April 2010 starting chemo
Comments
-
Thanks everyone for the well wishes (HUGS)!! Other than being tired and a lil nauseous, I feel pretty darn good!! But the bad days do not hit until Sunday, so I will be uping the prayers on that day:) Anyhow, I hope you all are going to have a great weekend!
Susiesue- How long did it take for you to get your BRCA test results? Just curious when I might expect to receive mine:)
Kad22- I am in Illinois, perhaps we are not to far from each other? Maybe one day all of those that live close to one another could plan a meeting:) I have been part of a Trying to Conceive board for years and have meet some wonderful women in person via that board--the support they have showm me during this cancer stint has been amazing!!
Well, for those of you who have undergone chemo. this week, may your weekend be side effect free!! And for those who have treatments up and coming, Good Luck!!!!
-
SGJ05, my results took about 3 weeks. The nurse apparently receives word that the results are on their way, so then she calls to set up an appointment.......that way she actually called and talked to me before she saw the results, that way she doesn't have to worry about being asked over the phone........
-
Kad22 and SusieSue - I am unsure if I am truly triple negative... but I am "close"... here's the deal. Initially my pathology from my tumor (2.6cm) came back 91% ER+, BUT when I had my oncotype DX test done, my score came back a 71 (!) and my tumor showed PR-/HER2- and ER postive at 4%~! (not anywhere near 91). My onc. reran the hospital labs and took my file to dinner with the Oncotype people
The hospital labs on the second run came back a 31% positive ER and the Oncotype people stood by their results as it is a very controlled and sophisticated test. SO... that said we moved forward with chemo. (I was going to forego it if my Onco score was extremely low.) I am on TC x 4. At this time, after rads, I plan to start tamoxifen because my onc feels that I must be at least slightly receptive to Estrogen. I am questioning now, after reading your chemo recipe if I am doing enough.... with just the TC. My Round two is Monday and my onc and I are going to have a talk...
(By the way, I do have a lot of confidence in her and feel I can approach her with anything.... she tells it like it is.) Hugs to you both!!! Have a wonderful weekend!
-
Oh also Kad22 and SusieSue I will get my BRCA results at my appt Monday.. I will let you know!
-
Thanks Catlady for responding! Had Rd 2 it went well until this Monday when I started experiencing a very sore mouth and throat. I couldn't eat, drink, swallow and barely talk all week. Went to the ER yesterday -- apparently the Adriamyacin is causing inflammation in my mouth and throat. Count was down to 2.5 but today is was back up to 4.0. On antibiotic now. Rd 3 is on Tuesday... Feeling a little better right now. I'm completely bald now... I took charge of this dreadful disease and shaved the remaining few strands on Mother's Day... Nails are starting to turn really dark. Top lashes are pretty much gone now... Eyebrows are still intact. Will have breast exam on Tuesday and US some next week to see if tumor is shrinking... Just hangin' in there...
-
Arubajan05,
I too attended the Look Good Feel Better Program in VA. It was an exceptional program. There were four of us so it was really a "personal" setting. I learned a lot about how to correctly apply make-up, to make your eyes look like you still have lashes, skin care, etc. I agree, if anyone has not attended, then you should make every effort to do so. We also got to try on wigs, scarves, etc. I had a wonderful time and met three incredible women, each battling a different kind of cancer. Other than myself, there was just one other lady who had breast cancer so we got to talk, compare our stories, etc. It was finally good to be in the room with someone who's going through the same thing as me. It really helped me!
-
JenC,
Kinda similar issue. Was in for Rd 2 of C+A, when my nurse noticed that a stitch was sticking out. She got her stitch kit and was able to take it since it didn't dissolve. My incision was red too and luckily, she said that I didn't have an abcess. Stay on top of that... Good luck!
-
Had my second AC (dose dense) yesterday, and so far treatment hasn't been that hard to take. At MSK they use a lot of premeds for nausea (Aloxi, dexamethasone, Emend) on the day of treatment, and sent me home with orders to take dexamethasone and Emend for the first 2 post-treatment days, and Reglan, Zofran, and Ativan if needed for nausea. The most daunting part has been injecting the Neulasta on the day after treatment, but I've already done it twice, and it doesn't seem to be as hard as it I thought it would be.
Started losing my hair yesterday (Day 15) and it's coming out even more today. Already have a wig, a side/back partial wig, and a few hats and scarves, to prepare for the inevitable. They may actually look better than my regular hair, which is straight and fine. Had a friend cut my hair shorter, but probably not short enough. She was scared of what it would look like if I didn't lose my hair (fat chance).
marcy4--The AC went OK for me. I hope that it goes smoothly for you too.
caltex_catlady--I can relate to your vein stick problem. My veins aren't great either. I went for 2 consults--the first group insisted on a port, while the 2nd group actually cringed when I mentioned that the first group wanted a port up front. For other reasons, I went with the 2nd group. At my first chemo tx, I needed 2 sticks to get a good vein (especially important with Adriamycin, which can actually cause bad burns if it escapes from the vein). This time, I hydrated for a day prior, and with a heat pack prestick, the nurse got it on the first try. I need another 10 sticks before the end of the initial treatment, and then about another 10 sticks for the full year of Herceptin, so I hope that my veins hold out.
susiesue--Have you looked into The Wellness Community, which has several branches in NJ, for a support group? They just merged with Gilda's Club, which has other branches in the area. I just started the process of becoming a member of Gilda's Club, and the process is more arduous than I had expected--an orientation meeting, a one-on-one with a social worker, and a final telephone call with another social worker before the process is completed. My husband and I had the 2nd step on Wednesday, and still haven't heard back with the final telephone call.
emme--Hope your 2nd treatment, scheduled for today, was better than your last treatment. Let me know how you're feeling. Also, how long did it take for all your hair to fall out the last time around? My hair has just started falling out yesterday, and I'm curious as to whether I should expect the process takes one week, two weeks, or longer.
Happy weekend to all. We'll all get through this. 2 down, 6 to go (plus another bunch of Herceptin) for me. Hope to be done with the major treatments before the end of the summer.
-
Well, head was shaved today:) Actually feels pretty darn good. I was really getting down about the long strands comming out constantly and finding them all over the house. Got my wig fitted today also but went out to dinner with just a hat. My 5 year old thinks mommy looks pretty funny without any hair. Gata love it:) I would rather him think I look "funny" than be scared of it though:) I let him try on the wig and he laughed histerically. It was adorable. Gata take the good with the bad I guess. Round 2 of AC is scheudled for Wednesday. Hope you all have a great and SE free weekend. Hugs to all.
-
I have a question for those of you who have attended Look Good Feel Better already. I'm assuming you go without makeup so you can start from scratch, right? And do women wear their wigs, if they have them already, or go without? I'm signed up for next Monday night and am looking forward to it.
Karen
-
Catltx_catlady
The ladies in my Look Good Feel Better group removed our makeup when we got there. Everything is given to you in the box. If I were you, I wouldn't bother wearing any makeup if you are comfortable with that. Everyone in my group still seemed to have their hair, although some ladies hair was really thin. The women in my group were all told to bring a friend along to the class, but I don't know if all the classes suggest that.
Curious One - I hope my AC goes well. I like to hear good things from the other ladies who are on it. It seems like starting all over again and not knowing what to expect. I only have 2 rounds of it so it I think of that as a positive.
Jen C - Glad to hear your little one is enjoying your new look. My kids keeping watching the bald spots grow. I am glad they seem ok with it, too. I think it helps since it has been so gradual. I am actually enjoying the fact that I don't have to spend any time on my hair. I am afraid if I use a hairdryer, the bit that is remaining will all blow away!
-
Hi Ladies!
I too went to the LGFB class this week. It was a small class of 4. We all had differnt kinds of cancer and were in different places in our treatments. We all sat and talked at the end of the class. It was nice to share and be understood. I would really recommend this to everyone. I didn't wear any makeup because I knew we would be applying new stuff! ANDDDDD what lovely makeup and skin care products were in that bag! At the end I tried on a blonde wig and wore it home! I will try to post a couple of pics of my wigs.
I had my second treatment of AC yesterday. I took Emend this time and no vomiting last night. thank goodness. I have a port, and I am very glad I had it put in. Initially my port was tipped. Once the nurses realized this *the first sccess was a hard day) they adjusted the position of the need and used a little longer needle. After having the gallbladder issues and having lost 40 pounds in the process....this round of chemo my port magically tipped back to the proper position and it is smooth sailing. Even with the difficulties I encoundered in the begining, I woldn't trade my port for my arms.(I have a year of herceptin to follow this round) It truly is much easier.
On to my hair...Curious One last time I had weekly Taxol so my hair thinned gradually, not falling out in clumps like I anticipate this round. It took about a month for all my hair to be gone. Every day it looked like I had a mini toupee in my turban. My scalp was very sore...it felt like I had worn a too tight pony tail all day.
My head started to hurt yesterday...that same feeling. But no hair has started to fall out yet...I keep doing the fall out test - I try to pul out a few strands between my thumb and index finger...sounds silly, I know but I can't help myself...and so far no hairs have come out. I have about an inch of hair regrowth from February. I am wondering if I should shave it closer. It is really odd to me....but this time the thought of losing my hair isn't bothering me. I have just accepted it as proof the Chemo is working and it's attacking any cancer cells that might be floating around in my body.
I know some of you are experiencing Nausea. My first round of AC I had some vomiting, diarrhea and nausea that was mild but persistent with all three anti nausea meds. My Onc. had me come in for fluid and a steroid pack...it made all the difference in the world...I felt refreshed...and no more nausea. If I have any of these symptoms this time around I am running not walking to get those fluid again! A word of warning...the steroid can cause you to become constipated...so stay on top of that with a stool softener.
I hope all of you have a day free of SE. Enjoy your weekend!
Remember, Fight like a girl!
Emme
-
It seems I have developed a cold/sinus thing. Have any of you been told not to take anything like sudafed? I want to take day-quil, I'm on AC, no fever, low WBC (.2)...
-
raerae7074--If you can get in touch with your doctor over the weekend, that would be the best course of action.
-
Four days of feeling human left until TX #3 (then I'll be halfway done!!!). I dread each treatment a little more than the last but also look forward to it because I'm closer to being finished. Talk about messing with my mind...
I have a question. Is anyone else's hair growing? I still have hair all over my head, although very thin compared to my normal hair, and DH cut it to 1/2" 3 weeks ago. It is now at least 1" all over and no longer falling out. Only have a few "new" hairs growing in but what was left is growing like weeds. Am I the only one this is happening to?
Jennifer
-
toughmom38
I am four weeks out of Treatment #1 and still have quite a bit of hair. Cut it tonight to 1/2 " since there were bald patches on the top and back which were too noticeable to go without anything covering them. Treatment 2 is on Monday. I think your hair news is awesome! I hope mine does the same thing. I have discovered through this that I look better with short hair and plan to keep it that way when I am done all of this.
-
Marcy4. I am with you on the short hair. I have always had long hair but had my head shaved on Friday and got a long wig from the wig shop. My hairdresser had a wig for me to try that waws short and "flippy" and I love it. She gave it to me and I think I am going to use that one rather than the one I purchased and when my hair grows back I may keep a short cut. At least some good things can come out of this whole experience.
Hope everyone has a great weekend.
-
toughmom - I feel like my hair is growing too! What was left seems longer, and I kind of feel like there are some new hairs. My husband says he can't see it, but I feel like it is longer - like it's softer to the touch and just looks darker on my head. Thought maybe I was crazy so I'm glad to hear it's happening to someone else too.
-
Hi all,
Had round 2 of TC on Tuesday,so I'm half way through.(WOO HOO!) Hair still falling out like crazy (I can't believe there's any left) but still haven't buzzed it yet. No one in family can bring themselves to do it (And my daughter is a hair dresser!) When can lashes and brows be expected to fall out? Last time, they didn't fall out until about 6 weeks after I finished chemo. I'm thinking about trying Latisse when chemo is over.
Hope everyone is doing well and feeling strong .
Jennifer Q
-
Hi Caltex-lady, Karen
At my Look Good Feel Better class we were asked to come to the class sans makeup, but some women ( alot actually ) still wore it. It was harder for them because we didn't have access to water; we just used a gentle cleanser and tissued it off. I , for one, was glad I didn't have makeup to remove. Also, we were told (different than marcy-4 not to bring anyone for privacy reasons.) The women who had already lost their hair, wore their wigs. I was in the stage of mine falling out in handfuls. It gave me a lot of courage after meeting the other women and I shaved my head that night (last Monday) and started wearing my wig. I am glad I am wearing it now. I have received so many kind compliments and after just one week I so much more confident. I have also gone out with a scarf and hat over top. It's not as bad as I thought. I get more discouraged in my home, when I am just wearing a buff or something and look in the mirror. Reality hits me in the face then... Literally, I have cancer. I really encourage anyone and everyone to attend the Look Good Feel Better Class. The comraderie was great! (I even meant KimW who posts on this website) and the free makeup even better! Also the scarf, wig and nail tips were extremely helpful.
I am off to round 2 TC tomorrow. Also finding out the results of my BRCA gene test and having a big discussion with my onc regarding my OncoType DX score of 71. It's 1:30am here... I can't sleep due to the decadron... I am trying to catch up on stuff I have put off before my "crummy" week, but maybe it's time for an Ativan!
HUGS TO ALL!!!!
-
Hi,
My hubby is riding the vitual tour of California in my honor to raise money for cancer research. He is currently position 15 out of over 13000. The top three riders get their "I ride for" sticker on Lance Armstrong's bike during the Tour de France. You can cheer for my hubby once a day to move him forward in the race. Please help. It just takes a second to put in your name and email. I will be in Santa Rosa today to watch the second stage of the race.
-
Had my second treatment this morning. It was changed from FEC to AC and I was able to take it with no problems. I am hoping the next few days go well, but whatever the case, it is one more treatment down. I was told I would have 2 more ACs and then weekly Taxol for 12 weeks. Lots more to go, but each one is a great accomplishment! Best of luck to everyone else this week.
-
Hi Marcy, Glad things are back on track. Good luck with only having a few (or none!) SEs
-
Well, I had my PICC inserted this morning, good thing too, since my next chemo is tomorrow, and I didn't want to deal with the vein troubles that I had the last time. Also tomorrow, I will be having my head shaved. I started to shed on Thursday and my hair is noticeably thinner. My daughter, who is 20, is coming to provide moral support and help me pick out a wig. So, it will be an eventful day.
Marcy, glad to here that things went well for you today, here's hoping that this is the right mix for you.
-
Hi all,
It sounds like everyone is doing OK and moving forward. I am 3 weeks post round 1 of TC. Round 2 is tomorrow. I had shaved my head down to a 2 a few days back and this morning in the shower I lost the rest. Back on the Decadron which gives me migraines, at least it's only for 3 days.
JenC: Yes, I agree, we have to take the funny stuff where we can find it. My 11 year old was soo funny when my DH shaved my head. I handed him the camera and told him to take a couple pictures, but he acted like a fashion photog- he kept say things like, "gorgeous, beautiful, act like a tiger", I swear I couldn't stop laughing!
Arubajan05: Looks like our rounds are only a day apart now. That should make it easy to get together for lunch, since we have to wait until we are feeling better.
Bye for now! Fight hard- stay strong
-
March4 - glad to hear that you had a good treatment and hopefully the SE's will stay away:)
-
I feel so sad today. My hair is falling like snow...I don't mind that it is falling, I wish it wouldn't hurt. my head is so sensative. I just want it all to be gone. i keep telling myself I am half way thru treatment...my husband is taking advantage of my weakness...can I just crawl in a hole? I am usually so upbeat...I hate feeling like this. thanks for listening...
em
-
Emme: I felt the same - sad, sad, sad - but now it is gone and I am looking forward to getting done with the chemo and having it grow back. Went to a new wig place last week and hoping to have them this Saturday. Can't get myself to go out in scarfs.
-
Oh Emme - That was me on Sunday.
Saturday Evening I sat watching tv and my hair was just coming out all over the place. It put me in such a downer on Sunday - I was grumpy with everyone. I was surprised as I'm not normally one that fusses over my hair so the fact that it hit me so hard came out of left field a bit. I wore my scarf yesterday for the first time - I haven't completely lost my hair but from Friday to Monday the difference so so much and I had a bald spot at the front. I'm feeling better now - have made the decision to shave what's left tomorrow morning (everyone kept asking when are you going to shave - I just couldn't go there until today and won't promise not to cry when the rest is shaved off!) and am going to a wig shop on Thursday (before TC #2 on Friday) to see if I want to get a wig.
I hope you feel better soon - like you said in your post your half way there. I guess we just have to continue to take it one day at a time and we are so lucky to have this wonderful group to help us through
-
Hi Ladies - Just checking in to see how everyone is doing. I spent the weekend taking the kids to all of their softball/baseball/soccer games. Kept me busy and because it was my weekend between treatments I felt pretty good. I am gearing up for tx #2 of AC on Thursday. I haven't lost any hair yet but I am starting to feel a little tingling of the scalp so I know it will be happening. I am just hoping that it holds out until Saturday since we have a wedding to go to Friday night and I would really like to have my own hair for it.
Emme - I am sorry you are having such a tough day. I am right there with you on this whole hair thing. It makes my stomach turn just thinking about it. I am sending you lots of hugs and thoughts for the rest of the day!
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