Illinois ladies facing bc

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  • [Deleted User]
    [Deleted User] Posts: 4,011
    edited August 2013

    Navy - I am so sorry your trip was cancelled. BUT...just think...December we'll all be freezing our butts off and you'll be basking and soaking up some Vit-D!

    Lisa - Welcome! Wow...four kids! Best wishes to you with your journey. We're here 24/7.

    Irene - How sweet of DH and the kids! Glad your milestone was fun!

    ------------------------------------

    Wow...it sure is a blustery one out there. Hoping we avoid weather related disasters here in the forest/hard hat area.

    Have a great day girls!

  • donnadio
    donnadio Posts: 674
    edited October 2010

    Lisa..  here for you and know you will find all the support you need here. Have a history of BC ib my family an d BRCA 1 that is a question mark but considered a mutation. You sound like you have a wonderful family and support system!!!!  always here for you.

    rene.....awwwwwww for your4 huby giving you a surprise 5oth!!!!Just wonderful!!

    Driving downtown for a Dr's appt. am I nuts or what? Sleep is still an issue.. chemo took it away, i am still struggling. Went to Ambien last night as I am done trying to do it naturally. I wake up every 3 hrs and accumaltively My legs abd body is weak.This morning was the first morning i could do excercise as i slept. AM I the only one who cannot regain sleep after chemo??? I am also goin to try Remiferen for the hot flashes, I am a very frustrated lady who wants a full night sleep.. and now it has progressed to not falling asleep.. two hours of that,.If I become addicted to sleeping pills I do not care anymore!!!! Sorry for my rant but I am sooooo frustrated and am done!!!

    Lago... good luck on tx today?

    Be safe ALL!!!

  • illinoislady
    illinoislady Posts: 46,506
    edited October 2010

    Donna....sorry to hear that you are having such problems.  Perhaps sleep meds just for awhile will help re-train your body.  It is the rare occasion when I can't sleep......but I do know it is a natural way for the body to help heal itself and drain off the stress and tension we all build up.  It is very important.....so whatever you have to do to get there....I would be willing to do  You have tried very hard to deal with it in natural homeopathic ways, but that hasn't worked out and your body needs the healing sleep --- just do it as they say. 

    Hugs, Jackie

  • gingersfavorite1
    gingersfavorite1 Posts: 134
    edited October 2010

    fever for me again today  :(

    I managed to do ok yesterday.   Rested aka:   did nothing all day, then scrapped with friends last night.     Was chilly this morning and temp says 100.5

    Waiting for a call back from my nurse/friend at the cancer center. 

  • lago
    lago Posts: 11,653
    edited August 2013

    NavyMom Really sorry to hear about your friend. Since I have been diagnosed I found out about 3 other women I went to high school with that are survivors. One sent me some scarves… so nice. Unbelievable.

    Wicked is commonly used that way in the Boston area to this day. My theory is it's from the Salem Witch Trial area. Seems  the idea of something being so good must be Wicked. Don't ask about pissa. I don't think they use that anymore but we are about a year apart in age so I knew she'd know what I was talking about.

    -------------------------------------
    gingersfavorite
    I really wish you would get better. Hope it happens soon. ------------------------------------
    Had a great day at chemo. Granted it took 5 hours but I expected that. My infusions alone took 2.5 hours. Taxotere took 1.5 hours! Nurse Ratched wasn't there so I discussed my SE with the Onc. Ratched made more mistakes than I thought. I didn't tell the Onc. I'm just dealing with Onc and chemo nurse from now on. Chemo nurse did say to page for any issue other than stuff she needs to fill out forms for. She had no problems with me paging her 2 weeks ago.  (Nurse Ratched called me down on this).

  • MsMarilyn
    MsMarilyn Posts: 27
    edited October 2010

    Question:  Is there anyone else here dealing with a reaccurance of cancer?  If so please let me know, because I have a ton of questions from a survivor's point of view.

  • [Deleted User]
    [Deleted User] Posts: 4,011
    edited October 2010

    Navy - So sorry about your friend's wife. I know it's tough...please don't lose sight of the fact that it will get easier to deal with as time goes by. After I finished chemo and rads, I had post trauma distress syndome too. I thought I'd NEVER feel normal. But in time, I did...and so have many others. We will never forget what we've been through and we'll always have a special place in our hearts for those who have dealt with this beast. Hang in there...

    Donna - Have you tried Cherry juice at bedtime? I'm sorry you haven't gotten relief. Damn girl...you deserve a good night's sleep!

    Ms. Marilyn - If I could offer advice, I would. I'm sure some of the girls here - who can - will chime in. Best wishes and hugs!

    Stephanie - I am sorry that fever is hanging on! I hope you're back to your ol' self soon.

  • gingersfavorite1
    gingersfavorite1 Posts: 134
    edited October 2010

    ok,  nurse/friend paged my onc.   He said bring her in for labs, oxygen level and chest x-ray.    Blood work was good.   Oxygen was fine.     My heart rate was 120 - that's high!     Then she called later to tell me chest x-ray showed MILD viral pneumonia.    She is calling me in a Z-pack and I will go pick that up here in a bit.

    Makes me glad that I spoke up and followed through.    That's a reminder ladies, anything abnormal needs reported!    I had been breezing through this thing on cruise control then felt like crap the last  4-5 days.    She said  "there's your first sign that there's a problem!"   LOL 

  • onward
    onward Posts: 229
    edited October 2010

    YEAH Ginger for being proactive. I cant tell you how many times I tell others to call and than three days later, I'm thinking, DUH make the call Caryn! Hopefully it will bring you back to the living.

    NavyMom: So sorry. Breaks my heart to see anyone these days with a scarf or those "knowing eyes". Let alone to see the obit and then find out it was someone you actually met.

    Lago: sent PM.

    Love to all. Onward

  • zap
    zap Posts: 1,850
    edited October 2010

    When I hear "wicked" I think of Boston which makes me think about my SIL which makes me think a dyed  in the wool Red Sox Fan.  My 3-year old grand daughter has a Red Sox cheerleading outfit.

    Stephanie, good you called!

    The wnds are so scary!  My cat is acting really odd with this weather.

    When I have trouble sleeping, Donna, I take one of those PM blue things (like Tylenol PM).  Once Wendy suggested a benadryl.  I am really sorry that is happening to you/.  I need so much sleep!

    Marilyn, I have not (knock on wood) experienced a recurrence.  I hope you get the information you need.

    Navy, tender story about the obituary and crying.  I think there is something within many of us that needs to connect with those who did not make it.  I actually went over to the cemetery where Irina is buried (in my town) and sought out her  plot.  When I saw a picture of her cat on the flowers I wept. I really did not know this woman in life.  We just need to connect.

    Take care!

    Susan

  • makmak
    makmak Posts: 374
    edited October 2010

    Hated today's winds but luckily they weren't as awful as I thought and hopefully it means I'll make it to my scan tomorrow.. so back to worrying about that instead of the weather... last time it took until 3pm to get the results.. thought I'd pass out waiting.. so hopefully I can get them by noon while getting my herceptin tomorrow.. since I'm also getting bloodwork I really need the resuts since last time my liver enzymes were going up..

    Keeping my fingers and toes and everything else crossed.. hoping I can sleep...

    By the way, another sleep aid is melatonin since that's what your body needs to sleep.. I tried taking it but 3mg which is a baby dose knocked me right out.. but then again so does alka-seltzer!!

    Good night and I'll be back to report tomorrow...

  • joan888
    joan888 Posts: 711
    edited October 2010

    Stephanie.. so glad that you got things checked out.  Get better quick.

    Laura... what is with the cherry juice?  I don't have any problems getting to sleep... but then I usually throw down one Tylenol PM every night.... works like a charm.  When I was going through chemo, my onc nurse said it was o.k.

    MakMak... I will be thinking of you tomorrow.  Stay positive.

    This wind is crazy.  Hang on to your hats, your wigs, your scarves, etc.!  Stay safe everyone.

  • illinoislady
    illinoislady Posts: 46,506
    edited October 2010
    ~ The truth is that our finest moments are most likely to occur when we are feeling deeply uncomfortable, unhappy, or unfulfilled. For it is only in such moments, propelled by our discomfort, that we are likely to step out of our ruts and start searching for different ways or truer answers. ~ send an e card M. Scott Peck
  • illinoislady
    illinoislady Posts: 46,506
    edited October 2010

    Hmmm, I was surprised by the cherry juice as well.  I have to remember though to one who can nearly fall asleep at the drop of a pin --  whatever you have to do -- is whatever works.  Is there going to be more 'wind' today.  Weather for about half the country sounded horrible.  Hope everyone does ok.

    I think our wind has lessened.....it did get down a lot of leaves......maybe we will have a few less days/weeks of having to blow them all into the ravines by us.  Dh will be happy.  He is having to do most of it.  Had to take the backpack blower in for repairs....so it is a difficult job right now with my smaller electric blower. 

    Hope you all have a fantastic day.  Good luck today Marina.  See you all later.

    Hugs, Jackie 

  • lago
    lago Posts: 11,653
    edited October 2010

    Living in a high-rise (I'm on the 17th floor) you can tell how windy it is by how fast your hanging lamps and mini blinds sway. Yes it is very windy by the lake in Chicago today! Granted I can also hear the whistling and the trees are swaying like crazy.

    I'm still going to go out and try to walk in this wind. Not sure if I will last the hour but I have the energy so I'm going to do it. My husband for some reason feels I should not go to the gym today. Wants me to take it easy after yesterday for a bit.

  • gingersfavorite1
    gingersfavorite1 Posts: 134
    edited October 2010

    fever up to 101-102 this morning.   Feel much worse.   Cough is more raspy (where it had been dry).   I have a heck of a headache and ringing in my ears.

    My longtime friend (my oncologists nurse) got me in to see him at 11:40.    I'm due for chemo at 1:00.     We'll see if I still get it.   She said my counts were good ..... so maybe (?) 

  • zap
    zap Posts: 1,850
    edited October 2010

    Marina, I am with you in thoughts.

    Lago, that os so funny....hang onto your hats, wigs and scarves.  That brings me back to being outdoors with the students.  You know how you can feel your real hair get tussled about but no feeling with the wig?  Mine was all over the place and an teacher  friend came over and straighted it out. That was impossible so I stayed in and watched from the window.  No one wanted me to lose that wig in front of 80 teenagers!

    Feel better, Stephanie!

  • lago
    lago Posts: 11,653
    edited October 2010

    Yes I'm thinking that the wind will remove some of those hairs that have fallen out but are still sticking in my head. Rather it falls outside then in my home.

    Steph I hope that temperature goes down soon.

  • makmak
    makmak Posts: 374
    edited October 2010

    Well, thanks to Lago's comment I remembered my wig this morning.. it was just too early to be leaving the house!!

    SOOOO... all is well here!!!!!!!!!!!!!!!!!!!!!!!!!   My numbers are still up.. :(  but that is now most likely due to supplements.. only one number, the other 3 are down.. AND... my scan was GREAT.. my lymph node is diminished even more.. and all the spots on my liver are still gone.. and the one left is either same or smaller.. they aren't sure because it gets tricky apparently based on timing of contrast dye from scan to scan..SOOO.. all the crazy stuff I do pays off and I'm not crazy for doing it after all.. I now scheduled an opinion with a surgeon though my Onc is against it (Susan he says hi to you).. but I need to explore.. I am also going to look into a clinical trial.. AND I get to to go and enjoy my trip to Panama on the 5th!!  What a huge relief!  My whites and reds are slowly coming back up and I have 1/4 inch of hair...

    Hope everyone is doing well in treatment.. Stephanie i hope your Dr's can help you out soon as well!!

    Relieved...

    Marina

  • zap
    zap Posts: 1,850
    edited October 2010

    Oh Marina, I jumped on the computer as soon  as I walked in and was scared to open your post and then I nearly hit the roof with joy!  Yes everything you are doing is WORKING! 

    Okay now for my huge confession.  I am very surprised our onc really remembers me and he  may be faking a "hey" for me as I have not (okay this is honest) seen him in three plus years and my cancer was four years ago.  He once told me to get on with my life and leave cancer behind me (which you all know I have never been able to do fully) and to come to see him only if I have a worrisome symptom.  I went once three years ago because my shin hurt Kiss and he sent me on my way and asked me again to get on with life.  So, I never have those routine visits you ladies all experience and dread.  I never get my blood checked and I won't until I start to get off arimidex (January 2012) unless i have a worrisome symptom. It feels good to lay this on the line.  I do  not suggest that others follow in my path (I do see the Breast surgeon annually) but this has worked for me as a Stage II cancer survivor.  When I did see him (active chemo treatment  we talked about his daughter, his father who is a Holocaust survivor and other deep topics,  I was teaching an English Lit.  Unit on the Holocaust at the time and so it was on my mind and obviously on  his as well, so that (not cancer) was the topic. We had both read Night by Eli Weisel and  When Bad Things Happen to Good People by Rabbi Kushner and so we talked about those books.

    I have so much respect for the man as I feel he has one of the hardest professions in all of life. So I am happy not to bring in things like "shin Pain" when he faces so much.  Oh Marina, I just know he was  happy to share that news!

    And Marina,  I would never contradict anything that goes against his wishes, but my friend with colon cancer that went to the liver considered a surgeon in Indianapolis who was willing to cut out the liver cancer.  I guess it is tricky but this doc does it on hard cases.  I know they generally do not do surgery on liver mets with BC, but I could get the man's name if you are interested.  I have no idea how he would handle your case, but I do know there is a doctor in Indianapolis who does tricky liver surgery.

    Susan

  • lago
    lago Posts: 11,653
    edited October 2010

    I saw a Eli Weisel lecture back in my sophomore year. Amazing man but although I understood his desire to keep people somewhat segregated (so the Jewish population and culture doesn't disappear) I don't agree with it. But that could be along discussion so I'll stop here.

  • joan888
    joan888 Posts: 711
    edited October 2010

    Oh, WONDERFUL, Marina.  I love it!

    Joan

  • navymom
    navymom Posts: 842
    edited October 2010

    Great news Marina.  Happy vacation dance for you too! 

    I go to Onc tomorrow to get Blood results and PET scan results.  ARRRRGG!

    Havea good night everyone

    Navy

  • saltykm
    saltykm Posts: 77
    edited October 2010

    NavyMom, Good luck to tomorrow!  Been thinking about you.

  • zap
    zap Posts: 1,850
    edited October 2010

    We have so much going on!  Now, Navy Mom, go get your good news!

  • makmak
    makmak Posts: 374
    edited October 2010

    Passing on the good news baton to you Navy!!  Let us know tomorrow!!

    Marina

  • lago
    lago Posts: 11,653
    edited October 2010

    BTW at the Northwestern lecture I picked up the NCCN Guidelines for Patients, 2010 version. It is available in pdf form online: http://nccn.com/patient-guidelines.html

    Might be useful for those just starting treatment.

  • ritajean
    ritajean Posts: 4,042
    edited October 2010

    Yea Marina!  A thumbs up on your news!!!!!!  Super!  You are doing the right things!  Hugs!

    Rita

  • illinoislady
    illinoislady Posts: 46,506
    edited October 2010

    Ditto

  • blackjack
    blackjack Posts: 771
    edited October 2010

    Good Evening Girls...I just want to say I am so happy for all of you who have been doing so well.

    I have not posted for a while as I too had a scare this past two week. MRI was read as possible malignancy in the good breast, off I ran to the bs and he did a FNB in his office. Waited 4 days for results inconclusive then off to have a MRI core biopsy big ouch!! and today it can back neg!!! My life was turned upside down for the past 2 weeks with md appts, tests, scans and those many phone calls. Now I am celebrating NED !! I didn't want to get anyone scared or upset so that is why I have been off for a while. But I am back and in happy mode.

    So doing all the right things to stay healthy is a work in progress. So keep up the good work girls!!! Just an FYI I would ask for copies of all your test results and get cd copies of all scans done. It makes it so much easier when you have to express over night scans to another hospital and you have them at home.

    Marina...keep up the great diet, be healthy and enjoy that well deserved vacation

    Navymom... I hope you get your vacation in soon too.

    Lago...hope you are doing well with chemo and nurse ratchet. Remember to rest. Thank you for the apt info. We are going hunting next week.

    Ginnger..feel better. Hope your temp is better. remember to push lots of fluids. my fav popsicles and Italian ice.

    Jackie... thanks for thinking of me. hugs.

    Zap.. are you enjoying the wonderful fall colors and yes Halloween this weekend!! I am going to a Halloween party. going as a flapper girl!

    Well off to bed for some needed sleep. Sweet dreams everyone....

    Remember to be healthy...be happy ..and enjoy life. Halloween is coming booooooooo to you!!!

    BJ