Starting Chemo October 2009

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  • Enjoyful
    Enjoyful Member Posts: 3,591
    edited November 2009

    That's miserable, Mary.  Can you take any stool softeners or isn't it allowed with your chemo?  Grapes help me a lot but it sounds like you can't eat much of anything.  Wish I had something more helpful to say.

    Good luck tomorrow, lainie!

    E

  • azdiva
    azdiva Member Posts: 201
    edited November 2009

    Hi All!

    Finished tx #3!!!  Half way there!  So far, I am feeling ok.  And you all saw my list, so I'd better get cracking while I still have energy!!

    Enjoyful - I asked my Onc if I could CUT BACK on my steroids because I am gaining so much weight!  He said No and that I would lose it afterward, and to enjoy myself.  HA!  He is a man and has no idea how hard it is to gain weight once it is on.  On my way home from chemo I met a friend at Olive Garden and stuffed myself to bloating.  Nice!

    He still says No to Zometa.  And I asked him about the new Zeloda information.  No to that as well (I guess since its still in mouse studies I understand that).  He did say YES to Black Cohash for the hot flashes, but NO to Folic Acid/B-12 (even though I told him my fingers were numb - but really, they're not. I just want to take it so I can still have my wine).

    I asked him if he thought I was at high risk for recurrence.  He said that I will be low risk once we are done with treatment.  He did agree to talk about Zometa again after the San Antonio conference, so I am slightly hopeful about that. 

    Hope you all have a good night!

    Laura 

  • Enjoyful
    Enjoyful Member Posts: 3,591
    edited November 2009

    azdiva - the steroids seem to have the opposite effect on me. Tons of energy, not much appetite.  Isn't it weird how we all react differently to the same drugs?  I wonder why your doctor says no to Zometa?  My doctor has said yes once I finish treatment, but then I'm stage IV and that might be the difference.

    Can't wait to hear what comes out of the San Antonio conference!

    E

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited November 2009

    Dear all,

    I signed up into the SWOG 0307 (bisphosphonates clinical trial) today and got assigned to the Zometa arm today.  will get Zometa by IV once a month for 6 months and then every 3 months for 30 months.

  • lieberman1
    lieberman1 Member Posts: 42
    edited November 2009
    Mom had her 3rd TCH Treatment today.  She is halfway through!  She was in such a good mood today and I think she is excited she is close to being done with the TCH part at least.  She will continue with Herceptin for a year but that dosen't have the side effects the chemo has. 
  • micheleboots
    micheleboots Member Posts: 1,993
    edited November 2009

    Mary my Dr have me both stool softener and a laxative as a precaution. I eat a lot of fiber so they have not been needed. I know TMi. I am sitting at the airport with nothing to do but type.

    Michele

  • MaryNY
    MaryNY Member Posts: 1,584
    edited November 2009

    lieberman1, I'm glad your Mom had no repercussions from not taking the Decadron last night. The nurse gives me the Decadron immediately prior to the infusion so I suppose you could have given it to your mother this morning. Good to hear she's halfway. Someone was telling me that she has no SEs whatsoever from Herceptin so hopefully your Mom will find the same.

    Michele: Which stool softener and laxative do you take? I bought Miralax tonight and took one dose. I've never used that before but someone suggested it might help. I'm afraid I let the bowel issue become too bad before tackling it. It would have been better to prevent it. Not sure what causes it, the chemotherapy drugs or the Zofran or Decadron tablets they give me prior to infusion.

  • puffins
    puffins Member Posts: 32
    edited November 2009

    Hi again BC sisters!

    For the those who sew, I was in a fabric shop today and found McCall's pattern 4116 that includes7 different versions of turbans, headwraps and hats...just like the ones being sold for $50-$90 online! Also found some beautiful colorful lightweight fabrics (from summer---for us with hot heads) being discounted for the winter season to try out the pattern. My thrifty side is happy to try making several for $5-10 max and also to discover my inner flair.   :-)

    Hugs to all,

    Shoshanna 

  • azdiva
    azdiva Member Posts: 201
    edited November 2009

    Onty - I am so glad for you!  As you know, everything sounds so good about this trial and I think the Zometa arm is really the way to go.  Boniva would be a good one as well, but isn't that arm closed because they can't keep up with the demand?  Did you read about the new Zeloda studies?  Using it as adjuvant therapy in early stage BC?  That sounds amazing - at least for the mice that it has worked on already!

    As you all can see, 1230 am and I am still awake!  Thank you, Decadron! I am going to take a Valium and try to doze a little.  Took some prophylactic Miralax as well.  Hopefully, it will work!

    Ate Chocolate Toffee Crunch ice cream out of the tub (from Schwan's) for dinner.  Why does it taste better from the tub and not a bowl?  I was having a hot flash and suddenly that ice cream just called my name.  I NEVER eat ice cream.  Just have it for the kids.  Oh well, less for them.  And calcium is good for me.

    Off to try to sleep!

    Laura 

  • jeanl151
    jeanl151 Member Posts: 146
    edited November 2009

    Tx #2 is done, one more smiley face for me

    .  Yesterday was a very long day. I had the port at 9 am, doctor appt. at 1 then chemo from 2-6.  All went well but was very tired. I was asleep by 9 pm.  Now between the steroids, achy port sight and the early night sleep, I am up at 4 am today!!!!

       Laura, I know what you mean about the joy of being with friends. My friends of 30 years, took me out Monday night. One girl made me a pillow case and they all signed it. It was to make sure I felt their support and hugs on bad nights when I was feeling done.  These women have been amazing support through this for me.

       I am planning on a restful day.  hope everyone has a good Thursday, Jean

  • Scoobydoo
    Scoobydoo Member Posts: 499
    edited November 2009

    Mary make sure you do not have an anal fissure.  You also might want to sitz bath a couple of times per day in warm water.  Also make sure you take your stool softners like Dulcolax and drink plenty of liquids.  I normally take 1-2 Milk of Magnesium tabs and 1-2 stool softners the night before.  But you have to make sure you are getting plenty of liquids.  I am the queen of these types of problems because I suffered from hemmies and anal fissure prior to chemo.  I have been able to have no bottom issues throughout this ordeal.

    Onty - please tell me more about these studies.  As we are both triple neg I am very interested on the thoughts behind this.  Do you take this while undergoing Taxol? 

  • lainieo
    lainieo Member Posts: 53
    edited November 2009

    I am off to my 2nd chemo in an hour. Looking forward to the time I can post it is my final chemo

    Scoobydoo I have hemmi issues too and use a producr called Heal Hemorrhoids. It is a product from Healing Natural Oils. There is another company called Amoils that makes a hemorroid oil as well. They both are miraculous.

     

  • one-L
    one-L Member Posts: 1,110
    edited November 2009

    mary,I had really bad constipation from my first tx.  I was determined that this time, I would take care of it before it started.  I started taking two stool softeners a day several days before my tx.  I also ate white grapes everyday and a high fiber cereal.  I also started taking Benefiber, just mix it with a drink, I like it in my tea, once or twice a day.  I am 7 days out from tx 2 and I have had no constipation problems this time.  It is painful, but that is because the drugs we are taking affect our mucus membranes and they are inflamed, sluggish and just cranky.  Anyway, it never got hard and I have always been able to pass the mass.

    jean and laino, congrats on one more tx down.  It is always good to get one out of the way.

    jean, what a sweet thoughtful thing for your friends to give you.  They must be so special.  You are one lucky lady.

    laura, a bowl of ice cream never killed anyone.  Besides nothing will taste good for about a week, so you should enjoy while the taste buds are still working.

    Shoshanna, you are so clever.  I sew, but it has been years and I never even thought about making scarves.

    onty, keep us informed on how the study is going.  I hope you do well.

    I am sending good wishes to all who are dong tx this week.  Hope SEs are mild.

    Juannelle

  • txstardust
    txstardust Member Posts: 599
    edited November 2009

    Chocolate Toffee Crunch....mmmmm.  Thanks for giving me something to lust after, Laura!  :)

  • micheleboots
    micheleboots Member Posts: 1,993
    edited November 2009

    Mary,  the stool softener is Soflax, and teh laxative is Senokot.  They are a prescription from the Dr.  She told me not to let constipation get out of hand as it is easier to prevent than fix...you could always call her and get a supposatory.  I know for the first couple of days after treatment I eat everything with bran in it or some sort of fiber.  Then on day 3 and 4 I go to the bathroom a lot...must be all the fiber.  But at least I know how my first 5 days will be. No, No, Go, Go.

    Jean,  yah for you being done #2....

    Lainieo,  Good luck with #2..

    Juennelle, You made me laugh so hard this morning.  I love the comment "pass the  mass' too funny.

    So I am trapped at home today.  My husband took the car.  I guess I should get some stuff done around the house..I have no excuses.  I could clean, do bathrooms, laundry, walk.  I hope I don't spend the day surfing the net, and wasting time.

  • MaryNY
    MaryNY Member Posts: 1,584
    edited November 2009

    Onty: I so regret not taking preventive action this time for the constipation. And yes, I think I must have an anal fissure as I now have such pain. I thought I was drinking plenty, but since I'm not eating much, I need to drink even more. I do eat a high-fiber cereal, my favorite is Weetabix. I'm now cooking some pinhead oats, which will do me for the next couple of days. Glad you got into the study. My understanding is that once you are in a study group, they monitor you really closely which has to be a good thing. 

    Shoshanna: I like the hand-made headcoverings idea. 

    Laura: Despite losing my appetite, one thing that tastes good to me is ice-cream. I also like Dan-Active, the drinkable yoghurt with live cultures. With the way this chemo is affecting our digestive tracts, I think we need to repopulate it with good bacteria.

    Good luck to anyone doing treatment today and hope all have a SE free weekend. 

  • micheleboots
    micheleboots Member Posts: 1,993
    edited November 2009

    Peanut butter cup icecream....in a sugar cone...yummmm

  • MaryNY
    MaryNY Member Posts: 1,584
    edited November 2009

    Michele: I wish my doctor was as good about staying on top of things as yours. She admonished me for getting constipated last time and told me the rectal bleeding really indicated that I needed a colonoscopy. My father died of colo-rectal cancer. But I really think now is not the time to do it, while my guts are inflamed. Anyway, the doc didn't give me any advice on preventing constipation.

  • Scoobydoo
    Scoobydoo Member Posts: 499
    edited November 2009
    Mary if you have an anal fissure then you must do softners and sitz baths. If the pain is excruciating and you see blood then it sounds like it is an anal fissure.  Anal fissure can heal on their own.  The warm water from the sitz bath will help it heal.  Sometimes if you have spasms then it will not heal on its own.  If not, there is an ointment your doc can prescribe that will stop the spasms to allow the fissure to heal.  The main thing is you can not be constipated.  The cereal you should be eating is fiber one.  One good bowl, plus plenty of water is all you need.  The fiber actually softens your stool.  However, if you dont drink enough water you will make cement.  (get the picture).  Along with stool softeners your bowel movements should become normal.  Also if it is a fissure do NOT use hemmie meds.  They will make fissure worse not better.  So make sure you find out which you have...hemmies or fissure.  Go see your normal doc and they should be able to look and tell you which one you have.  Also if you have a colonoscopy they will be able to see on the screen and let you know.

    Hope this helps.  I no longer have any of those issues, but had them long enough to become an expert of sorts.

  • Sunshine1958
    Sunshine1958 Member Posts: 22
    edited November 2009

    Hi everyone,

    I had my first treatment of FEC on October 26th and my second treatment yesterday and today I go back for fluids and Neulasta shot.

    I have a quick question regarding nausea medication.  Has anyone taken Metoclopramide and/or Ondansetron HCL?  Did either one of them work for you, and if you tried them both, did you find one better than the other?

    Thanks for your help!

    Sunshine Laughing

  • unklezwifeonty
    unklezwifeonty Member Posts: 1,710
    edited November 2009

    Dear SunShine,



    Love you screen name! Welcome to our support group.



    Zofran (ondansetron) works great for nausea. I haven't heard of the other one. I got Emend, Kytril and Compazine. But different women respond to different nausea drugs. You would need to try it the way your doctor prescribed. If it does not work as prescribed, try to experiment with the schedule a little bit so you would know what would really work and for how long for you.



    How did your first 2 chemos go?



  • MaryNY
    MaryNY Member Posts: 1,584
    edited November 2009

    Welcome Sunshine. I'll add your name to the rollcall up top. How many FEC treatments are you scheduled for? I get Zofran (ondansetron) the day of treatment along with Emend. Then I also take Emend on Day 2 and Day 3. The Emend works well for me as my nausea is less on those days than later. I don't have any experience with Metoclopramide. Neece in the Sept thread mentions that she was prescribed that. You can search all threads by hitting the search link on the top right corner of your screen and entering your keyword. 

    Scooby: I heard sitz baths help. Woke up in the middle of the night two nights ago and filled a basin with warm water but basin was really too small to fit my big butt in there Embarassed. Last night I sat in a warm bath for 10-15 minutes and that helped along with helping me sleep better. When people talk about sitz baths are they talking about sitting in a bath tub or is there another way?

    Ok, you sold me on Fiber One esp after seeing the amount of fiber in one serving! So I had a bowl of pinhead oatmeal for breakfast, then did a three mile walk and now I've had a bowl of Fiber One for lunch. I also bought some Fiber One bread, I never knew they made bread before. So might have a sandwich made with that later. And I have to remind myself to drink more water too. 

  • MarieK
    MarieK Member Posts: 911
    edited November 2009

    Hi All!

    Welcome new sisters and welcome back those that haven't been heard for a bit!

    Sunshine I'm on FEC too but I'm taking Maxeran, Decadron and Kytrel.  I have Semmtril too but haven't needed to take it yet.  I find by day 3 or 4 I have no need of anymore meds.

    Soshanna - great idea to make your own head toppers!  How great it is to be in touch with your creative side when all this other crap is going on!

    Mary - I feel for you....hope this too shall "pass" !

    1L - Pass the Mass - LOL!!!!  That was just too funny.  I'm not Passing the Mass quite yet - just Passing the Gas!  Boy the chemo gas is sure smelly!  I thought it was the dogs at first and I even smelled their butts - nope it wasn't them!  I will continue to blame the dogs though...

    Laura - nothing wrong with eating out of the ice cream tub - just a spoon to wash so you're actually being very efficient and preserving water!  Give yourself a pat on the back for being so clever!

    Onty - congrats on getting into the study!  Keep us updated on any "inside" info.

    Michele - get off the computer!

    Congratulations to those that can check off another TX and good luck to those that have one coming up today or tomorrow.

    Thinking of you girls often and sending my best wishes and e-hugs!

    Marie

  • MarieK
    MarieK Member Posts: 911
    edited November 2009

    I forgot to tell you that my PICC dressing allergic reaction is clearing up - looks all red and streaky but not blistering or infected.  The nurses are monitoring it closely and changing the dressing twice a week now until this clears up.

    For future reference or anyone who is doing a search I am now having the PICC area cleaned with iodine & saline only and using the white cloth Mepore dressings with success!

    Keeping my fingers and toes crossed that the PICC line holds up until the end of my chemo!

    Oh and I made a boo-boo today with my Neupogen injection. 

    I jabbed the same side twice in a row. 

    Anyone else doing neupogen?  Are you alternating sides? 

    I usually alternate but today the dogs were barking, I was expecting someone at the door and it was getting past time to do the injection (4 hour window).  I wasn't thinking and just hit my left inner thigh (yesterday was left belly flab).

    Just wondering if I'll be walking around this time with a left limp or if it makes any difference at all?

    Marie

  • Sunshine1958
    Sunshine1958 Member Posts: 22
    edited November 2009

    Thanks for the warm welcome!  I am SO thankful for this group of wonderful women who provide such great support.

    My treatment is FEC x4 and then Tamixifone x4 as well (I think).  My DCIS listed in my signature turned into IDC, hence the chemo.

    This second treatment has been AWFUL.  My treatment yesterday was 4 - 6 pm, and even though I'd taken Emend beforehand and later Ondanstetron, I started throwing up late last night and continued into today.  It was nothing like this with my first treatment (they gave me the Emend through an IV).  The most nausea I experienced was just a little queeziness but not like this.  I'm going back in an hour for fluids and she told me they'll be giving me 3 different anti-nausea medications through IV, so next time I'll make the 2nd appointment for first thing in the morning!  Of course, I will let her know what's been happening.

    I've tried lots of different things to help with the nausea:  peppermint tea, ginger snaps, Ginger Ale.  Someone told me that there are Ginger Lollipops that work really well.  Has anyone tried those? I'm just wondering how they would taste, because I can only handle the ginger snaps in very small bites because of the flavor.

    Again, thanks for your support and warm welcome!

    Sunshine Smile

  • micheleboots
    micheleboots Member Posts: 1,993
    edited November 2009

    Marie,  Can't get off computer, it is like my life line......I know sick..

    Michele

  • Scoobydoo
    Scoobydoo Member Posts: 499
    edited November 2009

    Marie - the only reason they tell you to alternate is because of soreness.  I think it is fine if you do it in the same spot twice.  I have a reprieve from neupogen on taxol until I get my bloodwork done to see my numbers.

    Mary - you must drink at least ten 8oz glasses of water.  Trust me.  Lots of fiber in fiber one and now you are adding bread.  Be careful not to overdo fiber because you will then have diarrhea.  Also take at least 2 stool softners tonight.  They sell these plastic sitz baths in drugstores that work really well.  Your whole bottom does not have to be in the bath.  I am a overweight woman so if I can fit in the little plastic sitzbath so can you.  They are pretty inexpensive.  A lot of pregnant woman buy them because of hemmies or to soothe their stitches.  PM if you need more info on anal fissures.  They are crazy painful.  But I think with attention, they can heal on their own.

    Welcome Sunshine.  Sorry to hear you were so sick from 2nd tx.  I sure hope your meds will help with that nausea.  I only used decadron, emend and compazine.  After several days I would not need any of the meds.  Ginger tea and ginger snaps really helped me.

    Well I am feeling much better from my first taxol treatment.  I actually went out to lunch with hubbby and then took daughter to Michaels.  We are going to make Christmas ornaments tonight.  She is 15 but still loves craft projects. 

    I sure hope each of you ladies have a wonderful SE free evening.  To those having txs tomorrow, I wish you the best and I am thinking of you. 

  • MarieK
    MarieK Member Posts: 911
    edited November 2009

    Sunshine I take 2 Tylenol Extra Strengths right before my Cytoxan infusion. 

    That really helps with the headache and resulting nausea. 

    I had a terrible first TX - smells, tastes, sounds, lights everything effected me and I could not keep anything down not even my anti-nausea meds!

    I spoke the to the nurse about it at my second TX and she suggested taking the Tylenol and even laughed at me like I was silly for not thinking of it myself.  I didn't even think of it because I thought I would just take what was prescribed and nothing else!

    Since taking the Tylenol have had much better results with absolutely no headache/nausea or vomitting.

    I would suggest that you try that for the next time - right before your Cytoxan take a couple of Extra Strength Tylenol (check with your nurse first) and see if that helps you.

    Marie

  • lainieo
    lainieo Member Posts: 53
    edited November 2009

    2nd cheno done!  Feeling ok for now.

  • micheleboots
    micheleboots Member Posts: 1,993
    edited November 2009
    lainieo  SmileWinkLaughingKiss, what else can I say.

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