November 2009-Starting Chemo

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  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Coolbreeze - kick you out?  NEVER !  I would think with the Herpecin injections and all you would get a port.  Call the oncologist and ask.  I don't have a port - so far we are hoping my veins hold up for my chemo treatments.  I guess 8 isn't that bad. 

    And yes Brenda you are appreciated ~ Your thoroughness in your posts is heartwarming. 

    Kimmy ~ sorry you had a nearly puke moment.  I had that the other day and sucked on a tums.  Thankfully it worked.  There is nothing I hate more then puking.  UGH !  I too feel like I will be a house when this is all over too.  BUT I will worry about it then.  For now I can just do the best I can.  :(

    This really is a great bunch of girls ~ while I wish I wasn't here...  I am glad it is at least with all of YOU.  We will get through this together.

    ((((HUGS))))

    Alicia

  • Melinda41
    Melinda41 Member Posts: 672
    edited November 2009

    I went to my "Look Good, Feel Better" class today, received a really nice tote full of great make-up. There were three of us in the class and one sister, small group and we had fun. Then I went to the ACS office and picked out a wig, the lady at the class told me they give one wig free. The color is good, the style is different, but it will work. I may take it to a salon and see if they can oomph it up a little bit.

    I don't know if I will wear it, but I am glad to have it. And I will be glad to donate it back when I am done with bald!

    So I meet the new onc tomorrow and see where I will be having chemo. I am trying not to read the post about port anxiety, I can't imagine someone poking me in this fresh wound! Denial is my friend with regards to the port poking.

  • CoolBreeze
    CoolBreeze Member Posts: 4,668
    edited November 2009

    Thanks for letting me stay.  :)

    Brenda, of course, weekends have to be for your DH.   I'm sure he's done so much to help you that devoting your weekend to him seems like a fair trade.  We'll miss you on weekends but family is more important.

    My onc's office just called me - they forgot to get my height.  I asked about the port and they said as long as they can find veins I won't need it.  I can't say I'm disappointed. 

    By the way, they aren't going to give me EMEND either, I'll get compazine and ativan.  I'm fine with that at first but will ask for the other if necessary.

    Melinda, I'm about to call for that class myself!  So many appointments coming up.  The more wigs the better, I say.  If you have to be bald, you might as well have fun with it.  :)

  • livelife
    livelife Member Posts: 38
    edited November 2009

    Just found this group and 'glad' I have. I am in the UK but have found the spirit of your discussion so helpful and similar to how I feel about my treatment- so hope having a member from 'across the pond' is ok.

    Had one dose of taxotere and cyclophosphamide, via a Hickman line on the the 4th Novemeber. Think ports get used more over in the States, but we are not quite there yet in the UK.

    Treatment every 3 weeks for 18 weeks, next one 23rd November. Had mastectomy 8 weeks ago, got an expander in, another mastectomy planned post chemo.

    This is my third treatment for cancer, my breast cancer seems to have resulted from the radiation I had 20 years ago for Hodgkin's lymphoma, had lymphoma 6 years ago too. I know this might sound a bit like I am feeling sorry for myself... I am not, I have felt positive each time. Just thought it would be a good place to start... aware that my on-line chat sounds very British ie. stiff... I am sure I will loosen up as time goes by. I look forward to getting to know you all xx

  • ccnani
    ccnani Member Posts: 46
    edited November 2009

    Good Evening all my Warrior Sisters!!! OMG this group rocks!! We have girls from all over the world with us here, just goes to show u how small the world really is and how all women are one in sisterhood, motherhood etc. Well, I called the nurse onc today but she called when I wasn't home,__ really??? I'm calling again 2marrow and won't stop until she orders my drugs!!! Well girls, I got both of my flu shots, regular and H1N1, I'm ok for the moment and hope I'll be fine 2marrow!! Figured I better not take any chances got 2 many kids running around here after they come home from school.  Welcome to sister Susan62! This group of lady warriors will be your shield in battle and we are sad you have BC, but glad you found this group!  JustmeAlicia, I'm so sad u are feelin so weak and tired. I think the other sisters are saying that once you get to day 10 things pick up really well and thats what I'm affirming for you today!!!  Reglau, glad to hear u slept well and if you feel like sleeping just go back to bed. A friend of mine who is a nurse said your body does the most healing while we sleep!!  Doronet, I'm so glad you have all your meds! I really loved your story about the bracelets reminding you of your kids , thats what touches our hearts and the one about your neighbor was a God thing, one of those aha moments, shes your neighbor and who knew she had been a survivor. Oh, sister Doronet I "learned the truth at 13", I was never pretty enough for that as a youngster, but I have been a cheer leader for all my kids & grandkids since before they were born, but all moms, grandmas and wives or SOs are definitely the worlds most loyal cheerleaders!! Thank you so much for your support!  AroninMia, I second that emotion sister Amazonian!! I definitely feel like no one should have to suffer needlessly when there are meds to alleviate the condition. National health care for all!!! NOW!! Thanks for having my back & I'm on a mission!! Sister what does TAWANDA mean?? is it your name or is it a word for  CHARGE!!  Shel, thanks 4 your encouragement, I'm gonna get my drugs. I'm sorry you are feelin tired 2day and sooo glad your neighbor, with his toy, is helpin you out. I hope 2marrow will be a better day for you..  Coolbreeze, my onc is very "conservative" about meds, ports, and scans, but I'm about to open a can of whip axx on him with a little taste of pissed off NANI Warrior! Neulasta and neupogen are as you said part of chemo, but he doesnt believe in them unless your white count crashes. Emend is the cadillac of anti nausea durgs, ativan is for anxiety and nausea, and there are various and sundry pain pills, vicodin, percosette, darvosette, oxcicodon etc. I believe we all should be getting the best possible medications no matter what our financial or social status, but evidently there are some problems with all that. Coolbreeze there is no way you should leave the group and ALL  the sisters chimed in on that one!! Once a Warrior always a Warrior!  Menevermind," yeah"!!! bon fires with your sweetie, I remember those, I think, thats the best, you go sister! You are no way a bummer just cause you had some bad days, you need to talk about the good, the bad and the ugly here cause this is your place to let it all hang out.  Shel, sorry your feelin weak and were not able to eat, maybe 2marrow you will have more appetite. Try to think of things that would really tempt you, you know those things we try to avoid because of our waistlines, then just go for it. Hot fudge sundaes, banana splits, key lime pie, cozy shack pudding and lemon drops for that ugly taste!!  BrendaSharon ,so happy that you are feeling good!! Day ten hooray!! You have been so busy, this group is getting to be enormous, all a bunch of amazing ladies!! Just think you started this roll. I know it has to be hard for you cause I haven't even had a TX and my brain is already on overload! Thank you for cheering me on about the meds and unfortunately I and others like me, are not equal under our current medical insurance laws. We need universal health care. Your attention to detail has been great and all the Warriors truly appreciate your efforts. Throw alot of love on that husband of yours and enjoy his company whenever you can. Carry on fearless leader!!   Welcome Livelife, from across the pond!! We are a rainbow coalition of women beyond borders!! Bravo sister warrior on being a true survivor!! Boy, if anyone knows what we are going thru or about to go thru it's you!! I think your attitude is amazing and you are more than welcome here with us all. We all look forward to your insight and wisdom on this fight we are undertaking! 

    Well my sisters, a Goodnite to you all, Portergirl, Mommy2two, Ann, Sueinfflu, RedheadPam, Sherri, Jkwick, Cafelovr, phillipa, and the Aussie sisters hoping you are all doing good or will be soon!! Could someone tell this digitally challenged Nani how to grab those cute little happy faces from up there and put them in my text!!! LOL, I'm not kidding!!

  • Sherri_V
    Sherri_V Member Posts: 159
    edited November 2009

    I went to the Look Good, Feel Better meeting in a local town tonight.  I was very anxious about going but a girlfriend met me for the meeting and my husband met me beforehand for an "alone dinner".  The bag of cosmetics was wonderful.  I also got a wig...nicer than the one I bought.  Similar style, one a little wavy, one straight - that makes sense to me.

    I'm going to try to keep busy tomorrow and Wednesday so I don't think about the port thing too much.  Hope I'm over-worrying about that!  But, my dr. did call in an anxiety med for me in case I need it :)

    My FISH report is due tomorrow....1st chemo on Thursday. 

  • BooBee
    BooBee Member Posts: 860
    edited November 2009

    Hi Ladies.  Sorry you all have to be here.  It brings back memories to read your posts.

    I have a video to share with you.  My friend's son needed a project for his media class in college so he taped my head shaving party. 

    If I had it to do over again I would have had my closest peeps with me and not made such a big fiasco out of it. 

    Best wishes to all of you.  Drink lots of water and remember that the anticipation is worse than the actual treatment.

    Although it doesn't seem like it, life does get better.

    Best wishes to all of you.

    http://www.youtube.com/watch?v=zznlRBX4wEg

    Hugs

  • livelife
    livelife Member Posts: 38
    edited November 2009

    Hi Ccani, Thank you so much for your welcoming words. I must definitely be 'loosening up' as I shed a few tears at your kind words.Just showing my Mum this discussion board for November 09 sisters (see I am getting in the lingo now!!!)- we think it is amazing. Catch up with you soon.x

  • MeNeverMind
    MeNeverMind Member Posts: 42
    edited November 2009

    Well good morning all.  It seems that morning is just not a good time for me.  I made a stop on my way into work to pick up some prunes and feel like I am going to die.  I got all hot and sweaty.  I had food with substance with me and it didn't work.  I downed half a bottle of water in hopes of not upchucking.  This is going to be harder to regulate that I thought.  It seems that my tummy is really only truly happy if I have soup in it.  So I will buy a plug in the car travle mug and just keep soup around all the time.  Now that I know that is what works best I can adapt.  Chocolate milk tastes good today, YIPPIE!  I bought some other drinks at the store in hopes of finding something good.  I made lemon aid last night, it was like drinking dirt.  Will not try that anytime soon. 

    My hubbie was so sweet last night.  He made dinner and cleaned up all the mess.  He also let me fall asleep in his lap while rubbing my head.  I love that man oh mine.  He could tell I din't have a great day yesterday and even asked me about it, but what the best part was that he listened, without telling me how to deal with it.  He just listened.  I was amazed.  Even thought this is a crap of a thing to be going through I really think we are learning to deal with each other better.  Silver linning?  You bet. 

    O.K. so now I have soup in my tum I feel better.  But I don't want to start working.  Now off to find a scarf from the earlyer posts.  Shopping is fun.  Hope everyone is going to have a great day.  lets all hope I am the worst today.  LOVE YOU ALL!!  ((((((((((((((((HUGS)))))))))))))) Love Kimmy

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Kimmy... so glad you hubby is taking such good care of you.  Hoping this is your worst day and you make it through it.

    Good morning ((((HUGS)))))  everyone !  I hope everyone has a good day.  Renee S thanks for the video link.  It was very heartwarming to feel such love.

  • Sherri_V
    Sherri_V Member Posts: 159
    edited November 2009

    Something that never occurred to me until last night at the Look Good, Feel Better meeting...

    IF you are planning on shaving your head in advance of losing your hair, leave about 1/2 to 1 inch so that your remaining hair will bend when you put on a wig.  Otherwise, there are lots of "pickies" and the ladies there told me that it is painful.  That alone was worth the trip!  There is a funny part...after that, she said to roll a lint roller over my head a couple of times a day until it all falls out.  If you can't tell, I do NOT want the shock of waking up to a pillow full of hair or the scary shower scene I have pictured in my mind's eye!

    My regular hairdresser is going to cut it down to the 1" mark on the Wednesday before Thanksgiving so I can give my new wig a try-out for the first time at a family gathering, not at work!

    Hope you all have a great day...only 2 days until my first chemo :)

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Sherri ~ I have read the old sticky roller lint brush trick.  I have mine ready for the pillow.  I too am petrified of the hair falling out.  I cut it into a short boycut already and will buzz it when it starts falling out.  I hope I have a good shaped head.  I just picture the ConeHeads on Saturday Night Live from back in the day.  That will be me.  You will be so relieved when you have TX #1 down.  The anticipation is the worst part.  Well it was for me.

    HUGS !!!

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009
    I'm so mad just posted the LONGEST note ever to you gilrs and it dissapeared into Cyber Space. We are in the middle of "IDA" toady. I will start again, just want to let you know I didn't forget y'all. Love "Warrior Sister" Brenda
  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited November 2009

    I'm still waiting for the 17th and actually can't wait. How dumb is that?! I just want to get better because I FEEL FINE. If I hadn't of had that pain under my arm, I wouldn't have went to the breast clinic. Good thing I listened to my body!

    I had a liver biopsy yesterday...hot spot on PET Scan. Keep your fingers crossed!!! Aparently I'm allergic to the adhesive on steri strips. I've got a rash surrounding the incision where my port went. Any ideas of what to do? The incision is fine and no pain. Just itching galore!!!

    Thanks for the advice SLV. I am planning on shaving my hair. It's the only darn thing I can control! Just remember to Fight Like a Girl! Oh me...the cheerleading squad is beginning :) Happiness is knowing that I'm not alone! Thank you for the posts!!

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Melinda ~ How did it go today at the oncologist? 

    Cafelovr ~ I am sending up prayers that your liver biopsy is NEGATIVE !!!!!!  Not sure on the rash by your port, maybe just let it air out?!  I hope it feels better. 

    Hoping today finds everyone feeling GOOD !

    :)

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    Here I go again!!!! LONG POST

    To all:

    "WARRIORS & SAVIORS"

    This is what we are for each other, we are warriors for sure (Whimpy or NOT"),

    Alicia & Kimmy,

    Good Morning to you also!!!! I'm not only feeling bad for you as well all CCnani, but I'm ticked off as well!!! I just don't understand what the hell is wrong with our country sometimes! Insurance should not be the cause of any women not receiving the proper meds she needs. I believe each of you go thru enough without having to suffer anymore than we already do!!!  Tomorrow will be 2 wks. since TX#1. I haven't yet been sick. CoolBreeze and CCnani aren't getting the "Emend" either, and I'm furious. What are you girls on for "Nausea"? CoolBreeze said she is getting compazine!  I had to completely INSIST on Emend before I got mine. They still won't give me "Ativan" though! WHAT are good drugs only for the rich and famous?? if my DH didn't have a job with the State as a FireFighter, I wouldn't have good insurance either and I know I'm a Huge Whimp, and I don't PUKE well either. I would have to want to die as to go thru what you all are!! I am burpy and gassey and that's it. Alicia, tooooooo funny about theconehead thing! I remember those days well!

    Melinda & Sherri,

    So glad you both enjoyed your LGFB class. I at first didn't think I would care about my looks after finding out about my cancer. At first i was sooooooo depressed, I couldn't do anything BUT CRY. I didn't give a crap about much at all. BUT, when I went I seen other women who inspired me. I even cried in the class and they all hugged me. One lady took of her wig and said see it's OK. It's like this site, we have each other to our strength when we need it. Sherri,glad you got your anxiety meds!!! Good for you girl! At least CoolBreeze did get that med as well.

    CoolBreeze,

    No NEED,to thank us!!  We are all so HAPPY you want to stay with us "Warriors" I had heard that the "Compazine" was good, let us all know. I asked Alicia & Kimmy what they where on seeing they both got a little "pukey". Hopefully not compazine. I am glad you got something for the anxiety though. 

    Yes, good for the Ativan, bad about the "Emend" Sorry!!!! Hope you a GREAT day!!!!

    LiveLife,

    Welcome from "Across the Pond"

    This truly makes us "Warriors" from everywhere. We have a couple of "Aussie" girls from downunder and now you from abroad!!! So, very interesting. Sisters all over the world coming together for one cause. BE CAUSE we care for each other. We are each others

     "SAVIORS & WARRIORS"

    I am correct in saying that your treatments are Taxotore & Cyclophosphamide every 3 weeks for 6 treatments.? I will add you to our list of "Warriors" today!!! Welcome abroad/aboard!! Smile, Oh, and youv'e already earned one of these. It will be posted!!!! By the way curious, what is a hickman?  I have a nephew and his wife whom are being sent on "Tour of Duty" to England this January sometime. My nephew is in the Air Force and his wife is so excited to be going to England. This was his choice of tour over anywhere else.

    CCnani,

    Finally, THANK YOU!!!!!!

    You are always so supportive of everyone, and more important so good at finding the helpful information us girls need. You are a ROCK to me. I understand the whole Nani and gramma's thing with the cheerleading, as we do tend to cheer our grandchildren on. I even cheer for my 12 yr. old grandaughter who cheerleads!!  When I can't post to the girls, you are always there to pick up my slack. Thanks so much. We are Saviours to each other.

    We are the "SAVIOUR WARRIORS" Some may be whimpy, some may be strong, some may be well educated, some not, some may be rich, some poor , some live on the West coast, some on the East, some across the pond, some from down under, BUT one thing we have in common, is that we are sisters, and we will help each other in this battle.

     Till the end sisters "Warriors"

    We will fight this battle to the end and we sisters will save each other!!!!

    A great day to all,

    RedHeadPam,Phillipa,JustMeAlicia,Toyah,SueinFlu,doronet,mouse6694,

    MeNeverMind,jwick74,AnnnHoung,Shel,portergirl99,reglau,Melinda41,AroninMia,Sherri,

    Susan62,Cafelovr,CCnani,CoolBreeze, if I forgot anyone forgive me!!!

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    Topic: Waah! I had a meltdown. I don't care who posts!

    You girls all need to go and check out his topic. It's all relative to the fact of the meds not being prescribed as needed to all. It is pretty funny some of the postings.  Just wanted to share!

    (((((HUGS)))))

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    I got all the meds.  Compazine really works when I have breakthrough nausea.  I also had the Emend for days 1-3 after chemo.  I hear it is a lifesaver.  I also got the ativan, although I use it more for anxiety the day of and after chemo.  hmmm I got another med too decadron.  I take that with the Emend.  I SAY GET all the MEDS you can girls.  NO one should have to suffer.  And with my prescription plan the Emend wasn't all that horrible.. well 34 bucks for 3 pills.  If it stops me from puking ~ PRICELESS..  Now I could use some vicodens for the backache and headache I have..  HMMM I'll be asking next week !!!!!!!!!!!

    Brenda ?  huh are you having a meltdown or is that topic in the forum I need to go look at ?  I'll check ! 

    Good day girls ~

    :)

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    JustMeAlicia,

    Hey Sweetie, No, I am not having a meltdown, I had that long ago. BUT, you got to check out the TOPIC. It is on this site of course and it is all about this lady not getting the MEDS she needs. Some funny stuff, yet NOT, if you catch the drift. It is such crap. Even some of our girls not getting what they need. Heck I know that Ccnani is as old as I and without the "Emend" I know I'd be violently ill. I don't think any of us should stand for it. I agree with insurance not too bad. Mine was $40.00 for the 3 pills. I asked how much they would be without insurance and they told me $400.00 for 3 pills. That in itself is BULL.  So not right!!! So, what they are telling us if your a poor sister, then tuff s@@t right, only if you have money or insurance your allowed to feel good.!!!

    I believe enough protesting will put an end to this crap for the "Warrior Women" of this world!! 

    Cafelovr

    We are all so glad to hear from you, we where worried. With reason to be I see.  I had an itch from my first surgery, I had a reaction to the povidine scrub because it has sulfur in it, which I'm allergic to. Then at the "Port" site I itched, they told me it was from healing. Anyways, they told me to put some Benadryl on the area to relieve the itch. But, be careful not to get too close to the area of the open wound.  SORRY, for your other problems with the liver and I hope all turns out OK with let. Keep us informed. WE will be cheering you on as well!!!!! Hey, I took control of my hair too, I cut it the morning of my first chemo, I said I would take my own hair before the cancer did. It gave me the power to use it for what I wished for, rather than watch it come out little by little from the bitc#%#g cancer. I sent it off to make my own hip-hat with!!!

    The whole time my hairdresser (Sweet, she came to my house) was cutting it I kept saying,

    (Ha-Ha, I got it before -C- , it's mine, it's mine, Ha-Ha,it belongs to me, not to the -C-)  

    Doronet,

    I was worried, but then I found you and seen you are OK.

    I had a really bad blonde minute

    (don't even have hair)

    Shel,

    Sorry the tummy is on fire. Do you have ulcers or acid reflex? Try a tums and see if that helps. I'm on previcid all the time so I haven't had any issues with burning in the stomach.

  • Shel
    Shel Member Posts: 41
    edited November 2009

    Dear fellow whimps and warriors, I wanted to wait and post until I could say I felt pretty good today.  Comparatively, I do feel better, but I had hoped for more.  If you are like me and having all kinds of stomach issues (like mine feels like it's on fire all the time), someone here at work has suggested papaya powder.  I am going to try it and will let you know.

    Thanks to Sherri on the advice about the hair.  I am thinking of getting it cut short (1 inch) this weekend and then just go with the roller from there.  Somehow I am really not into the clippers deal.  Also it was good to hear about the Look Good Feel Better program.  There is one here in my town, so maybe I will check it out.

    Hope everyone it having a good day and feeling stronger by the minute.

    Shelley

  • MeNeverMind
    MeNeverMind Member Posts: 42
    edited November 2009

    I am having a belly full of acid today.  And my mouth is RAW!!!.  YUCK YUCK YUCK.  So now I am off to get blood work done.  What a great day.  Hope everyone is doing good.

    ((((((((((((((((((((((((HUGS)))))))))))))))))))))))))))))Love Kimmy

  • doronet
    doronet Member Posts: 342
    edited November 2009

    Hey hey,  Thanks for womdering where I was, BrendaShar...I posted a couple of times on Saturday and Sunday, but not yesterday or til now today.  Sunday (day 6) was definitely my "break-through" day...uhhhh, for the ol' digestive tract.  And I actally almost felt like my ol' self.

    Sunday, I ended the day with a major breakdown about having the Neupogen injection that night from my hubby.  I get so upset about them, that I can't even look at the sringes in the fridge (we've hidden them), I can't look at the container we put the used seringes in (I put it out of sight), and I can't even look at the EMLA cream during the day.  I am so pathetic.  Afterward the injection, I cried thinking I still had 4 more in this round, and 28 left in all.  My hubby came in and said, "You're halfway there for this time!"  Ya gotta love him.

    So yesterday, I got on the internet and researched "Fear of needles," though I knew all the suggestions I saw and tried all of them.  Hubby suggested that I should start taking an Ativan when I put the EMLA cream on (Yes, I even use it for these injections so I don't even feel them.  It's mainly just the anticipation that gives me the anxiety.)  So that night, between the Ativan, digging my nails into my palm, listening to really loud music on my iPodShuffle, and deep breathing, I did it.  Still wasn't easy, but it was better.

    Monday, I felt like my regular ol' self.  Finally.  Had a dentist appt. though, for a broken filling and had to call my hubby to take me.   Was so anxious about going out of the house and driving my self, I was nauseous and was afraid I'd throw up on the dentist.  I called him in tears to see if he could take me,  I was ashamed I couldn't do it on my own, then I took an Ativan to calm my nerves.  He has been everywhere with me through this and reminded me, "I'll take you anywhere, anytime you need me to."  

    Today, had a TX follow-up with the onc to see how I was doing post-TX and to check the white cell count to see if the injections were helping.  They have, as the count was almost normal.  And she said taking the Ativan was fine...that the need for having the injections far outweighed any disadvantage to taking the Ativan.  I honestly don't know what I would have done if my breast surgeon hadn't given me the Ativan from the beginning of my diagnosis so  I could see it works for any dr. office visit.  ( FYI:  anyone taking Ativan pre-TX, do make sure you tell the chem-nurse you took one, as mine adjusted the nausea med. dose during my TX because I had taken an Ativan that morning.)

    Readng back over this and knowing the bigger problems other people are having, I feel like such a baby. Oh well.

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Brenda ~ so nice your hairdresser came to your house.  Mine did the same, it really was nice to have it done in the privacy of my home.  I told hubby I think we should buzz it off this weekend, before Chemo Monday.  He said NO.  He seems afraid of the whole bald thing.  Heck I'm not thrilled either but I don't want to wake up to clumps coming out.  :(

    Kimmy ~ I was using the Biotene for the mouth then I switched to warm salt water I think that works better.  I had a sore last week and the salt water worked wonders.  Make sure you are drinking enough. Kimmy/Shel ~ I use Mylanta for the acid belly and tums too ~ they make new smoothie ones that aren't so chalky.

    (((((HUGS Fellow WARRIORS))))))

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited November 2009

    Got to go home now girls~~~

    Love you all

    Till tomorrow, hope the acid tummys get better

    (((((GENTLE HUGS))))) to all "Whimp and Warriors"

  • Melinda41
    Melinda41 Member Posts: 672
    edited November 2009

    No mets! Just a glowing lymph node that showed up on the PET scan.

    So my first chemo will be 11/16 (they are trying to get me into a study and my glowing lymph node needs approval). I will be AC x 4 every two weeks, with the neulesta shot. I have heard bad things about the neulesta, will keep my fingers crossed.

    Going out to celebrate my cleanish scan!

  • Sherri_V
    Sherri_V Member Posts: 159
    edited November 2009

    Melinda - you go girl Kiss

    I'm so glad to hear a positive (in a good way, of course) test result. 

  • livelife
    livelife Member Posts: 38
    edited November 2009

    I think I am going to be having some very late nights now that I have found this group of warriors. Everyone is in bed, including the puppy - so a good time for me to catch up with you all. It was good to read your postings this morning but somehow writing back seems better at night when the house is quiet. I love your inclusive poem BrendaSharon, thank you. Melinda41 great news about your scan, I had practiced receiving a bad news result so many times that I am still getting used to the good news that I have no spread beyond lymph. Reading about trying to get hold of the best medication sounds similar and different to care over here in the UK. We have a National Health System which means that part of our tax goes to our health care, private health cover is very much the exception/luxury item over here. So instead we all get the same, the cheapest !!!!!!! I am fortunate in that I am being treated at one of the two leading cancer hospitals in the UK, yet even here only 6 people have had their chemo via a port- via a venflon is the norm.

    As a result our survival rates on cancer as a result are much lower than in the USA- not that I intend to let cheap medication lower my personal chance of survival- a warrior spirit and God in the battle will make up for cheap medication.

    I was wondering if any of you are using any special dietary approaches- I have skim read a book by Jane Plant who advocates dairy free and use of soya. I have read around on the science which seems to be inconclusive- so have decided to give it a shot- dairy free meaning that I have to get my food kicks from health alternatives rather than a quick fix with chocolate or cake. I am having a bit of soya but not gallons of the stuff. I feel really healthy on this plan. She advocates not eating meat in the active phase of cancer- but I am having a little.

    In terms of medication I haven't even heard of enmed, sounds good though. I am on ondasetron/zofran- which seems to do the trick. I am on those immune boosting injections too doronet and know what you mean about seeing them in the fridge. I give myself my injections- in my fatty tummy roll- it's not so bad there- I kind of pinch it up and slowly put the needle in. I do it at bed time then sleep off the side effects. In the UK we have District Nurses who come and visit you at home to do these- but I would rather do it myself. They are coming tomorrow to flush my hickman line- cheap version of a port, it is a central line with about 6 inches of tune sticking out from my chest. I am at a fancy do on Friday evening- hope it doesn't waggle out !! I am trying to get some tape to make my boobs look even, need to drag my old saggy one off to the left so that it matches my rock hard right new boob. oh well if I am odd at least I will be unique.

    Good night my new friends xx

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited November 2009

    Good news Melinda ~ my first Neulasta shot wasn't too bad with the SE's.  I will hope the same for you.  It is the headaches that are killing me the most !!!

    Natalie ~ Good luck matching up "the girls" for your Friday Fancy ~ I am sure you will do just fine. 

    Have a good evening everyone ~

    ((((HUGS))))

  • mommy2two
    mommy2two Member Posts: 130
    edited November 2009

    Hi Warriors!

    Melinda41 - GREAT news!  So happy for you.

    Brenda - How do you ever keep everything straight on here?  I have to spend 30 minutes re-reading posts every time to make sure I know what I'm talking about :-)

    Anyone that is having tummy problems as in acid, burning, pain....I was developing an ulcer from all the meds (I have a history of them)....started taking my Prevacid and it stopped and I feel great now.  Your doctor will prescribe some of that or another type of med if you ask them.

    I hope everyone has a nice restful evening!

    ((((HUGS))))

    Toyah

  • CoolBreeze
    CoolBreeze Member Posts: 4,668
    edited November 2009

    Lifelive, Soy is bad for you!  (Soya is Soy, right?)  You have ER+ cancer and there is estrogen in soy.  It will make your cancer grow, so don't eat it!

    If Soya is something else, carry on.

    I'm sorry you don't have the kind of healthcare there that you feel is quality.  We are told here that you have the best healthcare in the world, but that's a political statement I don't want to go into.  I'm surprised to hear your cancer survival statistics are lower than ours though.

    I made an appointment today with the Look Good, Feel Better folks.  I'll have my session on November 16th.   It will be good to do something that isn't a doctor's appointment!  :)

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