September 2013 Chemo Group
Comments
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LHL...Healing thoughts your way with No SE!!!
JellyK hope you feel better and the nausea stays away.
I am on Day 9 and feel pretty crappy...thought i would be feeling better by now. Water tastes like oil....I just rinsed with baking soda water.
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Something I hadn't anticipated, I think my nosehairs might already be gone - when my nose runs it RUNS like crazy, I can barely get a tissue up to my nose fast enough, lol!
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(((lovewins))) I'm sorry you're still feeling crappy, that's not fair. I hope the baking soda works, that nasty oil taste is awful. I've found that V-8 fusion seems to cut through that a little bit too.
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Good luck with the treatments today ladies! And I agree with JellyK: stay out of the sun! I wasn't told of the sensitivity (or I spaced it with all the other info to take in), and I was in the sun no more than 5 minutes waiting for my ride after chemo and got burnt.
JellyK: sorry to hear you are sick. I am so terrified of getting sick during this with 3 kids all in school, and all different schools at that lol. I thought I was getting sick after my first chemo too, but I am thinking it is just the way my body reacts, or like you said, the Neulasta kicked in and got rid of it.
So, I let the kids cut my hair this morning. A 4 year old and a 3 year old with scissors...I was glad to know my platelet count was adequet yesterday lol. They did good though, and had fun with it. I tried to do the mohawk but I had my friend cut my hair really short in back not long ago so I didn't have enough hair. Do you know how hard it is to cut your own mohawk?! I ended up going to my friends and having her fix it. It's only about 2-1/2 inches long, but I actually really really like it! I think I may do it again when I decide to cut off my chemo curls. Ah the things you discover when you get cancer.
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JellyK: my nose is constantly running! It is almost always tinged with blood too, and I guess I got more nose sores than mouth sores. It isn't very pleasant. I thought about nosehairs, too, and even looked up my nose lol. I dont' know how many were up there before, but there are still some. Still, when it goes, it GOES!
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JellyK: So sorry you are having a bad day with the cold. I was wondering if normal saline drops might help you. Also you mentioned that you start on Neupogen tonight. How is that given? I hope you start to feel better soon and have minimal SEs.
BabyRuth and Lighthouselady - I hope all goes well with this round of chemo. I'm thinking about you both and praying for you and others here on the formum. Now that I've a taste of what this experience is like I clearly sympathize.
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BabyRuth - (((HUGS))) I hope today goes well.
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Lovewins: I'm sorry you are still feeling pretty bad. I'm curious what chemo regimen you are on.
Mamawstewart: I'm sorry about your nose running. I wonder if normal saline drops might help. I was also wondering what chemo regimen you are on.
I'm on Day 7 and almost feeling normal but not completely.
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Sitting in the infusion room getting my premeds with my first cold cap on. Hope all goes smoothly!
I make quite a spectacle when we walk in with two wheeled coolers and bags and electric blanket. Ha! Nobody has ever used cold caps here I don't think.
They gave me Emend this time so hopefully the nausea won't hit me so bad. It didn't last long, though. -
I am finished and have been back at work for a while. Everything went well for me today and so far I am feeling fine. I hope it will continue that way! I will write more when I get home later today.
Here is my funny thought for the day: Men, Chocolate, and coffee are all better rich.
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Wishing everyone good luck with their treatments today - hoping the side effects are few!
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BayRuth, so glad you are doing ok. I hope it stays that way. Lighthouselady I hope you are doing good too. JellyK so sorry to hear you are sick. I hope everyone feels better soon. I will go for round 2 on Monday. Did anyone get dandruff after cutting their hair?Never had it before.
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hello ladies i also had my first cocktail of AC this morning. i was very nervous when i got there but all went well i didnt have any complications or side effects so far. i feel pretty good right now though i dont know what the night and morning will bring. Im hoping we all will continue to have good days with little to no side effects. any suggestions
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Deb...My cocktail...not by choice
id tch. I was feeling better on day 6....I am on day 9. I am wondering if my platelettes are low? I guess it kinda helps to think of this as a science project. Trying to see what I can do to better things for round #2. Yesterday I had the thought of this being like a boxing match and I have 6 rounds to get beat up and fight back. Tonight I am going to stay with afriend because she had a d & c today. Tomorrow I will drive up to my folks who live about 200 miles away to stay for a week. Glad you are doing better. Loved your fried chicken story.
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Well I guess my hair is starting to go.
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(((alfranco))) I'm sitting here with my buzz cut, pulling out 15-20 hairs at a time every time I tug ever so slighly on it :-( It's harder than I thought it would be. You are not alone.
Hugs also to the ladies having their treatments this week!
My cold sucks, there's no other way to describe it. But it's just a cold, and I'm a lucky lady because I don't have to be at work and both of my kids have school/daycare today, so I haven't really left my bed, lol :-)
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JellyK, I hope your cold clears up soon. That sounds miserable without the nose hairs...the things I have to look forward to...
I finally got notice that one of my wigs was shipped. It should be here in about 2 days. Yay! We are doing a big head shaving party next Wednesday. I originally thougt about 5-10 guys were shaving their hair with me. It looks to be much more than that. It will help make a tough situation so much more tolerable! I got a bunch of skull caps in the mail today that I ordered. I put them on with a wig cap underneat. I hate to say it, but I actually like them!!!! It reminded me of my OR rotations for paramedic school! I will be shaving my head all the way down. The plan is to put my hair into a whole ton of pony tails. I am goign to cut them off with scissors, cutting it as low and close to the scalp as I can. I am saving those to try and make a make-shift halo wig for myself. I then will let them buzz it/shave it all the way. A couple of the guys who ALWAYS are bald and never have stubble are even letting their stubble grow in this week to re-shave it. People can just be so incredibly kind and supportive! I have no idea if my attempt at a halo wig/headband will work, but if it doesn't, it will at least entertain me for a few hours trying.
One of the guys at work also made me a bet. He's a Nebraska fan and I am a Penn State fan. He has a Nebraska skull cap and I have ordered a Penn State one. Loser has to wear the winner's for a week. As long as I have to put up with this stuff, I might as well find some fun in it.........
Wishing everyone that had treatments this week comfort with few side effects.
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Kbee, your group sounds absolutely amazing! Our support networks are our lifelines, no question, because our survival absolutely depends on our attitude. Today I was feeling sick at all the hair coming out, but when I showed my son he thought it was super cool, then decided to count the hairs on my pillow. Took me out of my little pity party, thank goodness :-)
I can't decide whether to worry about this cold or not. I literally rested all day, didn't go out, slept, the works, but I don't feel even the tiniest bit better tonight. I guess I just keep monitoring if I get a fever, and deal with the rest :-( At least my pharmacist cleared me to take cold meds...
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Hi everyone, i got my hair cut off yesterday. Everyone really likes it but i cant get use to it. im really cranky because i rang today to check i was booked in for next Thursday and they said im not on the list. I now have to wait till Monday 23rd. That just doesnt suit with work or anything but i guess there's nothing i can do about it. Just wanted to get going with it. Im booked in for LGFB on the Tuesday so i hope im feeling ok. Good luck everyone with your treatments.
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Quote for the day
Recognize that you have the courage within you to fulfill the purpose of your birth. Summon forth the power of your inner courage and live the life of your dreams." -- Gurumayi Chidvilasananda
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JellyK: I suppose Airborn or anything like that is a no-no? I can't take really any kind of cold medications due to a heart rhythm issue so whenever I am sick I live off Airborn. It does do a great job of keeping things at bay and making it go away quicker.
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Thx Mamastewart, I'm not sure about Airborn, I'd have to check the ingredients. I'm sticking with Mucinex at the moment, since my sinuses like to clog up and get infected whenever I'm sick, and Mucinex tends to keep things moving. Every cell in my body hurts, and now my scalp hurts too because of the hair falling out. It's time to count my "thank you's" I think before I get too far into my pity party. Thank you to my colon for not clogging up today, lol; thank you to my son for letting his grandma take him to school without an argument; and thank you to On Demand for providing endless television to my 3 year old so I can rest :-P
Hope everyone is doing well today - for everyone who has started treatment, you are one more day closer to being finished, and for everyone waiting for their treaments to start, you are one more day closer to being done with the anticipation :-)
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Hi, all. Add me to the September chemo group. On September 16, I am starting taxol once a week for 12 weeks followed by a/c every two weeks for 4 cycles. Anybody else do taxol first? I've looked around on the boards and haven't seen many people do it in that order.
Getting ready to do some chemo-prep shopping this weekend. Any thoughts, tips, advice would be great!
Thanks so much.
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JellyK: Sorry you are down. I think it goes with the flow of the treatment. I know I had my keister firmly planted on the good ole pity pot last week. And thanks for reminding me to eat my prunes. I didn't realize you had a little bit too; my baby is three also. This too, shall pass! Hang in there! I haven't started shedding "down below" yet, but I keep checking. I feel like I am going to puberty again lol. I am still sporting my mohawk and I think I will dye it today and head to the store.
Hey Vanessa! Welcome to the group, but sorry you have to be here. I am just opposite of you (triple positive) so I just do all my three at once every three weeks. I suppose I have it pretty easy in that respect; less visits to try to coordinate and go to.
I didn't do a whole lot of shopping/preparation. I think this was partly due to the fact that I was/am in denial about all of it. It seems like a dream I am going to wake up from. If I did too much preparing I would have to face reality. I wish I had froze some meals. That would have been very helpful to me because the week after I didn't feel much like cooking. There is a list here http://community.breastcancer.org/forum/69/topic/706846?page=36#post_3436641 that is really helpful. I wouldn't go overboard with it though, especially if you have someone who can go get things for you as you need them. I did get the Clairitin to help with the Neulasta bone pain if you will be having that (not sure if that is on this list or not). Unfortunately, my clinic didn't go over any of the side effects or anything with me until the day of chemo. If not for this group and other survivors I've talked to I wouldn't have known about half of it and how to prepare until I had already had my first infusion. Best of luck and feel free to ask any questions!
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Ladies is anybody else's body shedding? Kind of dandruff or dead skin. I see it on my clothes and anywhere I may sit or lay.
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JellyK, Vent all you want. We are here to support each other. I hope you can get soem rest this weekend and kick that dang cold.
Vanessa, Welcome, but sorry you have to join us! I start next week too. I begin on Friday. I won't have Taxol, but will have Taxotere and Cytoxan. I am making sure to have a lot of the things on the list there on hand. I also am planning on bringing cold packs and bags of ice in a small cooler to ice my hadns and feet to help ward off neuropathy and hopefully save my nails. My MO okayed it, which made me glad.
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Vanessa,
My wife is getting the same order as you with herceptin added in because she is her2+.
Be well & good luck -
I had my long hair cut short yesterday too! It is spikey & funky.
I still don't have a chemo start date, week of 23rd but don't know the day.
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Well, I guess so far (knock on wood) this time has been a little better. The nausea still hit me right at the 3 hour mark (after chemo finished), but it hasn't been bad. Just a constant queasiness and nothing sounds good to eat. Hubby and I were a little rusty on the cold caps since we hadn't touched them since my last tx. It was kind of comical for the first one. But then we got back in the groove. The only thing was the caps were TOO cold, so he was having to sit on them to warm them up. He was like OUCH! LOL I told him imagine putting that on your head!
lovewins - I was able to finally drink water by like day 12 or so, but of course that only lasted for a couple of days and now my mouth is about to get yucky again.
I have been SO tired today. Holy cow... way more exhausted than I was the day after last treatment. And I slept so long last night. Not sure if my body is just catching up or if it's the Emend on top of my other medicines... or just a cumulative effect? I have a prescription for steroids for three days...do you know why we are supposed to take them? My MO only gave them to me after I called the next day last time to say my nausea meds weren't working. So if I'm feeling ok do I need to take them? I got it refilled (there were only 6 pills), but hate to take them because I can't sleep and I'm wondering if the "steroid crash" contributed to my awful headache last time.
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Have been reading but wanted to officially join today. Chemo #1 complete this morning, nothing really to write home about. My husband of 20 years kept me laughing by joking around with the nurses. Went to lunch afterwards and felt fine to eat then promptly came home and crashed for a 2hr nap (suspect the Ativan) Got up and although not nauseous per se, could NOT talk about a grocery list my husband was putting together. When he said the word 'salad dressing' i told him to please stop talking. He left for the store, I took my first phenergan and within 20 minutes called him, was ready to talk about food again and give him my list;).
I am a fitness professional and own my own yoga studio in our small town and I struggle with the hope of maintaining some activity so that I can still teach and have the mind and body energy to train my clients over the next few months. Luckily I have a Great network of supportive teacher friends who are jumping in and offering to teach some classes and workshops to help me keep paying my rent. I am also a runner and had major concerns about exercising while on A/C ...a board certified oncology naturopath told me nothing more than walking so as to not stress the heart, my own MO said just don't pick up any new activity I've never done before. We sought out a 2nd opinion about chemo options from the breast cancer oncology guru at OHSU in Portland...( AC-T DD for 16 weeks or TAC every 3 wks for 18 wks) in the end 2 less weeks made the difference for me. His opinion was ...do not just get lazy and stop moving. When I feel yucky and not like exercising to get out there and do it more. He said and i quote....go wrestle an alligator, go train for a race, go scuba diving, work on getting my bench press up...that really I have no limitations. It helped hearing him motivate me...although no way on the alligator! So We shall see. Thank you for letting me be a part. I hope to do my best to keep up with you wonderful ladies and share my own journey too!
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