Chemo May 2011

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  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011

     Cyborg, I hate this Hurry up and Wait. At this point I know for sure I am having chemo, Or atleast I better as they are putting in a port Monday 16. But it would be nice if they tell me what meds I am going to be on. LET ME RESEARCH!!

    Loviesmom2 I am trying to focus, but currently I feel up in the air with all this waiting.

    Marybe- Yes I am planning on having fun with her. I am also going to ask the people there how they make the hair extensions as my daughter wants some of my hair made into an extension for her.

    DebRox- I think you are right about the waiting. I wish I knew when I was starting,

    mccrimmon- my surgern told me that I have to be healed before chemo.

    Pop up add at bottom of this page, Breast milk may offer early cancer test. Like when you are breastfeeding you are thinking oh I need to be tested for cancer. All I was thinking about was is she gettig enought food, I hope that tooth doesnt come in sharp, and oh my breast are so full I need to feed her.

    Anyone know what to do about a pulled groin mussel, (happened at surgery april 21) cant seem to make it feel better. Hurts worst then the lump removal stuff. I am tired of limping around.

  • ---
    --- Member Posts: 197
    edited May 2011

    MamaV,

    Thanks for sharing about the 3rd day being the worst.  I really am hoping im on my way to crawling back because I don't think I can take this anymore. 

    Everything is really bad - nausea, queasiness in stomach, headache, fatigues, muscle pain.  I hate everything on that list!  Sorry to vent out.

    Take care,

    Laureen

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    We have to vent!!! I had one boot of nausea yesterday and today. I think I am getting my energy back. Man o man -- I can nap like crazy!!!!! Now I am in the fired phase.

  • ---
    --- Member Posts: 197
    edited May 2011

    Take care, Cyborg.  I don't want to jinx it but it's looking like today may be the potential better day for me.  I was able to write an e-mail to family and friends, post here on bco, and watch tv.

    Take care everyone!

    Laureen

  • Sue53
    Sue53 Member Posts: 63
    edited May 2011

    Just started TC X 4 chemo two days ago and decided I need to to join a support group so that I don't feel so alone in this journey.  Not feeling very well today but better than I did this morning.  Does it usually last a week before you feel better?

  • thinkpiece
    thinkpiece Member Posts: 7
    edited May 2011

    Hi, starting TCx4 every 3 weeks on Monday, 16th, ugh.  Local recurrance but chest wall involvement after 10 years clean and free.  Looking to shrink this sucker so I can have surgery in the fall to remove.  I went wig shopping today but I'm thinking ... no.  Just not me.  Love to all.

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Oh Stepahnie, sorry you are facing this again, mine is my second time, but with a new primary after 8 years.

    Sue53, I am still waiting for a week to pass to see if I feel better:)

    Laureen, so sorry you are feeling so bad! I had some sickness this mornig so I took the anti nausea meds plus lorazapam and went right back to sleep! I feel better now, hoping to go for a short walk, feeling housebound.My nurse did call this morning and said I was likely low on electrolytes or the low bloodpressure thing. She asked if I checked my blood pressure-well, no, I was too busy passing out!

    Cyborg, what day are you on? I am looking forward to more energy. I haven't felt really bad, just kinda weird and very tired, the meds seem to be halping me with sickness.

    So I had chemo on Saturday, they makes me 5 days out. I better find a wig or head coverings soon!

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Bkj66 I had my first infusion on may 2. I still get more tired than usual. Spent all day in a hospital cause my friend had surgery and I am wiped.



    Let's hope that this round takes the cancer out bkj66 and Stephanie.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

    Still no SEs and today I went for my neulasta shot....got it in my stomach.  I took claratin which someone told me would help with the bone pain I could get....thought that was pretty wild advice, but I did it and I asked a nurse and she said she thinks Susan Love recommended that in her book.  Too early to tell if I will even get bone pain, but if I do I think it's in a few days.  Next week I am off, but I will be going in for my Xgeva shot (for bones) and having blood work done. 

  • ---
    --- Member Posts: 197
    edited May 2011

    Hi Marybe,

    i read your post and saw that you still have not had side effects?  when did you have your tx done?  WOW!  I start battling SEs 2 hours after my infusion, oh man!  Lucky you!

    Laureen

  • lorenar
    lorenar Member Posts: 141
    edited May 2011

    MaryB; I go to the James Center. I go down on tuesday and stay in a hotel get treatments on Wed. and come home after that. What part of Ohio are you at. My sister usually travels with me, since it is about a 3and a half hour drive. We so enjoy going to the tuttle mall. Even though I never have money to buy anything. ha. They treat me so good at the James and I have alot of faithin the treatment I am recieving there. 8 more treatments of taxol/herceptin before surgery,.

  • lorenar
    lorenar Member Posts: 141
    edited May 2011

    So sorry I have not been posting ladies. Tryingt to get caught up on everyone. sorry for you feeling sick. I have found the worst side efffect eith the taxol/herceptin is leg and feet pain, and some fatigue. All in all it is so much more doable than the adrimyacin/cytoxin. I have noticed alot more hair stubbles but eyebrows and lashes thinning. I ordered some eyebrow makeup from qvc from the Mally line. Her makeup is so worth the cost. If you have any blood in nose from taxol it is a side effect. If it ever runs out doc said go to er they have to plug a hole of some sort so far not that bad. It is real tiring driving 3 1/2 hours every week to ohio but the great treatment I recieve is so worth it. Plus I stay in a hotel on  Tues. come home on Wed. I dont know about ya all but money is so tight with the cancer. So cant afford much. ha. Surgery is to be sometime in July now. I wish you all the best and will try to keep posted.

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Still no hairl loss and I am ten days out from tx on TC.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited May 2011

    Cyborg, I think it is too early still on the hair....mine took over 3 weeks.

    Lorenar....3 1/2 hrs is a long drive.  I live in Cincinnati.   My boss's wife went to the James Center...it is about a  2 hr drive from here.  Glad you are happy with your treatment there. 

    Oh Laureen, Just saw your post....my lst treatment was May 4, had #2 yesterday and a neulasta shot today.  I feel extremely fortunate because really I feel absolutely no ill effects yet. 

  • thinkpiece
    thinkpiece Member Posts: 7
    edited May 2011

    Guys, let's make the May girls mantra:  No Apologies!

    Let's vent and bitch and moan all we want, because I bet we are all doing the "game face" all day long, which is exhausting.  So no apologizing here, I decree it!

  • mccrimmon324
    mccrimmon324 Member Posts: 1,076
    edited May 2011

    Off to the drs this morning to go over the details of my treatments.  I'm so nervous it's ridiculous, then I actually have a 2nd opinion scheduled for later this afternoon.  For some reason I think he's going to tell me something absolutely worse, I don't know why I feel that way.

  • rondajean
    rondajean Member Posts: 74
    edited May 2011

    So I am new here and this whole DX sucks! I cut my long hair into a pixie before surgery.  I am so glad since I would never been able to fix it or sleep on a ponytail.  I would advise anyone to just cut it short and enjoy one less hassle in life.  I see my oncologist next week to discuss the "plan" and it it driving me crazy.  I feel like I am waiting so long and since I had 6 positive nodes, I just keep feeling like it's moving around in my body and will come back somewhere else.  I felt like I was in good hands and now question it.  Its a crappy feeling.  I look forward to meeting the MO and building a relationship of trust.  I need that more than anything right now.  Once I get the "plan" I will come back and get advise from all of you.  There seems to be some really good info here and I will use it wisely.  I look forward to all the "friendships" I will make here.  

    Ronda 

  • solds19
    solds19 Member Posts: 9
    edited May 2011

    I had my first AC yesterday.  It was a hard day.  I felt great through the treatment but about 3 hours afterwards, I started feeling nauseous and spent the rest of the night throwing up.  None of the meds seemed to help.  Also had a really bad headache.  I took my day-after nausea meds at about 4:00 this morning and so far am feeling fine.   I'll be getting my nulasta shot at some point today.  Hoping for a better day!  

  • Sue53
    Sue53 Member Posts: 63
    edited May 2011

    Hope everyone is doing ok today.  Feel better today than yesterday but kind of lonely here at home alone.  Hubby said he would try and come home early.

  • Sue53
    Sue53 Member Posts: 63
    edited May 2011

    Alosp, anyone notice that their body odor is like chemicals?  It's awful!

  • ---
    --- Member Posts: 197
    edited May 2011

    Solds19,

    I had the very same experience, so you are not alone.  I had my AC last monday and side effects kicked me 2 hours after the infusion.  Hang in there.  I am still nauseous today (5th day). 

    I was telling everybody I ahev been to hell and am starting to crawl back.  When I woke up this morning (5th day), I felt like I am back at the gates of hell:-(  No fun!

    Take care,

    Laureen

  • solds19
    solds19 Member Posts: 9
    edited May 2011

    Thanks Laureen!  Helps so much to know we are not alone in this journey!  We will all make it out of the gates of hell!!!  Ha ha!

  • Cyborg
    Cyborg Member Posts: 848
    edited May 2011

    Sue53 yes. I smelled like something horrible. Seemed more noticeable to me than others.

    I feel really week. Found out a side effect of my antibiotic or med for thrush causes dizziness. And diZZiness leads to nausea. not good.

  • txladysara
    txladysara Member Posts: 52
    edited May 2011

    Hello everyone I am new here, have been lurking and finally decided to post. Thank God I am doing better, started chemo on Monday 5/9, 6xFEC, Ughh it sucked. The first 3 days weren't too good. I had nausea and kept falling asleep. I couldn't even see anything on tv w/ out dosing off. The worst was constipation, which i believe made the nausea worse. I finally pooped yesterday, it wasn't easy had tons of colic, but tummy is feeling much better today. The main problem today seems to be acid reflux or heart burn. I also seem to have my clavicle (on the port side) swollen and it hurts a bit. I am glad that I am finally feeling like myself again and look forward to becoming a part of this group. 

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    I had a week followup appointment and my white blood counts were 800! That is low! I had a neuposgen shot 24 hours after chemo, then one today and they want to do on on saturday and sunday. Has anybodies white blood count got this low from the first treatment? No wonder why I am so tired. They told me to stay away from sick people and wash my hand alot-duh! ANything else I can do? What foods help? Doc found out I am pretty much vegetarian and told me that I can not be during chemo, he told me to go eat a steak! I had some beef enchiadas instead, I can't eat steak or chicken! I will eat fish though.

  • Beaglesgirl
    Beaglesgirl Member Posts: 287
    edited May 2011

    Welcome txladysara! This is the place to be to share our less then pleasant journey and we can celebrate our wrap up of this awful thing together :) when it's over!



    I start Tuesday my AC x4 DD I went to walgreens and bought what I was missing of the basics on my 'list' they had the biotine gum and mouthwash, miralax, colace, and 3 new scripts.



    I have done all I can to prepare, now I just have to show up on tuesday. The preparing kept me busy and now it's just the slow wait... I have to remind myself that I feel like i got ran over because I had surgery to remove the cancer, the chemo is for rogue cells that escaped the knife the rads the same. I am a "throw everything at it" kind of person I am not going without one heck of fight.



    ...now if I could just stop shaking in my slippers ;)

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011

    Today was a BAD day. I went to the surgern today. As you know I had a PET CT scan on Tuesday. The results were 4 hot spot on it. One in my lung, one liver, one right leg, and one left leg. I am still scheduled to get my medi port on Monday, and now Wednesday I am scheduled to get a biopsy of my lung. I am so scared! Cried in the doctors office, lucky hubby was there. The pain in my leg that I have had sence surgery could be from the hot spot on it. I just want to scream!!  I mean, yes I havent been to see a doctor for a check up in 3 years almost 4. But in 2007 I had a base line mamo and other tests and everything came back good. I found this lowsey lump myself. Other then my leg hurting and being sore from the surgery I feel fine, but no I may have cancer in 5 different places in my body. UGGGGG!!!  I feel sorry for myself, I know that we all are going threw this but why me is what is running threw my mind. Why anyone??

    Again HURRY UP and WAIT! I hate that!

    Other news, I am going to get my hair cut short (and donate) sometime in the next week. Daughter wants to come with me when I get it cut.

    Yummy news, I went to the local chocolate store (they make their own chocolate things) and got Chocolate covered oreos. Yummy!!

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Laureen, have you been getting yout neupogen shots? DId your white cells tank like mine? Now I have to go get 2 more shots over the weekend, after the 2 I already had. I really didn't expect this, the last time I went through this my counts stayed good, although I did not do dd, plus I am 8 years older now!

  • bak94
    bak94 Member Posts: 1,846
    edited May 2011

    Oh Candice, I must have been posting at the same time as you-I just want to give you a big hug! I hope it all turns out to be nothing, it just doesn't make sense and none of it is fair. We are here for you though if you want to rant, vent scream, cry, whatever, we are here.

  • 40-years-old-now
    40-years-old-now Member Posts: 309
    edited May 2011

    bkj66 Thank you, I am just so scared. I not even sure how to explain some of this to my 6 year old. She understands the cancer part, but thinks it is only in my breast. How do I explain it could be more? She already had picked up that mommy is very upset and has been trying to comfort.

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