Come join others currently navigating treatment in our weekly Zoom Meetup! Register here: Tuesdays, 1pm ET.
Donate to Breastcancer.org when you checkout at Walgreens in October. Learn more about our Walgreens collaboration.

More Tips (and a Shopping List) for Getting Through Chemo

1333436383968

Comments

  • badger
    badger Member Posts: 24,938
    edited January 2013

    bumping for the newbies

    with a shout out to rock for creating this thread, and my bump-buddies Nico & Soteria

  • Nico1012
    Nico1012 Member Posts: 1,152
    edited February 2013

    bumping for the Feb '13 chemo starters

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bumping

  • badger
    badger Member Posts: 24,938
    edited February 2013

    bump

  • Nico1012
    Nico1012 Member Posts: 1,152
    edited February 2013

    bumping in honor of 'badger' and 'Soteria205' ~ my bumpin' sistahs!

    And of course in honor of 'rock'!

  • badger
    badger Member Posts: 24,938
    edited February 2013

    bump!

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bumping with Badger & Nico for the newbies.

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bump

  • badger
    badger Member Posts: 24,938
    edited February 2013

    bumping up this thread to keep it in Active Topics

  • shadytrake
    shadytrake Member Posts: 69
    edited February 2013

    My wonderful barn friends took me out to dinner tonight and gave me 3 chemo caps handmade by So Southern.



    http://www.so-southern.com/products.php



    The lady who makes them made my saddle cover. They are so beautiful and soft. I pasted the link to her website if anyone is interested. I'm going to find some Tiger Blue and Grey and have her make me a custom one to wear to the Tiger games.

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Thanks Shady!



    Paula

  • chemicalworld
    chemicalworld Member Posts: 48
    edited February 2013

    -I have mentioned this in other threads (and I'm sure I'm soon going to sound like a product salesperson), but I found Witch Hazel and WH-containing products invalulable during chemo.

    I purchased a huge bottle along with unscented moist wipes.  Dumped half the bottle into the container with the wipes to have on hand for any soreness.  I also soaked gauze in WH to hold against any particularly sore areas.  I dabbed q-tips in it to use on mouth sores.

    And I swore by the Tom's Baking Soda mouthwash during treatment.  The one I had also had witch hazel in it which I think may have been discontinued, but hopefully can still be found.  The only time I got mouth sores was during a week when I had ran out of it.  The prescription mouth stuff did nothing for me. 

    -I had a P.I.C.C. line so the plastic sleeve thingies were invaluable as well, although the hospital gave me those.  However, I had to also wrap both ends in tape to avoid any water getting in.

    -Water, water everywhere......and I can't stand to drink.  I hated the taste of plain water during treatment.  My way of dealing with this was either drinking club soda (also good as a mouth rinse) or to use water flavorings (minus the vivid red stuff which reminded me of the red stuff they gave me during chemo). 

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Chemicalworld~Thanks for your input. It's great to have added tips to get through all this.



    Blessings

    Paula

  • Nico1012
    Nico1012 Member Posts: 1,152
    edited February 2013

    THANKS chemicalworld! I had the same experience using Witch Hazel products during chemo and continue to use them today. My derm told me that Witch Hazel is as effective as rx strength cortisone cream for treating external inflammation. It takes the itch and sting out of bug bites for me in a few minutes and calms my chemo-sensitive skin just by swabbing my face with a saturated cotton square. Thank you also for reinforcing the importance of FLUIDS! I've often thought we need a thread here just on fluids, including every trick of the trade to make them palatable.

    SPECIAL THANKS also to Paula and badger ~ you bc sisters ROCK!

  • badger
    badger Member Posts: 24,938
    edited February 2013

    BUMP!  Kiss 

  • shadytrake
    shadytrake Member Posts: 69
    edited February 2013

    Hi Ladies,

    I have the prescription for the Lidocaine cream to put on my port.  Can you tell me how, when, where you apply it?  I start chemo on Monday morning. 

  • badger
    badger Member Posts: 24,938
    edited February 2013

    hi shadytrake, I didn't have a port but wanted to wish you good luck for Monday.

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Shadytrake~Liberally rub the lidocaine (Emla) on the port site. Then lay a small square of Saran Wrap on top of it. There's no need to tape it. The lidocaine will keep it in place.

    Do it an hour or 2 before treatment. It works great.



    I hope you have an uneventful first treatment.



    Blessings

    Paula

  • Nico1012
    Nico1012 Member Posts: 1,152
    edited February 2013

    bump

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bumping with the best, Nico & Badger!

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bump

  • iluv2scrub
    iluv2scrub Member Posts: 16
    edited February 2013

    Thanks for all the tips...I got my port today and treatment x 6 starts tomorrow. Getting a cute short haircut Saturday...yay...have wanted to try short hair but been afraid to so I am so excited to have a really good reason to get it cut short:-)

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Iluv2scrub~I loved when I first found this site a few months ago. Such awesome tips!



    I see we're practically neighbors. I live in Reynoldsburg, Ohio! Where are you being treated? I'm being treated at the Stephanie Spielman Breast Center.



    Blessings

    Paula

  • iluv2scrub
    iluv2scrub Member Posts: 16
    edited February 2013

    Hi Paula, in am at Zangmeister and so far, its been good. Got a PM from another woman posting that she's here in my town and treated at OSU. Small world...all the best, most positive feeling to you and a great big hug...pm me anytime...I need some personal tips on hair loss...to wig or not to wig...((hug))

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Kathy~I got a wig before chemo. I got it at at Hope's Boutique in the Stephanie Spielman Breast Center. I wore it to church one time. It's a short bob in my own auburn color, but it just seems like too much hair for me.



    I don't usually wear anything on my buzz at home, but I wear hats, scarves, and my favorite, "T-shirt wraps" at church or anywhere else I go.



    I've heard great things about Zangmeister. My best friends husband was treated there 2 years ago for stage 3 colon cancer. He is cancer free. I also know 2 ladies who are cancer free now, who were treated there. One had BC, the other had Lymphoma.



    We're you speaking of Reneeinohio? I know she's in Westerville and being treated at the Stephanie too.



    It was more difficult at first, losing my hair than losing my breast, but I figured there's no sense in making myself miserable over something I have no control over. So, the day before I started chemo, I cut my long hair in a short pixie, then the day before chemo 2 I had my son buzz it. It's a lot easier than watching all those long strands fall all over the place.



    I'm a christian and my faith has really helped with my attitude.



    Please let me know if you have any more questions. You can pm me, or if you want, I'll give you my phone number.



    You can friend me on Facebook. I'm Paula BRUMLEY (Hendricks ).



    Blessings

    Paula

  • chemicalworld
    chemicalworld Member Posts: 48
    edited February 2013

    @iluv2scrub, I did what probably many did, cut my hair into a short sort of bob pre-treatment.  I also purchased a few new hats to carry me through the initial period of my hair falling out.

    I never shaved my head until I finished my last chemo and wanted that fresh start.  Everyone's different and that was best for me.  Shaving my head early on felt like giving in for some reason.  I was most comfortable letting mine fall out on it's own, and I mostly brushed it off my head after each shower.  I had a few little stragglers that hung around so that I was left looking a little like Gollum, but that was ok. 

    I purchased a wig through a shop after my first chemo, and hindsight being what it is, I would have avoided that as it wasn't a positive experience for me.  Found the wig person there kind of aggressive about sales, not what I needed then.  It cost several hundred dollars and I also didn't need that either.  Plus, much like what Soteria says, it was too much hair for me, too thick in contrast to my normally thin hair, and not really a style I would have normally worn (I was talked into a really short style because it was winter and it would have gotten messed up with scarves and such).  Whenever I wore it, I wore a hat over it. 

    What I eventually did later in treatment was buy a much much cheaper wig from ebay.  It was advertised as human hair and while longer than I wanted, it just took a quick trip to another wig dealer to get it trimmed up and looking just like I wanted and MUCH closer to my pre-chemo hairstyle, although still thicker.  It cost me under $60, plus a trim.  I wore that through the summer which was a p.i.t.a. with the heat and hot flashes, until I had enough regrowth to toss it. 

    Otherwise, I wore a soft cotton sleep cap around the house that I also purchased from ebay.  Looked like those kind that newborns wear with the little knot on the top !

  • [Deleted User]
    [Deleted User] Member Posts: 942
    edited February 2013

    Bump

  • Nico1012
    Nico1012 Member Posts: 1,152
    edited February 2013

    Bumping it up!

  • shadytrake
    shadytrake Member Posts: 69
    edited February 2013

    Hi All,

    I find that spicy foods tempt my taste buds. I also have a great recipe for fruit cups. I'll post it after the game.

    Ok - the recipe

    Frozen Fruit Cups - Makes about 2 dozen

    16oz sour cream

    2 tablespoons lemon juice

    1 cup sugar

    1/8 teaspoon salt

    8oz crushed pineapple, drained

    1 sm can mandarin orange slices, drained

    1/4 cup sliced strawberries, fresh or thawed frozen

    1/4 cup craisins

    1/4 cup chopped pecans

    3 peeled bananas, sliced or chopped.

    Combine all ingredients and pour into muffin tins lined with paper muffin cups.  Freeze until firm.  Store in a freezer bag and use as needed. Best if allowed to thaw slightly before serving.

    Trust me - YUMMY!

  • badger
    badger Member Posts: 24,938
    edited February 2013

    thanks shadytrake, that does sound yummy.  I was lazy and bought lemon ice at the store.  It tasted good and also cooled my mouth.