March 2010 Chemo Start

Options
1313234363767

Comments

  • LillyC
    LillyC Member Posts: 64
    edited May 2010
    Here's a picture of my team in the RFTCMy Team
  • Charley
    Charley Member Posts: 255
    edited May 2010

    Hello Fellow Marchers -

    I am better today -- not great --- but better so no ranting today!

    LillyC - I love your picture!! So great to hear how so many have gotten to participate in RFC! I too have been very tired and have no stamina.  The first 3 treatments did not effect me as much and I was able to get out and walk most days. These last 2 have been killer.  I tried to walk yesterday and did not get far.  About 10 minutes and I was ready to quit. LillyC - we have our last chemo on the same day ... 5/19?  I'll be thinking of you.

    hereandnow- You are very lucky to have your mom with you during some of this.  My mother passed away when I was 10 from BC and I have been thinking about her alot lately wondering how she made it for the 5 years she lived with Stage IV (all sorts of weird treatments- early 70s- w/ 3 little kids) so faraway from her sisters and other family.  Funny how this has really made me reflect on things.

    Suzanne - Not only does chemo give you bionic hearing (I too have had that sensation) but I have had bionic smell!  Never had problems with smells before but now I can smell every little odor!  And that is not always good! 

    llm822 - You are right.  You have to be reasonable about what you can and can't do at this point.  I have frustrated myself - physically and emotionally - because I really wanted to do something and then couldn't.  If you can, play it by ear.  A trip would be fun but I can tell, the way I'm feeling after #5, I would need more than week to get to the point where I would have fun traveling.

    Hugs to all, Charley

  • LillyC
    LillyC Member Posts: 64
    edited May 2010

    Finally figured out how to post a photo from the Komen Race for the Cure!

     

  • frosty1
    frosty1 Member Posts: 420
    edited May 2010

    Lilly -- my onc asked me about shortness of breath and said taxotere was to blame.  I told him it only is for a couple of days, doesn't wake me up at night, and goes away.  Since my lungs were clear and my heart beat good, he was okay with it.  But do check in with your doctor just to make sure.

     LLM - New York sounds lovely as a present!  You know your body, but your family wants you to visit -- can you go and do NY "Light"?  Maybe a show, sit in Central Park, enjoy the food?  I was thinking today that heading out somewhere sounded wonderful (especially now that I'm off the cranky truck - although I am refusing to make dinner this week -- I figure they are all capable, they can figure out what to make for dinner -- UGGHH - frustrating!).

  • Charley
    Charley Member Posts: 255
    edited May 2010
    Frosty - You make me laugh!  Are you sure you are off the cranky truck? Please don't let them starve! I think mine would if they didn't have popcorn or cereal. Don't even talk about actual cooking ...  I mean it IS a gas stove. Geez! Wink
  • hereandnow
    hereandnow Member Posts: 322
    edited May 2010

    Lilly that is such a beautiful photo. And what a wonderful thing for your family to do. I'm definately going in our version of the walk for a cure next year.

    Charley, I am in awe of those of you with kids and going through this. Your mum must have been an amazing woman to go through the journey she did, when she did. 

  • badger
    badger Member Posts: 34,614
    edited May 2010

    Hey all - this is so cool...yesterday a co-worker offered to organize a work team for RFC June 5.  I was so touched!  First inspiring mammograms (I know 'cuz they tell me) now this!  So I said yes.

    I'm getting teary-eyed just thinking about it.  Has anyone done these events - RFC or Relay for Life etc - and NOT burst into tears?

    The run is out for me but there's a 3k which is just under 2 miles.  Tx #5 is on 5/25 so I s/b OK by 6/5.

    Have a good day everyone, {{hugs}} all around.

  • staceyt
    staceyt Member Posts: 106
    edited May 2010

    Hello Ladies,

    LillyC - What a great picture - It made me cry happy tears!! 

    Good wushes to all

    Stacey

  • marilyn7
    marilyn7 Member Posts: 86
    edited May 2010

    I feel like I jinxed myself.  I was half-way through and feeling good, but now I have a blod clot in my port vein (non-occlusive thrombosis, subclavian vein).  It is not supposed to interfere with my treatment (#4 on Monday), but I am now taking blood thinners including 2 injections each day.  It has taken an emotional toll.  I feel like screaming - IT"S NOT FAIR!!!!!!!  But then again what is?

    Charley - glad you've turned the corner.

    Lilly C - great photo - Our Race in June 5th in DC.

    It is so great to hear that some folks are done! Wow, what a feeling that must be.  I am on a 3-week cycle, which has been great to have some recovery time, but it does prolong the process.  I won't be done until June 28th. 

  • sandiek9
    sandiek9 Member Posts: 54
    edited May 2010

    I'm off to my first Taxol infusion! Glad to be done with AC, nervous about what's next. Anyone had Taxol yet? xxoo Sandie

  • mamaof3bugs
    mamaof3bugs Member Posts: 198
    edited May 2010
    I am off to my last AC!!!  Then I will be starting 12 rounds of taxol....sandie how many rounds are you doing?  Wish me luckCool
  • horsedoc
    horsedoc Member Posts: 512
    edited May 2010

    I'm glad to hear someone else mention the super-sensitive smell thing.  It has been driving me CRAZY. 

  • frosty1
    frosty1 Member Posts: 420
    edited May 2010

    Didn't notice the smell as much this go round ... probably because I was focused on staying upright.  But the first two times, it was awful.  I had to ask my DD to stop using perfumed hand lotion -- it just about did me in.

    Now it is just the saggy, wrinkly face.  I feel so OLD going through this!  I know I'm not, but just feel like it.

    Charley -- maybe you're right -- I may not be off the cranky truck just yet.  I think I'm enjoying it too much.  Picture:  flatbed truck, me sitting on the back swinging my legs, and enjoying the h**l out of being so damn cranky.Tongue out

  • teemee
    teemee Member Posts: 122
    edited May 2010

    LillyC, love both of your photos! Especially your profile one, with a big pile of pink love and you somewhere in there!

    frosty1, also love that cranky truck. Make your family cook you dinner and heck, just serve it to you out there. That's my vote ;)

    Just to chime in on the shortness of breath--big YES for me. My lungs are clear, but I climb a flight of stairs and I'm about done in. And although I'm no super athlete, before the chemo part of my job was to hike around our very steep mountains all day. My onc also says it's the taxotere.

    And smell, OMG! Let me just say if one more person gets gas around me, I may poke their eye out with a pencil. I guess I need my own cranky truck. 

    I got a rental car today, luckily my insurance covers it. I haven't been willing to drive yet but I have (another) job interview tomorrow for a design job in a couple of months. It's really hard to be a freelancer going through cancer treatment. That is my complaint of the day. Anyway, wish me luck, I'm going to be super vigilant on the road!

    I'm going to try and upload a little profile pic now...

    Toni

  • Kayne
    Kayne Member Posts: 103
    edited May 2010

    Hi All,  I've been away for awhile, so much happened while I was in the HOSPITAL!!!  A week after my second treatment feeling so, so lousy, started to run a fever,  Went to a hospital in town for blood work, wbc was .07, put into isolation.  Looked for source on infection, transported by ambulance, (against my will) to Cooper Univ Hosp. where all my Docs are.  They were afraid my left incision was infected, Yes I still am not healed from my Feb 12 surgery.  So far so good, we are on a wait and see plan.  It is possible my left tissue expander is or could get infected and need to be removed!!!  This is my non-cancer side that I chose to have removed!!  If it does, my ps can put a new TE in in about 4 months.  Don't know if I can go through that pain again.  Just from being in bed for so long my chest muscles are tight and the TE are digging into me again.  PS was away while i was in the hospital.  Saw her associates.  Went for chemo #3 this past Mon.  but onc held off due to possible infection.  Sent me to my PS, she cleaned out the incision, now have an inch and a half crater on my left breast.  Hoping it will heal.  Go again today to have it checked.  Will possibly find out about chemo for Mon.  I have not had one treatment as planned.  I feel like I will never be done with this journey.  Felt so bad while in the hospital was ready to throw in the towel.  I couldn't imagine having chemo on top of it.  Thank goodness I feel better.  Gives you a different perspective.  Almost did my husband in -- he was so worried, poor thing.  It's taking him a long time to recover.

    Enough about me, so happy to hear about all the strides made!!  Many treatments finished, way to go. I love all the pics, so nice to put a face to a name.  As for the smell thing, it drives me crazy.  One night I got out of bed and came downstairs to put out the kitchen garbage.  I could smell it all the way up in my bedroom.  My husband thought I was crazy, it was 3:00am.  But it was keeping me from sleeping!!  Hang in there everyone.  Hope for a great day with minimum side effects.  Hugs those not feeling well.

    Michelle

  • jdootoo
    jdootoo Member Posts: 253
    edited May 2010

    Toni: I was reading your post and am curious about your job search. I, too, am a freelance designer. I work for one person, but the work has all but dried up, so I would love to find a full time job.

    How do you interview and deal with the fact that you are going through chemo? I thought about just wearing a wig and not saying anything, but this seems so dishonest. Basically, I have just been staying home thinking of going back to school!

    I wish you the best of luck on your interview!

    One love... Jackie

  • Yeshua4Me
    Yeshua4Me Member Posts: 77
    edited May 2010

    I thought this time around I was doing great...not so. Mother's Day the SE's hit hard and I thought I was dying. Wednesday brought some relief and today I feel as if nothing bad has happened to me! I actually feel great! Except my feet feel weird. I can't explain it. Just the bottoms of my feet. Oh and my mouth feels like it's scalded inside. Can't taste a thing. Even with these lingering SE's I can still say I FEEL GREAT today! Not looking forward to going back into the torture chair on May 24th. I think it's unfair I have to do this TWICE this month. But on the bright side, it will be my last A/C thank God. Then next month I start 4 treatments of taxotere which makes me a bit nervous. Wondering how that stuff will hit me. Hopefully I tolerate it better than Adriamycin and Cytoxan.

    Oh, I just started taking violin lessons. Yeah, I'm old (47) but I do weird things to keep my mind active and alert. Never played a musical instrument in my life!

    Walked my son out to his car the other day around 5:30 in the evening (California) and couldn't understand why all my neighbors were staring at me. Then it hit...I forgot to cover my head! At home I always go bald and completely forgot I was "naked" in public. Guess I gave them something to talk about.

     Hope everyone is well. Today I am putting on my red, kick cancer's butt cowboy boots and going shopping! I just gave chemo the last 10 days~the next 10 days are mine!

  • Ana1973
    Ana1973 Member Posts: 88
    edited May 2010

    Hello my fellow Marchers!

    I haven't posted in a while..I'm pretty much just going through the motions. I am happy to say Wednesday will be my last chemo! I am actually looking forward to sitting in that chair just 1 more time. I want to get it over with! I pray with all that I am, that I never have to go through it again. My rads consultation has been scheduled for June 2nd and my hormone therapy will be starting around the same time.

    I have a SE that I haven't read about in our posts. I have a 2 or 3 day stretch where all I want to do is eat! I wake up wanting hot wings at 6am, ice cream at 7am, steak at 8am....all day long! Just eating! I had my hubby go to the local store to buy $40.00 worth of ice cream cones, ice cream sandwiches, cookies and Klondike bars! Then in my steroid induced cranky voice, I tell him to go to bed at 9am so I can go back to the kitchen to eat some more! I started chemo weighing 119lbs and have gained 10lbs due to my cravings....I know it's unhealthy, I just can't help myself (laughing). Why can't I crave carrots, celery and salad? Anyway, I'm just wondering if anyone else is experiencing this?

    I hope everyone is having a good, SE free day!

    Hugs to all of you!

    Ana

  • hereandnow
    hereandnow Member Posts: 322
    edited May 2010

    toni, I love your profile pic, now you do good scarf. I tried but just couldn't do it well, so I'm a hat girl. I will try to figure out how to post a picture, any hints?

    Kayne, you are not alone with the boob wound drama. Mine has only just healed, (10 weeks post-op) but it went back and forward, and I was on antibiotics for 6 weeks, and I've been doing daily dressings. I had a skin sparing mastectomy, and they make the flaps thin with sometimes a problem with how much blood supply they have. So I had a moderate flap necrosis - needed 2 further small excisions of the dead tissue, and each time I've had chemo, it sets it back a little, but as I said, the wound is finally limping towards healed. In the middle of it, I felt low about it, until I realised that it was nothing that I was doing to make it worse, it wasn't my fault, and I started doing more with my arm and shoulder, and just made sure my nutrition was ace, as if we're not anyway.  There was a large study out of memorial sloan kettering that reported an incidence of around 4.5% of flap necrosis after mastectomy with TE placement - they range in severity, and do set things back a bit. I hope yours settles soon for you without any involvement of the TE. I took photos every day to chart the progress of the wound - hope no one ever opens that file accidentally :)

    Yeshua, I love that you have taken up Violin after never having a musical instrument background. The woman really loves a challenge, nice to do lovely challenge though. You should wear your red cowboy boots while you're going through the scales - now that would be a sight.

  • dawnn6th
    dawnn6th Member Posts: 4
    edited May 2010

    I was just about to post the same question! All i do is think about food and eat enough in one sitting for 2/3 people!! It's non stop! I haven't had any sickness luckily but getting tired of constantly wandering around the kitchen looking for food! 

  • horsedoc
    horsedoc Member Posts: 512
    edited May 2010

    I've been having the same eating issues too... I have some things that I just can't stand to think about eating, but then cravings for weird things, and it actually makes me feel better after eating.  Like macaroni and cheese, the orange cheese crackers, french fries, ice cream, ice cream sandwiches,  etc.  After my 2nd treatment I was wanting potatoes, and pasta with pasta sauce (not the mac/cheese like now.)   I am so frustrated because the healthier stuff I used to eat just seems gross to me.  And I really do feel better after eating this fattening stuff.  Maybe it's psychological.  All I know is that I'm gaining weight, and I'm so tired after working all day it's impossible to exercise.   The good thing is that I'm almost done; one more treatment to go, and after I recover from that I'm going to have to really work hard and start eating right and exercising again.  Once my stupid taste buds and smell gets back to normal!

  • Charley
    Charley Member Posts: 255
    edited May 2010

    Michelle - so sorry about the hospital stay but glad you are better.  Hopefully you can get on with the chemo now and get it overwith!

    I have had my cravings as well and have gained 5 lbs since chemo started.  It is strange though that the cravings have been different each time. Hamburgers, then hotdogs, steak ... normally not alot of sweets but fatty and salty. I certainly don't want anything that is GOOD for me like fruit or vegetables. 

    Ana1973 - Looks like you, LilyC and I will be having our last treatments next Wednesday.  :-)

  • Ana1973
    Ana1973 Member Posts: 88
    edited May 2010

    I'm sorry to say that I am so happy it's not just me with these crazy food craving. My hubby laughs at me because I have always been a healthy eater and exercised 5 days a week and now I'm so tried from chemo and eat nothing but junk...it's a whole new side of me. I'm relieved to know I'll be able to get back to my old ways in a few short weeks. Although it's my understanding I have to be careful about working out and the risk of Lymphedema.

    Charley- It will be a happy day for the 3 of us, I'll be thinking of you both :) I'll also be thinking of all the Marchers to finish after us...hang in there ladies. I know, easier said then done, but I am sending warm hugs and lots of strength to you all.

    On Monday I am going to the Look Good, Feel Better class. Has anyone else gone? Is it fun?

    Have a great, SE free evening to all.

    Ana

  • MNLinda
    MNLinda Member Posts: 204
    edited May 2010

    The first three treatments I had were always followed about a week later by a few days of wanting to eat everything in sight.  Not so much specific cravings, it was just that after I finished eating something, I kept thinking "Now what can I eat next?"  Cut back on the Decadron, and it wasn't really an issue for the final few treatments.  Steroids increase your appetite.

    I also found that when I cut back the Decadron and had less fluid retention, I also had less shortness of breath while walking.  Many, many things I found troublesome about chemotherapy were more related to the steroid than to the chemo drugs themselves.

  • frosty1
    frosty1 Member Posts: 420
    edited May 2010

    FOOD!  I think I finally stepped off the cranky truck.  That was a long ride.  I had to get me an armchair so I could wave and point at people I was cranky with.  Geez.  The food cravings are worse than when I was pregnant.  I'm trying to curb them but I just shove stuff in -- even when I have metal mouth and can't taste anything.

    Ah the dilemma of interviewing ... I had an interview 4 days after my MX and started my new job two weeks after my first round of chemo.  I waited until I was made an offer and accepted and then called my new boss.  She was great about the whole thing and everyone has been great at work.  I've been there 2 months now and am doing just fine.  Since most of SEs (until this last round) are on the weekend or don't floor me, I have only missed the days I'm getting chemo. 

    I'm so jealous of all of you that are finishing.  And I agree it isn't fair we have 2 this month!  My next one is the day after my 26th wedding anniversary.  Guess I'll have to wait to celebrate!

  • Charley
    Charley Member Posts: 255
    edited May 2010

    Ana - I went to the Look Good Feel Better class about a month ago. (Seems like it was years ago)  It is fun and you will get a bunch of free stuff!  I'm all about the free stuff. ;-)

    Hugs, Charley

  • marilyn7
    marilyn7 Member Posts: 86
    edited May 2010

    I signed up for the Look Good Feel Better, but ironically didn't feel well enough to go.  I'm hoping to go in June. It's a pain to get to during rush hour and its at the secured NIH facility so security is a hassle, but I'll try again.  I hear it's lots of fun.

    I had double chemo in April, so just one session in May - Monday.  Then I'm 4 down / 2 to go.

    As for food, I don't have cravings per se, but I find myself eating a lot of junk food that I normally wouldn't eat - potato chips,nachos, Taco Bell??  I think it's weird psychology that I have lost so much of my normal life, that I'm not going to deprive myself of potato chips for gosh sakes!  totally illogical I know, but I've spent the past 20 years of eating healthy and it didn't protect me from cancer, so what's the use.  I'm hoping / assuming I will get back to may healthy habits, but right now I'm either cutting myself some slack or throwing a bit of a tantrum - most likely both.

    Blod Clot doing OK.  Arm swelling went down a bit, but I've got some weird spider veins - I actually look like Iron Man (2).

    Congrats to those who are finishing.

  • teemee
    teemee Member Posts: 122
    edited May 2010

    I got the job, yay me! Now I have 3 clients with at least some work lined up through fall. Need a couple more jobs but sheesh it is hard to hustle while lying on the bathroom floor ;(

    jdootoo, I was a wreck for an entire week, a full week before I lost my hair. And it hasn't bothered me since. I bring this up because it's the most obvious sign of 'being sick.' (Ironic cancer never made me sick a day in my life, just treatment!) I quickly figured out I was not a wig person, so I typically wear scarves when I'm out. In my interviews I've just walked in like nothing is odd, and then at some point gesture to my head and say 'obviously I'm going through chemotherapy right now,' and they say some version of 'oh, I'm sorry' and I simply say 'thank you, I am going to be fine.' I make it no big deal, and I let them know the weeks I'll be down straight off. So far, the 2 jobs I've snagged since chemo, the clients seemed relieved to know how specific I could be -- ie no work here for 5 days -- and really comfortable with me.

    My guess? It's a combination of me faking how together I am (if I believe it so do they), identification (when you think about how many people are touched by cancer in some way, it's probably 50%) and I have been lucky enough so far to interview with women, who I think have an extra level of identification. It hasn't been nearly as uncomfortable as I feared.

    Ana, I loved the Look Good Feel Better Class. You get a huge bag of free, quality skin care products & cosmetics, and a priceless couple of hours with people who can laugh and cry right along with you.

    Yeshua, I love hereandnow's visual of the violin and cowboy boots. And good for you for taking up something new!

    Hereandnow your comment about my scarf made me think how interesting it is that we are all so different in how we cope with hair loss. We have the Wig Women, Scarf Women, Hat Women, and Brave Baldies! Every person seems to favor one. I've been having great fun on the days I feel good, playing with different ways to tie them, making scarf pins, etc. I probably have a head start since I come from a family of arabs ;) I'd say my second favorite is bald. How about you all?

    Happy day, wonderful weekend, and take care of your beautiful selves,

    Toni

  • Ana1973
    Ana1973 Member Posts: 88
    edited May 2010

    Ok, so I don't know if I need my head examined, but I have a job interview this afternoon. I have been in sales for the last 5 years and I have had it with the stress of the job. So, today I am interviewing for a supervisor position. I have my suit all ready to go, just can't seem to find suitable head wear! Baseball hat...no, beanie...no, scarf...just doesn't look right, and I am not a wig girl. I have to wear something on my head due to the fact I look like a baby orangutan with fluffy tufts of hair, so au natural is not an option either. I guess, I'll figure it out...I am totally qualified for this job, I just hope they can look past my current "situation" to see all of my attributes. So, wish me luck!

    Thanks for the info on the LGFG class. Did you take a friend or family member with you? Can you? I soooooo love free stuff, now I'm excited about going :)

    Hugs to you all, my March sisters!

  • hereandnow
    hereandnow Member Posts: 322
    edited May 2010

    Toni, congratulrions on the job. And Ana - good luck. I am inspired by all of you. Toni, I am a hat girl out of the house - I have little woollen skull caps, I have a turquoise hat that looks like the cat in the hat without the point, and a red one thats similar, lots of beanies, and mum knitted me a couple of woollen berets that look a bit like tea cosies, but they're really warm, and good for around the house. Otherwise, I'm a baldy.  

    Mbalcombe, glad to hear the arm is less swollen. I had fun at the LGFB I went to - I scored lots of goodies too, and I got 3 new lipsticks!  

    Lisa

Categories