Any secrets to Chemo? things they don't tell ya about?

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ShannonCannon
ShannonCannon Member Posts: 4
  • Hello ladies ~ please forgive me for being such a newbie as I do not know the proper "terms".. This chapter is so new to me almost unreal in a way. I am dealing with so many thoughts, fears and issues that you all have posted about and thought maybe you had some words of wisdom, or advise for a beginner with the same diagnosis might shed some light as I feel I am fairly lost in the process.
  • I am 37 mom of 2 young boys 11 and 7 and one day in June found a lump in my right breast sitting on my couch of all places…as I watched a movie with Meg Ryan called "In the Land of Women" where she faces breast cancer herself. Sounds like I am telling some "story" however, it is not... it is my reality now. At my first ultrasound in late June my tumor was 6-7cm and to date have had 2 lumpectomies. I now know my tumor was rapidly growing being the labs have come back combined size in late July was somewhere between 1.8cm and 2.1cm so my diagnosis is
    • IDC STAGE 1 GRADE 1 ER/PR + HER- 0/3NODES-
    • … Breaks my heart to even type those words.. I am scheduled to start TX chemo (4 rounds) this Thursday and was wondering if you had any advice, tips? I don't know just anything I need to know? I feel so incredibly "in the dark" so to speak…. Forever sending positive energy your way ll!!!!

Comments

  • blondedoris
    blondedoris Member Posts: 197
    edited September 2015

    Hey Shannon

    Have a look in the Chemo forums - Forum: Chemotherapy - Before, During, and After. There's heaps of good advice and pointers on there.

    Sorry you've had to join us here but we're all here for you

    {hugs}

  • mdg
    mdg Member Posts: 3,571
    edited September 2015

    So sorry you find yourself here. My son was only 4 when I was dx almost 5 years ago. I did TCx4 too. It was not as bad as I thought it would be...not fun, but doable. For me I kept exercising daily and drank tons of water. I never had nausea at all which I am thankful for! I was able to do most things I wanted to do except for the few days after chemo where I was just really foggy and tired with some body aches. I did take the Claritin for the bone pain due to the neulasta shots and that helped (I suffered horribly after the first shot and I did not take Claritin that time). I also used Cold Caps to save my hair. Most MO's won't tell you about that option, but I am glad I did it. Having hair made me feel "normal" when nothing in my life was normal at that time. You can do this....you will be done in 9 weeks. Best of luck!


  • ladyboss1997
    ladyboss1997 Member Posts: 202
    edited September 2015

    ADVICE FOR CHEMO:

    take the nausea pill regularly for the first 24-48 hours
    after chemo. Don't wait to get nauseous. The first 24 hours worked for me. I
    never got nauseous

    drink 10 - 8 oz glasses of water each day for at least 7
    days after chemo. I just started doing it every day, and still do

    if prone to constipation, drink one glass of metamucil or
    similar fiber drink each day for 7 days after chemo

    for 72 hours after chemo - rest. Let your body do what it
    needs to do. Sleep when you want to sleep. Be awake when you want to be awake.

    take short walks every day or do some type of light
    exercise daily

    eat/drink high protein foods. My favorite go-to was
    muscle milk, scrambled eggs, and peanut butter sandwiches

    the taste buds going wacky was the worst side effect for
    me. The only thing that tasted good was sweets, and you have to be careful with
    those. I kept a bag of low calorie mints with me at all times. And I drank flavored
    water because regular water was yuk.

    keep Benadryl and itch cream on hand in case you get
    hives. I only got them once.

    use Nail Tek daily on finger and toe nails

    Take Biotin and a probiotic daily

    get a night cap for your bald head, if you tend to get
    cold easy.

    Get a nice wig before you lose your hair. It will make
    her feel prepared. I bought my wig to match my hair color and style almost
    exactly. No one would have known I had lost my hair if I did not tell
    them.

    I cut my hair very short before I began chemo, then
    shaved it when it started coming out in droves. She can expect to lose her hair
    10-14 days after her first chemo. It might help to have her favorite
    hairdresser on standby to do the shaving. Throw her hair a goodbye party.

    When I finished chemo I began using Ovation Hair Advanced
    Cell Treatment on my head. My hair has come back prettier and thicker than
    ever. I still use it 4 years later.

  • hope49
    hope49 Member Posts: 370
    edited September 2015

    Hi Shannon,

    Sorry to meet this way, but it's a great place to find support! I searched and talked to a lot of ladies before I started treatment and compiled a list of chemo tips that I'd be happy to email to you - just send me a PM (private message) with your email address and I'll get them out right away. I had 4 rounds of Taxotere & Cytoxin and had really minimal side effects. I also used the Penguin Cold Caps and kept my hair, happy to talk with you about that as well.

    I remember the place you are at today well, but I'm happy to report that was over 3 years ago and life is great. I'd probably have to admit even better than prior to my diagnosis because of all i learned and the wonderful people it brought into my life. You will get through this, one day at a time, or one second at a time if that's all you can do some days. You're stronger than you may have ever known, and although hard to believe it now, one day you will be providing words of wisdom to others who are just starting their journey.

    hugs to you!

    Leslie


  • Sloan15
    Sloan15 Member Posts: 896
    edited September 2015

    Hi ShannonCannon, sorry you have to be here. Our diagnoses are similar, but mine is not tubular. Here are some tips I've learned:

    1) I'm having TC chemo --not the A like you-- but my Medical Oncologist (MO) gave me Emend as the antinausea. It's WONDERFUL as I have not had a minute of nausea. I get a drip of it right before my TC treatment.

    2) I also had skin problems before chemo --eczema, rosasea-- and the chemo aggravated them. So, they gave me antibiotics. Don't wait to go on the antibiotics; get in the same day you notice problems because with your weaker immune system, the problem won't get better without a little help. We are told to get to the doc if our temp is over 100.5, but we also don't have to suffer with other side effects (SE). I also got red bumps on my scalp right before my hair fell out --my dermatologist said it's a common reaction when every hair follicle goes eeeeek!-- and the antibiotics helped with that, too. Someone on my breast cancer chemo thread gave good advice: Expect NO side effects and live your live. When things come up, don't suffer with them!

    3) The other thing no one told me is that my white blood cells (WBC) would plummet after chemo. I freaked out because I thought I was doing so well. So, rather than starting the Neupogen shot to build WBC 2 days after chemo, I elected to have the neupogen shots the day after chemo so they start building up right away.

    4) Exercise and water really do lessen the side effects (and exercise and keeping your weight not too high and not too low will reduce chance of recurrence, too.)

    5) Join a chemo discussion group. I'm the August chemo group. All we think about 24/7 is cancer and chemo, but life goes on for everyone else (and we can't blame them for living life!!) But, it's like when you have had your children and now a new friend has a child and that is all she talks about.... We were there once, and others tire of it. BUT IT's CANCER, you want to say. Yes, and no one understands like other cancer patients going through this. So rather than driving my husband and friends away by always talking about me and my cancer, I talk about cancer in my chemo group and then I can talk about life and (occasionally cancer) to everyone else.

    6) Get out of town when you can. A change of scenery helps sooooo much.

    I really dislike having chemo and side effects, but it is doable. If you are not tolerating it, then talk with your MO about changing it. Plenty of women on these sites had to change medicines because of the side effects, so tell your MO everything.

    These are the things I have learned, and I hope it helps you.

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