Starting Chemo February 2013

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  • IamNancy
    IamNancy Member Posts: 1,158
    edited April 2013

    Katrine22

    My hands were (sorta still are) they shriveled and were so dry - they hurt.. I kept hand cream on them but it didn't help.. finally big patches of skin started peeling off my thumb and forefinger - thats when the doctor said to use cortozon cream - it really helped. I actually kept the thumb and forfinger drenched in the cream and bandaged to keep it in place.. I still use it as lotion to keep them softer and painfree. - hope that helps..

    I have shortness of breath and its awful... it does seem to lesson just in time for another treatment -but starts up again right away.. I just hope ts not damaging heart/lings but doctor didn't seem concerned.

  • Rdrunner
    Rdrunner Member Posts: 309
    edited April 2013

    Well stupid me decided to wait until yesterday for the mouth sore issue.. they were infected, my temp was really high.. anyway got the meds and a special mouth wash.. and my fever is gone. I have to swallow the mouth wash becaause I have sores in eosphagus also. The relief is amazing, but lesson learned.. dont wait :0

  • melody46
    melody46 Member Posts: 279
    edited April 2013

    Welcome Katrine, I can relate to the lung stuff, I've been short of breath and Nancy is right it starts to go away just in time for your next treatment and then its back. My treatment center has frozen gel gloves to put on my hands during treatment and I also use tea tree oil on my finger and toe nails. I use the Hollywood beauty brand and it smells like mint. Depening on the brand you get it can smell bad so take a whiff before you purchase it Smile

      

  • Heidi9256
    Heidi9256 Member Posts: 87
    edited April 2013

    Nancy, I had #3 last Thursday and am MUCH more tired this go around.  I've also had a lot more pain than I did with #1 or #2.  I'm not working this week so and I've sat in this chair until my butt hurts.  I'm gonna roll out today no matter what.  Just to the library or something - at least so my butt can get a breath of fresh air.  57 days until my last treatment!  Woo Hoo!

  • IamNancy
    IamNancy Member Posts: 1,158
    edited April 2013

    Heidi- hope you felt better after getting out a little - today was the first day I finally felt like the achiness has left BUT I started with diarrhea - hopefully tomorrow will be a great day ..

    Rdrunner - glad you finally got the mouthwash - sorry you suffered so much

  • melody46
    melody46 Member Posts: 279
    edited April 2013

    Nancy how are you feeling after #3? better/worse?  My third treatment today and no reaction which was such a relief. 3 weeks til my last treatment and I'm starting to perk up a little not too tired today but have the neulasta shot tomorrow. Rdrunner hope your feeling better with the mouth wash.

  • Katrine22
    Katrine22 Member Posts: 2
    edited April 2013

    Thanks Melody and Nancy for your replies. It is good to hear that others are experiencing what I am. somehow it just makes me feel better. Rdrummer gladyou got the mouth wash. Are you using Bioteen? I really appreciate the tea tree and  cortazone suggestions. I am starting Taxol or maybe Abraxane   onf April 10th. does anyone know anything about the difference between Taxol and Abraxane. It is supposed to be the same but somehow wrapped differently. If I take the Abraxane, I don't have to take the steroods, decadron, the night before and morning of the infusions. When I took the decadron before, I could not sleep hardly at all. so I am tryng to find out the difference because I would love to avoid taking the decadron if I can.

    To andy of you who are suffering from side effects, I send my healing wishes.

      

  • LW122713
    LW122713 Member Posts: 52
    edited April 2013

    I'm going in tomorrow for my 3rd treatment and will then be 1/2 way through. I feel like I'm getting somewhere now. I too have some sores in my throat but luckily nothing has crept up any further.



    I talked to my MO about reconstruction today. After my lumpectomy swelling went down I've been left with one D cup and one C cup. Plus the scar is so long when lifted up in my bra there's a giant crease more line a giant dent. It reminds me of an accordion now. Also it will get even smaller with radiation. One B and one D would look really odd so I think I'm going to get a new pair. I'm going to have them pulled up to where they used to be when I was 20. I'm going to get something good out of all if this.

  • leecy5
    leecy5 Member Posts: 14
    edited April 2013

    I am bt treatments 3 and 4 of TAC and I have been down for 7-8 days with the last two treatments. Really dont feel like doing a lot until day 10.

    I thought I was crazy because my recovery has been soooo slow each time. I am nearing day 14 and I am still weak. I have only been able two return to work in the 5-7 days before my next treatment - i take it every 21 days.

  • IamNancy
    IamNancy Member Posts: 1,158
    edited April 2013

    melody - on chemo day and the neulasta shot day - I felt good - thought, wow, maybe I am getting use to it.. LOL.. nah, 3rd through 7th day were awful.. tired, tastebuds shot, achy flu feeling, low fever..yesterday I started feeling normal again..hope you do better than me. I coming up on treatment 4 and final - april 17th.. will be glad to get it over with.

  • ywheels22
    ywheels22 Member Posts: 230
    edited April 2013

    LW: I think a new pair is a great idea! I love my new sisters. Perfect size B (300cc's in each). My permanent implants go in about 8 weeks after my last chemo, which is May 15. I am very happy with how they look now with the TE's in and I know they will look even better when my PS outs the permanent ones in. Good luck!

  • Wildlyshel
    Wildlyshel Member Posts: 48
    edited April 2013

    I have been researching Taxol trying to prepare myself for the new SEs--tomorrow will be my last A/C treatment. Hurray! I swear if this ever comes back I think I will have a melt down. I feel like I will always be looking over my shoulder.



    Anyways...I found this site for SEs and how to control things like nerve damage and mouth sores and the results of studies etc etc.



    http://www.truestarhealth.com/Notes/1451003.html



    Hope this helps.

  • tangles
    tangles Member Posts: 508
    edited April 2013

    Heidi how did your outing go? I feel like such a wimp. I dont leave the house for about a week after Chemo. I just dont have the energy. I think I had less SE with #3 but the fatigue is the same if not worse. I am 13 days post last Chemo and if I do too much I am still exausted. Last night I had to go to my sons school and just walking through the parking lot and into the school my heart was beating fast and I was out of breath. I feel so guilty not working. I have worked all my life. My hubby says forget about it and rest and get better during chemo, but I see others are working during their treatment. Maybe if I had a sit down job it might make a difference. I am hoping to get back to work during Rads, but after reading some of the post in the Rads section it worries me with everyone saying they are tired. UGH I just want to get back to work.

  • Rdrunner
    Rdrunner Member Posts: 309
    edited April 2013

    Well no chemo for me tomorrow. It was supposed to be my first taxol. Spiked a high fever, feel horrible and she doesnt want to do it until we get the blood cultures back. No obvious signs of infection so Im hoping is viral and that the cultures come back negative. 

  • Wildlyshel
    Wildlyshel Member Posts: 48
    edited April 2013

    Rdrunner -- I am so sorry. :( Hope your blood counts are up and you can get in there soon. I know it feels to want to get in there and just get it done.



    Tangles -- I am not working either. I am so envious of those able to work. I feel like a slug. Just the thought of doing laundry and taxes today is daunting.



    Shel



  • Rdrunner
    Rdrunner Member Posts: 309
    edited April 2013

    Ya my counts are great.. she thinks I might have a bacterial infection somewhere.

  • Wildlyshel
    Wildlyshel Member Posts: 48
    edited April 2013

    Last post for today...I swear.



    I was doing research about Livestrong at the YMCA because I want to gain some stamina back after the chemo and I found this comedian. Though he has testicular cancer, his video called Chemocation is relevant to many going through chemo. So, I thought I would share.



    Hope you ladies enjoy as much as I did.



    http://halanscott.com/chemocation-cancer-house-guest/



    Shel

  • Heidi9256
    Heidi9256 Member Posts: 87
    edited April 2013

    Tangles:  I am only working part time.  I teach three high school classes, three days a week.  I also take off the week after chemo.  Just not functional enough to be able to handle even three days.  I tried it one week and it nearly did me in - by the end of the day I was barely upright.  Even though I made it through the week I decided that week off would be a little gift to myself.  Not having to worry about whether or not I'm going to be able to go to school the next day is a big relief.  I'm 7 days past #3 and I feel extremely week and my balance is off.  I'll bend over and just keep on heading over till I catch myself.  I am VERY achy and painful this time.  The flu like aches are new for me.  I've had sharp pain but not this all over achiness. I actually felt okay Monday.  Tuesday was bad.  Yesterday was okay.  Now today is bad.  Ready to get off the ride.  Beautiful sunny day out.  I'm going to go plant myself in the sunshine and hope that helps.

  • tangles
    tangles Member Posts: 508
    edited April 2013

    Heidi on day #6 after Chemo #3 I thought I was feeling Ok so I ventured out too for about an hour to the store and paid for it. I got pretty sick, headache, dizzy, ect.... I think even if I feel Ok I need to stay resting for that entire week so 7 to 8 days after. Even now 13 days post chemo after some cleaning house this morning I am feeling it. Very worn out and tired. I seem to get a slight headache every evening. My hubby just keeps saying rest rest rest but it is hard to do!!

  • IamNancy
    IamNancy Member Posts: 1,158
    edited April 2013

    I work but I have a desk job - also I don't work for the first 5 days after chemo and it takes me another week to build up to a full day of work.. I am fortunate my boss is very understanding.

  • tangles
    tangles Member Posts: 508
    edited April 2013

    I am a hairstylist so on my feet, arms above my head,lots of smelly chemicals. Plus I nick myself allot when doing razor cuts. Funny how a tiny nick before chemo would do nothing but now puts you in the hospital!! We like any salon have people coming in sick all the time. We have a very small salon too. I cant even count the number of times I have had clients say they were headed to the walk in clinic after they get their hair done. Or they missed work the day before because of the flu. They can be coughing up a storm and say oh its allergies don't worry. People do not Cancel hair apt's for NOTHING! Major snow storms included! Then if I have to cancel or leave early because I cant do it I leave them hanging and I think that makes them more upset then having to find someone else. I do worry about losing a very good amount of my clients, but I guess if we can manage 6 months without the income we can manage with half my income when I go back. Im just so bored sitting around and miss the social part of working. Oh well 7 more weeks until my last Chemo. Of course I wont be done with treatment until Feb 2014 Rad's and Her2 but just getting this Chemo over will be a huge relief!

  • caitlin61
    caitlin61 Member Posts: 214
    edited April 2013

    Katrine, on my 4th round of AC, I had some dryness in the palms of my hands (mainly up the side of one thumb) and the soles of my feet. Only lasted for a couple of days, but during that time it was a bit painful to walk. Didn't think that was supposed to be a side effect of AC - expecting it more with Taxol.



    Had first round of Taxol yesterday and thankfully no allergic reaction. Only problems were that they practically had to stand me on my head to get port to work (now I'm on Coumadin) and Benadryl zonked me (fell asleep in chair for two hours). No Neulasta for me while on Taxol. MO does want me to take Claritin for a few days - thinks that will potentially help with joint, bone, muscle pain (but he did not advise Claritin when I was on Neulasta - had only minimal bone pain from that anyway). So far so good - but wouldn't really expect SEs to kick in for a couple of days.

  • Wildlyshel
    Wildlyshel Member Posts: 48
    edited April 2013

    Going in today for my last A/C treatment. I can't tell how glad I am this is the last one because there were some times when I thought I wouldn't be able to finish. (like the night I was getting sick out of both ends at the same time and was shaking so bad and so weak I couldn't get off the toilet - sorry if it's tmi. I had been constipated for almost a week and then took two ducalot sp? -- I will never do that again.). I cant wait to be off the nausea meds and to stop taking the stupid shot. Some of you have been through hell with the shot and it scares me every time I get it.



    Next is the Taxol which brings a whole new set of anxieties of the side effects. I hate this. I hate feeling like I am being swept down river in the rapids instead of steering the boat in my life. I really feel defeated right now and if it ever came back I don't think I would do this. Everyone says to stay positive and I try but there are days like this one (this not where I thought this post was going) when I want to crawl under a rock and give up. I know I am feeling sorry for myself and there are people who have it much worse but they must be made out of stronger spirit. Mine is on the edge.



    I won't be posting or reading for a few days. Reading makes me nauseated and dizzy after the infusions. I hope your treatments go well. <3
    <br />

  • ywheels22
    ywheels22 Member Posts: 230
    edited April 2013

    Tangles: don't be so hard on yourself. I am only working part time. I take 5 days off after treatment, then work five days, but only 5 hours. I work partially at a desk but also do photography so I am up and down. Everyone is different and we all react differently. You are not weak at all. Don't ever think that of yourself. You are a strong warrior fighting with everything you have to beat this. Work is just work. It will be there when you are ready and that will be before you know it. Chin up my friend. You will beat this all the way to hell and you will have your life back!

    Wildly: congrats on your last AC...it is a huge relief. I hope your SE's are managable. I just had my first Taxol 1/4 after finishing 4 AC's. Right now, it is much easier than AC. No where near the pain, yucky ass taste in mouth, foul stomach, etc.....I am tired and groggy feeling, with some aches but really not bad. I can sleep through it so that is good. I think you will find, as many on Taxol who also did AC have said, Taxol will be easier. Yes it has it's own SE's that you have to deal with, but, and I hope I am not speaking too soon, it is better. Hang in there. This road is so up and down, it is hard, but us Bellas are all here to support each other and help each of us when we hit a downward hill that seems nearly impossible to get up out of. We will pull you out, toghether. Chin up my friend!

  • tangles
    tangles Member Posts: 508
    edited April 2013

    Thanks ywheels like wildyshel I have my days. The last two I have been down in the dumps. I like everyone else just want this OVER WITH. Unfortunally I have a ways to go yet.......

  • ywheels22
    ywheels22 Member Posts: 230
    edited April 2013

    Tangles: I got sick during my last AC and I was so down. It sucked! Just keep looking for the bright days. They will come!

  • Rdrunner
    Rdrunner Member Posts: 309
    edited April 2013

    Well my first taxol was cancelled today.. I have had a week of high fevers of unknow origin, no infection can be found. Last night it was 104 with rigors for 3 hours. Im rescheduled for next Friday but dont know at this point if it will go ahead. I have to record fevers, and I have to go for an echocardiogram to rule out endocarditis. She said there is a slim chance it could be from the neupogen shots but it didnt start until I was done them. I feel so horrible at this point I would be quite ok with her stopping the chemo period!

  • slv58
    slv58 Member Posts: 1,216
    edited April 2013

    Rdrunner, I am so sorry you are going through this. First the mouth sores now this, please take care of yourself! Big gentle hug, I will be thinking of you- hang in there, you can this!

  • tangles
    tangles Member Posts: 508
    edited April 2013

    Rdrunner so sorry. I know how disapointing a week set back is. I have had one so far and pray I dont have another. We all just want this over as soon as possible!! I think that is why I have not gone back to work. I am so afraid of all the sick people that come into my work. I have pretty much stayed in my house besides doc apts to avoid getting sick again. I will say it is driving me crazy and making the days sooooo long. Good luck to you.......

  • ywheels22
    ywheels22 Member Posts: 230
    edited April 2013

    Rdrunner: very sorry to hear you are not well. Sending prayers your way for a quick recovery.

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