April 2011 chemo
Comments
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SaraSweety- Is procetomol your steroid?
I agree with you, this is all a learning curve that may get frustrating at times, but I rather go through this that live every day and wonder how bad my cancer is getting. So glad to hear you left he hospital the next day feeling ok.
KiwiMum- I don't think I have ever been this busy before in my life. The calendar of things to do keeps you going..lol
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I know what you mean about the calendar thing -- overwhelming at times. I think I went 23 years without going to a doctor (other than my chiro), and all of a sudden I'm running all over the place to various appointments. I had 8 in one week! Drove me insane! It's mellowing out a bit now, thank goodness.
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I really thought that the testing part was the worst! I was in a hospital SO many days! Now, it's just once a week, and so far I'm feeling really fine (started this past Thursday..so I'm 2 days into this!). The testing and the waiting for results was awful--so stressful--but once you start chemo, you are doing it. You're getting rid of your cancer--just like that great Pacman image! LOL. So, there's no more worry suddenly--no more news--just trusting that people who know a lot more about this than I do have given me the right drugs (and they'll be watching to make sure that's so!), and that this will be tough, but doable.
Jack ran a fever last night, so we're back to hoping that his seizure was febrile and not a sign that he has a serious condition. Fingers crossed...we can only deal with one truly sick member of the family team right now!
Oh, and when they were first scheduling my appts, I started to cry (which I don't do a lot), turned to my husband and said, "But there are days I don't have time to SHOWER, how am I going to fit in breast cancer?!" LOL!
Yesterday, I got a kicky little Hermione hairdo. I feel like mon-chi-chi a bit (remember that 80s toy?), but it's fine. Jack told me, "Mommy, I love you even if you're changed."
Enjoy the weekend, sisters!
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I think the testing is hard too....been to the hospital everyday this week and again all next week. Thank goodness for cancer free weekends.
I love the PACMAN image. I'm going to see if hubby can get the game for my kids DSI's and I can borrow it and play during infusion.
If you are on a budget...ask friends to lend you their scarves....I have about 3-4 in my closet that I never wear....(don't we all)...or wear once/twice a year...my friends are happy to lend them to me. I did go wig shopping (wow, expensive)...so not sure what I am going to do.
Is anyone getting neupogen shots rather than neulasta?
Kg.
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Kg--did you check your insurance? I got $350 for my wig from insurance. I had to go to an approved place, but it was $400. I need to call them too--it should have come in by now. hmmm. Also, if you go the American Cancer Society, there is a link for "local resources" and many wig places give free or discounted wigs for people whose insurance doesn't cover it. (I also heard not to bother with real hair wigs--they're crazy expensive!)
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If you go to a shop specializing in Cancer Image they can help you with the expense on the wig. My insurance does not cover the wig, but they were kind enough to give me a substantial discount and no sales tax because of my perscription.
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I just wanted to share some good non-cancer news this week. My husband has been out of work for a while, and just got a job! The finances have been very stressful, especially since I was diagnosed literally a week after we bought our house!
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Yay! Congrats Soon2! That's fantastic news!!!
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mdg - Thanks for the encouraging news. I am on the same treatment as you, only 6 weeks instead of 4. I was wondering if I should put my gym membership on hold, but I guess I will wait. I am having my Neulasta shots in daily doses instead of the 10 day shot. Doctor said this will cut down on the bone pain. How are your finger and toe nails feeling? Do you have any tingling? I start Thursday, 4/14. I am so happy that you are doing well and I hope to follow in your foot steps! How are the cold caps doing? Do you still have your hair?
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congrats on the job for your husband!!!
more good news here.. my husband and i just got back from our daughters senior prom!! she is sooo beautiful!!! we went and took pictures earlier and they turned out so great!!!can't wait to get them back then it will be time for graduation in may!!! i'll get back to cancer monday but for now i am spending my weekend trying not to think about my treatment starting then....
i hope all have a great weekend!!!
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SOunds like there is plenty of happy news this week! Hooray! My good news is that my Vermont daughter is coming in on Tuesday and will be with me for my first round of chemo. Havent seen her in a year!
Blessings on all! Pamela
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kg1234 So glad you like that Pacman idea brilliant idea to get it on the DSI, 'power to the pacman', chomp that cancer away.
Teckler2 My steroid is called Dexamethasone 2mg now Ive got the hang of this i take 2 paracetamol at the same time to stop the hot flushed feelings and a couple of rennie to ward off the bad indigestion.
scc218 I was exactly the same never hardly ever went to the doctors, infact the nurses on the chemo ward commented on how thin my file was, thank god last week is over.
profbee Thankyou for your kind words of encouragement regarding the test results, I only have one result left and thats the CT scan all the others were fine and I'm putting all my focused meditation energy into making the CT scans clear as well. Saying a special little prayer for you and your Jack, fingers crossed everything goes well.
I'm having a bob cut next week then the week following a shorter style pixie crop then shaved, in the gradual removal of my hair (cause its very very long and i've never had short hair so the shock of it falling out might upset too much).
soon2 Congratulations for your husbands job, it must of been a huge financial strain on you. I understand the stress this can put you under as well as dealing with this cancer nightmare. I'm a self employed designer/artist and have not made any money for about 6 months (due to the recession) luckily my boyfriend managed to get a job early this year which is supporting us and taking me through this disease as even though I am english and paid taxes and NI contributions I still dont get any benefits to help me through this so I have absolutely no money of my own, its really tough not to stress about money and practical matters but we must not worry, we need to be calm and collected and very very positive.
Lots of love and light to all of you
Sarah Sweety xxx
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Hi, thought I'd join in since I just started AC (adriamycin/cytoxan) on Wednesday. I was stunned at its impact and feel like I've been pummeled. Anyone else doing AC?
I was just going over this list in my mind. Since I have triple positive disease, if I go the whole nine yards this is what my smorgasbord looks like:
*Mastectomy
*Port
*AC x4
*Taxol x4
*Early (chemically-induced) menopause from all the chemo
*Radiation x 33
*Herceptin x 17 (in my case a clinical trial of a drug that is like Herceptin)
*Surgery to remove my ovaries
*Years of anti-estrogenic drugsIf I just stop here, post surgery, they give me a 0.9% chance of being alive and cancer-free in ten years. Which is abysmal. So I guess I belly up to the bar and dig in. *sigh*
I am not liking cancer at all today.
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Windlass - I HEAR YOU and am sending you lots of hugs and good thoughts! You will get through this! Got my port two weeks ago (along with a bone biopsy that thankfully was negative). I start my TAC cocktail on Wednesday tx every three weeks for 6x. Then surgery, then radiation. Then whatever else they think of. My daughter is already planning a fun trip for when this is all over! I agree, cancer sucks! But we are all here together.
What I really like about this site is that it is fullof incredible support and HONEST feelings. Friends and family sometimes want to avoid the real feelings and want us to be better - so we play along and may not be able to share how we really feel. Thank you everyone!
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artie cat -
I'm going to have acupuncture prior as well. Have you had it and if so does it work?
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artie cat -
I'm going to have acupuncture prior as well. Have you had it and if so does it work?
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axtella- i want to put my 2 cents in about acupuncture. I go every week for treatments for me, and i find it WONDERFUL. At the very least, it is great to relax on the table for an hour. But the treatments themselves help me with so many things. My adive would be if you do decide to go, tell your acupuncturist everything! They can put some things together to treat in a different way than our regular docs do.
Oh, and also do some research on who you see. There are acupuncturists out there that have only taken a 30-40 hr course and aren't as knowledgeable as ones that are herbalists and have had substantially more training.
Let me know how it goes if you decide to see one.
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Axtella - I have had three acupuncture sessions so far...a hip pain that has bothered me for 20years has stopped hurting! I start chemo next week and will continue with acup. throughout my process. I was a skeptic - but what the hey! It is worth a try and I am now a believer! There is research out there that acup. can help with chemo side effects.
My practitioner took a full health history at the first session - I also know that she volunteered her services at San Diego hospice, so has some insight into the cancer/chemo process (they often do prophylactic chemo for hospice patients).
And I agree with Techler2 - it is a relaxing time on the table - you have to be still!
Give it a try if it feels like a good choice!
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Massage and Acupunture is apart of my treatment at Cancer Treatment Centers of America. I was so lost in finding an oncologist. I did not care for the first one I saw. We are so blessed to have one of these four treatment centers in my area!
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I got to thinking today..
I was so violently barfy during my prenancies that I can handle this if it happens!
Funny how things pop into your head! -
Hi everyone
Add me to the group! I get my port in on Tuesday, April 12 and begin TCH (6 cycles) on April 19 and then H for a year, followed by Tamoxifin for 5 years. I had a BMX on Feb 16 w TRAM recon, so I am still recovering. I started back to work (I work at a college, teaching and in the Athletic Dept) and it feels so good to be "normal." again, only to have to start Phase 2 of Chemo life next week. I had a funky tumor - it was 85% HER2neg but 15% positive. I had the lab checked out, which turned out to be reputable and got a 2nd opinion as well. I feel like I did more research this past 3 months than I did for my entire dissertation!!! I have accepted I need to do chemo and feel a lot better once I stoped fighting it and being angry about it. I am going tomorrow for a wig fitting. My little son is very scared about the hair loss, so I am getting one good wig and then a bunch of cheap fun ones - like pink, ice bonde, jet black, etc... I think I'm going to try to have as much fun with this as possible, so that my 2 kids (ages 13 and 10) remember this as not so terrible (positive thinking). I went through this with my mom and I can't recall one positive thing about it, so it's pretty tough for me. Going to keep thinking positive and rock the wig look!
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Hi everyone! I have a prescription here for the numbing cream that was my daughters. I will have to check the expiration date but I'm sure my Dr. will give me one if I ask for it. I have a slight cold and my daughter is coming down with one so I am worried I will be sick and they will cancel my port placement on Tuesday.. keeping my fingers crossed! I want to get going and get this over with!
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Hello all! Got my port on Friday, not the best experience. My veins are really tired. I had two burst in the back of my hand and, after quite a search, they found one in my forearm. The "twilight" sedation was more like "the break of day." I was fully aware of all that was done, without any pain of course. I started weeping when the doctor was numbing me up and he had to take a break. It did finally come to an end. I'm sore, but managing to continue all that I need to do. I think I am just tired of being poked. I will be glad to get started Thursday on chemo and I'm hoping to get a routine back.
I went wig shopping today and yes, they are expensive. I am glad to hear that insurance may cover some of the cost. I guess I need to ask for a prescription for a prosthetic? Does anyone know the wording? Apparently the receipt needs to call it a prosthetic and not a wig.
I hope those of you who started this last week are all doing well and had a relaxing weekend. I feel encouraged that so many are not having a terrible time with SE's
Best wishes to those of us starting this week! Take care, xoxox
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To anyone considering getting a port - I did mine under full sedation and I'm so glad I did! I was a nervous wreck about it, but when all was said and done, it was a piece of cake.
Geocachelinda and seeay: Nice to see you both here! (Well, you know what I mean.
Linda: Take that cold seriously. I am sick with a cold now 5 days post chemo and I wish I had taken it more seriously when I could have. I wouldn't try to do surgery while fighting a cold at the same time. You need all your resources to heal.
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off to my first treatment with a headache i do believe that is from the dethamethasone i stated taking yesterday?? not real nervous just ready to go and hopefully get rid of this headachi hope all is doing well!!
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Hardy, the wig rx should say it's for a cranial prostethic. Also, if you check out your local American Cancer Society chapter, they donate wigs & headcoverings for free. In addition, crickett's answer for cancer will donate a wig or other services, and there's a website -franceluxe.com. Check out the GoodWishes portion of thier site, and you can get a free headcovering.
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Pawprint- I hope your headache eases up for you today. I had one too from the demathasone. I'll be thinking of you today
Michelle
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home from first treatment!! so far feel fine headache went away it could've been from stress and nerves too???i hope i can sleep tonight! the more i think about it i'm thinking i might want to get a wig..i have thin curley hair and it might be nice to get something cute?? maybe.....
i hope all are well...
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Pawprintgirl: Glad to hear things are going good so far. Best of luck to you sleeping tonight.
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