September 2013 Chemo Group
Comments
-
hi ladies, hope all is well with everyone! I have a new side effect.......heartburn!!! I have been taking tums, it seems to help a little. Even when I drink water I am getting acid reflux.... Anyone else have this side effect? I am on AC number three.......
-
Hockey - very common SE due to soft tissue irritation. Try Zantac because it is fast acting. Tell your onc as it may be better controlled with Rx meds.
-
Hockey mom, I have heartburn also, even with the water but I have a prescribed med that helps as long as I take it regularly. I had to add a pill a day to keep it under control but it's good now.
Rayna -
Thank you everyone for your posts and kind words, reading all of them made me feel better. I know it's probably the strain of three months of feeling like crap, it has to take a toll on us as time goes by and we don't ever feel better but now that I have finished chemo, I should start to feel better in a few weeks. It's just really hard to always stay positive and uplifted, that in itself is exhausting and no one knows but all of us here on this board who are all going through our own trials everyday. I thought wouldn't it be nice if life could stop while we are going through this and we only had the cancer to deal with but unfortunately life keeps going on all around us and we have to deal with what it brings as well. Anyways, thanks again and I hope everyone is doing okay.
Love, Rayna -
Hi, I started in August but will be having chemo until december so I am glad to have this space to join. I found that my very severe AC side effects including heartburn that prevented me from eating almost anything stopped as soon as I ended AC. I'm on taxol now weekly until nearly xmas.
Sheila, I had never considered that the chemo might be revealed not to work after my expected double mx and axillary node dissection in january. now I will have to rethink how i motivate myself to get thru this. i am always focused on the future: i'll be fine once i am doen with chemo, then surgery, then rads. So now despite a positive seeming ultrasound that indicted good repsonse, I spend some time thinking about being okay with my present.
V
-
I was also told by my MO that getting the flu (and whooping cough) vaccine would be fine...I wonder why different MOs are recommending different things?
Hockeymommy - I also started having heartburn for the first time after AC #3. I've been taking Maalox and Tums and it has helped, but mine isn't too bad. I think there are things your MO can prescribe if yours is really bad. -
Hi ladies. I have not been following for a while. I became so discouraged with my extended delays on starting my new chemo regimen and was also in a bad place with accepting the results of my bmx with delayed recon. But good news this week, I was finally able to start the Halavan on Wednesday and rads will start next week. I think I have has too much of a break from being poisoned every other week because this has hit me hard already. It also probably doesn't help that I am starting this one off pretty beat up as opposed to quite healthy, as I was the first go round. I'm still not 100% healed from bmx and I've also been sick with some sinus junk for a week and a half. I've been flat exhausted for the last month or so. But as bad as I thought I felt, it reminded me that it can't be compared to chemo. I had had a month break between finishing taxol and surgery, and initially thought the post surgery stuff was way worse than chemo. It's funny how our minds trick us that way. Forgetting so quickly how bad things really felt.
Now I suppose I should be in the October group instead. If it gives anyone a ray of hope, I can now report these things from my almost 3 months pfc before I got back on track:
Lashes and brows came back. They didn't go away until around my last tx, then became nonexistent over the next month. Brows have come in way darker than they were. Lashes are almost back to my normal length, which is long and they are as thick as ever. Biotin works.
My hair looks like hair again. Albeit very short hair. It's like a very very short pixie cut. I could go without a wig if I didn't have such a fat head.
Icing works. I only had minor lifting on two nails that I wasn't particularly villigent about keeping in the ice. And it grew out quickly.
Body hair came back. Boo.
Neuropathy subsided about 2 weeks pfc.
Period has not returned. Never thought I would miss that, but it makes me feel funny.
Hot flashes went away about 3 weeks pfc.
Now I'll see what comes and goes this time around. I feel like a walking science experiment.
Sorry for the long post. Steroids give me insomnia and make me ramble. Well wishes! -
Just had #2 t/c on Wed. Feeling not too bad. Had to get up to wee, eat & take pills. Ugh! Just want to sleep. eating every 2 hrs seems to help with nausea.
Got my loaner wig on Wed. Hair is coming out in large clumps. Strange how cold it is with no /very little hair.
-
I had heartburn too, probiotic drinks help.
Deliriumpie, hope you have a better weekend...
Viji
-
Welcome back DeleriumPie, I was curious how everything was going for you! Thank you for your insights, they've been missed. And I'm so sorry things have been so rough - some days are really hard to be strong. I hear you on missing your period - I got mine right after my first tx, and my NP told me that'd be my last one. But I got another one last week, and in a completely surprising reaction I celebrated. There are just some things that no matter how annoying they are they're a part of us and a part of what makes us normal. I don't know if yours will ever return, or if mine will continue, but I get the feeling you described.
Up at 2:30am again, uch. Why why why is day 3 post tx so awful? I almost feel like if I could wrap my head around the why I could handle it better. I felt so awesome on days 1 and 2 of this tx, granted I could tell that was maybe driven by the dexadron, but this morning (or actually I guess now it was yesterday morning) I woke up and could tell I was NOT ahead of the nausea anymore. And it didn't seem to matter what drugs I took or what I ate or what I did, I couldn't stay ahead of it. I had to just keep moving, but then by dinner time the fatigue set in, and of course that's when the kids were home and needing dinner and attention and a referee, and when I had to stab myself in the stomach with the neupogen, which then made me tired and spacey too. And now I'm up at...well now it's 3am I guess...and can't get back to sleep. Being on the computer isn't helping I suppose, if I follow my own earlier advise lol.
Anyway, sorry for the rant, just cranky. Every single tx has gone like this - I'm a mess both physically and mentally for days 3-5. The 1st tx was awful all the way around because I didn't know how to stay ahead of the nausea, but days 3-5 were when I completely understood people who just quit chemo, then the 2nd tx I had control until the cold set in on day 3, and my entire physical & mental stability crumbled, and now this time I had control until what feels like randomly evil day 3, when I'm yucky and pissed off again. My one shining hope is that I only have one more AC, and I'm PRAYING Taxol isn't like this.
Ok, taking my own advise and putting the pooter down :-)
-
Reading everyone's posts it seems like we are all going through so much right now. Not just physical but just trying to deal with everyday life. With the weekend coming up, I hope we can all get some rest that is much deserved. Jellyk, hockeymom, lengbong-hope you all feel better!
Finished my 4th round of taxol yesterday and so far so good. I finally gave up on the hair and had my husband cut it really short. There was just too much shedding and I was tired of cleaning it up every where. My MO gave me the flu shot 2 weeks ago. She did not seem to have a problem with it.
knightzoo-I did the genetic testing years ago with my first diagnosis. My mother had breast cancer also over 12 years ago. I tested negative.
Catoklyzmk-welcome to the board-feel free to jump in with any questions or insights!
Deliriumpie-I am glad that you were finally able to get started. The waiting is always the worst part. I wondered how things were going for you since we had not heard from you in a while.
Hvv- Glad to see you again and hear that taxol is much easier for you!
-
Jelly-I think of days 3-5 as recovery days, your body's systems have been beaten down and are working in overdrive to recover! Rest and eat when you can - you're doing awesome!
-
Hi lovely ladies
Does anyone have any remedy for an extremely sore throat that won't go away and is keeping me up all night please? Thankfully my body pains have cleared up so just need to get on top of this one now. Weird how some days you feel really strong and positive and other days you feel down. Such a roller coaster this cancer thing. K
-
Thanks for the welcome ladies.
JellyK- hang in there. AC #3 was the worst cycle for me. Major despair time. I had not joined the April group yet when I did #3, when I found it, I was amazed to read how #3 had kicked almost everyone's butt. Days 3-5 were always my worst too, but no other week compared to the one you are in right now, for me anyway. And taxol was a huge relief in symptoms, once you get past fear of the unknown.
This #1 still taking its toll on me. Staying in bed this morning. I've got that "chemo glow" and am freezing on top of it. -
Treat yourself for heartburn/acid reflux. My guess is that is the cause of the sore throat. Pepcid/Zantac? Do you have any meds for that? Also maybe sleep more upright to reduce reflux.
-
I think we all need a {{{{{{{{group hug}}}}}}}}}
Lots of yucky side effects, mixed emotions, anxiety, etc going around. I'm so sorry for everyone having a rough time.
I had a little bit of an emotional meltdown the other night.... partly because of my mother (she is having a really hard time with this and is SO clingy/needy... calling and texting me 5 times a day. Ugh - but that's a whole other rant) and partly because of my hormones. Unlike Deleriumpie and JellyK, I do NOT want my period. I was happy when I would learn I would most likely go into "chemopause". Unfortunately, I got my period three days after my first chemo, and then again three weeks later. This second one has lasted 8 days. Ok... so not only am I still GETTING my period, but it's here more often and for LONGER? Seriously? Enough is enough.
Other than the never-ending period from hell and a burnt tongue, I'm feeling pretty good. This is my non-chemo week, so no real bad side effects going on. I started taking L glutemine (in anticipation of neuropathy when I start taxol) and a prenatal vitamin (to help my RBC) and maybe those are helping me to feel good? I don't know.
Anyway, I hope everyone is able to enjoy their weekend. My daughter has a softball tournament and my son has a football game, so we'll be busy busy.
-
Off to the doctor again today! AFter over a month of passing stuff back and forth (and sneaking into my bed nearly every night), my children have finally managed to get me sick. I remember when you were sick JellyK and I am not looking forward to this. It started out bright green straight off the bat, so it is an infection of some kind. I am thinking maybe that is why the infection in my incision is getting worse (it has a lump under the skin and is getting painful now and I was going to go to the doc about that anyway), because my body was fighting this cold or whatever it is. Green mucuc does not equal cold, right? Maybe it's different when you are on chemo. Maybe since I somehow found the energy to clean all day yesterday, the germs will be reduced and the kids can stop passing it around! I need to get them a flu shot, too! I have been waiting for them to not be sick because that scares me, and I don't want them to end up getting sick if they are under the weather when they get the shot. Hopefully they will be able to just give me a antibiotic shot or something to get me all cleared up. So, lesson learned, I would say that if you have any little cut at all, keep it covered with antibiotic ointment on it. If my incision can get this infected from over a month ago, anything can. =/
Heartburn (sorry, I forgot who asked about this) I have had HORRIBLE heartburn!!! I started taking Priolosec the day before chemo, but I would say to start up to 4 days before because the bottle says that it could take that long to work. I should have started a day earlier than I did. It worked great. For fast acting, I took Zantac, but I don't know if you can take them together.
Palms of hands- mine arent' really itchy, but I did notice something strange. Opening things is extremely difficult for me! It is like the skin is super sensitive and the jars/lids tear into my skin. I can barely get anything open. Horrible time to not have a man around lol.
-
I hope the upcoming weekend brings rest, relaxation and relief too all.
Etkaterina, I had an extremely sore throat for about the first 12 days. For a few days in there, it seemed to even be blistered. I honestly ate anything cold. I froze Gatorade and made slushies, I ate every ice cube my icemaker could put out (it couldn't keep up so I went to work to get ice), and I ate a lot of frozen yogurt and such. It is finally feeling better...not 100%, but I can eat normal food. My mouth never blistered because I ate ice throughout the infusions, but throat was a whole different story. I do plan to bring it up with my MO when I go next week for #2.
-
Mamastewart, I'm so sorry you're sick - mine was not green right away, so maybe yours is bacterial instead of viral like mine was and antibiotics will get you cleared up. I'll be hoping for that, cuz yeah, being sick on chemo really really sucks.
LHL I'm sorry about your mom, clingy friends and family aren't helpful - they think they're trying to be helpful but they're not helpful. Turn off the ringer for a day, give yourself a break :-) And I'm terribly sorry about the 8 day period, that's awful.
I'm feeling like crap again this morning. Last night after I turned off the computer and laid down I had reflux like nothing else (tx #3 seems to be bad heartburn/reflux for a lot of us), so I still didn't get to sleep right away, and of course the alarm goes off at 6:45. So sleep may be an issue, but I'm definitely not functional, and of course Fridays are days when my 3 year old is home, and she's clingy and needy and well...three, lol. Uch, I've really got to figure out how to get more positive, cuz my attitude isn't helping anything. I am stronger than this.
Hugs to all, it's sounding like a rough week for a lot of us :-)
-
Hi to all the new ones joining us!!
I'm sorry so many are feeling bad, hugs to each of you today. I am finally past the SE's from round 1 & will have #2 on tues.
For those who have heartburn -- I had heartburn before all this happened & a natural help is apple cidar vinegar . You can mix it in water, it tastes nasty but it helps. There is also a drink of it that they add juice into so it doesn't taste so bad. And stop your caffeine, that will help too.
Keeo fighting ladies, your doing great!!!
-
My wife got the flu shot and felt more blah from that than the chemo so far. I'm getting mine today. She is on weekly taxol/herceptin but is really not losing hair (thinning a bit) and still has hair other places.
Is that unusual?
She was driving me crazy last night and saying maybe it's not working. I told her that doesn't mean anything.
Not really sure what to say to her or advice to give. Any help from you ladies would be appreciated.
Thanks. -
Let us know how it goes at your Live Well Feel Better. We were told we can go again but of course we wouldn't get all the freebies LOL But I think I would like to go again to maybe get some pointers for eye brows when all the hair is gone. I've always had fairly thick fairly darl brows so never had to draw or fill them in.
-
Hey SoccerMom
I go for my second round of A&C on Tuesday also. It's seemed like so long ago I had the first infusion. And I was sooo ready for another this week, impatient! Plus everyone *assumed* I was there this last Tuesday so kept calling & texting & emailing me asking. And having to wait 2 weeks gives me the weird feeling that I am not going after this cancer as fast as I should be, even though I know the treatments are scheduled as they are for a reason.
I hope you do ok next week!
-
Art, Two of my friends who did AC befoer Taxol had their hair start to grow in during Taxol, so I don't think it means it isn't working. I hope she continues to feel OK. She's lucky to have such a caring husband.
-
knightzoo - I hope you are not buried in snow! I just saw that parts of your state got about a foot of snow. I know I've said I am ready for hat season, but I am NOT ready for shoveling yet! Our cold front is just supposed to bring nasty thunderstorms and the midwest threats that accompany those. I am thankful for no snow yet!
-
There was a breast cancer walk going through my neighborhood this morning and it felt extremely triggering. People walking with shirts with pictures and "in memory of..." on them. I felt scared and tears swelling. Maybe because my mom's dx still seems so fresh but I'm not ready for this bc awarness month. Pink is everywhere and doesn't make me feel better. Maybe someday it will but for now i want to run from it.
-
(((((JellyK)))))!!! I totally understand on the the 3 year old issue. Mine doesn't have school on Fridays either and she has been super clingy and defiant and everything lately. I had a rough go of it last week when both her and her 4 year old brother were acting up and all I did was yell all weekend. I have lost site of the fact that they are acting like this because their mom has cancer and not just to be brats. I was wrapped up in my own struggle. I felt like crap mom of the year, for sure. We all have our down days. If you didn't you wouldn't be human. It doesn't mean that you are not strong. It is okay to be pissy once in awhile. You are going through chemo, for crying out loud!!! You are a superhero and don't forget it!
Art: I am on Taxotere which I believe to be very similar to Taxol. I am on a loading dose, though, so I get it every 3 weeks. I think that it is lesser of a dose to do it every week versus what us 3-weekers are given and that is why we lose our hair a lot faster. I think the end accumulation is the same though. I had thought about asking to switch to Taxol instead of Taxotere because Taxotere has the potential for permanent hair loss and had asked around about the comparison in effectiveness between the two and from what I found there is very little or no difference in effectiveness against the cancer. I decided to keep with the Taxotere because I just have no support system and finding someone to help with my kids every week is just not much of an option for me. I am sure if SpecialK sees this, she will have more knowledge about the details. Tell her not to worry but I know it can be maddening just waiting for it to happen. My aunt had breast cancer back in 1992 and she never lost her hair all through treatment (and she is still alive and cancer-free in her late 70's!)
-
vintage - don't assume you will lose all of your brows - I never did, they may just thin - particularly if you had thick brows previously. I used Anastasia colored brow gel to darken mine, but did not have to do any drawing. If you do lose them completely I recommend using stencils and brow powder - looks more realistic than drawn on ones. Anastasia and Too Faced make good stencil/powder kits - you can order them online from Sephora or Ulta. -
Art123: how long has your wife been on treatment , my hair didn't fall out until day 17, well that's when it started falling out, I shaved my head then. I just asked the onco about this because I was concerned my hair was starting to grow back while still on treatment but they said that's no indication that it's not working. I hope she continues to feel good and she is very lucky to have you. It's nice to see men post on here.
Love, Rayna -
Alisha (and lighthouse-I think...) I missed the conversation about Pinktober and if it bothers you. I really have very mixed feelings about it. It does bother me in a couple different ways: my mortality hits me when I hear/think of all those that have lost the fight. At this point, I think that I am just numb to it and still in denial. At first, I thought of it as a death sentence and that was horrible living like that, but now death rarely crosses my mind unless something/someone sends my mind down that road. It does bother me that so many companies use it to increase their profits as well. Besides that, I think it is a great thing. I don't' think there is any other cancer (and maybe not even any other disease period) that is so supported. I have made it my mission to inform people and I tell random people that I don't even know (people checking me in at the hospital for another test) to check themselves and even explain how/what they are looking for if they aren't sure. For me, the compassion of strangers has brought me to tears almost as much as the whole cancer aspect of it. I have thought about this a whole lot, and maybe I am crazy or something, but I think if I could go back and NOT have cancer, I don't think that I would. I hate so much about it, but if I had never had it, I possibly would never have gotten to experience this incredibly beautiful side of humanity. It also changed so much about me. It was the biggest wake up call you could ever get and showed me that I was really taking things for granted. It brought me closer to God. It provided me with so much strength and courage..... I know I write a lot of long posts, but this one could turn into a book lol. And maybe it should be. I am going to start writing a blog or something, I think.
Anyway, Alisha... what keeps me going is that everything happens for a reason. I firmly believe that. I have been through some very horrible things in my life but I can look back and see where they took me down a path that I wouldn't have traded for the world! In fact, one thing came apparent to me already about cancer. Long story....but if I hadn't been diagnosed, I wouldn't have been in the class I am taking (I was going to drop it but I found out about the cancer a week before it started) and this class finally, FINALLY showed me what I want to be when I grow up lol. Major change, a whole new set of classes I have to take, roughly half of my 41 credit hours are worthless, and an extra 1-1/2 - 2 years of school, BUT I am so very VERY VERY excited to have finally found something I am passionate about. It is science-related too, so maybe, just maybe, I can someday put all these people that have taken such good care of us out of a job. Nothing against them, of courseIt's one day at a time. I struggled with trying to figure out what that even means, but when you do figure it out, it is very peaceful. I had days when I was thinking I was living a death sentence and I would just tell myself "I'm alive TODAY! And that is all I am going to think about." Big ((((HUGS)))) to you! I was just talking to a lady the other day who was getting her last chemo and told her -and her daughters- congratulations. I know how hard it can be on kids and you are very brave and strong for helping her through.
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