April 2012 Chemo Starters?
Comments
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I found out Thursday when i went in for treatment that my red count & hemoglobin were real low. Talking about transfusion. Has anyone dealt with this? A little scared and not sure when to call onc. I have been so tired/fatigued since Thursday. Any words of wisdom?
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JR: Go to the April/May cheo starts group. There have been several women that have been in yor situation. YOu might want to PM them.
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JRyan~ go get your blood levels checked ASAP. Time for a trip to the ER (since it is Sunday & you can't go to the onc's office)-let them call the onc. This is not something to second guess. Do you have someone that can take you? Good Luck! You will be feeling much better soon!
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I have a call in to on-call onc. See what they say. Dont like this feeling of blah and no energy. Not like me at all!
Will keep you informed... -
I keep telling myself this was the last round of chemo, but I know that there are still side effects to deal with. My mouth is worse than ever this could be good for my eating habits. Another neupogen shot today so that'll probably kick me. All in all been feeling pretty good. Now just to get he 4-H projects done.
JRyan I sure hope you don't have othr complications
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JRyan: Let us know what the doc says.
SinginCyndi: I feel exactly the same way you do. Excited it's the last round, but dreading the S/E's. It's a mixed bag of emotions.
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I'm going in for bloodwork tomorrow. Lots of sleep yesterday. Feeling a bit better this morning, rested. Still nervous about transfusion possibility.
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And all I want to do is eat icecream.
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Yum. Ice cream sounds perfect!
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Just ate a bowl of frozen yogurt!
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Been so quiet in here for a few days....hope it is not because you are having bad SE's.
After my last treatment on taxol, I have neuropothy really bad in my fingertips and in my lower legs and feet. I called the cancer center and when they found out I was dropping things and having trouble walking, they ordered neurontin ... when you read about this drug (used for seizures) it really scares you. It is some strong stuff. I've taken only 2 times so far so don't know yet if it is going to help.
taxol is giving me so much pain ....to me it is much worse than my first sessions.
have any of you had the same experience?
I go for my 3rd taxol on Thursday and then, thank God, I only have one more on 7/19.
I can't wait.......
Carolyn
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I had a reaction twice with Taxol now I'm getting Abraxane. I got neuropathy, in my head, fingers, feet, arms, everywhere!!!!
I just read about the neurontin, very scary......but I hope it helps and the neuropathy those not get any worse...I was fine all day, but now my head and my fingers feel wired.
Did you have any SE from the neurontin?
Hope you feel better! -
Thanks .....
How does neuropothy affect your head? I know in my legs it makes it difficult to walk..you feel out of balance. I walk like a little old lady. That's why I decided to try the drug.
I have only been taking the drug a couple of full days....it will probably be a few more b4 I see any results. I'm not having any bad SE from it so far.
I hope you start feeling better soon.... where are you in your treatment?
Carolyn
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I had very sharp and short (like a second) headaches. I have no more tingling so far since i take the drug just some shooting pain in my hands. I'm sorry it is so bad for you. I hope the meds help soon!!! I think Taxane is the devil too!!
8 more weekly chmos and then surgery. -
I am officially done with chemo--yeah--June 28th! NO headaches for me, but sitting her with my dogs just trying to get some energy. I see the RO next Thursday and BS on Tuesday. Probably start rads end of this month! Yeah! I am so tired!
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kjiberty....that's wonderful news. I hope the rest of your treatment plan goes well. I don't feel like anything could be worse than the chemo.
please come back and let us know how you are doing.
I was taking neurontin for the neuropothy but it was making me so weak, short of breath and totally fatigued that when I called and told them how it was affecting me the took me off it. I don't think I can go take the Neulasta on Friday feeling this weak.
thursday is No. 7 for me and I will only have one more on July 19.......yeah......
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Two Steps: You are almost done! Congrats. Wishing you minimal S/E's and I am not leaving you wonderful ladies! We are in it for the long hall!
Happy 4th!
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Hi Ladies,
Sorry I haven't checked in in so long. AC #3 about knocked me out. Amazingly #4 wasn't as bad and I am SO GLAD to be done with AC. Start the final 4 rounds of Taxoterre next Thursday. Onc says he doesn't think I will have as much trouble with Taxoterre and I do hope he is right. School starts Aug. 6 and I really really want to go back to work. I tried to go back after my first round of AC and just couldn't do it. Biggest obstacle will be the heat. I know everyone all over the country is suffering from the high temps, but I think for us it's worse. The hot flashes continue to be terrible (although I sleep through the night now that I am on better anxiety meds). Still, I'll be walking around a big school, outside to portables and it's unbearably hot and humid in Louisiana in August clear through early October. Just will have to stay maximally hydrated and take it slow. Congrats to all of you who are finishing up your chemo. I am SO SO HAPPY for you and proud of you for hanging in there and being strong. May we continue to support and inspire one another!
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For neuropothy my onc. said to take a complex b vitamin with a really high dosage of b6 in it. I couldn't find any like that so I take a b-complex vitamin and supplement with more b6. Kicked my neuropothy right out the door in just a few days-the pharmasist told me that b6 will just be dispelled out of the body if it's not needed and so you can take alot w/o it harming you. I am 3 weeks past my last chemo but haven't been too perky - 3 radiation treatments in and am so tired can't even make it up our stairs to the bedroom without stopping for a rest-we're talking like 18 steps. I sure hope everyone continues on without bad SE's and wish everybody the best!
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Cyndi: So sorry to hear that. I am two weeks PFC as of today and still tired. Go to my RO today. I have been taking B6 since I started chemo.
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Had my last tx yesterday. Now just herceptin til next april. Feeling pretty beat up today but looking forward to getting back to normal, whatever thats going to mean!
Hope everyone is doing well. -
JRyan: Congrats. Wishing you minimal S/E's over the next few days.
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JRyan: Yeah!! I too will have to take Herceptin until next April. I am wondering what the new normal will be myself! Hope you have few S/E!!
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Hi Everyone. Been a little quiet on here lately. Hoping everyone is doing well, dealing with minimal SE's.
The last tx kicked my butt. Took me almost twice as long to get on my feet. But I am back on my feet! Now I am ready to start my trip back to normal. Has anyone seen anything on hair regrowth? I am wondering how long it's going to take to start seeing some hair.
I go next week for just Herceptin. Wondering what kind of SE's I will experience there.
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JRyan: I finished 6/28 and my hair is growing back so much so I have no bald spots and it's pretty dark, with gray/white mixed in. It's about 1/2 inch long. Chin hairs and leg hairs are back. Eybrows 1/2 gone.
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JRyan: I finished chemo a day before kjiberty and my hair is coming back too but it's thin and I measured mine yesterday it's about a quarter of an inch. Arm, face, and leg hairs are back seems I've lost a few more eyebrows but I'm not too worried about that. I too have dark with gray and white but it looks like its changing color to what I have no idea. I'm down to 4 more radiations!
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SinginCyndi: Congrats--you will be done this week!
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Well, I'm finished with chemo and have seven more radiation treatments. I had some SE during chemo, but it was doable. I had a few days after each treatment where I was hurting and miserable, but even that in retrospect wasn't that awful. I feel very thankful for all the support my family has given me. I haven't posted very often, but I was checking in on my 'sisters' and feel for everyone on this site.
Now, with 7 of 33 radiation treatments left, I am really excited. The 'sunburn' isn't much fun, but ... it's doable.
Keep the faith, and thank you from the bottom of my heart.
Diane
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Diane: I have 5 left! We are on the same timeline! My first boost is tomorrow. I will be done on Friday! Hooray!
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Hi Ladies,
I hope this finds you all well and managing the forwards steps with ease and good health.
I wanted to check in to see how everyone was doing and to get updates on where everyone is in their fight.
I am getting ready for my exchange surgery on 10/22. They are taking my ovaries at the same time. I had a hysterectomy several years ago and they left my ovaries then cuz I was young. I get a little anxious at times thinking they may find something bad on them, but trying to stay positive and relaxed.
Still waiting for my hair to grow. It has grown a little, but SO slow. Thinking maybe the Herceptin is keeping it from growing at full speed. But everything else seems to be getting along and mending pretty well.
I get really frustrated with well-meaning people who say "So you're all done. You must be all better now." How do you guys react to that? I really want to go on a rant about how I may not be done, and I'm not all better, but feeling better today... The mental part of dealing with this whole thing has really taken hold since the tx ended. I find myself down in the dumps a lot and dealing with a bit of anger too. Hoping time will bring "me" back, although I have a feeling that "me" will never be the same...
Happy to have a venting place
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