Sunday, April 26, 2015

TaTa... I mean TaDa!

I've been a bit hesitant to write the post, and if you know me, you know I'm not hesitant to say much. Honestly, now that I am feeling better, I am feeling a little more protective over my boobs.  They aren't trying to kill any more.  Yes, they are still a work in progress, but they are feeling more a part of me every day.  I am a little hesitant to share, but I am so grateful for the women who have mentored me on this path and if I'm able to mentor or help make someone else's journey a bit easier by offering some information, some humor and understanding then that would make my over sharing worth it.

Here's a bit of background: After my prophylactic mastectomy, performed by a breast surgeon, my plastic surgeon put in expanders.  These are basically empty shells (think like a small deflated ball) inserted in pocket he made in my chest muscle.  Every few weeks, I would visit with my plastic surgeon and he would use a syringe to gradually fill my expanders with a saline solution.  While I had a skin sparing mastectomy, my muscle still had to be stretched to create a large enough pocket to hold my permanent implant.  The expanders were quite uncomfortable and rock hard; I'd often compare it to having two cereal bowls in my chest.

On Wednesday, I went in for my exchange surgery. During this surgery, the plastic surgeon takes out the expanders and puts in permanent implants.  The doctor used the same scars he made during my initial mastectomy surgery.  I chose to go for silicone implants, as they look and feel the most natural and my doctor thought that would give me the best result.  My surgeon also took the opportunity to to shave an additional part off of my left chest muscle, as one of the margins to my tumor was very narrow.  The surgery took less than an hour and a half.  I checked in early in the morning and by noon was released and having lunch with Richard and my mom.  While any surgery is scary, this was one that I looked forward to... hopefully it marks the end of my reconstruction.

The pain with this surgery was much less than my mastectomy.  I took pain pills for about two days and ibuprofen one day after that.  While I must be cautious about my activity, I am able to do pretty much anything that doesn't involve heavy lifting.

I was instructed to wear this super tight sports bra for the next 3 weeks (quite a change for me since I haven't had to wear a bra for the last 7 months).  I cannot wait to take this beast bra off and try on some clothes.  Overall, I am happy with my results so far, although it can take some time for things to settle.  My right breast looks phenomenal, nicely shaped and perky.  My left breast still has some significant bruising and swelling, but that is to be expected because of the additional trauma.  I'm anxiously awaiting to see how things fall into place within the next few months.

I will draw the line at posting my pictures on my blog, however, if you are someone who is going through a breast cancer diagnosis and would like to see the progression, feel free to email me and I would be willing to share my pictures with you.  Seeing others' pictures was a big comfort to me and helped me know what to expect along the way.

No matter what my breasts look like, the key thing to remember is that they aren't trying to kill me any more and that is absolutely worth celebrating!  Admittedly, I'm also celebrating having perky boobs, too.

Tuesday, April 21, 2015

Behold I Make All Things New

A card my friend Sheri gave me... Fitting, don't you think?!
My sweet friend, Maria, had a surprise BBQ as a 'send off' into my final surgery and to celebrate my "new beginnings" (loved the way you phrased that Chris Summers!).  It was very much a surprise, as I arrived at Maria's for what I thought was our book study looking homeless in my comfies and in my coke bottle glasses.

Maria and her husband, Alex, can throw one heck of a party!  Usually something very entertaining happens, like someone catching the lake (yes the lake!) on fire, the buffet table falling, or in this case, we got to watch a big storm roll in on the lake.

After we all came inside because of the storm, it got a little crazy with several kids running around and Lia riding her bike in the house.  At that chaotic moment, I briefly shut my eyes and took in the moment: kids squealing and giggling, adults talking and laughing, thunder and rain in the background as I looked at the white caps on the lake.  It was perfect.  There is nothing better than families supporting other families.

Maria ordered this cake... I can only imagine what the cake lady thought when she found out it was for a family BBQ

Sunday, April 19, 2015

Nailed It

Okay, so, I've committed the good, the bad, and the ugly... Well, here's some ugly:
Chemo nails
About 2 months ago, my nails started getting very sensitive, almost like each one of them had been smashed with a hammer.  I struggled to do anything that required pressure on my nails, such as opening a package of fruit snacks (not good with an impatient 4 year old) or a bag of chips (not good with a hungry 36 year old who loves her carbs).  I also noticed that my nails looked very bruised, you can see the progression in the pictures above.  About 3 weeks ago, my nails started feeling better, but also have started separating from the nail bed (yuck!).  So far, I've been lucky to not lose any of them, but goodness, this is not an attractive look.

I guess we can just file this in with the random and sparse gray hair coming in, the lack of eyelashes (by bottom lashes are completely gone and my top lashes are dwindling).

I thought that finishing the tough chemo would mean my body would start bouncing back, but I am still seeing the effects, some worse now than during treatment (the case with my lashes and nails).  I think parts of my body have had enough and held on as long as they could...  I completely recognize all these little nuisances are minor ~ I'm cancer free and that is what matters, but it's still a reminder of the assault my body has been though the past 6 months.

Yes, I know this sounds vain, but I'm hoping my upcoming surgery (my exchange from tissue expanders to my real permanent implants) will detract from my bald head, my nonexistent lashes and my disgusting looking nails.

Blessings everyone!

Saturday, April 18, 2015

Party in a Box

Party in a Box ~ Such a sweet idea!  My friend, Debra, sent me a party in a box to celebrate the end of my chemo.  This lady...  Even though we live hours apart, she has been on this cancer journey every step of the way ~ Thanks for your support, D!  Your care packages always seem to come when I need them most.  And, they always include my favorites...  Your generosity and thoughtfulness overwhelms me!  

Along with my favorites (hello lemon Oreos and Good 'n Plenty) she also packed: party supplies (poppers, hats, blowers), a very generous Victoria Secret's gift card ~ I can't wait to treat myself to something special, tons of good smelling treats to pamper myself with, candles, a gorgeous coffee mug, a daily devotional, and some cute surprises for Mase.  

Every items was wrapped in brightly colored tissue paper and it was so much fun digging in...  

Have I mentioned how amazing my friends are?  They have spoiled me this past 6 months, but the truth is I have some of the best friends a girl could ask for!  Some are close and some are far away.  Some of them I speak to daily, and some I maybe touch base with a few times a year, if that... What I love about all of them, no matter how long it's been since we've seen each other or communicated, we can always pick up where we left off.  Thank you friends!
It's time to P-A-R-T-Y!
Such a thoughtful package!

Tuesday, April 14, 2015

A bit of Advice...

Mase and I are retiring from a week in Florida, where we visited my sister.  We had a fabulous time!

One day we visited the beach.  As I was standing, looking at the ocean, I reflected on the last six months.  I took in the moment, having the warm sunlight on my head, feeling my feet in the sand, looking back and seeing my sister who I missed so much, and listening to Mase and my nephew giggle while jumping over the waves.  It was perfect (well, as perfect as could be without Richard being there).  I'd fought hard to be in this moment.  The thought of this trip, this moment, was  what got me through some really tough treatments back home.  This was my reward.

Florida was a great place to rock the bald.  Have I mentioned the amazing feeling of feeling the warm sun on your head?  I almost feel bad for those of you who don't get to experience that feeling (okay, not really, but it really is a great feeling, especially after a cold Missouri winter).  My sister pointed out to me that at nearly every outing someone would come up to us and comment on my lack of hair. Some would offer a compliment and some would share that they, too, were a survivor.  One lady stopped us at the park and told me that I was rocking the bald look and that she was inspired by it to make an appointment for her annual check up.  Inspiring?  I don't know about that, but I LOVE that my bald head can bring some awareness (well, plus the fact that at times I can be an attention whore).  I also love hearing Survivor's stories and the sisterhood/family that we share.  While I'm happy my hair is very slowly growing back, I recognize that my gateway into the conversation is closing, and in some ways that saddens me.  Other stories and encouragement means so much to me ~ to meet someone who really gets it without you having to explain it ~ it's powerful.

My sister asked how she should handle it if she sees someone struggling with cancer.  She often feels pulled to reach out and offer comforting words, but she also recognizes it may not be her place, as some people may not want to share.  As mentioned in previous blogs, it really is a risk to say something.  Not everyone is as open about it as I am.  Personally, I appreciate when people mention the struggle (attention whore, remember?) or share their stories with me.  Let's be honest, when I rock the bald, the truth is pretty much in your face with my big, shiny peach fuzz covered, head.  Since I'm a people person and will talk to just about anyone, it is a great conversation starter.

A things to remember:
1.  If some one's struggle is obvious, I think it is okay to say something encouraging to them.  It feels good, for both the giver and receiver.  It's amazing how a stranger's words can make an impact on you.  I can still remember the woman who stopped me after walking out of a book store and complimented my newly shaved head.  I was scared and insecure about my new look and her encouragement really served as a boost for me, letting me know it was going to be okay.
Chances are if someone isn't open to talking about their situation then they would take steps to make the struggle less noticeable, such as wearing a hat or a wig (which would be dreadful in Florida!).
**Hold please, as I type this very post, a gentleman came up and started asking about my hair and sharing about his daughter's struggle.**
2.  Take cues ~ If someone is closed off after you say something encouraging, smile and walk away!  If someone is open and accepting of the encouragement, I've found that people, myself included, love sharing their story and educating others.
3.  There are lots of different types of cancer and lots of different types of chemo.  There are even multiple ways to treat breast cancer, depending on the various markers your cancer has.  I know some lucky bitches women who have had a lumpectomy and that was it.  They found and removed the cancer and no further treatment was needed.  Some survivors have to do radiation treatments (Ouch!  Think of getting a sunburn in the same spot 30 days in a row ~ oh, and I think they some how bolt you down to a table while this is happening).  Some must take hormone blocking drugs for 5 years.  Some do a type of chemo that doesn't cause hair loss.  Some chemo can be taken in a pill form, some has to be done through an infusion through a port. One friend of mine who is a straight up bad ass has had to do all these treatments.  Shout out to you Jenn!  Some drugs cause weight gain.
Me?  Oh, I was "lucky" enough to gain weight and lose my hair...  There must have been some sort of mix up because I was hoping to lose some weight and gain some hair ;).
4.  I feel like this is stating the obvious, but not everyone with cancer loses their hair.  On one hand, I find myself jealous of these folks... Although I totally admit that isn't fair.  Their struggle is just as real as mine.  Perhaps, their struggle is even harder because they don't have the chemo haircut that seems to open the door to connect with other survivors.  In a way, they suffer alone.  There is some comfort in walking through Target and not having to put on a happy face or even look presentable - I'm sick and I get a free pass.  No one expects much out of a cancer patient and I look the part of a cancer patient.  Those who don't lose their hair probably don't get that free pass.  Others may consider them less sick, while in reality they are fighting the same battle as every other cancer survivor.

Jill and I were trying to think of a good starter if she felt compelled to say something to someone.  Between well over $50k of education and two Master's in Counseling degrees all we could come up with was "Looks like you've been through some trials lately..." and go from there.  Profound? Hells No.  But I told her she needn't worry about being profound or saying the perfect thing.  Only worry about being sincere and genuine.  It isn't the words that are important, what really matters is what's on your heart.

In case you are wondering about what not to say, please refer back to the blogpost about that by clicking here.

Friday, April 10, 2015

You're Welcome

Dressing up... Just because we can.
In case you've wondered where I've been the last week, my crew and I have been busy saving the world.  You're welcome.