and I am sure you will find the same this year. I strongly recommend the Shopping List for chemo thread, and my own number one tip is - see a naturopath for supplements that can assist your body in withstanding the chemo.
best wishes
Rachel
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Count me in as yet another trekker out of the closet! LOL
When I went for my MUGA scan the other day they had to put EKG leads on me again as part of the procedure, at which I commented to the tech "Here I go feeling like a Borg again, just like after my surgery and while those darn drains were in!" He laughed and responded with "You will be assimilated.." which of course meant I answered with "and resistance is futile!" ;-)
groundhog, I am SO with you on the hair thing! I too am not really traumatized by the bmx (wasn't a heck of a lot there to begin with anyhow) but the hair thing really upsets me. I had mine cut very short just before I had the surgery because I figured I might not be able to raise my arms high enough to wash it for awhile and assumed that the shorter it was, the less yucky it might get. Plus I needed to psychologically prepare myself for the chemo-loss. First thing I noticed was how cold I felt without all that hair, even around the house which is kept at 67 or 68 during the day in winter. Brrrr! The more I thought and read about it, the more I felt that I just can't deal with watching the loss process, so am planning to get it all taken off (still can't bring myself to say the S-word!) the day before my chemo starts. I know I could wait but I also want to have it done before any chance of my WBC dropping, in case the hair gal accidently gives me a scratch or nick. It will be easier on me to deal with the initial shock of having the crownless Nefertiti look and move on, than watch it happen and add emotional stress to the physical ones from the chemo. -
Live long and prosper! OMG -- so glad to know other Trekkies are on this journey. So I have my implant and am ready to be plugged in. More stiff and achy today than sore from the surgery. Doctor said to do whatever I wanted as long as it didn't hurt. I now have my Halloween costume - the Borg Princess -- bald (well maybe hair will be growing back by then) and an appliance! I got my shorter 'do last week. And picked up a green wig from Target -- might as well have fun with this! I meet with the appearance counselor when I go in for my first treatment next and she will take me out wig shopping. I'll just be glad to get this first one over with so I know what the SEs are.
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Peace and long life! I like the idea of having fun with it, may as well plan to be bald for Halloween.
Hmmm, crownless Nefertiti, that has possibilities, or one of those gigantic Russian fur hats!
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i'm scheduled to start on the 15th, TCH. not sure of the specifics yet as far as how long the chemo will be but i know herceptin will be a year. a couple of things may delay treatment but i hope not!! i've had enough delays.
~M
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The delays are the absolute worst part of the whole thing. I just want to get started so I know what to expect. Then I feel I can deal with the rest. It was the same with the MX surgery ... I don't know how some of these ladies have done it when they have had things postponed forever. Hang in there!
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I agree. It still amazes me that I was diagnosed a few days before New Years, had my BMX on Feb 1st, and am starting chemo March 17th. I could start a little earlier but want to just give my body those extra 2 weeks to recover fully from the surgery before subjecting it to another onslaught. Plus, maybe enough Spring will be in the air by then to lift my spirits the way it always did before. Mental therapy. :-)
It does still amaze me that it's only been less than 60 days since I got The Phone Call. It both seems like forever, and also seems like yesterday.
I have a friend who had to wait almost 5 months between diagnosis and start of chemo (mostly red tape from insurance companies + medical incompetence) and it practically drove her over the edge. -
Hi all, just wanted to post well-wishes for our sisters starting next week:
EZH ~ staceyt ~ frosty1
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Good luck to all the March 2010 ladies! Just think - next year at this time you'll be the one posting encouraging comments for the 2011 March "newbies".
Hopefully one day there will be a cure or preventative, and no more need for March chemo threads.
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I'm starting chemo mid-March and am happy to find others doing the same thing. I'll have dose dense AC followed by dose dense Taxol, and then move on to Radiation. Your experiences will be very helpful.
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How kind of you to write to this forum. You've offered your strength, and I'm listening. Thank you.
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