Chemo in July 2015
Comments
-
You are all wonderful and beautiful and I'm thinking of you all.
-
Want2Bcamping - I have the same thing going on with regards to the scalp. Hurts, doesn't it? Mine started for getting bad on the weekend and I didn't want to call the MO on a Saturday because I had head zits, so I dug around and found some home remedies to try in the interim. It's largely resolved after about 5 days of washing my head 2x a day with baby shampoo and dabbing tea tree oil on the spots (which was pretty much my entire noggin; smelled like a forest gone wrong). Hopefully the meds work faster for you. Would you mind letting me know how that goes?
-
-
I LOVE how everyone looks with shaved/bald heads. Liberating, empowering...revealing new, undiscovered beauty and truth.
-
Hi everyone - we had a wicked storm blow through our town and it knocked out my power for almost 3 days. Chemo Monday - Tues, Wed, were good days. I felt pretty good! I even went running which makes me feel so much better. Today I feel a bit off - I guess it's Day 3 (chemo being Day 0). I haven't been sleeping well. Part of that is no power, no A/C and also the steroids I think disturb my sleep. Today is the last day I have to take them. So overall not bad. I have to catch up on all your posts. Right now I need to do laundry, run dishwasher and everything else I can plug in and turn on!
-
@inkster - seems to be starting to subside today. Haven't noticed any new spots on body and head is starting to dry up on the bumps. Itchiness isn't as bad so thankful it hopefully on the mend.
-
I am also TN (IBC) and on same plan as you, @Batesburg - carbo/taxol followed by AC. So far I have had one carbo and three taxols (every third week it's both), starting second set Monday (August 10th). I noticed changes immediately following the first infusion, and I have high hopes that this will continue. I no longer have the hard mass that once felt like it was about a third of the tissue in my right breast. I feel like there's a war going on in there each time I get the taxol since, like hot spots of not quite pain. I imagine that it is the drugs kicking the cancer's ass. I hope so, for sure. As far as SE's, I have been really fine on the taxol only weeks. The carbo week (which was the first one) did me in a bit a few days after with fatigue and fogginess but it was tolerable. Yesterday was day 14 and that was the day that i started having fairly significant hair loss. I had cut it pretty short (and dyed it purple) last week, but this morning I buzzed it even shorter. Who knew hair could hurt!?
-
RuthElizabeth Although it's dissapointing, I am definitely going to have a good time. Mostly eating some good food since my tastebuds are almost normal! Hoping you have no more delays in your treatment from now on.
Gretagirl My WBC went really low after 1st round. Got a fever and ended up in the hospital on antibiotics. I got a Neulasta shot the day after that was supposed to help prevent that. I don't think it worked.
I'm wondering how many of you are getting the Neulasta by auto-injector, and if you've had any problems with it. They're going to let me keep on the same treatment plan, but only if I come in to the office for the injection. My onc's nurse practitioner said that of the patients that have problems with their blood counts dropping, most of them got the Nuelasta using the auto-injector, so she doesn't totally trust it. There was no indication that it didn't work, but I don't think I trust now it either.
Cheesequake Love the pics! You're fakin' it in an awesome way! Although there is something empowering in seeing all the hairless heads too.
And I agree... it's amazing how much my hair/scalp hurts! Maybe it gets better when all the hair falls out?
-
@ Notdoneyet- Great we are on the exact same regimen! You don't happen to be having treatment at The Ohio State University - Stephanie Spielman Center, by chance? I know my MO and her team are doing this kind of treatment for the TNs (even though AC and taxol alone is the gold standard) - great research/outcomes on PCr with it- and especially effective with lymph node involvement. I have one confirmed lymph node that is involved- was palpable and now gotta "dig" to find it. (ouch!)
I have been having to deal with some bone marrow issues, though.....I have received 2 carbos and 4 taxols and head in tomorrow for my 5th taxol. Had a bit harder time with the second carbo/taxol combo from last week but tolerable. Minimal SEs for me so far except the neutropenia and thrombocytopenia. I have been taking neupogen and hope tomorrow's labs are OK- been a tad short of breath- have you experienced this yet? Not sure if it is chemo/neupogen or hgb dropping a tad or other related.
Good luck everyone!!!! We've GOT THIS.
-
Notedoneyet and Flaime, yep, my scalp hurt after I buzzed it on Monday, which is why I didn't shave it all the way down. I figure I'll let the rest come out on its own, though now it feels totally fine.
If I walk out of my house without something on my head I feel like I just walked outside naked, so I'm doing hats and wigs as needed. I've tried going "naked" a couple times - driving in the car, etc - I expect it'll get easier as I get better at dealing with people's reactions.
-
Well, my MO doesn't like ports so all my blood work, chemo infusions, etc. have been done so far on my right arm (can't use the left because they took 8 nodes from that side). But the nurses have been struggling with "valvey" veins. Guess I have a lot of different exit routes for my arm blood, good for for circulation, not so great for chemo. So I'm scheduled for a port install next week before the next AC treatment
Anything I need to know in advance?
-
ha, I somehow managed to change my language to Spanish on here for a few. No hablo Espanol.
Glad I fixed that.
Peabrain- I was awake (but loopy!) during my port procedure. They may knock you out, or not. I was pretty sore for a few days, and bruised up nicely. I kept activity to a minimum on that side, but other than that, recovery was smooth.
Suzanne- are you in RI? We had a bad storm Tuesday morning that knocked out power in my parts for a few days. If you are here, let me know where you're getting treated!
Thanks to all for the heartburn tips. I stuck with Zantac, and the heartburn is gone for now. It did get bad at the tail end of round 1 for me, so it may come back.
I met with my Radiation Onc today- was hoping I'd escape without it, but looks like it's in my future. Oh well. Anything to cure this and prevent reoccurrence is fine by me.
My latest 'do: my hair is stubborn, and is still holding on, so took it as far down as possible without shaving it. I kinda like it
Keep killin it ladies!

-
@ Peabrain,
I was on "Happy juice" during the port procedure and it was pretty smooth. Agree with Suzanne 1971- very sore for the first few days- I didn't take any pain meds because I didn't want to have to metabolize anything else- probably pretty stupid of me- and finally did take an advil when I saw that my platelets weren't low anymore. That first night without pain meds wasn't too great. Maybe you will be smarter than me and take some!!

I was infused through the port last Friday and it was nifty- no pain at all- just one quick insertion and all went well. don't even feel anything going in or out of it. It has healed up fairly well.
Suzanne- you are absolutely beautiful!
-
Loving the pictures of everyone! Great group we have here!
-
when did the hair on everyone's body start jumping ship
-
Hi! I'm also triple negative but stage 3A. Diagnosed the end of June and started with AC chemo July 1st. I will then have 12 weeks of the other weekly. After the chemo surgery will be discussed. I've been through 3 chemo sessions so far and the next one is schedule for the 12th of this month. You can do this, but I guess there's a reason why they call it "fighting cancer". It's been a roller coaster for me physically and emotionally. Steroids make me hungry but I have the strange nausea and fatigue. If you can take off work, do it and focus on healing. I am off work while I battle this. God, it is so good to read these posts and know we're not alone. I have an 11 year old daughter and I know that we all have so much to live for. About getting nails done.... Be careful because this chemo can bring your white blood cells down critically low and you won't want to risk infection. I've been getting my nails done for over 20 years and it was hard for me to stop. Yesterday I bought my first bottle of nail polish since high school.
To the sisterhood........ Keep fighting and
-
Jbandkb1 My scalp started to tingle and itch about day 11 after 1st round of chemo, then on day 14 it would come out easily when brushed or when I ran fingers through it. I buzzed it to 1/4" and more comes out when I rub or wash it, but I still have a lot clinging to my scalp.
-
Day 14 after chemo I could literally pull my hair out in chunks. I got a short cut prior to that... Actually let my 11year old daughter cut my hair and shaved it off soon thereafter. Otherwise it's messy and traumatic. I'm going in on the 12th for my 4th treatment
Hugs and support to you, sister
-
hi again, you won't have any problems with the port install. Mine went fine. They do give you meds to put you half under and it's like it feels like it goes shockingly quick. One word of guidance I will tell anyone and that is to make absolutely sure that you get a prescription for "numbing cream", prior to the first use of your port. I didn't do this the first time and wish I had despite a nurse reminding me to get it. You won't feel a thing with the numbing cream and remember that you might be sore and a little bruised and swollen in that area after the port is put in.
-
@Batesburg, I am in Milwaukee. I have only had the carbo once and I didn't actually see my labs from Monday so I am not completely sure where I am with numbers - good enough to have gotten the taxol Monday but not sure what is what. My WBC was getting somewhat low last week, which sounds like the norm. I am not taking neupogen (at this point) but will be doing neulasta during phase 2 with the andriamycin. Phase 1 is 12 weeks carbo/taxol, then 8 weeks phase 2 then surgery and rads (a given in my case). Hope your numbers stay good (enough) and all continues as well as can be expected, you are right, we CAN (and will) do this.
-
Yes, great pictures. You are beautiful.
-
Yes, great pictures. You are beautiful.
-
to "not done yet": I'm doing the same chemo as you, only backwards. I started with the andriamycin..I've done three out of four . And then start the 12 week regimen. I'm triple negative..... Do you have triple negative breast cancer? It's so interesting and comforting to hear what everyone is doing for their treatment. I'm so glad I found this place of support.
-
@Joy-Anna, yes, TN IBC. @Batesburg, I haven't had shortness of breath, is that something that you get immediately after the treatment? Does it get better after some number of days? I have had somewhat of a tightness across my chest like something is sitting on me while i am lying down, that may be related to what you are experiencing, but that feeling seems to last only a day or two then goes away. And YES, I am glad to have found this site too, there is so much gloom and doom out there. It is too easy to get sucked into the statistics and the scary stuff, we need some hope. Here it is!
-
@peabrain, I had no issues with the port placement with very light sedation (I was fully conscious and asked a lot of questions while they were doing it, it was kind of interesting actually). I had treatment that very day. The following week the port was quite sore and I learned the hard way that you should put the numbing cream on more like 90 minutes prior to when they access it, not the 30 minutes to an hour they say. The second week it was nearly painless, with a little more healing and the 90 minutes prior application of the cream.
-
Flaime I get Neulasta the day after chemo. I have to go in for the shot no auto inject
Peabrain my port surgery went well. My neck was sore for days but that was all
Suzanne1971 I love the picture!
Jbandkb1 I am 15 days out from first treatment and I still have all my hair. I have not had to shave my legs but maybe once a week compared to every night
-
3rd day after my 2nd CT round. I'm still upright and functioning. My mohawk still exists but with a lot more scalp showing every day. I'm finding I'm much more comfortable hairless than I had anticipated. My insurance company finally approved me for a neulasta shot after my counts dropped to zero last time. I had that yesterday and am feeling achy today. Claritin and some pain pills are making life tolerable. Not much nausea, thank goodness. But I do feel the need to always have a little something in my stomach. I do have a sore throat starting and am supposed to start up a round of antibiotics in a day or two. Now that the anticipation of starting chemo and some of the fear of the unknown has abated, I feel like I'm really in the trenches now. It is nice to read all of your posts and know I'm not alone.
-
Suzanne 1971 - I am on Long Island. This storm was so bad in our area. It was very short but winds recorded at top of our local hospital at 94 MPH! It ripped through a very small section of our community and created havoc. Unbeilable! But luckily have a generator. We have learned our lesson after Hurricane Irene and Super Storm Sandy. We were out for endless days. This was relatively "short". 3 days.
Today was a blah day. I felt blah. And now I can't sleep which seems to be my pattern. Last day for steroids so hoping that is the problem and then I will get a decent night's sleep. Sleep deprivation just adds to the "blahness". Tomorrow is a new day.
-
Peabrain: my port surgery went really well. I'd never want to blogspam and I only bring it up since you asked about experience, but if you want to read mine it's here: https://sweaterbunnies.wordpress.com/2015/07/13/he... It covers my port surgery from beginning to end. Please read only if you think it might be helpful...otherwise ignore! I also agree about the numbing cream, it works great. I didn't feel a thing and had no pain after infusion.
Day 12 today. Woke up to a tingly, itchy scalp...might not be long now! I'll have to model my wigs for you once it goes, I have some fun ones! Having my head shave party soon, I think.
Cheesequake you look fantastic! I love that wig!
Suzanne1971, another bald beauty. I'm just saying, some heads really don't need hair.
Suzanne50, I'm now the eternal insomniac. I feel ya! I'm in NYC so we're not too far apart. Just know someone in Manhattan is awake with you in solidarity.
-
morning everyone. Not done yet, I had the double mastectomy first, doing AC, and must say the first few days after chemo, I feel like I have a belt wrapped around my chest. It's a really odd feeling.
Had chemo 2nd AC Monday, and surprisingly Wednesday was my only day down flat. I still have the shakes, but feel pretty good. I am walking every morning early. Didn't even do that before, but it is helping my bowels and pain from the neulasta shot. I'm trying for a mile every morning. Drinking gator aid and pedialyte. Trying to stay hydrated. Eating little bits too. I wake up every morning between 1 and 3, with queezy belly. Eat a few crackers and sometimes just take a composine, hoping to get more sleep. It usually helps. And for insomnia, I take two Benadryl. I almost feel guilty for feeling good this time. I hope it continues. I'm even going to try to work a little today.
We went to an auction last night. Was weary about being around so many people, but it felt so good to just get out. Wore a hat, had a few weird looks, but didn't care. I like the short hair, haha. But must say, I wish it would just all come out. The stuble hurts when I'm in bed. I keep trying to wash rag it out, haha.
Love all your beautiful faces, hats, hair or the ole naturel. It's the beauty we all have in common. Love and peace to all of you. Here's to a good day to everyone.
Oh, believe it or not, my husband has been pretty good. I think when I wind up sick, really sick, he panics and turns away. So, here's hoping he gets a grip. men, I just don't get it......
😘. Ruth
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team