Starting Chemo February 2013

Options
1282931333459

Comments

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

    Hi ladies, hope everyone is enjoying the week end. Well, two days after my first docetaxol, I'm really feeling it. All my bones from hips down are aching. My toes feel numb/burning, I could barley sleep last night. My MO told me to expect this, but I guess I was hoping it wouldn't be as bad. Taking Tylenol extra strength and hoping to catch a few zzzz's. I just pray this isn't something that will last after treatment. Trying to keep smiling even though I sometimes just want to cry.

    To those celebrating Easter, I hope you find renewed strength, peace and love spending time with your families. Shari

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

    Shari - can you ask your doctor for a sleeping pill - getting a good nights sleep really helps.. we can face so much more if we have our sleep Smile

    My husband and I are just spending Easter together - this is treatment week and I don't feel like I feel well enough to spend the day with family - or even able to appreciate a nice holiday dinner.

    To all of you that celebrate Easter - have a blessed and happy Easter.

  • tangles
    tangles Member Posts: 508
    edited March 2013

    Ywheels do you use the tea tree oil to prevent the neuropathy? How do you use it?

    We too decided on not doing anything for Easter. Just dont have the Energy this year. There will be many more Easters for us all to celebrate!!

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

    IamNancy, thank you for suggestion, I may have to call her and see. I do know she said that if Tylenol extra strength wasn't cutting it, she could prescribe something for me. At this point I'm not sure if I should stay on top with the Tylenol or wait until the pain really bothers me. I know with the anti nausea meds they say to take it whether you actually need it to prevent nausea, wondering if its the same for pain. I just hate taking meds, but sleep is important.

    I'm curious about tea tree oil for neuropathy as well, since I'm feeling it in my feet and a bit in finger tips.

  • foxey2410
    foxey2410 Member Posts: 21
    edited March 2013

    I will do round #2 wednesday the 4th. my first one wasvery rough but hopefully round 2 won't be so bad the boards are a good way of support everyone is helpful so use them for a support team. Hope fully you will be one that just don't get sick many don't. I am 63 so at your age you should do ok honey. feel free to message me any time/ all we can do ispray and talke one day at a time lots of luck to you. JUST TELL YORSELF WE CAN DO IT. I will also do 6 week of radation 

  • melissa119
    melissa119 Member Posts: 172
    edited March 2013

    Hi ladies



    Just checking in. Hope you are all doing well with minimal SE's. wishing anyone celebrating a happy Easter.

    Regarding the tea tree oil. My mo suggested it to help with my nails which lifted and hurt at the end of taxol tx and after. It is supposed to help heal that. I wound up losing only one nail so maybe that helped. But it really smells! Lol. Don't put it on then go out anywhere! Everyone will be wondering who smells! Lol

    Hope that helps.

    Have a great weekend!

    Melissa

  • melody46
    melody46 Member Posts: 279
    edited March 2013

    My MO told me to take it for my nails also and so far no problems. SLV58 cry once in a while it helps ease the strain.  Happy Easter everyone!  Its going to be a beautiful weekend here in the Seattle area.  Starting to feel better just in time for round three on wed if my white cell count is way up over normal I think I'm going to ask to pass on the neulasta.  I had so much pain and weakness from the hips down after my last shot.

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

    Melody46, are you sure the pain you are feeling is from neulasta? I only ask because I have had 3 neulasta shots with each FEC treatment and felt no pain, now with my first docetaxol (taxotere) treatment (and neulasta shot day after) I am experiencing what sounds similar to you-bone pain from hips down. My MO warned me that this was a common SE of docetaxol and I'm guessing because I had no problems with neulasta for three times, my pain must be from that.

    Just a question, do you just rub tee tree oil into your nails? I always thought it was more of an antiseptic?

  • tangles
    tangles Member Posts: 508
    edited March 2013

    Melody I was going to ask to skip the shot too then my husband reminded me of how horrible it was in the hospital for ten days so I took it. I had pain last round but not one single ounce of pain this time. I did some research online and it says the way it works is the shot is making more bone marrow to create white blood cells so your pain is coming from the bone marrow expanding. Once it has expanded you wont have pain and that was so true for me. I still took the clariton and will each time just to be safe as clariton is not going to hurt anything. Now dont quote me with the way I explained it, I may have messed up a bit so look it up online and read on the way it works. I hope you dont get the pain with round 3 like me. One thing I have noticed with round 3 is I am starving all the time. Not sure why maybe that prednisone is still in my system. It is hard to be starving and have everything taste so bad. Frustrating.......

  • ywheels22
    ywheels22 Member Posts: 230
    edited March 2013

    Tangles: tea tree is to help keep your nails. Rub it in with a tissue or cotton swab. Rub it on nails and cuticles. It really smells though! Use B6/12 and l-glutamine powder for neuropathy prevention. I started B6(100 mg) and B12(200) and will take one every day through Taxol tx. L-glutamine is 2tsp 3x a day on day of and two days after tx. Mix it with juice. At least this is what I have been told. Hope this helps.

  • melody46
    melody46 Member Posts: 279
    edited March 2013

    Tangles I remember your trip to the hospital. SLV58 I've only had one neulasta shot and it was the day after #2 and when I had the pain start. My muscles are incredibly weak and I'm short of breath. Not sure whats causing what but hopefully I dont have it next time, so far each time is different. It may have nothing to do with the shot and could just be the chemo. I got a tea tree brand at RiteAid called Hollywood Beauty and it smells like mint so I just put a drop in each hand and rub it into the other side nails and watch tv for a while while it soaks in.  Is anyone taking bioten or using special hair shampoos or do you think its too soon to worry about hair?

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

    melody - I get short of breath also.. scary but doctor didn't seem concerned - its just another side effect of chemo

  • kkmom
    kkmom Member Posts: 54
    edited March 2013

    IAMNancy,

    I have also been short of breath - which started after chemo #2.  My blood pressure has been really low like 96/70.  Even climbing stairs when I go to bed, makes me feeling light headed.  My MO was not concerned either. 

  • Rdrunner
    Rdrunner Member Posts: 309
    edited March 2013

    Has anyone had a problem with really bad mouth and throat sores. Its so bad right now despite the constant rinsing with baking soda and water. I cant eat a thing other than a bit of ice cream. Im thinking I might go to ER tomorrow if its not better, it hurts a lot even to talk, my gums and my tongue are a mess and my throat is so sore and a bit swollen but not restricting breathing. Ive been lucky so far and not really had this, but every SE has been the worst with my 4th AC

  • Lmimp64
    Lmimp64 Member Posts: 219
    edited March 2013

    Rdrunner - do you have magic mouthwash? My mo gave me a prescription for it just in case. It's not the same as u can make at home. Can your on call mo call it in to a 24 hr pharmacy? I hope you feel better and get relief. Use the er if u need to. Best.

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

    kkmom - my blood pressure has been low too... hope the shortness of breath goes away when this is over..

    Rdrunner - oh I hope the mouthwash works - sounds like you have it bad.. I used a salt water rinse for my mouth but it was never as bad as yours.. how is it today?

  • Rdrunner
    Rdrunner Member Posts: 309
    edited March 2013

    I intially was using salt and water and it didnt really help so I switched to the baking soda and water trick. No difference today. I cant eat even mashed potatoes.. and I cant believe Im saying Im sick of eating ice cream lol!

    I wont be able to get ahold of MO today for sure, I see her on Tuesday anyway so Im not sure if I want to go hang out in ER for the day today. The pharmacist looked at it yesterday for me and said they were bad and normally the doc do prescribe something.  Not sure if I should wait until Tuesday or not.

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

    Rdrunner - don't suffer until Tuesday - try and call the MO - don't they have someone on call over weekends? the doctor won't want to know you aren't eating anything... you need to be able to eat to build your strenght up..

  • melody46
    melody46 Member Posts: 279
    edited March 2013

    I only ended up with one sore on my tongue after #1 but I talked through my teeth for about 5 days and barely ate anything. I agree with Nancy you should call him and he'll call a prescription in for the magic mouth wash. Somebody should be on call this is the formula they gave me but its not magic mouth wash.  1/2 teaspoon of baking soda and 1/2 teaspoon salt to 8 oz of warm water 3X a day.  I hope you feel better soon I know how those things hurt

  • Lori5B
    Lori5B Member Posts: 6
    edited March 2013

    Hello, this is my first post, I started act chemo on February 21. I had the normal side effects with dose 1 and 2 (nausea, constipation, fatigue, etc.). The third dose was a different story, I was so exhausted I couldn't get up, ended up my red blood cells were very low, so I had three iron infusions last week, then my white blood cells tanked (.400), so I am getting daily neupogen shots. I also received neulasta shot the day after each chemo. My question is if anyone has experienced this also, I have been mostly in bed for 7 days now. I am getting frustrated. Thanks for your help.

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

    Lori5B - hope you recovery soon.. sounds like this time you had a really horrid experience. Did they say the Neulasta shot didn't work?

  • tangles
    tangles Member Posts: 508
    edited March 2013

    Rdrunner your MO should have someone on call 24 hrs. Call!! With my MO if I need to go to the ER they have an agreement with the ER that Chemo Patients dont have to sit in the wiating room with all the sick people. Maybe your's has that too.

    As for thw short of breath I asked me MO and she said its the Chemo. I am 9 days post treatment and still very short of breath. I hate it!! I got the tea tree oil and OMG I almost puked the smell was so overwhelming.......

  • kkmom
    kkmom Member Posts: 54
    edited April 2013

    Lori5B - Yes, I had extreme fatigue with chemo 3.  All my counts were low, but the neutrophils were like .07.  I did have a neuropegen shot on Wednesday and they did come up.   Chemo 1 and 2 was also very difficult for me.  For this chemo 3, I received extra fluids on 2 different days after the chemo and I think the fluids made a world of difference. 

    Maybe ask your doctor about additional fluids.  I tried to drink as much water as I could, but at times it was so difficult to get water down. 

  • Lori5B
    Lori5B Member Posts: 6
    edited April 2013

    Thank you, I don't think the neulasta shot worked this time, I need to ask my oncologist this week if it will work for me in the future. I had hoped my counts would not have dropped so soon, and I worry that they will continue to be a problem with the rest of my chemo treatments.

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

    I try to drink as much water as I can - they stress how important it is after the few days after chemo - I try but seriously its the hardest time to drink water or anything... nothing tastes good and I don't feel hungry or thirsty..

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

    its been 6 days since my 3rd chemo treatment and I feel terrible - tired and my whole body is aching ... I felt tired the last times but by now I wasn't still achy.. I also run a low temp (100) now and again.. who else felt like this at the 6th day point?

  • melody46
    melody46 Member Posts: 279
    edited April 2013

    I felt like that too after #2 and I'm going in for #3 tomorrow and I feel so damn tired and still sore. I have a bad feeling the next ones gonna knock me down ugh!

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

    melody - I wish you all the best tomorrow..

  • tangles
    tangles Member Posts: 508
    edited April 2013

    Nancy you are getting different chemo then I am but I feel like it was day 7 that was the turn around for me. I will say #3 was easier for me then #1 and #2. I am 11 days post #3 and woke up feeling great so started cleaning house after two bathroom's and a load of laundry I was beat. Almost sick. I ended up climbing into bed for the afternoon. I have to remember no matter how good I feel I dont have the energy I use to. In fact I talked to my hubby about going back to work maybe part time but after working around my house for 3 hrs and getting sick Im not sure I am ready for standing on my feet at work. Tomorrow I am taking it easy. I hope you feel better tomorrow!!!

  • Katrine22
    Katrine22 Member Posts: 2
    edited April 2013

    This is my first time posting to this lsit. I started chemo on Februaru 8,2013. I have just completed four cycles of Adriamycin and Cytoxan. I will be starting Taxol on April 10th. I am hoping someone has had some of the same side effects I have so you can possibly recommend anything that might have helped you. It seems like in this fourth cycle I have really started to feel some of the toxicity in my hands and feet. My hands especially feel like they have been sturated in water too long. They are really shriveled but also super dry. I have not lost any nails, but my nails feel really sensitive as does my skin. I cannot even open a water bottle without something between my skin and the top. I have tried a number of lotions, but nothing seems to make much difference even vaseline. My fingers are even a bit numb. I went to a neurologist yesterday and he said I do not have peripheral neuropathy. Anyone had to deal with this? Any ideas?

    Also I  am having a lot of shortness of breath which seems to make me cough alot. I have mild ashtma so it seems like the chemo may have kicekd it up a bit. My  inhalers don't seem to make much difference though. 

    I have had many side effects, but these are not seeming to go away and really bothersome. It is pretty hard for me to think about starting Taxol when I feel so burned out and so weak and tired now.

    Thanks for listening and look forward to any ideas or thoughts.

      

       

Categories