Jan 2008--Ain't it Great?

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  • SISKimberly
    SISKimberly Member Posts: 762
    edited December 2007

    Good Morning Jewels,

    Again, I am amazed at all that's been posted since yesterday...



    KathyL and SheShe48-Shocking that a pediatrics office-an office that deals with medicine- can be so discompassionate to one of its own nurses. SheShe48-same to you...a BC Survivor fired you? I don't think that's even legal...firing someone on the spot for disclosing they were diagnosed with cancer. (Not that I'm advocating filing a wrongful termination suit- who would want to work for someone like that anyway). I feel for you both on the tightening finances.



    I am sooooo lucky to work in my school district. We have a Catestrophic Leave bank that we donate to each year. I applied to be granted enough leave to get me through the end of the school year. I am awarded 20 days at a time, and have been told there is enough to get me to the end of the year plus plenty of days for others in our district who may need it. Once that is done, if I need more time, my disability insurance will kick in at 75% of my pay.



    Kathy, I hear you about all the germs and being on your feet all day long. As a teacher, I'm in the same boat. Parents send their sick ones to school all the time, and I often don't get to sit all day long- except during my 36 minute lunch, if I take lunch as I often give up lunch to assist kids who need help- having 5 periods and over 130+ students in and out of the classroom. I had to take the rest of the year off...and it killed me...I miss my kids so much...but I had to put my well-being first.



    D1-Not only is FUBC totally appropriate....but FUSE (F..U...Side..Effects) too!!!! You crack me up...even when you're feeling like the Vikings snapped you the ball and let the other team trample all over you.

    I often say to the TV...like it can hear me...when pharmaceutical companies advertise their wares..."How can you put on that smile and do whatever it is you're doing with all those SE's?" Notice the SE's are stated quickly in the background like we won't notice. Who can function at all, let alone have sex, with a four hour erection, loss of hearing, and eyesight? And those SE's for the CMF chemotini sound dreadful...of course, not everyone experiences these SE's...and they have to be disclosed...but that's scary shit...oops, sorry...it just slipped out....must be an SE of BC.



    Vettegal-I hear you on being impatient...and agree with all the advice/support already given. I had nodes removed on the left side at the same time as my bilat, and healing is slow, but it does get better little by little and day by day. Hang in there...oh, you can't do that yet (neither can I now that I mentioned it)...ummm...Stiff upper lip dahling...you've got the right stuff!!! Love the T-Shirt idea.

    My DH was in landscaping for over 15 years before he blew his back out. After three surgeries ending in fusion, he had to give it up. He's now an energy analyst at a consulting firm working to get alternative energy plants built-solar, wind, biofuel, geothermal, and hydrogen.



    Carol- A Tugboater and a Truckdriver? That's great!!!! My father is working with a group to restore an old WWII tugboat from Pearl Harbor. He was in Hawaii when it was bombed-he was 5- and his father was a civil engineer hired by the govt to do things like work on the Panama Canal and stuff. Anyway, my dad feels his father may have been on this tug as he toured the damage and worked on a plan to clear away all the wreckage and repair docks and the like. My mother, who passed away at 58 of Pancreatic Cancer, was a wonderfully funny lady. She often stated that when she retired she wanted to be a poet truckdriver. Hee Hee. Sorry to hear your mom passed of melonoma. Anyway, I'm with you on making 2008 the year I show the world what this gal is made of...let's kick butt this year!!!!!



    Sharon-Thanks for the info on Neupogen and Nuelasta. I know I'm supposed to get a shot of something the next day after chemo...but can't recall the name of it. Still haven't heard from my oncologists office...I'm thinking they took today off and will do the same tomorrow.



    Welcome Julie K and Chris. You've found a great group here.



    Julie, I am 99% positive that I'll be getting a hysterectomy and have my ovaries removed, which is apparently not included in a hysterectomy (uterus only, I believe) in order to reduce my likelihood of ovarian cancer. My dad had breast cancer and prostate cancer(still living), and my mother pancreatic cancer (passed at 58), and all of those cancers are tied to the BRCA2 gene...so Dad's taken the BRCA test as of last week-my insurance won't cover it because we don't have enough cancer in the family line...go figure- If he's positive, then insurance has to cover my test....but more importantly, my twin will have no problems getting her test approved. I already did a bilateral mastectomy-which is one choice my oncologist would have strongly suggested had the test results been in hand prior to surgery...and I'm glad I did have a bilat...the right breast did have precancerous cells roaming around. Now, the test will determine if I have all my female plumbing removed, since my cancer is ERPR+.

    Sounds like your family history is full of this dreaded disease,too. I'm sorry your family has had to go down this road. Has your sister regretted her decision to remove her breasts and female plumbing? My twin is a bit unnerved by this whole thing...to be expected.



    I think I've gotten everyone...if not...know I'm thinking about you and wishing you nothing but dreamfilled nights, energy filled days, and clear headed minds :-)



    By the way, Charlie Wilson's War, was FABULOUS!!!! It's amazing what this man did...and how we find ourselves in the same position again...doing the same thing we've always done only this time without a man like Charlie on the team. When will our gov't learn from its mistakes?



    I read the Kite Runner, YuYuBear, and hear the movie is really good...but I loved the book so much and don't want to spoil what I imagined in my head...and heard the movie gives too much away too soon. I'll have to wait and see if I can bring myself to go see it. I'm a little weird when it comes to my characters in what I read...I literally have to grieve the end of a book...I can't pick up another for a day or two...OK,that's a lot weird.



    Happy New Year Jewels...tonight at the stroke of midnight, I'll be toasting us all!!!!



    Love, your SIS (Sister In Survival)

    Kimberly

  • golfer779
    golfer779 Member Posts: 1,378
    edited December 2007

    Kimberly, I was ticked to read that your insurance won't pay for the BRCA test.  How many more mom's and dad's with cancer did they expect you to have to promote getting the test?!   Thank goodness your dad is able to have it done first.  It took just short of a month to get my results, hoping that yours can help in some of your decision making.   Enjoyed your stories of your folks, I actually can't believe I'm a truck driver, was a secretary (work civil service for the gov), they had a entry position back in 1987, low and behold I got the job.  I work with some great men!  Any calls yet from the onc?

    Vettegal, hoping your on the phone this morning with some great news, I'm sending "negative" or is that "positive" vibes your way.

  • vettegal
    vettegal Member Posts: 287
    edited December 2007

    Hello Jewels,

        I called about my path results and the dr office called back, and they don't have them yet....CryI know its a holiday time but it is going on 10 days. I mentioned a to them a girl i knew from another state had the surgery the same day and she had hers back on friday! All they could say, another state. Anyway now that i totally going to freak out...I am so impatiant, She did say there was alot of us waiting for path results from the same dr.I wanted to get the 2008 off with good news so i can start my treatment and look forward to fight this FUBC(thanks d1)ok, sorry for the venting!

    thanks for the underarm tips, my scar too is lower but the pit has like a hole and then swelling. my breast really hurts today and my shoulder. i couldn't even wear my sportsbra it felt weird. so i am goling w/o bra today and wearing my cancer sucks t-shirt, my dh doesn't seem to mind the breast hanging a bit in the t-shirt (lol)

    i am so addicted to this board!!! Hugs to all!

  • KathyL
    KathyL Member Posts: 534
    edited December 2007

    OK, the little beasts are fed and I have some peace now! 

    Julie:  Welcome to our group!  It is great and most of us are addicted to hanging out here already.  I think we're all going to pull through this chemo thing well as a group.

    Vettegal: Great idea about the t-shirts!    And hoping each day of recovery after your sugery is a step forward for you and you feel better.

    Golfer: I also don't think the neulasta/neupogen is always a given.  My onc. told me he uses it for the DD (dose dense) regimens-- those given every 2 weeks.  For those doing every 3 weeks (like me), he doesn't do it unless your counts drop too low.  I'm hoping mine doesn't, but not a thing I can do about it anyway.  I agree with Sharon, I'd probably do the neupogen (5 days of shots) if I had a choice.  My friend is doing the neulasta and says it hurts (some of the others here said the same I think)!

    Sheshe:  Can't believe you were fired by a BC survivor!  That truly sucks (can we say that here???). 

    YuYu: Maybe what you're feeling from the expander is that your swelling has gone down and you're more aware of the expander edges.  I remember this happening for me and I was freaked that it was moving too.  My PS says they really can't do that, they are placed in a pocket the PS forms for them.  Glad to hear you're doing well anyway!  Wait 'til the next step-- getting rid of the expander.  It's heaven Smile  And the time goes by faster than you think.

    D1:  Yes, I'm doing T/C for 4 rounds.  But I got the port because I'm also doing a year of herceptin (IV only).  I hate needles and couldn't stand the thought of getting an IV every 3 weeks for a year.  That's why I'm getting the port.  Good news is my PS will take it out in the end, so less scarring!

    Kimberly:  I shoulda been a teacher.  You have great benefits.  My whole family is in education.  I'm the only one in healthcare right now.  My brother was a teacher but he's in Atlanta now doing PA school.  Just curious why you have to do breast, ovaries, and uterus?  I have a friend who is BRCA 1 AND 2 positive.  Her docs recommended b/l mast. and only ovary removal.  She's premenopausal.  I'm also so surprised you can't get the gene testing.  I have only one cousin besides me in our family that has had BC (she too is young-- in her thirties like me).  I saw a genetic counselor who said I was a definite candidate for the gene testing.  I had it done and my insurance (BCBS) covered it all.  I am negative for both.  Maybe you should push someone about your testing, or see a geentic counselor?

    If I'm not back later...  Happy New Year Jewels!  We're gonna kick some BCA in 2008!!

  • deb102307
    deb102307 Member Posts: 248
    edited December 2007

    Have to definitely agree with D1....hard to keep up with everyone.  I am so thankful that the ones that have already started are taking the time to keep us that are not so patiently waiting, up to date on how you are feeling.  You are right, the waiting is the hard part.  I don't start until the 8th and am getting downright impatient to begin.  Don't get me wrong, I am still apprehensive about the se's and how work will go but the sooner I start, the sooner it is over.  I am willing to put up with whatever I have to to get through this.

    One good thing for me I guess is that I don't have to worry about the hair loss.  I lost my hair about 3 years ago due to some weird, rare, autoimmune disorder so I am used to the wigs, doo-ags, etc.  Just have to wait and see what happens with the eyebrows and eyelashes.  I didn't lose those then so maybe they will be stubborn now too.Wink.  Who knows, maybe this will make my hair grow back!  Wouldn't that be a hoot?!?!

    To those recovering from surgery....it does get better each day.

    Lastly, I guess I'm a real doofus...it took me forever to figure out FUBC but I did like FUSE and will keep it handy in case the se's get me some days.

    Happy New Year Jewels.  "When one door closes, another one opens" and this coming year is OUR year!!  2008 is going to be GREAT!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited December 2007

    Still here and kickin'.

    The SEs were pounding me a bit the past couple of days. Thursday (treatment day) was ok, as was Friday, though I got pretty tired in the evening. Got the Neulasta shot Friday. Saturday I felt pretty icky and didn't do too much. Just vaguely nauseated and not wanting any food or drink. Even water was starting to taste chemical-ly. Sunday wasn't much better ... had to break down and pop some Senekott because of the Emend constipation. No way to wait it out. Did so again last night, and things are moving along better now.

    Today I feel better than yesterday, but not back to normal. My partner has been dying to have morning coffee, and I gave the all-clear for her to go ahead and make it this morning, thinking I would surely be feeling better, but as soon as the smell hit me, I almost went to my knees. Crazy how these things bother you. 

    The Neulasta bone thing has not hit me. (Though the shot itself was majorly irritating.) I have felt very uncomfortable since the shot, but I can't pinpoint if it's AC SEs or Neulasta. I just feel like I can't be still, fidgety, no position I sit in is comfortable, like I have acute ADHD or something (not my normal mode, I'm typically quite calm).

    I'm glad I'm off work for today and tomorrow, to get an idea of how this is going to go for the next 3 treatments. I had scheduled Thurs as chemo day, and Fri. as work-at-home ... maybe I'll work Friday instead and take Monday and Tues if needed as work-at-home. I wonder if every treatment will follow the same timetable of SEs?

    Still, let me grab a moment once again to thank those who came before us who tested and trialled drugs so we can get through our treatments more comfortably.

    Doesn't seem like my tumors have shrunk much ... is one treatment too hopeful to see a change? 

  • Determined1
    Determined1 Member Posts: 806
    edited December 2007

    Julie--warm welcomes to our club.  Your story made me so sad, I truly hope all the best for your as you continue your journey with us.  Whenever you need a shoulder, or a cheering squad, we're here for you.

    How ya doin' today, yuyu?  That da*n neulasta shot is a real kick in the pants, isn't it?

    Carol--get your butt in gear and exercise!  From previous postings, it sounds like you're as addicted to exercise as I am, so do it for your head!  I did an incredibly wimpy walk today (took me 35 minutes to do a mile + half), but by God, I did it.  My head is happy as a result.  I'm hoping for more tomorrow, and maybe even back to my beloved rec center to work out with the seniors on Weds.  (They make me feel like such a hotty, hot, hot!)

    May I say how indignant I am over the work situations for KathyL and Sheshe?  Remind me, in what century do we live????  That's just barbaric treatment.  I'm so sorry for both of you and hope that the financial hardships won't derail your full recovery in any way--not even for a minute.

    I'm hoping to see Charlie Wilson's War tomorrow.  Keeping fingers crossed that the chemo se's don't kick in, particularly now that I seem to have passed the worst of the nasty-lasta shot (do I really have to get 3 more of those????  No, no, let me rephrase--one down 3 to go--FUSE!!!)  And I'm with Kimberly--LOVED The Kite Runner as a novel and am a little shaky on seeing the movie.  It DID get good reviews, but I may wait for DVD as I'm sure I'm the only one in my house that would be interested in it.  The dh and 16year old watched the Marriage of Larry and Chuck, or whatever that Adam Sandler movie is, last night and har-harred their way through it.  I think everyone was ready for some simple slapstick and prepubescent humor.  Me?  I was in here trying to burb from my overeating...  Life's good. :)

    Vettegal--I saw someone talking about raising their arm to shave and it reminded me that I put my arm on the shower wall as high as I could to shave (actually, I'm still kinda doing that).  The wall helped to hold my arm up while I tried to get at whatever I could under there.  Try to remember it will pass soon.  You will get by, you will get by...

    So my dh is telling me that I smell like a dry cleaners now.  Guess that's better than a sewer...

    Today is better.  Just using max strength tylenol to stay ahead of the neulasta aches and am eating tiny amounts (piece of toast, then a banana, then 1/2 a sandwich, then slice of pizza, etc. almost every hour and a half without fail!) to stay ahead of nausea.  My tongue is thick and has some sores on it, but I'm trying to ignore them.  I'm swishing with the Biotene mouthwash after every food outing.  Think I'll go upstairs and shower and see if I can do my own hair.  I'm thinking I'll only have this cut for 10-12 days, bout the time I figure out how to do it, it'll be gone!

    FUSE!

    D1

  • Determined1
    Determined1 Member Posts: 806
    edited December 2007

    Hey LJ13--you musta been posting while I was in composition mode.  Good to hear from you.  Good of you to mention the chemically taste to water--I'm having trouble with it, too.  Coffee's still okay for me, but I don't seem to want/need as much.  I'm thinking I might try those flavored waters...

    Reading your plan of attack for work reminds me of my sister's chemo experience.  When I stayed with her, she was on tx#3.  Her MO was exactly the same as you (and I) have discovered--treatment day and the day after are okay--it's a couple of days out that you're hammered.  I'll bet you COULD work on Friday in exchange for Mon/Tues.  My treatment day changes to Wednesdays with my next one, but neulasta day will still be on Friday (meaning that following Sunday will pretty much suck).  (And how have you NOT had all the bone achiness???  That nearly KILLED me!)  I hope you continue not to have trouble with it--we all have enough crosses to bear, here.

    Oh, and you're not ADHD--I'm pacing about myself and I used to be very content to fold my legs under myself and read or watch tv in the evenings.  I'm justifying it by thinking the activity will move things through more quickly--you know, the mind works in mysterious ways!

    Keep smiling!

    D1

  • SISKimberly
    SISKimberly Member Posts: 762
    edited December 2007

    Afternoon Jewels,



    Carol-No call from the Oncologist's office. They must have taken the day off. So, I'll hear from them on the 2nd.



    Yeah, the whole BRCA thing was just so ludicrous...all my doctors were just amazed at my insurances' denial. The reason my Dad got tested so easily is because he's a man with breast cancer...he didn't need to have a family history... and Medicare paid for it. So, thankfully those results will be here by the end of the month.



    I think driving a truck sounds way more interesting and entertaining than sitting at a desk as a secretary for some govt' agency. Do you ever get to go out on the tug boat?



    Vettegal-I'm so sorry you haven't gotten your path results yet. It is frustrating isn't it? It might be different if it weren't the holiday season....and all the people waiting for the same doc to get their results...he's probably on a much needed vacation. In the mean time, enjoy the New Year knowing we are all hoping for Negative Nodes.



    Kathy-To answer your question about why take everything. I too am premenopausal, but apparently, with ovaries out to knock out any potential creation of estrogen, the meds I'd take after chemo and rads would be for post menopausal women, and it has the slight potential of encouraging uterin cancer, so I thought why keep any of it if I no longer need it? Wow, a family of teachers. You went into a service position, too, and one like teachers that isn't often recognized as a 'real' profession. So, I will raise a glass to nurses and teachers tonight...BRAVO!!!!



    Arkansas Deb- I don't recall seeing you here before...I could be wrong...but welcome. We have a teacher at school who lost her hair to a weird autoimmune thing, too. Wouldn't that be a hoot if chemo had the opposite effect on you since you've already lost your hair...kind of like stimulants given to ADHD kids have the opposite affect-calms them down...but speeds others up.



    Speaking of which, D1 and LJ13, I'm sorry that you're just buzzing and fidgety...I heard the steroids can have that affect.



    Glad things are moving along, in more ways than one LJ13. God I hope the smell of coffee doesn't double me over...I love coffee.



    I wrote a poem earlier today and wanted to share my New Years Wish with you all.



    After much rain, the sun is shining

    on this final day of twenty-07,

    and I think of the many dear ones

    watching over us from heaven.



    Massive pearly gates and golden-winged angels

    isn’t exactly what I imagine this place,

    but rather where souls give dissertations,

    accounting for their time in this Earthbound space.



    I imagine much hearty laughter

    as they recognize their many mistakes,

    and the futile agonizing they’d done

    causing their hearts to physically ache.



    I try to listen for my loved ones messages,

    but sometimes the mundane gets in the way

    screaming over their persistent whispers,

    making it difficult to hear all they have to say.



    The message that always comes through though,

    no matter how loud the man-made clatter,

    is the truth that we are all of one human race,

    and acting with love is all that matters.



    It matters not what religion we hold dear,

    nor what political party we call our own,

    for we can all agree we bleed the same,

    and will reap what we each have sown.



    So as I go into this newest of years,

    that message kept near to my heart.

    I will aspire to treat all with love,

    knowing of this universe, we are all a part.



    HAPPY NEW YEAR!!!!

    LET US ALL ASPIRE TO MAKE

    2008 MORE THAN GREAT!!!!



    SIS Kimberly

  • golfer779
    golfer779 Member Posts: 1,378
    edited January 2008

    To the Lady Jewels, I don't know what button I push on this darn laptop put this was the third time that I have typed a comment and I hit something and poof...it dissappears.  UUURRRRR!!!

    I'm hoping everybody reads Kimberly's poem, its awesome and will bring a tear to your eye.  I hope that you post it on a couple different threads to share.

    Kimberly, been on a tug a couple of times, my dh has been working in the office for the last couple years, thank god, when he was on the boat he would be gone for 15 days at a time.  I'd have a much tougher time getting through this without him.

    Vettegal, hoping when I got home you may have gotten some results later in your day.  Hang in there.

    Got my second op today from the Seattle Cancer Care.  She also suggest CMF for txt.  I let her talk for quite some time before I mentioned my previous appt at the onc closer to home.   Looks like I'll be signing up for the regimen, with radiation after that and hormone therapy for years.  The CMF sounds tolerable, only it takes 6 mo., the price to pay for keeping some of my hair I guess.  She said that a shot for white cell should not be needed.  I'll get some more scoops from the NP on Wed at the onc office.  I figure they hear probably more than the docs when it comes to patients yakking it up.

    I'm going to submit before I loose this post again!!!

  • sheshe48
    sheshe48 Member Posts: 338
    edited January 2008

    Hi Sisters,

    I hope this last day of 2007 finds everyone feeling better.

    Kimberly I loved your poam it was beautiful and touching. Sorry to hear your dad also has breast cancer. Is he in early stages? Oh my daughter is a elementary and middle school teacher.

    D1 sorry about the mouth sores, I'm afraid that is going to happen to me too.

    Vettagal waiting on the pathology reports is the worst part of bc hang in there.

    Lj13 My surgeon already warned me I won't be able to drink coffee during treatment. I had a chemo treatment before my first bc surgery and I have not been able to enjoy coffee since. Once in awhile I can handle it. I have been drinking green tea and honey and lemon tea and honey and all the herb teas. It settles much better on your stomach. Hot tea seems to make me feel like i'm still having my coffee.

    KathyL yes, we can say it sucks, life is not fair. I know we will both be ok and we will get on our feet again. I hope everyone has the best New Years Eve and Day, I hope the Se's don't get the best of everyone tomorrow. Cool

  • golfer779
    golfer779 Member Posts: 1,378
    edited January 2008

    Jewels - noticed the time and 2007 coming to a close, just wanted to raise a "small" glass of red to all you ladies that have been there, are here now, and will need us in the future!   We are now survivors and always will be, hoping 2008 brings a little less drama, and better times!!!!!

    Celebrating NYEve with the dh and a rack of ribs and hitting the hay by about 9:00, will watch the new year ring in on tv!!!! 

    Here's to healthier and happier times ahead...

    Carol

  • IowaCindy
    IowaCindy Member Posts: 341
    edited January 2008

    Hi, gang!

    Just wanted to stop in as 2008 begins to offer my assurances to the words of my other BC sisters. 

    You will cry. You'll be weak. You'll be weird - honestly, the chemo-brain thing happens. You'll miss your hair. Your nose will run. You will nap a lot. People will be either wonderfully supportive or astoundingly dense. Mostly they're wonderful.

    You'll hold your bald head high - covered or not. You'll find humor in the strangest things. If you haven't before - you'll start speaking out on your own behalf to medical personnel. You will find blessings in the strangest places. Your loved ones will struggle to be your absolute helpmates. Let them. Give them specific chores they can do for you - it will help them feel a part of the action, a part of your care and cure.

    Kids, it's the hardest, most remarkable journey of your life. So buckle up, choose some good traveling companions and make sure your map is current! :)

    The destination is worth the stress of the journey. It's definitely the absolute goal - LIFE!!! But that journey will include remarkable side trips that reveal unexpected treasures.

    I'd recommend that you journal or even start a blog. The blog is a great way to let family and friends know how you're doing (whatever you want to generically or specifically share) without being overwhelmed by phone calls or visits.  

    In a year, when you look back....when you rub your hand over your new, different colored hair.....when you're adjusting to a full return to life's activities..... when you're looking in the mirror at the new landmarks on your body......your journal or blog will be a testamony to the fight for your life.

    Gather round your fellow travelers. They will encourage, laugh with, cry with and hold you close.

    Blessings, sisters!

    Cindy from the Jan '07 chemo group 

  • vettegal
    vettegal Member Posts: 287
    edited January 2008

    HAPPY NEW YEAR JEWELS!!

        good morning, wanted to wish all of our new friends a wonderful and healthy New Year to you and your family. You are all probably still sleeping some with a mild hangover (lol)CoolSome like me made it a quiet evening at home with the hubby, A nice dinner a dvd to watch and hit the bed early, then my phone starting ringing at 11:45 from my brother to wish me a happy new year...we watched the ball come down at times square kissed my hubby and he was crying..he is so emotional!!! I told him i would be fine and to be strong I will need him in the upcoming months for support, and all he could say is he wish he could stop my pain. He is wonderful..

             I hope you all spend time with the family, friends, kids, relatives, pets (i love my oscar) when people like me don't have kids my furry son is a great kid!!LOL Enjoy the food, For all of you that started your treatments...keep eating like they said , take the meds and keep your chin upLaughing..the boards have brought us all together and that is helping each and every one of us to get thru this new year!!

               Hugs to all.......xxoo

  • deb102307
    deb102307 Member Posts: 248
    edited January 2008

    Happy New Year to all the Jewels!

    Thanks Cindy for the nice welcome of the new year for us. You said everything so well and I like the idea about a blog.  I started a page at Carepages.org at the Y-me website and maybe I will use that so that friends and family can know what is going on without having to always do it individually.  You sound so positive and knowing you have been there really lifts me up.  I haven't started yet and am tired of waiting yet apprehensive.  You definitely made me feel better.

    Vettegal, you sound like you are doing much better today.  I enjoyed a quiet evening too and am getting ready to enjoy a cup of coffee.  Think I will be trying to drink alot of coffee this week in case my taste buds change.  I would surely miss my coffee.  Your hubby sounds wonderful and Oscar is very cute.  My kids are on the furry side too!Laughing

    To those who started last week, hope you are still feeling well or feeling better anyway.  To those starting this week (((((HUGS))))). Hope you breeze right through it.

    Happy New Year all!

  • sheshe48
    sheshe48 Member Posts: 338
    edited January 2008

    Happy New year to all our sisters!

    Thank you Cindy yours words meant so much to me.

    KathyL  I also forgot to mention, I also use Barlean's Flax oil it has omega. It's all natural and good for your body. I buy it at a health food store it cost me $16 a bottle, it has to be refriderated, it lasts for months. You put a teaspoon in apple juice or in apple sauce. It gives me so much energy, someone here on this site said their oncologist that said not to take a lot of vitamens it does not mix well with chemo. I have a chemo class tomorrow morning, I will find out then. I hope everyone enjoys the day and hopefully the surgeries and se's will give everyone a break.

    Thanks Deb for the hug.

    Hugs

  • SISKimberly
    SISKimberly Member Posts: 762
    edited January 2008

    Good Morning and Happy New Year Jewels,



    Guess what my DH did? He went to Zales and bought me a beautiful gold on one side and silver on the other side, flat necklace that lays flat so you can put different jeweled slides on it...and he's having a customed made jeweled slide made for me...it wasn't ready yet, so I don't know what it even looks like...but how perfect to start the January Jewels Journey with my own January Jewel!!!!



    Carol- I hate it when the computer gremlins play tricks on me and arbitrarily erase everything I'd just typed...oh, they think it's hilarious and often play the same trick several times in a row, which makes me say words I shouldn't and want to throw my laptop. I'm glad to hear you made your CMF decision...that must feel good knowing you have a plan and a direction. Me...still waiting. Certainly, someone has to call me tomorrow!!!! Oh, and thanks for your compliment on the poem I wrote and for the toast...I was drinking a lovely Pinot.



    SheShe48- Thanks for your thoughts on my Dad...he's fine...hysterical as ever with his "Cyclops Chest".

    And HOORAH for your daughter!!!! Being a teacher can be the most rewarding and the least rewarding profession all at the same time, so many leave after the first five years...I hope your daughter has found her niche and sticks around a very long time...I'm in my 21st year of teaching. AAAHHH!!!! Another negative coffee message...I'm not liking this. I will be drinking as much coffee between now and chemo as I can...I am going to go through withdrawals (but I can just blame it on the chemotini SE's).



    Iowa Cindy- WOW, what a wonderfully insprirational message. Thank you so much for taking the time to come here and wish us all well and give us encouragement that it can be done.



    Vettegal- I just cried when you wrote about your DH tearing up and wishing he could take your pain away...what a man you've got there girl!!! OK, so you and me and Arizona Deb...we are going to hear from our doctors tomorrow!!!! Vettegal will find out she has Negative Nodes....and Deb and I will finally know when we get on the chemo train.



    Arizona Deb- Did you hear? There is negative talk about coffee again. I'm with you...I will be drinking up a coffee storm until I finally get word on when chemo will start for me. Looks like we're in the same boat on the not knowing part.



    Hope everyone had a wonderful time last night...my DH and I just had a quiet evening at home...listened to music, ate homemade navy bean soup, drank a great Pinot, and watched Big Night with Stanley Tucci and the guy from Monk...something Shaloub. Great flick about two Italian brothers trying to open a restaurant serving authentic Italian food.



    xoxoxo and HUGS to you all dear sisters.

    Your SIS(Sister In Survival)

    Kimberly







  • KathyL
    KathyL Member Posts: 534
    edited January 2008

    Happy Hew Year Fellow January Jewels!  Kimberly, your poem brought tears to my eyes.  It's beautiful; I hope you keep them all somewhere-- you should publish them all after you're done treatments.

    OK, I've read all the posts since I was last here yesterday (man we are a big, chatty group, huh?).  So a few comments, tips that it all brouight to mind...  what's biotene?  I think D1, you are using it orally?  I've not heard of it and wonder what to use it for and where to find it.  My onc recommends a mix of baking soda and water (1 tsp to 1 cup water), swishing 4-6 times a day to prevent mouth sores.  Sounds gross, but I'll do it anyway.  They said to start the day of chemo and do daily until all chemo (all rounds) are done; so for about 12 weeks for me.

    The ADHD comments brought a tip to mind, too.  My friend did radiation and of course was very tired from it.  Her onc (same as mine), put her on Ritalin while she was doing rads and for a few weeks afterwards.  She said it helped with the exhaustion-- something to keep in mind for those of you that have to follow chemo with rads.

    I also think I may start a journal-- someone mentioned this.  I write mass e-mails to friends and family and find it really cathartic and a great way to keep them up-to-date, but the journaling might be nice to look back on after this is all over.  Thanks for the idea whoever said it.

    I hope everyone waiting for test results, chemo dates, etc. gets some new tomorrow.  We'll all be waiting to hear from you about the news.

    As for me, 6 more days of work total before I'm out on leave.  15 days until I start round one, 13 until I get my port.  I've got a lot to keep my mind occupied.  My dad had a heart attack right before Thanksgiving and he's having his bypass surgery the 9th (the week before I start chemo)-- our family's a health mess, huh?  Anyway, I'll be thinking of him and hoping to get to see him before I start chemo the 16th.  Work won't give me a day off to see him, and he lives 2 1/2hrs. away (aren't they great?).

    Cheers, girls!

  • Determined1
    Determined1 Member Posts: 806
    edited January 2008

    Happy New Year, Jewels!!!

    First of all, good luck to Sherry/sheshe48 tomorrow.  If I remember correctly, you start chemo tomorrow.  It seems to me there were others in our group who started this week (wvgirl, maybe?/Diana63?), but I'm having trouble keeping track (can I blame this on chemo brain?).  Please remind me, everyone, of your big days because I really want to keep good thoughts for each of you on those days.  It's important to me to focus my thoughts on helping you all through this, just as I'm trying to keep myself under control.

    SIS Kimberly, you are our poet laureate.  You brought tears to my eyes.  Thank you.   (And you REALLY got Jewels!!!  How cool is that??)

    So it's CMF for you, Carol?  Must feel good to have your tx set.  I remember how impatient I got once I knew what was coming.  I just wanted to GET ON WITH IT.  Get your ducks in a row--tx day will be here soon.  And may I say I'm SO jealous that you don't have to have the neulasta shot?  That has been the worst of it so far for me.

    LJ13--get your partner a Starbucks gift card and tell her to get her java fix outta your smell line.  (And have her walk the dog--if you have one--while she's doing it!  Everyone wins!)

    I'm still having a cuppa joe in the morning, but just one.  And tonight I'm having a beloved bourbon and water.  Haven't felt like alcohol for a while and this tastes fabulous!  I'm more of a wine drinker of late, but I can't seem to enjoy it right now.  Maybe another night.  Water is tasting pretty vile--have switched to Vernors (I used to drink it whenever I was sick as a kid growing up in Michigan and managed to find it here in Virginia!).

    New weirdnesses to report:  I break into a full body sweat (not like the hot flashes I was having as I approached menopause), for no apparent reason.  I mean, I rub my finger across my skin and come up with so much sweat that it drips from my finger.  I also started my period today, even though they told me those would be over for me.  (You know, I don't believe this whole period thing.  I was told that I could avoid chemo if I was post-menopausal, so I took the blood test to check three different times.  Every time the test said I was post-menopausal, but I kept having periods.  So I'm doing the chemo.  Now, when they say I should be in chemopause, I'm having another one.  What's up with that?  And they told me not to use tampons because they were concerned that I would tear myself.  Well, I have never used pads and never will.  I'm bleeding already, for crying out loud.  Who would know if I tore myself???  Rant, sorry.)  Final new development--my scalp is numb!!!!  Did a respectable job blowing out the new 'do today, but I figure by the time I get good at it, the hair will be gone.  Ah well.  The cancer is totally f*cked, so what do I care?  FUBC.

    Keep smiling, Vettegal.  You sound good today.

    You okay, Yuyu?

    IowaCindy--thanks so much for the encouragement.  I know you understand how much it means to us.  Please stop by anytime.

    MAMHOP--YOU GO GIRL!  I'm pm-ing you.

    It's on, ladies--WE ARE THE JANUARY JEWELS!!!!

    D1

  • Determined1
    Determined1 Member Posts: 806
    edited January 2008

    Oops, Kathy, forgot about the Biotene.  I bought a toothpaste and the mouthwash.  It's supposed to be gentle when you have the mouthsores (no alcohol--hmmm, makes me wonder if the bourbon is okay.....Naw, bourbon's always okay).  I found it at Target, I think.  My mom was just telling me yesterday about the baking soda mix you describe, which is supposed to do the same type of thing.  Thanks for passing along the ratios, my mom wasn't sure about them.

    Oh, gotta tell you a laugh.  Last night I had this crazy dream that I was in the dentist's office (okay, it was a nightmare) and he was trying to pull tiny pieces of tin foil from between my teeth and it wouldn't come out.  When I woke up, I'd been drooling so much that my pillow and t-shirt were totally soaked!  Now there's a chemo-inspired dream for you!!!

    D1

  • golfer779
    golfer779 Member Posts: 1,378
    edited January 2008

    Hello 08 Jewels,

    Hoping New Year's Day has everyone feeling atleast a little bit better.

    Kimberly, I'm sure you atleast for the moment forgot about that darn onc office not calling.  What a cool "thoughtful" gift.  I had to tell my dh about that one, he atleast chuckled!!!  He did ask me if I told the gals online about my gift...it is the Ipod touch.  He thought I'd enjoy some video as well as music during appts, etc.  I have never watched Grey's Anatomy but my kids and friends all love it, so I downloaded all of last years episodes, I've already watched 10 of them with 16 to go.  Then I can get this seasons and get caught up.  Wasn't too sure about a medical type show during appts, but so far, so good!!!

    KathyL, so sorry to hear about your dad.  Sometimes these life's test are a little too much.  Do they do any sick leave sharing where you work?  I'm actually going to work tomorrow, want to save sick leave myself, and I think I can make it for atleast a portion of the day. 

    Hoping that something will work out for you, its so sad to hear of story like yours where there seems to be no compassion at all.

    D1 - just to let you know, I did get off my butt and went for a good long walk.  I had spent the better part of the morning taking down the tree, deco etc., asked the dh if that counted as my exercise.  He politely informed me "NO", okay he said it could be part of my exercise.  The wiener dogs we're all jazzed up for the walk!!!!  Felt great, and I'll get in gear!  Hoping your day has not gotten any worse than your last few, sounds like txt doesn't just ease into things. 

    Oven timer going off...yak later, Carol

  • Donna1955
    Donna1955 Member Posts: 24
    edited January 2008

    CoolHi January Jewels,

    Happy New Year to all..... I will start my Chemo on Thursday Jan 3 at 9am.....4 ac treatments every 2 weeks then 3 week break then 4 taxol treatments every 2 weeks....I will post Thursday pm let everyone know all the drugs they will be putting me on....I am ready to get on with this and get done... I guess with the every 2 weeks shit I will get thru it quicker, there that would be a positive.....

    Thanks to all of you for posting and helping us thru this and I will make my posts for the January Jewels behind me.....

    Az Donna

  • marshakb
    marshakb Member Posts: 1,664
    edited January 2008

    Hey Ladies, I'm Marsha from the Feb Chemo Cruisers.  Just wanted to stop in and give you all some encouragement. 

    Before you know it, this will be past you, one day you will wake up and think "what the hell just happened to me" and it will truly feel like some kind of oddball dream.  The Feb Chemo Cruisers of 07 are getting together Feb 08 in Florida at a beach house, you know why?  Cause we made the best friends of our life right here on these threads!  The journey sucked, no kidding you there, but the hair grows back, your energy level returns, your taste buds wake back up, and the shock of sitting in that chemo chair the first time subsides.

    Hugs to you all, I remember when we first started and someone came on from a year previous and it gave me hope that one day I would do the same.  Marsha

  • golfer779
    golfer779 Member Posts: 1,378
    edited January 2008

    Marsha, just wanted to say thanks for stopping by ... the anxiety levels are starting to rise again, just like when it got closer to each surgery.  Your kind words ease that stress if even for a short time,

    Carol

  • JulieK_11_30_07
    JulieK_11_30_07 Member Posts: 260
    edited January 2008

    Hi January Jewels! Happy New Year! I haven't been back online for a few days - wow, you all are an active group!! It took me forever to read everything I missed.

    For those of you who have already experienced your first treatment, THANK YOU for letting the rest of us know what to expect! My first tx is January 3 and I'm getting very anxious about it. I saw that many of you are also taking Emend and Decadron after treatments. My onc also has me on Pepcid and Zofran, along with Reglan and Ativan, if needed. He did not say anything about Neulasta, so I'm not sure if that's a shot I will need to get. After reading what some of you have said about it, I'm thinking I don't want to have to get it.

    Kimberly - I did a complete hysterectomy (including ovaries) - it's actually referred to as an oopherectomy when they remove the ovaries. Mine was done as a "laparoscopically assisted vaginal hysterectomy" - the recovery from it was not bad. I was back to work in less than three weeks and probably could've gone back sooner if I had to. I did not have the BRCA test, but my sister did b/c her insurance first denied her mastectomy - they thought she wanted to do it so she could have reconstruction to get bigger boobs - imagine that!!!! They said she first had to have the BRCA test to find out if she had the gene - she didn't, but fought the insurance company and they ended up granting approval for the mastectomy and reconstruction. She does not at all regret her decision to do it - especially now that I've been dx with bc and had previously decided not to do the prophylactic mastectomy. It was certainly not fun going through "the change" at only age 36, but the hot flashes, etc. have improved and I certainly don't miss the "monthly visitor" at all!! My mom's oncologist had told my mom when she knew she wasn't going to make it through her ovarian cancer that her daughters needed to have everything removed once we had all of our children. I don't think I mentioned that my grandmother also died of ovarian almost exactly a year before my mom did. With your family history, I would certainly encourage your twin to take every precaution she can to not have to go through all of this. I have definitely second-guessed my decision to not do the prophylactic mastectomy two years ago now that I'm facing six tx of chemotherapy.

    D1 - I have to say I so enjoy your posts and your honesty! I laugh out loud at so many of your comments. Thank you for starting this thread as I'm sure we're going to need each other as we all go through our treatments. I'm glad I found it!

    To everyone I missed, I hope you all had a nice New Year's and are ready to face the year together!! I agree with KathyL - we're gonna kick some BCA in 2008!!

    {{{{Hugs}}}}!!

    Julie

  • clsd
    clsd Member Posts: 101
    edited January 2008

    Hi Jewels.

    I love reading all your posts. I usually check in with Dec and Jan groups, but stumbled upon yoursthis morning...Great energy!!

    One of your ladies recommended a site for friends and family to check in ( when I am in my chemo fog, I don't return calls, etc, ), and I wanted to say I have had such great success with  www.caringbridge.org   It is easy, and friends and family can leave you encouraging messages, with out your phone ringing 24/7, and repeating how you are feeling a million times . If you wanted to check out mine, feel free, just enter code   cldiaz.

    I wish  you a WONDERFUL and HEALTHY 2008, and BEYOND! Prayers and Hugs, Love Cindy NJ

  • vettegal
    vettegal Member Posts: 287
    edited January 2008

    Good Morning Jewels,

           Hope everyone is doing well today! I see we have some people starting chemo today..Good luck to everyone and keep us posted on your status and hope everything goes as planned.

          As for me I am feeling better, going back to work tomorrow. Waiting for Path results today. Finally slep without any help frompain pill or sleep pill. I wanted to do it on my own, my dh says i am stubborn, that is the dago in me (oops) The italian in me.

         I am glad we have so many visiors from the other boards popping in on the Jewels for motivation and support. To all the new sisters of the board WELCOME ABOARD!!! This group has definately grew in the pass few days and I assume we will be getting more..

          Hope you all have a great day!!

                       Hugs

  • Determined1
    Determined1 Member Posts: 806
    edited January 2008

    It's chemo day for some of our Jewels!  Good luck.  Try to relax, take a book, iPod, knitting, whatever.  In a sick way, chemo day is okay cuz everyone dotes on you and you probably won't feel that horrible.  Try to keep your mind at peace and imagine the fear those cancer cells are experiencing when that see that cocktail coming down the line!  FUBC!!!

    Having back spasms today and I'm not sure why.  I'm pissed cuz I wanted to go to the gym to do some upper body work.  I'm relearning total flexibility in scheduling here (thought those years were gone once my kids got their licenses).  I go in for my first week bloodwork today.  Even though I'm not scheduled to see anyone on my med team, I'm going to ask for my case nurse when I arrive and hope she can come out to give me a wig rx, something for the acid reflux and something for the back spasms.  Otherwise, everything's still okay.  Now I'm going to try to complete the hardest task of my day--I'm going to motivate my college girl to vacuum the living level!  (Sh*t, I got up and cleaned the stove and sink with my back going like a disco--she can vacuum!)

    Life goes on.

    D1

  • SISKimberly
    SISKimberly Member Posts: 762
    edited January 2008

    Good Morning Jewels,



    It's a beautiful day in Lincoln today...the sun is shining, but a big storm is brewing and should come in tomorrow afternoon and last a few days, so I need to get out and take a VDW-Vit. D Walk today for sure.



    Kathy- WOW, thank you for your compliment regarding my poem. I do keep them on my laptop and on a thread I started on bc.org called Poetry Anyone? Good tip on the Ritalin if Rads should knock me over when I get to that point. I am so sorry to hear about your Dad...when it rains it pours doesn't it? The good news is...only 6 more days until you are on leave from work, you'll be able to be with him on the 9th, and he's only 2 1/2 hours away...not too far...at least you don't have to fly. I'll be thinking of you and your family on the 9th...sending out lots of positive energy into the universe. As D1 OLE stated, Biotene help eliminate dry mouth and keep your gums and mouth healthy. I prebought the toothpaste and mouthwash at Target. I now need to go get saline rinse for my nose. I so hate drugs/pills, but have heard Tylenol PM is a good idea for sleep when Decadron tries to keep you awake....anything else?



    D1 OLE-Thank you and sooooo cool!!!!! OH NO!!!! I won't like the taste of wine either? No coffee No wine...I hate bourbon and other brown liquor...am I too be without any vices????? Hysterical dental nightmare LOL I had a school dream last night...I was on my Prep period and ran an errand with my dh thinking I'd be back in plenty of time...but my dh has a tendancy to wonder and do too many little things in too short a span of time. I didn't have my phone...so I borrowed his...and everytime I dialed my school number some guy from Verizon said the number was not valid...I was paniced and crying hyterically, " You have to help me get through. My class is going to start, and I won't be there in time...my kids will be left outside. I need to ask someone to let them in and get started. I'll be there in 15 minutes." He of course just kept telling me there was no such number. As I began to wake...my rational mind kicked in and said, "Kim, you have a sub. You aren't working right now. Your kids are fine...they are safe." Man, that was intense!!!! They aren't even back in school from the Winter Break yet. I just love your posts...h*@# yes, the college girl needs to vaccume!!!! No convincing should even be needed. My 24 year old son wanted gift certificates to Target for Christmas so he could buy himself...you guessed it...a vacuume. Go figure!



    Carol-I did forget, and cool about the IPod. Isn't technology amazing and frustrating all at the same time? Good for you taking down all your Christmas stuff and taking the pups for a long walk. Today, i plan to take down what I can reach and put it on the dining room table...the Christmas storage box is in the garage...and I couldn't lift it even if i wanted to right now. My dh can get the box and the rest of the decorations down, and I'll put the stuff away in the storage box tomorrow. I also have the last of the Thank You cards to write.



    AZ Donna and Julie, good luck tomorrow 1/3/08...let us know how it goes.



    Julie, thanks for the info on your total hysterectomy...that doesn't sound so bad. I'll forward your message to my sis, so she can see that your sis doesn't regret her decision at all. Aren't insurance companies just ridiculous in their reasoning? "Oh, please put me through hell by surgically removing my perfect for the moment natural breasts, so I can get perky new ones!!!" Hello!!!! Who are they kidding? Did she do a total hysterctomy as well? With your family history, I'd imagine she did.



    NJ Cindy-Thanks for stopping by, and you are right...we are a positive energy group! Thanks for sharing the link...I just do a mass emailing, but others may find this very useful.



    OK, I think I'm caught up unless someone posted while I was writing this.

    Thinking of you all,

    Your SIS (Sister In Survival)

    Kimberly



  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2008

    Just checkin' in for an update.

    Good luck to our Jan. Jewels starting this week! You are the real Jan. Jewels, a couple of us just felt a bit too late to be December ones!

    Still not a hint of SEs from the Neulasta. I may have to turn in my Poster-Child-of-Side-Effects card. A couple of nights ago I had that jabbing pin feeling in my legs at bedtime, but I've had that before the Adventures of Chemo. Once read that it is tense muscles relaxing. Anyway, it was just the one night.

    Felt halfway decent yesterday, actually felt hungry for the first time in days. Some foods are even appealing. Who'da thunk? Water almost tastes normal again. Trying to maintain my weight but I think I'm down a couple of pounds. I'll try to pack them back on before next week's infusion.

    I was supposed to return to work today, but decided to be a big baby (I know, none of us are big babies) and take just one more day to try to get back to a semblance of normality.

    D1, the partner is such a gem, she felt awful about the coffee thing and I felt awful for her. I suggested that she take her coffeemaker to work, which was a brilliant solution (all modesty aside) and as she has her own office, that's working out well. 

    Sheshe, check with your dr/nurse about consuming honey. I too love it with my tea, but since it's usually raw and unpurified, if you're going on chemo, it's generally not recommended as your immune system, which could normally handle any nasties in honey without a hitch, may not be up to the task. I'm using organic sugar in lieu of honey until I have a real immune system again.  

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