Starting Chemo in September?? where are you ladies
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Hi Sheri,
I was wondering about the "potty break" question, I was happy to have that answered. As I stated in my posting I am not getting any pre-treatment care. No meds before hand or anything. This is making me very apprehensive. Should I call onc and ask or will they think I'm second guessing them?
Thanks for any suggestions.
Cheryll
Cheryl...I would ask if there are going to be any pre-medicine anti-nausea medication. This will also let your oncologist that you are aware of what is going to be happening to you and he/she will respect you for that. Also, it was suggested by my oncologist to take senekot during those pre-treatment days and after because sometimes chemo causes constipation and you don't want to have to deal with that on top of everything else. -
Hello! This is my first time on a discussion board. so be gentle
Biops y July 3. Lumpectomy Aug 21, 3 of 20 nodes positive. chemo in Sept and after chemo 7 weeks radiation. I am looking for a soft Bra to wear after I get the sucko tube out and don't want to continue to wear this corset contraption.
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Hi, I live in western Georgia, USA and was dx'd 8/2. I got my port last Monday, and start some kind of chemo this coming week. I'm er, pr negative, but my HER2 status is mysterious to the point that my doc has consulted with Johns Hopkins and some other colleagues, and will likely have me do another biopsy this coming week as well. I've chosen to do neoadjuvant therapy, so can only guess I'm stage II or so. I may have an axillary node biopsy done this coming week at the same time as the tumor re-biopsy, but not sure yet. Need to talk to surgeon. Thanks for the Chemo Angel info. I have a very, very limited support system, so it's great to get support anywhere I can. I'll also look into the Emla cream. (Is it expensive?) I'm worried about finances and work since I'm the sole support of me. I have no SO, just 2 cats and 3 goldfish. I'm especially happy that I have enough hair to donate it to Locks of Love. If anyone is interested, I keep a blog at www.tiding.blogspot.com.
Peace,
birdies -
I am in a clinical trial for Oncotype DX. I was tested (or my specimen was) and fell in the middle group with a score of 13. I was randomized and was selected to do the chemo, followed by rad and tomoxifen. Took 3 weeks to get the results back!Definitely tired of waiting. While I'm not super excited to start chemo, I'm thinking let's get this show on the road! Good luck to you!
Cheryll -
I know exactly how you feel. I have a limited support system also and am my only finacial support too. I don't know which is worse being scared of the diagnosis or wondering how to pay for it?!?!?! Someone recently told me that I will do well because I'm so strong and I replied I'm not strong and that I am just scared to death...but I will do what I have to do to beat this! So stay strong and take care and God bless us all!
Cheryll -
The learning curve for becoming a breast cancer patient is just jaw-dropping awesome. I don't know about the rest of you but I'm doing good to know about ER & PR & HER2 stuff. After that part people get all fancy about staging, and the fact that I'm doing neoadjuvant instead of adjuvant treatment and don't know (likely will never know) what stage I am, blows some people's minds. There's this whole body of knowledge that I haven't absorbed yet, and in some ways I'm scared to become sophisticated about. I want to be smart, but...it's all so scary. I feel like no matter what I do, I'll be explaining or defending my decisions to someone. Do any of you feel like this??
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Regarding your bra question...They have a wonderful post surgical camisole at Nordstrom called Ameona. It is soft and has drain pockets that velcro on. I only had a drain for one day, so I didn't need to use those. I found it very comfy to sleep in. It is made specifically for this type of surgery. Good luck! I start Chemo Sept 6 ...getting nervous/anxious.
Marietta -
This probably sounds doofey, but is it ok to sleep on the side that your port is on, as long as it doesn't hurt? Somewhere I read you shouldn't sleep on the port side. I tend to want to sleep on that side a little, not a lot, and I want to be sure I'm not going to screw it up.
Thoughts? -
Hi Ladies, just popping over from the August 07 group to tell you you'll make it! I'm halfway through, and life has now become a comfortable (comfortable? ok, predictable..) pattern of what I can expect. It will be for you too.
Have you seen the thread under "Going through Chemo" called "Tips for getting through chemo"? I printed out the list of possible side effects and what can be done about them, made a list and went shopping. Actually needed very few of them, but boy, was it nice to have what i did need without having to make an extra trip to the store.
Like another poster, the headaches and sinus congestion were the biggest complaint. I felt no nausea whatsoever, and constipation only the first treatment week.
I also didn't receive a lot of pre-treatment info, so I LIVED on these board, absorbing everything, doing a "search" on what I didn't understand. It's all here.
We're rooting for you girls, -
Thank you so much for your encouragement! I did find those lists of things that may be needed while going through chemo and thought it was really helpful.
Anyone have shoulder problems after port surgery? Mine is finally starting to loosen up a bit, but it is driving me crazy.
Anyone starting this week? I would love a chemo buddy.
Marietta -
Quote:
This probably sounds doofey, but is it ok to sleep on the side that your port is on, as long as it doesn't hurt? Somewhere I read you shouldn't sleep on the port side. I tend to want to sleep on that side a little, not a lot, and I want to be sure I'm not going to screw it up.
Thoughts?
Hey Birdies,
I'm so glad to see your question about your port (and no, it doesn't sound doofey)- I've been wondering the same about my port. I know that it is sure aggravating the heck out of me and I can't wait until time comes to get it out, but it's going to be a long wait 'til then! Hopefully someone will answer and give us some great (and reassuring) info! Take care and I wish you well!
Mary Jo -
Hi, me again from the July chemo group. I sleep on my port side all the time. (I wonder......does that make your other side the "starboard side"??) HAHAHAHAHA. But seriously, I couldn't sleep on that side right away. It probably took a couple of weeks. I wouldn't say the port is always 100% comfortable, but it's not bad.
Donna -
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Hi, me again from the July chemo group. I sleep on my port side all the time. (I wonder......does that make your other side the "starboard side"??) HAHAHAHAHA. But seriously, I couldn't sleep on that side right away. It probably took a couple of weeks. I wouldn't say the port is always 100% comfortable, but it's not bad.
Donna
Hi Donna and thanks for the humor!!!!!
I've had my port two weeks and it's still hurting at times, not badly but enough to remind me it's there. Glad to know it will get better.
Please come back anytime to our September gang and help us out-- you're great!
Mary Jo -
Hi there!
My port is causing me a lot of shoulder pain...anyone else? I put a call into my surgeon today...we'll see what he says...I don't sleep on my "port" side anyway, so that is not an issue for me. I'm having herceptin, so I've got this thing for a year! yikes!
Marietta -
OK, the sentinel node biopsy is scheduled for Friday the 14th, so that has likely pushed off the start of Chemo until after that surgery. You don't really want your SNB contaminated by chemo if you want accurate results. I hate putting it off another 10 days, but it kind of makes better sense for me if I have to invoke FMLA. That might get me through my chemo. I will have to worry later about how to handle time for the surgery, another round of chemo and then rads. Yikes! How can I do this and financially survive? Breathing deeply. One thing at a time. Just keep swimming.....just keep swimming.....(right-side-up preferred).
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Hi, Ladies -
I just wanted to mention that yesterday was the first anniversary of my first chemotherapy last year. I'm done with surgery, done with reconstruction, done with everything except tamoxifen, and I feel great. It feels like forever while you're going through it, but in the end, it'll just be a blip, though a very unpleasant one. I hope you're all posting notes like this in a year. You will get through it.
All the best,
Mindy
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Well I had Chemo A and C on Tuesday the 4 of Sept. It went ok the first day was pretty bad but today is day 4 and I feel great! I sat in the chair for about 3 1/2 hours not to bad i ate and talk to my best friend who came with me. Im on a does dense regiment. So its every two weeks for me.
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Sorry Ladies no idea why my comment is up here so much. Still kind of new at this!
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Well I had Chemo A and C on Tuesday the 4 of Sept. It went ok the first day was pretty bad but today is day 4 and I feel great! I sat in the chair for about 3 1/2 hours not to bad i ate and talk to my best friend who came with me. Im on a does dense regiment. So its every two weeks for me. I want to thank everyone for the encourageing words
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Hi again...I got my port put in Wednesday. IV's and giving blood never bothered me too much before all this, but now I feel a bit faint. Well, they couldn't get an IV in my right hand (thing swelled up all over from all the spots they tried). Brought in the IV expert and finally got that going in the other hand. I was awake during the surgery and he didn't numb me up enough so I screamed when he sprayed something that felt like fire. My whole shoulder hurts and I can't lift. I didn't use anything for pain except ibuprofen during my lumpectomy and node dissection, but I tried a pain pill after this port surgery. Didn't seem to help so back to the tried and true ibuprofen. Its still tolerable though.
I start AC chemo monday (10th). My boyfriend and I went to meet the nurse and do education. Seems like every health care person I've dealt with asks me something like, "so, what is it about this that's bothering you?" I always say, "you mean, besides everything??"
I asked about the ELMA numbing cream, but my nurse said she has better results with giving a shot of lidocaine (like they often do when they give you an IV). She said the cream can be tricky for timing. I don't really know what that means but it sounded like maybe it wears off if you're having a 2 hour treatment like I will. Not sure though.
I've read everything I can about everything so I feel like I know what to expect. I've had panic disorder for 10 years so I'm a bit afraid of panicing from some of the drugs they'll give me. But I'm doing my best.
Marietta: lemme know if u still need a cancer buddy. We don't have a running support group in my area so I feel kind of alone sometimes.
Well, take care everybody. It feels good to check in here.
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I had my first tx yesterday, the same day I got my port. Everything went well. I have a nasty taste in my mouth but that's about it. The port is a little sore but not taking any meds for it maybe at bedtime I will. My chemo is AC and it really didn't bother me. The first bag hung had an anti-emetic and steroids in it then they gave me atavan directly into the port. If the rest of the tx goes this good then I'll be happy. I know I may feelcrappy tomorrow or the next couple of days but hopefully not too bad. Hope things go/went well for you. When is your next tx date? Mine isn't until 10/4 as we delayed a week for preplanned vacation time.
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Hi Paxton, I would love to be your buddy. I had my first chemo on Thursday (taxotere, Carboplatin and Herceptin). It was such a long day. My shoulder was still bothering me from the port so my surgeon wanted me to have an MRI, so that put my chemo off by a few hours and I was wreck. Oddly enough, once the meds went through the port it felt so much better and I have very little pin in my shoulder now. So thats good.
Thursday night was really rough for me, I will spare the details. The anti-nauseua meds had to be changed and things are better now. I survived my first chemo. I will be thinking of you on Monday and sending you postive thoughts. I took all of this great stuff to keep me occupied at chemo but was so tired (from not sleeping the night before) that I just wanted to close my eyes and relax. Let me know how things go. You can always send a private message as well, ok?
Good luck!!
Marietta
Marietta
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Hello everyone well its day 5 for me (chemo was on Tuesday 4th) Wasnt to bad at all still feel a little tired but the ativan works pretty good. I dont go back until the 18 th so wish me luck. Ill be sending out all my prayers for you gals starting this week remember think positive try to get up and walk drink a lot of fluids and you will be fine.
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Hi Ladies,
I'm going to be a September Chemo lady as well. Got my port 9/5 and will get first chemo 9/10. It's been so long since my surgery (6/14) that I've forgotten some of the details of my cancer. I had a bad infection in my lumpectomy incision and had to wait for it to heal from the inside out. The waiting for chemo has been very difficult for me, but thankfully it's finally starting.
This is my first visit to this site and I must say it's been very informative. I've written down lots of notes for my chemo doc.
Thanks to all of you and I look forward to sharing the journey.
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Welcome Delachaum!
I hope all goes well for you tomorrow. I had my first chemo on Thursday (6th) and survived, yay!! Still a bit queasy. Achy from laying down a lot. But I am well enough to go watch my little boy play in his baseball game today, so for that I am thankful. Also, September ladies, I applied for a chemo Angel and got one! They notified me this morning. I'm very excited, it will be great to have that support and something to look forward to.
Be well
Marietta
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marietta: glad to hear things went good overall. I had my 1st tx at noon today. I was so nervous but it wasn't so bad. My port hurt before, too, so I was nervous about that but once she took the bandanging off and put the iv in, it wasn't so bad. I've been home awhile and feel kind of shaky (prob the decadron) but its not too bad so far. I was worried about that too because I have panic disorder already. My oncologist gave me two perscriptions to get filled right before chemo which was a bad idea. I had trouble getting them filled and ended up late for chemo. My insurance won't cover the emena so they're trying to figure out what to do since its like $370 for the 3 pills you take each tx. Keep me posted marietta.
Dela: I'll be thinking of you and hope you're ok.
This site has been so helpful with the tips (especially since the docs and nurses don't tell you a lot of this stuff).
Take care everybody.
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Harley, Did you respond and say you were taking Taxotere and Cytoxan. How is it going, any side effects, I start on thursday for 4 treatments every 3 weeks. Also my onc. did not think I needed a port? Anyone else go thru without one?
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Hi Paxton,
thinking about you today. I hope the treatment went well and you are doing ok this evening. I'm slowly feeling better. I found a great anti-nausea supplement that is also helping me with my low blood sugar...It's a mushroom capsule called Maitake D-fraction. I have also had massive indigestion, so I called the nurse and she said I could take zantac...wow, what a difference. I felt like I was burping up gasoline
So intense!
Ok let me know how things are going.
Delachaum, are you there? How was your first treament?
Marietta
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Had my first dose today - it went well, no problems, no unusual sensations. Got home about 12:30p.m. and took a nap from 1:30 - 4:30. Woke up with a migraine. Threw everything besides the kitchen sink at it to no avail (excedrin migraine, lavender oil, peppermint oil, ice, valium - you name it). As a last resort I called my onc. doc and he called back. After discussing everything, he said if I had migraines in the past, it would not be uncommon for me to react this way. Since I had taken Zomig (similar to Imitrix) in the past, he ordered them for me from my local 24 hr. Walgreens. I just took the pill and do seem to be having some relief already.
I must say I have sinus involvement as well - also not uncommon for me this time of the year. Soooo, tomorrow I'm starting on Mucinex to get rid of the drainage that upsets the stomach.
I'm on the dose dense regimen as well (every 2 weeks). I asked about Emla cream after they had already successfully placed the IV needle in my port (really astute of me, don't you think). The nurse just sprayed some numbing agent on the port and I didn't feel a thing when she put in the needle. She said you have to put the Emla cream on at least 1 hour before they place the needle. Lucky for me the numbing agent worked well because I didn't have any Emla cream.
Hi to Marietta and Paxton. If I can get through this migraine and know what to do for future migraines, I'll be fine. Thank you so much for your concern.
If you guys see lots of "edit" notes, it's because I can't get used to pressing the return once for a paragraph. I hit it twice and have to back space up to the correct distance.
(just did it again). Marietta, what is Maitake D-Fraction? Also, I think I'll ask about Zantac because my food seems to be staying in my stomach and making lots of gurgling noises.
Thanks again to everyone in the September group - I always learn something.
Delachaum
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The maitake D fraction is a supplement made from Maitake mushrooms. I've been reading a lot about it, not only does it help with nausea and low blood sugar, it helps the immune system and supposedly helps the chemo work better.
So sorry about your migraine...that sucks. I love Excedrin tension headache. I can't tolerate aspirin well, and that one is aspirin free. It gets rid of the worst pain. I've had a little post nasal drip since chemo. My sense of smell is so heightened right now as well. Lots of food smells make me queasy.
Hang in there!!
Marietta
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