Lumpectomy Lounge....let's talk!
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I was so overwhelmed by the response from my Bar Show castmates when I e-mailed them before rehearsals bega to drop out of this year's show--as well as from fans, colleagues in the folk music community, and online Acoustic Guitar Forum buddies, most of whom I’ve never met but with whom I’ve corresponded. Several of the latter are bc survivors themselves, and gave me tips on how to deal with rads & AIs even before I found BCO. When I went to my annual regional folk conference (FARM) in Iowa City this past Oct. after originally having had to take myself out of consideration for showcases due to having expected to be deep in treatment, everyone was amazed and totally solicitous. (I also had a gig in that town that weekend that I was not going to miss even if it meant flying or taking the train there). People who’d previously only nodded to me in the corridors came over and sat with me during meals, insisted on carrying my instruments, asked me if I was okay--and one showcase room host made room for me at the last minute in one of her writers’ rounds. As for my circle of close friends, we’ve all been through the health-crisis mill over the past decade or so: lung cancer, COPD, scleroderma, and of course bereavement. At this point, few of them drink anymore, and of those who still do, we got through New Year’s Eve without even finishing one bottle of champagne. I guess being older, with older friends in pretty much the same boat, has its advantages.
I am very lucky to have an amazing support system. (As for family, it’s just my sister, niece and a couple of cousins--and I’ve been out of touch with most of them in the past 5 years--yet somehow the word had gotten out and they called me out of the blue). Even friends of friends have e-mailed to offer moral support if I needed someone to come along with me for doctors’ appointments or to meet for coffee after. I’m sure that there are acquaintances who’ve been scared off, but I haven’t noticed them.
I do feel embarrassed about one thing, though. About half an hour ago, two little girls came by to take orders for Girl Scout cookies. I apologized that I can’t have sugar anymore. A few minutes later, it hit me that one of them was a girl from about three or four houses down who likes to talk over the fence to our housekeeper and when she was little, liked to play with one of our cats (who passed away last year at 19) who liked to escape into the backyard. I told Bob, who replied, “You can’t have sugar. Gordy & I merely shouldn’t. Get her back here and order some chocolate thin mints.” Unfortunately, it’s 0 outside, I’m in my PJs, and I don’t know her last name or phone number--maybe my next-door neighbor does.
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Awwww, Jersey and Mel....you are so right...there are silver linings in everything and EVERY day is a day in OUR LIVES! We have to make each one count with people who count! So glad for you all even though we are not in the same location..you "get" it...and, also glad we are each figuring out what friendship REALLY is and making the most of it with the ones near who are REAL friends. We ALL ROCK!
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Sandy- precious story about the little girl and your cat...they sell for awhile so am thinking this story will have a happy ending for her..you...and, Bob and Gordy...the nice thing is that the Thin Mint cookies freeze well. (Learned this when only niece was selling them and we were helping her make her goal.)
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thanks for the tip 1step. Now she is on performatrin diet dry food, a quarter cup in the morning, and half a cup at night. Maybe I will switch the morning food to wet (Kids give her the evening meal and I'd like to keep it that way but wet will gross them out lol!)
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definitely have some amazing support. My mother gets on my nerves, but she is always there for me, as is my mother-in-law and my sisters in law's. My best friend has dropped the ball, but some other friends are definitely there for me. I have a few to drop off food all the time, which is a bit of challenge since I am both vegan and gluten intolerant! So far I haven't really needed much help, but I definitely know who I can call on if I do.
It's not like I really needed anything fro my best friend, it's just hurt me how much she has not been there. Especially ironic because she recently went on a educational trip to Israel, she came back talking about how inspirational and life-changing it was, and all these goals she has about being a better person and all the "sisters" she made. All I can think to myself is "really? This is being a better person? And do your "sisters" even know you've basically ignored your bff who has breast cancer while you are posting on FB every minute about all the fun things youre doing? I wonder what they're think of you then?" People must ask her how I'm doing? Isn't she embarrassed that she barely knows?
Sorry for venting
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Peggy...glad you resurfaced...that damn "decluttering" can be all encompassing....hope you are finding some things that spark JOY and that the memories bring peace and comfort....was thinking about you and how this past Christmas was your first without your DH...and, now you are going through your life as you "declutter"....hard work so am glad you are coming up for air every once in awhile.
You are right...we are "sisterfriends" and the real deal. It is heartbreaking to learn that close friends really aren't sometimes and then, those who you didn't know were so important turn out to BE real...people grow and change and often grow apart...it isn't personal a lot of the time, I don't think...it just IS. Keep the good and push the bad or hurtful to the curb...we all now realize for sure....life is too short!
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MLP3- LOVE the "meatheads"...what could be better than that?
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LTFly- venting is good....gets the bad stuff out of your head....sorry about your friend, though...know that hurts your feelings.
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I haven't said anything in FB about my dx, but will if I end up with chemo. I'd rather tell people what's going on rather than have them wonder. Other than my best friend flaking (which I think has more to do with her inability to deal with an unpleasant reality than anything about me) mostly everyone in my life has really stepped up and shown me unbelievable support. The other day my husband said "wow, you really have a lot of people who care about you".
. He's a bit antisocial and can't believe the outpouring of support coming our way.
Amy
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LTF - sorry about your friend. Mine is doing the same thing. It really hurts and sucks big time!! (((Hugs)))
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It does suck Amy! (((Hugs)))
I feel like you, I don't think the issue with my friend has to do with me particularly, she just is not good at dealing with difficult things. When my brother was in the psych ward for three months last year, it was one of the hardest things I've ever gone through, honestly as hard as this even, and she also really dropped the ball then. I texted her one day because I was having a crying attack outside the grocery store in my car, even though she lived around the corner and I knew her husband was home so she could've come to me (which is what I was hoping and what I would have done in a heartbeat) she just said she hoped I felt better and was able to go home soon!
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What an amazing group this is!
The pet pics are so great! And lovestofly... Sexy badass is definitely becoming on you;)
It is amazing the support that I am getting... Food chain once I have surgery, mantra bracelet that says "stay strong", journal, BC water bottle, daily check ins... It's just that one rotten apple after a 15 year relationship. But... I'm HER loss😎
I have only told a few close friends and two of them are BC survivor/troopers. But news travels fast in my town as my kids reached out to their friends for support. I haven't posted a thing on FB... Only pictures of me enjoy life as i should. But I was thinking of posting something next week as I head into my surgery. And the only reason is that I don't want my kids to hear the tumors of stage 4 and that its mets to my organs... That's the rumor!!
But then again... I may not. Let 'em wonder and have egg on their face when I come out of this like arockstar;)
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I have a question. I had my lumpectomy on dec 30. I still have swelling at the sight of the incision. It's about the size of a baseball is this normal? I have been icing it on and off. The swelling goes down at times throughout out the day. Anyone else experience this? What else can I do?
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Some people have surprised me by how they were unable to deal with a cancer diagnosis, though far more have jumped to offer help and encouragement. Many who I barely knew. That's the silver lining.
Sadly, my best friend passed away suddenly last December at 49. She developed an abscess on her liver which went undetected because her symptoms seemed like flu. It burst and killed her. Its formation was related to her medication for rheumatoid arthritis. She fought RA mightily and refused to let get her down. Though she is not here, I've adapted her approach. And know she'd be telling me "No feeling sorry for yourself. We're going to get through this."
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blamoms you mean sticking out or under the incision?
If you mean sticking out, I think you should have it looked at.
If you mean under the incision, yes I had that. I remember squeezing my breast and having it feel like half of it was a baseball! It was like that when I went to see my surgeon for my postop, at 11 days after lx. I told her I was scared that instead of my lump being removed, half my breast was full of a huge tumor. She assured me that it was fluid and was quite normal, and as long as I did not get hot or exceedingly painful, it would go away on its own. I think it started receding about a week later.
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MLP....you ARE rock star...it IS her loss....
I do love, for all of us, that those we do not know are in our corners come out and make the dif when those we think ARE there, aren't...ROCK ON!
(It is interesting that no matter our circumstance...we seem to have a similar experience...friends we thought were...weren't and some we didn't know we could count on...we can...LIFE!)
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peachy I am so sorry for your loss.
I'm glad your friend was able to teach you something. I try to always keep in mind that there are so many other things besides cancer, I blog a lot about my experience, and try to remember to always mention that I think what I'm going through similar to what a lot of people go through with a lot of different diagnoses!
Definitely had a lot of silver linings. The biggest one is that my husband can no longer bug me to remove my beloved tattoo, because it's on the arm where I had lymph nodes removed! Sucka!
Also, a good friend I had a falling out with in the fall reached out to me when she heard the news, we are good friends again. It's not exactly like it was and probably shouldn't be, we had thefalling out for a reason, but I am very glad to have her (and her family as we were family friends) back in my life
I'm looking forward to not have to deal with my mustache, random chin hairs, and bikini line for a while!
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Blamoms - that sure doesn't sound right to me. Please call your BS tomorrow and see if you can get in to see her.
HappyHammer, my decluttering has had one very UP side for me. I have discovered a whole lot of information about my dad's sister who died long before I was born. I knew she had sleeping sickness (turns out it was Encephalitis Lethargica) and that she was hospitalized. But it was so sorrowful for my grandmother and dad that we never asked about it. I came across the letter my aunt was writing and died the next day. It gave me a hospital name. The hospital in a new incarnation is still around (and no longer called a hospital for imbeciles) so I wrote and requested any hospital records they had. Mind you, she died April, 1938! Yup. They did and printed off the microfiches for me. So now I know a whole lot more about my aunt. That was fun.
However, all the lifting and moving stuff around is not that much fun. I find I can't lift as much weight as I could prior to my Lx. That's a bummer. So lots of extra trips up and down the stairs (which I will NOT have in my new home). And crap everywhere. Hopefully my mover will be bringing boxes by so I can sort and pack at the same time. I think the AAUW will come and pick up my 600-800 books - that would be wonderful.
End pity party! For the most part I'm not minding going through everything. I just want to get it done NOW!!
HUGS!
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it's under the incision. It's exactly like you described yours. I'm going to call the doctor in the morning and get it checked out just to be on the safe side. I go Tuesday for the results of my lumpectomy. It's not painful or warm just bothersome cause I know it's there
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You are right, HappyHammer, we are living parallel lives.
Gemma, I didn't post anything on Facebook until October, when I posted the photo that is my profile pic. Most of my FB friends are industry friends and former classmates, and I needed to able to keep FB the one piece of normal in my life. By the time October and breast cancer month rolled around, so much was behind me. I had talked to more than a few colleagues who admitted that they had skipped their mammograms, which I often had. It took until the end of the month for me to get up the nerve, but I felt the need to do a PSA.
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Love all the pets Omg you guys they are all precious! This is mine but...I rarely see her a casualty of the divorce he got her. She's beautiful a Siberian husky and talks....awwww!
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blamoms, sounds like a tumor-cavity seroma. Nature abhors a vacuum (so does my cat, who runs away from it in terror); so when the tumor & surrounding tissue come out, fluid fills the cavity. Same thing happens in many different surgeries--my husband had one after his hernia repair. They usually resorb fairly quickly--but ask your doctor.
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614 wow! So glad you know now, it's half the battle...who would have thought cramping inside your chest? I also had to have a heart ablation done a year after rads as I did suffer palpitations but it was horrific after rads. Now I'm great! Well haha as can be
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Peachy I love your profile pic. You look gorgeous and such an important message!
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Lovestofly - I lost every hair on my body haha saved money on my Brazilian haha only want hair on my head! You looked fabulous too for date night!
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Peachy - I am soooo sorry for your loss! I can't imagine what you're going through.
Happy Hammer - Well said about friends and just life.
Gosh I have to go back and re-read uuuugh I go out catch up ironically with my wax lady for coffee because I dont need her services still haha! and the thread blows up.
Peggy- I think you're amazing, losing your DH must be so incredibly hard and now the clearing out and moving forward.
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MelClarity, I think that the fact I will be moving to be near one of my sons has been a blessing. Something positive to look forward to. DH had been sick for a number of years and the past year a huge decline. But even knowing that, it was still a shock when he was actually dying. I've got so many years of good memories to keep me happy. So while I am missing him, I'm glad I can finally live near one of the kids AND be in the same time zone as both of them.
HUGS!
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Peggy - Well yes even with the many years of being unwell, still a very hard thing. Yes you have some wonderful things to look forward to!! and certainly a new beginning and change for you, it will be great!
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Thanks LovesToFly. And truly, not having to use tweezers or razors for a while is awesome. (I am now finding that I forget to shave my underarms. And need to again. Good thing it's winter!
)
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MLP -Beautiful, beautiful picture and a good attitude to go with it! Yes, I'm not sure if I'm living with urgency now or if I've just decided to make positive changes since the bc, but it's wonderful. I remember seeing a bumper sticker on a little sports cars a while back, and it said, "Drive it like it's stolen." Like this bumper sticker or the sign that says dance like no one's watching, it's nice to just live freely again... like when I was 6! haha I just retired--technically quit since I'm 51-- so I think that has a lot to do with my feeling so free.
ChiSandy- Oh, you'd love a RS tour because they incorporate lots of little gems and surprises in the tour. It's not for everyone, though, because they choose proximity to action over comfort sometimes, but I like it. We always put an extra week of Hilton at the end for a little luxury.
You sound like you travel a lot, too. Where's your favorite place to go?
SouthernCharm - Glad the chemo did it's job! That's great!
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