April 2011 chemo

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  • scc218
    scc218 Member Posts: 163
    edited May 2012

    You got that right, Bernie Ellen!

  • KiwiMum
    KiwiMum Member Posts: 704
    edited May 2012

    Suzy - had my Zometa infusion a couple of days ago. It was pretty uneventful.  It only took 20 minutes via IV and then I was back at work feeling fine.

    I think maybe I had some mild SE's on night two. I was awake much of the night with flu-like chills.  By the morning they were gone and nothing since.

    The worst part was being back in the room where I had chemo. The best part was seeing my nurses again.  The same two ladies who gave me chemo were there and it was great to catch up.

    I had forgotten all those horrible chemo room smells!

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited May 2012

    KiwiMum, I had a check up with my MO today and I went into the chemo room to say hello to the nurses. You are right. It was nice to see them again, but it felt strange to be back in that room.

  • axtella
    axtella Member Posts: 88
    edited May 2012

    Just checking in. It took me an hour to catch up. I have been doing pretty good. All my scans and mammo was clear. I was put on Femera and doing good. The only thing I have not been able to shake is the lasting joint pain! Anyone else have this?

    My hair grew back brown and very curly where is was blonde and fairly straight. Crazy stuff!!!

  • scc218
    scc218 Member Posts: 163
    edited May 2012

    Kiwimum -- Glad it was relatively uneventful.  It must have been quite strange to be back in the chemo room for an infusion.  I can only imagine all the things going through your mind at the time.  I still haven't gotten my teeth issues resolved, so the Zometa is on hold for now.  I guess I need to get on the stick.  Part of the problem is that we are volunteering as campground hosts for 3 months in an area where I don't know the doctors and dentists, so I have to find somebody to go to. 

    Axtella -- Sorry to hear about the joint pain.  My only issues with the Femara are hot flashes and night sweats, but they're not terribly severe -- not bad enough to switch medications.  Hope the joint pain problem goes away for you.

  • geocachelinda
    geocachelinda Member Posts: 223
    edited June 2012

    Hi, I have been put on Arimidex and one of the side effects is joint pain.  I have been having a lot of that, plus the hot flashes, plus being exhausted all the time.  I feel so guilty because my daughter wants to do things and all I want to do it sleep or lay in bed.  She gets so angry with me and just doesn't seem to care or understand...

  • profbee
    profbee Member Posts: 858
    edited June 2012

    Hey pals!

    Linda...so sorry to hear about your daughter.  Yeah, it seems like everyone thinks crisis is over, but I'm still so terribly tired too.  I'm having a hard time motivating--still getting all my work done, but it always feels so last minute and stressful.  I hate that.  I can't remember how old your daughter is.  Maybe she's got something else going on?  ((hugs))

    Annie, my hair is curly too!  I HATE IT!!!!  It's ridiculous looking!  I can't believe I'm going to type this, but I think it may have looked better BALD! Sheesh. 

    Love to you all.

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited June 2012

    I agree about the hair. 

     

  • scc218
    scc218 Member Posts: 163
    edited June 2012

    Linda -- I'm so sorry your daughter isn't being more understanding.  You don't need more stress; you need compassion and understanding.  Like Profbee said -- maybe something else is going on?

    Profbee -- I HATE my hair, too!  Very curly and short and ugly.  I actually think I liked the bandanas better.  But I just keep telliing myself I'm just happy to be alive....and the hair will eventually grow back to something better than this....I hope!

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited June 2012

     Give a thought, say a prayer or thank you of the men and women of D-Day today. THANK YOU FOR YOUR SERVICE!!!
    June 6, 1944, 160,000 Allied troops landed along a 50-mile stretch of heavily-fortified French coastline to fight Nazi Germany on the beaches of Normandy, France. General Dwight D. Eisenhower called the operation a crusade in which "we will accept nothing less than full victory." More than 5,000 Ships and 13,000 aircraft supported the D-Day invasion, and by day's end on June 6, the Allies gained a foot- hold in Normandy. The D-Day cost was high -more than 9,000 Allied Soldiers were killed or wounded -- but more than 100,000 Soldiers began the march across Europe to defeat Hitler.

  • Elizabeth1889
    Elizabeth1889 Member Posts: 1,036
    edited June 2012

    Hi everyone, I am exactly one year PFC today. I never thought this day would come. I do not especially like the hair I have now, but I am so happy to have any hair at all. Today was an especially good day for me because the medical center where I received my surgery, chemo, and rads had a cancer survivor celebration and luncheon today. There was an inspirational speaker who is now 55 years old, but he lost his right leg and left lung to osteosarcoma when he was in his teens. He does every kind of sport imaginable now and he never gives up hope. I am guessing he has bad days and exhausting days just like all of us, but we are all in this together for the good and the bad times. Thanks for your support.

  • scc218
    scc218 Member Posts: 163
    edited June 2012

    Beautifully said, Elizabeth!  And congrats on the PFC! 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2012

    I think I was the last straggler to finish chemo in our group! My last one was May 23.
    I am going in next week for my one-month-out checkup and blood tests. It's weird to be done.

    I have a tip for taming the super curly, poufy hair: After shampooing, towel dry and apply a ton of extra-hold mousse.
    Then part your hair and comb it into shape. Let it air dry, do not blow it dry.

    Voila, an actual hairstyle!

    (p.s. I have avoided this new BCO for the last month because I feel so dismayed and betrayed by the damage they did to it.)

  • geocachelinda
    geocachelinda Member Posts: 223
    edited June 2012

    I like my hair!  It is curly but waves too and all I have to do is brush it and it looks like I went to the salon and had it done!  I have to color however because it came in mostly white!

  • KiwiMum
    KiwiMum Member Posts: 704
    edited June 2012

    Agree Windlass.  I do not like this new layout at all!

  • scc218
    scc218 Member Posts: 163
    edited June 2012

    I agree, Windlass and KiwiMum.  Hate the new layout and tend to stay away.  Thanks for the hair tips, Windlass.  I think I'll try that with the mousse. 

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited June 2012
  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2012

    Just dropped in to say "hi." Hope the silence on here means everyone is doing well.

  • sarahlou1967
    sarahlou1967 Member Posts: 153
    edited June 2012

    Hi Ladies,

    Its been a long while since I posted on the american site and on this thread, (was known by name of sarahsweety and live in the UK), but just wanted to bring you all up to date with my story and hope it inspires and brings some hope, I did chemo (last april)/surgery/rads finishing Jan this year, I already knew I had spread to lymph nodes and both lungs, basically as of the last ct scan done this May the results are and I would like to quote the dr "The results of your ct scan are very good, the stuff on your lungs is unchanged and is the same as a year ago, infact I'm not convinced that it is cancerous nodes on your lungs it could just be scar tissue from the chemo or from an unrelated flu/chest infection, the rest of the scan is clear!!!!!! As you can imagine this news has blown me away, as I've spent the past year since dx thinking that I had it on my lungs, anyway ladies (profbee, windlass, berniellen, merilee, anyone else who remembers me) just wanted to bring you up to date, sending you all big hugs and wishing continued good health for all.

    Love and light

    sarah xxx 

  • KiwiMum
    KiwiMum Member Posts: 704
    edited June 2012

    That's the best news Sarah!  I am really really happy for you.

    Thanks for coming on and sharing.

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited July 2012

    Really happy for you Sarah.  Often think of all the ladies.

  • profbee
    profbee Member Posts: 858
    edited July 2012

    Yay!  Sarah!  I immediately knew it was you by your profile pic!  I'm so happy for you!  Yay!!!!  Seriously, how often do we hear about coming down from a Stage IV dx?!  Ah, this is a reason to smile tonight, my pal across the pond!  Sending you a great, big ((HUG))!!!

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited July 2012
  • pawprintgirl24
    pawprintgirl24 Member Posts: 173
    edited July 2012

    hi all! i never come here anymore..too busy on facebook!! lol!thats great sarah!!! sorry i never updated yall on my surgery.but everything was fine. thank god!! i dont think i could've went through all of that again!!!not a year later!! wow give me a break for once!! gees!!! now just dealing with these hot flashes in this summer heat!going to the mountains in a month to celebrate our 20th wedding anniversery!! can't wait!!i hope everyone is doing great!we made it!! i go the 3rd or the 8th for my 2nd mammagram! crossing my fingers!!! :)

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited July 2012

    Pawprint, great to hear you are doing so well.

    I had my one year mammo in March and have just had a check up.  all looking good 

  • profbee
    profbee Member Posts: 858
    edited August 2012

    Love you all!  I'm busy as HELL, but I keep reading up on you!  Miss you!

  • BernieEllen
    BernieEllen Member Posts: 2,445
    edited August 2012

    Hi Profbee, glad to hear you are sounding so good.

    I'm doing well just a dodgy hip and breast pain.  Hubby says that's no excuse for sitting around.

    Love B. 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2012

    So glad to hear all of this good news from everyone! Sarah - I am thrilled for you. Congrats :)

    I am going in for a DIEP in a few weeks and getting nervous. Anyone else done recon?

  • seeay
    seeay Member Posts: 56
    edited August 2012

    Hi All!

    It took me forever to get caught up on our b oard, as I've been away from it for so long. It was so nice to read above where everyone is in their "new normal" lives. Sarah-that was such terrific news! Windlass - I had DIEP - it was difficult to make that decision, but I am happy I did. Are you doing one? I can't recall. Just this month, I had my nipples and tattooing done. I really didn't care about doing either one. The thought of someone touching my boobs with surgical tools for cosmetic purposes seemed ridiculous, but once completed, I have to tell you - something about it - makes a big difference! I had the time off, so I figured I'd go for it. It's as if I feel somewhat normal again. I was also surprised at how much feeling I have! I have all my feeling (except the nipple area) in the left, but not a lot in my right. Windlass - if you have questions, PM me, and I will be happy to answer them. 

    On another note, how does everyone feel about this new label we carry - Survivor? I am having trouble with it. I feel like the name needs to be something else. I feel as if soldiers are survivors because they made a choice. We were just handed something and plowed our way through as best as we could. When people say I am an inspiration, I think, "really? I just did what I had to because I had no other choice." At my place of employment, I have become the face of BC. It's not who I am, nor whom I want to be. Does anyone else get this feeling?? I just turned down opportunities for 2 speaking engagements. As an educator, I know it's important to educate, but...I don't know...maybe I'm just not there yet. Thoughts?

  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2012

    Hi Seeay!  I'd love to learn more about your DIEP. How long before you were up and back on your feet? How long did it take to feel like it was your breast again? I'm amazed you say you have feeling in the skin. Is that the skin they moved/grafted?

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