Starting Chemo October 2012
Comments
-
lou4of7 / halfcan - I also had the constant teary eyes, but then I caught a cold and was taking extra strength tylenol cough/cold - sure enough it helped the cold but my eyes stopped tearing and it didn't come back
However, I still also have the sore legs (calves and thighs), I am exercising though and trying to stretch a lot. Right now I'm typing with hot water bottles on my legs, helps a bit and epsom salt baths are good too. But yes, after sitting/lying and then to stand I feel like I'm about 90!
-
Evening/or Morning everyone (well in Bermuda its evening 10:02pm)...I should be over happy this evening but I think my hormones are getting the best of me. Wednesday March 13, 2013 I had my last chemo taxol and the blocker herceptin. I am super excited that that part of my treatment is now come to a closed.
I am now awaiting for my doctor for the schedule of surgery to remove the cancer from my right breast then start on the radiation. When I was in Boston at Beth Israel Hospital my doctor there didn't mention being on herceptin only for 12 months like the doctor said here in Bermuda, so I am a bit confused...Has anyone been on herctptin by itself for one year once finished with taxol/herceptin? I did send an email to my doctor in Boston to confirm this because he never mentioned anything like this to me before.
Also, I believe what really making me unhappy is the side effects I am having. I am taking the Vit.B6 but the hot flashes and now my finger nails and feet are just gone a-wall. I don’t feel my toes and half my feet is so numb. The tips of my fingers are numb and one nail is already lifting up as like the rest of them. They are breaking off where the white lines are..I notice its super thin there. I am getting so depressed I feel so not myself.
On a good note I do see some fuzz growing on my head. It looks like thee fuzz that are on peaches…its growing grey but today my husband said he sees some dark hear growing…my color was dark brown so we will see what grows back.
I am sorry if I sound so down…I don’t mean too…I guess today just insent my day today…I hope tomorrow gets better.
Everyone please have a wonderful weekend! As I will try to shake whatever this feeling I am going through away. Take care. . .
-
I don't get Herceptin, but from what I've read it is typical to get it for a full year, yes.
This group has been pretty quiet lately, everyone feeling better and getting on with whatever is next? I'm happy to report that I am starting to feel much better. If anyone had asked me at 4 weeks PFC I would have told them I really wasn't seeing much improvement yet. But now here I am at 6 weeks PFC and all of a sudden things are better. The "taxotears" have subsided, stuffy/runny nose much improved, the annoying eyelid twitching has almost completely stopped, and best of all my sense of taste is starting to come back. Eyebrows/lashes thinned, but hanging on. Numbness in fingers slowly improving. The worst thing is the muscle pain, and that is still there, maybe a slight improvement, but everyone says it will go away eventually, it just takes a long time.
Next week starting rads..... on to the next phase.
-
Ten weeks PFC of Taxotere/Cytoxin. I finish rads tomorrow. I have the muscle aches and tired body but that may be due to rads also. Still have some hair loss after washing.....probably should stop soon! I used cold caps and have overall alot of thinning but no wigs. I have to keep my port until July.....cautious doctor. Hope to never have to go back to chemo.....and so glad that part is over. I iced my fingers and toes so never had the numbness and nail issues. Anyone going to rads look into Aloe Force online. I used it and had minimal skin issues. Hope everyone is doing well.
-
Bermuda: I am on track to get a full year of Herceptin-only. I started it with my chemo and continue it alone now that chemo is over.
-
Last chemo was 2/1 and I still have no sign of hair
-
Halfcan..& LouBar ..Thank you for the reply...just wondering...how long will this last?? I forgot to ask my oncologist..Yes the constant tears just keep dripping down my cheeks...& the muscle pain does not improve from day to day. I am doing aquafit classes right now, & walking 3 miles ..2-3 times per week.. trying to strengthen my muscles..Every time I get up or get out of bed...especially the thighs...are very sore. But also noticed the upper arms are sore as well ...Still feeling very tired as well... Anxious to see improvement.
Will have my surgery (mastectomy & ax. node dissection) next week. Hoping things will improve...
-
hello all..
sorry i have not posted in awhile.. finished chemo on march 6th...finaly got rid of the migraine that was plaguing me since january...and now i have a really bad cold..
going for my pre op tests tomorrow.. probably going to cancel my MRI...cant see myself head down, for 45 minutes staying still...
also started up a dragon boat team... raise some money for cansupport, they have helped me and my family alot during all this...
sending all some purple bubbles.. be well
love
flower
-
Hi Ladies! For those asking about se's PFC.....I have a similar experience as others. The tearing stopped about a month after tx, my thighs stopped screaming about the same time. Right now I have about 1/4 " of peach fuzz......but that will be leaving me soon. I'm feeling that familiar itch and prickle. Grrrrrr Melissa- your hair will come in, I'm sure of it! I'm sorry it's taking a while. I can't wait to have hair again!! So tired of my head screaming CANCER PATIENT!!!!
Well, went to MO appt yesterday fully ready to tell him no to AC Thurs......I have just had enough & it makes me SO sick & emotionally crazy. Physically felt like there wasn't a break at all & AC slammed me. My 24th wedding anniversary was yesterday & I finally got out of the house Sun. to spend the day w/my husband.We had an amazing day doing simple things. I went in & talked to my MO & told him that I wasn't going to do it......but I changed my mind. I hold onto those positive days to get me through the bad. Thursday is IT!!!! Hopefully NONE OF US HAVE TO DO THIS EVER AGAIN!!!
Ya'll are amazing!!! -
Po-ke - I read somewhere that hair regrows slow while we're still on Herceptin...
Celine - Congrats on being done! Yay!
Andrea - I hope your final dose is better than the previous. I know AC affected me in the head, chemo-brain and just feeling down, but at least the end is in sight for you.
My chemo experience has been so atypical... After my last AC on December 17th, I didn't resume chemo again until February 18th so, despite having to deliver a baby and recover from that, I was still in pretty good shape (cell-death-wise or whatever) when I had my first taxol/herceptin. My hair had started growing back but then all fell out again at the beginning of March. Taxol is weird though, seems like the hair follicles only respond once and become immune because about a week after it fell out, it started growing again - right after my second tx. With all the partial falling out and regrowing, my hair looked ridiculous so today I just shaved my head again! I'm not sure how fast it will regrow but it's pretty stubbly so maybe that's a good sign. Besides that, I pretty much feel totally fine. I have two more to go so I sure hope this trend continues. I guess if you have to do chemo while pregnant and then with a newborn at home, no one should begrudge you a relatively easy time with chemo right...?
Hope you are doing well.
-
Marlene: "cell-death-wise" hahahaha this had me laughing out loud, thanks.
Andrea: I'm so glad that you got to go out with your hubby and that you decided to stick it out. As much as it sucks, I want to see you get the maximum benefit from these awful treatments!
Still not a sign of hair, the grows-slower-on-Herceptin thing is a comfort but that also sucks so who am I kidding why am I trying to see the bright side this is totally lame.
Celine: I'm glad you are feeling better. Don't back out of the MRI - they can give you anti-anxiety meds. You'll be ok. My first and only one was scary, too, but I took a xanax and I closed my eyes the entire time and visualized all of my friends standing around me in a circle. I never looked into the machine, but when it was over I realized the end of it by my head was open the entire time (just as I was hoping in my imagination). I'm so glad that I did it because the more information we have the better (I hope).
xoxo
-
Well i ended up cancellingall my pre op appts today as well as the MRI...put off till april 3rd
I have a horrible chest cold... my god i could not envision myself in that mri machine, with the pressure on my sternum and head facing down..not moving for 45 minutes...
the other appointements, including pre op "class" i post ponned because theres a storm out...
i feel crappy... so the nurse said it wouldnt delay surgery ... and not to worry everyone is sick right now.
She suggested i call my onc if i need any meds.... sigh, i hate taking pills, trying to kick it with vit D and C.... but i just might need more help
My hair is growing back... but i look like a clown... lots on sides and back, barely any on top. My husband calls the collor light brown... hes sweet... but its mostly grey..lol
Loosing a few toe nails too... so sensitive, neuropathy is in my toes and pads of feet... hope it goes away soon...
Looking forward to more normal days... till then...
*celine blows purple bubbles *
-
Oh... and btw.. anyone know iof its ok if i got to a nordic spa next week? 3.5 weeks after ending chemo?
And what about a massage..? i have this gift certificate im dying to use
-
Celene...hope that cold goes away quickly!
Po-ke... My last chemo was Jan 16 and I'm just seeing a bit of hair. Yours will come soon. :-)
Andrea... I'm also glad you decided to continue. It sucks but you will get through it.
Marlene... So glad you are feeling pretty good this go around with chemo!
LouBar and Lou4of7... My legs are finally feeling much better at 9 weeks PFC. Guess it just takes time!
I'm 2 weeks since last rads and still fire engine red and raw peeling now in my armpit. Glad that area is a bit numb from surgery nerve damage. I got my port removed on Friday and was back at the hospital yesterday as the glue came apart from my incision. They trimmed some of it and then Steri strips. So both sides if my chest are a sore mess now. The fun never ends. Still have toenail issues. Now the other big one is turning white and probably going to lift too. Now??? Geez..... On a good note ... I've lost 5 chemo pounds of the 15!!! And with no effort or diet. Must be just cause I'm more active. :-). Hope you are all having a good day today! Hugs. -
halfcan....good to hear that your legs are better..9 wks post chemo...it gives me hope. I am almost 4wks post last Taxotere & my legs & arms are still quite sore especially when moving after a rest period. Have not seen any improvement yet. Still have the teary eyes too...But hoping this will change soon. I have been pushing myself to do more exercise these past couple of weeks to see if it make a difference, but nada!!!Still hurts!!Especially the thighs & upper arms...
On a positive note..I have a bit more energy now..especially in the morning....fingernails & toenails are doing o.k. a bit of yellowing so I keep them trimmed short. I also keep polish (nail hardener) on them. I think that has helped.
Yeah!!!Congrats on losing 5 chemo pounds!!!that is so encouraging...I am also working on this...Did you feel you had water rentention ? I feel like I have...
Hope your skin is healing after the rads burn...it must be painful..good luck!
Celine...hope you are feeling better from your cold! I too am having some hair re-growth...especially on sides & @ the back of my head(slight peach fuzz)...not much on top yet!! I am hoping that by summertime I should be able to go out without a wig!! As far as a massage...check with your oncologist first...it should be someone knowledgable in lymphedema...my massage therapist is CDT (Combined Decongestive Therapy) certified..or at least knowledgable if you have lymph node involvement...
Marlene18....I am in awe... giving birth & resuming chemo?? Good to read your SE are minimal...best of luck with next 2 chemos & congrats on your new baby!
alcb70..good to hear the SE did not last long (1 month post chemo)i.e. tearing & muscle issues... I too may need more chemo post surgery...& I feel the same as you do...no more... but I know when & if I have to make this decision I will most likely do it again..Hang in there..& good luck...it will be over soon!
Wishing everyone a great weekend! And gentle hugs!
-
Jennie93 ~ thanks for letting me know that Herceptin for a year is what others are doing as well. Glad things are starting to feel somewhat normal for you now. How are your rads going for you?
Toots ~ thanks my dear. I so look forward to see how my hair will grow back. It seems to grow fast for what I see so far…time will tell…lol…Also, how is the Anastrole (hormone therapy) going for you? It’s something they gotten it incorrect the first time around…how odd. Is there known side effects?
Po-ke ~ How was your exchange surgery? What type of surger is it? Is it to remove the cancer from your breast is that what “exchange surgery means? I hope it all went well for you. Thanks for letting me know regarding the Herdeptin!
Caitgrace ~ I hope your feeling better from the chloroprep reaction. I am glad your still dancing.
LouBar ~ How is the radiation going so far? I still have surgery first then radition so I need to read more about the side effects.
Schoolmom ~ Good for you for finishing up with your radiation? How was it for you? My time is coming and trying to get all the inforamtion I need before I see the doctors. I am writing a list of questions so I can make sure I am full aware what to expect.
Halfcan ~ Congrats for finishing up with your rads! Thanks for saying better days are coming because I sure hope so! Lol
Karen3231950 ~ Congrats for finishing up with your chemo on March 13! I've finished my Taxol and Herceptin on Wed. Mar.13, 2013 too! It feels great to move on to our next phase does it? All the best!
Lou4of7 ~ Congrats for finishing up with your chemo as well! I also have watery eyes but I thought it was not having eye lashes…my thighs always seem to feel heavy when I get up too.. I need to get out walking 2/3 miles like you then perhaps my thighs wouldn't feel like heavy weights...I hope anyway...
CelineFlower ~ Congrats to you for finishing your chemo on March 6! I hope you start to feel better soon!
Alcb70 ~ Happy Belated Wedding Aniversary to you and your hubby! So glad to read you had a amazing time out even if it was a simple outing!
-
35smiling- I had 28 full breast radiation treatments and 7 boosts to the tumor site. I used a lotion called Aloe Force religiously and only had a little pink and slight peeling once but no real pain, scarring etc. It is Aloe with bark and some other added ingredients. I found it online when another girl was using it successfully in a trial. I am now 6 days past and my color is almost normal on the radiated side and only have some residual soreness in my left arm that goes up above your head during treatment. My dr. said it was just muscles that were not used to being used. I am hoping it gets better in the next few weeks.
Good luck
-
schoolmom ~ wow that sounds like good news. I got to get me some of that Aloe Force too but then again do you think the jelly from the natural aloe plant will work just as effective too? Here on my island aloe plants grows wild and I have a lot of aloe plants in my yard too…if it works…I would have to look it up how to skinned it for the jelly and put it in a container. I hope your left arm heals quickly too. Thanks again and good luck to you too!
I hope everyone is doing well this evening...and is having/or had a great weekend!
I received an email on Friday regarding my next phase for treatment which is continuing the Herceptin every 3 weeks until December 2013. My next treatment is scheduled for Tuesday, March 26, 2013. Then I fly to Boston for two consultations meetings on Tuesday, April 9, 2013 and my Lumpectomy surgery is scheduled for Friday, April 12, 2013. I am so nervous for this. I have very low tolerance for pain…I am like a child...I am trying to read up on as much information on this surgery...sighh
-
35_smiling Best of luck to you on your upcoming surgery; after all you have been through with radiation and chemo...a lumpectomy will be a piece of cake. You will be in my thoughts and prayers for a successful surgery on April 12.
-
karen3231950 ~ Thank you for holding me in your prayers. I still have another round of 7.5 weeks of radiation after this lumpectomy. The surgery for August 2, 2012 ~ Underwent Laminectomy and fusion of the lumar spine and the August 3, 2012 ~ Underwent L4 vertebrectomy and lumbar fusion. After the those surgeries a portion of my spine was replaced by rods. Then I had 9 rounds of radiation in that area to make sure they got everything.
-
Hello ladies-- after a week the rash went away so now I'm feeling better. Still struggling with hot flash city, alternating with being so cold and not able to warm up. We had snow for spring here so back to hats even though I finally have enough hair I often go without.
Had a dream last night that I caught my reflection in the window and had long flowing hair, long like mid-back length. Me and my hunny were both surprised in the dream "oooo look how long it's gotten" heehee
Hoping good luck with everyone on their radiation experiences, their continuation of chemo and/or surgeries yet still to face. Remember we are stronger if we stand together, share openly, and love profoundly.
Keep dancing ladies. -
Great to hear everyone's updates and slowly but surely we are all getting there.
35_smiling - I concur with karen, a lumpectomy after all you have been through will be a piece of cake, nothing to worry about...you underestimate yourself and obviously considering what you have been through and are still smiling you are a warrior
Try not to be too anxious.
Caitgrace - can't wait to have enough hair to ditch the hat - mine is growing and I even had to shave my legs and see some very small but definitely there eyelashes!
Finished radiation #20 of 30 today - so I'm on the final 10 countdown!!! yippeee. Skin is burning and my collar bone and armpit area seem the most affected. I'm doing all I'm supposed to so just hoping to get through the next 10 with minimal damage. Should have tanned topless when I was younger and toughened up my skin
Haven't filled my tamoxifan prescription yet...procrastinatingl Anyone else who's premenapausal looking at Zolodex?
Hugs to you all
-
Lou4of7 Finished my chemo 7th February, my last 4 also taxotere. eyes which were iritated, itchy and watery but have cleared up just in the last couple of days. Musle pain experienced, mainly in legs and thighs,now improving by the day calves still play up in the evenings but definitely getting better. Have found the exercise at aqauaerobics 3 times a week help, but also just a hot soak in the bath................ hope it improves for you soon x
Have lost the stone I gained whilst going through the chemo woohoo!
Sorry haven't bee popping in much lately, not so much time on my hands at the moment, trying to get 'life back to normal' whatever 'normal' is supposed to be x
Take care all, and things do get better, lots of hugs, Toots x
-
Hope everyone is doing well here. I have been in and out reading up on everyone.
I had to have a thyroid biopsy yesterday on 4 nodes they found during my CT scan in Sept. I was hoping all was well since I had not heard anything from my endocrinologist after the ultrasound in Dec. The procedure was not bad, needle biopsy where they withdraw cells from the nodes to send to pathology. Hope all is normal. Not really wanting another surgery at this point.
Keep your fingers crossed for me. Results back in a week but my appt isnt for a month. Take care all.
-
Hi ladies! I am a February chick but had a question for anyone who did 6 tx of Cytoxan/Taxotere. I am starting to struggle with some increasing fatigue since the week before my 3rd tx. I am now a week after #3. I am curious about how much worse it may get. I am still working full time but it kicks my butt by the end of the day. I REALLY want & need to keep working. If it stays like it is now, I think I may make it, with naps & early bedtimes! Any other SE's to watch out for during the second half of this ballgame?
-
Lisa, I worked right through 6x TC and found it very do-able. The later rounds were no worse than the earlier ones. In fact overall I think #2 was the worst. Everyone is different but I had very little nausea, easily controlled, and virtually no GI issues. All the other SEs pretty much fell into the category of annoying but not incapacitating. The worst thing for me was the muscle pain, really bothersome, and taking a long time to go away, but 8 weeks PFC now & finally noticing some improvement. Slow but sure. :-)
-
Schoolmom - really hoping everything is fine with your results please let us all know the outcome, prayers with you honey x
LisaMM - think everyone was different with the SEs from the Taxotere, I was real bad after the 1st Taxotere but the dr lowered my dosage from 170 ml to 140 for the next two seconds and they were a lot better, still had issues with the muscles but cleared over the last week, last session was 7th February!
Take care all, lots of hugs, Toots x
-
Happy Good Friday for those who celebrate it! I hope you had a great day.
Caitgrace ~ So glad to read the rash went away! I feel you on the hot flashes…they suck. I wish mine will be over soon. I rock my bold but wear hats when it gets too cold. Your dream sounds interesting…who knows it just may come true! Good luck.
LauBar ~ Okay I’ll take you and Karen’s word…I will calm myself down and not get too anxious. Thank you for your kind words! I hate surgeries and since Aug.2012 this will make #5 for this cancer…sigh…I can’t wait until I am completely over. As far as your 20/30 radiation wow you’re almost done! I hope your last ten comes by fast and you don’t have to worry too much on the radiation SE’s, all the best to you.
Toots ~ Hello there. Glad you popped in. All the best to you too.
Schoolmom ~ Praying your thyroid biopsy comes back normal. I have my fingers and toes cross for you.
LisaMM ~ When I was on Cytoxan and I was sick from the third, fourth and fifth day after but that was me…I hope it doesn’t affect you too much. All the best!
Jennie93 ~ Wow, glad it worked out for you…this should give LisaMM some hope.
-
Thanks for the info ladies, I appreciate it! Happy Easter!
-
Happy Easter to you too!
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