Starting Chemo, November 2013 Group
Comments
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HI all-
Thanks for all of the love and encouragement! I am feeling better today, thank the LORD!!! I actually slept til 8! So 3 full days of hell from neulasta shot, nice. I do NOT think I will be asking for that again...
LOVE all of the photos and the scarf tying info!!! sounds easy, hope I can do it!
Taking daughter with husband driving, not feeling that good yet, to a friends...Yay! to get out of the house is such a thrill!
The little things...:)
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Okay, ladies, this is my brain on drugs:
Saw a friend of mine tagged in a photo of a group of women on the statehouse steps for a memorial of Newtown today. Off to the right was a woman with white hair, dark sunglasses and looking tough like I wouldn't want to meet her in a dark alley.
Focusing on that woman, my first reaction was "Oh s%$^, another bad picture of me" (I have a long history of such pictures).
Took a moment for some mental review: (a) I don't have hair (b) I don't have sunglasses like that (c) I wasn't in Denver today (d) I haven't been out of the house and barely out of bed today .......
Definitely had to laugh at myself! -- Ellen -
Hi ladies: It feels so great to be sitting on my computer
instead of typing away on my Iphone.Paulette: I hope
& pray you’re feeling much better. Lisa:
I notice you have chemo the day before me.Audra: I hope you’re feeling much better! Flu like symptoms
I’m not feeling nausea or dizzy for the past week. I’m
drinking like an elephant on diluted water (3/4 glass of water and ¼ canned
green tea). I can’t tolerate just drinking water. Oh, I feel like a pregnant
lady. Any kind of strong odour just make me sick. I feel like I’m ready to throw up. Anybody had those
symptoms? All of my hair is almost gone and I’m very sensitive, but not itchy.
Thank God! I like wearing turbines, just like someone is holding my head. I can’t
wear glasses cuz the arms of the glasses make big dents on the edge of my head.
I’m just about bald like a little duckling. Lol. I don’t get headaches from not
wearing them. I eat six times a day and eat small portions instead of a big
meal. I found that help my stomach from being bloated or nauseated. My stomach is shrinking. Can’t eat big meals
like I used to. I’m HER2+ so I can’t eat red meat.Amazonwarrior: Hugs
love your scarf. On Thursday I went to Look Great Feel Good workshop. I really
enjoyed myself. My self-esteem went sky rocket lol. We learned how to use
makeup and hide those dark areas like under our eyes. They gave us a makeup kit
with all kinds of accessories. I volunteer to try on a wig and they all cheered
when they saw my baby duckling head lol. I had fun with the ladies. I order
another partial wig where I would wear that when I wear a hat or toque. It was
fun going Christmas shopping. I need to go shopping again before my next chemo
treatment which is Dec. 24/13. I will say later as I enter into chemo land lol.
I am happy that I don’t have that much side effects. I will try to make it to
our annual Christmas late night service. I don’t feel nauseated or dizzy
usually till the next day, which is Christmas. PatAlameda: my mind went blank will come back to you later lolThe port underneath my upper arm is healing nicely, but its
still a little sensitive. I’m exercising it gently. I still need to exercise my
left arm due to surgery. My oncologist said you need to lift it up high. He
lift it up and it felt kinda funny, like being stretched. I’m working on that
arm. My BC surgery has healed.Wren: welcome to baldness. My head is like a baby duckling. On
my head I have long strands of hair here and there. My chemo nurse suggest that
I keep my hair 4 inches long.VirginiaNJ – cool pet – Piglet. I use a cushion when I go
out somewhere for comfort. It’s comforting to hold it where my operations was –
left side.QuickGirl – hugs what kind of pain you’re experiencing? Hope
you take a nap and forget about the world. Paulette23:
I’m reading your posts. I hear you! Inks: welcome to chemo landEllen: way to go! Five miles of walking, that’s excellent.
Proud of you! I don’t go for walks because of the cold spell, but I use the
exercise bike as much as I can.SpirtBless: Hope your infection is healing nicely. Audra67: Hang in there. We are here for
you.
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I'm sitting here watching the snow fall. I feel I'm getting a cold. It's not good. Chemo #4 is this week. It's suppose to be the last dose of AC. I hope I get better fast. -
hey ladies.
Seems like the weather front is hitting many of us northern folk - -32 deg here today with wind chill. I froze my butt of walking my furry beast. The hatches are buttoned down for the snow that amazon is getting already. Yuck! Btw Amazon, love the wig - looks like the same model as mine.
Paulette, I'm sorry your getting hit so hard with the last chemo. My thoughts are with you my chemo sister.
Ellen - I hate those steroids they put us on - l'm not sure of their exact purpose but I was under the impression it was to help with nausea - HA I say to that!
I've had a rather emotional couple of days. My elderly parents are coming to terms with my cancer and it is really breaking my heart. Both have not been well and I have been supporting them in their struggles over the last year. Now they are trying to help me but are really not able to do very much, making them feel helpless. I found myself reassuring them that all would be fine as I was running my fingers in my hair and big tuffs of it were coming out, which just added to their sadness. It's hard to seem strong when that sort of thing happens.
I know we are all going through a physical hell with this, but I find the emotional impact this has is far harder.
Take care ladies, and keep warn
Judy -
Phebe -lol with the duckling references. I look like a soldier- my hair is as close as my sister could buzz it
. I'm glad you enjoyed the Look Good Feel Better program. Sounds like it has been pretty much the same for all of us. Yay for you modeling the wig!!!
Our snow is turning over to rain which is expected to turn to ice. Yay for us!! My neighbor did my driveway once early this afternoon, then I did it once with my snow thrower, and I just shoveled it.......here's hoping for a better nights sleep with this little bit of exercise....
Judy- so sorry about your folks.. It is so sad and emotional. My father was with me my first occurrence and I know it crushed him that I got cancer so young. Hugs to you for strength!!!
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jab - Judy - You are so right. The physical part of this, for me, is annoying and not plesant; rather like having a particularly nasty flu that comes back every two weeks and causes hair to fall out, but still..... The sickest I've ever been was either when I had mononucleosis at 15, or when I had pneumonia at 17, and so far chemo hasn't been nearly as bad---physically--as either of those were. Emotionally is a whole different ballgame; I hate what this has put my husband through (and he's being a super hero,) and my elderly parents and ...well, my entire family. So I find myself in a position sometimes when I am reassuring THEM that I'm gonna be okay, when I'm not 100% sure myself that I AM gonna be okay. It's tough!
Our weather sure is different from everyone else's; just heavy rain here tonight, and there are tornado watches a couple of counties away. Hopefully none of the nasty weather willl come our way. I'd rather have snow than tornadoes, but honestly, I just don't like weather. Any weather. Give me a day with an 80 degree high and a few puffy clouds in a blue sky, and a night that's just barely cool eough for a long sleeved shirt, and that's about as extreme as I want the weather to be.
BigT16: I'm looking very forward to being able to say "my next AC is my last." I've got two more to go. Course, then I have taxotere and more cytoxan to look forward to but I'll whine about that when the time comes, I reckon. It'll all be over before we know it! Right? Right!
Phebe: over the past couple of days I have become SO sensitive to smells. Didn't really get that with my first round of chemo, but it's definitely hitting me this time, and with two dogs and a cat in the house, I sure do wish it would go away! I can't drink plain water either, at least, not much of it. I mostly drink seltzer water with a splash of cranberry juice because it's one of the few things that taste the way i expect it to. also managed to drink some coffee earlier that was GOOD....it just required me to put three times the usual amount of sweetner in it to achieve goodness.
Ellen: LOL thanks for that laugh. I needed that! -
Just checking-in to say "hi" and to tell everyone you have been in my thoughts and prayers all day long.
Snowy day here...8" or so...I had a mini-meltdown panicking about making it to my pre-chemo check on Monday, my 2nd TC on Tuesday and my Neulasta shot on Wednesday...sigh. Some days are easier than others. Will be glad to get #2 chemo over with...praying for no delays.
LOVE reading through all the posts. Absolutely LOVE seeing the photos and getting to "see" you all!
Paulette, Pat & Amazon...you ladies are beautiful and you look GREAT without or with little hair, you really do!
Amazon...LOVE LOVE LOVE what you did with your head scarf...it looks so pretty and so cool, it really does! You look pretty! And I LOVE your wig...it looks so much nicer than mine :0) I've not had the guts to wear mine yet...wearing funky turbans.
Wrenn...guess what...I ALSO STARTED LOSING HAIR IN DROVES YESTERDAY...MY 1/16" STUBBLE IS EVERYWHERE :0(
Judy...I really feel for you regarding your elderly parents...it's got to be so hard for them AND you... I can totally relate to the "emotional" part of this being as hard, if not harder than the physical...(((hugs))) to you all
Phebe...hang in there and take it one day at a time...you're doing better
Audra...continue to feel better...take it slow...one day at a time
Quirky, Gayle & Lisa...please feel better soon
Fond thoughts and prayers to everyone else...Melrose, Virginia, Veronica, Quirky, PomPom, atlbraves, Ellen, northwinds, smrlvr, BigT
Sorry if I over-looked or left anyone out...it's not intentional. Not a great day.
Have a restful night everyone!
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hi all...still feeling pretty rough.......thunderstorms rumbling and lots of rain! have put off er cause family outing today been waiting for. not the wisest thing but I'm tired of missing my kids! feel dzzy.earz ringing and weak but I HATE hospitals.don't wannnnnna go.....I know they'll keep me....pooo.....just gonna enjoy being w family....then go....hoping great day for -
goodness....seems like I've been bald forever now! everyone is dealing with stubble...lol...ichose to wack it off when it began cause I saw what was coming! in one day I looked like the walking dead and buzzed it all! I know they don't want u to sh ave but did twice with new razor and BUBBLED my head with lather! sure glad I did! been using nivia lotion w tanning stuff. mmmm...makes my head all soft and glowing....I think my head is like a babies butt now!!!! -
Woo-hoo, I slept in yesterday and today. Stayed in bed until 6am which sure beats 4:30. Appetite, smell, taste, and bowels are all back to normal, just in time for AC #2 to mess it all up again.
Jab, I'm so sorry that you are having such extra stress about your parents. As horrible as it may sound, I'm almost glad that my mom passed before this happened. I don't think she could have taken it. People who haven't taken this particular trip we're on can tell us to worry about ourselves, and take care of ourselves, but they don't understand that we also have to worry about what we're doing to the ones we love also. No, we aren't really doing anything to them, but the emotional part overrules the intellectual part and tells us that it's our fault they are worrying and stressing. I can't imagine watching one of my kids go through this. I really believe that would be harder than facing it myself. Try to keep your brave face on for them, sure it will be hard, but also helpful to all of you if you can convince them you're good. If you can somehow help them unstress, it would actually take a little stress off of you too.
Phebe, be careful about exercising the port arm. They can shift, especially before they are healed all the way.
Virginia, watch out with the snow blower, don't fall or try too much at once. We rarely get enough for a blower, but Hubby has a plow blade for his riding mower so he can get the driveway.
Audra, did you get your drive in? It's great to get out a little if you can.
BigT, Hubby brought a cold home for me too. The MO said to use Mucinex. It seems to be helping a lot.
Paulette, you are going to make all of us jealous with the pics of a green yard with no snow. And I shaved the stubble too.
Smrlvr, what time is your AC Monday? I go at 10, maybe we'll be there the same time and can send good vibes to each other. My oldest daughter is also a teacher. At one of the worst high schools in town. She's had chances to transfer to other schools, but she thinks she can make more of a difference where she is. I know she's dedicated and cares about the kids, so maybe she can be the sort of roll model they don't get outside of school.
Northwinds, my MO said I could have a glass or 2 of wine as long as it didn't seem to upset my stomach. I've only had it twice since I started and it went down FINE.
Amazon, thanks for the scarf tip. I couldn't figure out what to do with the long ones except to tie it behind my bald head and drape the ends over my shoulders
Lisa, have to agree with you on the weather. The older I get the more I hate the cold. And to me anymore, anything below 80 is cold. I don't even want it cool at night anymore. Give me swimming weather ALL year round and I'd be happy.
Toni, hope your weather lets up and you get out okay tomorrow. What's a pre-chemo check? I get all the blood work done right before the chemo and go back 7 days later for blood counts.
Here's hoping everyone has a good day. -
We had a nice time last night; had a couple of musician friends over, plus my little brother and his 5 year old, did a little jamming, ate too much pizza. My side effects cooperated by being mostly non-existent, other than being tired.
Followed that up by having weird dreams -- and some nightmares-- pretty much all night long, so I reckon I'm gonna be due for a nap or three today to make up for being up-and-down all night.
Okay otherwise though; I'm only on round two, but already loving it when my morning routine of medication only includes my vitamin D3, my claritin (which I'm takng all the time now because nevermind bone pain, I can BREATHE lol) and maybe a klonopin if I'm likely to have a stressful day at all. Feeling pretty good this morning, so maybe, MAYBE, I'll be feeling pretty good all the way up til my next chemo which isn't until the day after Christmas....
A girl can dream, right? -
Is anyone else running an ongoing fever?
My docs insisted on Friday that I go to the ER when the fever got up to 100.6 by early afternoon, but they couldn't find anything with the blood & urine tests they ran and meds brought fever down. Got to 100.6 yesterday, then took ibuprofen, which gradually brought it down to 99 by evening. Woke this morning with 99.4, ibuprofen again, wondering what will happen by afternoon.
I had so wanted to go out to a couple of things today, particularly a show in a small theater. Seems like too much of a risk if I continue to run even a low-grade temp. I'm keeping my doc posted, but definitely don't want another ER session unless there are some more definite developments. I would prefer this not get worse, but feel like I am hanging in limbo. I've been in bed since Tuesday mostly due to pain and then crashing from steroids. I feel more like doing things today, but we'll see.
-- Ellen -
Ellen, my fever has spiked like that a couple of times; 100.6 actually was also the highest that mine got, that I'm aware of. Mine seems to especially do it if I have the *sensation* of being hot, and if I uncover and cool myself down, it goes down. It also spikes up to 99 or above if I get upset or overly anxious or anything like that. My onc doesn't seem to be all that concerned about it so long as it *mostly* stays below 100, though I did tell him that it wasn't unusual for me to have a slight fever like that anyway for no apparent reason.
Personally I think I'd keep throwing the ibuprofen at it....and I probably would not go out (sorry,) and just keep a very close eye on it. If it goes up any farther, I'd go back to ER, or at least call for advice. Better safe than saddled with a tough hard-to-pinpoint infection!
Edited to add: I checked because you made me curious, and my temp is 99.1 right now.... but I feel perfectly fine. Maybe it's a chemo thing? -
Ellen, I recorded my temp every day. it was a great source of frustration. My usual temp is about 96-97. Days 3-10 after TC, I ran a temp in the low 99s during round 1....round 2, it was in the high 99s...round 3, it was in the 100.1-100.3 range. MO would not see me at 100.3, but when it went to 100.6, I was sent to ER where it was 101 and I was admitted because my neutrophils were so low. Round 4, I got neulasta. I ran a temp from days 3-8 on that, and this time it was 101 each evening. I was sent to the ER... both times, there was no infection ...and I got a complete workup in the ER. I was so frustrated because my MO kept telling me no ibuprofen, and he would say "no way chemo causes fever like this." My response was that, "apparently in me, it does." Luckily, the MO on call the second time I went to the ER said I could take ibuprofen, so I did, and was much more comfortable...this was only after a complete work up to rule out infection. It is frustrating. I hope your fevers ease. Mine was always a couple degrees higher in the evening than during the day which was an added frustration because they would not see me during the day because the temp was not high enough, and at night, they would just send me to the ER. I hope your fever eases soon. -
Thanks, Lisa. Maybe this is the new normal.
I should have mentioned two things:- I just had my 3rd chemo infusion on Tuesday, so this shouldn't be the nadir yet. When I did a dive in week 2 after the 1st infusion, my temp was as high as 101.4 and I would definitely do something if it got that high again.
- I usually run low on temp, around 97. Pre-cancer, I would feel crummy with a temp of 99.
Ellen -
I just had my second chemo on Monday, so schedule wise, we aren't that far off; so it cold be a chemo thing. I'm doing AC though, so don't know if that makes a difference.
I'm the same as you though; my temp used to be below "normal" most of the time, and even though it was fairly common (especially during PMS week) for me to spike a temp up to 99 or above, I always knew when it happened because I'd feel awful from it.
For some reason, cooling my *feet* off seems to make a huge difference. Maybe I am part Cocker Spaniel? ::::sniffs feet to check for "frito paws":::::: -
I can walk again. Thank God the bone pain finally let go. Thanks everyone.
Sorry to hear about the fevers, Ellen. It feels so random. I was running hot, for me, this morning but MO on call said to just watch it unless it goes over 100.4 (I've had a fever and chills at under 100 in thd past). Hope it gets figured out and you feel better. Loved the photo story earlier. -
Good morning everyone ~
I sort of checked out the past couple days...glad to have last AC behind me and on to Taxol, but this treatment wiped me out more than others. I've been sort of a zombie, saving what energy I have had to try to muster Christmas spirit for the family. I have been reading posts, but it's so much to get caught up on, so I'll jump in this morning where I last left off. (Been up since 4 am -- thanks, Decadron!)
Love all the pet pics! We have a cat and some fish. Kitty became a lap cat when I came home from surgery and realized I couldn't pick her up. She's been my buddy.
I can't remember who did the fabulous scarf modeling and wig (Amazon?)...beauteous!
Audra, glad you're felling better. I'm on day 4 post-Neulasta which is when I usually start with the aches. I almost am welcoming it after the nausea of the past few days.
Ellen, ha! I can't rely on my brain at all anymore, especially as a thought gets to my mouth and things unrelated to what I was thinking start coming out!
Phebe, it sounds like you're muddling through pretty well these days. I'm 2 1/2 months post-surgery and can lift my arms above my head pretty well. Keep working at it. It still feels like things are stretching, but in a good way. I also eat all day, squeezing in lots of small bites between regular meals. It seems to help.
BigT16, I did my last AC last week...glad it's over! Are you doing Taxol after? My MO says nausea is mild at most with Taxol....woo hoo!
Judy, I hear you about parents. When I first told my 86-year-old mom, she had a terrible time. She had to be hospitalized b/c she literally worried herself sick. It was so hard to help her go through that phase of grief and be strong at the same time. She lives a little over and hour from me and is now rallying to do what ever she can, which has been wonderful. I can tell how good she feels to be needed, which is hard for me b/c I HATE being needy!
Northwinds, my MO said three glasses of wine a week was okay...all at once even! I start Taxol 12/26, so I know I'll feel my best on Christmas. And I am having a fabulous cabernet with everyone with my roast beef! I've stayed away from wine (miss it!) when I'm taking any medication, but I don't think it would have been a big deal as long as no driving.
Hey, Ellen, watch the fever. It sounds like everyone is on top of it, but maybe stay in until it normalizes?
Has anyone else done Taxol yet? I'm doing it dose dense, and my MO says that damage to finger and toenails might be lessened doing it over a shorter period of time. Nausea should be less, but body aches more. I'm doing Neulasta for the first round, but she says my WBC may be high enough to discontinue it for the other three rounds. Also, Decadron only with the infusion and not at home...yeah!
Well, the first kid just woke up and is off for a Starbuck's date with his girlfriend...so cute!
Good vibes for today, girls! -
we got a foot of snow between yesterday and last night. I really don't find it charming anymore. Would love to live In a warmer climate!
Amazon, love the wig. It looks really good on you. I wore mine out the other day and ran into a former coworker. He didn't know it was a wig.
Phebe, I feel like you. Not nauseous but like when I was pregnant. Not knowing what foods will taste good.
Wallymama, my appointment is at 130 tomorrow. Bloodwork first then AC #3. I can't wait for that to be over. I am starting to feel like I have less energy. I hope I will be fine for Christmas, then I will crash before my next infusion. We are traveling, so it may require more of my energy.
Ellen, I have taken to listening to my body, and I would not go out if I were you. I know it's hard and staying home is boring. But I think recovery will be faster if we rest as much as we can.
I am sorry to hear some of younger not feeling well. I agree the mental part of what we are going through can sometimes be more overwhelming than the physical. We are dealing with so much at once. I still can't wrap my arms around it and I am thinking about counseling.
Good luck to everyone this week. -
I have a question for those running low-grade fevers, or those spiking fevers. Are you receiving Neulasta injections? Do you think the Neulasta helps and/or creates fever?
I'm confused about the cause for the low-grade fevers and why the 100.5 F cut-off is so important. And then a trip to the E.R.???? Ugggggghhhh. Cannot imagine with the weather here PLUS the craziness of ALL of the E.R.s around here during this time of year...all the flu-carriers and virus carriers. Seems like an E.R. is the worst place to be...
Forgive me...I think Virginia asked...my cancer center does a physical with bloodwork 24 hrs pre-chemo day before they give the all-clear for the round of chemo. I'm not sure why but it's their protocol. Pre-physical, chemo then Neulasta. No bloodwork afterward unless I feel very ill.
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I don't think Neulasta was related to my fever. As for blood work before chemo, I think it just varies slightly by MO. Mine do blood work the morning of, chemo if okay, Neulasta the day after and then blood work a week out to see how the counts looks. With a compromised immune system the low cut off is high enough to indicate potential infection. My MO uses 100.4. -
Tonilee - so you sent the snow to us???. Thankfully it was so cold that it was super powdery. I didn't actually ask about the blood work. I only get bloodwork a couple of days before chemo via a finger stick. They draw blood only once per month. I never get my blood checked right after chemo.....I never even take my temperature!!! (I remember them telling me to my first go round....but not one person (nurse or doc) has told me to take my temp, so I don't lol
Paulette - thinking of you........I am an insomniac too so I am always reading your posts at all hours of the night :O
WallyI was careful.....used the snow thrower once and shoveled a couple of times. Was careful as my PS doesn't want me "working" my chest muscles too strenuously. Was actually grateful for the fresh air and exercise as I was laid out from e last chemo treatment (last Monday).
Lisa- lollllll RE frito paws! That gave me a flash back to our dog growing up.....perfect description.
Quirky- I had he bone pain too---sooooooo debilitating. It's amazing how it just subsides......
Managed to wrap presents today... Yippee. Giants stink so now I am thinking I should bake a batch of Christmas cookies
Sending warm thoughts to everyone!!!!!!! -
Re: why 100.5 is the flag level where we should call the doc: On page 2 of this article http://www.altmedrev.com/publications/11/4/278.pdf it notes that when the normal temperature was established at 98.6, the doctor/author also noted that variations from 97.2 to 99.5 were also normal. Maybe 100.5 is the flag because it is a degree above that normal range.
I did do Neulasta on Wednesday, and fever is listed as a potential side effect -- but most of the Neulasta side effects are identical to chemo effects, so who knows. I do know that on my first cycle, when I didn't have a shot and hit 101.4 degrees, it was quite real and landed me in the hospital for a few days with extremely low white blood count almost no neutrophils. They never identified a specific infection, but pushed IV antibiotics.
On frustration with ER visits: I am right there with you. The only reason I relented and went to the ER of Friday was that particularly living alone now, I didn't want to face the weekend with a possible unidentified infection. I got a follow-up call from the ER today and realized from the discussion that in my 4 hours there, all they had done was general blood counts and differentials, and a totally unnecessary lung x-ray -- all of which could have been done in 15 minutes at an outpatient site. The only saving grace was that I was in the middle of a 24-hour sleep (steroid crash?) and dozed through most of the ER visit.
Ellen -
Today is my down day. It's probably because I am experiencing my PMS symptoms, and have had a bubbly stomach all day, with low appetite, and my nurse didn't show up, so I ended up packing and dressing my own wound (the drained abscess site), and because I feel the wound is not healing faster, and each day I feel I am falling further and further behind this group's 'chemo bus', that makes me want to shout: Hey, wait for me! I am frustrated with my own body's healing abilities, and not getting my chemo treatment on time, for being stuck at home, for not being able to decorate for Christmas because my arms hurt, for feeling sorry for myself, and not having the energy to respond to you. -
Amazon, I was late to start chemo because of wounds. I was told by onc that because I was triple negative I should start chemo 8 weeks after surgery but my surgery was August 16th and chemo was Nov. 25th. My wound continued to heal after chemo started and is almost closed now 3 weeks after infusion. I hope yours continues to heal but I can sure see why you are so frustrated. It doesn't help that you wish you could have started something sooner that makes you feel like crap. :-) Hang in there. -
hugggggggs Amazon.... So wish there was something more I could do/say. Thinking of you and sending you all the best karma possible!!!!!! -
Amazon -- Knowing just little bits and pieces of each other on this board, we get to do all sorts of speculating about each other. Just from the fact that you chose a screen name like Amazon Warrior, I picture you as someone who is used to taking charge, getting things done and moving on to the next thing. Ordinarily, nothing would stop you in your tracks. I picture you as someone who has perhaps been an executive, or had major job responsibilities in addition to running a household and raising kids.
If you are anything like that, you are a lot like me. And the worst thing you can ask either of us to do is wait. And you have been asked to wait for so long. In fact, just before you wrote, I was thinking that the biggest sign that I had a bad week this week was that I was too tired and hurting to be throwing fits at being stuck in the house.
Somehow, some way that Amazon Warrior will triumph -- if for no other reason than to spite the fates! Hang in there.
BTW, I love the pictures of your scarf and wig where your phone hides your face. Made me giggle because it reminds me of the episodes of Home Improvement where they never, ever showed the full face of the next door neighbor -- named Wilson I think. Did that show play in Canada? Did you have that in mind?
Ellen -
amazon, waiting stinks! I was close to 120 out from my op when I started last Monday. It made me totally crazy. The bus will not leave without you!
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- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team