Starting Chemo March 2015
Comments
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revup-65 how did the port placement go? Do you have any residual pain or problems so far? I think I'm more worried about that than the chemo. I've just had so many other surgeries (and haven't even had BMX yet) that I get anxious about procedures.
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Hello, all,
I was out and about today for a while. Visited my Mom, who lives about 20 minutes away. She is very frail, and is mostly housebound, but is scheduled for cataract surgery next Tuesday. We had a nice visit, but she is focussed on my chemo starting soon, so the conversation tends to drift there. It's pretty draining, really.
My sister cut her hair last night "in solidarity" with me. She didn't go down to skin, but her long hair has been transformed into a cute pixie cut. I almost feel embarrassed that I haven't buzzed my hair yet. Maybe tomorrow, after my port placement.
I'll stop by tomorrow after my port is in. Gentle hugs to all
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Hi ladies...... unfortunately I too am starting chemo in March, probably second week. Almost 2 weeks ago i had mastectomy and exactly 2 weeks later (on 26th) i am having a complete hysterectomy. I'm nervous about healing enough before chemo starts. Onco thought that if i could get it done this week i would heal better than after treatments down the road.
I'm glad we will have others to do this together with.
Xoxo
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Msmath, Rleepac - Yes! I'm having one breakdown after another. This part of the "journey" seems the toughest to deal with so far, for me. I'm trying to get all the ducks in the row before my chemo starts on Tuesday, and nothing seems to be working out. I've made numerous phone calls and I'm getting a lot of run around, especially from my health insurance company.
Cancerisnotmyhappyplace - Thank you for chiming in, it's always nice and reassuring to hear from those who walked the path before us. I also agree with your nickname!
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Going for my pre-treatment echocardiogram today and I think I've got DH convinced that doing the port on the same day as first chemo treatment is an ok thing. Planning a weekend out of town this weekend for a relaxing getaway and then I'm ready for my first treatment next week.
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Does everyone get pre-treatment echocardiogram? I know they will be monitoring my heart function every so often once I start going to treatments, but they did not mention doing one prior to the first chemo.
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Unfortunately there seems to be a few of us now, starting soon. BB I had my heart checked last Friday. Today I'm taking part in a study. It looks to the risk of chemo on the heart and diabetes. Then I'm getting my hair cut!
I went away for a couple of days. Needed a break before this all starts. My boss came to see me to talk about me doing some work if/when I can.
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BB - I believe anyone on Herceptin is supposed to have a baseline and then monitoring cardiac testing because it can have negative effects on the heart (although with Herceptin it supposed to be reversible). Also, I was told that Adriamycin can cause heart damage (non-reversible) so that's another one that gets monitored.
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Hi ladies,
I'm a March 2014 alumnus, stopping by to say hey. A couple of other veterans have already covered a lot of what I would have shared, so I'll keep this short.
1. You will survive this. There will be times when you might doubt it, but you will get through chemo.
2. Everyone is different. You won't get every side effect (SE) on the list, but you will get some combination of them. Contact your MO (medical oncologist) as soon as you start experiencing symptoms. There are a number of meds that will help you, but you have to ask.
3. Take it one day at a time. And if there are times when a day is too big a timeframe, take it an hour at a time. Just put one foot in front of the other and keep going. Everyone will marvel at how strong you are. Accept their positive reinforcement even it you know your strength is an illusion.
4. Ask for what you need. The most surprising people will come through for you. Be prepared, though, that some surprising people will be unable to help.
5. Nurture each other. This group will become a tremendous source of support, comfort, and inspiration. You will find yourself sharing stuff you would never dream of telling your nearest and dearest. Celebrate your victories.
Best of luck to you all. Remember -- you can do this! PM me if you'd like. I'll try to answer if I can.
PS: I have a full head of snow white hair now. It was brown when I started. Go figure.
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Just got back from having my port placed. I was told to expect that the procedure would take less than an hour, but to plan for being at the hospita for about 4 hours. That estimate was spot on, as I arrived at the hospital at 10:30, and we were in the car on the way home at 2:25.
When we arrived, we met with the doc who placed the port, and he had an actual port in the meeting room to demonstrate its size. I was a bit surprised at how deep it is. After checking in, and giving DH a kiss, he went back to the waiting room, and I was wheeled into the surgery. I did opt for sedation, so that was first, followed by a local. The procedure seems to involve a fair amount off tugging and pushing, with dissolving stitches "inside" and just a few steri-strips at the incision sites. I'm allergic to tape, so the steri-strips were then covered with Tegaderm, and I was off to the recovery area, where they monitored vital signs for 2 hours. During that time, snacks were available, but I couldn't lie down fllat - head had to be raised at least 45 degreess.
Back at home, I've taken a tylenol, but it isn't really uncomfortable. I'm tired, though, after the drive (1.5 hours each way) and the sedation.
I go back tomorrow morning, for echocardiogram and CT scans. Looks like this is really going to happen, and soon!
Gentle hugs to all.
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Deep breath. This too shall pass. The anticipation of the first dose is the worst, and then waiting to see what happens to your hair. There are a lot of women who have been where you are right now and thankfully some of them started this wonderful site so we could support each other through this most trying of times.
A year later I see things with new eyes, find a lot more to love about life and know more than I ever dreamed about myself and what matters to me most. Yeah, somethings could be better (eyelashes) and I certainly wouldn't wish it on my worst enemy, but I am grateful for treatment that dissolved my tumor and left me cancer-free.
I would recommend adding to your team and not just sticking with the western, allopathic treatment. I've used Chinese Medicine, massage, naturopathy (I have a naturopathic oncologist I sought out separately who has been invaluable), etc. Cancer docs are specialists and they tend to see things from one perspective and there are other practices that can help your body through this experience. I used Chinese herbs (from my practitioner) to boost my white blood cell count instead of getting the Neulasta shot for instance. Be your own project manager because they won't give you one and you deserve a bigger plan for healing.Ann
March 2014, member of The Chemo Sabes -
rleepac I am sorry I am late getting back to you. I am having more discomfort then I thought I would. It sticks up more than I thought it would also. I go for chemo tomorrow so worried about it being painful. What can you do but just keep going. Maybe they put it higher on my chest than usual because I am still healing but who knows. I will tell you this is nothing like 20 yrs ago when I went through all this. But you may have a better time than me, it seems to be different for each person. I hope yours goes well, send good thoughts your way. I did work the day after, maybe should have stayed home and rested. It is all so frustrating, I cant wait to see what happens tomorrow! I will have to try and find my happy place
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Good evening Ladies - You can do this, and it's game time so Game On! I finished chemo 11/25 and I just wanted to let you know that while chemo is no picnic, it is doable. It is a huge investment in you and you are all worth it.
The good news - My hair is now 1" long/short and it is dark brown and white, but mostly dark! My eyebrows have grown in, and the eyelashes are all back and thicker and fuller than the ones I lost. So nice bonus there.
My fingernails are almost all grown out, one more trim and file and they will be as good as new. My thumbnail has grown back and another month and it should be just like the other one. My toenails are looking good too! Lots of lotion on the hands and feet helps too. So I should be all together by Spring, and sporting nice short hair and pretty nails. Another bonus, my nails are coming back very hard, not brittle like my old ones.
For the AC chemo ladies, they did a baseline ECHO before I started the chemo so they could keep an eye out for heart damage to the EF percentage. Just watch for any cough or shortness of breath that may point to heart issues. I have reduced EF from the Adriamycin, but I cannot do it again. I'm sure my age doesn't help, 58, but I still have the permanent heart damage.
Ok ladies, get your game on! Good Luck
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such fantastic advice! Thank you you all for spending time helping us. It helps when people That have gone through it share and give tips that have worked for them. I had my haircut today. Stage 1... I'll probably get it buzzed when it starts to fall out.
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Hi Everyone- Just jumping in to introduce myself. I'm a newbie. I'm 46 and just had my lumpectomy and lymph node removal last week (7/26positive). I have my port going in on Monday and I'll find out on Wednesday what my chemo schedule will be. I've started reading these forums and am noodling around trying to find out as much information as I can. It's very helpful to read other people's stories.
I did purchase a fancy wig a few weeks ago and am going to my stylist to have her cut the wig and my own hair short. It's weird, I've never had short hair, let alone no hair. Who knows if I'll even end up wearing it. I've heard that your scalp can be super sensitive.
I guess I'll know more next week, eep!
xo
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Count me in with the March group. I start chemo on March 5th. I had my port put in on Tuesday. I'm still a little sore from it but glad that I got it done. Getting an IV in gives me the heebies and I have a really bad arm. It took them almost an hour and 5 pokes to find a vein when I had my mastectomy on Feb 3.
I have a 5 year old and he's getting used to mommy having doctor's appointments. I got my hair cut short last Saturday and returned to work on Monday. I haven't had short hair in 30 years (I'm 41). I have very curly hair so I was always afraid of what it would look like. So far everyone loves it! My husband says I should keep it short when it grows back
I bought some cute hats through TLC and plan on getting a wig -- just waiting for my insurance company's approval (they pay up to $500 for a wig).
I'm pretty positive minded about the whole thing. I'm grateful that my cancer was caught early enough and that we have these medicines (no matter how crappy it'll make us feel) that will help us heal.
I plan on working through treatment. I'm fortunate that I can work remotely and even while having the infusion. Which brings me to question, how long is an infusion treatment? I'm trying to plan around it. I'm glad that I live and work 10 minutes away from the doctor's office and the hospital.
Thanks everyone and best of luck with your treatments! Stay positive!
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Hi, all. Back from echocardiogram and CT today. First AC is scheduled for Monday morning. It seems to be both taking too long to get started, and so soon that I can't possibly be ready. I suppose it's just another of the endless uncertainties that go with this strange new country of Cancerland. I'm always scared of the next thing, then when it comes, I seem to manage to deal with it somehow. I often feel like I'm still in denial - after all, I'm not just curled up in a ball, shaking with fear. On the other hand, I haven't been able to do get very much done since my surgery. I did have a nasty infection, post surgery, but I've had lots of fatigue.
Gentle hugs to all. Let's do this
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Looks like I am a week behind you avmom in treatment. I have a lot of the same feelings. I haven't been able to get much done since my surgery which has now been 4 weeks. These drains are really driving me crazy. I keep telling myself if I can get rid of the drains I will feel like going out and getting all this stuff done before chemo starts on March 9th. I also think I maybe just be putting off doing things out of denial.
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I think Avmom has hit the nail on the head when she talks about being scared of the next step, then when it comes along somehow she can manage it. That's exactly how it goes. Although I never stopped being scared of the next step, as time went on I began to develop confidence in my own strength that I could manage whatever the next step brought. I'd done it before, so I could do it again. That growing confidence in my own strength and abilities made it a little easier as time went on and I was faced with the next step.
Even now, seven years later, I find I'm much more open to trying new things. If I like them, great. If I don't, oh well. I think that attitude is leftover from being forced by cancer to take several scary steps like surgeries and chemo, then finding that somehow I was able to manage them. This whole process made me realize I'm a lot stronger than I ever thought I was. Whenever I'm faced with a new challenge now, I think, "Heck, you got through chemo. After that, whatever this is will be a piece of cake by comparison!"
SC - you asked about how long infusion treatments were. My infusion treatments took about 4 hours, but yours may be different depending on exactly what cocktail of drugs you're getting.
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Got my Mediport put in yesterday. No general anesthesia, just the "deep sedation", I'm still a little woozy.
Not in much pain, just discomfort, can't turn my head well to the opposite side, as well as I'm limited in my movements on the port side. I'm hoping this will go away shortly and I'll be able to forget I have just another artificial part under my skin.
Also, just a thought of having this thing close to my neck and going into the heart makes me squeamish again.
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MSMath, I understand about the drains being crazy-making, but I'm pretty sure my post surgery infection was the result of the drain being taken out too soon. Several days of IV antibiotics later, I was exhausted from the trips to the hospital every 12 hours for the antibiotic infusion. (I live in a rural area, and it's about half an hour's drive to the town with the nearest hospital.)
BBwithBC45, my port went in on Wednesday, and was quite sore and swollen yesterday, but I've been icing it last night and this morning, and it's a lot better today.
NatsFan, thanks for the encouragement.
I'll be out and about today, doing last minute things. I think I'll buzz my hair today. Onward!!
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BB and avmom - I have to admit that you have me a little nervous about the port! I know everyone reacts differently but I'm just getting so squeamish about procedures. I know it is the absolute best thing and I really will be happy to have it in the end but I think I'll be taking some Xanax the night before!
I had a mini-meltdown last night. I was giving DH the rundown of appointments next week and when I finished he said "are you ready?" I told him I was and even if I wasn't, I have to do it anyway. Then he told me that I don't have to be tough and strong. To that I burst into tears and said "good...because I sure don't feel strong or tough right now" Ten minutes, a box of tissues, and lots of hugs from DH and DD later...I recovered and I'm moving forward.
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Shaz - I'm so sorry to see your long hair go but the short cut looks good on you. I cut mine about a week ago and I cringe every time someone tells me it looks cute or it suits me. I want to scream at them "Nooooo...don't tell me it looks good...I didn't do it because I wanted short hair!!!" Uggghhh.. I know it's weird but only my fellow chemo sisters will understand.
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Isn't it amazing that all or thoughts and feelings are the same. My chemo starts on Tuesday and I'm at the stage now of it can't start quick enough! I haven't really been on the forum lately as I keep waking up with migraines. Today was the 5 day in a row. The drugs get it under control but it still takes 3-4 hours and wipes me out for the rest of the day.
My oncologist hasn't mentioned a port. Is that standard?
Rleepac. I feel the same when anyone mentions my haircut! So I totally understand. No one else really gets it.
I'm planning on a nice weekend. My sister and mum are coming around soon to do some cleaning for me. Followed by a bbq for dinner. I feel embarrassed having them clean my house. But I can't scrub anything with my arm yet and movement is still limited. I really want to clean shower!:-) have a great day everyone xxx
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rleepac, try not to worry too much about the port. Mine went in on Wednesday, and it was tender yesterday, but today it's basically resolved. It isn't pulling when I move my arm or turn my head, and although I'm aware of its presence, it's easy to ignore by concentrating on something else. I'm confident that by the time it's accessed on Monday, it will be just fine. I changed the bandaid today, and the incison is closed up, without a single stitch or staple. Even the steristrips are gone.
In other news, I did buzz my hair today, and wore my wig into the office. The wig is much more comfortable without all of my hair underneath it, and the only comment my "hair hat" is getting is how it makes me look younger. I stopped colouring my hair about 5 years ago, so my natural hair was quite grey. My wig is not- it's the same colour that it was when I was about 12 years old, and matches my eyebrows perfectly. Not that it matters much, as my eyebrows will likely be history soon, but it's a good match for my complexion. Overall, the wig improves my appearance. I'm surprised that buzzing it offf didn't bother me much. I just went to a walk in salon and had it done. I think it would have been harder for me to have made an event of it. This way, it's another item on my to do list, checked off. Maybe I'll figure out how to get photos from my phone onto this board over the weekend, and I'll share some "before and afters".
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rleepac I too had a little crying/hugging session. It felt good to get some emotion out. My husband and I have never had family live close by. My mom was visiting over Christmas when I was diagnosed. She went back to Ohio for a few weeks but returned the day before my surgery and is planning to stay for my first chemo treatment. It is weird because I can't cry in front of her. I'm trying to show her that I am the strong person she keeps describing to everyone who calls or stops by. So needless to say my session was done late at night and my husband was a good sport and didn't mind the lack of sleep. Next week my mother-in-law is coming to stay for 3 weeks. Then my dad just sent his flight info and to my surprise he is planning to stay for 7 weeks! How am I going to "stay strong" until the end of May? Don't get me wrong I'm thankful to have family that are basically putting their lives on hold for me but going from no close family for 20 years of marriage to them staying with us an adjustment. Any advise on how to deal with my visitors?
On a lighter note any advise on what type of sports bra to wear for chemo that won't interfere with my port? Today was my first day wearing a sports bra instead of the the surgical binder thing.
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I guess I am now joining this group so I'm popping in to introduce myself. I just received my oncotype score and the MO recommends chemo. At this point I simply feel relieved to finally have an answer. I started this whole process back in late November when I found a lump so this answer had been a long time coming. What a roller coaster! Anyway, I am ready to get this started! Shaz101, I remember you from the January surgery board. It is nice to see a familiar face here. I hope all is going well with healing. I didn't post much on the other board but life was just so busy at the time. I'm going to slow down now and take some time off of work once I start chemo so I can make sure the energy I have goes to my family. I haven't even looked into head coverings or anything like that. I am so style challenged that I am going to need an army of friends to help me - lol! I have the weekend to digest the news from the MO and then I will give him my final decision on Monday about chemo - even though I already know the answer in my heart. It sounds like I'll start the process the week of March 9th and will be on taxotere and cytoxan.
Have a good night!
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Msmath, Didn't ya'lls families get the memo: Fish and house guests stink after three days! Seriously, it's just chemo, you will not be an invalid. My advise to you is to have them house-sit while you and hubby get some nice quiet time away on long weekends.
Go braless during chemo. They will place a 3 inch square clear bandaid over your port to hold everything in place. Wear a button front shirt or a low cut, very loose top.
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Just had a really nice relaxing day and a half in Monterey - thoroughly enjoyed the beach and bought about 7 scarves to start playing with. I need to order some Buffs for my head though because they are so easy and comfy but I'll do that later tonight.
Now, I'm totally 'nesting'!!!! LoL!! I've mowed the lawn (1/2 acre) and used the awesome gas leaf blower to clean up the rest of the yard. I will let DH do the weed-whacking though because that thing scares me 😜. I've scrubbed the bathtub and cleaned out the fridge. I went to the store and made sure I have stool softeners, good lotion, Biotene mouthwash, and a really soft kids toothbrush. I'm doing laundry and already went grocery shopping. I know I don'tstart chemo until Thur but I'm just trying to be as prepared as possible. I feel like I did when I was 39 weeks pregnant hahaha. Anyone else do this?
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Starting chemo tomorrow, March 2, 2015, (Taxotere/Carboplatin/Herceptin), and am somewhat nervous today. Or maybe that is just the Dexamethasone kicking in? I feel like I took in a super heavy dose of caffeine today, and I have to take the next two pills in about a half an hour - eek! My HER2 had to go through an additional level past FISH, and basically came up as slightly HER2 positive (low level amplification) on the HER2 Breast Equivocal FISH Panel amplification. So not sure if that is a good thing or a bad thing, given that I am ER/PR-. Trying to be positive about chemo, but the closer tomorrow comes, the more nervous I think I am becoming. I know it is the right thing, I just wish the first one was over so I know what to expect.
I somewhat short-cutted the process to begin with. Once my ultrasound showed a spiculated lump, I went right to a lumpectomy with Sentinel Node Biopsy, and I did no other biopsies after reading about women getting breast cancer back in their biopsy tracks. Lumpectomy smallest margin was .5 centimeters, 3 nodes removed, all clean, no lymphovascular invasion. Tumor was at 2 o'clock on left breast, some DCIS with the IDC. The only concern is now that there is no tumor left, not sure if anybody will be able to tell if the chemo helps. I've been through an ultrasound, diagnostic mammogram, MRI with contrast, PET Scan, bone scan, and MUGA scan, and so far all show clean. Nothing like starting out chemo toxic to begin with!
Best of luck to everybody starting chemo in March!
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