Chemo June 2010
Comments
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Ladies: We are all doing great, handlng the ups and downs. I agree with Vicki - I finished last week and thought I would feel great but guess what, I forgot to keep drinking fluids and had a crappy weekend. I am going to do a "spa day" at a nearby hotel with a friend - just a massage and a facial - as a little pick-me-up to celebrate the end of chemo. And I keep needing Ativan and Restoril to sleep - my sleep cycle is totally out of whack, but when I get tired, I get weepy. Make sure you are getting enough sleep!
Hugs to everyone. Toni
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carrol2, your gonna do great!!! it will be over before you know it, i have a total of 16 treatments, yuk!!! but only 7 left now, we will help you through it!!!!
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Wow, Chey. I can't believe you only have 7 tx left. Time seems to have gone by fast. Today was another blow. I did not get to have chemo because my blood counts are too low, a first for me. My oncologist started out by telling me he was going to adjust the dosages of the chemo meds for me. He is really very sweet and seems to be concerned about me and how I will do with chemo. But he said today that my white count is too low and he's a little puzzled by that since I am two weeks past my last Taxol tx. I will go next Wednesday and have my blood drawn and checked again and if it's okay, will start my new tx then. I asked about a shot, but he said he doesn't want me to have one. Not sure about why that is, but I do like him and trust him, so I guess I'll wait one more week. Had myself all psyched up for today. Wasted a couple of good Ativans! ! ! LOL! Now, it has thrown my schedule off. We had planned a short trip to Texas for a family get together during my fall break in October which would occur a week after my second tx. Oh well - this is life with cancer I guess! I HATE IT!!
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But I do LOVE all you guys! Didn't want to end on such a negative note.
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Sherry sorry to hear about the delay in your chemo. I guess that is something that can happen at any time. Hope you get back on track asap.
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sherry- Dang! You just don't get a break. Okay, you will be strong next week for your treatment. When my white count was low, I initially declined the Neulasta shot. When I had second thoughts about it a week later I asked the Onc if I could have it. She explained that it could only be given within 24-48 hours after chemo or it wasn't effective. That's probably why you didn't get it yesterday. As you are planning a trip, you might want to get it after this next chemo to make sure your white counts are strong while traveling. I would ask your Onc. Are you still working? You need to be extra careful if your white counts are low so you don't catch something. Wash those hands a LOT. I'd stay away from eating out too. Praying for you Sherry.
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sherry, dam! just one thing after another! im glad you trust him though,as we all know the wait is the worst! It will be over soon,as Dmom says, be careful, remember its the start of flu season. i would lay low for the next month... im sorry about your trip, but you need to be strong before you take off... im thinking of you always, yes!!!! 7 left, yay!! it still seems forever away! I hate it it too!!!!!!!!!!!
love Chey
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Hi All,
I have not been on in a while because my month of Sept has well shall we say been rather eventful. I started with Febrile Neutropenia on Sept 1 and spent 6 days in the hospital and then after that on the 14th had another Docetaxol tx . Then low and behold had such abdominal pain from severe constipaation that I am now in the hospital again. I have been here since last Thursday. When I have another bm I will be able to go home. X rays showed I was more shall we say full of poop than anyone they had seen. The unit I am on is fabulous. It is a little 5 bed funded oncology ward and it is just for people like us who have had bad SE with chemo. This unit has been a savior for me and I wish there where more like it. The hospital is brand new and the RN staff is AMAZING. I am being brought back to life and feeling much stronger. Really it is the job of the oncologist to cure the cancer and they are going to give you as much chemo as they can without killing you. I have my next and my last Docetaxol treatment on Oct 5th and I am thankful that I will be finished because this Docetaxol is kicking my ass much more than FEC did. I am also seeing my PS next week and my radiation oncologist on the 14th. I will then have either radiation or surgery first depending on whether or not I do implants for both sides or a one sided DIEP with reduction to the other side. You cannot radiate a DIEP graft... so there is the difference and implants should be done prior to radiation. I am having immediate reconstruction. I just have to make te one side or two decision. Well that is my story. I hope you are all well and for those of you who have finished chemo ....a big congrats! Now we can stand up walk and move forward to the next phase.
Take care,
Trusting
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Trusting- Oh my! Sorry for your set back, glad the hospital isn't that dreadful. I can relate to the constipation problem,. My first chemo had me blocked up for 4 days, awful. I started taking these great fiber supplements made by Yerba Prima. I think it is just all natural psyllium in capsules. I take them with meals and water ALL the time, a few extra on days before chemo. It has really helped. As they are capsules, I actually take them regularly. I hate all the mix-it-up Metamucil slop. Hoping you "get to go" in all ways soon and that your final chemo is uneventful.
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Hi Designer Mom,
Four days is yuck but try twelve! How are you doing ?
Take care ,
Trusting
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DMom: I am back at work at the school. I work in the principal's office at a junior high (8th grade only). I have always been a germ freak, so I continue to wash my hands a lot, and I don't come in contact with the student population at large. Just a few here and there throughout the day. Being at work has saved my sanity. For about 6-8 hours a day I forget I have cancer - well most of the time. My wig is itchy and I can't feel the bottoms of my feet and my face and hands are puffy from steroids so maybe I haven't forgotten after all! LOL.
Chey: I so remember having the same feelings as you while on Taxol. Each week when it was time for tx I would tell my husband that I didn't want to go and I felt like I was never going to come to the end. And then the end FINALLY came. I guess we all are at some point where someone else was or is and we know exactly how it feels. That's what makes this web site such a blessing - to have the support and encouragement of someone who really understands what we are going through.
Trusting: What a mess you have been through. I sure hope things are taking a turn for the better for you. You are so close to being through - just one more tx. Praying that your body will stay strong and be able to withstand your last tx without any nasty SE's.
Bon: how are things going with you?
Carroll: nice to meet you. I will pray for you to as you go through your tx.
Don't know what will happen with my trip to Texas next month. We are waiting to see how I do on the new tx plan. I hope I get to have a tx next week. WOW! Can't believe I just said I "hope" I get to have a tx. LOL! I was so hoping to be finished by the first of November so I could feel better for the holidays.
Now I'm going to partake of my favorite supper ever: chocolate cake with fudge icing, pecans and Blue Bell ice cream - YUM!
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Trusting--I feel so bad for you girl. I REALLY hope and pray that you will get through your last tx with NO horrible se's!
Sherry-Hope you enjoyed that supper!
Chey--It seems like your treatments are going fast. You sound so great! And you're such a great support for all of us on here. We're almost done girl!
Tonight I'm having a lot of pain from the Taxol (had #3 on Monday). I've just been taking one percocet at a time, but I think I'm going to go take a 2nd one soon (I can take 1 or 2 every 6 hours). I had my grandson here today--boy does he move around now! He'll be a year on Sunday. Thankfully my mom was here to help me with him, so I could sit and rest for a few minutes when I needed to. A few more days of this pain, and then I'll feel pretty good (hopefully!)til the next tx. Overall, I still have to say its better than the AC. Oh yeah, I better remember my colace tonight--the percocet is hard on the system!
Have a good night ladies!
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Trusting: you poor dear! It's so great that you are getting wonderful care as you deal with things.
I hope things get moving well for you. I am one girl with the opposite problem! Grrr. can't wait for this to be done with.
TMarina: Bone pain sure sucks. Is this your last infusion? Hang in there!
It's Day 8 for me and the bone pain continues, but it's manageable. Other side effects continue...
Does anyone else feel like their teeth are tingly and loose? I wonder how long before we start feeling like ourselves again.
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Hi everyone!
Sherry- sorry about your delay... what was your WBC? Mine is just below normal, so I'm concerned about going out to public places... how low is too low??
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Trusting - hang in there girl! I hope you are better soon and back on your feet.
Sherry - sorry about the delay. Maybe another week will get you back on track. Just remember one foot in front of the other.
I had #6 Taxol today. So far so good. I swear some days I wonder if I am really metabolizing this stuff cuz I am missing SE's. Actually not having many at all. Kind of scary actually. Isn't that sad - you guys are struggling with SE's and I am in doubt because I have none. I swear this disease is going to make me crazy! For all of you having the SE's - hang in there and I hope you find relief soon.
Love to all my sisters out there!
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Good morning everyone!
Trusting- What a miserable time you've had. I am so glad you are getting good care now. A friend who teaches Pre med stopped by when I was in the middle of chemo and told me I should have been half dead from chemo. So, unfortunately, as you say, the Onc is doing his/her job with your chemo.
tmarina- I am so sorry about your bone pain. You are such a good Grandma to babysit while in pain.
Northern Girl- My teeth and mouth feel similar to yours. I know it's a side effect and have no idea if I will have permanent damage to my teeth. Need to find a new dentist who accepts my insurance because I think I will be spending alot of time and money on my mouth soon.
grneyday- I am glad you don't have side effects. I am sure there are many more women out there who are doing well. They just don't take the time to post.
Chey- I am so happy to see that you are feeling better.
My fingers and toes still tingle and burn. My energy is coming back. My one weird side effect seems to be whenever I groom my dog I develop a face rash. It responds to Benadryl. But if I take the Benedryl I sleep the day away.
You all are the best. Hang in there.
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Morning Ladies!
Just wanted to say, for those of you facing rads after chemo, I am totally thrilled with the Canadian protocol so far. I have 4 more regular tx, then 5 boosts, then I'm done. So far, no skin issues, a few shooting pains that I'm told are normal (ie. everyone gets them apparently), a little fatigue, and sometimes a mild sore throat right after the treatment. I am so happy that I will be done in another 1.5 weeks!
Julia
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Trusting, Whew, you have been through the wringer this time. My onc nurse told me that docetaxol wasn't that bad except that people who do FEC first, then the Docetaxol really get knocked on their but. I can attest to that! I figure it must be good at killing cancer cells as it seems to KILL EVERYTHING ELSE IN THE BODY TOO. This time with reduced dosage and neupogen shots has gone a little better but still was no walk in the park. I have my 4th and last one Oct 8th, right behind you. Hang in there girl, we are looking at the finnish line. I am jelous of the local hospital unit. It sounds nice, we just get stuck on any old ward with grouchy nurses here.
Sherry, sorry for the delay and the missed trip. I have had two delays on this journey and would have been done next week! I have learned to not make definate plans about anything.
I haven't seen my 4 grandbabies (2 sets of twins, same family) in months. There is never a time that one of them isn't sick or I am sick or my counts are too low. I am going into withdrawal from this.
Love and Hugs to all my friends, Mimi
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Those of you planning on taking tamoxifen--- Have you taken a test for tamoxifen metabolism?
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PS Anyone on Taxol with steroid IV pre-meds... how much is your dose?
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Rs711-->I was getting 10mgs as a pre-med, but the last time (my 3rd of 4 dd Taxol) I asked for a reduction and my onc cut it down to 5mgs. And I still couldn't sleep
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RS711 - I am getting 10 mg now. Started at 20 mg. I also had them cut my benaryl from 50mg to 20 mg. I am like TMarina I am still wound for sound from the steriod after the benadryl wears off.
Also what is the test for the tamoxifen metablism you are talking about? I probably won't be on Tamoxifin because I am post menopausal but I am curous abou tthe name of the test so I can ask abou tit.
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RS711 - I haven';t done the tamoxifen test yet, but I do plan to. From what I understand, it is not recommended for pre-menopausal women because they have no other alternative, so even a low metabolizer amount is better than nothing. The reason I am going to do the test, is that my onc wants me to keep taking tamoxifen even after I have my ovaries out (which i plan to do after BC surgery and rads) - she says there is no reason not to use tamoxifen also post-menopause, and this way i will get 10 yrs benefit - 5 from tamoxifen and 5 from an AI.
i get 10mg steroid IV before weekly taxol, and it keeps me up the entire night too!
grneyd - the test is to see whether you have the cyp2d6 gene deficiency. I found this online: "Women with an inherited deficiency in the CYP2D6 gene, which is important for the metabolism of tamoxifen, have a nearly fourfold higher risk of early breast cancer recurrence compared to women who have not inherited the deficiency." "It is estimated that 7% to 10% of Caucasians are poor metabolizers of tamoxifen based on specific CYP2D6 alleles".
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I FINISHED CHEMO TODAY! It has been a looooong 18 weeks, but I did it, I did it...I can't believe I did it! All you wonderful, encouraging friends have been my lifeline and kept me sane. I don't know what I would have done without you! Next it's on to rads. For now, I am going to chemo crash one last time.
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HAPPY DANCE FOR DESIGNERMOM!
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Dmom,YAY!!!!!!! holly crap!! another one down..... heheheYOU DID IT! i cant wait to get to get there...we started in June and here we are end of September, WELL DONE LADY!!
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Rs711, i take no premeds the night before and in my IV i get 12 mg of steroid, im gonna take it down to 10mg or lower.. i too am up all night. it sucks!!!
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designermom congrats you did it! I am starting on oct 5th and would like to thank you for sharing your strength it really does help give me courage.
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YAY Designermom!!!!! You did it!! Now rest up, then on to rads!!
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YAY Designermom!!!!! You did it!! Now rest up, then on to rads!!
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