Chemo June 2010

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  • JFV
    JFV Member Posts: 795
    edited July 2010

    Glad it made you giggle!  Hang in there

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    Well, I got a script for prednisone from the onc but he still isn't convinced that this darn rash is from the Taxotere. I shoved the literature in his face and had highlighted the part about 'Generally it will appear between treatments ...' and his comeback was "it normally will happen within two or three days of the infusion, not 12 days later".  I'm gunning for bear now. Have to find a phone number for the manufacturer in Bridgewater NJ and will phone them tomorrow. If they publish this insert to go with their med, they need to back up the info with fact. I want to know more about this rash and it's rate of occurrence and timing of such. I'm not a crock or a hypochondriac and resent being treated like one. (Hey, the prednisone hasn't even kicked in yet and I'm feeling aggressive. Imagine what I'll be like tomorrow after a couple of doses.)

    And Danielle and Janny, I ended a long distance long term relationship in January and was diagnosed with BC in March by mammogram and April by biopsy. I have never regretted kicking that guy to the curb for one minute. I got tired of worrying about his practice or his grown sons issues. His stuff. I wasn't going to move there and he wasn't going to move here. It was time. Yes, it is tough going through this stuff alone. But I have been blessed with a wonderful array of friends, some whom I've probably known longer than you are old. And I get support and understanding from them without reservation. Whether near or far, there is always someone to talk to or lean on. My good old girl friends will get me through this. I feel freedom to do as I please and to take charge of my life. This a time I need to focus on me. It IS all about me now. I can't be worrying about his issues or trying to make him feel better.. He kept calling for a couple of months and I never did tell him about the BC. I just asked that he please leave me alone. I had to be blunt. And the PS here is that I don't think that if we had still been together when I was diagnosed that he would have been able to handle it very well. I imagine that I would have had to console him and tell him it will be OK. What a load of crap.

    What's that song?  Oh..."Got along without you before I met you, gonna get along without you now.  Un hu, my honey, un hu my honey, gonna get along without you now"..

  • cheyenna
    cheyenna Member Posts: 379
    edited July 2010

    Bon you give them hell!!Smile

    well all bloodwork good i get my last AC friday at 8 am, then i get 3 weeks off and then Taxol x12.

  • Sherry9316
    Sherry9316 Member Posts: 294
    edited July 2010

    I want some of what BON has! ! !

    Jennweg: I just finished tx #4 of weekly Taxol.  It's not bad at all. My tx time is 3 - 31/2 hours and I sleep about 2 hours of that time because of the Benedryl so it goes by fast.

    Chey, honey.  Don't be so hard on yourself about your emotional state - it will cause you too much stress during a time when you need to eliminate as much stress as you can.  Friday is going to be a milestone for you and I'm praying it will go very smoothly!  Our dx is similar (except I have node involvement) and yet my body wouldn't tolerate the A/C tx.  So you have accomplished much!  Focus on that and not the negative.  YOU CAN DO IT!

    Danielle and Janny:  My thoughts are especially with you two and having to go through this alone.  It's hard for me to imagine and each of you get a special CROWN with jewels for forging through by yourself.  I hope each of you has good family/friend support.  HUGS to you both!

    <twirling and dancing> in my mind anyway!  LOL!  My decadron high is about to crash I'm afraid, so I shall exit here and get ready for bed.  See you all tomorrow (maybe).  Curious to see if the new nausea drug regimen will work for a second week.  Stay tuned.

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited July 2010

    Okay, chemo brain must have kicked in big time.  I just came across this video of a Pug singing the Batman theme and I just can't stop laughing.  We all need an Action Pug to help us fight BC.  Forgive me, I hope it gives someone else a good laugh!

    http://www.wimp.com/pugbatman/ 

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    DMom...I won't ask how you found this video, but it's priceless! Thanks for the laugh. 

  • Sherry9316
    Sherry9316 Member Posts: 294
    edited July 2010

    Oh my STARS!  This video is even funnier when it's 11:00 p.m. at night and your pre-treatment steroids are still hanging on in your body!

    Going to bed now.  Zzzzzzzzzz

  • janny99
    janny99 Member Posts: 119
    edited July 2010

    Designer Mom ~ That was hilarious!!!  My daughter had a pug that looked an awful lot like the "singer" in the video....lol....thanks for the laugh.

    JFV ~ Love the T-shirt slogan!!! Laughing

    When I start getting sad about not being in a relationship with my former male companion, I think this quote by Marilyn Monroe says it all....

    "If you can't handle me at my worst, then you don't deserve me at my best"....

    Goodnight ladies!!!  

  • Latte
    Latte Member Posts: 1,072
    edited July 2010

    I'm back!! So much to catch up on while I was gone.

    Danielle123 - I hope the Taxol gets rid of your ex for you - I think that's a great idea :-)

    i've been really sick - the first week after my last AC was bad, but just regular bad. I never got my good second week after AC :-(

    Instead, I had to have surgery on my port, because somehow it twisted around the wrong way. then I had a reaction to the bandages etc. and got these huge painful blisters around the stiches. then I got an infection in the site of the surgery, and had to go to hospital to check whether there was an internal abcess (there wasn't) , so just got antibiotics. then got a bad cold (3 days of coughing, throwing up, sneezing, and ear ache) but the antibiotics seem to be helping with this too. I seem to get every possible complication out there...

    now i'm coming out of it - just seems like a regular cold now, not like i am dying...   But i won't be able to use my port for my 1st Taxol on Monday, which is traumatic because it usually takes a couple of hours and many attempts to get a vein - they run away at the sight of a needle!

    about hair loss or lack of it - my head hair came out in huge clumps after 2nd AC, so i shaved it very short. but it never all came out, and i feel like a badly plucked chicken! it also seems to be growing again slowly - i have one specific hair in the middle that is getting quite long - like the "zeds"  in Dr Seuss's "One Fish Two Fish"? Leg hair is still growing fast (annoyingly), underarms have stopped, eyebrows and lashes and nether regions are thinning but still hanging in there.

    re male/female toilet fun - i was at the onc center the other day, and I know which toilets are male and female because i am there a lot. but when i went to the ladies, i saw a guy coming out looking confused, and then i looked into the mens (the door was open) because I thought maybe i got mixed up and saw a woman in there washing her hands, which explains why the guy was in the ladies looking confused :-)

    re diet - i also know that everything everyone is saying re diet it right, but it's just too hard to follow at this point - if i can eat something and keep it down then i do. maybe if the taxol symptoms are better then i will try to eat better too. i do try to eat lots from the brocolli/cabbage family as i know this is good.

    re periods - i've had 2 since starting tx - both on their normal dates, but the last one seemed more like i was haemorraging or something - it was so heavy and unusual. But that's TMI! but i remember reading somewhere that this is also a SE so i wasn't worried. Tampon info seems logical, but I'm glad I didn't know about it before :-)

    thanks everyone for all the funny stuff you've been posting - it's nice to see we can keep our sense of humor :-)

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    Good morning and Welcome back, Latte! You've been through a really tough time but sound like your spirits are up and you're ready to fight that good fight again. I'm so sorry to hear about your port and sympathize. Mine is tilted and it makes for a difficult time each infusion. One of the stitches holding it in place was snipped to alleviate the pulling. But that means it's lopsided and I can actually manipulate it under my skin. Creepy!  Sorry your new one won't be ready for the next round. How long do they intend for you to wait? I got my port on a Friday and had chemo that next Wednesday.

    I'm with you on diet. Right now I intend to eat whatever I can keep down and what appeals to me. I will worry about the healthy stuff when the chemo and rads are over. The one thing I'm trying to be careful with is fresh fruit and vegetables. They are supposed to be a no-no while having chemo since there is such a high incidence of produce contamination. Even cantaloupe is supposed to be one of the biggest harbingers of contamination because of the rind...and when you slice through the rind you spread the bacteria. But I cannot give up lettuce and tomatoes. Or celery. So I scrub the heck out of them, bruise the lettuce and wash it like mad, but I still eat them. Everyone can tell when I feel well because I have my salad.

    Rash update...I've had almost a full day of prednisone to squelch the itching. But as I sit here typing this it is spreading down the inside of my left arm from shoulder to elbow. This is maddening. I'm on my way to eat some cereal and take the morning dose. Then I'm going to find the number of the manufacturer and get to the bottom of this rash thing from Taxotere. It may take me a while but I'm determined to find out more before they try to give me the next IV dose. The literature says that rash is common but only serious in 5% of cases. Well, I think that this is mighty serious after 4 days, benadryl and prednisone...and it's still going strong.

    Song of the day..."Hot fun in the Summertime....Hot fun in the Summertime" (Sly and the Family Stone

  • mimi9186
    mimi9186 Member Posts: 127
    edited July 2010

    Cheyenna   Good Luck tomorrow.  It is supposed to be my last FEC before starting the taxol.

    Bon, I can identify with how worried you are.  I hope you obtain some relief with the prednisone.

    I am headed off to the hospital today.  After a weeks delay because of the gut infection, they will do bloodwork, an EKG and MUGA scan to check for heart damage.  My pulse has been running very high and I am winded all the time.  If all is ok, I will have the LAST FEC tomorrow.  I really hope everything is ok and I can do this last yucky triple chemo and move on to the taxol.  More later.

    Hugs and blessings, Mimi

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    I just got off the phone with a pharmacist from Sanofi-Aventis in Bridgewater, NJ. She is emailing me controlled study and SE info on Taxotere that is not part of the 70 pages prescribing document the oncs get. She is also sending my 'report' to the next level for review. She said to expect a call from them, too.

    And, 'between treatments' means any time between treatments. Not just 2 or 3 days after. 13 days after qualifies as 'between treatments', too.

    I am really serious about getting to the bottom of this. Never mess with an itchy, bitchy chemo patient!

  • cheyenna
    cheyenna Member Posts: 379
    edited July 2010

    sherry, thank you, im trying i get 3 weeks off so i can regroup and maybe be me for a week or so.

    bon im so sorry that rash is still there. i cant believe there is nothing else theycan give you, i pray you get some peace soon,its not fair all the extra crap everyone is going through.im thinking of you.

    designermom, you are too funny, how did you find it???

    Latte. wow you have been through hell and back! im so sorry, im glad your back.

    sounds like your spirts are up? i was just saying its so un fair to have to go through all this extra crap while dealing with the chemo!!! you guys are my hero's, i have had no problems on the AC but emotional, i feel like such a baby and spoiled brat compared to what you all have been through! i dont know how you get through it? your amazing!!!!! i think ive learned im very weak, lol im so trying to stay positive but cant help but cry every couple of days.

    ive had two periods in two weeks, i wonder does that mess with your emotions as well.. DR gave me something lite, she said she did not see depression in me just high anxiety cause i worry about everything, it seems to help, i think.lol, maybe we should ask my husband.lol

  • JFV
    JFV Member Posts: 795
    edited July 2010

    The pug is too funny thanks designer mom.

    Bon you tell them what is what!

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    Cheyenna, You can't 'fail' chemotherapy. We are all going through a terrible thing. Breast cancer is not a walk in the park. Everything is different for everyone and we learn from and help each other to cope. That's the beauty of 'hanging out' on-line with other women going through this mess at the same time.I know you're grateful for lack of serious SE and we're all happy about that for you, too. This is a highly emotionally charged event in your life. I'm sorry that you get weepy but if that's how you can cope with it, then grab a box of tissues and cry it out. Then pick yourself up and move on. Remember, there's nothing wrong with a good cry. Keeps those tear ducts moist and functioning so chemo doesn't mess them up, too. But do take that RX to help with anxiety. This is scary stuff we're dealing with. Whatever can help you through is a blessing. You are probably too young to remember the old Monsanto tag line... Better living through chemistry.

    Personally I think I've channeled my 'emotional' stuff into fighting this damn disease and worrying that the treatment will get me before BC ever does. I came to this website about 11 days before I began chemo and started a forum "I'm terrified of chemotherapy". Still am, but I'm trying to work with it now.

  • julia2
    julia2 Member Posts: 183
    edited July 2010

    Ok, I'm due for my next TC on Monday, and I don't think I can do it.  I am changing oncologists due to the complete disaster of my last infusion, and when I talked with the new onc about extra premeds for my next infusion I was good with it, but now 5 days from the infusion I am really scared.  I am worried that I am going to have a reaction again during the infusion, but I am more worried that I'm going to spike a huge temp and have liver pain 24-36 hours post infusion like I did last time and end up on antibiotics or in the hospital.  I feel like I'm being systematically poisoned.  Called the onc's office to get an appointment to discuss, she is out today and fully booked tomorrow.  I guess I'll call back tomorrow.

    Julia

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited July 2010

    About that Pug video.  I swear I don't normally go for silly, internet videos, usually delete them from my inbox.  However, Mom had a Pug and he looked and sounded just like this one.  He hated the garbage man and squirrels and loved oranges.  I have to think my Mom was looking down on me and just wanted me to have a good laugh.

    Latte- Aye, yay, yay!!  I am so sorry for your extra suffering.  I am praying that it is smooth sailing from here on out.

    Bon- I KNOW you will get to the bottom of this.  The drug company's attentive response makes me wonder if they have had problems with this.  Stay on top of it.  Instead of that "Achey, Breaky, Heart" song, you could come up with a "Itchy, Bitchy, Witch" version!

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited July 2010

    Oh, I forgot to ask.  My Oncologist told me NOTHING about avoiding fresh fruits, salads and vegetables...or tampons.  I'd be curious what all your Oncs say.

  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

    Julia, Changing oncs was a big step. Good for you. That's not easy to do. And yes, you are right to be concerned, but take a deep breath. Tomorrow you will hopefully be able to speak to the new onc and get some reassurance. She knows of your past experience and reactions and if she's worth her salt, she will be on the lookout for anything and everything during this next infusion.

    Try to spend the next 24 hours thinking of the best outcome...completing chemo and being cancer free! That's the goal we all have. We'll all do whatever we can to help you get there.

  • TMarina
    TMarina Member Posts: 692
    edited July 2010

    julia-->I hope you can get in to see the onc before your next chemo!  I don't blame you for being nervous.  I don't think it happens very often that someone gets an infection twice in a row.  I know I was worried about that last time too though, but i got a little fever, then I got the back pain from my neulasta shot, so i knew that was working!  Hopefully that's all I'll get this time too!

    Bon--> still thinking about you!  Thanks for keeping us updated!

    Chey-->Like Bon said, we are all happy for you that you don't have too many se's.  We like good news too!  :)  You are a strong woman!  Don't ever doubt that!!  Hope all goes well with the last AC! YEAH!

    Latte-->sorry you are having so much trouble!  Hang in there!

    D-Mom-->FUNNY video!  Thanks for sharing!

    JFV--> I think you are the one with the t-shirt slogans?  Keep thinking of them!  They are GREAT! 

    Mimi-->Hope you can get that last FEC!

    Hope this makes sense--kind of out of it right now!  Yesterday I was "awake" in the am, and had a nice time with the g-baby, but I had more nausea than usual.  Took my Zofran and Decadron at 7, and then a Compazine at 10.  Realized I had forgotten to take my Emend on Tues., so called the nurse and she said go ahead and take it today (yesterday), and tomorrow (today).  I was so relieved!  I was really worried about how sick I might feel if I didn't take it!  Not much nausea today, and was able to do some dishes, etc., but I'm sure I'll be sleeping most of the afternoon (I try to stay awake until after lunch!).

    Hope I didn't miss anyone--but know that I'm thinking about you all!

    DSA Deb?? how are you doing?

    TinaKiss

  • jenweg
    jenweg Member Posts: 195
    edited July 2010

    Well had my first taxol treatment yesterday.  All went well.  Of course felt like I was having an out of body experience from the benedryl!  My dd went with me and after the nurse stayed with me for the first fifteen minutes and monitored me, she left because I was fine.  A little while later my daughter told me I was all blotchy on my chest and neck so she called the nurse over.  The nurse stopped my drip and called the doc to check on it.  The doc said I was fine and to continue.  The rash disappeared and I was fine.  I might add that I felt fine when the rash appeared.  I am at work today and feeling good, of course the ac effects usually didn't hit me till two days after so praying I still feel good tomorrow!!
    One strange thing I have had with this chemo business is my eye sight is totally out of whack.  I wear contacts and my vision is blurry even with them in.  It sucks but I don't want to pay for new contacts now on top of all my other bills.  Anyone else have vision problems???

    Bon - - - Good for you for being so proactive!!  I hope you get to the bottom of it soon.

    Cheyenna - - Good luck tomorrow, hope all goes well!!  We are all moving closer to the end of chemo, YAY.

    Sherry - - Hope your meds help your nauseau again.

    Designermom - - Too funny, made me laugh!

    I got a card in the mail the other day from a dear friend I met here on the message boards.  It says "chemo sucks" on the front, then you open it and it says something like "But if it sucks the cancer right out of you, Yay chemo" 

    Haha they truly have a card for everything!!  Thanks T!!

  • cheyenna
    cheyenna Member Posts: 379
    edited July 2010
    thank you Bon and TSmile, i need to get out of this hole and like bon says channel it into something else. I too am scared to death of the Chemo!!!!!!!!!!
  • PearlGirl
    PearlGirl Member Posts: 549
    edited July 2010

     Below is most of the text from Foods to Avoid During Chemotherapy on the site www.breastcancerwarrior.net.

    It addresses the issue of fresh fruits and veggies as well as soy products for ER+ women. It all makes perfect sense. I never asked my onc about this...heck, he already thinks I'm a crock. Can you imagine if I start questioning him about fruit? He;ll have me in the funny farm pronto. I envy you who have a decent PA or ARNP to deal with. I have Brunhilda.  Actually, this specifice food info was brought to my attention by a classmate who is an anesthesiologist in WV and a former roommate who is an OB/GYN ARNP in PA. Both sent it to me indpendently. So thought it couldn't hurt to keep in mind. Still, I brave the salads since I really can't live without lettuce.

    *******************************************************************************************

    When you have Estrogen-positive Breast Cancer, Estrogen is your enemy (because it is your cancer's best friend), and any "Psuedo-Estrogen" is also your enemy.  A ‘Pseudo-Estrogen' is easily mistaken by the body for a true Estrogen, and, in fact, your body does a little tap dance with ‘Pseudo-Estrogens' and actually turns them into virtual copies of Estrogen.  Soy is a "Psuedo-Estrogen', as is Licorice. (Oh darn!)
     
    According to many researchers, Estrogen-positive Cancer gains strength not only from Estrogen, but from ‘Pseudo-Estrogen' as well.  As a result, many health care professionals advise that Breast Cancer Warriors (BCW's) avoid Soy in its many and varied forms (Soy Beans, Soy Sauce, Tofu, Tempeh) as well as other ‘Pseudo-Estrogens' such as Licorice. 
     

    When you have Estrogen-positive Breast Cancer, Estrogen is your enemy (because it is your cancer's best friend), and any "Psuedo-Estrogen" is also your enemy.  A ‘Pseudo-Estrogen' is easily mistaken by the body for a true Estrogen, and, in fact, your body does a little tap dance with ‘Pseudo-Estrogens' and actually turns them into virtual copies of Estrogen.  Soy is a "Psuedo-Estrogen', as is Licorice. (Oh darn!)
     
    According to many researchers, Estrogen-positive Cancer gains strength not only from Estrogen, but from ‘Pseudo-Estrogen' as well.  As a result, many health care professionals advise that Breast Cancer Warriors (BCW's) avoid Soy in its many and varied forms (Soy Beans, Soy Sauce, Tofu, Tempeh) as well as other ‘Pseudo-Estrogens' such as Licorice. 
     
    Having said that, we should also point out that there are others in the health care field who believe that the potential health benefits of Soy (when eaten in moderation) outweigh the potential harm.  For more on the subject of Soy, click here: www.breastcancer.org/tips/nutrition/ask_expert/2009_10/question_14.jsp
     

    The toxic effects of Chemotherapy and Radiation can also decrease a body's supply of natural Digestive Enzymes and healthy bacteria, both of which are used to help us digest food and to deal with many of the common forms of bacteria that typically adhere to virtually all fresh foods.  It is this decrease (or even complete elimination) of healthy bacteria that can open us to a potentially dangerous complication.  
     
    When you are undergoing Chemotherapy or Radiation, there are several other foods that can be problematic.  Unpeeled, uncooked fresh fruits and vegetables are chief among them. Raw Eggs are also on that list of ‘no-no's', which means say goodbye to Egg Nog during the Holiday Season. 
     

    During Chemotherapy, any uncooked, unpeeled food can pose a significant health hazard to BCW's.  Foods such as Lettuce, tomatoes, celery, apples, peaches, grapes, cherries.....in short, any raw, unpeeled, uncooked food can make a chemo patient very, VERY sick, very suddenly, and very seriously! 
     
    We know of dozens of BCW's who, within a few hours of eating a simple green salad, have found themselves suddenly and severely sick -- projectile vomiting, their fever spiking to an alarming 104+.  (More often than not, the culprit turned out to be bacteria on the lettuce).  This is nothing to fool around with.  This can be life-threatening.   While on Chemo, a body temperature in excess of 101 is reason for concern, as your Oncologist should tell you.  If, however, you suddenly find yourself being violently ill, and feverish, you should immediately (and we do me IMMEDIATELY) get to the Emergency Room.  

    Our advice:  while on Chemotherapy or Radiation, avoid all uncooked, unpeeled foods.  That means NO LETTUCE.  If you want to eat fresh fruit (apples, peaches, pears), make sure that you scrub them with a professional anti-bacterial food wash, AND PEEL them!  (no kidding!)  If it can't be peeled, don't eat it!  Unless you have mastered the fine art of peeling grapes, strawberries, blueberries, cherries, etc, etc, etc....forget about eating them while you're on Chemotherapy.  In fact, we recommend that you do what many BCW's have done: while on Chemo or Radiation, say goodbye to green salads, as well as all unpeeled fresh fruit or veggies and eat only cooked, or thoroughly, seriously scrubbed and then peeled foods, and if a food can't be peeled and can't be cooked, then don't eat it.   (And, if you're going to eat foods such as melons, oranges, lemons or limes, make absolutely certain that you seriously, thoroughly, severely SCRUB the exteriors of each before you cut into them, so as to get rid of any bacteria that might otherwise move from their skins or rinds, onto your knife, into the sweet, tender insides of the fruit, and from there, into the sweet, tender insides of you!)
     
    Other edibles to be wary of while fighting Cancer include Sugar, and Acidic foods.  Extensive scientific research has proven that cancer cells thrive in high Sugar and high-Acid environments.  (To learn more about the dangers of Acid, click on the article entitled: "The Acid Trip".)  Better safe than seriously sick!!   You're a BC Warrior, we know you can handle it.   

  • Latte
    Latte Member Posts: 1,072
    edited July 2010

    thx everyone for your encouragement - the antibiotics seem to be kicking in and i am starting to feel better.

    DesMom - you asked what our oncs had said - mine didn't say much. i was told to avoid soy because i am ER+, and eat veges from the cabbage family, and try to avoid sugars. apart from that, nothing. no mention of bacteria on fruit and veges, or avoiding tampons.and when i asked about taking glutamine, she brushed it off as not necessary.

    jenweg -  i'm also having vision problems (I wear glasses, not contacts) - i find that some days i can't focus properly. since it doesn't happen all the time, i haven't done anything about it. i thought i'd get through the next 3 months of chemo and then see if i need new glasses. but I do know that one of the chemo SEs is dry eyes - so maybe this affects the way your contacts fit? and i love the card you got :-)

     is anyone on taxol using ice packs during tx to protect your nails?(my onc brushed this off too as unproven)

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited July 2010

    Bon-thanks for all the food info....I think!  It got me looking in other places like chemocare.com.  There they refer to the American Cancer Society, suggesting lots of fruits and vegetables, both raw and cooked.  I live on lots of fruits, vegetables and salads too.  I just can't imagine eating less nutritious canned fruits!  Having said that, I do think I have to be more vigilant about washing everything well (and DH barely washes stuff at all).  I stopped buying the pre-washed lettuce, got my good old spinner out again.   I think if your blood counts are very low, it would be wise to avoid raw anything and definitely restaurants too.  There's only so much I can deal with while going through chemo.

    On a completely different topic.  Has anyone else had a skin eruption that feels like a big, itchy mosquito bite?  I didn't go out for three days after chemo and WHAM, this big, itchy red bite right on my butt!  I thought it might be a hive, but it did not go away.  Maybe it's just more chemo nonsense.  Maybe a spider bite?  I feel like Forest Gump "somethin' bit me on the A$$"!  I couldn't see it closely, so made DH take a close-up photo with the camera.  Nothing like being way too familiar!

  • mimi9186
    mimi9186 Member Posts: 127
    edited July 2010

    Bon, thanks for the info.  I live on bananas and grapes.  Some how I can't envision myself patiently peeling the skin off of each grape. Oh well, another thing to lose.  Spent 3 hours at hospital getting tests done.  EKG was normal. Pulse was high.  The MUGA was done and they will have results today.  It looks like the last FEC is on tomorrow.  Finally!

    DMom I did have a spider bite about 1/2 inch over from my port.  It swelled and itched like crazy for days.  Good thing is was not over the port.  I hope it died from chemo poisening.

    Julia, good luck Monday.  We will all be there in cyberspace holding your hand.  Keep us posted.

    Love to all, Mimi

  • julia2
    julia2 Member Posts: 183
    edited July 2010

    Hey designerMom, I got something sorta like that on the back of my head, first I thought it was sunburn, but it didn't feel like sunburn, it felt like an insect bite and super itchy!  About the size of a quarter.  I got it a week after infusion, it took about 5 days to go away.

    Julia

  • NorthernGirl
    NorthernGirl Member Posts: 67
    edited July 2010

    Hey ladies... reading about everyone's side effects reminds me of the phrase someone used some time ago:  going through chemo is like having an alien take over your body. There's so much going on with our bodies, and so much that is unpredictable.

    Like Chey, I feel such trepidation about the next infusion. After a week of yuck, I am feeling better, and stronger. It's hard to think of going to the next chemo and getting sick all over again. Gotta find my big girl panties and get over it.

    To the girls who don't have supportive partners in their lives:  I hope you have great friends and family by your side. You are the priority. You don't need to spend precious time and energy on fellows who just can't step up.  I like Janny's Marilyn Monroe quote; "If you can't handle me at my worst, you don't deserve me at my besst"  Love this!

    When I got diagnosed, the timing was unbelievable. We've been through a tough year with my youngest son who had a complicated tumour growing through the tibia of his left leg. It wasn't cancerous, but his doctors used really cutting edge stuff to save his leg from amputation. After lots procedures and two surgeries, things are looking really good for him now. A few months before my son's last surgery, we find out I have breast cancer. My second excision surgery was 10 days after his second surgery. I was being treated at a cancer facility 4 hours from our home, and my son at a children's hospital 8 hours from our home. My daughters were at universities in 2 different cities across the province.

    I kept apologising to my family that they have to go through this. They've been through enough. My husband and kids have been so wonderful. This cancer thing is actually drawing us closer together. This is the first time that my husband has really been my caretaker. It's a whole new dimension of caring for each other. He's great at it. And it's been great for both of us to slow down and spend lots of quiet time with family.

    At one point my hubby said, if this was happening to him, wouldn't I step up and take good care of him... which is true, I totally would.  And he reminds me we're in this, "for better or for worse"  He says I have given him plenty of the "for better" part, and he has given me too much of his "for worse" part.

    I really wish every person facing the cancer beast had a good quiet loving soul to lean on, no matter what... it's like potent medicine in facing this cancer monster.

  • cheyenna
    cheyenna Member Posts: 379
    edited July 2010

     Well tomorrow is Friday and ill be having my last RED DEVIL cocktailSmile 8 am is a bit early for a drink for me but we do what we need to do! i hope all goes well, everyone have a great Friday and i pray no se for all of us, i shall try and sleep now, Ha!!! no way,lol

    love Chey

  • kittycat
    kittycat Member Posts: 2,144
    edited July 2010

    I finished my last AC yesterday!  Woo Hoo!  I feel okay today.  Kind of like how I felt the 1st go around with chemo.  Maybe it's the chemo nurse?  I got the same chemo nurse that I had the 1st time.  Of maybe it's just my imagination.  Hopefully I won't feel to awful tomorrow.

    So, I called a couple allergist's offices today.  I have a consult with one of them next week.  The girl that answered the phone said that they might be able to tell if I can tolerate Benadryl or Claratin.  That would be cool to know.

    So, my onco was on vacation this week, so I saw her partner, who is my FIL's onco. He was very concerned that I had low level nausea.  So, he told me to take Zofran, then Compazine (a couple hours apart) - then take Adivan at night.  So far I've taken the Zofran/Compazine combo.  I had a maid coming to clean my house this morning, so I didn't want to sleep through that.  So, I didn't take the Adivan yet. 

    So, my house is so nice and clean.  I haven't had the energy to do it.  I've kept up with it best I could, but I hired a housekeeper (she cleans my inlaws' house and used to clean ours pre-recession).  It was worth every penny!!!  I feel like I spoiled myself!  :)

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