Anyone starting chemo in Aug. 08?
Comments
-
Nico
-
Three days until chemo starts. I hope I'm ready. I am supposed to get dose-dense ACT, but don't know how much my recent dx of IBC is going to change the game plan. This inflamed, cancerous breast is painful and looks really deformed. I'm praying that the chemo will start shrinking it. It is so large, with the tumor protruding from the skin, that I amy actually be able to see it decrease in size. That is what I am trying to focus on, instead of how bad the SE will be. Tomorrow I am going to shop for the stuff on the chemo list.
Bette
-
I am starting chemo finally on August 27, 2008 (this Wednesday). I was schedule to begin two weeks ago went in for it and my oncololigist took one look at my reconstruction flap wound and said no. Last week it was off to the plastic surgeon who told me to give it another week. So hopefully it will happen on this Wednesday. I am very nervous about getting chemo and it being postponed hasn't helped. I will be getting cytoxan and taxotere.
-
Good evenings ladies,
I had my first FEC tx on Tues & Wed. very few SE, but I don't think I'm being carefull enough. I've just gone about my life as normal because I'm feeling OK. I've been washing my hands all the time but not really staying away from crowds etc. I think I'm going to be much more carefull this week. I'm so sorry that some of you are having so much pain. I'm really going to be praying for you. The food obsession is what's got me. OMG.....I'm eating like a horse. If I don't slow down it's going to get really bad.......I don't even want to think about the scales. I ate my bosses half of sandwich last week at a meeting.......holy cow....
stacy, we miss you!!
Have a great evening ladies.....peaches
-
No food obsession here yet, not much of an appetite actually. Maybe that will come in a few days. I've mainly been eating soup, but managed half a sub today for supper. Just feeling very slightly icky, napping every afternoon and falling asleep watching movies in the evening. Decided not to go to a movie today, went to Subway, the park and Blockbuster - woo hoo!
-
Hi, all ~ Hope everyone has had a nice weekend without too many SE's. Personally, I am having a harder time dealing with the hair loss than I'd expected. I'm sure I'll get used to it, but today it was just kind of a downer I hadn't anticipated.
It was disappointing to learn that this board isn't as private and safe as I think we'd all assumed it was. I guess we just have to be careful about what we choose to share here.
Stacy - You and I started our chemo on the same day, 8/6, as did Hood, I think, and maybe Tonya, who I think is dense dose, so no longer on our same schedule. (Forgive me if I'm overlooking anyone else who started on 8/6, but we need a chart or something.) Anyway, Stacy, I hope you won't really leave because, not only will I miss your wonderful sense of humor and warmth, but I will miss having you as a chemo sister who is on the same schedule. And if you're not here, especially because we are on the same schedule, I will continue to think about you and wonder how you're doing.
Jeannine - I never seem to get to the Whittier area (I'm out near Palm Desert), but knowing you're there, it would be fun to try to get together one of these days.
Thinking of you all ~ Deanna
-
Sorry ladies i Have not been on in a while.. i started ti run a fever and had a lot of things going on. I lost my hair and had a little bit of a hard time dealing with it. But I am okay. I go for my second round of chemo on wednesday and i am not looking forward to it. everyone keeps telling me it gets better and soon i want need someone here with me everyday. I am so ready to have my house back to me.. My family will be coming once a month for 4 months. just so someone can be here with me during chemo. I cant work my doctor told me that they are not going to let me. i feel bad cause everything is on my husband. 2 car payments and a house that we just got in december of 07. its like i need to find a source of income. i try not to let it get me down. but i feel bad cause he is working 2 jobs.i am trying to look at the bright outcome after this.. but sometimes its hard. i feel like someone stole part of my life from me.. i just keep telling myself i am going to beat this. even though the cancer started to spread it isnt in my brain and other major organs which is a blessing in itself. I want to thank all you ladies for praying for me.. i go back and try to read everything i missed when i get on. sometime I cant.. but i do try.. stay blessed ladies and i will continue to fight this cancer that thinks it is going to steal my life.. have a wonderful and blessed night ladies..
-
Hi everyone! I had to take the weekend to regroup.
Very rough weekend. Hair is all gone - had to shave it off today as it was making a big mess throughout my house. My sweet hairdresser came in off of vacation when I called her in desperation! She even let my younger 2 help shave it off. But, first we did a mohawk into which she shaved I (heart) U and we sent it by phone to my dh who has been gone for 5 days. It made it alot easier to deal with! I then tied on a bandana and took the kids to the country club (note - lots of pretty people with HAIR!!) pool and stayed the rest of the day. I was so proud of myself. Did stop at the store on the way home for a lint roller for my stubbly head. I have been told that as the stubble comes out it pokes your head when you lay down and a lint roller helps. How weird! My older dd was approached by a friend at the pool who asked if her mommy didn't have any hair. She told her no she shaved it off. When her friend asked why she replied "breast cancer" to which her friend said "bummer". Then, off they went to do whatever 9 year olds do. I guess it was good practice for the first day of school tomorrow when all of the kids friends will see and ask. My baby starts kindergarten tomorrow - another reason for the rough weekend.
Tx #2 on Wednesday - half way!!
I just want to close with a thank you to all who posted words of encouragement, understanding, and acceptance this weekend. It meant more to me than you will ever know! I take great pride in my compassion for others and was devasted when I felt that something I said, even though it is a reality we all face, would have made someone uncomfortable. Also, I do not do embarrassment very well at all! Therefore, I needed some time to "get it together." I will admit that I am not quite there yet, but working on it. Thanks again!!
Good Night!
Stacy
-
Nico
-
Hi all - well shaved my head this morning before I took my 13 year old daughter to school - threw my wig on and away I went. Feels weird here at work but everyone tells me how good it looks - oh well if not I am stuck with it for awhile!!!!!! Stacy I haven't posted since all that took place but NOTHING I HAVE EVER READ FROM ANYONE has offended me. I am glad you came back. I go in on Friday for my 2nd TX treatment and I guess I am ready - I only have to do 4 so I keep telling myself - after Friday 1/2 way done!!!! YIPPPPEEEEEE!!!!!!! Hope everyone is feeling good or as good as can be expected. Lashon2008 - I feel for your situation - I am working thru chemo and if my doctor would have told me I couldn't my hubby and I would have been hurting - BADLY. We too have a house payment and 2 car payments - I got my car 10 days before I was dx so if I could ONLY go back - I love it but I wouldn't have gotten it!!! Hang in there - we are all here for you!!!!! Loves to all!!!!!!!!!!
-
Hi,
Seem to have a "good day" then a "bad day" when it comes to exhaustion and nausea. Today so far is "good" so trying to work. Actually looking forward to the kids starting school next week! Too tired to type! Hope everyone else is well. Hugs to all!
Dawn
-
Hair is coming out in clumps........
-
Hi All, I have my 2nd treatment tomorrow. I hope it goes as well as the first one did. Not much to complain about, no nausea, vomiting or diahrea. Felt a bit fatigued on day 4 but that passed. Am working full time and keep my other schedules too. But if I need the time to rest I do. Hair has started to come out, have it cut very short, no bald spots showing yet. Hope everyone has a good week!
-
Hi Girls,
See-time is going fast now with some girls starting #2 already. Stacy, Alibug, and Maria-good luck with #2! I feel okay after mine last week. Maria, glad you are doing well-hadn't seen a post from you for a while.
Some tiredness today-could barely do my walk. Still some taste changes and feeling less hungry. I bought some Carnation instant breakfast-just sounded good as I was walking by it. I haven't gone to the bathroom in 3 days-not feeling bad from it, but I will take something "mild" tonight to help it out. Didn't have any problems with this during TX1. Oh, well...
Kids came back to school today-felt good to be back in the normal routine. Had a bad night last night because a couple of people went to my good friend at work and asked if everything was okay with me (guess the wig didn't fool everyone). She told them yes-I just want to go to work and not have everyone look at me differently-that's why I want to keep quiet there.
Roya, sorry about the hair-I still have some hanging on after TX2, enough to cover and stick out of a cap, but I think my time is running out, too. So sad to know it's going for a while.
Lashon-hope you are doing well-it sounds like you are having a rough time, but hopefully, things will turn soon!!
~Misty
Stacy-
-
HI ladies.. just wanted to come and say hello.. Nico, misty1,alibug05.. thank you for the words.. it helps me to read those when i get on-line.. I am doing good today.. seems like everytime i go out i am buying a wig.. it has become a drug just like clothing.. but i am getting better with it.. I have decided not to wear a wig to my chemo session.. just dont feel right when i see so many other strong ladies in there with there lovely bald heads and with pride. but i will wear my head wrap.. i am not ready to go totally without just yet.. i still wish i could work.. i need to find one of those work from home things.. that way i can do something with my time.. its so hard to find someone to do lunch with or be around that understands what i am going through.. I really dont want to go for this second session.. but i know i have to.. i get depressed when i go in there and know what i have to go through.. i know it could be so much worst.. but its like i have to have 6 sessions of this after wednesday it will be 4 and i am so ready for november to get here and that will be one thing marked off.. well ladies. lets continue to kick some cancer butt.. and thanks for the kind words.. praying for us all..
Lashon
-
Hey everyone
Lashon - I can relate to your post. I am not allowed to work per my onc dr either. It's boring even when I don't feel good. I had my first chemo last tuesday and my white count is already way down according to the dr today, plus I have thrush. I will be having six treatments alltogether ending sometime in December so I'll be counting down with you. We will all kick cancer's butt together - I'm so glad to have found this site,
tired - so goodnight ladies - everyone rest well tonight and feel better tomorrow!
Monique
-
Hi everyone!
Lashon I 'm so glad that you were feeling up to posting and letting us know how you are doing. You have been in my thoughts every day. I know at times things can seem so hard but we are kicking cancer butt and like you I am counting down the days to November when I'll be done with this treatment.
Stacy, I'm lovin the pic! We're going away this weeking and I think I may bit the bullet and shave my head Thursday night before we leave. My DF wants me to wait and if my hair starts to come out we can shave it in the hotel room. How seedy is that! I'll feel like I'm on the run from the law. Go into the hotel room with one hair do then come out in a wig a big sunglasses.
Roya, you're in my thoughts. I'm trying to stay up beat for the hair loss but I don't know how I'm going to feel the first time I look at my bald head.
Cheers to the ladies that are down 2 tx, one step closer to the end of treatment. I'm keeping my fingers crossed for no SE's.
Hope all have a restful night.
As always you are all in my prayers.
denise
-
Hi everyone... I'm a long time lurker and a first time poster. I am 30 years old and scheduled to start my first round of TC chemo on Thursday 8/28.
Although I had my lumpectomy back in June, it has taken me almost two months to get my head around actually doing chemo. Although I am a generally positive person, I am REALLY struggling with the idea of pumping what is essentially poison into my veins. I know it kills both the good and bad cells, but I just feel so fundamentally opposed to going through with it. I feel so normal and otherwise healthy; it's next to impossible for me to really believe that I could still have some microscopic rogue cancer cells drifting through my body. My nodes were clear, my margins were clear, but I had (have?) an aggressive form of triple negative breast cancer. The ONLY thing that convinced me to do it is that my onco told me that if I didn't I'd have a 1 in 3 chance of recurring metastic breast cancer and would likely have to deal with it for the rest of my life.
I am a huge planner and the unknown following chemo absolutely terrifies me. I understand that everyone's side effects differ, but I have to admit that just reading through what some of you have gone through has brought me close to tears.
Any suggestions for calming down and changing my attitude? I'm worried that I might wake up on Thursday and not be able to bring myself to my first "poisoning" session.
-
Nico
-
Nico
-
Hi, Rosemary ~ I think anyone who has had bc understands what you're talking about - feeling absolutely fine, but being told you have to do things that will probably make you sick. It's such a hard concept to get your mind around! And yet, I think the odds of recurrence you quoted (1 in 3 without chemo) are not something most women would feel comfortable risking.
Prior to my mastectomy, I was agonizing in much the same way you are, vacillating about the recommended surgery and chemo, and my BS said something that helped me move forward. She said the only reason we don't feel bad with bc is because it's the only cancer that starts outside your body's core. But if it gets inside, it's a whole different ballgame. So, it's important to do everything we can to be sure it never gets inside.
Something that helped me see chemo in a more positive light is a guided image CD I've mentioned elsewhere in this thread. The website is http://www.healthjourneys.com/, and it's available as an MP3 download.
So sorry you are joining this sorority, but we'll all be here for you ~ Deanna
-
Hi and welcome rosemary ap,
You're correct, it is a difficult concept to get past...pumping ourselves with "chemicals" in order to get well. My strongest influence has been my family. My grandmother and mom are both breast cancer surviviors and did everything they were told by the doctors. Back in my grandmother's day, the treatments were very different from what they are today, but she did everything she could to live.
My sister-in-law (DH's sister) passed away two years ago from breast cancer at the age of 43yrs. She was such a free spirit...open in her thinking and actions...terrified of chemo and radiation, so she did neither. She went the holistic route. Now that I have breast cancer I feel like I can understand her actions so much more. The entire family was very judgemental in their thinking when she was terminal...that she should have sought treatment and didn't....outside of the holistic route and lumpectomy. I still would never judge her decision. She asked for chemo during the last month of her life, but it was too late. Her breast cancer was aggressive, but totally treatable from a medical standpoint. She lived far from all of us and was very quiet about what was happening to her at the time. None of us realized until it was too late how very sick she was. I wish we could have been there for her to help her feel strong enough and less afraid. To help her fight.
I know we are all so afraid. I know I am. I believe we need to do everything we can to save ourselves from this horrible disease. I have had one round of chemo and at night I imagine it is attacking the cancer and killing it. I need to be here to raise my kids and live life.
Know that we are all here to support you and help raise you up.
I hope this post isn't depressing. It's not meant to be. I just know my sister-in-law felt so alone when she needed help the most. I hope no-one ever has to feel that way when dealing with such a serious illness. We can and do support eachother. You can do this. You can do this.
Hugs.
Dawn
-
Rosemaryap, I too am triple neg and had 0/5 lymphs, clean margins. When you feel good and 'normal' it is so tempting to forego the chemo & rad. Why trade feeling good for feeling sick? Triple neg is sneaky, quick, & extremely aggressive. It is carried by lymphs, blood, and however it can get around inside you. Clean lymphs are just one segment of the diagnosis. We don't have the tech to find every single cell that may be there. Taking chemo is like taking out insurance against recurrence. I told my kids that all this that I am going through is a small premium to pay for assurance down the line. My doc says to treat the aggressive aggressively! like, halpino, I lost someone close who chose not to undergo chemo or radiation. This could have been prevented!
Nico, Thank you for the info on some of the websites for triple negs. I was not aware of some of them.
Misty, did the Carnation instant breakbreakfast work for you? I can get quite a few of these things here in France.
Lashon, glad you are back online. Just 6 sessions after Wednesday! Just watch how fast this all goes!
-
Roya,
I bought the sugar-free vanilla instant breakfast-I had one mid-morning at work today. I mixed it with lowfat milk-went down much easier than water. I feel this is one way to get some nutrition into my body when other foods are just not cutting it!! Try it and let me know what you think. I'll probably do one again tomorrow morning until I get over the first week after...
~Misty
-
Thanks Misty, all went well this morning with #2, the half way mark. And again, as with treatment #1, the blood counts were perfect so NO "Big N" shot tomorrow. I was asked to consider being in a trial treatment for Bone Density Loss. Told them I would review the information and let them know. Looks like 4 weeks of rads, I have to see the Rad Onc shortly. Hope everyone else had/has a good experience with this week's treatment.
-
Good afternoon ladies,
Lashon, great to see you back....you have been in my prayers specifically. I hope that as the days go by you will see more and more blessings that can come from this journey.
Stacy, so good to hear from you. I loved the picture! I know my hair day is coming in about 8 days. I'm glad that you are feeling good. I know what you mean about people at work. I really wish that they wouldn't look at me like I'm about to fall out. I know that they just don't understand , I didn't either a few months ago.
Well, I have had one side effect that I've noticed. Chemo took my patience. I have very little patience with stupid questions and procrastions from co workers. I have no idea why....maybe I better double up on the Lexipro.
It's great to hear about so many of you already done with #2 Way to Go!!
Rosemary, Welcome to the group....I know the thought of chemo is hard but I guess I'm just thankful that God has provided a way to lessen the % of it coming back. I don't know what kind of tx your on but my first tx (FEC) was not bad at all. I"ve known so many people that have gone through it with very few SE. I'll be praying for you!
Talk more tomorrow...peaches
-
Hi Everyone, Sorry I haven't been around much lately....trying to get everything done before my 2nd T-C tx tomorrow. My ds, who I take U of MD on Thursday, is taking me tomorrow. Hope he can handle it!
My husband thinks it will be a good experience for him, but secretly I think it gives dh a day off from taking me! LOL! I really feel like I can do it myself, if it goes like the first one, but they want to "be there" for me. Isn't that sweet, in an almost suffocating way??? All kidding aside, I am truly Blessed to have them here with me! I will be praying for you Lashon too as you go for your 2nd tx too! Take care! I love you all! XOXOXOXOXOX
-
Hi all!
Hood1980 - I go for #2 tomorrow too! We can be Wednesday buddies. I am going alone this time. Maybe I will sleep. Who knows since I am back on the "roids" again!
Rosemary - Welcome! We have a great group of ladies here! Hope we can all be of some help and support for you, too!
Misty - Hope school is going well. Have you noticed the cumulative effect of being more tired this time?
peaches - my patience is gone too! You are not alone. Trying my best though to no loose it. Luckily my kids are back in school now.
Maria - glad #2 went well for you. Hope my is the same as last time. Went pretty easy although my onco gives neulasta on the 2nd day no matter what. Hello bone pain here I come again!
Alibug - yea for halfway this week!!! Good Luck!
Lashon - I am soooo glad you are doing better! You have been in my thought and prayers daily!
Roya, Dawn, Deanna, Nico, Denise, Monique,Bettylou, Longhorn, and anyone else my hyper-steriod brain may have missed at this late hour - Have a great rest of the week!! Hope it is stress and se free.
My dh shaved his head today and realized he didn't have as quite a full head of hair or good of a hair line as he thought!!! He said he will keep is shaved as long as I have no hair!
Good Night all!!
Stacy
-
Hood, Stacy - I'm with you on tx #2 tomorrow! It will be soooo great to have the second one behind us!! Bettelou - I seem to think tomorrow is your tx #1. Good luck if it is! Agnes - Good luck to you tomorrow, too! Lashon - So glad to see your most recent post, and I hope and pray that things will continue to get better for you. Nico - Did you speak to your onc about the severe muscle aches you were suffering over the weekend? Maria - Hope your tx went well today. Apple - We haven't heard from you in a few days. Are you okay? Rosemary - Good luck with your first tx on Thursday!
Sending caring thoughts to every one on this board, even though our numbers make it difficult to address everyone individually each time. May you continue to feel well and strong this week! Deanna -
Hi Rosemary,
I am glad you found us on this topic. I wrote to you on the other thread you had started. I felt the same way as you before I got started. Now that I am in the middle, I feel a little different. I just want to get this over with, kill any possible bad cells, and move on with life. Once you get over the hurdle of TX#1, you will probably change your feelings. Everyone on this thread is great, and we are all getting through this together.
~Misty
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