Starting Chemo in July 2009
Comments
-
Hi ladies
I have numbness in my fingers and surprisingly in my cheeks!! My onc says I'm only the second person he has had this happen to. But it gets better as time goes on. As I am done with taxol I am looking forward to the end of the SEs, just not sure how long I will have to wait.(4 weeks like Josybee perhaps) I am VERY tired now, probably the cumulative effects of all the chemo, and not sure if having it all dose dense makes me more tired. I feel like I've done pretty well over the chemo time despite having a sinus infection, broken bones in my foot and shingles.
I THINK I have been getting thrush too. Is it the white tongue thing? That would account for things not tasting great. But by the time it's my next appointment it has always gone.
Those of you who have already started rads, how long between your last chemo and first rads? I have the consult on Tuesday and am worroed about starting quickly when I am so tired and still have shingles etc. But of course if it affects tx I want to get going!!!
Hope you are all having a good weekend.
-
Gillyone - I started rads 4 weeks after last chemo tx (T/Cx4). Hope the cumulative effects of chemo wear off quickly for you and that your shingles go away soon.
-
Gilly, I had 20 days between last chemo & 1st rad (Sept 10-Sept 30) I took naps almost every day for the 1st 3 weeks of rads-either came home at lunchtime for a power 20 min nap or took a half hour or so one right after work, but this last week, I didn't nap at all. My rad onc said that sometimes with chemo after it's out of your system, the energy level is increased even while undergoing rads--seems to be that way with me (so far!)
Joni2
-
Hi everyone just thought i would come say hello its been awhile i have finished chemo and now taking tamoxafen all is well just some hot flashes once in a while....
-
Eliz-how long have you been on Tamoxafen? Did you chose that over Femara, Arimidex or Aromasin? Or did your onc just chose that for your treatment?
-
thanks Joni2 and chrisct
-
Hi to all,
So far taxol #5 has gone smoothly do not know whats different but I am doing much better. I even felt like going out day after chemo and had more engergy than normal. I am sure by Fri. or Sat. Fatigue will set in. At least I can eat and function more normally. Thank goodness!! 7more weeks of Taxol girls and I will be finished with chemo YEAH!!
Take care,
Edie
I
-
Just checking in...just finished Taxol #3 on Monday. 9 to go. Feeling good, no side effects to speak of. Eyebrows and lashes gone, but hair returning on head...YAY!! Some unpleasant taste sensations, but nothing like A/C. Hoping this continues to be tolerable.
Hope all is well...July seems like ages ago in some ways. We've gone through so much since then it seems.
Enjoy the fall,
Joni1
-
Glad to hear the treatments are going well for all. I am finally starting to feel better. Met with PS and surgrey is after the first of the year. Can't wait for the exchange. Ready to live life again. The hair is coming also. Have a great day Dianne
-
Hi everyone... it's been a while since I last posted... I had my Taxol #4 (weekly) on Monday... although Taxol is sooo much better than Ac was... the neuropathy is getting worse. I too have it in my face... my cheeks, lips and tongue... I feel it down my back and in my ears! I would say I have flashes... but I can't tell if they are hot or cold.... kind of like icy hot. My feet are kind of numb and tingling and on my right side I have it half up my leg and all of my right arm and into my shoulder. I was put on Neurontin and was told if this does not help I will start on Taxotere on Monday instead of the Taxol.
My hair is fuzzy... my fiancé says it feels like a tennis ball... he is right!! lol but when I step outside... I can feel the wind blowing in my hair... makes people laugh when I tell them that
... lol
Prayers for all!
Elizabeth~LovingLifeToday
-
Eph 3 i have done alot of research with some help from my onco. i also went to some support groups to find out about all the different drugs out there for bc i choose tomoxefen for my ++ hormones. i havent had any side affects other than once in a while i feel tight in my hands but i do have some arthrites anyway also hot flashes but everything is very managable. i did also research vitamins and the projestrone cream but i am not going to fool around with my body .....I have been considered a health nuts since i was young and also brought up with homeopathic medicine all my life .this is very much a change in my life. haveing cancer has change my life. if things change than i will check into other options ferema is to new on the market its still in the testing stage .....i do have a health doc i go to also and yes i still take homeopathic meds
-
Lovinlife
I also have white fuzz and some hair coming back. Looks like a newborn babys head LOL. I guess time will tell if Taxol will make it fall out..
-
HI ladies, Started rads yestrday, today is only my 2nd day(can't wait to be finifhed) They wouldn't give me my Herceptin last week due to the fact that my mugascan showed ejection fraction at 50%. Now I have to see a Cardiologist on Thursday. I know I will probably have to have an echocardiogran but I don't know what else they do. Anyone have any info on that?? Any info would be helpful. Thanks,Joanne
-
Popping in to check on ya'all. Sending prayers to those of you having yucky SE and rejoicing in all that have finished Chemo. Hard to believe we all started this in July and here it is almost halfway through November!
Stay strong ladies!!! Lisa
-
Hello triple j's. LovinLife, I just got done with taxotere and very little SE's. The only thing that I got was from the steriods. Little sleep the first night and thrush and fungus on the arm. they can be handled. The taxotere makes the bones ache but that might be the neulasta shot. Sleep when you need it and take tylenol or advil for the pain. it usuually popped up for me on days 4-6. Otherwise not bad. The hair is getting where you can see it. Going to ditch the hat if the hair on top thicker. It is coming. Had to shave the armpits and going to shave the legs tonight. Have a great day Dianne
-
Yes, Quarter405... baby fine!! I have my hand on top of my head every time they are not busy doing anything else.. hehe As soon as I don't see scalp anymore, I'm going out in 'my' new hair :-)
Thanks Dianne! I do feel much better on the new meds, but he did say they only mask the systems not fix them. I did decide to stay on Taxol for a couple more weeks and then make a decision. With the meds, I do feel much better... I just don't want long term effects from it. I'm glad to know that the se's are minimum with the Taxotere and you are doing well :-) I'll be ditching the wig too when I no longer see scalp!!! And I may treat myself to some new earrings as well... I've tried on some that I already have... but they looked sooo much better with the much longer hair... lol
I can't wait to get my eyebrows and eyelashes back again!! I have some... but you have to look really hard for them and my eyesight is not the best anymore!! lol
I hope everyone has a beautiful day as we are all beautiful women!!!
LovingLifeToday~ Elizabeth
-
ok....I have a new question. My last chemo was Sept 9 and I have been on tamox for 1 month. I now have fine, fuzzy hair all over my face! Will this go away, or what can I do to get rid of it????? Exchange surgery next Thursday....cannot wait!!!!!!!!!!!
Hugs,
Linda
-
I also have fuzz on the side of my face so I would like to know if it will go away?
-
I've always had fine, light hairs on my cheeks, even before all this. Maybe with your head hair gone you are just noticing it now or is extremely noticable? Mine's not.Joni 2
-
My fuzzy face fell off with Chemo. and hasn't come back. Small favors to be thankful for. I think Eph3-12 is right. I know I have seen freckles I never noticed before but I think it's from lack of hair on my head.
-
I can't have my Herceptin treatments, ejection fraction was 50% and had to see a Cardiologist today. Have to start taking 2 pills for the heart and have echocardiogram and stress test in the next 2 weeks, so I don't know if and when I will be getting the herceptin again. Anyone else have this problem??? Still doing rads though, #5 tomorrow.
-
I can't have my Herceptin treatments, ejection fraction was 50% and had to see a Cardiologist today. Have to start taking 2 pills for the heart and have echocardiogram and stress test in the next 2 weeks, so I don't know if and when I will be getting the herceptin again. Anyone else have this problem??? Still doing rads though, #5 tomorrow.
-
Hey Triple Js-Just thought I'd report in. Finished radiation yesterday!!!!!! Start Femara on Monday-seems never ending!
Joni2
-
Joni2 - Congratulations on finishing RADS!!!!!
-
Hello Triple J's. I hope you are all having a good weekend.
Congratulations Joni2 on finishing Rads.
Josybee I hope you get your heart issues sorted out. I cannot really comment on Herceptin as I am HER2- and cannot take it.
I haven't started Rads yet, I'm going to be marked up on Tuesday, not sure yet when they will start. Can't say I am looking forward to it, but it is the next stage and I should be finished by Christmas.
My hair has started to grow back a little, I have the fuzzy baby hair on my head and not much in the way of eyebrows or lashes. I am ready for my nasal hair to come back too, I'm fed up with the constantly running nose!
Sending a wish for minimal SE's to all still going through treatment.
-
Hi Jayne
I start rads today. Got my tattoos and dry run last week. I am beginning to post on the November rads thread. So many of the Js are on the October thread.
Congrats on your hair!! I have not noticed the return of any hair yet, but I am only three weeks out from DD taxol so I probably need to be patient. Like you, I would love for nose hairs to return - I am sick of constantly wiping my nose. On the positive side, I am definitely less tired now than when on chemo.
Have a good day everyone.
-
Good luck with the rads gilly! How many? Joni2
-
Joni2 - you get done and I get started!! 33 is the total.
-
Gill good luck with your rads.
I'll have to start reading the November rads thread to see what to expect. Today I went for my marking up, had a CT scan and 3 very small tattoos. My dry run will be 26th November and my first real session is 30th November. I am only having 15 though, so will be finished before Christmas.
-
Jayne- great news. I am looking into my crystal boob and I for see that everyone is going to do great in Rads.!!!
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