April 2011 chemo
Comments
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headaches anyone? the past two days I've had a dull pain on one side of my head on and off, not sharp but like a headache, a little like that squeez kind of ache, anyone have anything like that?
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Oh gosh...I totally her you all about people comparing troubles. If I said the things I think sometimes I'd have no friends at all. I mean really, this week on Big Brother was HELL? REally?! Come ON! You're upset and crying that you've been torn apart from your fiance?! He left a day ago and he's just on the other side of that wall. No patience for the petty lately.
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Hi All!
Had to share my breakdown with you..So I was back at work, giving a brief beginning of the year presentation to my colleagues - a room of about 80. After, I simply wanted to thank them all for their support, but what occurred next, I couldn't control. Out of nowhere, I broke down..sobbed, trying to thank them in between and trying to let them know that I kicked cancer's butt, but was ridiculously bawling! yikes! Then, what's worse, I found myself woken up at 3AM with tears rolling down my face, jjust thinking about the scenerio. It was like I finally realized all I had gone through - the 16 hour surger, 2 weeks of living in a recliner, 2 months of recovering, then getting slammed by chemo - and I finally realized that this nightmare we are all living in -was over. Wow! Pretty intense. Has this happened to anyone? It was almost as if I'd been holding my breath through it all and finally exhaled...
I guess it is really over, as I spent the day cleaning my house and putting my kids back to work. They must be soooo happy that Meanie mommie is back! ha!!!
Geri - thanks so much - good to hear!
Ginger - from what I've read, everyone's hair comes back white or grey at first, which is because the pigment cells come back slower. Eventually, when the pigment cells come back, then so does your color.
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had my ct scan today, and now sport 5 "cute" tattoos dots. I envisioned a huge machine, but it was about size and shape of an 18wheeler tire - just shiny white and worth lots more money and loaded with laser. So silly when there's a ct scanner in my town, but the only radiologist in the area works thru a center 100 miles away, so had to go there for mapping and simulation. I won't start rads tho until 6september to give the month after chemo.
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Seeay - big hug. I can see how the "normal" of a presentation to colleagues followed by thanking them for their support thru all the not-normal might overwhelm the senses. I think we're on overdrive thru all this, trying to tread water, keep functioning...it hasn't hit me yet that it's over, as I'm just starting phase 2, with rads, but...
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Windlass -- I, too, had several sessions with a lymphedema therapist after my surgery, even thought I didn't have LE -- it was kind of a preventative thing. I think I started about 3-4 weeks after the surgery and went about twice a week for 3 weeks. She was really helpful and gave me lots of self-help tips and exercises to do on my own. I've also called her with a question since then -- I started swimming laps in the pool occasionally, and I wanted to know if I had to wear my compression sleeve while swimming (swimming was on the list of beneficial exercises for LE). She didn't know the answer right away, but she found out and called me back -- the answer was that I didn't have to wear it while swimming.
RangerMom -- You might ask your surgeon to recommend a good LE therapist for after you recover from your surgery, especially if they end up taking a lot of lymph nodes (as was my case). She can be a wealth of information.
Geocache -- Sorry you had to cancel your trip to Atlantic City, but I hope you have a wonderful and relaxing birthday celebration. I, too, had to cancel my boat trip with my husband because I just never know if the incapacitating abdominal pain is going to hit again. I had also planned to take a trip to Maine to see my parents and my sister -- during chemo (I would do one session up there) -- but came to my senses and decided it was crazy (all the airports and airplanes with germ-infested people). Like you, I just try to fit one-day or partial-day adventures into things now. Need something to look forward to, yet afraid to stray too far from home. Anyway, enjoy your birthday!
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Good morning all
Ranger Mom I will be thinking of you Tuesday. I didn't find the surgery bad at all. Especially if you compare it to the chemo. For those drains I used an ace bandage around my hips that I could tuck them into while showering and such. I had a few spares so I didn't mind getting wet then changing it out. I ordered dinner delivered for a few days too, just so I could stay on the couch and rest my body but I was able to do a lot more than I thought. With the exception of sweeping the floor, don't try that or your body will yell at you LOL
One thing I have missed is traveling. I am planning a get away in the fall once I am done with Radiation.
People comparing their healthy aches and pains to chemo side effects are just ignorant, lucky them eh? I would love to be ignorant or down right have amnesia to the whole hideous thing LOL
I have asked two therapists if they can hypnotise it out of my head and they both said no.
Healing Rad blast #12 this morning at 7:20
Hugs to all.
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Profbee- I know, seriously with that Rachel on Big Brother. Funny thing for me is that when I am on the steroids she really irritates the crap out of me! I think I take it out on her because I get so nasty during that time LOL....
Seeay- Thanks for the insight on the hair, good to know... and on your breakdown, I'm not to that point yet, but soon so I don't know how I will feel then or react. I am sure you needed to get it all out and good for you!
I know this may sound dumb, but what exactly is lymphedema? and what happens when you have it? does it only happen to those that have had mx?
Hugs
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Taxol 6/12 is done! My lovely oncology nurses brought me beautiful flowers and cake to do an early celebration of my birthday next week Wed. One will be on vacation and did not want to miss out helping me celebrate, so they decided to kick off my Birthday week! Gosh, it takes wonderfully special and caring people to help nurse us back to health and I am so grateful for them.
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I got bummer news today that the spot that showed in my r lung on the PET scan back in April is showing now in the chest x-ray they did for presurgery. The BS said she will be doing follow up in 3 mos. Its probably nothing but with cancer in your history, its got to always be a nagging whisper in the back of your mind. I'm going to think positive that its just some scarring from past pneumonia or something I had.
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RangrMom - we'll keep the faith with you!
Carla - what fun - and must have felt good to be so cared for!
My news: surgery scheduled for August 29!
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Ginger_mea -- In a nutshell, lymphedema is fluid retention and swelling caused by a compromised lymphatic system, which is what happens with lymph node removal. The more lymph nodes removed, the more compromised the lymphatic system -- the lymph nodes aren't there to allow for proper drainage. Some people might never get lymphedema (I HOPE I am one of them), whereas others will, and I guess it can be quite uncomfortable and even debilitating.
RangerMom -- So sorry. Thinking positive thoughts with you......
Carla -- Happy early birthday, and how nice of them to honor you like that!!
Artiecat -- Glad you have a Sx date.....moving forward......
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Hey gang!
Happy birthday, Carla! How NICE of them! I love the uplifting stories of people going the extra mile in the midst of all this.
RangerMom, I'm sorry. Bummer that they can't look more closely or do an MRI or something. I'd HATE to have to wait like that.
Ginger, oh it's not you Brenchel is a two-headed monster!
Merilee--I can understand wanting to forget all this, but meh...we lived through it! I guess I want to remember it--but as a DISTANT memory! lol!
Love to all!
C
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I don't want to remember any of it. I keep waiting to wake up and find it has all been a nightmare. I don't know about the rest of you but I am not the same person I was a few months ago. Just so beat down my this shit, the worrying, the fatigue, the lack of feminine appearance. It really gets to me some nights and makes me cry for long spells.
I am sure my poor son thinks I am a nut case.
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Oh, I hear you. We're in it. It SUCKS. I was crying yesterday and said, "I think because I smile and still sound like me that everyone thinks everything is okay and NOTHING is okay. Not one thing is okay." I'm SO tired of it all too.
I just meant that someday, someday not too, too far away, we'll be able to say we lived through it. This is some serious crap, and more than most people ever have to deal with...and so that's totally unfair, but it also means we're pretty diesel for getting through it...even if we cry the whole time.
Hang in there. You're not a nut case, you're in the nuttiest situation!
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I agree cancer SUCKS! I try to be happy and positive and get so mad at my daughter and stepson because they show absolutely NO compassion for my situation what so ever. Maybe its just that this generation of kids are so selfish and wrapped up in their own business. I don't know. I know I never tried to raise my kids to be so selfish.
Anyhow, the Taxol pain has really kicked in today and I am taking the Lortab which helps to some degree. Wish I could sleep but it makes me sleepy but because of the way my brain works on overdrive all the time, I can't sleep unless I take a sleeping pill. I am so sick of looking like a fat, one titted bald woman. I hate the hot flashes! I hate being trapped at home being so tired all the time. I'm mad because I have to stay poor in order to keep my health insurance. I get so sick of everything and I should be grateful because I am alive and able to get the kind of treatment that I do. I could have it so much worse. Ok enough ranting!
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I agree Merilee, I am definately not the same person since this whole thing, and this past year I've cried more than ever! I truthfully don't know if i can forget it... I guess time will tell.
RangerMom, praying for you and positive thoughts.
Scc218, thanks for the explanation... I do not have that, thank God!
I had a lump all of a sudden show up in my groin... In reading my paperwork about the meds it says any lumps call the dr. I get so confused because its the old, what Dr. would I see for that???? I am almost done with Chemo (next Thurs.) and I don't want anymore issues delaying anything. So I guess I will call my onc. office tomorrow and seek advice...
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I finished my Chemo two weeks ago and still have Taxol related pain in my feet. I sure hope this goes away! I found out yesterday because I did not have a masectomy I will be having 33 RADs. I had my port removed yesterday YAYHOOOO! Today I go in for RAD simulation.
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Axtella- so glad you are done and got that port out! Yippy!
I still have pain in my feet also. Especially when I first get out of bed or if I set for a while then stand, my feet yell at me.
As I am trying to figure out my mood and such It has occurred to me that much of my self talk sounds very much like a discouraged soul. I have never been like this. Anyone else relate?
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Axtella: I had a mastectomy and I am still getting rads. We'll all support each other through it.
I've been feeling weird lately, like this is all going to end and we'll get our hair and our energy back, and then WHAT? It's like no honor will have been paid to this year (for me, two years). It will just fade away and be gone, like going to college or being pregnant, or anything else that we did and then moved on. People are going to look at us and say "get over it already, you're done!" And we will look and feel done. I know that should be making me leap for joy, but it's leaving me discouraged today. I'm feeling like cancer came in and messed up my life, and then just dumps me by the side of the road - "have a nice day."
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Beautifully said Windlass I feel the same way. I want my joy back and I can't seem to find it.
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Windlass - P E R F E C T !!! and I could cry reading that.
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My thoughts exactly, too, Windlass. At least we're all in the same boat and can commisserate together.....even if nobody else understands what we're going through, what we've been through, etc.
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I can't remember who's got this in her signature, but I thank her, as I think it often - it's exactly how this experience has made me feel - the one about cancer is like crossing the mafia and getting away with it, you get to live, but have to look over your shoulder for the rest of your life.
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i cant get the imaging thing to work!
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i have had one of those weeks....hopefully this weekend will get better for us.i just feel helpless all of a sudden.might have something to do with the jello arms and legs i still seem to have! just want my life back and now that chemo is over for me i guess i expected to feel better already!!!but i guess that was wishful thinking. atleast food taste great!!!
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I can't wait to get my port out! You know I wonder why I have to get rads after having surgery and chemo? Guess they aren't taking any chances due to my Stage.
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Geo - I can't wait to get my port out either. I want it done right away when I finish chemo in 7 weeks.
I'm also having rads (after chemo and surgery). I start 2 weeks after finishing chemo (mid October I think). We are the same stage. I think its because of the number of positive nodes.
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Looks like a lot of us will be having RADS together. I start about 4 weeks out from surgery which should be somewhere around Sept. 16 or so. I found a place that will take me at 4:30 pm so I can put in my full day's work. yeah! I thought I'd prefer to do at the end of the day then go home and rest instead of in the morning before work. I have white fuzz growing out of my head now! do you think that might be hair coming?? I've never seen so much white hair or at least it looks white.
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Geo and Kiwi- sounds like we are ont he same path. I, too, have had chenmo, now surgery, then rads.
Pawprint - I am jealous tht food tastes good! Cant wait for that moment!
Sounds like many of us are having a bit of an emotional dip - but weshall go forth!!!!! Stronger than ever!! Onward, Warrior women!!!
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