I am terrified of chemotherapy

Options

I am going through the motions of preparing for chemo but honestly don't know if I can go through with it or not. The description of the possible side effects has me in a panic. I know that not everyone has all of those side effects and that the ones with sever complications are rare, but I'm not feeling lucky. On the outside I am a picture of positivity, telling all around me not to worry and that I'll be fine. On the inside I'm having a melt down.

Diagnosed by mammogram and ultrasound in March, by biopsy in April. Surgery was May 20. My tumor was nearly 2 cm, no nodes invloved, stage 1 but grade 3. ER- , PR- and HER2 positive. Suggested chemo regimin is Cytoxin, taxotere, along with herceptin for 1 year, beginning June 23rd. Then radiation 5 days a week for min. of 5 weeks. By sometime in November it all should be complete (except for the Herceptin), barring any difficulties along the way.

I keep wondering if these drugs aren't worse than the cancer? I know that my type of cancer has a good chance of recurring elsewhere sometime. But I'm still not convinced. I'm just more frightened of the treatment than I am of the disease.

And I'd dearly like to have my life back. Cancer has taken over and I'm sick of this already.

Yes, you can all say, 'BUCK UP and stop acting like a baby'. Easier said than done. As I journal this cancer journey to family and friends I am the poster child for hope and positve thinking. But in private I'm a mess.

*Check my post from July 21, 2010 (page 4 this forum) to see what I learned 1/2 way through chemo

*June 27, 2010 started the Taxotere rash saga. 

*Completed chemo on August 25, 2010 and began the first of 33 radiation tx September 21,2010. Completed radiation tx November 5, 2010.   

Instead of saying 'BUCK UP',  I'd tell anyone facing the chemo and radiation journey to "BUCKLE UP"...it's one heck of a ride.

«13456710

Comments

  • jeanl151
    jeanl151 Member Posts: 146
    edited June 2010

      Having gone through it all, I can tell you chemo sounds worse than it is.  I was not sick to my stomach one day. I was just tired for a week, had two weeks of no chemo (worked those days), then did it again for 6 cycles.   It truely is one day at a time.

       Trustn in your doctors and tell them if you have any symptoms of not feeling well. There is no need to suffer. They can give you things for the symptoms you feel.  

       My last advice is stay on this website.  There is so much help and info.  Find a group starting the same time as you.  You willl feel so connected and it is the perfect place to express what you are really feeling.

      good luck,, Jean

  • lorrhaw
    lorrhaw Member Posts: 751
    edited June 2010

    Sorry to hear that you are going through this.  I am quite sure no one on the forum would tell you to buck up and stop acting like a baby because we all do it from time to time, and I think we have every right to do so.  This is scary stuff but thanks to the forum you will find out that you are not alone and that there are many, many people who can relate to what you are going through,

    I was also terrified of chemo but after 4 treatments of FAC I can say that it hasn't been as bad as I had feared.  They give you really good meds that help control the nausea so other than being really tired during the first week after treatment I have done pretty well.  I do gag sometimes over weird stuff and have a bit of nausea but I haven't actually thrown up.  There is a great post in the chemo/ before/during/after section that gives a lot of great tips to help anticipate side effects and help deal with them.

    This forum is a good place to come and rant, rave, vent and cry as much as you need to because we all understand how you feel because we feel the same way at times.

    Good luck and keep us posted.

  • TMarina
    TMarina Member Posts: 692
    edited June 2010

    You're not acting like a baby--you're being real!  Everyone is scared!  I'm so glad you found this website, its been very helpful for me, and I hope it is for you too.  Its a good place to get info, and vent when you need to.

    I think I saw you on the June chemo group?  That's a great place for info about side effects and such.  I agree with jeanl151 that you need to tell your docs about EVERY side effect.  They can help with almost everything!  And with the cytoxin, make sure you drink tons of liquids to flush it out--it can cause bladder irritation.

    I've been down this road before with colon cancer last year, and there were times when I wondered if I could do another round.  But then I would think of all the things I had to live for--family, new grandbaby--and the determination to fight came back.  Counting my blessings helped me--even making lists of things I was thankful for.  And I have a lot of people cheering me on--and you have all of us here on the forums cheering you on!

    Keep us posted on how you are doing.  And ask questions!

    Take care,

    T

  • maltomlin
    maltomlin Member Posts: 343
    edited June 2010

    I'm nearly 18 months post chemo and was absolutely terrified. If it wasn't for my husband I know I would have made a very quick getaway from the chemo ward on the first morning.

    It honestly wasn't as bad as my mind feared. The first couple of days I thought that they'd given me the wrong drugs. I just sat and waited for s/e to kick in. They did but nowhere near as bad as I'd feared.

    Everyone is different but I think most people get some s/e. Mine were mainly concentrated on the mouth. Sore throat, sore mouth (thrush) and the awful taste. Oh and the runs! Fatigue is a problem that seems to affect most people, but go with the flow and rest or nap whenever you need to.

    I am the biggest softie going and if I can do it and come thro' then so can you. You will get thro' this. Just mark the dates on the calendar, batten down the hatches and you'll be thro' it before you know it.

    Life will be good again - not quite the same, but you will appreciate things that you didn't before, and before you know it you'll have your life back.

    Mal x

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2010

    Thanks to each of you for responding so quickly to my SOS.

    Still scared but making appointments and moving forward. MUGA yesterday. PET scan this coming Wednesday, followed by port implant Friday.

    Getting lots of support from friends but none first hand like what I can learn from all of you. Everyone of my friends and family means well, and they will do whatever I ask, but I end up trying to cheer them. I'm exhausted from trying to be up beat. WA WA WA WA WA...there, I've had my melt down. Thanks for listening.

    I am so glad I found this website.

  • lovetosail
    lovetosail Member Posts: 544
    edited June 2010

    Bon - I was scared too.  It really isn't that bad, I had the same regime as you did.  Here are my tips for you:

    1.  Did you get a port?  It really makes chemo easier.

    2.  Take an ativan about a half hour before the infusion.  I'm sure your doc will prescribe it for you if you ask.  It's a mellow anti-anxiety drig - I can't help but think everything goes better when you're calmer

    3.  Start drinking ~2 quarts of water a day starting the day before chemo.  Good hydration helps flush the toxins (the ones produced by cell death).  Just keep forcing fluids!

    4.  Suck on ice chips during the infusion - helps to prevent mouth sores

    5.  Biotene worked great for me for any mouth sores that popped up, they were gone in a day!

    6.  Take a B complex supplement to help with neuropathy, also L-Glutamine helps.

    7.  Walk every day, no matter how tired you are.  Exercise helps with fatigue.

    8.  If you think you want a wig, go shopping before your hair comes out (usually after day 14 or so).  It's way less depressing to shop for wigs while you have hair.

    9.  In the pre-meds they'll probably give you Benedryl, which combined with ativan made me woozy/sleepy.  You may need someone to drive you home.

    10.  I also never got sick once, but if you feel sick, nip it in the bud and get your doc to prescribe you something!

    It will be over before you know it.  Like the others said, there is great information here, use the search function for any SE's you have to read about how others dealt with them.

    This is do-able!  Take a deep breath.   And let us know how it goes!

    Sue

  • jancie
    jancie Member Posts: 2,631
    edited June 2010

    Bon:  I was so terrified of chemo when those words came out of my doctor's mouth.  I didn't remember a thing he said after those words "you will need to do chemo".  Thankfully my dh was there taking notes.

    I had most of the SE's but I still pulled through.  I am a total wuss - zero tolerance for pain, etc.  I am not going to say it was easy but it is doable and looking back (1 year later) I am so glad I went through it because at least if I have a recurrence in the future I will know in my heart that I did everything I possibly could to prevent it and so I will have no regrets.  

    Keep coming here for help and encouragement.

  • flash
    flash Member Posts: 1,685
    edited June 2010

    We all get scared of the unknown.  It really isn't as bad as you think.  Remember an important thing:

    The side effects are for everyone who takes the drug, not a list of effects that all happen to each individual. You won't experience everything, you may even experience NONE of the se's.  Every person is an individual.  My experience with chemo was easy even with taking the red devil.  You really will get through it.

    Hugs

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2010

    In the last two hours, you've all made me feel like I can do this. Maybe not without some bumps in the road, but I can do this. I think. Just have to get past next week's PET scan and port implant. And the hair loss thing. I feel trapped when it comes to that. Can't just test chemo once to see if it is tolerable for me...before the 2nd treatment I'll be bald! Seems like it's the 'hook' to keep going. As they say, in for a penny, in for a pound.

  • Jayne_in_UK
    Jayne_in_UK Member Posts: 517
    edited June 2010

    You are certainly not acting like a baby, this IS scary stuff. You have already had lots of great advice from others who have been through it.

    I am about a year ahead of you, diagnosed April 2009, surgery May 2009. I had different chemo and I can honestly say that it was not fun, but it was doable. I just took it one day at a time and told myself that I did not have to be brave, I just had to show up. I finished my chemo at the end of October 2009 and I am feeling good again now, exercising again, back at work and generally getting my life back. My hair started coming out on day 14 and on day 15 I had it buzzed off, I was glad to see it go at the time as I had no patience with it. I found the hair loss not as difficult as I expected and it has been interesting seeing how it grows back. That is just me, I may be a bit weird :-)

    I bet you will be surprised at how quickly the time goes and you get to the end of it. That is the best place to be, looking back on it.

    Good luck, I wish you minimal side effects. Keep us posted on how you get on.

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2010

    Jayne...I will keep repeating your words over and over in my head...

    I don't have to be brave, I just have to show up.

    Thanks for that.

    And to everyone, thank you. I really can do this now because all of you are here, knowing first hand the issues, and still cheering me on.

    Yes, Jayne is right...I don't have to be brave. I just have to show up.

  • lovetosail
    lovetosail Member Posts: 544
    edited June 2010

    Great advice Jayne!

  • jenn3
    jenn3 Member Posts: 3,316
    edited June 2010

    Bon - You are not a baby, your feelings are normal and valid.  Chemo isn't as bad as you invision it to be and I won't lie, there are side effects, but they are tolerable.   I found that by walking everyday, even on my bad days and keeping a routine of getting up dressed, walking, breakfast, housecleaning, errands(on good days) and socializing with friends and family both at home and outside of the house kept me sane.  I did avoid large crowds like football games and concerts and the mall during the holidays at peak times.  I still went to lunch and dinner with family and friends, maintinee movies, shopping during the day and parties if I was up to it.

    The support on these boards helped me to realize what I was going through and feeling was normal........everyone here is wonderful!  The earlier advice given is great and you can and will do this, we are here to hold you during this time (((HUGS)))). 

  • Cowgirl13
    Cowgirl13 Member Posts: 1,936
    edited June 2010

    Bon, I don't post here that often but I had to post today.  I was terrified about chemo--in fact I said i would rather be dead than have chemo.  I had no idea how i was going to do it.  A friend went with me for my first chemo. I wanted to cry when they started i was so freaked out.  I thought i would blow up in the chair.  Seriously.  I want you to know that chemo is very do-able.  Never once did I have nausea.  The second day after chemo I was riding my horse! (that's becuase the side effects hit about 4th or 5th day). My chemo was Carboplatin, Taxotere and Herceptin.  my last Herceptin will be next month.

     Just show up for your appointment, don't worry if you are terrified.  You can even tell the infustion nurse.  My advise would be to not worry about looking positive for other people becuase it takes energy==save your energy for yourself.

    Now, I actually like going to chemo!!  In fact, i have it on monday and i'm looking forward to it--i love the chemo nurses and people are really nice--the receptionist, the person who takes my blook, takes my weight and blood pressure, my doc.  Believe it or now I will miss seeing them when chemo is over.  I couldn't have asked for a more wonderful team.  

  • TerriD
    TerriD Member Posts: 591
    edited June 2010

    When do you start?  I worked thru my entire treatment "C" for 4 rounds every 3 weeks and Taxol 12 weeks and 36 Rads. Chemo was a breeze!  I hope you have great nurses.  Ask for Lidacaine to numb your port area, put it on an hour b4 they poke you (I covered mine with a sticky note).  God Bless!

  • CoolBreeze
    CoolBreeze Member Posts: 4,668
    edited June 2010

    Everybody is afraid of chemo.  But, it's not nearly as bad as you imagine!  I was scheduled for six rounds of TCH and then because I began getting neuropathy,halfway through i was switched to weekly taxol along with the every three weeks carboplatin.  I was tired at the end but I had no nausea ever, no severe side effects.  I was tired at the end but there are worse things than being tired.  The neuropathy went away and I'm fine.  (My last chemo was March 31st and I finish herceptin next December.)

    There are things you can do to take control of the situation:  read up on how to prevent constipation and eat properly, drink lots of water before your treatments, give yourself time to rest.  Apply to the chemo angel program - they sent me lovely little trinkets in the mail to keep your spirits up.  

    Even losing my hair wasn't so bad.  I bought a whole bunch of wigs, thinking I would change styles with clothes but I didn't like wearing them - too scratchy, so I wore scarves. Now it's grown back enough so it looks like a pixie cut and it's platinum grey!  I'm trying to decide if I like it or want to dye it.  I never, in a million years, would have chosen a pixie cut but I get lots of compliments now.

    went back to work before chemo was over and it was fine.  

    The people I met in the infusion room were really nice.  Everybody was cheerful  - very few complainers.  The whole experience was positive.  I wouldn't want to do it again but if I had to I could without fear.

    Tell your nurses you are nervous and they'll give you ativan, but after the first one is up, you won't need  it anymore.

    I went out to eat after each chemo - the steroids made me hungry!  Even though I had the metallic taste, it didn't matter much.  :)

    You can get trhough it - millions of people a year do.  Good luck!

  • coonie
    coonie Member Posts: 7,618
    edited June 2010

    Hi Bon

    I pretty much had the same treatment except I didn't have radiation.

    My main concern with chemo was the nausea/vomiting. I told my doctor I was worried about that most of all. He prescribed a wonderful drug called Emend . I can honestly say I NEVER got nauseated or threw up. I didn't have an appetite and experienced some diahrreah and alot of fatigue, but other than that, it was doable. I just DID NOT WANT TO BE PUKING!!! Thank God for the drugs to handle most side effects of chemotherapy. Ask your doctor for anything you need to make this easier for you!!

    Good luck!! I hope all goes well for you!!

  • swanseagirl
    swanseagirl Member Posts: 393
    edited June 2010

    Wow, it's great to see so many folks from the UK on this site.

    Originally from Wales now living in WA.  Hi fellow Brits!!!

    I am meeting with the onc and radiologist this week.  I am scared to death also.

    I didn't think I could get any more scared, then they mentioned chemo and port.  I didn't know what a port was so I researched.  That reduced me to tears.

    I only had a lumpectomy a week ago and I am still coming to terms with me having cancer. Like you I feel like a baby, always crying and having pity parties.I want to know when I am going to wake up and say "I CAN DO THIS".   Will that ever happen?

    There are so many brave women on this site.  I'm just not part of that club yet.

    I send everyone love and hugs

    Jules

  • myboysx3
    myboysx3 Member Posts: 4
    edited June 2010

     Everyone is right you are not being a baby. It is a very scary thing to hear that you have to go through chemo. It truly is not as bad as you think. You will probably get very tired and have some side effects but it isn't that bad and they go away. I worked the whole time I was going through it. I did take a few days off the longer I went through it because I got very tired . Just keep thinking it will be over before you know it and it will be behind you. Good Luck  

  • tkone
    tkone Member Posts: 511
    edited June 2010

    Well who wouldn't be scared?  They are pumping poison into us for goodness sake.  No one WANTS to do chemo.  Everyone is scared.  I know it doesn't always look that way, but it is true.  Don't feel like all of us are brave who have gone through it.  We aren't.  But we all felt like we had to keep putting one foot in front of the other and that is how we get through it.   You will get through it also.  Put one foot in front of the other, ask for help when you need it, take the drugs they give you and take it one day at a time. 

    Cancer sucks-there's just no two ways about it.  But I guess I feel like if you have to have cancer, breast cancer is a pretty good one to have.  There is a ton of research and doctors have done a pretty darn good job of figuring out what works and what doesn't.  Trust in your doctors and ask lots of question. 

    Take a deep breath and take that step.  That is all anyone can expect of you.

    We are here for you.

    Tracy   

  • readingteacher
    readingteacher Member Posts: 7
    edited June 2010

    Bon-

    You have put my feelings into words. I have my first chemo tomorrow and have told my husband and daughter they might need to carry me into the infusion room. Most of the chats I had been reading were very scary with all the SEs they were experiencing. Thank you to all who wrote the encouraging words and letting us know that chemo is doable. I am not as scared as I was 30 minutes ago. I will keep telling myself I just need to show up.

  • PearlGirl
    PearlGirl Member Posts: 549
    edited June 2010

    Readingteacher,

    I'm so glad you found this site and know that you are not alone. This breast cancer diagnosis creates a sort of sisterhood...all these wonderful women who wrote their support and experiences here are with you on your journey, through the chemo and beyond.

    I heard a motivational speaker say that fear and faith are both grounded in the unknown. Fear thinks all is negative. Faith looks ahead to the positive.

    We can't let fear overpower faith. We can do this chemo thing. We've come this far and we can do this, too.

    Tomorrow just show up...and we'll show up there with you in spirit.

  • Karen09
    Karen09 Member Posts: 320
    edited June 2010

    No one here would tell you you are acting like a baby.  lol  I think the waiting for all the tests and waiting for the results and waiting for the chemo is the worst part of the whole thing really.  You can do this!  You will get through and get your life back.  Hang in there! 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2010

    I remember the first couple of times going for chemo. I was not handling it very well. I told my husband I wasn't getting out of the car. I got out. I told him that I was not going to walk in. I walked in. Everything I had to do I would tell him I wasn't going to do it. I told the nurses the same thing too. They laughed. The nurses were great. They talked me through the whole thing explaining very step. I sat there and cried but I got through it. By the end of the sessions I was being funny and fooling around. It's been 8 months since I finished. You will find your strength and make it through.

  • thenewme
    thenewme Member Posts: 1,611
    edited June 2010

    Hi Bon and Readingteacher,

    You can do this. Seriously. 

    I like Jayne's quote too - you don't have to be brave; just show up.

    Someone a while back posted another one that I like (but I sometimes have trouble following it):  Keep your head where your feet are.

    Best of luck!

  • shannon56
    shannon56 Member Posts: 73
    edited June 2010

    Bon -- The first day of chemo there was a wonderful woman at the center having her blood drawn.  She was just about finished with chemo for her 3rd primary cancer in 25 yrs, so 3x through chemo.  She told me that chemo wasn't nearly as bad as you think it will be, to speak up to the onco nurses and/or your doctor if you're have any se's.  I did just that.  Carboplatin gave me a terrible headache so the nurses slowed down the infusion from 1 hr to 2 hrs and if I felt the headache coming on gave me compazine (it was a migraine type) which got rid of the pain and any nausea.  My herceptin was given of 1 1/2 hours instead of 45 min to 1 hr.  I was definitely one of the blessed in that I didn't have any se's to speak of.  Mild nausea that compazine cleared up with one dose and extreme fatigue.  In fact I felt so guilty about not having bad things happen that I quit coming to the site.  Now I realize it's important for those of us who haven't had such a bad time to be heard.  Also, I still have my original port.

  • NatureGrrl
    NatureGrrl Member Posts: 1,367
    edited June 2010

    Jayne's words are prefect:  you don't have to be brave, you just have to show up.

    The anticipation is, for most, far worse than the event.

    I would only add a couple of things to all the great advice you've gotten:

    Don't be afraid to share with people how you're really feeling.  You don't have to share everything with everyone, obviously... but don't be afraid to share and let some of that out. You'll feel better and so will the person you shared with -- really.  As someone who's been a caregiver to two people who had terminal cancer, I can tell you caregivers/family/friends can feel pretty helpless.  Sharing with them lets them into your heart and your journey and, at least for me, it brought me a lot closer to people when I learned to share as I went through my own cancer.

    Don't be afraid to ask for help.  Same reason as above -- people do want to help.  Let them know how they can, rather than wear yourself out.

    Finally... you already are one of the brave ones, even if you don't feel like it.  Being brave isn't about not having fear.  It's about doing what you have to do regardless of fear and other emotions. 

    I know you can do this.  I know you will.  I know you'll get through it.  We're all here for you.  Warm hugs....

    Carol

  • vision4utoo
    vision4utoo Member Posts: 138
    edited June 2010

    Bon - just saw your post(s) ~ Yes, it does look scary before hand - You don't have to be soooo perky, well adjusted, optimistic, "I'm fine" all the time  - I found myself taking care of those around me who seemed to be more upset than I...Taking care of you, honor what you are feeling and yes you will be okay!  This is a grieving process for all of us, life as we knew it...but I am much better today as a person (not in the 'nice" category), stronger, more faith, more motivated to accomplish things I have put on backburner...dreams...Losing hair - I LOVED being bald!  I knew I wasn't going to wait for it to fall out - one dear friend came over and we shaved our heads together with our daughters helping with the cutting/shaving!  We made it a party - I knew in my heart I didn't want to wake up with handsful of hair on my pillow or in my shower...Be well! 

  • vision4utoo
    vision4utoo Member Posts: 138
    edited June 2010

    BTW:  I am one of those with most of the side effects ~ and I am adjusting to those too ~ better to be among the living, with my children, I can deal with the longer term SE's that have plagued me.

  • Char2010
    Char2010 Member Posts: 532
    edited June 2010

    Bon - Tomorrow is my 4th and final dose of TC - I work full-time and have only taken off the days that I get the treatment - so it is very doable for many of us.  Just think of one day at a time and you will get through it.

Categories