August 2013 Chemo Sisters
Comments
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Hi Sharon, i could not agree more, we need to do what ever we need to do to live and welcome.
shary
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I was diagnosed may 28, 2013, I think I'm definitely in the denial stage. Or disbelieve I'm only 29, and got diagnosed 10 days before my wedding. The wedding itself was stressful...At that point I was stage 1a and not even 2 weeks later I jumped to a 2b. I just started chemo 1 week ago and I am more that freaked out about loosing my hair, my hair is me I mean I already lost my breasts now my hair! What part of me will be left?! This is my first time venting publicly I hate to sound so pessimistic but I am very salty about loosing my hair, I've been trying to stay positive through the headaches, dry heaving, acid reflux, etc but loosing my hair is definitely going to be the worst. It's nice to know reading some of your posts that others have the same concern, thanks everyone for sharing it really did make me feel better!
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Ashley-so sorry that you were diagnosed right before your wedding. That should have been such a happy time for you. I think that the hair loss is one of the hardest parts of chemo. It is like chemo strips everything away from us and then the hair loss exposes us to everyone. It is not just a vanity issue but also a privacy issue. Everyone deals with it differently. I choose to wear a wig at work but would take my wig off when I got home. I did wear a scarf or hat when I went out of the house. My kids hated my wig as did the dogs who always gave me weird looks. Choose whatever path makes you comfortable. All of us are here to support you.
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Ashley, First welcome you came to the right place. It is hard to loose our hair. Just today 15 days after chemo my hair start shedding. I was really believing it wasnt going to come out. (im still thinking its not going to come out haha) Im sick to my stomach right now. I think most of us are in some kind of denial. Loosing our hair makes it real. I did hear someone say it was depressing at first, but when it comes out alot of stress goes away. Its always the unkown that bothers us once we get through it, it feels better.
Im sorry here I am welcoming you while I go through my little crisis. Thats the nice thing about this group you can cry and let out your feelings. The next day be uplifting to someone else.
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I started AC on 8/8 scheduled every 21 days for 4 cycles. Then followed by Taxol once a week for 12 weeks.
I cut my hair short before any hair loss. I also picked up a wig prior to hair loss. I will be participating in an American Cancer Society Look Good Feel Good session next Monday. I am really looking forward to this class.
I have a great support system but find it difficult to share how I really feel with family and friends because I don't want to be the negative, feel bad for type of person. Does anyone else feel this way? I feel that this forum will help provide me with the outlet to share the true side of how this diagnosis and treatment is impacting me.
I experienced extreme pain following my chemo port placement. Later found out that the pain was likely from swelling pressure on a nerve. The pain subsided after a day or two. I found the chemo treatment a much easier process than the surgery. It was recommended by my oncologist to take an allergy type med to help with the effects of the Nuelasta. One note that I have learned is to make sure the allergy med is a non-drowsy. My mind has been so overwhelmed that I forgot to check for non-drowsy and was wondering why I was drowsy.
I have not had any surgery nor radiation. The first course of treatment is chemo since my last scan showed three millimeter size masses in my lungs. The oncologist recommended to start the chemo first to treat the possible breast cancer masses in my lungs. -
Wishing you strength and support during the trials of this disease. It is difficult not to think of our mortality. You are not alone. I am doing as I am told and keeping the positive thoughts pumping. It really helps me to have "cheerleaders" around me to remind me that I can continue to fight.
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Question: How long after surgery is it okay to start chemo and radiation?
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Lyndsey32, Today is day 15 for me and im starting to shed., Im sick to my stocmach about it. Im also going to the Look Good Feel Good given by the american cancer society and looking forward to it. I know what you mean I dont want to be the feel bad for me person either so I also try to be positive at least on the outside but cant always do that on the inside. You have come to the right place for an outlet to share emotions and get lots of knowledge and support.There are alot of wonderful ladies. welcome
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I worry about losing my hair too but I feel armed with my wig, my scarf, my Buff. I also want a skull cap like the ones on sparklingearth.com especially one with flames!
The biggest pain I think about losing your hair is that everyone can identify you as a cancer patient. I actually would not like people staring at me so I kinda decided to be outrageous to give them something to look at. Anything to boost my spirit and help me fight.
I went to an ACS Look Good Feel Better workshop a couple of weeks ago. I felt a bit bad that I had my hair when all the others did not but they were very kind. It was a wonderful experience and the others were so unselfconscious about their baldness I was so moved. And frankly a couple of the ladies were amazingly beautiful bald it was so cool.
It was all so empowering and they gave me TONS of very expensive makeup. I highly recommend the workshop to everyone. -
Lindsey-we all try to act stronger than we are. That is the good thing about the forum, you can let you guard down and say what you are feeling. We all support each other here.
Sharon- I had to wait 3 weeks after surgery before starting chemo.
It is sad that with everything we are all facing with our treatments that the hair loss has such a big impact on us. -
Sharonannebaker,
My surgery was 6/17.
My first chemo was 7/29.
Chemo was then delayed.
Chemo resumes 7/26 (had a TE removed due to severe pain and seroma issues).
So to answer your question, about 5 weeks btw surgery and the start of chemo. -
My hair fell out in clumps around day 16. I then had it shaved to a #1. I wear the wig outside of the house. I sometimes wear a bandana scarf in the house. My kids and bf took the hair loss better than me. I try not to over think everything and am grateful that I am alive. Acceptance of my TE loss (for now) and hair loss have been very hard though. I feel for all of you and your suffering.
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I totally agree about the hairloss being a privacy thing. The actual losing the hair thing I think I'll cope with but everyone knowing is really difficult. When I was first diagnosed I didn't want anyone to know, I told no one, then the weeks went by and I realised that when my hair went there would be no hiding. I teach 125 kids a day, there are about 900 kids and staff at work. With my hair theyd spot a wig a mile off. I am such a private person normally, this has been really difficult. A staff member told the rest of the staff the day I went for surgery that it was the C word. (see still cant do it) and I didn't want the kids to be told. I thought it would dawn on them (high schoolers) slowly but some do know I think. I just have to get it together before B-Day (BaldDay). Haven't told anyone its breast...Something out of this has gotta be private.I just cant cope with the idea of thinking the guys will be sitting in class playing 'one of these is not like the other...one of these just isnt the same'!
With scars from breast and port, and maybe after the chemo no breasts, tattoos from the radiation, I'm never going to be unaware of it, so Id rahter the rest of my world was.
Like some of you have also said, I feel like Im going to have to be the brave courageous, positive hero for 100s of people , so here I just want to be how I really feel.
Ashley, I cant begin to imagine how difficult things must be for you having to cope with so much, when you were expecting a time of joy. Your picture shows a stunningly beautiful person and the thing to hold onto is you are still her!
Thinking of you all.
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Welcome to all the newcomers! Prayers out to all who aren't feeling well, those who are stressed + who are afraid. Face your fears head on and put the enemy of cancer under your feet. In Christ we are more than conquerors!
Thank God that our tumors were found + are being treated. I thank God that He is working through my medical team to bring healing to my natural body! Let's trust the process and be gratiful + thankful for every minute of every day we are given. Let's take this opportunity to love more, live more and laugh more! Yesterday is gone + tomorrow is not guaranteed! All we have is today + this moment. Let's be present!
We are so much more than chemotherapy, radiation, mastectomies, lumpectomies, cancer, ports, side effects + meds . . . we are WOMAN, created in the image and likeness of God! Hear us ROAR!!! This dis-ease can only touch our bodies (+ possibly our emotions); it can NOT touch our Spirits (the part that connects us to God). Stepping off my preaching stand . . .
Like other's here, I have not shed 1 tear. 4th day since 1st treatment . . . still feeling good! The say having a positive attitude helps heal and we all know that laughter is the best medicine!
Does anyone know a good + funny joke?
Blessings, Joy + Peace to everyone!
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It's been a week since my first chemo session and I've been sidelined since Friday (it's now tuesday) with awful diarrhea. My appetite is gone and even if all I eat is cottage cheese, bananas and white bread, there it still the diarrhea. I go to the doctor tomorrow for a lab draw and a check in, I suppose. Fatigue is pretty heavy too. I watch tv or try to do whatever and end up lying down for a long long time. I'm taking Imodium and lots of Aleve, but no coffee because of the runs. Gatorade goes down well so I shall stick with that.
How is everyone else?
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Welcome to our new comers but I am very sorry this has happened to you, Ashley dear you are far to young to have to deal with this in your life right now, I pray for peace of mind for you, " The peace that passes all understanding" that comes from Christ and he will give it to you if you just ask. I was Dx on may 31st and I was just wondering today " Do I really get this? Really get this?" I don't know but in 2 days I will start my chemo and that just freaks me out!!!!! Ashley I am 50 and I don't get it:-( This is such a great thread and we are all here for each other, so cry, scream, laugh and encourage, care here for all of you🌹
Shary🌞 -
I am on the same regimen: AC x 4 and then T x 12. Will have my second AC infusion this Tuesday.
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FMG, got a good one.
A man arrived at the gates of heaven and was ushered in by St. Peter. After an long tour of everything, they decided to get something to eat. So they stopped in a cafeteria and though there was a long line they patiently waited.
When they were finally at the head of the line, a man in a long white coat with a stethoscope around his neck rushed in front of them and demanded immediate service.
The man who just got to heaven was amazed at such behavior and asked St Peter, "Who is that guy?"
St. Peter replied: "Oh that's God, he thinks he's a doctor." -
Beeve, Gatorade seems to do the trick for me. Also, watermelon and chicken soup are sitting well.
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Beeve, rice, cola beverages, and best of all, chocolate are all constipating.
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Beeve, chicken broth and saltines have helped me. Also make sure your doctor know of your issue. He may want you to come in for fluids. They have me scheduled regularly for fluids along with my neulasta shot.
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Good one Lisa😄
Beeve, so sorry you are feeling so crapy😰let's of good suggestions here, my thoughts and prayers are with you for healing.
Shary🌞 -
@LisaSp, good one. It made me laugh; thanks! BTW God better be THE doctor . . . we're all depending on Him!!!
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Thank you JN, My surgery was July 12 and my chemo has not been scheduled yet due to the fact that I went to check out a clinical study for Triple Negative Breast Cancer. As it turned out, there was no trial into which my stats fit, so I had to go back to my original oncologist. My appointment is Monday, Aug. 19. I don't know how long after that appointment the chemo will start. I'm 68, so I'm expecting a lot of tests beforehand, not sure. My cancer, being TNBC, is grade 3, the most aggressive. That is why I'm chosing to have chemo, although I could opt out and only have radiation. I am afraid to do that since there is no targeting medication for TN like there is for positive ER/PR cancers. I want to hit it with everything they have since it will be a 5 year waiting game after everything is said and done. That is the scary part. I am gambling either way. If I do chemo, I may have permanent side effects. If I don't do chemo, I may get a recurrence in the first 1-3 years. TNBC is famous for recurring quickly. It is about 12 times more likely to recur in the first 3 years as the positive breast cancer. I'm so new at this. I'm so glad all of you are here to discuss these scary issues. I feel for the young people who get this disease. I am a great-grandmother and have had a great life. I still want to live on, but I can't imagine having it when I was young and had my children. God bless all of you and thanks so much for being here for everyone to vent their fears. Sharon
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FMG, you're right! By the way, a nurse told me that joke. Seriously!
Beeve so sorry to hear about your situation. BRAT diet like everyone said and just plain pasta should help. Please let the docs office know maybe there is something else to do that can help fast.
I go in to get my first blood checkup Monday wish me luck! Hoping for good lab results. -
ForMyGrandaughter, thank you for putting things back in perspective and reminding me who is in control. Preach it any time l need to be reminded every so often. Thank you
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Getting my port placed in the morning...UGH! First chemo tx on Friday is fastly approaching. I want to thank you all in advance for sharing your stories, suggestions and support it has truly helped me prepare for what MIGHT be coming my way.
Hugs to all and to all a good night.
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Candi, my port site is still sore after 4 days, but you should have seen the chemo nurse beam at me for having one! Besides the Emla cream she used a numbing spray and it didn't hurt one bit. I was really glad to have it! I guess it's like a drain, as much as they are a pain in the butt, it's great what they do for us!
Beeve, how awful! I was surprised to see you list cottage cheese - I always thought dairy was not good for diarrhea? Bananas rice, applesauce and toast. If you re concerned about protein maybe ßome plain sliced turkey? So sorry for your troubles.
Thanking God for a goodDay 1. Cooked dinner and.dessert, ate, felt a little off so took a Compazine. Headaches so some ibuprofen. And now bed. See you all tomorrow! -
Joining in...was scheduled for lumpectomy on Monday but at pre-op appt docs measured me and tumor grew from 3.2cm to 3.7cm in one week. Changed my plans to chemo starting Friday....nervous since I haven't done any research on chemo since I didn't think I'd be worrying about for a few months! Diagnosed last month, clinical stage 2, grade 3, ER+, PR+, HER2-. I'm currently six months pregnant with my second son, first is a toddler. My biggest hope is to still be able to have the strength to put my son to bed while undergoing treatment, and of course deliver a healthy baby.
I will be doing 4 rounds of AC (taking a break to deliver baby) and then 12 of Taxol.
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Oh, Cougarlicious, what a challenge for you! I had a friend who had cervical cancer when she was pregnant and both she and her baby boy did really well, but I'm not sure what drugs she was on.
So I had my first session picking wigs from a catalogue today, get to try them Saturday. My 19 year old daughter came to help and we loved the dark one with purple spikes but the wig lady didn't take us seriously at all. : ( she said I'd look like a clown with a very small head...and there I was trying to be adventurous!
Then chemo education with the nurse. Mmm. I was trying to feel upbeat but I always seem to come out of these meetings feeling a bit squashed. Saw the chemo room. 9 chairs in one smallish room, more like a hospital ward. No ice available. ( not a private hospital - I'm in NZ with free health care, generally good but financially squeezed in the current economic climate. I'm just really grateful I don't have to worry about paying for it).
I'm booked in for next Wednesday 21st. I get the port in under local anesthesia then I have my first chemo immediately. I'm wondering if I'll manage work the next day? If I tell myself this is just no big deal perhaps it will be : ).... Perhaps not.
Kid Joke: what do you do if you find yourself on a horse, with a giraffe next to you and a lion chasing you? - get off the carousel.
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