One down........5 to go!!!
I made it through my first chemo treatment. Well at least THIS far anyway. I was there for 6 1/2 hours.......whew!!!! They said the next one won't be as long.......sure hope not!!!
I was terrified.....to the point of tears......and they wouldn't give me anything to calm me down because with the allergies I have they wanted to make sure I could tell them if something was going wrong. The nurse I had was WONDERFUL. She calmed me down just by talkin to me. And the pharmacist that mixed my chemo, came in to talk to me. She is a breast cancer survivor......and she was on the same chemo I am on. She has been in remission for 2 1/2 years now.
If anyone knows anything I should expect in the next few days.......would love to have some advice!!!! I've been drinking........LOTS.......and peeing lots. I go back tomorrow morning for a shot of Neulasta. I have an appt. on Oct 8 to see the Dr. and have my blood counts checked. Then my next chemo is Oct 15th.
I told my nurse......next time just put my chair in the bathroom.......cause that's all I did was PEEEEEE......lolol
Thanks to all of you who have been so supportive and helpful......hugsssss
Comments
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Hi Genia,
Congratulations on having the first one finished. What are you getting? Probably in a couple of days, you will feel tired
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Taxotere, Paraplatin (Carboplatin) and Herceptin. I will be on the Herceptin for a year........doing a treatment with it once every 3 weeks.
This is all so foreign to me.......I understand some of it........but not all!!!!
They gave me Zofran........Decodran and Benedryl.......I guess to kinda counteract the side effects some!!!!!!!!
Right now.....the only thing I am experiencing is some bloating........and my head feels like it is in a FOG.......lol
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Genia,
Congrats with getting through your first treatment!!!!! My first treatment was the longest and hardest to get through (I have treatment 6 of 6 on Monday).
I am on different chemo drugs, but on the same regimen. Take chemo, next day get Neulasta, the next week get blood drawn and doctor appointment.
The hardest time for me was chemo week (especially day two and three after treatment but things get better).
Are you on Claritin? One of the side effects of taking Neulasta is soreness the in large joints (I would get it in the hips and knees...I felt like an old woman). I was put on Claritin to take every day. According to the nurses they don't know why but it helps with the soreness. It really helped with me.
Decadron is given so you don't get major swelling in the legs.....unfortunately it makes you go pee all the time. How often do you take it?
The best advice a friend (cancer survivor) told me is to drink lots of fluids (Crystal light has been a life savor....I use a half a packet) to flush out your system. For me colder the better. Also for what I call the hairy tongue (I would get a bad taste in my mouth) I was told to use Biotene mouthwash.
Hope this helps......just remember we are here for you!!!!!
kim
Remember to laugh at least once a day( or at least do something silly)!!!!!
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I am drinking LOTS.....I think that is where some of the bloating is coming from. TEA tastes so good to me........at least right now........that may change tomorrow.......lol
I have a horrible bitter taste in my mouth already........everything I eat tastes bitter.......but I'm making myself eat something!
I got some Biotene mouth spray.........I sprayed it a little while ago and it seemed to take some of the horrible taste away.
They just gave me the Decadron in my IV today.......it was part of the regimen!!!!
Thanks for advice........any way to get through this I'm willing to give it whirl!!! I'll go get some Claritan tomorrow before I get the shot.
Thanks!!!
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Hey Genia!
I too am on a different regime then you, but I did get the Decadron on my IV prior to starting the first chemo drug. The nurse told me it was going to "disrupt my sleep", but what she should have said is that it would ELIMINATE it! I finally starting sleeping better last nite and it has been 7 days already! For me the hardest thing was first thing in the mornings... I just had no energy to get out of bed and drink water or eat. But once I did I felt so much better. I was also taking extra strength Tylenol for 3 days after the Neulasta shot by recommendation of my onc. in case I had some aches and pains. I really had no side effects from this shot anyway.. but it might not hit me until the 2nd shot. Try to get up and do a little even if it's going outside in your back yard and walking a few steps! Keep your mind off of what is going on and don't let it rule your day! I was back to work for full days on Day 5, I probably could have come in for half a day on Day 4, but I wanted to play it safe. For the metal taste in your mouth brush your teeth a few times a day especially after eating and I would highly recommend the Biotene mouth wash, there's no alcohol in it so if you unfortunately get mouth sores it will help with that. Exhaustion can get pretty bad so do take it easy if your body is telling you to.
Happy thoughts to you!
Sue
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I am surprisingly feeling good today.......I went and got my hair cut short......just so when it falls out it won't be so bad. The lady where I got it cut gave a gift certificate for a full year of free hair cuts!!! She also said when my hair started to come out......to call her no matter what time it was.......and she would go in and shave my head for me........bless her heart........I almost cried!
I got my Neulasta shot today.......took some Claritan before I got the shot.......so far the ONLY thing I am feeling is a bit of a headache. I am trully amazed and thankful that so far I don't feel bad at all.
My mouth is very dry......and my vision is a little blurry........and I still have that bloated feel that I had yesterday, but I was feeling SOOOO bad BEFORE the chemo started........I couldn't imagine feeling any worse. I remember when my husband and I were on vacation in June......I told him SOMETHING was wrong with me.......I didn't know at the time I had cancer.....but I constantly felt horrible and had NOOOO energy at all. And by July 24th I had my reason for feeling so bad........
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Oh and Sue I was wide awake at 4 this morning.......and have been going strong all day long!!!! So the Decadron IS disrupting my sleep. They didn't tell me that......lolol
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You go girl! And keep up that drinking. I posted extra info somewhere else because I had some quite bad SEs after the second go. I started having a teaspoon of slippery elm bark powder in water before bed and this really, truly eased my feeling of having half a mile of ulcerated and inflamed gut. Another girl gave me that tip. That bloody bloating! And use the biotene toothpaste and mouthwash religiously. My mouth ulcers hit me from nowhere! Take care, Genia. It will fly. XX Kerry
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I'm using the Biotene and I still think I am getting them. The roof of my mouth is hurting tonight.......what else can I do for them???
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Genia,
The nurse giving me my chemo gave me a cup of ice chips to chew on during one specifc drug infusion, I can't remember which one it was but she said that that specific drug can cause mouth sores and that chewing on ice chips while it's going in your veins does something to your mouth so that the sores cannot produce.
Glad are you feeling ok!
Sue
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Sue....it was probably the Adriamycin that you were taking when she gave you the ice chips. I think it's that drug they recommend you chew ice chips while you are taking it. I may be wrong......cause God knows this is all very new to me right now.....lol They didn't give me Adriamycin.......so not sure if that would work for the other drugs they gave me or not!
Not feeling the best in the world today........just feel draggy and tired!!! Plus my stomach still feels like I am one good BURP away from feeling better........lol
Thanks for all that have offered suggestions........hugsssssss
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I had the same problem......I have noticed that I since starting Chemo I tend to burp a lot more. I also felt like I had "hair ball" in my stomach for a couple of days. According to my Nurse Practitioner, she said I was experiencing nausea type symptoms.
Just remember you can get through this! Usually on my "bad days" I would just sit on the couch and veg (but I would still go outside every so often and walk across the street). Like Sue I usually returned to work (for short periods of time) by day 5 post chemo. The two weeks between I would return to work (just make sure you don't over do it). You have to listen to your body.
I would call your nurses and ask what you can do for the mouth sores (especially the one who had the same drugs you are on). They are there to help you.
kim
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I wish I remembered the mouth rinse I was prescribed for mouth sores. I only got them once but they came on fast and hurrt bad. I had the rx and DH had it filled. It was red, really nasty tasting and had something floating in it, but it worked immediately and I had no other problems. I'm almost a year out from my last treatment and threw it away a few weeks ago. I've had one haircut and feel good. Sometimes my bones ache but friends say that will go away too. Keep the faith!! It will be over before you know it.
mary
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I've been using the Biotene and it is feeling better today.......thank God!!! Thanks everyone........much appreciated!
Genia
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Hi to all of you,
I was recently diagnosed with multiple areas of IDC, each 1 mm X 2 mm or less, positive for vascular space invasion. My doctor offerred Taxotere and Cytoxan.
Dumb question, but does everyone get diarrhea or hair loss?
Thanks,
Liz
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Liz, there are no dumb questions. Of course we would not know these kind of things before going through it. On the Chemotherapy forum there is a thread for those getting Taxotere and Cytoxan. You will find many, many answers there.
Everyone does not get diarrhea, some get constipation instead! But I am afraid that on taxotere and cytoxan we will all lose most or all of our hair. Let us know how you are doing.
Chris
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Unfortunately from all I've read.......there is hair loss!!! Small price to pay for my life........that's the way I look at it!!!
Good luck Liz.....
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Hey girls! I finished chemo on Friday AND ordered a new wig..something a bit shorter for our summer here..and felt great about it. A very different experience to the first time!!
Genia: stay on that biotene religiously..don't forget! And chew the antacid tablets when you get that stomach thing happening. They are a 5 minute miracle. XX
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Good for you Kerry............get a pic with your new wig..........would love to see it!!!!
And the antacids........were a miracle..........my hubby just handed me one and said try this.......maybe it will help. And it DID.........I got to sleep without being sick!!!!
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Hello to all,
Genia....I carry TUMS (with Calcium) with me everywhere......plus try to eat smaller meals and don't eat anything at least 3 hours prior to bed.
Liz.....most likely you will lose you hair, but cutting it short before treatment will help you lose it slower. I would buy a lint roller. When I started to lose my hair I would use it on my pillows in the morning. I would also use it on my clothes throughout the day. After the second treatment I started to lose my hair (I am on Taxatere, Cytoxan and Adriamycin). Like some people, I decided to have my head shaved....I got tired of cleaning the shower drain, plus the hair that was left really looked dull and limp.
kim
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Never thought about the Tums with Calcium.........that would be a plus!
And the lint roller sounds like a great idea too........
I got my hair cut on Thursday. The day after my treatment. I had a gift certifcate for a free hair cut and thought I would just go ahead and use it after I had my treatment.........so I had never been to this little gal before. When I was ready to leave.....she hugged me.........and handed me ANOTHER gift certificate for 1 year of free haircuts........and she told me when my hair started to fall out........no matter what time it was.........to call her and she would come in and shave my head. She was such a sweet woman!!!!
I'm finding there ARE people out there that are still very helpful and nice.
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