**NEW** Starting Chemo March 2009

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  • PattiB
    PattiB Member Posts: 421
    edited April 2009
    Oops Bwbly - I think your Bubbly too.Cool
  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009

    sakura73... I am so very thankful that you are feeling better today!

    Janet0527... Sounds like you had quite a day yesterday!  Are you taking the Claritin?  My Neulasta bone pain hit me the second go around between my shoulder blades.

    Carol... I missed your comment about the birds!  That is hilarious... I agree with Marshall2000... use the "best" hairs possible.

    Ricki13... So your 000 must be like like our 911 (emergency call).  Also, I certainly understand what you mean about chemo fatigue.  It is getting very hard to get out of bed in the morning.

    McLouLou... I have the opposite problem after chemo which requires imodium.  Your pictures didn't come through for me...

    DonnaDio... Thanks for your words.  I DO feel that way sometimes.  I take the decadron 2 in the morning and 2 at night... I take a sleeping pill called Trazodone (prescription) to help with my sleep issues.  Is Lorazapam the same as Ativan?  If so, I've been taking Ativan about an hour before my sleeping pill at night as well.

    annadou... Welcome!  Ask any questions you might have... we have an absolutely great group of women here.  And... lucky you living in Greece!

    Carol... Can't look at you tube here at work, BUT I'll look at the video when I go home for the day.  Very cool... Also, have you tried Aleve for your headache?  I've been plagued with migraines for years... the only OTC meds that help a bit is Aleve for me.  OH... and good luck today!

    BethR... The fatigue has been my biggest factor overall.  The SEs are the worst that first week, BUT they do get better with each passing day for the most part.

    luv2sing... WOW, working on your MBA thru this "stuff"?  I'm impressed!  Good luck today!

    bwbly... I've been in that particular praying position myself as well! 

    Marshall2000... I'm in the lumpectomy category, but that doesn't mean I haven't had some second thoughts.  Hopefully, that's normal!

    Chris... I don't know... Does it mean if you have a bilat that you will never get BC or cancer again? 

    Patti... Struck me as cute/funny about the 1st grader... wish more people would just shrug and go on... I think more of us would just go bald if that were the case!

  • buddy1
    buddy1 Member Posts: 750
    edited April 2009

    Hello,  I havent chimed in for a while.  This place sure is busy.  I had my second DD AC on ue. Nuelasta on Wed  Went back Thur for 2 IV bags and antinausea drip.  I slept all day and all night.  I feel ok today.  Just real tired.  My hair is more than half gone.  I think I will cut it tonight.  I can now say I am half done with the AC part.  Hang in there everyone.  We need each other.

  • ginagina
    ginagina Member Posts: 327
    edited April 2009

    Hey everyone - I love the boob size stuff. Keep it coming. I think I am going to turn it into a graph. Or chart. At least a spreadsheet. Should be interesting. What should the other variant be? Something to keep it fun - Surgery type? Eye Color? Hair Color (natural or otherwise)...(before it fell out/stopped growing/buzzed or shaved)? And lets just not be limited to lumpetco gals (for cyin' out loud, I am a bilateral mx gal) so anyone who wants to play, chime in.  

    I just realized this am that next week is, um, Spring Break for us. We aren't going anywhere, but 6 year old wants to know what I have planned. Yikes! Thank goodness I have my energy back...I got to figure this out pronto.

    I will catch up on posts later...

    hugs

    gina

    Chick717 - we chanted your name this morning, both at wake up and in the car on the way to school. 6year old definitely thinks I am crazy now...but she went along with it anyway! Thinking of you and ALL INFUSION BOUND GALS TODAY!!!

    Annadou - WELCOME! I saw your post, and I will add you to our roll call list.  

    McLouLou - I can't see your pics! Is it me or are others having trouble too?

  • annadou
    annadou Member Posts: 221
    edited April 2009

    Carol,Bethr,Janet,Luv2sing

    Thanks so much for your replies-I am english married to a greek and have lived here for 30 yrs-have a holiday complex in Crete where I work from March till sept.rest of the time in Athens.Daughter No 2 is helping me this year as she is out of work due to the economic crisis and now my crisis! I have to go to Athens every two weeks for the chemo and am terrified of what I will feel like after and if I can  return to work.etc .Its all happened so quickly think I am still in shock or denial or whatever. Have you heard about the vaccination against recurring  BC-its all in the news here doing clinical trials in Athens,

    Take care xxx Anna 

  • annadou
    annadou Member Posts: 221
    edited April 2009

    Hi ginagina Thanks for the welcome!

    xxAnna 

  • IowaDiva
    IowaDiva Member Posts: 76
    edited April 2009

    Janet:  You and I are the same age, girl!  I'll be 46 in May.  I'm pretty proud of my girl.  She is the one you see.  The whitish pants are actually old sweat pants with a black leotard showing underneath.  In some of the other videos, she has the plaid shirt and black shorts.  And on the one with her sister, she has a black and white baseball-type shirt.  It gives me so much joy to see how much of her heart and soul she puts into her dancing.  She dances because she HAS to...she can't survive without it.  

  • cpanasci
    cpanasci Member Posts: 35
    edited April 2009

    Hi all;

    I had a busy day in CancerWorld yesterday (aka Dana Farber). Got a wig in the morning -- looks pretty natural, but not sure I will wear it. Then saw the nutritionist and then off the Infusion Center. I asked my onc abot SEs in round two and she said VERY rare. Maybe 1%. Guess what? Red face, breathing, spasms, SWAT team. You all had it pegged! They got me back on eventually, and say next time we can pre-empt. What fun. Thank you all for the warnings. No matter how many people say stay off the boards, thank dog you're here! BTW, feeling much better today than last time at this point... go figure! -carol

  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009
    cpanasci (Carol)... OMG!  I am soooo very sorry.  Again... again... I feel very fortunate I haven't had that kind of reaction.  I had read on the TC board that the second round might produce an allergic reaction, but thank God none for me.  Are you seriously feeling better now?  Any different meds for you now?  Will you be able to still do TC the next round?
  • crusader1
    crusader1 Member Posts: 1,222
    edited April 2009

    Hi,

    Ladies I got the free head wrap today from Franceluxe..L. Erickson USA Free Good Wishes Scarves and Triple Negative Breast Cancer Foundation

    What a lovely free gift. they even sent me a card signed by all at the office. How nice can you be. Do call the lady ,she loves to get people from different places.

    Welcome to our site..Annadou.. We are  becoming more and more global.great to have you here..

    Buddy- Glad to hear you are doing okay and tolerating your chemo..

    Carol- I agree that this board is wonderful. You can learn so much. Glad you made it through your treatment.

    Chick-How are you doing after the treatment today..

    Rachel- Hope you are doing fine..

    My breasts were 36 to 38 C after having children.Not big but not small. Then I had my lumpectomy and a quarter of my breast was removed. Quite lopsided for a while. Then two months later I had the mastectomy due to bad margins. No breast at all. Then I had probelms with dying skin. I just got my prothesis a few weeks ago.It is large, heavy and looks real big. But I do feel more whole now..Took a while to get used to it. Almost like the wig..Good quality, fully covered by insurance.If I ever finish with chemo I will have lat surgery and get a new breast. Hopefully someday this journey of mine will end.  

    I am still trying to research the question of 4 TC's over 6 TC's. I sent Otter , An expert on this board a PM and she replied. I don't think there is a right answer. I will just have to wait and see what happens.

    Have a great weekend.

    Hugs,

    Francine

  • chick717
    chick717 Member Posts: 58
    edited April 2009

    Hi All,

    I'm home from round 3!  woo hoo!  Nurse fumbled the IV, went to get another nurse, then finally had to call in the head nurse.  She popped it right in and on we went.  There was lots of waiting around - computers down, labwork took long time, nurses had lunch hour, etc.  Apt was at 9 and I walked out free at 1.  The actual drip took about 1 hour 15 minutes...and the rest was waiting.

    Planned a nap but a well-meaning friend wants to come for tea.  crap.  Even when I said I was planning a nap, he wasn't to be diverted.  Ok tea, then a nap later will be good.   

    "talk" to y'all soon!

    -Trac 

  • pickle
    pickle Member Posts: 1,409
    edited April 2009

    What a busy site....wow. So much wonderful input from everyone. So sorry to hear of the reactions and side effects that some of you great gals are experiencing. This F'N cancer is a bitch but we will all get through it....This is a great place for encouragement, support and of course the humor....I love the humor!

    I had my first AC tx on Monday and my scalp is driving me crazy. I don't know if it's from the chemo or the Nexium Shampoo. How soon after the first treatment did anyone else's scalp start to feel funny.

    I have been told that by day 14 my hair will be falling out. That's Easter weekend so I am thinking of getting it buzzed before Good Friday (which would only be 11 days from first treatment) Can anyone please comment on this. Should I wait or just go for it ahead of time?

    Thanks

    Beth P

  • Alyad
    Alyad Member Posts: 817
    edited April 2009

    BethP- My hair started just a little by day 14- didn't really start going til day 16 and I had TAC. I think you might be alright to put it off a few more days. my scalp did  feel weird for a couple days before I really started shedding at all. I have seen where others have said the pubic hair starts going first and that was true for me- so you might be able to use that as a litmus test- see if you can pull them out there before seeing if they pull out of your head.

    I had committted to shave my head evening day 16 - days 14 and 15 I was careful brushing my hair and lost very few. Tried to brush my hair morning day 16 and a whole bunch came out so I just put it in a ponytail and wore a bandana until the party to shave it. Day 29? after first treatment and I am still growing hair definately thinned- but I don't seem to have patches that I can tell- tho I have shaved it down to skin twice. I started losing stubble again after second treatment.

    Some folks choose the cut it sorta short but still try to hold on the hair for as long as possible. It just depends on what works for you.  I suspect if I had done that, I still might have enough hair to look okay for awhile yet. But then you get to deal with longer hairs falling out everywhere and I just wanted to get it over with.

  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009

    Francine... Good luck on your decision.  I know that's a tough one!

    Tracy... Congrats on your completion.  GRRRR on the well-meaning friend.  On my day 5 this past time, I finally drug myself out of my bedroom and into the living room.  Still felt pretty miserable.  A well-meaning friend dropped by unannounced and then proceeded to tell me what a bad day SHE had!  We'll learn to NOT answer the door, won't we?

    BethP... I'm on TC and I think the "T" is what got my hair.  Day 14 was my "D" day.  That morning, I couldn't have pulled a hair out if I had tried.  By evening, it was shedding.  I personally had a "party" of sorts with friends and snacks at my wig lady/hair stylist to have my hair cut down to about 1" and to have my wig fitted before I started shedding or even had the "tight ponytail feeling".  For me personally... and as Alyad points out... everyone is different... I wanted the control (my other "C" word) of knowing when my hair was going to go.  My wig lady/hair stylist also liked the idea of me wearing the short hair for a while so I would know how it would look growing back someday -- and, although I had never had short hair before, I really liked it!  BUT, on the day 14, once it started obviously shedding... I had it buzzed completely. 

  • ginagina
    ginagina Member Posts: 327
    edited April 2009

    BethP - You already have a cute short do, but maybe you want to try an ultra short (super-duper pixie short style) first before you buzz. It's a good time to experiment.


    My sore scalp began around day 14 (I described it as bonking my head on the edge of a cabinet door.)...it was a good warning sign for me, but I don't think everyone experiences it. Mid day 15 is when it started to come out (just the stuff on my head. The other stuff hasn't budged!) but only if I gave it a gentle tug. Day 16 I headed for the slopes with my daughter with ski beanie on my head and I refused to remove it all day. Morning of Day 17, I woke up and the pillow was COVERD. Eeew! I also tried to style it and ended up with a messy-hairy-disaster (think gel-mouse-hair covered bathroom). That afternoon my brother came over with his kids and we buzzed it off! Instant sore scalp relief for about...12hours. It started to ache again the next day. And as Dayla put it, it will continue to fall out, even though it is only 1/8" long...looks like metal shavings. And this is where a good sticky lint roller comes in super handy!


    Have you thought about head covering? Wig? Buff? Hat? Scarf? All of the above? None of the above? I hated my short do, but loved the buzz. Then, once the buzzed bits came out, the confidence dissapeared again and I haven't been comfortable totally bald, and generally stick to my tan/flower baseball hat.

    I got a free wig from ACS last week - its ok with the buff but not alone (way too fake). Went to a REAL WIG SHOP this week in my chemo/steroid intoxicated state and got a REAL wig (that cost some $$ but will hopefully be covered by insurance) that is actually...comfortable? The family loves it. Not sure about wearing it out and about everyday because the kids all know me at school as the bald mommy. Would they flip again if they saw the wig? Who knows. I think I will save it for special occasions. Hubbo conclusion: you get what you pay for!

  • BandanaGirl
    BandanaGirl Member Posts: 11
    edited April 2009

    Hi!  I actually started chemo in February but I saw your site and wanted to join....I am halfway through my dose dense A/C biweekly-4 cycles...Next week I will start dose dense Taxol for biweekly-4 cycles.  I was given a strong  group of anti-nausea meds so I made it through the 4 A/C cycles without too much nausea...I take a Neulasta shot the day after each treatment..My main problems are very sore legs and feet and an anal fissur that started right before I got diagnosed and was too busy with the diagnosis to take care of it properly...Use lots of Miralax to keep it under control but the weight is falling off me...I'm a little nervous about switching over to Taxol because they say all the anti-nausea drugs won't be necessary.  If someone could write to me and tell me about their Taxol experience...what kind of anti-nausea meds did you use and did it do the job..I appreciate being on this site with you great gals!!!

  • Mom_of_boys
    Mom_of_boys Member Posts: 556
    edited April 2009

    Travelgal... Welcome!  I can honestly and without reservation tell you that the March Princesses are a great group of women.  If you made it thru 4 A/C cyles without too much nausea, I'll bet you'll do fine on dose dense Taxol as well.  I am NOT on dose dense... I am on Taxotere/Cytoxan every three weeks.  The nausea med I've relied on after each treatment (I get something or another in the IV as well) is Zofran.  Others seem to do well on Emend (although Rachel didn't).  Hopefully, others can chime in with their suggestions.

    Gina... Is that your new wig?  If so, it looks GREAT!

  • crusader1
    crusader1 Member Posts: 1,222
    edited April 2009

    Gina...  Love your wig. Mine is also very comfortable.

    You look like a real hot Mama...I guess you probably are  a real hot Mama...

    Beth..I cut my hair short on day 14. The short hair lasted for one week. Then each time I washed it, it came out in clumps.You couldn't even touch it ..Day 21 I had my husband shave it off. We knew it was time. I am also on TC...

    I am real comfortable with the bald look. It is amazing how we all adjust. You will do fine..

    Francine

    Get those free headwraps...

  • pickle
    pickle Member Posts: 1,409
    edited April 2009

    Thanks to everyone for the input on the hair.

    Gina-Your wig looks great.I love it! Smile I have purchased a wig and have some buffs and scarves

  • crusader1
    crusader1 Member Posts: 1,222
    edited April 2009

    Photobucket

    This is me with the new head wrap..Not bad...

    Francine

    Here is the site again.

    L. Erickson USA Free Good Wishes Scarves and Triple Negative Breast Cancer Foundation

  • michele54
    michele54 Member Posts: 152
    edited April 2009

    Hi travelgal - I'm also on dose dense treatment.  I'm in a study so I'm doing the opposite of most. Tx4 and then A/Cx4. Just had my 2nd treatment and it's pretty easy.  My onc prescribed heavy duty steriods the first time which made me feel like Wonder Woman - the steroid crash headache sucked a little but nothing Tylenol didn't help.  Took half the amt of steroids the last time and things were fine.  From what I understand, the Taxol infusion takes a little longer than the A/C infusion - I was in the chair at noon and done by 4:00.  First they give you Tagament and then Benedryl because of allergic reactions. 

    For me the s/e are minimal.  I get the Neulasta shot the day after treatment and that causes bone pain for me too.  Women on here suggested taking Claritin and that really helps.  Even though the box says take one per day, take two the day of and the day after - what is one more drug in our systems.  I have the infusion on Monday and take Thursday off from work mostly because I have a lot of sick and vacation time so I figure why not use them but I really could go to work.I have anti nausea meds but haven't had to take them.

    Hope this helps - if you have any other concerns, please feel free to pm me.  Any A/C suggestions/hints you have would be greatly appreciated.

  • ginagina
    ginagina Member Posts: 327
    edited April 2009

    MOB and Francine - ah, schucks.  Yes, this is the new wig. It is also what I looked like 8 years ago when I got married.  It helps that I put some make up on before I took the pic.

    Hope everyone who had a date with the chemo clinic today is faring OK. Chick - hope you were able to get your guest to leave quickly so you got some good nap/rest time. Jdeking - Hugs, hope you are doing Ok with today's drip/drip/drip. Luv2Sing - ditto!

    Hi Travelgal - welcome!! Ok, off to read yesterdays posts (yep, I am that far behind) and will update our class list. Wow what a group!!!

    Francine - love your scarf. The colors look really good. Thanks for posting the link. 

    Ciao

  • michele54
    michele54 Member Posts: 152
    edited April 2009

    Looking good crusader1.  I wish I looked that good in a scaf.

    ginagina -You look beautiful..

    My hubby buzzed my hair the other day and I've been wearing a wig to work and I hate it.  It's too hot and I don't think it fits right but I ordered it online and it didn't cost much so I guess I can't expect much.  I have an appointment at a wig salon tomorrow so hopefully I find one that I actually like.  I ordered a couple tee shirt material caps from Ebay and wear them around the house and got a free scarf from francelux.org and it's beautiful.   If you haven't ordered one yet please check out their website and call Francine - they are no charge to anyone suffering from hair loss.

    I always wondered what I would look like bald and now that I am, I'm not liking it very much.  I think I have an odd shaped head.  Maybe due to an excess of brain matter lol.

  • Luv2sing
    Luv2sing Member Posts: 145
    edited April 2009

    Okay ... I'm apologizing right now, I can't remember who said what, my SEs kicked in quicker than the first time and I've taken something to help me sleep.  So here goes ...

    The actual chemo tx went well, but I started feeling light-headed as soon as I walked out the office, then I lost my appetite, so I was just eating because I knew I had to.  Drinking plenty of water.  MoB - Yes, I'm currently working on my MBA have been in accelerated classes with plans to graduate in March of next year, but I'm taking a break after this course, so my graduation (tentaltively) is now June 2010.  I don't plan on anything stopping from reaching this goal. 

    To everyone - Have good nigh's rest and anyone else who went thru today and/or will be going thru soon ... you are in my prayers and I send you big hugs and kisses!

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

    Dear Ladies,

    Sleep?  What is sleep the first two weeks after chemo?  Rest is best.  Rest like you are the Queen of the land.

    laurie41- I need my stubbles, too.  As long as I look a little better than Homer Simpson, I will not take a razor to my head.  Yeah!  Let's hear it for the stubbles.  Do not mistake stress for chemobrain.  I want my cancer markers to go down, and I have to  NOT worry about it.  As long as they don't accelerate upward drastically, that is good.

    marshall2000  - I think the kitty knows that you would appreciate some company even more now.  Do not underestimate any of God's creatures - good or turned bad.

    Mom_of_boys- You mean the one (SVU) with the child soldier from Africa grown up, or a different one?  Yes, it is always cruel to see animals abused.  We are charged by God to take care of them!  Don't you just love it when Elliot stands there are narrows his baby blue eyes to give the person speaking a showcase on his exposition?  It's like he's saying, "Do you really believe what you are saying?  Are you for real?  What is going on with you?"  Cutie pie Christopher Meloni.  I don't want his character to hook up with Olivia Benson's ever.

    To All - Last month's Reader's Digest had an article about cancer testing, and this month's Newsweek (?) has an op ed piece about early detection.  I don't like the message in either article.  The thing about cancer is that everyone is different, and you have to look at yourself as an individual.  You also have to get a darn good oncologist that you trust and want to work with.

    I think the public needs to know that you can fight cancer, and that some people are more successful in utilizing and benefiting from the treatments available than others.  I think the public needs to know that if your health is weak to begin with that you need to especially weigh in the quality of life issues - and don't let anyone scare you into chemo or rads.  Doctors are not gods and you are not a number.  I think people with cancer need to consider the effect their decision will have on those that they love the most - it's not just about you.

    I think that people need to stand up to clean up our foodchain.  These poisons are in the air, water, soil, etc.  We should not genetically engineer our food, it's full of enough stuff that shouldn't be in it already.  When that goes up against the corrupted innards of our bodies, the result is not positive.  Sorry, United Nations - but boycott food from China - that place is too dangerous to accept any foodstuffs from.  They have their own people cowed, IMO.  I don't know what triggers autism in children, but something is egging it on more and more. 

    I think people with cancer should not be cruel to one another, and be bitter about a dodged bullet in the proposed treatment.  Shame on anyone who has done that on these boards.  I say, shame on you.  I hope you find it in your conscience to ask God and the person you hurt to forgive you.  That is the mark of a mean spirited person, to do that kind of stuff, and we don't need those kind of mean spirits on the boards.  I'm calling you out.  Yes, Christians can do that.  Christians aren't weak and passive - get that out of your head.

    I am three-to-five days out of Cycle 2.  Yes, I have the hot head woozies with a small pinch of nausea.  That's it.  Too dizzy to go many places in public without feeling like I might faint.  Feel very weak, some bone pain, lay in bed most of the time.  Hair band of head (what's left of my hair band) hurts especially in the a.m.  Eating plenty of protein.  Will go buy Ensure at store as soon as I feel up to it.  Ginger ale is better than 7 Up, IMO.  Guess it's time for that Claritin-D, huh?  God is good, and He is able.

    Love in Christ,

    Sessna1

  • Alyad
    Alyad Member Posts: 817
    edited April 2009

    I kinda miss the stubble- I've shaved down to skin twice cause my scalp felt gummy and nasty.I can't say I would reccommend it to anyone else.  I am BALD BALD BALD!!! cold head!

    been running a fever for the last 24 hours or so- low grade- less than 100- didn't go to work- had body ache, had this last round too but this time seems a little worse.  I'm ready for this round to be over! tired of feeling like crap. hopefully tomorrow will feel better- heading to bed.

  • ginagina
    ginagina Member Posts: 327
    edited April 2009

    I know I owe Reeney a celebratory drink. This is from the archives of one of my favorite blogs TheKichn.com for a twist on the traditional martini. Cheers Reeney!

    Dayla - I have shaved down my head as well. I am glad I did because I couldn't handle the fuzz and patchiness that was left when the stubble was falling out. Now it is prickly every day, so when it bugs me, I shave again. But I dont use a wet razor (blade) but an electric razor; it is an upgrade for my hubbo. He will get it when I am all done with this. While some gals do shave with a wet razor, generally it is not recommended (nicks, cuts, infection etc...) but everyone just needs to make the right decision for themself. You know your bods.

    night-night.

  • moborn63
    moborn63 Member Posts: 70
    edited April 2009

    Hi All.

    Had a Double Mastectomy in December. Had to wait to start chemo. Had to get an unknown ulcer under control and get my Hemoglobin count up. It was around 7 which is Highly anemic. (did not know I was anemic until they told me LOL) now counts are up to 10 and ulcer in under control so they allowed me to begin Chemo on March 13. I go every two weeks. I am on the E5103 trial which is a Double blind study phase 3 using Doxorubicin and Cyclophosphamide followed by Paclitaxel with Avastin or Placebo. I follow my treatments 24 hours later with a shot of Nuelasta. I have had 2 treatments so far and my third is scheduled April 9. So far so good. No sickness, only a couple of aches and pains from the Nuelasta those aches usually hit me on day 5 after the shot. After the second chemo treatment my hair started falling out in handfuls. I am currently wearing scarves because I am uncomfortable in the wigs the cancer center gave me. I think I look stupid in the wigs. Have not lost my lashes or my eyebrows as yet. Hopefully I won't.  The Chemo is making me gain weight which I hate. But the good news I got my fake boobs last week. I had been a 44D before BC. So I liked being flat chested LOL. So I had her fit me for an A size. and I am just loving it.

    Thanks for all the info in the forums it is a great help

  • BandanaGirl
    BandanaGirl Member Posts: 11
    edited April 2009

    Hi Michele54...I have so much trouble writing now especially if I don't have your post right in front of me...so if I forgot something or get it wrong..I apologize...I hope all my brain function returns...Now that might be the result of my A/C regimen especially with the anti-nausea drugs...I got kinda freaked out when they showed me all the different meds I would be taking but I never really felt sick..They all did their job! For my A/C regimen I was taking Emend, Zofran, Ativan and a little Dex. The infusion is pretty quick..You'll be out in two hours. My chemo day is Thursday so I pretty much relax all through the weekend.  That's why I've been nervous about switching over to Taxol...I've had my guard up and now they say I can let it down..They say this drug is not as rough..So I'm glad to hear, that especially, nausea wasn't a big problem. I'm nine days post chemo and my feet still ache..I'm scheduled to take 5 dex, 12 hours prior and 5 more, 6 hours prior...and Zofran and Ativan...but I'm nervous to let go of the Emend...Thanks for writing...I think I've needed to join you gals for a long time..

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

    Dear Ladies,

    "Gummy" scalp?  Oh, dear.  I think we still have to wash our scalps at least 1x every two weeks at the most.  I really do like the antibacterial wig cap from headcovers.com , it works very well to aerate your cranium, and it's light.  Massage that scalp like a baby's head, don't neglect it until it itches up.  Don't forget to moisturize your whole body.  It's easy to forget to do "the right thing" in the midst of this journey.  So many ups and downs.

    Love in Christ,

    Sessna1

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