Sept 2012 chemo

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  • jojo2373
    jojo2373 Member Posts: 662
    edited September 2012

    When are u starting? Other than my foods, meds,and my bag to take along to chemo I bought or made sure I had the following: thermometer, colace, imodium,eye rewetting drops, good lotion, neosporin for ur port incision, benadryl.



    Not a big list, but i have used it all.

  • jojo2373
    jojo2373 Member Posts: 662
    edited September 2012

    To all, Amy recommended Melatonin to me for the cancer benefits plus as a sleep aid. I must say it works for me :-)

  • Cindi74
    Cindi74 Member Posts: 363
    edited September 2012

    Patriciahurtado,  I think I used ice pack first two days for a little, but no pain with port.  Don't remember taking tylanol.  But, I read where seven women on one of these threads were all doing the same medications with seven results in terms of effects on their bodies.  My brother, dentist, impressed that on me in the beginning.  We are so different.  Am so sorry if you are uncomfortable with your port now.  Am sure it will get better.  Hugs

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @bearcub Thank you so much. I too was surprised at how many young mommy's there are dealing with this. I have a 12 yo daughter and a 9 yo son. Still young, but old enough to be somewhat independent and so helpful to me.



    @sheryllynn Thanks for the tips. I was going to Sephora first, but when I couldn't find a parking space at the mall for 10 min I got frustrated and went to Ulta. I will have to go during the week.

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @amylovesbubby I started same regimen on August 20th. So far so good. The SE have been tolerable. The nausea seems to be well controlled on the meds (compezine and adivan). My biggest SE is fatigue. I feel better when I try to stay active. I did start losing hair at the end of my first cycle, so I shaved it.

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @timbek I think the anticipation for me was worse than the reality. Don't get me wrong, it's not fun, but it is totally doable. We are warriors. I believe that God does not allow us to have trials beyond what we can bear. My hubby told me this happened to me because I am the strongest. We all are, and we will get through this together. I'm really tired, but not really sick. The meds are good for that. I am still mommy. Still get up at 6 and make lunch and get the kiddos off to school. I just take nice naps while they are gone. You will feel better once you get through your first cycle so you know what you are dealing with. The not knowing is the worst. Good luck to you sister.

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @jojo7323 yes I live in No. VA just south of DC. Are you in the DC area?

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @patriciahur I did not find the port pain to be too bad. Of course I still had some Vicodin from my TE fills so that helped. That's good stuff. I am almost 4 weeks from port placement and I don't even feel it. Only time it kinda bothers me is with my seat belt. I'm gonna try to get one of those fuzzy cushions. I think that might help.

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited September 2012

    Patricia=- Here is the link to the Important Chemo Threads for Newbies where you will find links for tips and more tips & shopping list, etc. and other chemo threads you might find helpful.

    http://community.breastcancer.org/forum/69/topic/785189?page=1#idx_1

    I used the shopping list and of course I didn't use everything I purchased.  I used a rolling packback that I kept all of my chemo gear in that I always took to the infusion center. I had a ziploc bag of snacks  (peanut butter, ritz crackers, fruit cups, nuts, candy) that I always kept in the backpack in case I got hungry at the infusion.  I also had another plastic container box that held things that I didn't think I needed during the infusion like OTC meds for constipation, diarrhea, extra Biotene products and also extra duplicates of Tylenol, Advil, etc. and  an extra thermometer.  It was my go-to box for home so I wouldn't have to digging around in that backpack.

    I also kept a daily record of the drugs I needed to take and when to take them as well as a daily food record and symptom record.  I also made a list of all of my doctors and their phone numbers, addresses and what specialty they practiced abnd also the name phone number and address of the pharmacy I use and also a close by 24 hour pharmacy.  I also made a list of all of things I'm allergic to ( drugs, foods, tape, etc.) All of these lists helped me  track of everything.  I also marked the pill bottles caps with some large circle color coding labels and noted on the label the name of the drug and dosage.  (As you can tell, I'm a little type A personality....lol)  When I developed a high spikey fever/chills after my second chemo, I made sure I jotted down my temperature and the time I took my temps.  it was helpful when I called my onco to let her know I was having the fever/chills and my symptoms. 

    If you have more questions about the shopping list, just ask.  I'm happy to help you and everyone else here.  Hope you start feeling better after the port placement. 

    Wishing for minimal side effects for those who have already started chemo and calm and restful times for all.

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited September 2012

    Hey everyone,

    I started 1/12 treatments yesterday. They hooked me up to an iv and started the pre-meds something like a zantac, then a benedryl or antihistamine and then a steroid. After that we were good to go and start the Taxol. My nurse literally turned on the Taxol on the iv and started explaining the possible SE to me and in less than 5 min I experienced every  one of them. My arm started to hurt, my stomach cramped, my ears were ringing, my mouth got fuzzy, my jaw and lips felt like they were numb, my face flushed and I started seeing shiny spots. They immediately turned off the Taxol and gave me more benadryl and steroids. I guess I had an allergic reaction to the Taxol. And then they started up the Taxol again but very slowly. An hour infusion ended up taking 1 hr 45min and I was fine. I am wondering if I reacted that way because I have really low blood pressure. This only dawned on my when I got home. I am going to phone my nurse today and ask her. But before we got started with anything she took my vitals. She took my blood pressure twice and asked me if it was always so low. It is. Low blood pressure runs in my family. After that I had the herceptin and without any SE, thank God! I was pretty foggy through the whole thing with the extra benedryl and steroids and of course since it was my first visit, lots of people came to see me - my doctor (of course, because I had the allergic reaction), a dietician, a social worker and the lovely volunteers. I cannot remember much. I had brought a bag so heavy that my DH had to carry it for me. And yet I didn't use half the stuff but one thing that I DIDN'T bring that I will next time is my own blanket!

    Melrose, always the best at handing out the info! I wish I had seen the shopping list before my first trip. I might have brought more useful stuff with me! I started my daily food and temperature journal as soon as I got home.

  • jojo2373
    jojo2373 Member Posts: 662
    edited September 2012

    Forever - glad your ok and thanks for sharing all the details.  I get that in my second round mid October.

    Donna - I am about 1 hr west of you in MD.  Hi neighbor! 

  • aliasismo
    aliasismo Member Posts: 16
    edited September 2012

    Hi everybody, this is my first post! What a roller coaster the last 3 months have been! After being 100% certain I wasn't going to have to go through chemo, I start theTC regimen tomorrow. That's what I get for trying to diagnose myself! I am dreading it, but a girl's gotta do what she's got to do.

    I'm saddened but glad you all are here; it's a big help knowing I'm not alone in this.

    Mo

  • Cindi74
    Cindi74 Member Posts: 363
    edited September 2012

    September Team   of the Exclusive Club No One Wants to Join

    (If anyone wants to be left off, send me a private message.  If I have accidently left you off, also let me know.  Since we are sharing so much together, I thought it would be interesting to see where we are in this trip.)

    AmylovesBubby

    Bearcub                                Prince George, British Columbia

    Firestorm531                        Texas

    Melrosemelrose (visitor from April)                    Houston, Texas

    Cherioo                                Florida

    Whenlifegivesyou lemons       Minneapolis

    Jojo2373                           Maryland                                                                                                                            

    Mycancerjourney                   Illinois

    Sheerbab                              Dallas, Texas                                          

    Foreverchanged72612            Chelsea,  Quebec

    Amy4978                              Howard City, MI

    Cindi74                                 Apopka, Florida

    Terri07-11

    Joemommy                            Portland, Oregon

    Cgesq                                    New Jersey

    SandeeAR                              Conway, AR

    Timbek2

    Laura_g

    Runnergirl71                             Fort Collins, Colorado

    Lokimax2                                  Siler City, NC

    Sparkysbrat                               East Tennessee Mountains

    Momto5children

    SugarlandlDC                              Houston

    PatriciaHurtado                            Miami, FL

    DonnaDo8

    Mariposa123                                Washington, DC

    Damiana9                                    Burleson, Texas

    Timbek2                                       Peoria, IL

    Movinonmom

    Aliasismo

    Ergirl

    Kstillie

    Damiana9           Burleson, TX

    301724                Vermont

    Nickythebean        

    That's 34. So many enduring together.  

  • sugarlandIDC
    sugarlandIDC Member Posts: 23
    edited September 2012

    Forever - I'm right behind you - start Taxol on Thursday and have port placement same day. I too have really low blood pressure so I'm going to quiz them before they start. I hope you read this and are having ZERO side effects.



    To all the mommies of young kids - mine are 16, 14, and 11 and I think all the time what I would do if they were younger. I won't say it's easier with their ages but it is easier to explain what's going on and why things are happening. And being a single mom the help is needed. PLUS, we all know teenagers..give them the bad news they are distraught for a bit, then," hey, can I still go to the movie?" The world revolves around them, I relish those days.



    Thank you to everyone for sharing - I don't have time to individually answer but I sure read everyone's experiences and it really helps bolstering my attitude for mine.



    M

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited September 2012

    GOOD LUCK TOMORROW CINDI74 !!!!  Hope your day in the BGC tomorrow is an easy and calm one and your side effects are minimal!!!  I'm sure you have packed a few things in your chemo bag  and are ready to go.  I know you have done everything and read everything you can to prepare for tomorrow.  Try to hydrate today so your veins/port will be easy to access and ready to go.  I know you are anxious and perhaps a little scared and ready to get started; all of those range of emotions are normal.  Just remember you aren't alone and will not be left alone and unattended during your chemo.  Yes, you can do this and tomorrow after you get home- you can say out loud and very loud---- "I AM DOING THIS!!!"

    Sending lots of HUGS and positive, calming and healing prayers, thoughts and energy to all of you as you make your way through chemoland!!!!  For those who have started, wishing for minimal side effects. 

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited September 2012
    Sugarland: zero side effects today! Went for a long walk with a friend and there was even a big hill  - no problem! Wishing you all the best on Thursday!!!
  • Ergirl
    Ergirl Member Posts: 18
    edited September 2012

    I'm starting TC x 4 on Monday the 17th. No port. Really scared to lose my hair. Bought a wig yesterday that looks like my real hair so that helped. Good luck to everyone!!

  • jojo2373
    jojo2373 Member Posts: 662
    edited September 2012

    Melrose - what do you know regarding exercise and Adriamycin?  I have been doing some lite walking this week, but read on the site to be careful especially week 1 post when taking the red devil (not that I was planning anything but resting week 1 lol).

  • Melrosemelrose
    Melrosemelrose Member Posts: 3,018
    edited September 2012
    jojo2373- Unfortunately, I don't know much about exercise and Adriamycin.  I would tell you that I try to keep moving and probably moved less Week 1 following the chemo round.  I know I always walked whenever and wherever I could even if it was just walking around Target or the grocery store.  I have an exercise fan bike parked in front of the tv that I can hop on for a few minutes here and there.  One wants to be careful about doing strenuous exercise, especially if one hasn't been previously been exercising a lot before chemo.  It is my understanding that Adriamycin can be hard on the heart which may explain why one may not want to go full force exercising after the Adriamycin chemo.  I wasn't a huge exercise person but was always on the go and move before chemo.  During my chemo, I tried to get out everyday to go for a walk, whether it be around my neighborhood or someplace like a shopping mall, Target or the grocery store.  I opted not to go to a gym or any kind of exercise class during chemo since I wanted to avoid close contact with people and somehow became a little germophobic.  My red blood counts slowly dropped over the course of my chemo rounds and reached a point towards my last rounds that my onco told me to start eating foods to help get those counts up.  She and I agreed that I would try to eat high iron foods rather than take a supplement since I don't like to take meds/ supplements unless I absolutely have to.   When the red blood counts drop, you can feel it.  One feels more fatigued and winded.  Whatever your mode of exercise is, take it easy ( not too much too soon), listen to your body and use your common sense.Cool 
  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited September 2012
    Sugarland: I just got off the phone with my primary nurse and she said that my low blood pressure wouldn't have an effect on how my body reacted to the Taxol - I just reacted differently than most people. She promised that we would take it slow again next Monday.
  • whenlifegivesyoulemons
    whenlifegivesyoulemons Member Posts: 184
    edited September 2012

    Here's a simple, empowering, and thought-provoking reference for those of us in the Exclusive Club No One Wants to Join (so well put Cindi):  

    • From This Moment On, by Arlene Cotter.

    A little something to keep on the bedside table, to page through a bit at a time.  Worth checking out.  It's on Amazon.

  • sugarlandIDC
    sugarlandIDC Member Posts: 23
    edited September 2012
    Foreverchanged72612 - port is out!  I'm finally apendage free :).  Thanks for the info on the low blood pressure - we shall see.  I'm glad you are side effect free.  I left the hospital feeling the pain has been worth it when my PS said my "boob" are looking fantastic.  Long road ahead but positive always helps.
  • damiana9
    damiana9 Member Posts: 389
    edited September 2012

    Well, I am now 6 days out from my first treatment.  I had it on Wednesday, friday had a bit of diahrrea and a little tired, saturday I was a zombie.  monday I started getting really achey knees and TERRIBLE heartburn, and today I have a lot of knee and hip pain and stiffness.  Other than that, really very good!  Trying to keep up with protein and fluids.  My son has a cold which of course made me very nervous but we have been obsessive about hand washing and so far it seems to have worked.  I have also not been good about staying home- I have gone out shopping/eating alot this past week.  I am careful about germs but I think getting out has really helped me to feel better.   My hair is not falling out at all yet.  It was kind of tingly for a few days but that has stopped now.  This is all so WEIRD!

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012
  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @aliasismo I know exactly how you feel, When I first found out my tumor was small I though I might be able to avoid chemo too, but once I was diagnosed triple negative it was a veritable certainty. It was a real kick in the stomach, but in time I learned to accept it and embrace chemo as my new best friend. If it's going to be the thing that keeps me from hopefully ever having to get cancer again, bring it on.

  • DonnaD08
    DonnaD08 Member Posts: 128
    edited September 2012

    @daimiana9 Congrats on getting through your first treatment. That is a huge step. I think the anticipation of chemo is worse than the reality. I too felt like a zombie the first few days and I got horrible heartburn on days 5 and 6. I found Maalox worked well for me. I am allergic to prescription PPI's like Nexium. I also realized I was eating a lot of tomatoes. I cut them out and the heartburn went away.

  • bearcub
    bearcub Member Posts: 485
    edited September 2012

    JoJo, I have been exercising everyday on the red devil, day 7 now. I have been on the stationary bike doing 16 km. a day. Before chemo I did 22 km. a day.



    I have had minimal symptoms, a bit lightheaded yesterday at the LookGood Feel Better, but it was 2 hours sitting and for the last hr at 2 in the afternoon listening about wigs. I kinda would have liked a nap at that time. Made it through and the makeup kit is fantastic.



    They did say no false eyelashes with adhesive while on chemo???



    I have spent today sewing a few chemo hats from a McCalls pattern...they are pretty cute. Anyone Sept. girls losing there hair yet?

  • Foreverchanged72612
    Foreverchanged72612 Member Posts: 223
    edited September 2012

    Bearcub: chemo hats? Do you have any links to look at some pictures?

  • bearcub
    bearcub Member Posts: 485
    edited September 2012

    Checkout McCalls pattern #6521 and 4116

  • Cherioo
    Cherioo Member Posts: 305
    edited September 2012

    Hello Everyone, I hope you all are doing wonderful. I went to the cancer society today and was shocked at all the stuff they give you. I received a wig, scarf, binnie, and was fitted with boob inserts and a bra . It felt good to look like I had boobs . You all should check out in your neighborhood if you have not already done so .





    Question? Is anyone having problems going number 2 ? I have the worst constipation . That is probably my worst symptom so far

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