Dear Me,

Day 6 of the WEGO Health Activist Writer’s Month Challenge nearly made me give up on the daily task of blogging about my “condition.” I don’t like my “condition” and I don’t like the touchy-feely side of dealing with that “condition.” I like to keep my word, though, and I said I would take on this challenge, so here goes.

Today’s prompt: Write a letter to an older you. What lesson do you want to make sure you remember?

Well, with my dilapidated body, blown-out knee, and menopause-induced lunacy, the older version of me scares the hell out of the current version of me, so I’m going to write a letter to the younger version of me.

Dear Younger Me,

Listen up, missy: that college dream of yours to light Madison Avenue on fire with clever advertising campaigns isn’t gonna happen. You don’t like the Big City — too many people and way too many germs. That other dream of writing children’s books isn’t going to happen, either. You do end up reading a whole lot of good ones, though, to a couple of precious kids who look so much like your baby pictures it’s scary.

Your smart mouth will get you into a fair amount of trouble. I’d tell you to be careful, go easy, and use restraint, but we both know you’d flip me the bird and keep right on sassing. I can tell you that eventually you do learn the fine art of holding your tongue, but it will never come easy.

That sweet, loyal, smart, cunning and unmatched yellow dog who grips your college-aged heart will never let go. She will protect you, and then your children, for nearly 15 years. She will guard the entrance to the nursery and sleep under the crib. She will show you her back when you get out your suitcase, because she knows you’re leaving, if only for a few days. Her time on this Earth will grow short but she will stick it out longer than anyone expects because she will insist on seeing you through an even rougher patch: the death of your sweet mama.

Guess what, girlie? Your sweet mama keeps a tight grip on your heart, too. Not a day passes without you feeling the loss, in big ways and small ways. (Note to self: don’t give up on trying to make her pie crust. It won’t ever be like hers, but keep trying.)

Just about the time cancer steals your beloved mama, you’ll start getting an annual mammogram. You’re ahead of the schedule thanks to that mama-stealing cancer, and every year the mammogram will come back funky. Don’t settle for the “dense tissue” rationale. There’s a tumor growing, and it ends up taking up a lot of space, both in your body and in your life.

Look, I know you’re going to be busy living your life and raising those two little kids when the diagnosis comes, but please, brace yourself, because it’s going to get ugly fast. And say a little prayer to the environmental-services gods who control your operating room on the day of your mastectomy; maybe we can avoid that post-mastectomy infection that will reorder your life. And BTW, the bilateral mastectomy was totally the right choice. Good girl for following your gut. There will be no hint, not a single whiff, of cancer in your left breast, but it’s there.

Give up right now on thinking your cancer “journey” will be “one and done.” It will be more circuitous than you can ever imagine, and it will change you in ways you won’t discover until years later. Oh, and before you even begin that circuitous journey, you’re going to have to deal with melanoma on your right foot. I know, who puts sunscreen on their feet, right? Hate to tell ya, that even though you catch it early, the surgery to remove the melanoma will be the most painful thing you will experience. Yes, it’s worse than childbirth and a bilateral mastectomy. Oh yeah, about childbirth–when your water breaks, the baby is coming. Yes, he’s early. No, you haven’t finished the birthing class or packed your bag, but it doesn’t matter. And you’re going to get teased for decades for reading ahead in that “What to Expect” book on the toilet in the middle of the night when your water has broken and your much-better-prepared spouse sleeps peacefully, unaware of your foolishness.

It turns out fine, the baby is healthy (but hard-headed). Even the cancer thing is manageable. Not easy, but manageable. I think we both know you can handle it. You’re going to learn a lot, whether you want to or not. Your limits will be tested. You’re going to make some true and life-long friends along the way. You’re going to unload friends, too, in one of many hard-learned lessons. You see, there are people who are willing to give what they want to give, not what you need. This is a very important distinction. Trust me, you’re much happier without ’em. A couple more pieces of advice: first, don’t ignore that knee pain while you’re running. Stretch before and after you pound the pavement. Listen to your body. Pain is its way of saying something is wrong. Ice your knee after each run. I know it’s a hassle, but so is living with constant pain. Years down the road, you’re going to be embarrassed by how you hobble down the stairs like a woman twice your age. You’re going to be frustrated by the ways in which your body fails you. I don’t have an answer for how to deal with that, because I haven’t figured out how to deal with that. I do recommend drinking champagne as often as you can. I don’t have to tell you to never, ever pass up an opportunity to drink some bubbly. The lesson I want you to remember is that the sound of that popping cork will soothe your soul, every time.

Love,
Me

 

 

 


Cancer Vixen

Day 5 of the WEGO Health Activists Writer’s Month Challenge:  “If I could do anything as a Health Activist…”

My first thought was to cure cancer. Today’s prompt said to dream big, so I am. url

 

Since it’s my dream, I’m claiming two superpowers. In addition to kicking cancer’s ass, I would eliminate all the stupid/inane/insensitive/uncaring/clumsy/offensive things people say to those of us in cancerland. Yeah, yeah; I know sometimes people mean well and just don’t know what to say, but that’s no excuse. No cancer patient needs to hear a comment like this, or certainly not this, no matter how well-intentioned the awkward speaker should be.

So if I could do anything as a health advocate, I would ensure that no one in cancerland ever had to hear anything like this. Ever. 00518B46-24C7-46E0-B621-C284213E7976


Care page, HAWMC day 4

Today’s mission in the Health Activist Writer’s Month Challenge: Create a “care page” – a list of your best resources that someone who is newly diagnosed could go to when starting to advocate for themselves or a loved one.

Consult the mainstays such as Breast Cancer Action, and Think Before You Pink, and Dr Susan Love Research Foundation, and breastcancer.org, and The Rose. Consulting “Dr Google” once a diagnosis has sunk in is something most people do.

Follow a blog that appeals to you. Whatever flavor you prefer — spiritual, snarky, research-oriented, or off-the-cuff like this little blog — there’s a blog out there to meet your needs. Among these blogs, you’ll find posts such as this and posts such as this with practical advice from those who’ve been there. Much of this information is rather like on-the-job training; you don’t know what you need to know until you need to know it. Take the hard-won wisdom from those who have walked this walk before you.

My best piece of advice, in a sea of good advice, though is this: Do what you believe in your heart of hearts is best for you. Whether a prophylactic bilateral mastectomy instead of a lumpectomy, whether undergoing reconstruction or flaunting the flat & fabulous look, or whether pursuing a second or a third or a fourth opinion. Follow your instincts and listen to your gut.tumblr_mefqlvRiq41qlp3rfo1_1280

 

 

 

 


Wordless Wednesday, HAWMC

Day 3 of the Health Activist Writer’s Month Challenge:

“Wordless Wednesday. Post a picture that symbolizes your condition and your experiences.”

My first thought was of the many powerful images in David Jay’s The Scar Project. I’ve written about this amazing body of work here and here. The photographs are raw and real, just like cancer itself.

David Jay Photography

David Jay Photography

 

 


WEGO HAWMC

day2

 

The WEGO HAWMC is quite a mouthful! WEGO Health describes itself as “social media’s most active online health community — Health Activists. These influencers, organizers, connectors, leaders and contributors are passionate about helping others lead healthier lives.” WEGO Health Activists have thrown out a challenge: the HAWMC, or Health Activist Writer’s Month Challenge. It’s a post-a-day challenge taken on by several bloggers I greatly admire. One of them asked if I was planning to participate, so here we are.

I missed Day 1, so will start with Day 2, which is pretty scrambled logic for this Type-A girl, but part of the challenge is thinking — and blogging — outside of our comfort zones so I guess I’m in.

Today’s prompt:

Introduce your condition to other Health Activists. What are 5 things you want them to know about your condition/activism?
Yikes. I hate to think of breast cancer as “a condition” but I suppose it is. I certainly don’t think of myself as an activist, but for these purposes I’ll assume I am.
Ok, so introducing y’all to breast cancer. Y’all, this is breast cancer. Breast cancer, this is y’all.
It’s safe to say that everyone knows about breast cancer, thanks to the pink-ribbon brigade, so on to the 5 things you need to know about breast cancer. Those who have it already know. Those who care for/care about someone who has it already know, too.
#1 — “Early detection is key.” Yes, and no. Early detection is important in that it can prevent breast cancer from spreading and progressing to a more complicated prognosis and a less favorable outcome. But it also leads to overtreatment and contributes to our skyrocketing health-care costs.
#2 — “Breast cancer is a “good” cancer. This is rather loaded. Yes, it is “good” in the sense that it occurs in a body part that is nonessential to sustaining life, and in a body part that can be removed, ostensibly also removing the cancer. But let’s face it, no cancer is a good cancer. And while have a lumpectomy or mastectomy is perhaps easier than removing a lung or other vital organ, the aftereffects for women are brutal, both physically and emotionally.
#3 — “Taking Tamoxifen every day for 5 years is a pretty easy way to manage the disease.” Tamoxifen is rough. Its side-effects are numerous, and even if a women suffers just one or two of those side-effects, they’re quite disruptive. And quite sucky. For those of us diagnosed before menopause, Tamoxifen fast-forwards us to the land of hot flashes, night sweats, mood swings, and other lovely challenges. Within days of starting my Tamoxifen, brown spots appeared on my face. My skin grew noticeably thinner while my body tried to grow fatter. My anxiety level soared while my endorphins crashed.   Having to remember to take my little white pill every day stresses me out: taking it ensures these awful side-effects, but stopping it puts me at risk of recurrence. What part of this is easy??
#4 — “Your breasts don’t define you.” True. Very true. This is true for all women, whether they have breast cancer or not. Huge strides have been made in women’s rights and it’s a wonderful thing that society “allows” us to be more than window dressing. But pick up any magazine and look at the ads or watch any random commercial or walk through any suburban grocery store and notice the boobs. They’re everywhere. And they’re big, round, and perky. If we aren’t defined by our boobs, then why is losing them so traumatic? If we aren’t defined by our boobs, then why do more than 300,000 women a year in the United States undergo elective, cosmetic surgery to enhance their breasts?
# 5 — “Being diagnosed with cancer makes you stronger.” Perhaps in some ways it does. I am no longer afraid of needles after the bazillion shots and injections I’ve received, and can now give myself a shot if need be. I barely flinch when the phlebotomist pierces my skin with a wide-bore needle to extract a blood sample. I know that I can endure an awful lot — physically and mentally. But did I need to be diagnosed to become stronger? Doubtful. And that newly gained strength is a pittance compared to the things that cancer costs me — physically, mentally, and financially.

 


Hacked off

Susan Gubar has done it again. She’s written another fantastic post for The New York Times‘s Well blog. This one is about The Scar Project, which is near and dear to my heart. Perhaps it’s a theme this week: scars, invisible and visible, and how we cancerchicks live with them for the rest of our lives. The women pictured in The Scar Project will have a long, long time to figure out how to live with those scars, as they are all under the age of 40.

Says Gubar of the young women portrayed: “The youthfulness of David Jay’s subjects wrenches me. Unlike them, I had a good span of my adult life — more than 60 years — before treatment. Their bodies stopped being their own too soon. Did their selves also stop being their own too soon? Cancer scars are physical mutilations of and on the body; but, more than that, cancer scars the psyche, the soul, the spirit. The ‘me’ before cancer is not the ‘me’ after cancer. Nor can these identities always be sutured.”

Yes, Susan Gubar, I think it’s safe to say that our bodies and our selves did indeed stop being their own too soon. I was 40 when I was diagnosed, which is old by The Scar Project standards, but I can say with certainty that it totally sucks to have been denied a good span of my adult life before cancer . It’s a drag. Because estrogen feeds my cancer, and many other varieties of breast cancer, I had to shut off the supply of that vital hormone. Being forcefully fast-forwarded into menopause also sucks. Aging on an unnatural timeframe, well ahead of my peers, does too. Having to face mortality decades in advance extracts a heavy toll on us cancerchicks. We want to live long, healthy normal lives; we want to see our children grow up. We hope that cancer doesn’t have other plans for us. Gubar touches on this, too, writing this about the young women portrayed in The Scar Project photos: “The ones that grip me stare at the photographer — at me — defiant. They want to live. I want them to live. Like Barbara Ehrenreich, David Jay seeks to unsettle a ‘public anesthetized by pink ribbons and fluffy teddy bears.’” Unsettle away, Mr Jay.

Gubar writes that “David Jay’s portraits contain images of women whose bared breasts look crumpled, concave, synthetic, reconstructed without or with reconfigured nipples, stitched horizontally or vertically or at an acute angle, lumpy, lopsided, wounded, or hacked off. Bravery resides there, beauty elsewhere.”

Wounded. Hacked off. Those descriptions apply both to my body and my soul. My body is wounded, and like my cancer-ridden breasts, I am hacked off. That this disease happens. That it takes so much from those who are so young. That it steals so much beauty, both internal and external. That the scars that remain are so upsetting, so unsettling. That this disease robs us of our youthfulness and our peace of mind. That the cancer experience changes who we are, forever, and not always in ways that are good or positive.

Gubar says that before cancer, she may have been perceived as being “ungrateful for an intact body, taking for granted organs that functioned normally, arrogant about the boons of health, ignorant of the preciousness of life.” As the old saying goes, we don’t know what we’ve got til its gone, and so too it is with cancer. Pre-cancer, I didn’t think about an intact body, fully functional organs, the boons of health and the preciousness of life the way I do now. While there are days I’m grateful to be up and about and not confined to a hospital bed or tethered to an IV pole, there are many more days in which I’m hacked off. While I take notice of air filling my lungs and appreciate my stamina at the gym, that appreciation is tempered by sadness at what I had to go through. While I am happy that I’m capable of achieving strength and fitness again after the cancer, surgeries, infection, and treatment took their pound of flesh (literally), I’m pissed that my triumph is bested by the omnipresent fear of recurrence.

I can identify with Gubar 100 percent when she says, “I remember the ‘me’ before cancer nostalgically. My earlier self could … connect with family and friends spontaneously and lavishly. At times I visualize the diagnosis as a gun aimed at a flying bird — pitched down from the sky in an instant to lie fluttering on the ground.”

Bang!

translations.deviantart.com

translations.deviantart.com

Susan Gubar ends her beautiful article by pointing out that “the young women in The Scar Project were gunned down while just trying their wings. With courage, the wounded survivors bear invisible scar tissue beneath the physical scars of cancer: the haunting lost person each might have become, had it not been for the disease. They live, but not the lives they would have led.”


Invisible scars

Last night, while pretending I was watching “Dance Moms” with my favorite girl, I saw this Facebook post by Stupid Dumb Breast Cancer:  “Had a ‘friend’ ask me when I was going to ‘get over this whole breast cancer thing’..ummmmm when my chest stops feeling like bricks, when my arm stops swelling, when I stop having doc appts, when I do not have to have another MRI, when there is a CURE!!!”
Shortly thereafter, while still fuming from that FB post, I came across this blog post when it was shared on Twitter by several blog friends. When more than one blog friend shares the same post, it’s worth reading. Surviving Survivorship by Cindy is most definitely worth reading.

This post about the invisible scars from cancer on Surviving Survivorship blew me away. I had to go back and read it multiple times to take it all in. Her depiction of  “the darkness of hovering clouds for the cancer survivor” are so right on, so completely telling. That darkness and the invisible scars aren’t something people like to talk about. The darkness and invisible scars fall into that category of things that make people uncomfortable. I don’t recall seeing anything in the “now that you’ve been diagnosed” literature about the darkness or the invisible scars that would come. I didn’t give  them much thought before my own diagnosis. Even watching my sweet mama die from cancer didn’t clue me into the darkness and invisible scars, because she was an all star when it came to downplaying the horror of this damned disease. Me, not so much.
Cindy writes that “invisible scars are well hidden, not often seen, but most definitely felt.”
Most definitely.

In Cindy’s words:
I wanted to post my thoughts on the topic of invisible scars, and the darkness of hovering clouds for the cancer survivor.  Throughout this document the words “cancer survivor” are loosely used, as cancer survivors are not always quite as fortunate as the words imply.  Yes, their cancer is in remission, and that is incredibly wonderful!  However … the survivor continues to spin, fearful of what may come next. 

Our visible scars are reminders of each step and path along the way of disease or injury.  The invisible scars run much deeper.  Even when the physical scar starts to fade in color and blend in with surrounding skin, the invisible scar residing just below it continues to prevail.
For me, going through major health events, resulted in a darkness like no other.  The darkness hovers, and follows me around like Charlie Brown’s friend PigPen’s cloud of dirt.  This pesky dark cloud of dirt doesn’t magically go away, or even diminish.  It’s a lifetime event.  Actually, it grows with each late-effect side-effect issue discovered.  I may be tricked into thinking it has finally subsided, but its still there, poised and ready to strike at any moment in some new unknown way.
I will say, the invisible scars can show themselves in unkind outward ways.  They are indeed ugly and evil on their own.  Holding inside the frustrations of the incredible physical changes I’ve encountered over the past 7 years takes a toll emotionally and messes with my psyche.  Occasionally, the frustration pours out, like a burst of bad energy. It’s the darkness of the cloud that never gives my pea brain a rest.

We all definitely have our day to day issues to deal with.  Work, the car, the kids, the spouse, the toilet overflowed, the dog ate the cat, etc.  A cancer survivor has those plus these invisible scars weighing them down.

I’ve been weighted down lately. The PigPen darkness has been swirling. My invisible scars are prevailing. It’s something that’s hard to understand unless you’ve been there. We’re told to think positive, be grateful, and savor what we have instead of focusing on what we don’t have. Good advice, in the abstract, but pretty worthless in the ongoing pursuit of surviving survivorship.
If I had a magic wand, I would wave it over the invisible scars (and the visible ones, too, because those suckers are ever-present and an oh-so-powerful reminder of all the evil that’s been inflicted upon the bodies of those of us in cancerland). I would wave that magic wand over the darkness that envelopes even the most intrepid cancer warrior. I would get carpal tunnel from waving that wand over the PigPen-like clouds of dust that choke out even the most persistent rays of sunshine. I would dislocate my shoulder waving that wand over the morons who ask us cancerchicks when we will “get over” our cancer. (I would likely have my magic wand privileges revoked for whacking those morons, actually. But it would be worth it.) I would tear my rotator cuff waving that magic wand over each and every resident of cancerland to rid the kingdom of darkness and invisible scars.
If only.
dark_clouds-wallpaper-1440x900

A good deed that’s not so good

On my way home from carpool #1 this morning, I was driving down my street, minding my own business, when I saw a tiny white dog running full-speed down the sidewalk. With no humans in sight, I figured this little dog had escaped. I pulled over to get a better look at the dog and to see if he had a collar and tags. He had both, so I got out of the car and called him over. He came right away and was quite friendly, and his tiny body was shivering from the 43-degree morning chill. 

 
I called the number on his name tag, after learning his name is Maxwell Chambers, and got a busy signal. With an eye on the clock and carpool #2 in mind, I put Maxwell Chambers in my car and took him to my house. 

IMG_1050He’s a friendly little guy, and was happy to drain the water bowl I set out for him. I tried his owner’s phone number a dozen more times, each time getting a busy signal. Just as Pedey the Weasel Dog was getting upset about our visitor, and just as our queen-bee piggie was considering whether this littler furball was edible, inspiration struck and I called the vet listed on Maxwell Chambers’s rabies tag.

The vet said that yes indeed Maxwell Chambers was a client of theirs, and she gave me another phone number to try for his owner. I told her that my animals were about to riot and rather than keep Maxwell Chambers while I tracked down his owner, I’d just bring him to the vet and let the owner pick him up there.

Maxwell Chambers was happy to play in my bathroom while I got ready to get out the door. IMG_1051

Clearly he’s used to being indoors. He made himself quite comfortable on the bathroom rug and tunnelled under the wet towel a certain girl left on the bathroom floor this morning.

Maxwell Chambers enjoyed co-piloting carpool #2 and was a good passenger. IMG_1052

Briefly.

He was a good passenger briefly.

After my #1 son got out of the car, Maxwell hopped into my lap, and before long, he barfed all down my shoulder, covering my seatbelt, spraying the inside of the door, and drenching the carpet in the backseat.

Gross. Really, really gross.

There wasn’t a good place to pull over for a while, so I could feel the undigested kibble he had for breakfast seeping through my sweater. The smell was less than pleasant. I scooped out as much as I could into the street as soon I pulled over, exhausting my glove-box supply of napkins and dousing myself in hand sanitizer.

When we got to the vet, I handed Maxwell Chambers over and big him adieu. I was tempted to tell the vet tech to have Mr Chambers’s owner call me to discuss the car-cleaning bill, but I did not.

I sped home and employed every cleaning technique I could: first sucking up the remaining chunks with the shop vac, then using the Shark hand-vac to get the gunk in the crevices where the driver’s seat moves back and forth on the little track. Who knew there were so many nooks & crannies in which bits of doggie barf could land? I sanitized the door, seatbelt, seat, and carpet as best I could with Lysol wipes, then finished it off with a coat of Meyers Clean Day lavender all-purpose spray to get the smell out. The final step was to Windex the windows and leave the car wide open in the garage to air out. IMG_1053

Perhaps no good deed goes unpunished, but this is ridiculous.


48

 

Apologies if you receive this post twice; something went wonky and the post disappeared. Here it is again. IMG_1031

On this day 48 years ago, an accomplished and driven schoolteacher from humble, rural beginnings married a confident, athletic Greek who was making his way in the petroleum engineering industry. The mother of the bride had passed away nearly 15 years before this wedding. The father of the groom, who had immigrated to the United States from Greece with limited funds and even less English in his vocabulary, died before being able to watch his son’s life unfold with his new bride.

That bride’s life was cut short, too. By cancer. Stupid cancer. While that bride lived to see her son and her daughter into adulthood and she welcomed and adored four grandchildren, her life–and her marriage–ended too soon. Stupid cancer.

That bride was my sweet mama, and I miss her dearly every single day. I’ve written about this topic in this space a lot. And I will continue to do so. I know my dad misses her every single day, too. He still refers to her as The Bride. In caps. I’m sure he’s missing her even more than usual today. Because today he should be celebrating with The Bride. They should be celebrating 48 years of marriage and a life full of happiness. She’d be laughing right now, recalling her simple wedding and her sweet pale yellow suit and pillbox hat. She’d be self-effacing about the number of years that have passed and the wrinkles etched in her face and the extra pounds settled around her middle. She’d be tempted to surrender the battle against the grey hair, but would continue seeking the ash-blonde color. And she’d be infusing our lives with her unique blend of meddling, hovering, and loving.

Happy anniversary, Mom.IMG_1032


Scenes from the rodeo

It’s rodeo time again. The Houston Livestock Show & Rodeo is a big deal. It’s been going on since 1932, and in those years the rodeo has raised more than $330 million for agricultural scholarships, research, and educational programs.  It’s the largest livestock show in the world, and my fair city is the epicenter for all things rodeo. For 3 weeks every spring, people come from all over this great state and from farther afield to compete in all kinds of events. From bareback riding to calf roping to showing prized animals to producing works of art, the rodeo has it all. Then there’s the carnival, with rides and the most inventive fried foods ever conceived.

The first year we went to the rodeo, my kids looked like thisrodeo 007

 

rodeo 017

and they rode carnival rides like thisrodeo 020

Now they ride rides like this,img_2640

the highest set of swings in the world,

and this. Yikes166785_4879392221273_985662432_n

Read about our trip to the rodeo last year here, in which I feared for my life on one of these carnival rides.

While they’ve gotten bigger and more adventurous, one thing hasn’t changed: they still love to see the animals at the rodeo. IMG_0981

From the show ring to the petting zoo, the animals are the main attraction. IMG_0982

Some of the kids showing animals in the ring look so young, but they handle their animals with ease.IMG_0983

This little girl handled her 250-pound pig without a backward glance. IMG_0989

We took special interest in the pigs, of course. This one has similar coloring to our little piggie, but thankfully is a different breed. If Piper ever got this big, we’d be in trouble. IMG_0985

IMG_0986This black & white beauty grabbed a nap in the midst of the festivities, while this guy was wide awake and curious. IMG_0987

How could we resist that snout??

Watching these giant pigs walking to and from the show ring was fascinating. Although they barely glanced at each other as they passed, I kept expecting them to turn and sniff each other, and maybe even scuffle, the way dogs might.

IMG_0988

Their handlers kept them on the right path by tapping them with a thin stick. We must get one of those for our wayward piggie.

These rodeo volunteers use yardsticks to keep the crowd back when it’s time for the larger animals to make their way to the show ring. IMG_0984

This pig needed to step on the scale before going to the show ring, but she wasn’t too happy about it. It took two guys to get her into the pen that holds the scale.

IMG_0990We stuck around to watch the battle, which the pig lost, and to see how much she weighed: 252 pounds!

Lots of babies are born at the rodeo each year. This little lamb made his entrance into the big wide world and was on display soon after.

IMG_0991This sweet Hereford was born just a few hours before we arrived. Mama looked proud, but tired. IMG_0995

Two litters of piglets were on display, as well. The Little Rascals were born last month and were running and playing. Their next-door neighbors, the Baconators, were a couple of weeks behind them but catching up fast. IMG_0993

 

IMG_0994_2

There were more pigs in the petting zoo, including this little cutie. IMG_0997

There’s a phenomenon in our house called The Pig Flop, in which Piper enjoys the petting so much that she literally flops on the floor all at once, in one smooth movement. My favorite girl attempted to get a Pig Flop from each piggie in the petting zoo.

Including the pregnant piggies.IMG_1002

Of course she succeeded. She is the Pig Whisperer, after all.

IMG_0996

We wondered if our little piggie would smell her rodeo relatives on us when we got home. It’s perhaps more likely that she smelled the deep-fried Snickers on Macy’s breath!

This llama won top awards for best haircut at the rodeo. IMG_0998

Not sure what that’s all about, but it was memorable.

And this little girl took the award for best t-shirt at the rodeo:IMG_0980

“If I can’t wear my boots, I ain’t goin” sums up the rodeo experience quite nicely. Lucky for her, boots are most welcome at the rodeo!