Chemo May 2011
Comments
-
LAureen
On decadron pills one day prior and one day after the infusion. I also get it in the infusion. Affects my sleep. Going on a sleep binge today. CAn feel it. -
Laureen: I'm on decadron as well, day before, day of and day after. Plus infusion as well.
I did not have the super energetic effect or sleeplessness from them, they made me an emotional wreak. Today I'm not on them and feel better, more stable.
Hope you're feeling better.
Cyborg: my period started day before chemo. Stopped almost completely after infusion, not long enough to finish my cycle. I hope it starts again as the lining needs to shed. Maybe our periods will be abnormal for a few months. -
Cyborg and DebRox,
Thank you for the Decadron input. My oncologist puts me on day of infusion, 2nd, and 3rd day after. So far, it's just the sleeplessness that drove me wild.
You mentioned about period. I missed my period 12 days after my first infusion. Just got it back on day 16, day of second infusion. I thought i was the only one with the period problem!
Laureen
-
Laureen, they give me decadron in the iv and that is it with the second treatment. The first treatment they gave it to me for 3 days after, 3 pills each. I told the mo that it made me crazy so they didn't give me any this time. They said it was only for nauseousness and since I have been somewhat ok with that they said I did not need it, and I am ok with that. I take zofran, compazzine, and lorazapam for the nausea, I don't feel too good today, kinda weak and it is my doctor appt. day. So i am 5 days past 2nd ac. My naturalpath doc put me on digestive enzymes and it really helps with the constipation, weird, huh? Maybe ask your mo about that, mine said it is ok.
-
bkj66,
I hope you feel better soon. I'm on 4th day today and still a bit shaky and weak. I will ask about digestive enzymes. Constipation is still with me despite colace 2x a day. i will add prune juice to my regimen later today.
Laureen
-
Bkj66
Sorry about the constipation, kid. Drink a lot of water! Maybe even a cup of coffee will help. -
I got through round 2 of AC yesterday. i have been sleeping a lot but feeling much better this go around. My MO changed my meds up so I've not been as sick (threw up for 12 hours after the first treatment). I did have the horrible headache for about 12 hours but it seems to have gone away now. I am alternating Zofran and lorazapem every 6 hours. Still taking Emend in the mornings as well. I'll get my nulasta shot this evening.
But overall, I feel pretty good! Praying that continues!
-
I am getting the steroids (Decadron) as pre-meds for Taxol, which I am doing before AC. So, the steroid does cause me to "buzz" around. I feel better than normal for about a day and a half and then it seems to wear off. If I get the infusion too late in the day, then I do notice I am up late the following night. I think the Benadryl pre-med prevents me from having a sleepless night on infusion day.
I think AC is a different story, however. When I start that, my Onc is suggesting taking the following, in this order:
Emend
Zofran
Compazine
Ativan
Colace -
Looking forward to any tips you lovely ladies can provide for the AC regimen.
I have a vacation (driving, not flying) planned right after dose #2. I know that sounds ridiculous. I am just not willing to delay it, even if the first half of it is spent in bed or on the damn couch!
Here's hoping everyone is feeling good. -
Hello all, Hoping everyone is having a good day. As for me, it's not a good day
. My hair is coming out in clumps, I have a huge bald spot in the middle of my head and I leave hair all over the house. I am 17 days after first fec chemo and I am sad
. To top things off I got my period on the 21st, I thought I would be through w/ my period and today it started super heavy. Heavy to where I have to change my pad every hour and a half, and I'm talking the overnight heavy duty pads. I read that tampons shouldn't be used on chemo patients so.. no tampons. I'm on my period, I usually have two heavy days per period and then i'm ok again, and my periods last around 2 weeks. I actually feel like crying, but I wont! I refuse! I have to look at the bright side of things, but it's difficult when i'm feeling sorry for myself. I am glad I had my hair cut a shoulder length, niece cut at least 9 inches off. I thought I was prepared for loosing my hair but... I still feel sad.
Hoping everyone is having a good day God bless!
-
{{{{{{{{{txladysara}}}}}}}}}
-
Thank you Neecee.
-
Patriotic, it all depends on how you specifically do on ac. I take all the meds they give me and have not thrown up once. I do get very tired on days 2-4, but I could ride in a car no problem if someone else is driving, as I don't get car sick very easy, I actually enjoy road trips. With my second ac I drank much more water and gatoraid (nurse recomended) and I have done much better with round 2. Also, just got back from doc appointment and my counts did not tank this time. Not sure if it was the build up from my 1 neulasta shot and 3 nueopgen shots from last time, but I will take it. I also followed my doctors advice about not being vegetarian during this time. I had some lean, grass fed organic beef that I incorporated a couple times a week into my diet. So who knows what exactly helped me, I just am much better than last time.
-
Post part 2! I don't know why I got so sad sitting waiting for my blood draw, as a group of us were chatting. There was a young man, another woman about my age just starting out, and a younger woman. All having a great conversation, talking about hobbies, laughing and having a good time, despite everything they are all going through. Why are all these wonderful people having to deal with this? Just made me sad.
On another note I asked my mo about the parp trials, he had nothing good to say about them. He had a patient that responded well to traditional chemo, then they worked hard to get her on a parp trial as she wanted, and her cancer spread and became more aggressive while on parp. I was feeling like the parp could be my back up if all this other stuff doesn't work, but he was not liking it, even for brca+ like am and this woman that did not respond well to it. I know it is all a crapshoot, but I have heard such good things about parp, this deflated my balloon bigtime.
-
Txladysara- I am bleeding a lot too. Feeling more sad today. I am hoping that I won't feel so sad. I know that losing hair is really sad. At first I was sad. Then I felt ok. Yesterday I was called sir twice. Today, feeling sad tired and sore. I am feeling scared about my sex drive . I know that my boyfriend is patient and loving but I am really worried about that. I fell so in sexual. Started a thread about this and hopped on another. Can I just say that ALL food tastes horrible and so dies the water. Even flavored water. Waaaaaaah!!!!! I'm just sad. I hope our days get better and I just have to keep reminding myself that I am LUCKY to have treatment.
-
txlady....was going to write earlier but my daughter called. Your experience above sounds a GREAT deal like what I've experienced, especially after my first chemo treatment. My hair was falling out in clumps up until last night and I became brave and shaved!!
-
Cyborg, I guess it's just part of the process, we must grieve a bit because our lives are changing so drastically
. I really wish I could be done w/ my period, that's what chemo does to most ppl. My sex drive, what sex drive lol, it's non existent right now, poor hubby, and of course I worry about him not having his needs met.
I too try to remind myself, I am alive and things will get better, I just wish I could be 6 months from now and things would be normal again.
Linda, sorry to hear that you were loosing your hair in clumps too, I have only had one treatment and was told by the time I go for my second I will have lost my hair, I guess they are right, having second treatment on the 30th. I don't know if I should shave mine. Did you buy a special shaver? or did you use a regular razor blade? Well they say that when it grows back it comes out really nice and healthy, looking forward to that.
bkj66 when I got my first treatment there was a variety of patients there w/ me, and I felt bad for them, first a lady w/ her daughter, she was wearing a scarf and she started vomitting while reciviing her infusions, and she would close her eyes, you can tell she was feeling bad. Next to her was an old lady w/ a turban, and she had no port and she was w/ her daughter too, she cried when they poked her and couldn't get the vein, they had to poke her in her other hand, her daughter comforted her and was telling her, please mami you need to calm down or your blood pressure will go up. Next to that lady was a very young man, no older than 20 I would say, w/ his mom and his girlfriend, he was totally bald. My heart went out to all of them
I hate hate hate cancer, I usually don't even say the word, I hate it so much.
Well on my side there was another lady, she left very quickly, she had something like a fanny pack, and left, and next to me was a lady, she was getting her last chemo, she had family members come and go, and when she finally finished, I could hear them all clapping. So that was positive
Hope we all get there soon!!! I hope the days go by quickly and before we know it we are all done w/ chemo and back to our normal lives.
God bless us all
-
txlady...I had my my period on Mother's Day...5 days after my first treatment. I thought the same as you. For me the end of periods was going to be a blessing. I haven't had it since. Going for third treatment on the 31st. My hair was fine until about 2-3 days after second treatment. I got tired of the shedding. It was too sad. I used my daughter's clippers (she use to do hair) and then used my leg razor (Infusion- Ironic!! or something like that). Razor had soap around the outside and it was almost impossible to cut myself. I started out crying as I began and ended laughing. You have to laugh at the way your body had done a 360. If you are really depressed though, call you doc. They gave me antidepressants right from the start. Adavan for sleeping at night and mood adjustment as I sleep.
-
I have a mirena iud so I have not had to deal with my period for awhile but my mo said he wants that out asap even though I am triple negative, he says that no one really knows the effect of it on triple neg. I just can't bring myself to have it out yet, thought i would get a few chemos under my belt to knock me into menopause first then have it out. It is a quality of life issue for me, as I too was having horrendous periods before i had the iud and i just can't deal with that right now. So sorry you gals are dealing with it, I know how awful it is, plus the se from the chemo.
My hair is crazy right now, shaved it with a half inch clipper guard and it is THIN. It sticks up all ovr the place and itches under hats. I have a wig arriving tomorrow, hopefully and then I work on saturday (i work in a hair salon of all places!) If my head is still itchy I am gonna say screw it and just were a hat and not a wig, and they are just gonna have to deal with it! Honestly, the other employees and clients are so nice they wouldn't care if I went in bald or with a paper bag over my head, they will just be happy if I feel good enough to come in. Once again, I ramble on.....Hope all of you are feeling better.
txlady-that sounds hard to deal with. I was just doing labs. So far I have had all my chemos in a hospital where I have a private room with room service and nurses at my every whim, this is because my mo is doing a 24 hour ac drip on me, it is how he does ac, says it is easy on the heart and he also believes it is more effective, and I already had ac 8 years ago. Once I go to taxol/carbo I will be in a community setting, although they do have privacy curtains. I hate to say it, but if someone is getting sick next to me, it will set off a chain reaction, and I know I would start crying if I see anybody else in pain or crying, that is just how I am.
-
I dont think it is fair that we are having periods. I think we are going threw enough with out that too.
Today I saw the radiologist, I will be having radiation on my leg and arm as apparently the cancer is there too , starting next Wednesday. I may be starting chemo on Thursday. The leg is very sore, there is damage to the bone. But with any luck the pain will go away after about a week of the raditation.
That is about it for me.
{{{{{{HUGS to EVERYONE}}}}}}
-
Dear May Girls.
I am from the March chemo lounge and just thought I would pop over to give you some good and encouraging news. I go for Tx #4 tomorrow of TCH-I am neoadjuvant. I had my midway thru scan this week and I have killed off (with the help of the drugs) more than 50% of my cancer. Had 1 tumour go from 3 inches to 3mm. Others have not resonded that dramtically but everything shrunk by at least half. All nodes appear normal in size shape and density.
It is a drag but the good results make it so worthwhile. It will be over before you know it. A lot of the March girls have finished up in the last couple of weeks. Stay positive-exercise daily-drink fluids-did I say stay poitive??? Good luck to all of you.
-
Lilylady,
Thank you for the encouragement. It is alsways nice to see that it is working well. It Helps Alot!
Candice
-
38 years old, glad you are finally getting some treatment started. So they will start chemo and rads for you the same week? You mentioned having a pin put in your leg in one of your posts, are they still talking about that? I hope you get quick relief from the rads.-Big hugs to you!
-
38yearsold, I agree it's not fair to have our periods when we are already dealing w/ SE. I really hope that radiation helps you w/ your pain in your leg and arm. {{{{{{{{{HUGS and LOVE to You}}}}}}}}}}
lilylady thanks for encouraging us!
bkj66 I know it's sad to see others going through this.
but how cool that you get your chemo in the hospital, VIP
Linda, I wish I owned some clippers than maybe I would get the courage and just clip it away. I don't really feel depressed, it's just that I am a bit sad, but I am sure I will be better once I get this hair issue over w/, once it's gone and i get use to it, I am sure I will be fine. But I do suffer from anxiety, was even agoraphobic for a while, but I am way better. Have a bottle of xanax in my cabinet, I am thinking maybe its time to take one.
Have a good night Maygirls
God bless and sleep well.
-
Lilylady! That is great. I am so happy for you!
-
Onc prescribed dexamethasone (same as decadron) am and pm on the day before, day of, and day after. They keep me up late and make sleep restless, wear off by 2 days after I'm done with them. Only take them every third week when I'm doing TCH, so, so far it's not too bad. Onc said I get it to avoid the edema in the legs that Taxotere causes.
-
I just want to say big hugs to you all! I had taxol #6 today and have experienced all of the same emotions as you all ~ sadness and anxiety have been so bad at times. This is definitely not
The time to work these things out on our own! We are fighting for our lives so are going to have many sad and anxiety filled moments in between better moments. Take all the help you can get and dont be afraid to get meds to help with all of these crazy side effects - mental and physical. And by gosh if you feel like crying - do it! It's ok! It's part of the grieving process of the way our lives have been and continue to be forever! I cry, get angry, get scared, and laugh a lot too! All healthy emotions!
God bless you all - we are strong (-most of the time) and together we can do this! Hugs to all!
Vicky -
Thanks MamaV for the encouragement to embrace all different emotions this journey brings us all. Take care everyone!
Laureen
-
Thanks mamav
-
hello sisters,
im so sorry you have joined us, but, you could not have found a better place!! im here to give you some encouragement, and some tips. my heart goes out to you, no one can ever understand what we are going thru, except us sisters.. i finished chemo last Nov 1, 2010, i was on AC x4 and taxol x12, i want to let you know a few things for all our new girls, there is light at the end of that long tunnel
its not fun but doable, and you will get there!
The main thing id like you to know,is to please let the chemo do its job, don't fight it, go with it.. ask for help if you need it!!! dont suffer through it alone... i cried,got mad,laughed,hated my hubby many times, so scared of whats to come, and its all very normal! you have been hit hard! but you will get through it!
remember, you are doing this to kick Cancer cell ass. i remember i felt like a scared kitten on the freeway, but it really does get better.... water,water water, you want to keep your kidneys and liver flushed from all the hard toxins, that was the hard part for me, water taste like metal, but so important, for all my new AC sisters, drink a lot of water while being infused, as you know you will pee red and you want the red gone before you go home, AC is hard core ONC's call it the (Red Devil), been around for 30 years, It sucks!! as they all do ... For all of us girls on any chemo, i was advised to flush twice with the lid down for a couple of days. the half life on the Adriamycin is about 28 hours i believe, and the Cytoxin is about 17 hours, and its out, im sorry i dont know about Taxotare or others. but lots of fluids..please stay on top of your meds!!, i was very blessed that i did not have any se's thru 16 treatments, but i did hit a bit of depression, well a big bit!!! PLEASE,PLEASE, if you feel it coming on tell your ONC, dont suffer through it.. know that is is only situational depression, and is part of the game sometimes. get a mild anti depressant i did...Take what you need to take to get you through this. I also had the famous Chemo Fatigue, third chemo was the worst it really helped to get up and take a walk and a shower, if your so fatigued that you cant, pop an Ativan and sleep through it,dont fight it..Remember Ativan is your friend, hehe this is your time to be selfish and take care of you!! listen to your body, wash hands always, AC girls you will have to have the neulasta shot 24 hours later,as you know, the Adriamycin wipes your white cells out. but the shot will super charge you, hehe, then they will drop again about the 9th day or so, some women have had bone pain from the shot for a few days, i did not, remember when your on chemo and your white cellsl are low, if you get sick it will come out in a fever, they call it an infection, u wont get sick like a non chemo person cause you do not have a lot cells to fight it off, so u will have a fever. Keep an eye on you temp,if you you think something is going on, and if your not good,dont take a Tylenol, it can mask the fever. no fresh fruit or veggies, they r touched all the time, you never know... now that im done, i know i did not need to be as scared as i was of getting infection, so please dont worry about it (i know easier said then done), but hand sanitizer always, and dont be afraid to tell a guest to sanitize when they walk in,or any nurses or DR if you notice..i was able to take down my pre drugs, i didnt like the Ativan in my port (IV), it made me too loopy all night, so she took it down to like 10, the decodron pills before taxol, i had 2 the nite before and 1 in the morning of, i always forgot plus it would keep me up, so i was allowed to go off the pills, but it was still in my port, talk to your ONC if something is not working for you,
BTW, Taxol was a piece of cake compared to AC, i went back to work, thanks to happy pills
taxol does not hit your white cells or red like AC and Taxotare, you will have much more energy,
i used Biotane mouth wash and tooth paste, and gargled w/ the salt water and baking soda 3 time a day, never got mouth sores, i did it all thru chemo everyday but really dont know if that was why? chemo really effects the mouth membranes, for the girls on the Taxotares and Taxol,these are very drying on the nails, and they can fall off
I used nail oil,not hardener, you want them moist
none of my nails fell off, but two toe nails turned a blackish color, again,who knows if it worked,or i was just lucky.....i think its worth a try... The Taxotares and Taxol are very famous for bone, joint pain and the dreaded neuropathy, i took glutamine
in powder form,1 tablespoon 3 times a day in about 4 inches of water the day after infusion for four days, i never got the neuropathy... that is the tingling, pins and needles and the numbness that can be permanent... i took B6 and B12, i never had bone or joint pain, i mean really its so hard to say if it works, everyone is different but, UCSF recommend it. i never lost my eyebrows, i used Latesse every night on them and my eyelashes, lashes thinned a lot, but very little on my brows, i started just doing it on my brows cause it cost so much, I did lose every ounce of my hair, except my brows and the hair on my head,( i used the PCC (cold caps) and it really worked, i saved my hair, it thinned a lot, i lost about 65% of it evenly... i know they have a Generic of latesse in beauty supplies that is about 50.00, much cheaper then Latesse, i heard it works as well, mind you i do have thick brows, and they did thin a little but only i could tell, hair on the head is gone by 18 days
im so sorry for that, they have beautiful wigs now and scarfs, remember it will come back,
down stairs hair was the gone by my third AC, that was kinda nice, hehe, as well as all body hair, nose hair goes as well, so u will prolly get drippy, friends who lost their head hair said they use a pet roller for all the lil fuzzies at first... where my hair thinned, on my head, i noticed it started growing back about my #5 Taxol, and really came in fast..Taxotare is stronger,the girls i know didnt start growing hair back till done
but before you know it, it will be there.. please girls no razer blades on your head, u dont want to cut yourself, im so sorry,
I started chemo june 16 or so, i had a normal period a week later, then i had a normal one July 22, that was my last, i had my hormone levels cked in September and my levels were like a 10, not putting out hormones, my ONC said that because of my age, i was prolly not going to go into menopause, so she still wanted me on the Tmox when i finished chemo, last Feb, we cked my levels again, and it was 85, im producing lots now, but my period has not come back,im taking the Tamoxfin and have had no problems its been 6 months...
Stay positive,and let it do its job!!!
wow im sorry for rambling on, please know you will get through it!!! your in my heart and prayers, if you wanna talk please PM me,and i will call or you may call me, i dont care day or night!! i made a lot of calls to wonderful women, and would love to be there for you!!! imno DR but i have learned a heck of a lot!!!
biggest hugs and love
Chey
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