Starting Chemo March 2015
Comments
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I'm sick of people telling me to "stay strong", "think positive". Ugh.
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I get text asking how I feel.
I say its been really tough but a bit better today.
The response: I'm glad your better!
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Ugh. People. I know. Stay positive. Like that makes any difference.
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Hello Ladies.. Checking in 4 days out from my first round of A/C I have been reading and my heart goes out to everyone struggling! I so want to hug each one of you! This is the worst of times and we will pull through by reading and ranting here!
This first one wasn't so bad for me. Thursday was the day and Thurs night was a bit nauseous and I think the phenagren and the steroid were fighting each other but I did sleep. I took Friday off from work and really just layed around. I just rested. Sat and Sunday I made it to the ballpark to see all my boys games. I took lots of naps here and there and was in bed for 8pm each night. The only thing I can compare the way I felt was like I was just getting over being sick. I wasn't sick but didn't feel quite right. Still feel like that today but I am back at work and plan to hit the gym tonight if I can. My biggest thing so far is food aversion. I literally have to make myself eat. I have zero interest. I know I need to keep my strength up but unless someone puts a plate of food in my face I am not searching it out. Anyone on 3 week A/C? Does your appetite come back at all?
Now that the first one is down (15 more to go!) I am just waiting for the dreaded hair fall. That's when I think the depression, moodiness will hit for me. Right now I look fine.........Not for long....
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In my room. I just had breakfast. My fever is down and my WBC count is inching up. It was 1.4 yesterday and 2.5 today. I'm just so sad that I'm missing my son's first trip to legoland. I've been messaging with my husband. They're on their way in an hour.I might be here through Wednesday. They want to wait to have the test results back. Most likely my chemo infusion won't happen this Thursday.
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Leigh,
My hair started falling out on Friday. It was painful and a pain in the ass. I wrapped my head in a scarf and had my stylist shave me on Sunday. For some reason I felt 100x better once it was all gone. I do miss my hair (my old healthy hair), but I guess no hair will be the new normal for me.Losing my eyebrows is going to be the big deal. I have a hard enough time putting make-up now and now I have to add eyebrows to the normal regime.
PS...ladies...I'm a huge swearer. I can't help it.So I apologize in advance for any curse words. Working in the construction industry makes swearing too easy and just a normal part of the day.
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Katy,
Love the bird picture! Obviously I love the doggie picture too. My dog (Brandy) has been my sweet companion. We like to go outside at 3 am (her to pee and me to cool off).
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Are we not supposed to swear? Rut-ro. If I slip up, I apologize in advance, as I'm positive it'll happen. If it hasn't already.
Royalties have started streaming in so I ordered my purple dreds wig and the extra ego boosters from the TLC catalog just now, but still feeling blue. I've decided to just go with it. I don't have to be "up" all the time. It's allowed and definitely falls under the parameters of what I would consider a natural & rational response to current events. Especially this week. Wrapping up production on this next project so the big reveal (about the new book and my BC) will be this week. Unless something dire goes wrong, within days actually. Mr. Lumpy may be vamoosing, but the vile, nasty booger is taking my privacy with him. What a jerk. LOL. Stil, better to get ahead of any rumors, control the message. I'll feel better once that's done, I'm sure. Just a bummer-rama at the moment.
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Joanna: I am glad to hear you are feeling a bit better. I know it must be so hard to be missing that trip. But you have to take care of yourself now so you can go on the next ones.
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oh Bekah! Thinking of you. I know there's nothing I can say. A big, big, hug
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Avmom. That was nice you got out a bit yesterday. A bit of semi-normal time with your mom.I like how you wrote about what you were feeling. And glad you have the best of "rides" coming up for the dreaded next.
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Diane - I still have your little cozy room made up. I'm sorry you're going through hell. I hate the idea of all of this concentrated pain, torture, depression. When you said you read others' posts and think it could be yours, I realize anew the depths of your struggle.
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You called it on the name. I am from Indianapolis!
I broke out in an awful rash about 5 days after after my first chemo. My doc thinks it was a reaction to Taxotere. He gave me 5 days of Prednisone, and that helped, but I'm still blotchy too. Bald and blotchy is the new sexy, don't you know? Ha!
You guys are cracking me up with the list of dumb things that well meaning people say. I feel like we should publish a book of them. I appreciate every word of kindness that I receive, but some are certainly more helpful than others.
Ex. A friend tagged me in a picture on Facebook that was taken about 5 years ago. A mutual friend commented, "Wow! [You] look so full of life here!"
Geez! I'm not dead yet, People! God willing, I fully intend to survive and carry on that way for a good long while
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Ugh on THAT comment, Indy. lol
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Bekah: I wish there was something I could do to make you feel better. I think of you all the time.
Katy: I missed your lovely pictures yesterday. I enjoy them so much. I LOVE birds AND dogs.
Let's see if I can post a picture of my favorite place.
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Princess Karen- well done on the cash cow! Glad you had a bit of a spin with your cc. I'm sorry bc is taking away your privacy. I know it is imperative for you to have it to do your best at what you do. Nobody is watching me but Jack. But he knows. But I should imagine being the prey isn't much fun. A bunch of worried mini eagle eyes. Would be hard.
And NinjaMary- as our princess has said, I never got the memo on swearing. I have to say I lol'd and was going to try to put on my profile ER/PR/SWEARSLIKEASAILOR+++ . I'm terrible. I grew up with a salty ole sailor for a Dad and I just like how it sounds. Makes me laugh when someone turns a mfk$78)(n phrase just so. Ha! Got my first laugh of the day in.
You ladies are each and every one a lifeline to me. I hereby strike the word "whiner" from my vocabulary.
I'm day 5 chemo 2. My neice comes today. I'm so tired. Bone pain. Still have the mfg🐳 dmx pain. Every gd day. Never ever goes away and it's been 3 months.
And our dear SC Coqui Joanna- I can't imagine the loneliness you must feel being in that hospital room. Glad the vitals and wbc are improving. You must try to close your eyes and visualize all of us here in March chemo. Standing in a circle holding hands. You are in the middle of the circle. We are keeping the bad guys out. xoxo
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Trvler! Where is that! A beautiful place
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Backatcha with a pic
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My sister told me today that in spite of the fact that I have BC, she thinks my OTHER sister will be the first of us to die. That made me sad. It's because she doesn't take care of herself, eats total junk, hasn't exercised a day in her adult life, etc. She complains of feeling old and she is only 56.
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Princess: Yeah for $$ coming in. I am sorry about the loss of privacy. I guard my privacy so I can understand that being hard on you. I am still on the fence about going public. I probably won't. But I understand your reasoning.
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Trvler- uhhhh.....I don't think your sister gets it. Not helpful. My jaw dropped.
There is an absolutely hysterical thread called "Stupid Things People Sat" started by Raidergirl. IT was very active last month, so it might be hard to find but oh....so worth it. Sad and funny, but when funny....very very funny.
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and Shaz- I've been sitting here trying very hard to say something right. To say the right thing. For you and for Bekah. I also think about you all the time. On top of the unfairness of the condition itself- to suffer constantly is beyond my comprehension. I wish you could have just even 24 hours of relief. But I can't find the right words. I'm sorry. I care, somehow, after knowing you such a short time, very deeply for you, and wish I could do something. I will continue to send my fiercest wishes for some relief. Any relief
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I just saw my PS and it turns out I need a revision surgery. My TE is way too high up on my chest and it needs to be dropped. He wanted to do it asap, but I reminded him I was going through chemo and had 8 more weeks of it.
I'll ask my oncologist tomorrow, but I don't think they'd want me to go through surgery while on chemo, right?
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It must be spring. I'm starting to shed.
It finally occurred to me as I was reading your posts, Katy, that I could hit the reply to post button as I read through the posts instead of reading everything and then trying to remember all the details at the end. I'm going to blame chemo brain since I can, even if it isn't true at this moment. For now, though, I am going to have to stick to my old (and ineffective method) of trying to remember because I've run out of time to be on my computer for now. Bekah, Sharon, those of you who also have SEs that are driving you crazy and making you miserable, and SC, I'm thinking of you today (and always) and wish some relief will come for you soon.
Had my daughter's 8th birthday party last night and it was tons of fun! We invited the "mommy group" over. This is the group of moms and their kiddos I met at a breastfeeding support group when I had my first daughter. The adults drank wine and the kids played until well after bedtime and I smiled more and laughed harder than I have in a long time.
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BB- I'm no expert, but I wouldn't think they'd want to do it while you're having chemo. Better question maybe is do you? You haven't had the easiest time of it either. I'd try to take it easy.
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how wonderful Amy to have some smiles and laughs. We all need them don't we? I say use the chemo brain card whenever effective. I've tried using that post a reply button but it still takes you to the bottom and then I have to scroll backup to find where Iwas responding. Can't win. Or maybe I just can't figure it out. Feeling pretty fuzzy.
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I never figured out the reply button either. lol
BB: Are they TE's causing pain? I would tend to think chemo would not be a good time to have surgery either. I guess the one to consult would be the MO.
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My TE is not painful, just uncomfortable.
My arm and fingers on that side sometimes hurt or get numb, but this is probably from some nerve being pressed on, although the PS says it is caused by nerve damage from mastectomy.
It is not going to be major surgery, it will be outpatient, quick and easy, but still a surgery! I consider this a setback. Now instead of just looking forward to the end of chemo and resuming somewhat normal life until the exchange surgery in fall, I'll be looking forward to the end of chemo so I can have revision surgery. At least I won't pay for it out of my pocket, because I already met my out of the pocket maximum for the year. Still, not happy.
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Here's my pup, Penny. She loves riding in the boat.
When we all kick BC's ass we should have a get together at the lake!
I've been thinking a lot this morning about this whole BC/chemo thing and the million ways it's effected all of us on this site. SEs, relationships, friends who have stepped up, friends who have disappeared, stupid things people say, getting through each day.....I don't post much, but this site - esp this group helps me in so many ways, even if I'm mostly hanging out on the edge.
I've been lucky to have a lot of family/friend support through this. I do need to give a shout out to an amazing family though. My daughter, now almost 24, had a best friend in middle school named Sivan. We did a few dinners together with her family over the years, lovely parents, etc. As the girls went through HS/college they lost touch, but I am still Sivan's friend on FB. I made a FB announcement a while back about my BC and then a note when I was starting chemo. This family swooped back into my life after 8 years. They brought over 5 night's worth of dinner last week and checked in on me this morning to be sure I didn't need anything. I've been just floored. I know others have commented on people who disappeared one the dx was given, I have those too, but it's so nice to have folks step up when there is absolutely no "obligation", nothing is expected of them at all. Makes up a bit for those who should be there who aren't.
I can't decide how I feel about the ones who have faded away. Should I be hurt (well, I am), should it be a "deal breaker", do I assume people have their own stuff going on and that my BC isn't their first thought? The 2 that bother me the most are folks who have had trauma of their own over the last many years and I've been there for them. They seem most interested in being friends when you can help them, not so much interested in helping me.
We are spending Easter weekend at the lake with one of these couples. The husband has been such a help to me both when my husband & I separated last summer and now. Checks on me, has given me rides to things, etc. Checks in with my husband to be sure he's holding up ok, so surprising because he is sort of a curmudgeonly sort. His wife, nothing. Not even a text since I was dx.
ok - enough of today's musings. Off to give myself my first Neupogen shot.
I hope everyone has as good a day as possible.
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Thanks for all your kind words. I feel better emotionally this morning. Might have been lack of sleep that brought it to a head but it felt good to vent.
Physically...meh. I'm still tired, can't focus my thoughts well, and have intermittent bone pain but I managed to get my sorry arse out of bed and go to work. What do I find when I get there? A patient with early symptoms of a stomach bug...good thing I read the chart notes before I went in so I could maskup!
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