Showing posts with label The Healing Chair. Show all posts
Showing posts with label The Healing Chair. Show all posts

Saturday, June 3, 2017

This One's for You, Cara

It is with a heavy, heavy heart I wrote this post. I've been mentally writing blogs in my head over the past few months, but haven't had the actual drive to sit down and write one. I honestly don't know if I can find the words to say, however this one needs to be written.

My beautiful friend Cara (this pic is of us at the Making Strides Against Breast Cancer breakfast last August) finished kicking cancer's ass last year. She did not let several rounds of intense chemo, followed by a mastectomy, and then a clinical trial (maybe radiation, etc, I cannot remember) slow her down - this chick has been running marathons since then! Before I even met her I had a bond with her, as she had the Natalie healing chair for her mastectomy recovery (I love all those women, it's a special bond I will never be able to describe...the Healing Chair is a sisterhood unlike any other, even just the regular breast cancer sisterhood...it's amazing). Cara is an amazing woman, friend, wife, and mother. Even as she was doing treatment, she sent me things like cards made by her first grade class (which I still have, and are FREAKING adorable). I pulled those cards out last night and looked through them, after I heard the news. For all those who are not Cara, here are my thoughts and feelings, and how you can help (prayer and encouragement please, and etc); and Cara...these are my words to you, and please excuse the profanity.

Cara, I can't even imagine having heard this news, and it physically pains my heart to think about it. You go in for some simple stomach aches, and come out with the news that you have tumors on your liver and both lungs now?! Stage 4 metastatic triple-negative breast cancer.

Fuck you, cancer. Fuck you.

I am angry and sad and scared for you, and your family. And, of course, for myself. This is what all of us survivors fear, yet try not to live in fear of. You have inspired me so much, more than you will ever know. You and your husband are such incredible and positive people, and you take such good care of yourselves; how the fuck did this happen?! HOW?! I won't even begin to ask why. I have changed my own diet and lifestyle (more whole foods, gluten free and dairy free, almost completely given up alcohol [as it can increase my risk of recurrence 90% since my tumor was estrogen-positive], exercising more, stressing less, etc), but you were like PERFECT about all that (as far as I know). I feel guilty for complaining about "having to" make those changes, and about having to take tamoxifen. A little brain fog is nothing compared to that triple-negative bullshit you've had to deal with. I am a huge believer in spiritual warfare, and I am so thankful for yours and Josh's examples of incredibly strong faith. I cannot thank you both enough for you guys just being who you are. I am just pissed off that you have to deal with this; yet I know if anyone can fight this shit, it will be you. I know God "gives" (I don't believe he GIVES them to us, Satan does, but I know God will use this journey for good) his toughest battles to his toughest warriors, and you are the toughest warrior I have ever met (besides my grandma, who has kicked stage-4 ovarian cancer's ass twice...thus, I know you can do it too...as she is still alive and kicking 10 years later). Ok sorry that was so rambly, but I wanted you and the world to know how fucked up cancer is, and how we need a cure for all types of cancer.

Fuck you, cancer. You've messed with the wrong woman twice now - she will KICK YOUR ASS AGAIN.

Here is info on how to help...I will be ordering a shirt, please let me know if you want one as well!!!!! And please please PLEASE keep them in your thoughts and prayers <3




Sunday, July 17, 2016

Mastectomy and Radiation Tips

These are things that I came up with that helped me when I was going through treatment, and hopefully they will help you too! If you have any additional tips, please comment below so I can add them. Thank you!!! ❤


  • After mastectomy: Go slowly. Have patience with yourself. Allow yourself to slow down, as tough as it may be. It may take you 20 minutes for your first bathroom run, but don't worry about time; just focus on healing. 
  • Stay on top of the pain meds (as in taking them as prescribed, not waiting extra hours between doses), at least for the first few days. I didn't have too much pain at all while resting, as long as I stayed on top of the meds! I only needed them for less than a week post surgery.
  • Movement is the most painful part, including shifting around, reaching for things, standing and sitting, etc. I was surprised to find that it was more of a burning pain (from nerves being cut) than a sharp stabbing pain. It was honestly intense at times but never more than I could bear, so do not worry too much about the pain because the meds help tremendously. Bracing my chest (basically hugging a heart pillow across my chest as hard as I could) helped TREMENDOUSLY!!!
  • If they wrap you in an ace bandage, watch for skin irritation. If skin irritation occurs, try using some aloe vera on the skin (being careful to avoid any incisions or drain openings). Something else that worked good for me was to wear a tank top or camisole over the bandages, and under the ace wrap. I was scratching several spots on my back.
  • Remember that if you are having a mastectomy with reconstruction, remember that what you see the first time you see your chest with the bandages off is NOT the finished product! While it may scare or disappoint some, remember that you did this surgery because you are strong enough to handle it; you did this because you chose life. And now the cancerous breast(s) are gone.
  • Get a recliner (buy one, borrow one, etc), preferably one with a lift-up feature. The transitions from laying to sitting, and sitting to standing can be very painful, as things shift around as you move. I didn't sit or sleep anywhere other than that recliner for weeks after my surgery. If you're in the Kansas City area, contact me or Google The Healing Chair Kansas City to contact us to sign up for a recliner to borrow after your mastectomy! The girls are great, they deliver it and set it up and when you're done they come and get it! Plus they're amazing women! St. Louis hs a Healing Chair charity too.
  • Connect with other breast cancer survivors. This one is especially important in my opinion, as during the really tough moments I thought of them. Drawing on their strength, and the strength and hope I received from crying out to God, kept me going.
  • Accept and enjoy help. You will most likely have several or more people who want to help you before and after your surgery. This was tough for me, because I always prided myself on being very independent, and being the one to help others. I resisted assistance in every way initially, until a friend (and fellow CA survivor) reminded me that people WANT to help. You may also be surprised, as was I, at how much people really do want to help; especially strangers. Don't reject offers for help; embrace them! I needed helped even feeding myself for the first day or two, so I'm so thankful for my momma!!! ❤
  • Don't get scared about what you will look like. I was terrified to look at my new breasts the first time they took bandages off, but I saw what looked like a regular breast, minus a nipple, and plus an incision. But they were beautiful, and cancer free.
  • Buy oversized button down tops. I bought 2 sizes up, and I am so thankful I did! I allowed myself to splurge on 3 pairs of Victorias Secret pajamas, because I figured they would help me feel pretty after my surgery. I also wouldn't let myself wear them until after surgery, so that that had something to look forward to! Other than getting the cancer out of me, of course ;-)
  • Don't be surprised by odd sensations. I experiences pain, swelling, numbess, tingling, pressure, stiffness, soreness, and even a bizarre "bubbling" sensation at times. Even having studied the nervous system extensively, I was surprised at how many different sensations I would experience in just my breasts after surgery! Even sometimes all within the same day!
  • Heart shaped pillows and drain pouches were my life savers! I had a cousin of mine who wanted to help and is a rock star at sewing make some of these for me, and they were absolutely perfect! I would have been miserable without them!!!
  • I also used a heart shaped pillows to put in the small of my low back at times, when my low back started getting site from sitting around so much. 
  • Ice was my best friend! 20 minutes every couple of waking hours helped take the edge off the pain, swelling, and itching (from under the ace wrap).
  • Keep the drain cords close to body, and be cautions where your walking, and what you lean up against. I.e. don't get your drain cord hooked around a drawer knob, and walk away...only to feel the the pull from the drain site! Lol
  • Keep a blog or journal. It's fun to reflect upon how far you've come. You can do a journal, but blogging allows you to share your journey with as few or as many people as you want. It's also an easy way to help friends and family keep up with you.
  • Dry shampoo, face wipes, and baby wipes were all live savers!
  • Wedge pillows were awesome for under my legs, and for sleeping on after I was done with recliner. 
  • Drain removal - no pain! Only felt something where they insert! So freeing!!!
  • Remember the good and sweet moments. I remember my mom washing my hair in our kitchen sink, patiently waiting for me when I winced in pain. I remember my boyfriend gently washing my fave with a Burts Bee's facial cleansing cloth. These sweet, beautiful moments that many people don't get to experience. When my mom hand fed me at the hospital because it was too excruciating to move my arms.
  • Radiation - I used strictly aloe vera on the entire radiation sites twice per day, and I maintenance a healthy diet (lots of water and vegetables, low sugar and alcohol), and I didn't have any real burns or skin changes until the last week. Be prepared for fatigue, but also for brain fog too! Random symptoms can happen. Oh and make sure it's pure aloe vera gel, not oil or anything! And don't apply it less than 4 hours before a treatment! I also had some itching inside my breast, which benadryl helped with. 
  • After mastectomy, start moving as soon as you can, and as doctors allow. Getting range of motion back in shoulders and stretching out the chest and torso was so helpful in my recovery, and continuing it through radiation was crucial too. Commit to doing stretches EVERY DAY, even of you don't feel tight. Every time I've skipped a day of yoga and stretches, I've felt so tight the next few days! 
  • As with all treatments, REST REST REST!!! 😊😴😪

Sunday, February 28, 2016

First: Rant. Second: Fun!

First:  Rant.  

As I approach my fifth (and second to last!) round of heavy chemo, I'm anxious.  Nervous.  Scared. This fourth round was tough; a lot tougher than I expected.  I knew that as my toxicity levels increase, my symptoms will increase; but I did not expect it to be THAT much worse than my third cycle.  In the scheme of things, it was not that awful; but what scares me is knowing that I have two more doses of that heavy stuff.  And that each one will most likely be worse.  I know I can handle it, I know I will get through it, but it is the going through it that scares me so much.  

I've also started feeling frustrated with it all.  Mostly the constant nausea (and occasional vomiting), mouth pain and sores (this time my throat got mega irritated also), ever-increasing fatigue (the intermittent insomnia helps, hah), body aches and pains, skin discolorations and rashes and splitting, nosebleeds (which thankfully are not painful, just more of a nuisance), and lately my fingernail tenderness has been really making me frustrated.  My nails are often just straight up painful...if I bump my nail or even just the finger, even the slightest bit, it sends shock-like pain through my entire hand.  I can't scratch an itch (which is probably a good thing, because I would probably shred my delicate skin lol!), open containers, and even writing and typing sometimes bother them.  If I do try to scratch my skin or use my nails, it feels as though they are lifting off of the nail bed...literally like they are about to pop right off!  Creepy!!!  And while I do think it is kind of cool how there are what I call "chemo-cycle lines" in my nails (like tree rings!), my pinky nails have started darkening.  For some reason, losing my nails freaks me out more than losing my hair or any of the other gross or annoying things.  I don't know why, maybe because I've never seen anyone who has lost a nail, but it's got to look creepy and just...WRONG!  LOL like what the heck does a freshly-uncovered nail bed look like?!  I could Google it, but I won't...I SHOULD remember from grad school, but my (and yes, this is my favorite excuse!) chemo brain isn't letting me recall many things! ;)  

Aside from the physical junk, I just feel so off...I just don't feel like myself.  I feel like I am disconnected from myself, like I'm just not me.  I'm so thankful my family, friends, and coworkers all still put up with me, because I feel like I'm a really crappy version of myself lately!  I know everyone is understanding, and hopefully none of them perceive me that way, but ugh I just want to feel like myself again!  I am so thankful that I will feel like myself relatively soon, and that I only have a few more weeks of this stuff.  

Second: FUN! :D 

But in the midst of all this crap, I've been fortunate to have had a lot of good times over the past few weeks!!!  I've gone out to lunch with friends and have done some shopping which is always fun, and gets me up and moving!  I've also got some cute new clothes to wear this spring and summer, and every girl loves having new clothes to look forward to wearing! :)  While part of me feels guilty that material things such as new clothes excite me, another part of me knows that I need to do everything I can right now (within reason, of course) to give myself all the motivation and excitement about the future that I can get!  

Last week I found out that I was chosen to be a Portrait of Hope for the American Cancer Society's Making Strides Against Breast Cancer program, which I'm super excited about!!!  Basically I get to share my story and talk about various things with the media and at Making Strides events and what not. I will find out more in the next few weeks, but I am so excited to share my story on a larger platform, and hopefully encourage and inspire many more people!  When Claire McCaskill announced her diagnosis last Monday, I was able to talk to Fox 4 about my story, and I had a BLAST talking with Abby Eden!  She is an absolute DOLL!  Click HERE for the link for the article and news clip if you want to see it!   

I also got to go talk to the Olathe East girl's basketball team, who raised enough money for more Healing Chairs!!!  They are an AWESOME group of girls, and I was so blessed meeting them!  


Surrounded by amazing women!!!

Talking to the girls, and my Italian blood is coming out!!!  LOL!  


Yesterday my mom hosted a little craft party, and some family and friends came over and we had a BLAST!!!  Oh my, so much food and fun and craftiness, I slept soooo good last night lol!!!  We made these super cute Easter wreaths (ok, well, I'm STILL working on mine...haha), and it was so nice to hang out and talk and laugh with everyone!!!  

 Work in progress!  

This little blue one still cracks me up, LOL!!!   

I also got to see Newsies Thursday night, which I HIGHLY recommend, it's awesome!!!  And thanks again Ashlea for taking me!!!  :D  So all in all, life is good...I'm so thankful to be alive, and enjoying this beautiful life that God has given me (and this beautiful weather as well!).  Thanks again for all your prayers, love, and support...it's still what's keeping me going!!!  

Sunday, December 13, 2015

Days 4-10 of Chemotherapy

Day 4

Today was just not a good day.  I didn't feel too terrible (other than just tired and flu-ish), but emotionally I was a WRECK.  I feel like I look terrible, as my skin has broken out all over my face, neck, chest, and back; I feel like I'm a teenager again, without the unlimited energy!  I went to work for a few hours, and I was almost paranoid to get out in public.  Just driving through traffic I felt like there were all these big, scary germs everywhere, waiting to attack me.  But I survived, of course ;)

Day 5

A much better day today!  Felt a lot better, still just tired. Work went pretty smooth, so that helps!  Went out to Tequila Harry's for some Mexican food for a fundraiser for The Healing Chair - Kansas City, and I am so glad I went!  I want to be at everything I possibly can be at for this charity, since that chair (recliner) seriously helped me TREMENDOUSLY after my double mastectomy!  Not to mention the four women who head it up are amazing, and always know how to raise my spirits.  I even ate an entire cheese quesadilla myself, and some chips!  That's like, what I ate in an entire day last weekend!  Not to mention it even tasted pretty good (thank you taste buds for coming back a bit)!!!





Days 6-10

All these days kind of ran together, but overall they were good.  My mouth had started to feel TERRIBLE on day 6 (I felt like I'd eaten a cactus!), which was frustrating.  I was having trouble eating and drinking, but it mostly cleared up a couple of days later.  We had our office Christmas party, which was a blast!!!  I was pretty worn out by 10:00 pm, so we cut out a bit early, but it was a lot of fun!  It was also good to see and spend some time with my boyfriend, who came in town for the party.  I'm feeling pretty darn good today, almost back to normal!!!  I accomplished some things today, which is always good...even went for a walk in the rain!!!  :)  I also found out that "my" healing chair (the Natalie chair) was delivered to it's 2nd recipient today! I can't wait to meet her, and I hope she feels the love from it!