November 2011 Rads

Options
12021222325

Comments

  • ptdreamers
    ptdreamers Member Posts: 1,080
    edited March 2012

    I agree with Natters, it sure seems scary. Best of luck rn4babbies on your surgery and figtn4fam on your tests.

  • Flautalee
    Flautalee Member Posts: 118
    edited March 2012

    Hi everyone,

    I've been reading your posts after posting a little bit in the Fall/Winter. I had my radiation ex (28) in Dec and Jan but I think that your group meets my needs, so I'm...,back. I have a question. Is it normal to have most days be ones where you want to stay in bed the entire day? Fatigue, I guess. I just started a very light walking program, hoping that the exercise might help. What has your experience been post-chemo and post-radiation? Best to everyone, Lee

  • Flautalee
    Flautalee Member Posts: 118
    edited March 2012

    Hi everyone,

    I've been reading your posts after posting a little bit in the Fall/Winter. I had my radiation rx (28) in Dec and Jan but I think that your group meets my needs, so I'm...,back. I have a question. Is it normal to have most days be ones where you want to stay in bed the entire day? Fatigue, I guess. I just started a very light walking program, hoping that the exercise might help. What has your experience been post-chemo and post-radiation? Best to everyone, Lee

  • kdajay
    kdajay Member Posts: 90
    edited March 2012

    Flautalee - I do know that it is hard after treatment because everyone thinks you should be back to "normal" and it is not like that at all. It takes some time to come to terms with everything you have gone through and to discover what your new normal truely is. sometimes after the anxiety of chemo and rads not to mention everything that goes with it, people get depressed. What you are describing sounds more like depression than the fatigue from treatment, but I am not a doctor. If you are taking any medication, sometimes the side effects can cause the feelings you are having. In either case, I would tell your doctor how you are feeling and see what their suggestion is. Keep us posted...We are here for you.

  • rn4babies
    rn4babies Member Posts: 409
    edited March 2012

    Natters - Unfortunately, my grandmother passed away yesterday morning and the funeral is on Wednesday so  I will be having my surgery on Friday as planned. He is doing a SNB this time. These are ER/PR+, HER2 - tumors so that's good. I see the surgeon tomorrow AM to discuss the MRI results and hope he has the Oncotype score back.  I'm sure I'll need to continue my Tamoxifen. I started it on February 1st and have had no intolerable SE's yet. Occasionally my face and ears get really hot for a few minutes but it is better than the terrible night sweats I had before I started taking it.

    Now I'm just hoping and praying for clear nodes and no chemo!

  • Flautalee
    Flautalee Member Posts: 118
    edited March 2012

    Kdayjay---Thank you so much for responding to my question. I think also that part of my "fatigue" is depression. I'm on meds for this and am also seeing a therapist who is wonderful. But I guess I don't have the right cocktail of depression and anxiety meds yet.. Unfortunately, because of all of this, one of the pharmacists knows me by name. LOL! She's very sweet. I asked her about the fatigue and the fact that I only feel normal if I take a 12 hour real Pseudoephidrine and 200 mg Cafeine pill in the AM and in the afternoon another 200 mg Caffeine pill. She said this OK if it makes it possible for me to function. She said the profound fatigue is normal. Fortunately, I normally have low blood pressure--I've noticed getting higher since I started the real Pseudofed. (When I had my mastectomy last July, I wasn't permitted any additional pain medication because my BP was about 80/50. So I just got up and walked around for a while and my BP came up.) I have to say that I woke up feeling good for the first time in a while. I started a very gentle walking program 2 days ago. Today I went around our circle 5 times. It has trees in the middle that my children loved to climb on until they got to big. 11 times around is one mile. Tomorrow I will aim for 6 times around the circle. Thank you all for being behind me, Lee

  • Natters
    Natters Member Posts: 361
    edited March 2012

    rn4babies - so sorry to hear about your grandmother. You have so much going on this week, it's insane. I am really glad to hear about the ER/PR+ and that Tamox is treating you OK. I still get night sweats occasionally but not often enough that I want to go off it or try Effexor. Fingers crossed on the oncotype now. I'm sure you've been doing your research about the SNB and all that entails. I'm wishing you no nodal involvement and a fast recovery.

    Do you have something nice planned as a treat for yourself afterward? A video you haven't had time to watch, and maybe something special to eat? You definitely need to be good to yourself right now!!! If you ever come into town for any special tests or whatever, let me know if you want to get together and I will buy you lunch or dinner or what have you. You deserve some pampering these days!

  • Natters
    Natters Member Posts: 361
    edited March 2012

    flautalee - my friend that had chemo + rads is still battling fatigue many months later (she had rads a couple months before me). I didn't have that debilitating, fatigue but I did struggle to get back into shape for a good 6-8 weeks, even without having had any chemo at all. My RO said that he only radiated a "clinically insignificant" amount of my lungs, but let me tell you, it took me a lot longer than normal to get my wind back this winter. It's so hard to be patient with this process and allow our bodies time to heal, eh? Maybe by "clinically insigificant," he meant that I wouldn't end up in the ER with radiation pneumonitis.

    I still have some pretty significant swelling (edema) and my skin still looks weird (darker + peau d'orange) on that side. My MO told me that the edema should go down within the year but that my skin may remain discolored even longer than that. I can live with these SEs - it still beats having my skin peeling off from rads. That breast is still a bit sore and tender, though, which makes me dread my next mammo.   

  • tvacrat
    tvacrat Member Posts: 60
    edited March 2012

    rn4babies - I'm so sorry for your loss. I hope you have wonderful memories of your grandmother to help ease the pain. I hope her passing was peaceful. The MRI results are encouraging. I hope the oncotype score will allow you to skip chemo. I think they should do that test for all of us diagnosed with DCIS. Maybe then they'd have a better idea of who needs rads, too. Our prayers are with you this week.

  • tvacrat
    tvacrat Member Posts: 60
    edited March 2012

    flautalee - I didn't have chemo, I finished rads on Dec 14th and I've always been pretty active, despite two knee replacements. But there are still days when I feel wiped out and it's an effort to get moving. But I think if we keep pushing through it, we'll find ourselves more able to move on. It can get discouraging, though. Hang in there. Are those trees budding in this warm weather?

  • kdajay
    kdajay Member Posts: 90
    edited March 2012

    Rn4babies I am so sorry for all the bad stuff you are going through right now. Keeping you in my thoughts. (((((((HUGS))))))))

  • Natters
    Natters Member Posts: 361
    edited March 2012
    rn4babies - just wanted you to know that you were in my thoughts today. Best wishes for a speedy, uneventful surgery and clear nodes on the SNB! Also a very low oncotype score, because you have been through enough in the past year. Treat yourself well this weekend -it sounds like you are used to being a caregiver but it's important to take care of yourself, too, especially now.
  • rn4babies
    rn4babies Member Posts: 409
    edited March 2012
    Natters - I appreciate so much that you have been thinking of me. I feel as if I know you personally.... I had my surgery yesterday with clear margins and nodes! Yeah!  I have an approx 9-10 cm incision from my armpit across the breast. I haven't seen it yet but that's the way he described it. The surgeon hasn't mentioned chemo again but it could be because of my reaction the first time he did. I have an appt with my MO on April 26th. He would be the one to tell me what the recommendation is. I don't know if they'll move that appt earlier or not. I'm still taking my Tamoxifen with only the occasional hot flashes as a SE. At this point, I can't believe I was considering NOT taking it. This was also a strongly estrogen positive bc so I'm more than happy to take it now. I'm just relaxing at home catching up on Dr. Phil and maybe a Lifetime Movie or two....lol....I never get to watch daytime TV since I work so much. I'm planning on going to the movies on Monday to see the Hunger Games with my co-workers. I read all 3 books so I'm looking forward to seeing the movie. Thanks again for thinking of me. I'll keep you updated with my treatment plan after my appointments.......I will be thinking of you and praying for a normal mammo for you in June!
  • kdajay
    kdajay Member Posts: 90
    edited March 2012

    Rn4babies good news about the margins and nodes. You sound in good spirits with everything you have been through! Keeping you in my thoughts.

  • tvacrat
    tvacrat Member Posts: 60
    edited March 2012

    rn4babies - super news! I hope you enjoy your "time off." And I hope the news continues to be good - a low oncotype score and no chemo. 

  • Natters
    Natters Member Posts: 361
    edited March 2012

    rn4babies - that sounds like a pretty big incision but CLEAR NODES and CLEAR MARGINS??!! That is definitely a cause for celebration!!! How did you find out so quickly about the clear margins? I thought they made us wait for a final path report on that? That is SUCH good news!!!! What a relief!!

    I can't imagine waiting until April 26th to find out if you need more than rads. Can you get your hands on your oncotype score before then at least? As for your reluctance to take Tamox, I can totaly relate because I was super reluctant on my rads and put it off 2 months. Here's hoping that I don't regret that decision and lose that breast. I will sleep a lot easier after a clear mammo in June. 

    I read all the Hunger Games books, too, and I cannot wait to see the movie. I would have gone this weekend but the girl I'm seeing now wants to wait until she reads the book, though. All weekend long, though, I kept reading things on Facebook about how good the movie is, and how it's not a disappointment after reading the book. That will be a great outing for you tonight. 

    Thanks for the update,

    Nat 

  • rn4babies
    rn4babies Member Posts: 409
    edited March 2012

    I had my mother measure the incision yesterday and it is a little over 6 inches which is actually 15 cm! I'm used to using cm since I work in OB......lol It is much longer than I thought. The surgeon told me he got clean margins several times. I think they sent it to pathology during the surgery. As for the Hunger Games, I guess we are going to see it on Saturday night, now. My best friend said it was great and she didn't read any of the books.  I'm looking forward to it. My brother is here from Colorado (he came in when my grandmother got sick) so I will be going to the airport tomorrow for his flight back. I'll be back to work before I know it! Ugh!

  • Natters
    Natters Member Posts: 361
    edited March 2012

    That is really long but I guess it's good if that's how your BS got those clean margins. I remember with mine they also sent it across the street to Pathology at the Hillman while I was still in the OR, but they made me wait until the final report before they were able to confirm that I would not need re-excision. And I remember thinking that the wait was excruciating, even though I had specifically asked my BS for wider margins so I wouldn't have to be cut twice. Hey, it's nice that you got to see your brother even though it wasn't the happiest of occasions for him to be flying home. I hope you don't get stuck in any Pittsburgh traffic tomorrow (i.e., not driving in between 6-9am or driving out between 3:30-6pm).

  • RealtorJackie
    RealtorJackie Member Posts: 91
    edited March 2012

         rn4babies:  I am so glad everything is going well for you.  Just keep your chin up, and relax while you have the time off.

  • Joan811
    Joan811 Member Posts: 2,672
    edited April 2012
    Hi all,
    am catching up - glad to see you back here, Lee.  Yup it is really hard to get the right drug combo after BC and treatments....I know mine is not working for me right now but am experimenting with the times of day to take pills before I change things.  good luck...exercise should really help to gain energy.
    rn4babies - so glad your surgery is behind you.  I wish you a good recovery and uneventful pathology reports.  I am so sorry about the loss of your grandmother during such a stressful time.
    BC is no respector of life's events.....it amazes me what the women here go through while dealing with BC. As if life itself didn't bring enough.....
    I will check back to see how everyone's doing.
    It's late and sleep is supposed to be important....
    Nite all.
    Joan
  • tvacrat
    tvacrat Member Posts: 60
    edited April 2012

    I had my first mammo post-treatment today. I spent four hours (!) getting films, waiting, getting more films, waiting, until finally they told me I was good to go for another 6 months. That was a great relief because they thought they saw more calcifications and I was already trying to figure out what my options were. My husband was going to take me out for a drink, but we ended up at Smashburger when the other places were too crowded.

  • Joan811
    Joan811 Member Posts: 2,672
    edited April 2012
    congratulations on the good visit and clear mammo.
    What a relief!
  • Natters
    Natters Member Posts: 361
    edited April 2012
    tvacrat - contrats on the clean mammo. I had figured mine might take a couple hours but....FOUR? Yikes. I guess I better clear my calendar that day, just in case. Did it hurt like hell? My rads breast is still very swollen and tender. Sometimes it hurts when nothing is even touching it, never mind benig squeezed and compressed. I am dreading the first mammo but also sort of looking forward to it, just so I can stop worrying about a recurrence.
  • kdajay
    kdajay Member Posts: 90
    edited April 2012

    Congrats on the clear mammo! Here is hoping we can all post such good news.

  • tvacrat
    tvacrat Member Posts: 60
    edited April 2012

    Thanks for all the support. It really is a great relief! Natters, I was anticipating much more discomfort than there was. The technician actually put some kind of padding on the machine before she positioned me during the first go-round and it didn't feel any different than all the previous mammos. When they brought me back to do more, they left the padding off and it still didn't feel too bad. Of course, I was more focused on what I was going to do when they told me there were more calcifications to deal with. But I guess what they saw were artifacts and not anything to be concerned about. Phew!!

  • Natters
    Natters Member Posts: 361
    edited April 2012

    Major phew!!! Congratulations!!!

  • Joan811
    Joan811 Member Posts: 2,672
    edited April 2012

    Nat,
    I don't have post-rad swelling; but as the swelling has gone down a lot, the pain is increasing.  My scar areas feel tender and bruised.  There are so many lumps in there, I wouldn't find a new lump - no chance.  But as far as the mammos, after all the wacky things I've been through, I don't think the next mammo can be any worse.  Remembering the mammo scan with the needle in place for the guide wire....hideous!
    Here's to good mammos for everyone here in 2012.
    Hope things are going well for you, Nat.
    Joan

  • Natters
    Natters Member Posts: 361
    edited April 2012

    Well, for the mammo-guided wire placement, I had them give me drugs (Ativan) so I was actually pretty chill about the whole thing. I don't think I can get anyone to prescribe me a pill every time I need a mammo, though. 

     I am doing fine, thank you, Joan. Feeling very strong and fit again, despite some little aches and pains that I can luckily mostly ignore. Which is a good thing because I'll be racing in Hong Kong in July :)

    It's a pain in the butt about the swelling because I still can't fit into some of my bras and tops, but really that's such a small thing to complain about. I will be very relieved and able to fully relax into my Spring/Summer after that mammo in June. 

  • Joan811
    Joan811 Member Posts: 2,672
    edited April 2012

    Natters,
    Hope all is well.  Sounds like you are doing great.  I remember when you first checked in to BCO and had the same fears we all have - will this beast take over our lives???  I feel very fortunate to have my life back even though there are a number of adjustments.  It sounds like you are doing the thing you love.  Enjoy your trip to Hong Kong.  Awesome!
    I am traveling at the end of the summer and looking forward to it.
    Enjoy the spring!

    Joan

  • Natters
    Natters Member Posts: 361
    edited April 2012
    Fingers crossed today for rn4babies, that her visit with the MO goes well!

Categories