**NEW** Starting Chemo March 2009

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  • DonnaDio
    DonnaDio Member Posts: 905
    edited March 2009

    Thanks PattiB..good info and tips!!Have a pile goin..the mouth wash and all the good toileteries needed!!  Hope you conitnue well and good to know you are goin back to work as well!!!That really would make a difference to have some sense of normalcy during such a day to day journey. Will keep you posted when I start!!!

    Hugs,

    Donna

  • kellerka
    kellerka Member Posts: 49
    edited March 2009

    I did the head shave last night. After all you wonderful women shared your stories I thought I would be OK. How wrong I was. I feel worse today than I did the day after my bmx. I guess they should give out drugs with the shave. This is too hard.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    kellerka   Patti and I are right behind you and I wish there were drugs to make us forget this whole ordeal sometimes......  All I have done today is pull my hair out literally and I got myself a bit choked up about it on the way home from picking my daughter up from school (didnt need the tissues though).  I am wearing one of the buffs I got all day to prepare myself for tomorrow.  The hair has to go.  Hopefully I will talk myself into not being a big cry baby...but if I do, so be it...tears it is  :(  I love and will miss my hair but yes, I know it will come back.  Just one of the many steps we need to take to get through this BC BS.  Sorry for the foul language.

    2 arms around you,

    Diane

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Quick update......OK I have been home 10 minutes with my 3 kids and guess what?  They have all noticed mom's new scarf and are taking turns trying to get their grubby hands on my head.  I ask again....does anyone know where one can find a wig that can be superglued to my head for the next 6 months which doesn't need to be washed AND where my "new" hair can grow back in.

    I am sure I am going to have about 50 funny stories about sorted head wraps and wigs in the future with my kids as the main characters.

  • gymmom8
    gymmom8 Member Posts: 86
    edited March 2009

    I buzzed my head on Wed.  I've never thought of myself as beautiful but the compliments I have received have been nice.  Apparantly the shape of my head is condusive to baldness.  Yeah me!  I am having one big problem though.  I am soooooooo tired.  Any suggestions on handling fatigue?  I am much more tired after this round. 

    I will now check out the website for a free scarf.  That is awesome!

    Good day to all!!

    Cyndi

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Cyndi, sorry you are more tired this round.  I, too fear that round 2 will cause more SE's and fatigue......I really tried to drink a lot of water the first 5 days.  I carried water bottles around with me everywhere...and walking the first 3 days helped me, too.  I started feeling crappy day 4 and 5 but still tried to stick with my program.  Good luck and thank goodness it's the weekend again.  Get some rest.

     I also took extra strength tylenol for the first 5 days.....and took my compazine.  I found that some of my fatigue was attributed to the nausea.....hope this helps.  

  • chick717
    chick717 Member Posts: 58
    edited March 2009

    Cyndi,

    I've read both extremes about the fatigue.  Mine has also been worse second time around, but onc blames it on changing from Taxotere to Abraxane.  Doc says to do what I feel like doing, no more and no less.  Lie around all day if that's what my body says, go running if my body thinks that's ok.  Other websites say that 30 minutes of walking a day helps with the fatigue, even if you feel too tired to do it.   On days that I've felt crappy (9 of the last 11), I tried to walk around the neighborhood some of those days, but would even get light-headed doing so.  

    Anyone else got advice on fatigue management? 

  • knowledgeforpower
    knowledgeforpower Member Posts: 184
    edited March 2009

    I usually follow medication directions too.  However, I took two Claritans on Wednesday, one in the the am and one in the pm, when I had my Neulasta shot.  I also took two on Thursday.  Today I took one and I think I will take one tomorrow.  So far, no bone pain.  My onc. had never heard of taking Claritan but was all for me trying it and said to report back to her how it worked.  I am so happy I read about it on these boards.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited March 2009

    So, I just returned from tx # 2.  Unfortunately, like a few before me, I had a reaction to the Taxotere. Thanks to having read other descriptions I recognized it immediately.  I was about a minute in and thought, great no problems.  Then I became bright red and had trouble breathing.  I tapped the nurse next to me on the shoulder and  said " Houston, I think we've got a problem".  They were awesome in their response.  My blood pressure had shot from 106/68 to 168/90.  We did the whole benadryl, more steroids and waited.  Then they started it up again slowly, increasing it at 5 minute increments and got through it.  I mentioned that I read about some folks having a reaction.  My onco replied, so did we do all the right things?  I don't think the medical profession appreciates patients with TOO much knowledge.

    Other than a little scare, 2 down, 4 more to go.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Geez Deb......that seems like more reactions than normal....Do they want to see if you can tolerate it again for round 3? My girlfriend had really bad neuropathy on taxotere a year ago and they switched her from the TC to AC as in adriamycin for her final 2 treatments.

    Good for you for getting through.....how scary but again, nice to know the nurses are on top of this.

    Relax this weekend.

  • laurie41
    laurie41 Member Posts: 61
    edited March 2009

    Mom of boys...i'm pretty sure I'll continue the Taxotere, when they started it back up, I was fine. When I see the doc again I'll have to ask him to make sure. I don't want that reaction happening again.

    Laurie

  • Anonymous
    Anonymous Member Posts: 1,376
    edited March 2009
    didle20diane  Yeah, they think they can keep me on the same regimen.. The plan is to load me up on the benadryl and such at the beginning.
  • Alyad
    Alyad Member Posts: 817
    edited March 2009

    I just got home from tx 2 and it went WAY smoother than the first! Whoo-hoo! They gave me the benedryl after the A and then gave me the C, then finally the Taxotere I had reacted to before. last time benedryl wasn't enough and thye had to give me more steroids too. This time, just the benedryl was fine and I was hooked up 2 hours less than before!

     Dh's aunt and her friend who had BC 2 years ago came up for a visit and then all went to lunch with another of his aunts. he brought me bac good food from that and I ate it and then was all done. Very tired from the benedryl right now-

    Michellein SJ, Bellydancer, Bethr, WLL, NYdeb48- hope your treatments today went well and I hope all of us have a SE free weekend!

  • WLL
    WLL Member Posts: 96
    edited March 2009

    Hello all. Thanks ALYAD for asking. I am doing good, just a little tired. They gave me something to relax me, it made me very tired, I sleep through the whole treatment. The treatment was very fast, it lasted about 1 1/2 hours. From what I had read, the side effect do not start till 3-5 days into it. I am crossing my fingers all goes great. Hope everyone is doing great!!!!!!!

  • DebbyB
    DebbyB Member Posts: 16
    edited March 2009

    I had my first treatment yesterday and everything went fine.  Like everyone has said the anticipation and waiting was FAR worse than the treatment.  It was a long day but had no problems.  I was actually very calm when I finally got into the room and sat in my recliner chair.  Went back today for my "shot" and so far so good!  I met a woman who was getting her shot at the same time and she also started her treatments yesterday for BC.  She was very eager to talk to someone who is going through the same thing and we will be having our next treatment at the same time, so I look forward to talking with her more.  I will let her know about this board and how very helpful and comforting it can be. 

    Because I was supposed to start on March 12th, which was the day after the port was put in, I'm actually glad I had some time for the port to heal.  I think having Chemo right after would have been very uncomfortable.

    Thank you all for the kind words and just being here.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Yeah Debby and WLL!  Congratulations on getting through your first chemo treatment.  Get some rest, drink lots of water, take your compazine even if you don't need it and walk if you can.  Day 4 and 5 were the worst for me BUT all doable all the same.

    We have a page on Facebook for any of our newer posters.  See my signature for the group name.

  • PattiB
    PattiB Member Posts: 421
    edited March 2009

    Kellerka & DidleDiane - I must be right behing you both.  I am still not ready for the shave, I procrastinated today calling my friend/hairdresser who will shave my head and trim my wig.  She thinks shaving before gives us the power not the cancer treatment.  I'm just not ready, even though I have always "hated my hair".  Don't think I'll say that ever again.  I guess I will call her tomorrow morning after I see what falls out in the shower.  I have some buffs I picked up at an REI store (I wanted to see them first).  I do like them and will purchase more on-line and can't wait to see the Franceluxe headwrap. 5 more days to round 2 then we are 1/2 way through - Yeah!!!

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Patti, I have my buff on tonight...hair is falling faster and faster. My head isn't hurting but tomorrow AM I think I am going to buzz it myself.  The way I look at it is we have about 6 more weeks of treatments before our hair starts growing back in.  Surprisingly, I like wearing the buff and will probably not miss the 30 minutes it takes to wash and dry my hair.  Thank goodness its not the dead of winter. I will talk to you tomorrow.

  • WLL
    WLL Member Posts: 96
    edited March 2009

    PattiB, what treatment are you receiving? Yes check out franceluxe, I ordered my FREE head wrap today.

  • PattiB
    PattiB Member Posts: 421
    edited March 2009

    WLL - TC x 4, then radiation, then Tamoxifin - I did call and ordered the Hip Geo in Graphite (gray) yesterday.  Laurie said she would email when it is shipped - she said it would probably ship have been today, but I didn't get an email yet.  Seems we are the same size,grade, & nodes but different ER/PR HER2.  Did you have a Lumpectomy?  I did.

    DidleDiane - My head is not hurting yet either, although it kind of tingles (could it be psychosematic). I like the buffs too.  I wore one around my neck yesterday, amazing that I got a lot of compliments just because I had some color around my neck. I tried the different ways you could wear them, during my lunch break.  They do sell Jr. and baby sizes at Planet Buff, maybe you could get a few for your kids, then they would have their own.  When our hair grows back it will be nice that they can be used as a scarf too.

  • PattiB
    PattiB Member Posts: 421
    edited March 2009

    DonnaDio - I have a golden also.  He is huge and bad. Kind of a Marly.  He likes to mouth me whenever he wants something, which is often.  I walk him at least 20 minutes each day and was able to even right after the chemo - I wanted to stay active and it also helps him leave me alone after he gets some attention on his walks.

    WII - Sounds like you're feeling pretty good, hope that continues.

    Everyone - Have a really great weekend!!!

  • WLL
    WLL Member Posts: 96
    edited March 2009

    PattiB, I did have lumpectomy. My treatment is A/C. Still feeling good. Thanks so much

  • Anonymous
    Anonymous Member Posts: 1,376
    edited March 2009

    Mom_of_boys, I was told to take the -D version, and I too, for bone pain took 1 every 12 hours.  It seems that as soon as it wore off my nose started running like it had "dried me up" and was now letting go.  Odd.  I thought the twist of bitters and Tylenol sounded like overkill...er...over doing it, but I'll take some Vicodin if the pain is that bad.  (Oh, that was a nasty Freudian slip, and I put on on over my Freudian bra.  Pardon me. We are not goin' nowhere.  Nope, we have things to do on this planet, ladies!)

    I, too, have felt like I am taking drugs under the counter, over the gums, and look out tummy, here it all comes.  I'm gonna talk to my chemo nurse about it.  It is just not right that some doctors say "no extra vitamins," because it may interfere with the poisons.  If you survive the treatment, then you can get better - for now, you can just get well.  Good grief, Charlie Brown!  Not lookin' forward to the liver filter queasies @ four/five days out later this next week.  Taxotare, oh, Taxotare (sung to the tune of "Galveston").  No offense meant to any one in Texas or anywhere else.

    Love in Christ,

    Sessna1

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Round #2 gals - Yeah! We did it.  Marshall2000, Alyad, MichelleinSJ, NYDeb48...crazy taxotere side effects aside.

    Round #1 gals - CONGRATULATIONS on your PREMIER!

    BellyDancerinNJ, Bethr, WLL. This one is for you.

    And if you are worried it is too early (depending where you are) Undecided  I give you options....

     Classic Bloody Mary

    Mimosa (yum, yu), Or....

    Oh and my personal fav..a double espresso.YUM YUM

    I made it as well with no drama (thank goodness) and a nice, unexpectedly short fusion time...so short in fact that we were out of there at 1pm and went to lunch! My hub and I. With no one else. What a nice surprise! Feeling OK so far, though my head is hot and prickly and my tongue is numb (already!!!) I am up to take some Ativan so I can sleep...this is just a quickie post because I really need to try and get some sleep-o-rama. 

    I will be back to reading and posting soon.  Love to all!

    hugs

    gina

  • McLouLou
    McLouLou Member Posts: 8
    edited March 2009

    Gina, would you please add my name to the roster for March? 

    I really like this forum.  It is great to have a group within the larger chemo group, just for women who started their chemo in March, 2009.  We are not alone Laughing .

    I started my chemo March 12, 2009.  I am in the heavy shedding of my hair stage.  I have an appointment with my hairdresser on Monday (day 18 post chemo one) to take off what ever is left.  I am okay with it.  I knew from the beginning that this was a definite possibility, so am ready to let it happen.  I placed an order from planet buff.  I also have a wig.  Had it styled on Wednesday and will have it adjusted (with no hair) on Monday.

    Have a great day everyone.

  • laurie41
    laurie41 Member Posts: 61
    edited March 2009

    I thought that after i shaved my hair real short the pain would never come back. Boy was I wrong. The top of my head is tender. After the 2nd round I'm more tired and cranky. My kids think I have lost my mind and at times I think I have. I'm at work right now and I can't wait to go home and crawl into bed and sleep all day. Sleeping is my favorite thing to do.



    Holy cow...I'm having a hot flash right now....now I know what my mom is going through..yikers.



    Today is my wedding anniversity...17 years. All great too.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Happy Anniversary Laurie!  Get some rest after work and then go celebrate!

  • WLL
    WLL Member Posts: 96
    edited March 2009

    Thanks GINAGINA, I would love the espresso--Its way to early and 2nd day after treatment I dont know if I could hande the harder stuffLaughing

    LAURIE41-- Happy Anniversay!!!!  17 yrs that is awsome.

    Glad to hear everyone is doing good. This is my second treatment, but first treatment on A/C. I have lost alot of my hair--taking it great--I thought it would be more difficult. I am feeling good. I am having some face hot flashes though. 

    LAURIE41-- what type of work do you do--did you miss much work?

  • Luv2sing
    Luv2sing Member Posts: 145
    edited March 2009

    NYDeb48 - Yeah .. 12 steps my butt!

    mmdj43 - I'm definitely singing that song now!  My husband had to shave my head this morning because I decided to wash my hair while in the shower.  It all became matted and no matter how hard we tried we could not comb thru my hair! Cry  So now he and I are twins.  He finished cutting, turned off the razor, stepped back to look at me and said "You're still beautiful."  I cried the entire time.  I know it will come back, but still ... so now I'm trying to figure out what to do with my head because I don't have one of those perfectly shaped noggins.  Anyhoo ... while I'm at home, I'll just let it go Cool  I uploaded my new look.

    Ricki13 - My husband and I went out for breakfast last week and I was extremely flattered when several men paid extra special attention to me while my husband was away from the table.  Two even got up the nerve to actually tell me I was very pretty Embarassed.  That's something that definitely keeps a smile on my face!

  • PattiB
    PattiB Member Posts: 421
    edited March 2009

    Luv2Sing - You do look very beautiful!!!

    McLouLou - I started TC on 3/11 and since I don't have a lot of hair to begin with a lot came off in the shower today but did not knot up. I have not dried it yet but when that's done I'll see what's left and then call my hairdresser, she will shave and trim my wig, I'm thinking Monday or Tuesday, next chemo is Wed.

    GinaGina - Glad 2nd round was quicker

    & Round 2 girls - Hope the SE's stay away or to a minimum!!!

    Premier girls - hope for the same!!!

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