Taxol Chemotherapy
Comments
-
JulieLynn- congrats on finishing up! It is reassuring to know that many of us are feeling the same anxiety at the end of treatment. I have always been such a positive person..but like my BF tells me..after having the crap kicked out of me for the past 4 months its gonna take a little time to recover mentally as well as physically. {{Hugs}}
-
Kelley and Julie yes I too am convinced that the pet scan is wrong and dr is lying to me. I keep telling my mom and she laughs and says they wouldn't do that. I'm not so sure. I guess only time will tell. Do they do MRI or cat scan at end to see if anything shows up? I'm paranoid I know, thought I would be celebrating...
-
FLislander- I guess there is no real way to check to see if the cancer is gone..we just have to have faith..I just feel very challenged in the faith department these days..
-
I haven't asked yet how they will follow me for recurrence - That's on the list for this week. It's hard to have a little faith when you've been smacked down so many times.
-
Hi everyone, I'm new to this thread - I have just received my second dose of Taxol (every week for 12 weeks). I am experiencing a lot of difficulty sleeping, this didn't happen to me on AC, in fact I slept really well on AC (DD every 2 weeks for 8 weeks). I'm hoping they can cut down on the steroids, maybe that's causing the insomnia?
-
Hi Marina
Yes that is another SE of taxol, dr put me on tramadol or something I forget but it gave me nightmares for 3 nights. Only took one and quit. I am taking anxiety medicine, still have surgery coming up soon. It could be steroids, but the emotions seem to outlast the steroids. Try and let us know, Quaatsi quit the steroids check with her. -
marinakaplan, I have my 2nd dose of Taxol (4 very 2 weeks) and finished A/C also. I have not slept well through any of it and am thankful for a decent night of 5-6 hours. I almost always wake up at some point. I try not to nap to help me do better at night. One Tylenol PM helps me get through a longer stretch. My first 3 days were difficult with the steroids but that has been better on Taxol too. I'm diabetic, so the steroids kicked my sugars in a nasty way, but even that was better with Taxol. Some nausea a few evenings, but not as much as A/C which was constant. No appetite, but food tastes better. I keep my Kindle by my bed so I can read when I am awake at night, till I can fall back to sleep. We all need rest so much! I pray you can get some good, deep, restorative sleep.
I told someone yesterday, when they asked how things have been for me, that it hasn't been easy, but it also hasn't been impossible. I have not had the worst of SEs, but am not breezing through either. This past treatment, I got a whopper of a cold on top of everything and am praying that it won't affect my blood counts for this next treatment. I'm not usually negative, but am expecting a call tomorrow telling me I need to bump my treatment for a week. I hope not! Happened once - it is probably when I caught this cold! I've been doing alot of resting and staying in, and am feeling better, so we will see.
Overall, the Taxol is easier. When I look back at my list for SEs from A/C, there are many more. But the leg/joint pain was nasty. Couldn't get away from it. I still have my eyelashes and brows, but they are getting thinner and thinner.
I was hoping they would hang in there!
Always amazed at the variety of treatments...I know it depends on so many things, It just amazes me.
-
Hi Marina- welcome to taxol..sleep issues seem to have happened to all of us. I take a benadryl and an ativan every night to sleep..I'm gradually stopping the benadryl but I also did not have this issue on A/C.
-
Hi Marina, not sure how many days you're on steroids, I get them during infusion and have been gradually cutting back. Still greatly affects sleep. The benadryl does make me sleepy and I'm sure that takes some of the edge off too. Sometimes an Ativan that night too.
I've been taking calcium/magnesium before bed, supposed to calm things a bit.
I hope you can find something that helps.
Andimom I hope you recover quickly from your cold and are able to have treatment as scheduled.
Feel well, Laura -
I only get steroids on day of infusion and still don't sleep well for two weeks between hot flashes and getting to sleep
-
Hi BethU-I'm on weekly taxol x 12. Started end of Dec and have four to go with one delay b/c of low WBC. Because I'm on weeklies, I can't have neulasta as it has to be administered and then followed by a 14 day wait, so I'm getting neupogen shots 3x a week from now on. Tx on Wed, then neupogen Th/Fr and Mondays.
I'm taking effexor for hot flashes and so far they haven't been at all bad--mainly just interesting. I have a hard time believing my white count was low because I felt so good considering I'm getting Taxol. I can say that the neupogen shots seem to have helped me feel better--I think you aren't supposed to feel SEs from low white count itself--but I was pretty fatigued. My RBC has always been normal. I hiked six miles RT yesterday in Sedona at my normal crazy pace--and felt fien throughout. My onc. said that exercise was a really great thing to boost WBC so I'm stepping up my activity levels.
Getting through these Taxol txs is like watching the glaciers recede. It seems to be taking SOOOOOO long....
But my hair is growing back--in a few weeks it looks like my prison haircut will be more like a Sinead O'Connor look. I'm going topless more and more in public and I don't even think about it much...was white and fuzzy, now getting darker and darker.
Claire
-
Wow, thank you all for your responses! I will try attivan, I loved attivan during the AC phase, it was my rescue! i try not to sleep at all during the day and try and excercise regularly.
good luck to everyone on this roller-coaster journey.
-
Marina- I see that FLislander mentioned that I quit steroids and yes, that is true. I had two doses and not very high doses either. By the third one, I refused it, which is our right. Here is the reasoning--
first of all Taxol can produce an allergic response which is preempted by the steroids. Therefore, you either do not know if you are allergic to it or you know that you are by your response shortly in the infusion process. Buyt the 3rd time, if you do not have a bad response-as my ONc told me- you are unlikely to have one in the future.
That said, they do keep hydrocortisone handy in case you do react and then, you get a hefty dose but you need it and it saves your life.
I had no reaction and therefore, felt no need to bombard my body with any more drugs than those that were needed.
Be careful with ativan-- you can develop immunity to its lovely sleep effect!
Good luck with Taxol-- I am done with it and off to another set of new chemo. Q
-
Q- I hope all goes well for you during your next round of treatment!!!
-
thanks Kelley.
I rode my horse for over 5 hours yesterday (about 15 miles) and I ached from head to toe-- BUT, I still can get out and do things I love. This new chemo (Navalbine) has its own unique profile of side effects, intense fatigue being one of them.
Thanks for your support! Q
-
Quaatsi, sorry about the achiness, but that sounds absolutely wonderful!
-
Q
Hi good to hear from you , and still getting out there with the horses, what a peaceful treat. I only take steroids the day of infusion and I'm trying to cut that back, thanks for the info that it's ok not to take them, they give me a terrible time. -
Hi Ladies,
i just had the first of 4 Taxol treatments (every other week) last Friday after completing 4 treatments of A/C every other week. Prior to the Taxol treatment I had hand foot syndrome with my last A/C treatment but it seemed to have gone away by Friday's treatment. It came back with a vengeance on Saturday and Sunday I spent in bed because my feet hurt so much. Today my feet seem better but my right hand is still swollen. Has anyone had HFS and if so what did you do? On Friday the doctor claimed that it was rare to HFS on A/C and didn't seem overly concerned. But not being able to walk to me is a big deal....
Claudia
-
Marina: Q was a little head of me on the weeklies. I finished a few weeks ago. Anyway, I got them to cut back my steroids to 6mg in IV only with premeds no orals. I still had insomnia for a few nights with that
So I think the taxol can add to the sleeplessness. Anyway, most of the time a phenergan and a xanax were enough to help me sleep the first few nights. Other than the sleeplessness, I hope the weeklies are smooth sailing for you!!!
-
Hi all, This is my first post to these boards, but I've been lurking since my diagnosis. Has anyone else had problems with high BP, fast heart beat, or palpitations on Taxol? I've had 5 of the scheduled 12 weekly treatments and my BP is really inching up. My onc sent me to a cardiologist who did an EKG (fine), but he was concerned with the BP and a resting heart rate of 94. He is prescribing a low dose of a beta blocker to slow down the heart.
I've completed the four DD AC treatments and did well. I have a little finger and toe neuropathy that seems to resolve towards the end of the week after each treatment. I must admit, that after the visit with the cardiologist, I just went home and cried! I feel that I just can't stand any new meds.
-
Hi Elaine, sorry you have to be here but welcome.
I have been troubled by a fast heart rate since beginning AC. I am now approaching my 4 of 12 taxol.
My heart has been as high as 115! Prior to chemo my resting rate was in the 70s.
Lately it has been in the 80-90 range. While this has me concerned, the onc is not as worried. She always checks again and finds it has slowed down. Glad your EKG was fine.
I do find it is worse when I am anxious or more fatigued and from the steroids. Are you taking them more than one day?
I hope you and your Drs find the best way to ease your symptoms and your mind.
Laura -
I have my 2nd of 12 weekly taxol's tomorrow. Its seem liks I am on a crazy number of steroids. 10 pills the night before for a total of 40mg, IV the day of, 3 pills the day after and 1 the 3rd day. I was a jittery mess last week. BUT the deep bone joint pain didn't hit until the night the steroids cleared my system. They lasted about 36 hours. If you are taking less steroids, what has your bone pain experience been like? And was the pain consitent across the weeks? I work out and am used to muscule pain- the bone and joint pain was like nothing I've ever experienced and it was BAD!
-
KCD - I just finished 12 weekly Taxol today. Yippee!!! I had steroids Sunday thru Wednesday but not nearly in the amount you are getting. Thursday night my leg aching and weakness would start but I would not call it deep bone pain. Definitely some weeks were worse than others - I don't know why but it doesn't sound as bad as yours. I'll take my last steroid on Wednesday and I'm anxious to see how long the achiness and weakness lasts. I always felt better Sunday night after I started the steroids again. Do you tend to overdo it or do you get lots of rest? Have you tried any pain medicine? What kind of other pre-meds do they give you before the Taxol? The only medicine I take after the steroids at home is Ativan to help sleep at night and Zofran on Tuesday and Wednesday only to help my stomach. But I get steroids, Prilosec, Aloxi, Alavert, Benadryl, and calcium and magnesium before the Taxol and just Tylenol before the Herceptin. If you don't get it, the calcium and magnesium might also help. I hope your next tx goes much better! Definitely talk to your oncologist or nurse about it - They should be able to do something to help!
-
JulieLynn congrats on finishing Taxol!! Today I have # 6 of 12 weekly Taxol. So far I have had minimal achiness and weakness. I did 4 DD of A/C prior to this treatment. I am looking forward to my last infusion
-
I'm currently sitting at my second Taxol (every 2 weeks, DD) and doing okay. Not looking forward to Thursday when leg pain starts. I have had a fast heart rate off and on, but no high blood pressure...quite the opposite!
I get a steroid, benadryl and Pepcid as pretreatments and have pain meds and anit-nausea meds at home if needed. Have never taken steroids orally for this. The dose they give is a 3-day dose.
Doing okay but will be so glad to be home.
-
Wishing you well Andimom
-
Week 7 of 18 done, still feeling ok, more or less. Feet are a bit tingly and sensitive but it eases off when I walk around. On a steroid high now so hoping to get lots of work done tonight. Sending positive thoughts to all.
-
Right there with you on steroids, Ank066. I just caught up on a bunch of "Words with Friends" games, watched 3 old "Greys Anatomy" shows and now am here. Actually got some work done at chemo today, so I'm curling up with my Kindle in a few. Taxol first night, definitely not as awful as A/C. Thursdya...yuck! I'm glad your feet aren't unmanageable. Last time it was painful to walk for 4 days. Positive thoughts and prayers right back at you!
Sleep well, everyone. Sure am thankful for your support and wisdom.
-
Just had my fourth taxol,
I've been wearing crocs shoes since I started taxol and those shoes have saved me fom hitting my toes at least 20 times. They are serving me well
Good night
Cindy -
Sandlake - Thank you!! I had the four DD of AC before too - Taxol is definitely easier but not exactly a breeze either. My last dose of steroid is tomorrow - I'm soo happy to be done with those and hope the extra weight comes off easily and quickly.
For any of you that are icing, I found that holding frozen water bottles in my hands instead of putting them directly in ice worked pretty well. My numbness, tingling, and prickling has been pretty minimal and short lasting when I have had it. I did put my feet on top of an ice bag instead of completely in ice with the same results for my feet.
Wishing all you luck and few SEs as you finish your Taxol treatments! The end of it will be here before you know it!
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