Chemo June 2010

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  • grneyd5600
    grneyd5600 Member Posts: 420
    edited June 2011

    Bon

    I completely get now why the Onc originally said he hesitated to do scans because they often led to areas of concern that were hard to distinquish.  I am actually comfortable waiting for another (3) months and seeing what changes (if any) happen.  What I know about mets is that if it is mets the pain will progress.  Not that I want pain but I am ok waiting and seeing.

    You guys are the best. 

  • Latte
    Latte Member Posts: 1,072
    edited June 2011

    Chey - so sorry to hear about your brother in law, sending my love to you and your sister and nephew.

    Jackie -  so sorry that you didn't get clear results and are now in limbo. hoping that the next scan will bring good news. I know that rads can affect how ribs show up in scans sometimes.

  • SarahT
    SarahT Member Posts: 4
    edited June 2011

    I started chemo today 6/2.  Port placed yesterday

    AC every other week x 4; Taxol every other week x 4. radiation to follow

  • mimi9186
    mimi9186 Member Posts: 127
    edited June 2011

    Sarah, sorry you had to join this group.  chemo is not fun but we all made it through with the support of each other.  You will find these gals very informative and helpful.  Wishing the best for you.

    Chey, My condolances to you and  your sister for the sad loss of Rick. He sounded like a really wonderful man.

    Jackie, as Bon said, we will wait with you, worry with you, and pray with you. We are family now.

  • JFV
    JFV Member Posts: 795
    edited June 2011

    Sarah T-  Welcome.... we all know what you are going through and send you our best wishes.  Any questions you have feel free to post.  We want to help you !

    Chey and Jackie AAAAAAAAAAARRRRRRRRRRRRGGGGGGGGGGGGGGGGHHHHHHHHH!

    That is the sound of me screaming from the shores of Long Island.  I want the world to stop beating both of you up ! 

    Jackie- I believe you are just full of non cancerous holes and cysts and nodes.  I believe your next scan will be clean.  But, I believe 3 months of waiting is h#ll.

    Chey- I don't know how you survive the pain of the loss you and your sister are suffering.  But, I believe you are a strong creative woman who will find a way.

  • flopsy
    flopsy Member Posts: 365
    edited June 2011

    Chey,  I was stunned to read about Rick for I truly thought you were going to be able to get him the help he needed.  My heart bleeds for you and your sister.  I will keep you in my prayers.   May God bless you and your sister with peace and acceptance.

    Jackie,  I don't know about you but I think all medical test that are non conclusive should be banned.  Of course that would mean we would have only a handful of tests left and that would not be good, but it is so frustrating for them to say, "We just don't know for sure!!"    I will be praying expecially hard for you and am sending you good vibes and thoughts right now.  I also am sending you one big  (((((((HUG))))))).  When I had my Bone Scan and CT scans last year before Breast Surgery they saw several areas that were questioned.  Have not had re-scans but am thinking they would still be there if I did.  I work with radiologist all day so I know their weaknesses and limitations  Believe me there are many of both.  

    Sarah T,  Good luck with your treatments and keep us posted.  Ask any questions and we will surely try to answer them.  So sorry you are having to go on this journey, too.    

    Hello to all of my Chemo-Sabes!!!!   I sure hope we can meet at one of the trips we have talked about.   I can't wait!!!!!!!

  • TMarina
    TMarina Member Posts: 692
    edited June 2011

    oh Chey---I just don't know what to say. I am SO sorry!  Your family has been through so much already.  I am lifting you up in prayer--May God wrap His arms around you and your sister and carry you through this difficult time.  Love you!

    Jackie--sorry you didn't get definite answers, but glad you are ok with the waiting.  I think you are ready to just get on and enjoy life!

    Sarah--we all started chemo a year ago this month, and would be very happy to help you in any way we could. You have the same chemo I had, and I had rads also.  Please ask any questions you have, and you can send me a pm (private message) also!

    Love you all!

  • BirdyRobin
    BirdyRobin Member Posts: 105
    edited June 2011

    Hello ladies,

    I am coming over from the surgery section, I am past (just) surgery and saw my oncologist yesterday, boy what a lot of info. So it seems I am a part of a phase 3 trial just tweeking dose and timing otherwise drugs (cocktail) are the same.

    Ya know I started on this sight with the not diagnosed but worried section, then onto surgery before during and after, now I am in the June chemo group. Some of the people I have met along the way have been very kind and I appreciate there support. Now I am moving into a new group and they are staying behind, at least for now. I look forward to making new friends and finding new info and levels of support. I have to admit though the thought of chemo is daunting.

    I am gratefull to those that have been here done that and I am sorry for those that join me here this June. There is strength in community and numbers and I believe we will get through this together and from here move on, after here is radiation therapy and then reconstruction for me.

    Thanks for reading, god bless.

    Robin

  • grneyd5600
    grneyd5600 Member Posts: 420
    edited June 2011

    Chey my dear - I am so sorry about the loss of Rick.  We wil keep you and your sister in our prayers.  Remember that the wind on your cheek is really the flutter of angel wings.  Now that you both have a special angel feel the wind my friend! 

    Sara and Birdy - welcome to our group.  We certainly understand where you both are in the process and will lend any support we can.  Just remember that healing comes with the process so getting through it is important.  Keep your outlook positive and your smile on and remember that each day is a new chance for sunshine!

    As for my situation - I am convinced it is all good.   I think God is teaching me a lesson that when Onc says he avoids scans because it ends up leading to more questions than answers he is right.  I am good with the waiting game and determined to keep smiling!  Kiss

    Hugs!

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited June 2011

    Cheyenne-I just don't have words, little sister. Too many tears this year. I am on a remote island right now. Thankfully, prayers travel anywhere...and mine for you will continue.

    Jackie- You have such an amazing strong attitude, sort of, "okay, we'll look at it again in 3 months.  I will continue to pray for you.  I do think that all we have put our bodies through (did I really do that to my body?)  makes our bodies hurt and rebel for quite some time.  Let's just pray your body is regrouping.

    You will not believe my last two days!  We traveled 20 hours straight to get to our somewhat remote island home without sleepovers.  We arrived to find:  no water (something wrong with pump), no heat (needs water) and yes it is 50s here in Canada, no internet therefore no phone, no place to buy bottled water after 8 p.m. car won't start and, just for the fun of it, I have some kind of whopping flu or virus and have a wracking dry cough which won't let me sleep.  DH had to return our rental car today and just piled everyone in, took the ferry to Vancouver, checked us into a hotel for the day to shower and rest.  We are trying to line up all the workmen (not much to pick from with 1,000 residents)  before we return on the late afternoon ferry.   NYC is looking awfully good to me about now.

  • JFV
    JFV Member Posts: 795
    edited June 2011

    BirdyRobyn-  I'm an ILC gal also.  It takes a long time to figure our all the doctors are telling you.  When it is all said and done we all ended up with similar treatments even though we are from all over the world on this group.  My two big pieces of advice are take whatever anti nausea meds the doc prescribes for chemo, keep a notebook and write everything down and drink more water than you ever thought humanly possible to drink. 

    Dmom-  Does not sound like a great vacation.  Good luck getting the place back in shape.

    My daughter will be going on date #2 tonight.  She still won't talk to me.  She wants to join a gym this summer and take Zumba classes.  She has suggested I join too.  So, I will be Zumbaing in order to try to bond with my daughter.

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited June 2011

    Joan- It sounds like your daughter is still wanting to "hang" with you, even if she doesn't admit it. Not a lot of young girls want to Zumba with their moms!

    I just read this study linking elevated CRP blood levels to breast cancer outcomes.  I will be asking my doctor to test this along with my D3 levels.  Another good reason to focus on anti inflammatory diet and fish oil supplements.  It irritates me that our Oncs don't advise about these lifestyle things that are obviously very important.  Here's the BCO link (sorry linky thing won't work)

    http://www.breastcancer.org/symptoms/testing/new_research/20110603.jsp 

    Birdy and Sarah- Welcome! Do you guys realize we are the June 2010 chemo group? Of course we will all try to help you as much as we can, but there is something extraordinary about going through chemo at the same time with people. We have all become such close friends this past year. There is a new thread called "Jun 2011 chemo" that you should also check out. If you copy and paste this link, you will find it. Wishing you the best of luck as you go through this next phase!  Let us know if we can help.  Golly, we are veterans by now.

    http://community.breastcancer.org/forum/69/topic/769067?page=3#post_2429074

  • JFV
    JFV Member Posts: 795
    edited June 2011

    Dmom you're right.  She may not want to talk to me about her dates.  But, at least she is willing to be seen in public with me.  There is hope

    Update on the life coach plan.  I try really hard to avoid spending money so the first thing I did was research life coaching on the internet.  I got 5 free life coaching lessons from a Leslie Gebhart sent to my email.  I have printed them out and tucked them away for later.  After reading the first two I became anxious and depressed.  So, then I knew I had to try to slay those demons before I could move on to life coaching.  After doing more internet searching and spending alot of time looking at book exerpts and book critiques on Amazon I picked up the book What You Can Change...and What You Can't.  It talks about what studies have shown as effective forms of self improvement.  I have read it through quickly and will try the anxiety ideas as well and the depression ideas.  The life coaching idea is on hold for now.

  • renee2010
    renee2010 Member Posts: 93
    edited June 2011

    Hi,Renee Rodgers hereLaughingJust checking in a seeing how every one is doing.I can not believe it has been a year.I think of everyone often and pray for all  of you.My hair is coming back Curly and grey.Put on 30 lbs ...Adjusting to Armidex...been a challnge,still not smoking,not my self at all ,no sex drive..ugg.Happy to b alive,but trying to figure out who I am ...or just getting threw each day.Look forward to hearing from al of you.You all where my life line.Thank you.Still are.

  • JFV
    JFV Member Posts: 795
    edited June 2011

    Hi Renee !!!  So good to hear from you !  I always wonder how the ladies we don't hear from as often are doing.  I have curly grey hair too.  I did dye it brown and it needs to be done again.  I think my hair is averaging a quater inch a month.  It will be a long time before I have as much hair as I want !  Glad you are staying away from the cigs.  That must be tough.  I am on Tamoxifen and don't really notice any changes.  How has the weather been for you this Spring ?

  • julia2
    julia2 Member Posts: 183
    edited June 2011

    Chey, So sorry for your loss, and I can't begin to say how I feel about Rick's doctor.  Be strong.

    Julia 

  • kittycat
    kittycat Member Posts: 2,144
    edited June 2011

    Hi girls!  Long time, no talk.  I hope you're all doing well.  I've been busy, working and doing stuff.  I had my bone scan and CT scan of my abdomen last month.  Everything came back clear!  YAY!!!  The pain in my leg has subsided.  I really wonder what all this chemo and rads did to our bodies.  I'm sure it will take a while to get back to "normal" ... whatever that is anymore!  :)

    We did the Susan G Komen walk in Las Vegas.  My survivor friends and I had about 35-40 people on our team.  One of my friends got stuck trying to fly back to Vegas and didn't make the walk.  There were a ton of people there.  We had these really cool t-shirts made up for our team, The Pink Ribbon Mafia, "Going Gangster on Cancer!"  My mom and cousin took the short cut without telling us and ran into some reporters.  They got on the news.  Afterward they kept saying that they wanted my husband interviewed because he designed the shirts!  WHAT???  Even my husband thought that was the most ridiculous thing he's heard.  It's a breast cancer walk and I had breast cancer... TWICE!!!  And I've done public speaking for Susan G Komen.  Oh well, whatever.  I had a lot of friends there that walked for me and that made me feel really great.  Even our friend Joe walked with his neck brace (he broke his neck a few months ago).  He had surgery and is doing better.  Thank God he's alive!!!

    One of my survivor friends here in Vegas has taken a turn for the worse.  She has stage 4 BC (triple negative).  She's had BC twice and has liver mets.  She's been struggling since last November.  Our onco has put her on every chemo imaginable.  She is no longer getting chemo and has hospice coming to the house.  I am sooooo sad for her and her family.  She is a wonderful person, very graceful and composed.  Her husband doesn't think she will last much longer.  I hate cancer!!!!! 

    I was supposed to have my hysterectomy/oopherectomy on May 18th.  2 days before the surgery, my obgyn's nurse calls and says the gyn onco got "called out of town" and they needed to reschedule my appointment.  It wasn't an appointment, it was surgery!!!  So, I did the crazy patient thing and went to the gyn onco's office to confront them.  They offered me nothing!  Ugh!  I had already gone to the hospital twice to do paperwork, labs and x-rays.  They wanted to reschedule it for June 6th, but I pushed it out to July 20th.  We have a vacation planned for July 4th and I don't want to cancel it again.  I've canceled the same trip the last 2 years because of breast cancer. 

    It's good to get caught up with everyone (although I must admit that I need to read the last 3 pages).  I have to go to bed because I'm seeing my plastic surgeon in the morning to deal with my poor hardened foob from radiation.  I'll probably need surgery to fix it.  I'm going to ask if I can have it done while I'm under for my hysterectomy.  Doesn't hurt to ask. 

    I love you gals and miss you!!!!  :)

  • kittycat
    kittycat Member Posts: 2,144
    edited June 2011

    Chey, I am so sorry to hear about Rick.  This must be incredibly hard for you and your sister.  It has been a tough road and your family will be in my thoughts and prayers. 

    Jackie, I'm sorry to hear about your scans.  The not knowing is terrible, but I'm hopeful that it is nothing.  The scans can show stuff that is nothing.  My sister had a bone scan over a year ago that the doctors were certain was a chest wall recurrence.  She had it biopsied and it turned out to be nothing.  So there is hope.  You will be in my thoughts and prayers, as well.

    For those of you who are starting chemo, we are all here for you.  It was a tough road, but doable.  Keep hydrated (even if water tastes yucky).  Find ways to flavor your water or drink smoothies.  Eat, even if you feel yucky.  It helps with the nausea.  And take your meds to stay on top of the nausea.  Ask questions if you are uncertain about anything.  Don't feel stupid or crazy if something bothers you.  Trust me, I am crazy patient!!!  Squeaky wheel gets the grease!!!

  • toni30
    toni30 Member Posts: 252
    edited June 2011

    Hi Sisters: Just checking in to say hi. Caught up on the ups and downs of everyone - what a CRAZY year it's been, huh?  I was at a meeting today with two survivors - one for 29 years and one for 32 years, so I was inhaling their good karma and I send it your way.  My hair is back - it looks old-ladyish but what the hell, I'm not complaining. Otherwise I feel great, healthy, knock on wood.  I have gotten active with National Breast Cancer Coalition which is pushing for a cure by 2020 - about time, huh?  For the newbies on chemo - my advice is: take any drugs they give you and don't be a heroine.  You are ALREADY a  heroine, so you don't have anything to prove!

  • JFV
    JFV Member Posts: 795
    edited June 2011

    Hey Toni and Kitty !  So good to hear from you !!!!!!!  My hair is slow growing Toni.  I love, love, love the idea of a cure by 2020.  Let's kick cancer's b*tt !  Kitty you are just so strong !  You impress the heck out of me.

  • DesignerMom
    DesignerMom Member Posts: 1,464
    edited June 2011

    Kitty!  Toni!  So good to hear from you!  You both sound like you are busy getting on with life.  Good for you!

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2011

    Hello, my lovelies.  Glad to see that we are all busy getting on with life. Prayers continue every day for everyone's good health and happiness.

    Just wanted to tell you that today my best friend, Karen, participated in the annual Alaska Run for Women in Anchorage. She walked in honor of me and all the women of the June 2010 Chemo Group from bc.org.  More than 7300 women took part.  They raised money and awareness...hopefully both will save lives. 

    Love you all.  Bon

    PS/ Chey...let us hear from you to know how your dear sister is doing. We are all so terribly sorry for your loss.

  • TMarina
    TMarina Member Posts: 692
    edited June 2011

    Renee, toni, kitty--good to hear from you!  Hope more ladies check in to let us know how you are doing.

    My hair is getting some of it's blonde color back!  I got it cut a few weeks ago to shape it up better.  Mostly straight, but some weird waves that are hard to tame down!  A while back I lost some eyelashes again, and then they all grew back, and today I lost a few lower lashes!  I was hoping I wouldn't lose any again!  Hopefully it was just those few.

    I still don't sweat as much as I used to--must be a menopause thing?  I can get by with a cheap deodorant, when I used to have to buy the expensive clinical stuff.  Also the hair on my legs takes longer to grow and is more sparse.  Just weird little things that have changed!

    I have been searching for a mastectomy swimsuit. Land's End has some, but of course they are too small.  I hate to order from a store I can't easily return to, but I might have to.  Monday I'll call the place where I got my bras and prosthesis to see if they have any my size. I remember seeing a small selection there.  I don't swim often, but I'd like one for the hot tub when we go on vacation in July!  And I might start using the pool at my daughter's apartment building--good exercise :)

    My grandsons are doing great!  I'm not needed as much for babysitting so I have had some time to do other things, like volunteering at church again.  The children's pastor is a friend of mine and I help her with her copying and such.  I have also been getting out for lunch with some friends. I'm not looking forward to going back to work in Sept.!

    Please say a prayer for my dd's best friend.  She is 19 and waiting for biopsy results for Melanoma.  The first test took several weeks and they think it might be melanoma, but needed another sample to test. She had more removed from her leg on Monday.  She is leaving in about 2 weeks to go to Asia for a month on a mission trip.  I'm praying for B9!!

    Take care ladies!

    Tina

  • mimi9186
    mimi9186 Member Posts: 127
    edited June 2011

    Hi Ladies,

    Joan, a little birdie told me it was your birthday this weekend. HAPPY BIRTHDAY! my friend.

    Tina, will be praying for your DD friend. Way too young to start this game. I find the hair on my legs is very sparse too.  That goes for my head too.  The hair is just so sparse you can still see my scalp.  I am going wigless anyway.  People stare a little because of the hair, the compression sleeve and glove too.  I feel like a walking advertisement "I had breast cancer."

    Bon, tell Karen THANK YOU from all of us.  It is an honor that people so far away would do walks for us.  We appreciate it.

    It's so good to hear from group members.  Keep us updated and check in more often.  Life is good these days.

    Love and Hugs, Mimi

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2011
    JOAN....Another Birthday?  HOORAY!!!! Happy Birthday...and many, many more!!!!  Hugs...Bon
  • kittycat
    kittycat Member Posts: 2,144
    edited June 2011

    Happy Birthday Joan!  Here Here for many more birthdays!!!

    Bon, that is so nice that your friend walked for us.  How awesome!!!

    I'm going to need another surgery after my hysterectomy to fix my hardened radiated boob.  My PS is going to cut the capsule and add Alloderm.  Then it will look more normal and I won't be so lopsided.  I'm having the surgery August 30th.

  • Haljen
    Haljen Member Posts: 45
    edited June 2011

    My husband started treatment June 8th. TC (taxotere/cytoxan) 4Tx-3 weeks apart. Yesterday was his first at home neupogen shot and last night he was in such immense pain all over his body that he had to resort to thy oxycodone which he hates! Tomorrow is another neupogen shot and I hope it is not as bad! :( He says this is the worst side effect so far. I am not sure if it is bone pain or just joint pain? I see some of you recommend claratin. His onc never mentioned it. Today he is so fatigued, he is resting.

  • JFV
    JFV Member Posts: 795
    edited June 2011

    Hi Ladies! Thank you so much for the birthday wishes !!!!!!  I hit the big 5 0 today. Considering where I've been I am happy to be 50.  We had an oversized family party yesterday.  It was fun.

    Good to hear from everyone.  Tmarina have you looked at llbean suits ?  They have free shipping and returns. JCPenney ships free sometimes.  Sometimes you have to have it shipped to the store.  I live in a beach town and usually have more than one suit.  I rely on Land End and Llbean tankinis alot because I can get a different size top and bottom.  Glad you are planning on soaking in the hot tub!  My hair on my head is coming in very slowly.  I seem to have had some extra hair grow on my body this past week.  I had eyebrow hairs growing really low on my upper lid.  Also my legs seem more stubbly.  Armpit hair is slower than before chemo which makes me happy.  I have also lost and regrown eyelashes a number of times.  Every few weeks I think I need to buy new mascara because it's not coating my eyelashes.  Then I realize it's not the mascara it's the lashes.

    Bon- tell your friend she is wonderful for walking for us. 

    Halijen-  So sorry you must go through this with your husband.  Best wishes.  I have heard people get relief from claritin.

  • Haljen
    Haljen Member Posts: 45
    edited June 2011

    Happy Birthday!



    Thanks for the advice, I have been reading about it in the threads and am going to pick some up this afternoon along with a NEW toothbrush for him! <3</p>

  • TMarina
    TMarina Member Posts: 692
    edited June 2011

    Haljen--I, too, had  a lot of pain from neupogen and Neulasta shots.  I alternated ibuprofen and Tylenol every 2 hours and that seemed to work for me.  I started it before I even got the shot, so it was already in my system. Taxol gave me even more bone/joint pain and for that I took percoset.  The pain from the shots is the bone marrow being stimulated--the pain is actually in the bones!

    JFV-- Happy Birthday!!!!  Aren't birthdays wonderful?! Laughing  I'll look at LLBean--I had forgotten about them.

    Kitty--sorry about more surgery!! Hoping that will be the last if it!

    Bon--Yes!  Thank your friend!  That really touched my heart--sorry I forgot to mention it before!

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