Starting Chemo in September 2017
Comments
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hi everyone thank you for your well wishes
just checking in. Port insertion is done. there's a liiiittle bit of pain but bearable
and mostly when i laugh or yawn. 😂 taking it easy for the next few days just to make sure the incisions heal properly until my next chemo (this friday). and taking my first painkiller since the procedure finished this morning at 830am.
i have a habit of avoiding meds that are not required.drinking smoothies and tea with lemon and turmeric to naturally keep inflammation down and boost vitamin A, C, and E and staying hydrated for healing also eating food with protein and zinc to make sure i heal as fast as my body can manage. Thank you all for your words of encouragement. virtual hugs to all of you

The port feels strange but i think my mind and body has welcomed it long before it was even actually installed. i remember being fascinated by it when one of the doctors was explaining the entire thing to me.
I wish you all a good week. i will be here lurking for the next two days. and maybe laughing at myself when i get a crick in the neck from trying to stay still. 🤣
hugs from my side of the world
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mkn - you are ready to rock now!
Travel - we have to look at the good days and enjoy it. Forget the bad days.
I was thinking how this journey taught us to focus on the good things in life, value what we have.
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Glad it went well, mkn!
The weather here has finally gotten a little cooler. I went for two walks this weekend! I was at a height of activity in my life when I was diagnosed -- I'd recently gotten a bicycle and was riding regularly. All this has knocked me back, so I'm trying to get back into walking at least. Maybe biking again in a bit, although my trips will have to be short.
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Chemo #3 for me tomorrow. I will be halfway done, 3 down, 3 to go! I wish tomorrow were the last treatment. I hate the way it makes me feel for the first week and a half after. It seems like the first week is awful, then the second week I start feeling slightly better and then by the 3rd week, I feel almost normal and want to do things and eat good food again. At least the big "D" went away this time and I didn't lose any more weight. The mouth sores and fatigue was about the same.
I also tried to drink some wine between treatments #2 and 3. In week 2, I tried to drink a glass of chardonnay at dinner for my parents' anniversary but it tasted awful and I couldn't even finish it. Then we went to a comedian show on Friday and I had a glass of red wine and it tasted good. I like to have a glass of wine every now and then, so I hope chemo doesn't ruin my taste for good wine.
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2 weeks almost since my 2nd treatment. I'm so emotional this time I can't stop crying.
So many new people here it's hard to keep up. Congrats to everyone on your milestones.
Keep your eye in the prize. Next week will be my half way Mark! I can't wait to be done with chemo.
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Hope, First of all ((HUGS)) I'm so sorry you are feeling so sad. Have you talked to your oncology team about your sadness? They can help you! If you are open to it, they can prescribe a mild antidepressant and/or refer you to a therapist to talk through things. I've actually done both and it has made a huge impact on the way I am handling things. I was struggling with anger after diagnosis and then major anxiety before surgery and chemo. I'm now taking 20mg Prozac (very low dose) and Ativan .5mg as needed. I went to a therapist and told her about how angry I was about why this happened and talked to her about my irrational fears of chemo. In some ways, just talking about it helped. She helped me rationalize my fears and anger. I went a few times and she said I can always call to make another appointment. Just knowing that it's there as an option for when things seem to spiral out of control is comforting.
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Travel, the study I'm on is testing immunotherapy (Keytruda) in early stage breast cancer (as far as I know, it is already approved for Stage IV tumors that express certain protein). Apparently, when tumor expresses that protein, Keytruda can disintegrate the tumor in a matter of weeks! In fact, what happens is that it strips the tumor of it's "defensive shield" that makes it invisible to the immune system, and our plain old white cells take care of the tumor. Anyway, I'm in the control arm, so I'm not getting "miracle drug", but I was told there were some dramatic results in the treatment arms (sigh)
I do get MRIs, and lots of them. For that I have to give them my flesh, literally. Today they took one more biopsy of my tumor (final one!) I was so uneasy about them inserting needle into my known cancer, but oh well. I was rewarded though - my MRI shows some shrinkage of the tumor, after only 3 Taxols! I knew the sucker was smaller and much softer to touch, but having it quantified and confirmed on what is considered most reliable imaging for breasts, is very comforting.
mkn, glad your port went in fine. You will soon get used to it.
toughcookie, good luck tomorrow, and I want to say I completely understand your mental state and probably need to hire a therapist myself. Today, before the biopsy, I was a wreck. It ended up with hubby staying home from work so he could take me, I was not in shape to go myself. Now, of course, I feel bad, because in addition to missing half a day at work today, he will miss most of Thursday. He keeps wanting to take me to chemo, and I can't resist - having him sit there makes me feel so much better.
And yes, so hard to keep up, but I wish everyone easy treatment and good news!
Oh, my hair is still here, all of it. I will have Taxol #4 on Thursday. Is it possible it won't fall out?
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To all -- I started w/ a therapist the weekend after I was officially dx -- this is my second time around and I can tell you - I wish I had done it the first time - which is why it was the first thing I started with.
Even if it is just a few times, you can talk to them about fears that you can't talk to others about. Reach out and get help -- its not weakness - it is human. Especially as females, I think we try to manage it all and be strong for our families. Talk therapy, drugs to help you through - whatever you need - you have to give your immune system a break to help heal -- don't hesitate. (oh and they all have big boxes of tissues !) I think they can also help take some of the pressure off your family/friends - meaning giving you another outlet. My 2cents for the day
Faraway - thx for info on the study, either control group or not, you are doing a great thing to help further BC research. I looked up that Keytruda, interesting! I did a study the first time, it was comparison of tamoxifen to aromotase inhibiters - 12 years ago. They have increased tamoxifin to 10 years now, I like to think that I am part of the bc journey that others are benefitting from today -As far as wine goes, I have had a glass or two the third week that tasted ok -- it is really that 1st and second week, yuckers! Virtual Cheers to us all! We are strong -
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These clinical trials are interesting. My MO said he wanted to talk about getting me in a clinical trial when I'm done with radiation that combines Ibrance (which is for metastatic breast cancer) and Anestrazol in early stage breast cancer. It's the same deal where you get either just the anestrazol or both and have to be followed for a certain amount of time. I'm game for trying it. Anyone else looking at clinical trials?
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OCDAmy -- go for it if you can.
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Hi! Hope everyone is managing!
I feel like I have dementia. I posted Monday I I must have edited typos and hit delete instead of sumbit!!!
So I had my mid cycle follow up with onc. He let me know that after my next two ac treatments (yay only two more!) I get an mri then I start weekly taxol. I forgot to ask where the herceptin and perjeta fit in. Maybe I'll have weekly taxol, herceptin, perjeta. That will be for 12 weeks. The. Mastectomy and 6 weeks radiation to the chest wall neck and armpit.
It's funny but this ac stuff is brutal to me and being half way through it I feel like I've climbed half way over the fence! I'm assuming the weekly treatments will be easier.
Then to gain even more of a feeling of knowing what's gonna happen ( I need that in my life, I hate wondering) I met with the plastic surgeon!! He wants to do to diep flap yay! BUT I have to be 6 month out of radiation. So I'm gonna have to get used to being flat for quite a while. Shouldn't be too bad. I'm bald and already getting used to that.
So today I'm feeling good cause I've gained a pretty good timeline. I needed that helps me feel like I'm not just along for the ride.
Back to this last chemo. I've felt more run down this time. It's taken a little longer to bounce back. I always am so nauseated even with all the meds. I found that a cbd with very low thc oil vape pen (legal here in wa) is good for that break through nausea.
This round I got thrush in my throat. That wasn't fun.
Also wanted to ask, always around the nadir I get this really back ache in the low back and pelvis. Am I crazy? It comes on the exact same time both times now. Anyone have this? I would say it's more of a pelvis pain. And hip. I figured the neulasta pain would have been gone by day 11. But that pain aside and aside from getting tired faster I'm having my good days right now.
Round 3 is Monday. I'm seeing the light at the end of the grossest chemo tunnel. My dr laughs that I refer to ac as “the gross chemo". But the end is near!!
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mojo, having a plan really does make a huge difference. I'm so glad you are moving forward! We are all getting there!
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OCD having a plan you are right makes ALL the difference. I think it helps us to feel in control. I will be at my halfway point with chemo next Friday..YAY!! I don't think I will radiation even if they recommend it.
It's beautiful here in Michigan so I did some yard work and satoutside enjoying some sun on my cheeks😁
I think I have the hand and foot syndrome.....anyone else?
Enjoy the weekend!🌞🌞🌞
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hope - are you having numbness on your hand and feet? I have and I spoke to my MO so he cut back 10% dosage now. Why aren’t you going to do radiation
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Mojo - did you take Claritin and Advil for your pains? AC can take you down fast and take longer to bounce back. But you have second week to rest up, verse weekly taxol you only have couple days to bounce back
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checking in and bringing some good news.
chemo session 3 (EC) DONE!!!
good news all around. doctor saw improvement on my red patch. so he decided to give me one more dose of the same meds. my port incision healed very quickly doctor said and they used it yesterday. nurse also said the incision looks so clean likely that it will not even be a keloid when it heals. and also my 2D Echo showed improvement instead of any damage and also my blood tests were all normal before chemo 🙂
I am riding out the first three days with nausea meds and also continuing with antibiotics for my port incisions.
just finished a tiny bowl of non-fat yoghurt with fresh mangoes and chocolate granola (locally made, no artificial flavoring) and prepping food that has ginger in it to ease any hyperacidity and citrus fruit to put in my water for when the metallic taste comes in.
hopebringscourage, congratulations on your halfway point!
i am celebrating with you! paulette, hang in there you are almost done with your weekly treatment

have a good weekend everyone!
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Mkn - that’s such a good news! You will see the end of the rainbow soon!
I reached the half way of my taxol treatment , 6 more to go! 😀😀
Have a good weekend ladies, and minimal SE!
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hi all,
I had my first round of AC on Friday. I felt spacey in the last 15 minutes of my cyclophosphamide, which persisted 12 hours. My hubby said I was clumsy also and my chemo nurse friend who saw me a few hours later said yep that's cyclo. I had warned friends that chemo on top of blonde is a bit funny, not.
I also got reflux about 4 hours post completion lasting about 12 hours, all gone now. I was given akenzyo ( apprepitant/ neupitant combo) oral that lasts up to 7 days. Also had 8 mg dexamethasone iv. Anyone else had the redux and what did you do ? I had read that some require eg omeprozole, ranitidine, mylanta or gaviscon. Anyone else had this?
I had an extra blood test day before chemo. My own onc had seen my newts at 3.1 but my pre 1st chemo dose they were back to my normal of 1.3. Anyone else had this.? I have a pathology form for day 12 to qualify for pegfilgrastim but hope it doesn't drop before then. I'm going to get my nurse to discuss it with my oncologist.
I feel pretty good now about 36 hours post chemo. So hope it's that same for all four doses.
Hope everyone else is travelling a bit better, stay strong
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Binnie, I had horrible reflux/heartburn. My MO told me to take Nexium daily and it has helped. I also keep a bottle of Tums in my purse. I'm also on cytoxan. I notice it makes my nose burn at the beginning of the infusion. I get that last and by the end am pretty tired
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Amy, I’m on taxol it gives me acid reflex plus gas also. I didn’t have that problem with AC, this is new SE for me.
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i am celebrating your halfway mark with taxol too Paulette! 😊
it's day 3 post chemo for me. fingers crossed that SEs are not too bad
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mkn - thank you so much, I’m happy also, wish I can reach to the end of the rainbow soon. Prayers for minimal SE for you and me also. MO cut my dosage down 10% I hope it will help my stomach gas.
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OCDAmy,
Thanks I picked up nexium. Hopefully may only need a dose day of chemo. My akenzyo lasts up to 7 days so may even need nexium after that.
We're stronger together
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just finished AC #2, side effects were more intense this time but only lasted 4 days. Like a light switch I woke up today and felt fine.
I still have my hair, we shaved my head proactively a week ago, so far no patchy spots noted but I feel like I have a pony tail in that’s too tight, it’s the strangest thing
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Wonderwoman, you description of a too tight ponytail is exactly what my MO and nurse said I would feel before my hair started to come out, but I never really felt it and I definitely have lost my hair. Now I think my eyebrows are thinning and my lashes, but I should only have 3 more treatments (fingers crossed) so maybe they can hold on?
I'm on taxol as well and take Pepcid for a few days after each infusion. It helps a lot.
I have lots of appointments this week! Echocardiogram on Monday, MO on Tuesday, chemo on Wednesday. I'm having a work friend sit with me part of the time this go round to give my husband a little break
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Ditto that on the ponytail feeling when I went from longer hair to a pixie cut just before starting chemo! Just had round 4 of taxol / Herceptin on Thursday, and this morning I noticed my hair starting to shed. This has hit me harder than I thought it would. I've been very lucky with almost no side effects other than horrible constipation. I will probably get my hair buzzed down soon before it starts looking patchy. I know it's all part of the journey, but it still sucks!
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Fleur, our hair must be on the same schedule: I had Taxol #4 on Thursday, got itching/burning feeling in my scalp Friday night. Shedding became unbearable yesterday, so today I shaved it off. It's so liberating!
I think I was afraid of this for a while, but now that it's done, I feel relief. I did have a good cry at the beginning when we were just buzzing it off.
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Hi Warriors - the start of a new week. Today is my last 'some what normal' day before the chemo cycle starts again.
Tomorrow (day before chemo I get blood work and see my oncologist) -- and then Wed is #4 (of 4) TC Chemo cycles.
I am both dreading it and looking forward to it being over at the same time. One of my close friends is traveling to see me Friday eve to Monday am, just to help me push liquids and catch up on on the couch while I go through my first recovery weekend. Friend therapy.
I am sure on Wednesday afternoon, after the chemo session, I will feel different, today -- just kind of full of dread (yes, I know it comes in waves ....) . I am also a bit angry that I will be feeling 'yuck' during my friends visit -- silly I know -- she is coming to visit to help me through it ...
Ohmm, I came to the board for inspiration and to change my Monday morning attitude. Thanks for all of your posts and support - it helps. I keep reminding myself this too shall pass ....
Cheers to everyone managing the SE's and pushing through the down thoughts.
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Travel Girl...#4...LAST ONE AND DONE! I also see you have a surgery date already set in December? You are really getting there, light at the end of the long tunnel! Can't beat a good friend. Mine have also been here for me through this whole experience.
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Travel Girl- You're almost there!!! One more to go and then chemo will be a memory. I hope your last treatment is easy on you and you can enjoy the time with your friend.
My third (halfway done!!!) treatment was last Wednesday. The side effects were not as bad this time, just more tired. I sucked on ice during the Taxotere and my mouth sores aren't as bad this time. I am dreading the remaining three treatments, but each one gets me closer to done. It's like running. I'm at that point where I want to stop so badly, but I need to keep pushing through.
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