Starting Chemo June 2013!?!?!
Comments
-
Lstewart--were u out for it??
-
Alibeths~~I was given twilight sleep and a local. I was very relaxed, but awake. I actually watched the port placement on the ultrasound screen. The doctor told me everything he was doing, and they kept making sure I was comfortable. I had no pain at all during or after. I even slept on the port side that night.
I finished chemo 2 weeks ago today, but I opted to keep my port for awhile. It will need flushed every 6 weeks. No biggie. I'll decide after rads whether to have it removed.
Blessings
Paula -
Hi starting chemo June 6th - FEC-D for 6 treatments . I'm 46 and very afraid also! Got my picc line on Tuesday.. Finished all my scans today... So fed up of being poked ... Touched.. Scanned etc... Good luck everyone and be sure to post how treatment went
-
Hi Everyone,
Joining the June Chemo Group with you fine folks. I had originally posted in the May group but had some delays and additional tests that pushed my start date to June. My actual day for starting is on Thursday June 6th.
I'm up and down with emotions. Lots going on. I feel I'm all set and ready to go. Seems like I've been waiting for a very long time to get treatments started.
Sorry we all have to be here but looking forward to sharing the journey with others at the same time.
Hoping everyone has a restful weekend.
-
Hi Val, I had my first FEC chemo 10 days ago May 22. I feel fine now. Main side effect was nausea for 1 week. For 3 days after chemo I was on decadron, emend and Zofran. I also took a gravol at night . I slept well. I never threw up and I ate often. Drinking fluids was more of a challenge with the nausea. I also had a bit of heartburn the first week and a few sore spots in my mouth.
Are you getting Neulasta day after? Take Claritin daily starting 1 hour before Neulasta- it can help prevent bone pain. I only took it for 5 days and got bad pain in my legs hips and back on day 7. Next time I will take it longer.
Not many of us doing FEC. Let me know if you have questions -
Hi lily28. Thanks for the response. Yes I will be getting neustala injections also.. Wow Claritin is that for allergies? Should I discuss with my oncologist before starting to take ?
-
Val~~You can discuss Claritin with your onc, but they aren't all up on the benefits of using it. The nurse/practioner at my onc's office told me, she had seen it work too often not to tell her patients about it. It is an allergy medication, but maybe the bone pain is an allergy we have to the Neulasta. You can get the generic (Loratidine) which is much cheaper but works the same.
Mouth sores can be prevented by using the baking soda/salt rinse.
Mix: 1TBS salt to 1TBS baking soda in a quart of water and rinse several times daily.
Swish for about 30 seconds and spit
I did it everytime I went to the bathroom. In 6 months of chemo I never had mouth issues.
Blessings
Paula -
Just dropping in to tell you all that you can do this. The side effects are no picnic, but the nausea meds do help. You do not have to lose your hair either. I used cold caps and kept all of my hair-and my privacy.
-
Hi Ladies,
I was just wondering if any of you were told that they would wait and evaluate whether you need Neulesta until after they looked at your blood counts after first chemo?
I mentioned to my Oncologist that I heard the Neulesta shots were the worst part and that is when he told me we would wait. Now I'm scared if I don't get the shot I will end up getting sick or an infection. What do you think should I tell him I want the shot? -
Hi Sunnyskys, re the Neulasta. The main benefit as explained to me is that it promotes formation of white blood cells. With chemo's effect on white blood cells the count can go dangerously low (neutropenia). Which in turn means you can get a bad infection and also means chemo will have to be delayed until the counts recover. You may know all of this already. My onc only asked me if I was covered for it as its very pricey. And I told him I was ready with the Claritin - he only said it "might help" the bone pain. But the chemo pharmacist told me that any antihistamine may help prevent the bone pain.
So I suggest you read more about it. Check out the April or May chemo group postings there's a lot of stuff about Neulasta or you can search this whole site for postings specifically about Neulasta- most ladies did ok with it. And then talk to your onc again. -
Fab 1 and Alibeths - thank you.
Jojogal123 - Seems like there are some medical professionals that down play things. I hear that there some that get minimal side effects. Meanwhile, getting informed is valuable. List of items to have on hand just in case, etc. Good luck to you.
Lgfoster123-Hope the next few days go o.k. for you.
Sunnyskys-I too had a tough time anticipating chemo. I feel you girl. We will get through this.
Paula-Congratulations completing chemo.
Had mybfirst chemo Thurs May 30th. Day of chemo and next day went fine. Pepicid was really all I needed and it worked. Swiched my mouth with baking soda salt, water combo for prevention of mouth sores, also did the same with coconut oil. Got my shot on Friday, Saturday, even with clariton, my body hurt, also brain fog. Felt weird but no nausea or mouth sores. Food tastes good, just wasn't into it. It's past 1 a.m. Going to try and go to sleep.Maybe I will count sheep.
For all that are starting your chemo soon, best wishes for you. Actually, best wishes to all.
Carla -
Hello Ladies,
I am in this club (that no one wants to be a member of) too. I start TCH on June 13th. 6 sessions over 18 weeks, followed by 1 year of herceptin and 5 years of an aromatase inhibitor. Doc says I will get neulasta day after chemo. Trying to make the most of the next couple of weeks.. still healing from lumpectomy with reduction....
-
To all of you starting chemo in June--
You can do this!!! It is scary, but it is doable.... make sure to ask for help--- get lots of rest and drink lots of fluids. Your body will tell you what you need (mine said only eat white food!).
Your onc will give you instructions on the anti-nauseau meds--- follow them!!!! they do help. You can live your life while doing chemo, albeit a little slower.....
I am almost 5 years out--I remember the fear of the first visit and how I just wanted to turn around and go home. I didn't, and now it is a distant memory, as is breast cancer. I had kids, a job, etc..... just like you. this really will fade into the background at some point, but for now, it is front and center..... take all the support offered. You are doing something that will hopefully eliminate the need for you to ever have to think about bc forever!!!!!
The first step is the hardest... good luck!
-
Thank you momand2kids
It really helps to hear from those who are at the other end! It really is inspirational to hear from you and keeping our spirits up and sharing your tips of how you for through it.
Many thanks
-
Hi everyone,
I am starting today also, sitting in the big girls chair as we speak..
Scared too... And I don't think from looking at all the advice here from previous chemo goers that I have drunk enough water.. Does coffee count???
Anyway...good luck to anyone else starting today, I am in Australia so will have a head start on you...!
I decided to do the chemo based on my oncotype score of 18. Not quite in intermediate zone but almost... And because I am 43 with four kids, aged between 12-7..
Thanks for all being here!! And as Fab said thanks momand2kids for kind words.. Good to hear!!! -
Ingrid~~Water is always best, but I don't like water. You do want most of your drinks to be non-caffein though. I drank decaf iced tea, but it wasn't very good once I started AC. I found that for me Raspberry Lemonade Gatorade quenched my thirst and was very tasty. I also drank flavored waters. Caffein is a natural diuretic, so it wouldn't hydrate you at all.
Blessings
Paula -
Hi
Thanks Paula for your advice... I do quite like Gatorade so think will get some. I had an uneventful first session of chemo, no adverse reactions.... So far...
Wish I'd tried the cold caps though, am regretting not giving it a go.. Saw Allibeth that you were on the cc thread.. I just thought it looked like a massive amount of work on top of a stressful situation but now that I've had the treatment can see that it could have been worth a shot..,
Eyes feel a bit odd, head a bit weird but other than that ok so far..
Fingers crossed...!! -
Hello there Bc friends ive decided to go aggressive with treatment and believe. Biting amdoing act...so afraidbuts its mybestodds putting it off till week of june10 need more time to process it.
-
Good on you Dlm,
I will be starting a week after you. We can best it thank god we have treatment no matter how unpleasant that can give us a fighting chance of beating this invader. I've decided to see chemo as a weapon to blast the cancer out of us, and god willing we will never have to use it again. Good luck any let us know how your treatment progresses. X
-
I must have been way out of it I do remember nurses talking but don't remember anything else nothing about the port placement or them putting it in just got done sore the next day but it was manageable. Chemo tomorrow have to leave the house at 4:00 am to have an MRI for spot on spine chemo blood draw isn't supposed to start til 12:30 hoping they'll take pitty on me and let me in earlier
-
DOES ANYONE KNOW THE CLARITIN REGIMEN FOR THE CLARITIN??? THANK YOU!
-
Take Claritin starting the day before Neulasta and continue for 5-6 days after. You can use the generic which is much cheaper. (Loratidine)
Blessings
Paula -
Thanks! I got the 24 hour, so I guess just 1x a day..
-
Im starting in 7-10 days!!! Im so scared I could scream and run away....... Trying so hard to be brave and positive but Im not at all!!! 4 rounds of AC (Or maybe it was AD) followed by 12 two combo something, paclitaxel?? Port going in as soon as they can fit me. Feel to scared to read up on drugs and what I need to do. Its been a crazy roller coaster for 3 weeks since diagnosis. At leased they did find the primary source and now what they are dealing with.
-
I am one of the May girls just thought I would share about the claritin. My chemo nurse said to use claritin and aleve. I am also in my early 30's there seems to be quite a few of us. Lets kick some cancer @$$
-
Annika - it is scary I try and concentrate on one thing at at a time. And appreciate any of the good days or hours. If not, then it all becomes way to overwhelming and the good moments lost. When you do decide to research any topic regarding your procedures etc., I suggest setting a limit on time per research. It really is good to have knowledge behind you, but sometimes too much research at one time can be a little depressing. At least for me. Sometimes I have to remind myself that this is too will end.
Best to you - Carla -
What about fingernails do they fall off?
-
Fingernails do occasionally fall off as well as toenails. This is most commonly associated with Taxotere. I believe it is one of the more rare side effects. I have seen people talking about icing their nails during the infusion of taxotere. I have had two rounds of taxotere and have not seen or felt any nail changes. I am hoping for the best.
-
Hello to all my fellow June Bugs. Take a deep breath girls – we will get through this.
I am relating so much to what many of you are saying. Scared, confused, WTF. It’s a confusing time and SO much info coming at us – and none of it is anything we want to hear. It makes it really hard to absorb it all. I’m making a few mentions here for posts that I’ve read. I’m sure I’m missing saying “hey” to some of you, sorry about that. Just trying to get the ball rolling with a cheerleading squad. (selfish reasons – needing a bit of pumping up here) Start my first of 8 cycles of AC in just 3 sleeps – Thursday June 6th is my day.
Really happy we have a group here to follow and support each other. Catching up on the posts and hope to be an active participant as we navigate through this. Sending encouraging and supportive energy to all of you.
Paula- and everyone else that is farther down this path – thank you, your info is awesome.
Kaydeesmiles – hope today went well for you, let us know how you are doing
Lstewart51 – go time for you tomorrow – best of luck – we are here for you
Jojogal123 – we are starting together on Thursday the 6th same # of cycles.
VAL1966 – starting on the same day as well, this Thursday – gulp. No kidding, sick of being poked and prodded. They put us through an awful lot.
Stay strong everyone – we can do this.
-
Hi all June girls,
Had first TC yesterday... Infusion was no drama at all.. Since home have felt ok so far.. Headache seems to be worst se so far..drinking lots, and eating fibre, prunes to help digestion. Apparently probiotics helps so might start acidophilus. Still have hair......
Asked the nurse re the Claritin she said next cycle they will check white blood cell count and if low will give me the neulasta then, so will need Claritin at that stage I presume..
It isn't so bad so calm those nerves!! We can do it..
MichelleRN78- how was the second round?? Any diff to the first? How did you cope w hair issue??? Please advise as this is my dread at the mo..
Dim425- it will be ok, decision is the hardest part..
Allibeths- have you decided on cold caps, am regretting not giving them a go but my hair is pretty fine also so maybe wouldn't have worked, although I have read of others with fine hair who kept maybe 60-70% so that's better than nothing hey!!
Thanks Ocean Warrior for uplifting words-
Good luck Lstewart51, thinking of you hope for smooth sailing!!!!
Good luck to everyone, lets get this over and done with...! As I read in another post somewhere, will all soon be in the revision mirror where it belongs!!
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