Starting chemo January 2009?

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  • ktym
    ktym Member Posts: 2,637
    edited March 2012

    Hope things are going well with chemo today Phyllis

  • BerkeleyKim
    BerkeleyKim Member Posts: 390
    edited March 2012

    Phyllis--What chemo are you doing? Thinking of you and hope you see good results quick.

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited March 2012

    I hope you are doing okay after your first chemo tx, Phyllis.  Thinking of you!

  • Renrel
    Renrel Member Posts: 497
    edited March 2012

    Phylis - I hope you are doing OK.

    Is everyone experiencing an early spring?  My Sping Bulbs are seriously springing out of the ground already!  

    We just finished a super crazy week,  DS had Russian math class on Wednsday night, as usual.  On Thursday he had his first math competiion - a standarized test given to kids on the same day all over the world.  Then a friend took him out for dinner and bowling.  Then Friday we had three families from DS's Sunday school over for a Shabbat dinner.  Then Saturday DS had Tennis and then a playdate and then the kid who hosted the playdate came over with his Mom for dinner.  Then this morning was Sunday school, followed by theater class, followed by going to see a community production of Joseph and the Technicolor Dream coat that DS dropped out of because the rehersal schedule was too much.  Looking forward to a much quieter week.

    We are finally painting our foyer after living with plaster board for 3 yrs. That what happens when your diagnosised with BC 4 months after moving into your new home. (new for us the house is over 100 years old).  DH had his heart set on having a red wall in the house somewere so we are trying to find the right bright but not primary colorish red.  And the other wall, that goes up the stairs we are trying a rich pumpkln type color.  Having a heck of time getting the colors just right and making sure the go with each other but we really really love the life they add to the house.  Makes us happy and alert everytime we look at them, but as they are in the foyer the don't overwhelm or exhaust us with their energy because you don't stay in the room with them.  You walk through and glance over.  

     DH is also trying to buy a table saw off craigs list and going crazy deciding how much saw he needs/how much he wants to pay.  He does not plan to do alot of work but he wants a safe saw for what he does do.  

    Where I work things are a bit crazy as in the past 3 months, my direct supervisor has transfered without warning to another position, her supervisor decided to demote herself back down to my position and the director of the whole department resigned to go home to Ohio.  And all this while we are trying to roll out a whole new computer system which is supposed to change the way we all do our jobs and the way the public interacts with us.  It maybe that roll out that made these people deside to leave their positions.  But all I can do is keep plugging along trying to do the best I can and provide support to others where I can without overdoing it.  

    I am back to working out using our Wii.  I am doing a golds gym cardiowork out which I assume is working as I am sweaty and out of breath when I finish and sore the next day.  Weight loss is slow though.  

    Thats the low down over here in Massachusetts.

    Renrel

  • kt57
    kt57 Member Posts: 425
    edited March 2012

    Phyllis,

    Found my way back to the January Jewels and read your posts.  i am so sorry this is happening to you.  If my estrogen free brain is remembering correctly, you were the last of the Jewels to complete chemo and now here you are again in the throws of it.  Take care of yourself.  ((((Hugs))))  

  • PLUTZ
    PLUTZ Member Posts: 133
    edited March 2012

     Hi Ladies. Sorry I haven't been in touch. My chemo treatment was Mar. 13th. It wasn't too bad.I was really nauseus the next day.I think I'm on Taxotere again but not sure. I'll find out next treatment. I'm also on chemo pills, called xeloda. I'm on them for 14 days, 1 week off  then start them again when I get my iv chemo. The side effects are terrible. My body aches (reminds me when I had to get the neulasta shots), headaches, dizziness and fatigue. Starting to lose my appetite but not the taste. I have to be careful of mouth sores. My mouth was sore for a couple of days but its gone now. I have to wash my hands after handling the pills and the nurse gave me udder cream that i have to use after. My hands could crack and turn red, but they haven't so far. I have neuropathy again. It never went away in my toes, but its back in my fingers. My next treatment is Apr. 3rd. I'll let you all know how that goes. I hope everyone is doing well.

  • Renrel
    Renrel Member Posts: 497
    edited March 2012

    Phyllis -

    I am so sad that you have to go through this again.  It just sucks!  I hope this time the chemo kicks the cancer's butt out of the house for good.  I will send you some Reiki energy if you like. Just give me the go ahead. 

    I am trying to do some Reiki volunteer work at the local hospital but I have to get a TB test and the department that does the test is only open during the week day while I am at work. I either have to make a special arrangement with them or take time off from work.  So annoying having to jump through hoops to try and do some good. 

  • ktym
    ktym Member Posts: 2,637
    edited March 2012

    That is annoying Renrel

    Phyllis, hugs, I was so hoping the chemo wouldn't be so bad.  I'm so sorry you're going through this. I hope it starts helping the breathing go easier

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited March 2012

    Phyllis- I agree with Kmmd, I hope the tx will help with the breathing.  That has to be so tough.  I hope you get through this tx without the crappy side effects and then move on to NED land again!

     

  • PLUTZ
    PLUTZ Member Posts: 133
    edited March 2012

      hi ladies.  I'm not feeling too bad. Still get the headaches and dizzy spells. I haven't used my oxygen in over a week but i still have shortness of breath when I go up the steps or overdo things. well i woke u this morning and Im losing some hair. I found it first down under if you know wat I mean so I thought I would comb my hair and sure enough, a few strands came out. I was told not all women would lose their hair. Hopefully it won't all fall out. I will let you all know how my treatment goes next week. Have a good week

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited April 2012

    I am glad you are feeling better Phyllis.  I hope you week is better and you get through the treatment without too many hitches in side effects.

  • PLUTZ
    PLUTZ Member Posts: 133
    edited April 2012

      Hi ladies. no treatment this week. my blood counts were too low. i go tomorrow for blood work because i have a dentist appt. Mon. but if the counts are too low, can't get my teeth cleaned. I'm scheduled for my next treatment next Tues.

  • ktym
    ktym Member Posts: 2,637
    edited April 2012

    Thanks for checking in Plutz, you know we all want to hear how you are doing.  Keeping my fingers crossed for your blood counts

  • BerkeleyKim
    BerkeleyKim Member Posts: 390
    edited April 2012

    Phyllis--hope you're feeling better this weekend and your bloodcounts go up for treatment. That xeoda is strong stufI and worked great for my sister-in-laws sister. Hope it does for you too.

     I saw my onc a couple weeks ago. She's going on maternity leave and I'll see another doc for my June visit. I'll be done with the bisphosphonates trial at that point. I think I'll need a bone scan to follow up. My onc asked if I wanted an mri of hip since I have so much pain at night. Funny she leaves it up to me. Anyone else with hip pain? I'm also getting another referral for LE Physical therapy. My elbow on that arm really hurts and onc thinks it's bursitis due to arimidex. Maybe I'll try to get accupuncture during spring break next week. I am really needing that break!!! Trying to figure out what the family should do for Easter tomorrow. HUGS to all!

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited April 2012

    Hi everyone--Just checking in. 

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited April 2012

    MRI results next week.  Yikes!

  • BerkeleyKim
    BerkeleyKim Member Posts: 390
    edited April 2012

    Jess--Hope you get the all-clear on MRI. What's it of? I get a breast MRI every June--so coming up. I hate them but since mammos didn't see my tumors (and ultrasound only got one), I feel like it's the best diagnostic tool for me.

     Phyllis--hope you've been able to get your treatments and they are getting you to NED. Sending hugs your way.

  • Renrel
    Renrel Member Posts: 497
    edited May 2012

    Had my 1/4;ly check up last week.  Everything looks good.  I am having hip pain too.  Mostly in in the groin area if I stand or walk to long.  Last time we did a bone scan and it showed no issues.  This time he did pelvic xrays and is going to recommend a orthopedic doctor to diagonis and recommend a form of threapy.  I was on vacation the week before the visit which means I was up about about alot so I was hurting alot at my appointment.  Vacation was visiting my inlaws in Boca.  DS was running a fever on the plane ride down and was sick for the first few days then DH did not feel quite right the rest of vacation.  But we still got to Butterfly world and Seaquarium and the pool.  DH and DS got in some tennis. We ate out alot and DS watched way too much TV and played too much DS.  The worst part was sleeping in the pull out couch for 10 days.  I don't think we can do this for a week anymore.  We need to split the time with a hotel or sometime. 

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited May 2012

    My mri of my other breast and of the foob incision area came back all clear.  I get one in April - yearly now instead of just the mammogram-

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited May 2012

    Hey, sisters, how you be???

  • kt57
    kt57 Member Posts: 425
    edited May 2012

    Hey Jess,

    Great news on your recent MRI!   

    I had a bit of a scare this week.  I finished the bisphosphanate trial and had my bone scan last Thursday.  After the bone scan, they came back in and wanted more images of my pelvis....then they wanted x-rays, first of the left hip then back for the right hip.   I am trying to remain calm-- nobody is saying anything, but I know this is not typical.   I talk the the tech and tell her I recently fell squarely on my right hip -- her response was, "Oh, the 'hot spot' they are looking at is on the other side."    Holy Crap!   The next day I walk over to the cancer center and talk to my chemo nurse -- she pulls the report.  It says there is a spot that lights up and "osteoblastic metastasis cannot be ruled out".  Holy Crap!  Then I wait the weekend -- trying not to worry -- staying busy and distracted til my scheduled appointment with my onc on Monday.  He is calm, thinks it is probably nothing but needs to be sure -- so off to MRI I go.  Today I learn it is the tendon that attaches my hamstring to my pelvic bone -- it's inflamed.  No mets.  What a relief!    I guess in my head, I knew it was prob nothing -- but you can't help but imagine the worst.   It is probably the yoga class I started -- better quit trying to touch my toes!

    I am in Relay for Life mode.. our event is in a few weeks.  Always makes me think about the January Jewels and how we helped each through a tough time. 

    Take Care all.

  • momand2kids
    momand2kids Member Posts: 1,508
    edited May 2012

    greetings all

    hope all is well--I also had hip pain- which I swear is from the lupron/femara--- but did PT this fall because it was really sore when I exercised.... it seems to have resolved-- Onc meeting today--she said she is only concerned when things come on and get worse--something that comes and goes does not worry her.

    had my annual MRI-- told her not to bother with the results until next week--- don't need to know over the holiday weekend... and I figure if something was wrong, she would have called me anyway.....

    We did negotiate my going off lupron for the summer to see if I am in menopause--I am thrilled-I think this drug is causing many of my slight but really annoying SE's.... or at least I will know if it is the lupron or the femara.....

    have a great weekend!

  • ktym
    ktym Member Posts: 2,637
    edited June 2012

    Hi guys stopping in quickly.  Wanted to see how you are all doing and especially how you are doing Phyllis. 

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited June 2012

    Hi everyone.  I hope all is well.  Hey, has anyone heard from Phyllis??'

  • ktym
    ktym Member Posts: 2,637
    edited June 2012

    No, I haven't, been wondering also

  • kt57
    kt57 Member Posts: 425
    edited June 2012

    HI Jewels.

     Well it's that time of the year again -- American Cancer Society Relay for Life. We have been fundraising up a storm and have raised over $16,000 so far. 

    As I have for the last 4 years, I will carry the Jewels with me.  And I will trek mindfully and prayerfully for you, Phyllis. 

    Here we are -- the best support group in the world!!

    lisalisa brendafromflorida holtbolt renrel ddlatt

    GriffinSong jrgolomb sjr585 BevR Sunflower45

    Babyc Jas­_man bookgirl Misty auriga jillyG

    mamasarah mimi07 AZStacey08 eadsla Hawaii808

    Webwriter BerkleyKim sweeeetpam Butterfly2008

    amyjane Snowbird ChrisBern Carol0371 Brenny lester63

    rsben70 PinkLady Shavoners yrawleigh dpstarr REKoz

    principessa kmmd bfb0123 susan13 mabels Kim25

    newalex Yearof theHat marlenet carlajane ladyjane54

    Alo123 marymoir Dpstarr aprilgirl1 living4today stitches

    luvmyself silverlining KM47 susan13 carpediem bobcat

    SallyJane blackmailtx Triciaski ChrysalisPa kimberlyjo

    rmsilver shockedat39 Sister3 Horselover44 csbsk123

    07rescue Lisa810 Misty123 PLUTZ Shannon7 knots Ninja

    tyra PrincessKauai59 spooky EvaPerone JanetC826 cil326

    LucyMichaels SusieQue momand2kids   and me kt57.

    Take Care - stay strong

    Kathy

  • BerkeleyKim
    BerkeleyKim Member Posts: 390
    edited June 2012

    kathy--that's a great tribute to our jewels. Thank you!

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited June 2012

    I agree, Kim, thank you Kathy.

    I had my six month and all is okay except I noticed my bilirubin was a bit high....onc said it looked okay........I never will understand what all this means!

  • jrgolomb
    jrgolomb Member Posts: 1,236
    edited July 2012

    Hey!!  HOw is everyone doing???

  • BerkeleyKim
    BerkeleyKim Member Posts: 390
    edited July 2012

    Hi Jess! Hi Jewels! I'm waiting to hear results from bone scan that I did yesterday for end of bisphosphonates trial. Tech needed to do extra pictures due to slight uptake in neck. Then more of my sides that he didn't explain. I'm a wreck. Hoping for arthritis.

    3 weeks relaxing at brother-in-laws house in Maui was great. Back to reality and worry. I guess my breast MRI early July was ok. Didn't get a letter this time so I called, and the receptionist just whispered "don't worry".

     Hope you all are having a great summer.

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