I don't even know where to begin. I feel like this has been the craziest morning. Just bizarre with all these little snippets of stories running parallel to each other yet intertwining on beautiful upholstered sofas and then in hallways in passing, then on tables, and under machines. It's a bizarre globe of swirling matter that seems a little surreal in this fog of coughs and sneezes and masks and such. I feel horrible as if this cold is purposely out to contain me. And I am certainly contained. I need some sleep. But despite this swirl of intersections, and weight of snotty noses and barking seal coughs, I feel calm and peace,
I will cut to the chase. You can immediately stop praying for fat. It's not fat, and I don't want that prayer to back fire and me take on fat in areas I don't need it, so let's nix that prayer right now. Don't utter those words again. My hips are counting on that! But thank you for your diligence all the same. So we know it isn't fat, and now we also don't think it is malignancy (more on that below) nor fluid, nor calcium deposits, nor...well to use her words " I have absolutely no idea what this is."
It started with me sitting in a waiting room of 12 women, that number would fluctuate as as I sat, all clad in the same two layers of muddled grey gown. What struck me first about the room was the 3 daisy shaped light fixtures hanging above my head, and then the modern wood paneling draped on the far wall and the sage green paper on the back walls. I felt as though I were in a luxury hotel lobby. I kid you not. This place goes all out to make you forget the sterility of the halls leading to this particular imaging area. After absorbing that awesome scenery, I was left with the utter silence of the room. I mean not a word. Not a spoken voice, not background noise, not a TV or a phone call. Just twelve women clad in gray sitting in silence. The silence would come and go as the morning went on as women exchanged themselves out for another and as technicians called out names thus prompting the exchange. But the silence left in between spoke a novel. There were untold stories in this room. Ongoing stories. And I've never heard such heavy silence.
I went back for my ultrasound and the radiologist poked and prodded. There is was the black blob next to my implant. "Ms. McCollum, I was really hoping I was going to get this up on the screen and immediately say "this is nothing" and send you home. But honestly, I have no idea what we are looking at here."
Me: "is it a mass?"
She: "I don't know. Let's get the mammogram and see what comes up."
So she sent me back out in to the luxurious waiting room where now new faces sat (all staring at the mask I was wearing), but the same silence remained. Then I got called back to mammogram. Shove the boob into the slot - picture. Turn the boob shove back into the slot- picture. Shove the side of the boob back into the slot- picture. "ok, you can go back to the waiting room." Back to the silence and yet more new faces. It's as if they passed out a sheet of paper to everyone who entered asking them to respect the silence. But i knew what it was. It was a room full of worry.
"Ms. McCollum?"
I go up to meet the radiologist who says we need to re-do the mammogram. "I am seeing something and I just can't tell what it is." Ok, at this point she had my attention. I was perked first when she said the ultrasound is non-conclusive and sent me to mammogram. But now TWO mammograms? You have my attention. Insert boob, squish boob - picture. Insert boob , squish boob- Picture. Back to the the luxury waiting room.
Now we have found ourselves down to 4 women (myself included). Also in silence. Until....Until the lady next to me turns and looks at me and says, "you look like you feel really bad. I hope you are ok? (me, yeah, I just had a cold that won't let go) I know this sounds crazy but, do you believe in heaven?"
What?!?! No you can't make this stuff up. I sputtered, then clamored to think quick on my feet and said "yes, It's what gets me through these kind of waiting rooms. It's amazing how you can find peace in the knowledge of a heaven". Well, the flood gates opened and the whole waiting room started chiming in. Some told stories about how they got there. Others talked about how heaven played a role in their journey. The women kept asking the touch questions. And I just kept praying God would give the words she needed to hear. Right smack in the middle of that rush of conversation "Ms. McCollum?" I got up and grabbed my stuff and walked over to her and said, "I have to go now, but whether or not you ever believe there is a heaven, you can believe in relationship here on earth and that as a result I will be praying for you and let that give you hope." Mercy, I'm sure I flubbed that up but it is what I had in the 4 second walk out of that room to meet the radiologist! Surely, I could have laid out the saving grace of Christ and all the grace of that, but alas my mind landed where it landed in the split second I had. What a crazy dialogue at such a time as this!!! I'm hoping the conversation continued after I left the room, I'm hoping just the right words were uttered to get her through her day. Something to give her the hope she must have been looking for. Those 4 women will be permanently etched into my brain. Their stories. Their search for hope. Their hunger for more. I was broken by that. On my way out, another women stopped me and said "I'm praying for you, and crossed her heart." Here I was feeling like death warmed over with this awful infection and the mental strain of being anywhere but in my bed and God brought me this little nugget. I know this isn't what you opened this page to read, but it truly is the highlight of the story. Relationship. Trial is a lonely place. And if you don't hear me say anything else today, here me say that. We absolutely have to support people in trial. I've never felt more lonely then in the middle of "stuff" and I know you feel the same. These women proved that to me.
Ok, now I am back with the radiologist in a dark conference room. "Sally, I have no idea what this is. I can say with certainty it is not fat. It is not calcium deposits. And it's not a malignancy, because I have never seen malignancy look like this. I called Lead Plastic Surgeon and spoke with him on the phone about you. I wanted him to look at the scans, but he is out of the country right now, so we decided to have you go see him for an exam and for him to look at the scans with you. He's going to call you to set it up. I'm suspicious it is the sling that is under your implant (to help hold the weight of the implant), but I have no idea what a sling looks like on imaging. I even googled it and there are no pictures out there. So I want him to see it. But for now, rest that we don't think it is malignancy, because if it is, I have never seen one look like this. It looks 'man made' in a lot of ways because it is so dense. Very dense. But it's not the implant itself" (paraphrased slightly off my memory). No malignancy from what we can tell, that's really all I needed to hear.
So, I'm now back in normal clothes, sitting on my bed, very eager to climb under the sheets and take a nap for I feel rough, but I totally feel at peace. This whole day was somehow peaceful, despite 3 sets of imaging, despite knowing they were seeing something, and despite having no idea what it is. God totally orchestrated this day. And I now have 4 women who broke the silence to keep my mind company. That's a score!
I will keep you updated. I imagine my plastic surgery appointment will be next Wednesday. Maybe a biopsy is in my near future, but definitely another exam and lookey loo (there's little dignity in malignancy as you pull out body parts at every turn). I've emailed him and Lead Breast Surgeon who I saw yesterday and am waiting to hear back. He's going to laugh, because I had promised him at my last visit over 6 months ago that I planned on never seeing him again and to not take it personal. Be careful what you promise ladies, Life has a way of tweaking itself as you go.
To access previous blog posts - click HERE.
It began as a story of prophylactic mastectomy and became a smattering of every day life. I write so I can remember. I write so I can advocate. But mostly I write to overcome.
August 24, 2016 - "The McCollum"
I've said it many times before. There is something about a cancer center waiting room. You can do the best of interior design, the most brilliant placement of soft lighting, and the perfect combination of artwork and still, your heart skips a beat when you walk in. It's been almost a year since I've been in that waiting room (for a visit, I am often there for work) and it did its thing, changed my mood.Mine was the last appointment of the day so the waiting room was deserted minus one couple also waiting their turn, so the calm of the wait brought me back to center and away from the initial heart gallop. Lead Breast Surgeon was as delightful as usual. She has an almost supernatural ability to put someone at ease. I didn't necessarily need easing, but she certainly maintains status quo. I told her if you are going to have a breast lump, you might as well enjoy the great people along the way. Present company included.
The appointment went exactly as planned. Strip down, bare a boob, touch and feel, get dressed again. She agreed there is something there that shouldn't be there and in her supernatural ability told me she wasn't worried yet. I said "okay then, I won't worry either." To which she responded, "but let's image it." She picked up the phone right then and there and called over to ultrasound and landed me an appointment tomorrow morning. I chuckled at that and made her promise me she still wasn't worried. I pinned her down. "What is on the differential?" I guess she was expecting that question cause she dove right in with a response. "I'm very hopeful t is one of 2 things: A collection of fat necrosis (dying fat cells),or scar tissue." (Us gals have been laughing that never before have we been so willing to pray for more fat! LOL). I said "and what else?". She said, "well it could be the negative things: a mass of malignancy or fibroma. If it looks like a mass on ultrasound, we will biopsy it. But let's just assume it won't come to that." See, she is awesome at putting someone at ease. I had to push her to list the last 2 because she wanted to leave on a high note. Despite her super optimistic approach to medicine, I really do think she is leaning toward fat necrosis, or else she has an awesome poker face (and I think she does, but that is besides the point). So we will continue to pray for fat and for a good night sleep and see what comes tomorrow. Oh, and while you are praying, I have the nastiest of respiratory infections going on right now too and could use a pick-me-up from that. It's really pulling me down, and I don't want to be down. I want to be up.
Funny story. During show and tell she says, "I really can't believe how great this all looks (refering to my reconstruction). You've had 6 surgeries and I was expecting to come in and see a railroad of scars. Sally, you should be thrilled. (she went on to remark about my cleavage but I will save face and spare you those details)!" So there you have it, we have a thrilling breast job! I could use that good news. I chuckled a little saying "well he (Lead Plastic Surgeon) told me he was going to do his best work ever! (well I made him promise that)". She said "speaking of him, do you know that we now refer to the procedure we did on you as 'The McCollum? (mastectomy, wait 2 weeks, start reconstruction)". I said "huh?????" "Yep, that was the first time I had done that (wait to do recon) in prophylactic mastectomy." I don't know if I should be thrilled or not, but it totally got a laugh out of me. So if someone says to you, "do you want the McCollum and all the works?" Know you may be "thrilled" with the results. (Chuckle!) I reminded her I did have 4 more surgeries after that so the jury is still out. She reminded me "The McCollum" was still a huge success.
Oh the joys and ins and outs of mastectomy. It's never boring.
Ultrasound tomorrow. Pray for fat, or scar tissue is fine too if you want to overachieve. and pray for this respiratory infection to resolve too. Might as well shoot big! Hoping to have good news to report back to you in a few days.
Ta-ta for now!
To access previous blog posts - click HERE.
The appointment went exactly as planned. Strip down, bare a boob, touch and feel, get dressed again. She agreed there is something there that shouldn't be there and in her supernatural ability told me she wasn't worried yet. I said "okay then, I won't worry either." To which she responded, "but let's image it." She picked up the phone right then and there and called over to ultrasound and landed me an appointment tomorrow morning. I chuckled at that and made her promise me she still wasn't worried. I pinned her down. "What is on the differential?" I guess she was expecting that question cause she dove right in with a response. "I'm very hopeful t is one of 2 things: A collection of fat necrosis (dying fat cells),or scar tissue." (Us gals have been laughing that never before have we been so willing to pray for more fat! LOL). I said "and what else?". She said, "well it could be the negative things: a mass of malignancy or fibroma. If it looks like a mass on ultrasound, we will biopsy it. But let's just assume it won't come to that." See, she is awesome at putting someone at ease. I had to push her to list the last 2 because she wanted to leave on a high note. Despite her super optimistic approach to medicine, I really do think she is leaning toward fat necrosis, or else she has an awesome poker face (and I think she does, but that is besides the point). So we will continue to pray for fat and for a good night sleep and see what comes tomorrow. Oh, and while you are praying, I have the nastiest of respiratory infections going on right now too and could use a pick-me-up from that. It's really pulling me down, and I don't want to be down. I want to be up.
Funny story. During show and tell she says, "I really can't believe how great this all looks (refering to my reconstruction). You've had 6 surgeries and I was expecting to come in and see a railroad of scars. Sally, you should be thrilled. (she went on to remark about my cleavage but I will save face and spare you those details)!" So there you have it, we have a thrilling breast job! I could use that good news. I chuckled a little saying "well he (Lead Plastic Surgeon) told me he was going to do his best work ever! (well I made him promise that)". She said "speaking of him, do you know that we now refer to the procedure we did on you as 'The McCollum? (mastectomy, wait 2 weeks, start reconstruction)". I said "huh?????" "Yep, that was the first time I had done that (wait to do recon) in prophylactic mastectomy." I don't know if I should be thrilled or not, but it totally got a laugh out of me. So if someone says to you, "do you want the McCollum and all the works?" Know you may be "thrilled" with the results. (Chuckle!) I reminded her I did have 4 more surgeries after that so the jury is still out. She reminded me "The McCollum" was still a huge success.
Oh the joys and ins and outs of mastectomy. It's never boring.
Ultrasound tomorrow. Pray for fat, or scar tissue is fine too if you want to overachieve. and pray for this respiratory infection to resolve too. Might as well shoot big! Hoping to have good news to report back to you in a few days.
Ta-ta for now!
To access previous blog posts - click HERE.
August 22, 2016 - Wherever we will go
I’m still lying in wait. But I did it “Sally Style” by going
to the Caribbean for a week. This trip was planned well in advance, but the
timing could not have been more perfect as breast lumps seems almost
non-existent while swimming along with seemingly weightless sea turtles in St.
John’s. My world was weightless too as I bobbled up and down with the
undulating waters around me. I purposely floated alone, away from others. The
sea was mine, if only for a few quarters of time, but it was mine as my view
held only the waters around me. (I will spare you the intricate details of
snorting water up my nose almost sending me into a flopping display of panic,
but know that moment was there along with also almost losing my swim bottoms as
I dove off the boat). I’m a sucker for creation. And the creation in these incredibly
blue waters provide nothing short of mental healing. One rolling tide can sweep
away any angst that lie at your back doorstep over to be discarded out over the coral
reef that protrudes up from below. It’s therapeutic. And it’s simply glorious
to lose yourself in the vastness of magnificence under the water line. But now,
well now, I’m back. Back to the ins and outs. Back to THIS side of the water
line. Back to the timeline of the ticking clock our society spends so much time
trying to tame. There is no clock in the ocean, or rather I found none in my
weightless stroll, but now I am back. Back to waiting.
Habakkuk 2:2 has been ringing in my ears non-stop ever since
stepping on the plane heading back to my reality. “I
will wait to see what the LORD says and how he will answer” (NLT). The verse
flooded my thoughts before leaving town and again flood my thoughts now that I’ve
returned. Aren’t we particularly horrible at waiting? Do we not conjure
up every known horribleness that could possibly be while we wait? Anxiety is
real. Worry is real-ER. Fear is real-EST. Somehow, for I know not how by my own
merit, I’ve been able to keep these predators at bay. They creep in (mainly in
the middle of the night), but then they creep back out. Crystal blue water surely
played some role, but I struggled more as the week went on. Flying home was
more like flying back to this breast nodule and all it may hold. I’m adoring
the statistic of 8 out of 10 (8 out of 10 breast nodules go on to be benign
cysts), but I’m finding less comfort around my own statistics for I know not
what they are. I did this prophylactic double mastectomy to keep breast cancer
at bay. So what does it mean when my risks were so high pre-mastectomy to now
find a lump post mastectomy? You can roll that around in your mind until worry
is all you know. I’m not there. I am not worrying. But I worry I will START
worrying while I wait. See, that is the vicious cycle of worry so easily portrayed
by us Type A folks. We truly can worry about worrying. Worry serves no purpose
here. Waiting serves all the purpose here.
I’m so gracious in knowing that even through this nodule, and
its imposed waiting mode, I am being refined. Ron is being refined. Our “We” is
being refined. And for that I give thanks as I lay in wait. In turmoil we get
glimpses of our self that we don’t see in the ins and outs of everyday life. There
is a camaraderie that can be found in struggle. There is a depth that can come in turmoil. The
lack of guarantee of tomorrow brings a filter which strains out the superficial
and brings back a focused lens aligned on the irreplaceable moments of life. I
don’t want even a single second of that surreal focus to be muddled with the
spoilage of worry. Worry is a predator that lurks behind each corner ready to squeeze
out any blessing that lies just underneath. It’s a thief of everything great. So I very much want to choose to get ahead of
that so my lens of perspective remains cleansed by the hope and clarity that
comes during refinement. I want more time in the irreplaceable moments
and in the sifter of refinement, and less time flooded by the corrosive nature
of fear.
To access previous blog posts - click HERE.
August 10, 2016 - If it takes a nodule...
I’ve mentioned before that I often struggle with what to keep
private (my introverted heart protecting my everything) versus what to share
here openly. It’s a constant internal battle of vulnerability versus honoring my
commitment to model “doing life together” and letting my Story be His Story. It’s
not always easy doing life His way. But I know that when I do, He honors that,
and He uses that. Three days after my double mastectomy, I made a commitment to
God that if He brought me to mastectomy I would do everything I could to be
open to Him using my story. All of my story. So I’m laying my vulnerability on
the line, and stepping in to His command for us to do life with other people,
not in solidarity. And also because it is related to my mastectomy story that
you have been following for 4 years now, and I want to stay committed to my transparency
in that for hopes it helps one of you should you find yourself in similar shoes
one day.
It was 1:30 in the morning and I was jolted out of a very
deep sleep. I sat straight up in bed, eyes wide open, heart racing, and my mind
attempting a record speed to orient myself to time and place. I originally thought I must have heard a
noise, but no, that wasn’t it. The house was very quiet. Beyond still. Beyond
quiet. Often Oliver (the cat) comes up and hits me on the forehead when he thinks
I need to be up and about. He’s brutal about it when he thinks it is time, but not
this night, he was tucked in at the end of the bed on Ron’s side heavy in sleep.
I laid back down and immediately felt a “twinge of something” in my lower right
breast. Earlier in the day, I had done an arm/chest workout and now the muscle was
in a cramp, no doubt its way of getting me back for what I had done to it hours
before. I reached up to massage the area back into submission as I laid back
down to fall back asleep, and there it was.
It’s the perfect text book “lump” I’ve heard described so
many times before. Small, round, peanut sized, rubbery, non-tender nodule. It’s
location: one inch to the left of midline and ½ inch up from the base of the
breast (ok, there, that IS too much information, but location matters). Had it been in any other quadrant of the breast, I would have thought
it to be a swollen lymph node, but lymph nodes don’t live in this region of
breast tissue. But here it is, all the same, in MY quadrant of MY breast where
it had not been invited. Something. Something that shouldn’t be there. Something
that wasn’t there before. Immediately, I mean immediately, panic set in. And
then a furious investigation of the situation (thankful to have only found this
one). Then, the wondering of “what in the world?!”, “I had a double mastectomy”,
“there is little to no breast tissue in my breast”, “It’s August! My heavy
month! My Celebration Month. My Mastectomy Month. My ARE YOU KIDDING ME month”
and then all the other things that run through your mind when you are in panic
mode. Then, no sleep for many hours as I watched the room get lighter and lighter as the hours ticked on (I may or may not at one point reached down and tapped Oliver unrelentingly on
his forehead until he raised his head. Just because I could. But don’t worry he
got a lot of belly love too).
We often think God’s story comes when we have a “known”.
Once we know the outcome (a diagnosis, a decision, a plan), we then bring our
inner circle into our story for moral support. It’s as if we need to have it
all figured out before we allow God to publicly do his work in us. I think it can
be a rookie mistake, and a mistake that I make often. I’m learning we can miss
some crucial moments that are ripe for the blessing that can come in chaos. These are the core moments of this “period of
wait”. There is huge value in this period! Where prayer may have its biggest
outcome. Where friends can rally and remind you that your story is also their
story, because they love you and they want to do life beside you. Where anxiety
can be repurposed into astounding faith. Instead we sit in silence and in the
privacy of self, and often rob ourselves of the beauty and restoration that can
come while waiting with others in tow.
This journey of mastectomy has been all about this for me.
Teaching myself to do life with others in the moment that life unfolds, and
teaching me that every aspect of my story can be used for something. It may not
mean a hill of beans to me, but it may mean something to the young wife who
finds herself in tears while standing in front of the mirror the week after her
surgery, or the middle-aged friend who doesn’t know why she feels so
overwhelmed while emptying her breast drains, or the forty-something mastectomy
soul who wakes up in the middle of the night and finds a lump. There is always
someone out there who is just like you. And maybe they too need to know they aren’t
alone, they aren’t a failure for feeling what they feel, and they aren’t strange
for the thoughts that creep in when they don’t expect it. God is re-training me
to be the version of me he designed me to be. And maybe 25 years after my
lymphoma remission is the perfect time to remind me to stay aligned with faith
in His plan. For His way is perfect, even in the waiting, and there is much to be
learned (I’m working on this, but boy is it challenging! Be gone, negative thoughts! Be gone, fear!).
Lead Breast Surgeon (who did my mastectomy) is taking me
back under her wing. She wants to see me in her office next week for an initial
“touch and feel” session, and then I imagine imaging or biopsy or something is
likely in my very near future (update: the appointment had to be moved to the
following week due to a scheduling conflict on my end). But let’s look at the
totally reassuring statistics that we all need to remind ourselves of in these
situations. 8 out of 10 breast nodules are benign. 8 out of 10 ladies!!! That's only 2 being breast cancer! That’s
for you too! So let’s relish in that truth when we find our lumps and bumps! Not
worth worrying about 20% right? And for me, I had a prophylactic double
mastectomy. These boobs are man-man, “his best work ever” he promised me, I
have little to no breast tissue left (picture and orange, you cut a slice, then
chew the fruit off the skin. You get almost all of the fruit, but there are
bits and pieces left behind on the skin. Same with the boob after mastectomy,
most but not all). So having so little breast tissue there, I am wondering how
this nodule even found its way here. I must be very likable for it to choose to
do all that work to reside in an area where it will have no friends. But it’s
here, and we are going to pray it to benign-ville! The outcome just may lie in
our prayer, not because God is our puppet, but because we grow closer to him
through our prayer. Hurry is the death of Prayer. There are times we must wait and listen. And if it takes a nodule, it takes a nodule.
I’m a work in progress, and maybe because of His work in my
story, you are too. Hello, nodule, welcome (eeek!) home.
Habakkuk 2:2 says, “I will wait to see what the LORD says and how he will answer” (NLT).
You guys are my people, for such a time as this.
To access previous blog posts - click HERE.
Habakkuk 2:2 says, “I will wait to see what the LORD says and how he will answer” (NLT).
You guys are my people, for such a time as this.
To access previous blog posts - click HERE.
August 1, 2016- Deflated Balloons
Tomorrow is August 1. August as a month holds a lot of
memories for me. Twenty five years ago my lymphoma when into remission in
August. Ten years later, I was labeled as “cured”, also in August. Four years
ago, I had my double mastectomy, also in August. Four years ago, I had surgery
number 2 in the breast series to start breast reconstruction, also in August. Last year, I had surgery number 6 in the breast series, also in August. August holds a lot. August is a heavy month.
I’ve never been one to celebrate cancer mile stones. I don’t exactly know why I don’t do that. Almost everyone I know does that. I love celebrating your
milestone with you. Balloons, cake, dinner, trips, whatever, whenever. It’s all
wonderful and something almost everyone does, and does well! But for me, I
always held this moment as a memory, not a celebration. I don’t know if this is
survivor’s guilt? I don’t know if this is because I am terrible at celebrating
(really, I am, I build something up in my head and it turns into deflated
balloons and a molded piece of cake that never got eaten)? I don’t know if this
is because it feels awkward? Most likely it a combination of all of the above
plus a few more for good measure. I have plenty of friends who don’t get to
celebrate milestones because they didn’t survive the diagnosis. I’d much rather
celebrate their journey and the lives they touched even in their death rather than
my “success”. It also always felt a little weird to celebrate an achievement because
when it really comes down to it, I didn’t do a single thing to survive. I
simply showed up each day when they asked me to and got my treatment. My
survival is no great achievement on my part. So it just felt weird flaunting
this stepping stone year after year. This year, it was a biggie. Twenty-five
years lymphoma-free! That's crazy. So I wanted to try this attempt at celebration …..And I
even flubbed that up. I wanted to go simple. Ease my way in. I can pull off
simple, or so I thought. I bought two slices of cheesecake (guess Ron should have one too,
huh?) on a whim while doing my grocery shopping earlier that day. Dinner rolled
along, I pull out the cheesecake, popped the plastic lid open, grabbed a fork, and
took a bite….and then…well what am I supposed to do next? Make a speech? Thank
Ron and Oliver for attending the celebration? Give Ron a high five? Give a
shout out of “I did it! I survived!”? It just simply felt awkward. Really
awkward. I took my one bite (I was too full from dinner to finish the slice),
close the lid, put it back into the fridge and we headed back out to the garage
to finish cleaning.
Maybe I didn’t do it up enough. Maybe I should have planned
a dinner out and invited people over. Maybe I should have set aside something
other than just opening the fridge and pulling out a piece of cake shoved in a plastic
takeout container. Maybe I should have realized that today was July 31 and not
August 1st. Yeah, I remembered that just before sitting down to
write this tonight. Maybe my thoughts shouldn’t have been on the people that
didn’t make it.
Hours later, it was getting dark outside and I could hear
the thunder rolling in so I went outside and laid down in my driveway. I wanted a few moments to decompress from the
day. And while staring up at the lightning show God had given me, it hit me. I’ve
had it wrong all along. Just as I was feeling let down and out of sorts, God
gave me my favorite thing: A thunder storm. And it was spectacular! And I was
reminded that none of this celebration rig-a-ma-roll should have ever been
about me. I was missing the boat! I was trying to feel something I didn’t feel:
accomplishment. My celebration should have instead been about God’s
accomplishment: His provision. He gave me the thunderstorm to remind me he gave
me survival. For some, death comes and even in that God has provision,
particularly for those left behind who may grow closer to him and to others around
them in the process of loss. In death he can bring restoration, forgiveness,
longing for something outside of ourselves, a purpose to propel us forward as
we grieve. Sometimes we don’t understand what he brings us, but it’s there,
just waiting to be discovered. For others, like me, He may give survival. He gives us provision in and through our
stories that follow survival. We have the opportunity to be a conduit of his
grace and mercy as our stories unfold. I think had I had THIS be the focus of my celebration of what he is and has
done in my life for the past 25 years of surviving, my celebrations would have
been heartfelt and purposeful (for me who struggles to celebrate self). My celebration
simply needed to be realigned around his provision to me, my family, and my
friends by keeping me around to finish My Story.
So I’m having a do-over (or I am at least going to give it a try!). I am finishing my piece of cheesecake
tomorrow actually ON August 1st. It’s kind of late, so I am not
going big for tomorrow. I’m sticking with the store bought cheesecake that is
still sitting in my fridge, but then I am going to have little celebrations
throughout the month (maybe a dinner out with a close girlfriend, maybe asking
for cards or posts here on social media with bible verses of provision to be
sent to me by friends - would you do that for me?, maybe set aside a day with
Ron to just love on life, find and cherish time spent with family) as a
testament of God growing me through the last 25 years. This feels manageable, something
I actually could get in to, and better focused by focusing nothing on my
achievement and all on Him, because really, all I did was show up.
Here’s to twenty five years of awesome memories, incredible
friends, life changing moments that I hold dear, storied shared, mistakes made,
boobs removed, lungs challenged, hearts touched, challenges accepted, Christ-focusing
journeys journeyed, lives loved, and even lives lost for in your loss I continue to
find myself. He’s not finished with me yet. I am better for knowing each of you,
and I hope you are better for knowing me too.
Hear ye, Hear ye! Let the celebration month begin!
Click www.tradinginthetatas.blogspot.com to access other posts.
Click www.tradinginthetatas.blogspot.com to access other posts.
July 22, 2016 - Long live Saul!
Since I was running very short on time, I quickly threw
on my swim suit, my flip flops, grabbed a towel and headed out into the garage
in record time flat. Normally, I would have been a bit more organized (throw on
the swim suit, A COVER-UP, flip flops, a bag stuffed with sunscreen, a towel, a
book, a snack, a drink, goggles, headphones) before heading outside, but today I
was in a hurry and needed to get there, get my swim in, and get back to finish out
the tasks of the evening. I also usually walk, but since I was in my swimsuit
only (I never do this!) and needed to get there fast, I jumped in the car and
opened the garage door to drive the few short blocks. It was sweltering outside
and the glare of the sun was reflecting off my window making it difficult to navigate
the drive way, but soon enough it was all clear with lots of squinting and I
was pulling into the street.……..oh no.
There he was right in front of my car, oblivious to me,
making his sluggish way across the scorching pavement. “Saul” (because that is
what I do), an adorable rather large turtle about the size of a football, had
become the perfect target for, if not my tire, the tire of some fast driving
teenager who takes the corners on two wheels. And somehow all of this was now
unfolding all on my watch. Because I have an almost supernatural ability to
find myself in the company of animals in distress (a recent few: Gertrude, the dehydrated
sea duck with a bum wing; Stormy, a pond turtle crossing the soun Id bridge; Franklin,
the sea turtle who had been kidnapped by beach goers; Blinco, the belly-up fish
attempting to die in the surf; and now Saul), I'm not totally surprised this is my task for the day.
So here I was with a choice:
- Drive by slowly so that I don’t clip him and head on toward the pool
- Get out as fast as lightening (cause I am in my swim suit!) and run like the wind to pick him up and take him to the other side of the road.
- Sit and wait in the car acting as a crossing guard in hopes that no other cars come around the corner, but for now the coast is clear.
Number 1 was the obvious choice for any sane adult, because
did I mention I was driving my car in my swim suit? Yet Number 3 was a totally
plausible option were I not Sally, who absolutely can’t let an animal be in
distress or risk of distress, and I, not knowing if Saul was out for his fast
paced stroll across the road or a gingerly lackadaisical wobble that would be
hours on end to reach the curb (and could he even climb the curb?) forced me
into risky decision number 2.
Ok, so it’s Number 2. Come on, Sally, you can do this! I
slide into the very middle of the road (to prevent another car from coming
through) and put the car in park, though leaving it running so I could make my
fast get away when the rescue was complete. I check the windows, the mirrors,
the windows again, the mirrors again, while craning my neck as far as I can to
ensure no one was out walking or driving by (I’m in my swim suit!) and determine
the coast is clear. I open the door, jump out of the car, run fast as I can to the
front of the car and pick up football sized Saul in both hands to which he
promptly responded with hissing and aggression of “oh no you didn’t!” while I ignore
the hiss and purposely whisper sweet sentiments of “you’re so precious”, “what
a lovely turtle you are”, “smooch, smooch, smooch” into what I thought may be
his little Turtle Ear. We make it to the curb quick like lightening and then I
realize, I have carried him back in the direction he had just come so that was surely a slap in his face for all of his
efforts for the last however minutes it had been since he stepped into the road.
Then I also remember, glancing in the direction he was heading, that there is a
pond in the woods right around the corner, and I imagine this is where his turtle
family surely was out camping for the holiday weekend. I simply had to get Saul
to the pond! I glance around again, coast is still clear, and pick up poor
hissing Saul once again and carry him (arms straight out in front of me) back
across the road and now down the street a little in the direction of the corner
next to the pond.
(Chatting, laughing, conversations off to my right)
Holy guacamole!!!!! The front door of my neighbor’s house
has just opened and out pours what surely was the census of Texas right into their
front yard. And there I stand, IN MY SWIMSUIT, holding Saul, BOTH of us now
hissing at the outcome of this moment.
Promptly and prideful with head held high I continue my 20
foot jaunt to the grass at the corner and place Saul down facing the pond, walk
back to the car, climb in and close the door, then lower my head back down in
embarrassment, pull back into the driveway, drive into the garage and close the
garage door.
The moral of my oh-so-very-true story is five-fold:
- Take the time to grab the cover-up. While I am working so hard not to allow self-shaming, embracing my body flaws does not mean I have to parade myself (carrying a football sized turtle mind you!) in the middle of the street while wearing a swim suit.
- Maybe Saul has his own plans and who am I to thwart them? (Ok no, the turtle needed saving and I was just the person to do it. Save the turtle every time!)
- Every animal deserves a name as it makes endearment absolute and therefore follow-through a lot more likely when the situation changes.
- It’s ok to change your original plans after embarrassment. Nothing shameful about re-prioritizing vacuuming over swimming.
- Sometimes we simply need to learn to look for reasons to laugh. The world brings us so many reasons for heart ache so we need to celebrate with laughter when we can.
July 8, 2016 - I know it's not that simple, but really it is.
To say the last few days, weeks, months have been full of
heartbreak would be the understatement for sure. Black lives, police lives, Turkish
lives, homosexual lives, American lives, Christian lives, refugee lives, children lives killed by
parents, parent lives killed by spouses…the list goes on and on. Then there are the
individual lives we hear nothing about on the ever scrolling news reels. And then there are the
day to day heartbreaks over every day lives. It’s too much! My heart nor my
mind know how and what to process with this ongoing onslaught of “one more
death” day in and day out with no reprieve. I don’t want to get into the cause
of it all because mine would be an uneducated dialogue in a pool of many, but
my summary thought is we have not a gun problem, but rather we have a devastating
heart problem. We’ve lost our focus, and we have yet to find our way back.
So while I am leaving the cause there in that one sentence,
I find myself in need of exploring my role, which I dare not say would be
trivial. We are all to blame. We are stupid to think we are not. I have racism.
I have anger. I have “elitism” thinking I am better than the next. I have
jealousy. I have pride. I have education gaps. I have financial gaps. I have
stupid thoughts and even more stupid reactions. I have a heart that is tender…for
certain things. I have things that make me the cause, and I have things that
make me the target. I am not immune to being a contributing cause to the
problems of this world. We are just as fallen as the next person, but maybe we
have better resources, better coping mechanisms, better…whatever. Encompassing
it all, I am stupid to not at least acknowledge that I am not immune to making
bad decisions, to saying I am one thing when I am really the next, to being part
of the problem and not the solution. Our pride keeps us from acknowledging it.
But it’s there. We need to quit
diagnosing the person next to us and instead start diagnosing ourselves. We need an intervention and we need Divine intervention.
It’s time for purposeful action. I don’t have measurable
effects on legislation. I don’t have measurable effects on our response as a
society. But I do have widely significant effects on my response as self. And I
need to be held accountable to looking inward. I need to sum up the passion I
know lies underneath the muck and make tangible impacts in my immediately
surrounding 100 square feet. I have a choice to make. And it’s knocking at my
front door. So I’m looking for people next to me that I can love on. I’m looking
for that friend that needs an extra “pick me up” today as they navigate their
life. I’m paying kindness forward to my waitress. I’m seeking out opportunities
to offer praise and moments to provide a compliment to that
coworker. I am healing from the inside out and not waiting for you to change. I
am squashing my poor actions and taking responsibility for where I failed you.
I am working to focus on your strengths, for you already know your weaknesses
and need not for me to point those out. I
am reaching out to the friend I haven’t spoken with in quite some time. I am
contacting the person I need to ask forgiveness of. I am offering forgiveness
without waiting to be asked. I am
reminding myself you are driving slow because you have a broken rib. I am
bringing to light that your rude response was sprouted from your domestic
violence. I am saying the words to you I
left unspoken. I am going out of my way to put your needs above my own. I am
seeking to be more grateful and to offer more grace. Even mal-intent can be met
with the kindness of humanity. I can hold you accountable in love, and not in
spite. I can dig deep to find my racism and pray it into extinction. I can be
open that I am not perfection, but rather a fallen soul covered in God’s grace,
which should propel me into a more suitable response. I need to consistently choose to go out of my way to exude kindness. I can root out my failure and replace it with
warmth and hope and joy, for those will win out every single time when chosen! I
am starting this very moment with realistic steps that positively impact my
circle of being.
We think the answer lies in the government or the ___lives
around us (insert your own solution), but I absolutely would be a fool to not
find my role in the destruction of this humanity. That should keep me busy for
many moons to come. As Christ grows my heart, he reveals my responsibility. Our
fingers should first point inward and work outward from there. And we should
hold each other accountable, but only after we start with self. I have a long
road ahead. I know it's not that simple, but really it is.
#prayersforhumanity
June 28, 2016- For lying in wait simply leaves us….Lonely
It’s so easy in this life to find yourself on any given day
feeling rugged. It’s a ruggedness of being worn out, emotionally drained,
emotionally conflicted, physically challenged, and on the verge of being out of time for the monstrosity
of the never ending to-do list. All
while attempting to raise little ones with any chance of them being
contributing members to society. All while wondering where our time goes when
we are single and working hours on end. All while being married and trying to pull together 2 schedules into one. All while approaching mid-life, or
passing mid-life, and looking back and wondering what we have to show for it
all. There is nothing like navigating mid-life to get our attention around the
value of life’s accumulations.
I’ll venture a guess to say that on top of this incredibly chaotic life we spend so much time building for ourselves surrounded with a calendar
so overflowing that that no one would envy, a work ethic over shadowing our
home ethic, and such a sense of imbalance that we don’t even know what comes
next, that most, if not all of us, would describe ourselves as lonely. I ask
myself how in the world we could ever be lonely with a calendar overflowing
with tasks. How could we be lonely when we are surrounded by person after
person in this place of work? How could we be lonely with the constant
bombardment of events, and sound, and cohabitation? How could we be lonely with
a spouse and 2.5 kids? Yet it is exactly what we are, isn’t it? Lonely. And burned out. And run-down.
It’s evident as we navigate challenges, and we long to
dialogue the experience with women that we trust. It’s evident when we are
confronted with heartbreak, and we long for the phone to ring with someone
calling to check in on us. It’s evident when we see fellow friends showered
with attention during loss, and we long for attention ourselves as we mourn in
silence. We don’t want more tasks or things. We don’t want more calendar
commitments. We don’t even want another
acquaintance. Rather, we crave to our core people that bring value and who are
willing to do the tough road with us. Doesn’t it really simply come down to the
fact that we crave authentic relationship? And as we search this out we ebb and
flow in this rat race of the American Dream in hopes of finding a reasonable
substitute that will give us a sense of value, a value which we didn't realize was intended to come
through relationship. But with that missing, we fill the void with
a to-do list, one more vacation, another night on the town ,
just one more accolade for our children, or one more promotion while spending
our days away in the cinder block lined hallways. We are shoving our lives so
full with substitutes that instead of coming out on the other side purposeful
and recharged as genuine relationship can bring, we come out in a perpetually starved
substituted version of our selves. And there is no wonder we suddenly find
ourselves worn out, emotionally drained, emotionally conflicted, physically
challenged, and out of time.
So having pondered this for days/months/years on end, and as
midlife has not only knocked on my door, but somehow been invited in, I find
myself still floundering in finding the fix. Having accumulated all that this
life can offer, how do I better focus myself on what life was intended to be
and encompassing more of relationship and less of things? It’s not as if we can snap our
fingers and “poof!” genuine relationships are on your front porch. Yet we live
our lives as if they do, sitting in wait for our best of friends to gather at our
doorstep. And it’s not as if what genuine relationships we do have will meet every
need of every circumstance, though we wait in anticipation of unsubstantiated proof
that they do. After much churning of thought and reflection, I think the
culprit lies in that fact that we have become passive in an active process. We
sit in constant wait for something to happen TO us. We wait for people around
us to prove their self-worth. We lie in the shadows of life and anticipate
someone else coming to our rescue in our hour of need. And THIS is where I find
that I have been fully in the wrong. And THIS is where Christ is growing my
heart. It’s not a revelation of any sorts. You’ve heard me type similar words
on similar pages. It’s my awareness that deepens as I continue to ponder and thus hopefully propelling
me into action: I want/need/should/must model what it is that I think I want from other
people. Instead of unrealistically setting a list of expectation of what I expect from people around me, I imagine I am much better served
to place those expectations on myself in proof of their worth. It removes the focus
off of what others are or are not doing for me, and instead pushing me to focus
on what I am or am not doing for other people. For do genuine relationships come not
from waiting for them to happen, but rather in my active pursuit and
nourishment of those around me.
Loneliness is not a place I one day am surprised to find myself, but rather a place
I most likely cultivated for myself by my lack of action and investment in others. This statement isn’t absolute, I know, but
I would say it is a huge contributing factor at the very least. I know this
that God will provide my every need, even in loneliness. His is a Hope that will
anchor the soul (Hebrews 6:18). But God also created the value of earthly relationship that
doesn’t replace His, but instead embellishes this life on this side of heaven.
So while I can sit back in the Hope He offers, I can also nourish this life
with the joys that genuine relationship here on earth can bring as well. And it
deserves to be actively cultivated, sought out, and nourished (not to be replaced by an enticing substitute) for lying in wait simply
leaves us….Lonely.
I’m asking myself how can I expect less of others around me
and more of myself instead. How can I accumulate less tasks, things, accolades,
and instead better cultivate myself for genuine relationship? How do I leave time in my life so it can be spent with people in a sense of community, and not running the rat race we set up for ourselves? It’s a long process of
ups and downs, but it is certainly worth the pursuit. There’s proof in the
pudding. I’m stirring my pot.
To access previous blog posts - click HERE.
To access previous blog posts - click HERE.
June 22, 2016 - It could change your everything
I was running late. The meeting would be starting in no
time, so I really needed to hurry. I
grabbed up my stuff and out into the hall I went and soon after realized I had way
too much stuff to carry having left my book bag back at my desk. I shuffled it
all around in my arms over and over again and quickly realized the tiny stuff
(the credit card, the note) simply had to go elsewhere. Up until now I’ve not
been one to repurpose the bra for a pocket but when you find yourself in a bind
and in clothes with no pockets… I reluctantly decided on my bra.
I stopped in route to grab a drink, a snack, and some napkins/utensils,
and after paying for the items, I returned the card and now two more items (receipts
and napkins) back to my bra for safe keeping and off I went to the meeting. Now
mind you, this was mid-day and after the meeting I attended two more, finished
out my day seeing patients, and then gathered all my belongings and made my way
to the car and back home. I got home, fed the cat, made dinner, did odds and
ends and then several hours later was ready for bed. I went to the bedroom and
took off my clothes, took off my bra….and literally about scared myself to
death when the now long forgotten items started tumbling out of my bra and
noisily onto the bedroom floor. Who
walks around for 5+ hours having no memory or sensation of several items shoved
into your bra during a moment of haste? See, I told you I couldn’t feel
anything. Four years later and I still
have large portions of boob 1 and 2.2 that can’t feel a thing. It’s comical if
you let it be. Lesson learned: Choose taking your bag, no matter how
cumbersome, every single time.
Today was simply a mastectomy kind of day. The forgotten
items in the “bra stuffing”. Earlier in the day I ran into my surgeon who I
haven’t seen around the office since my last surgery 9 months ago. After my
meeting, a lady in the elevator asked me if I could point her in the direction
of the breast clinic as she was running late for her follow-up mammogram. Thing after thing today. Some days it’s
nothing. Other days it’s like the whole world is there to remind you. I’ve
decided both days serve their purpose.
A little nugget from today? My coworker brought a little
nugget right to my doorstep for the taking: “I’ve decided I am going to start
being selective about what I let in my home.” We had been talking about
downsizing our lives. Purging our closets, uncluttering our drawers. I was
thinking very literally about the discussion. Having just moved earlier this
year, I was acutely in tune with the tasks, both emotional and physical, of
unloading stuff from our closets. I simply didn’t want all the stuff I had
collected over the years packed up in another box only to be stored once again
in another attic. I wanted less. She had recently gone through a similar task
of pulling things out of the closet and setting them aside for donation. We
discussed a little while longer about duplicated items our cabinets held and
the freedom found in tossing them in the donation box. The day got busy and
then the conversation was abandoned.
Or so I thought. As the day went wound its way forward, her
words hung close. “I’ve decided I am going to start being selective about what
I let in my home.” Hum. Those were simple words uttered in benign declaration
of a literal thought. You know, I need less sweaters. Who needs more books? A
statement of the typical clutter of excess found in the American home. But on my way home as I was navigating traffic
(with credit cards shoved in my bra!) those words dug deeper. They started to
eat at me in that maybe each syllable carried not only literal implications of
this shoe or that kitchen ware tucked in the nook of that cupboard, but what if
there was a deeper implication of that statement. And I found myself wondering
if literal is what she meant. Was there a deeper meaning in her words? What if
I truly did carefully dissect and evaluate each item (literally or
figuratively) that came through the doors of my home. What if I carefully
thought through in a way of saying “by bringing this item (or thought, or
whatnot) into my home, what would the ramifications be”? Do I care enough about my home and marriage
that I assign this degree of thought to the things I introduce for each? I know someone who took internet out of their
home because the husband didn’t want the temptation of pornography in his life
. If he has an email to send, he waits until he get into the office to send it.
He needs to look something up online? His wife offers to look it up for him on
her smart phone. To my knowledge, he doesn’t have a pornography addiction, but
he loves his marriage so much that he doesn’t want to risk it. He cares more
about protecting his vows than he does the convenience of life online in their
home. Powerful, huh? I know plenty of other people who have a rule of not
riding in a car alone with someone of the opposite sex. While there would be no
mal-intent on their part, they value the appearance of their marriage more than
they do the convenience of getting a lift to the meeting. They don’t want to
risk someone else seeing them and starting the rumor of “I saw Johnny with Lucy….”
We all know how the appearance of things can destroy a reality when placed in the
wrong hands. So while you sit there reading saying to yourself “Sally, these are
pretty drastic examples!”, I find myself
now wanting to reply with “are they?”
What are we bringing or allowing into our homes (our lives, our minds, our
hearts) that we shouldn’t be? What are we allowing to come in that is now an
unintended risk to the things we hold dear? Got kids? Oh that list probably
just tripled. What are we addicted to that are destroying our finances? One
more pair of shoes? What words are we allowing to be said in the confines of
our home that are destroying the self confidence of our pre-teen? What words
are going unsaid that portray to our children that we must bottle up our
emotions? Got teenage sons? I’d say we need to take heavy inventory. Do you
really need cable TV? Got teenage gals? Yep, choose wisely! Are you single? How
do you need to structure your home to preserve yourself? I imagine each “risk” is going to be different
for each of us, but I would say the “call for action” lies within us all and
most often remains untaken.
If I were to search my heart and search the atmosphere in my
home I know without a doubt that I could be more selective. More protective! It’s
not always our intent that matters. It’s the outcome. The perception. The
onlookers that can roll right over your reality, and I find that without being
proactive to protect our home, we just may find ourselves in a place we never
intended to be. You don’t usually see disaster coming your way. You just one
day find yourself there. You also don’t always consciously choose with disaster in mind. It’s a subtle temptation that one day plops
itself from un-tempted to tempted in no second flat. I think we now live in a
society and a cultural environment where we just may have to, at times, choose
the drastic choice in order to protect our home and all we hold dear. In what ways should I choose inconvenience in
an effort to put my marriage to my spouse first? In what ways do I need to change
thoughts and behaviors to uphold the sanctity of family? How should I better
model what comes in and goes out of my home. We need to be proactive, not
reactive, and we just may need to be drastic because everything could be
hanging in the balance and we don’t even know it yet. And if you don’t know
where to start, start where I am: Douse your home in prayer. Pray that you
choose to be selective. Pray that you aren’t afraid to make the drastic choice,
if need be. Pray that you are able to see the risks by looking through the eyes
of your spouse and children. Pray that you don’t consider yourself immune to
the risks. Pray, pray, pray! And then start evaluating your front door and what
you are going to allow to come through it. Just because something knocks doesn’t
mean you have to answer, and just maybe closing a door on it could change your
everything.
“I’ve decided I am going to start being selective about what
I let in my home.”
Psalm 51:10: Create in me a pure heart, O God, and
renew a steadfast spirit within me.
To access previous blog posts - click HERE.
To access previous blog posts - click HERE.
June 7, 2016- Dodged the bullet
I used to jokingly say “I need a lung transplant” anytime I
got a nasty cold. The hacking fits that would double you over, you’ve been
there yourself. Well tonight as I am sitting here feeling like crud and hacking
up a lung, I say that no more. Isn’t it
interesting how something so benign and trivial said in jest totally takes a
drastic turn to not so funny when faced with the real possibility? I dodged the
bullet back in December (and “dodged the bullet” certainly wouldn’t be funny in
someone else’s circumstances) and it left an impact. I no longer joke about my
lungs. It’s too close to home.
Interesting how we can go from being carefree/comical
in tossing around colloquialisms about certain scenarios, and then drastically
in 24 hours time with one brush of fear we can transition over instead to an
advocate. “I need a lung transplant”, “He
rides the short bus”, “ we certainly dogged that bullet”, “it made me want to blow my brains
out”, “I’d rather jump off a bridge”. Carefree, right?... until you have to
face one of them for real. You would
never use these latter words so carelessly with someone who lost a daughter to
suicide. Words carry a different meaning once you've been there.
And take the advocate into play. Isn’t there always a story
there? Who actually advocates for something they know nothing about? Chances
are, I mean super high chances, if someone is speaking out for or against
something, they’ve had a brush with it themselves. I have a friend who is highly visible in the
world of human trafficking. She’s had a brush with it herself. I work with
parents who devote their lives to raising awareness for genetic diseases. They
lost a child to its horrible grasp. I have another friend who lost a spouse in battle.
They now serve on a foundation for helping widows of war. Think about the
things you are passionate about. Are they not fueled by experience? We want
women to be more open about infertility and miscarriage. If you advocate for
that, I bet you’ve been there. I
advocate for women in mastectomy. Yep, I’ve been there. It’s so easy to care
about issues we have traversed, either first hand or second hand), and in
contrast it’s simply so hard to have lasting care for things we have not. Experience
carries forward a motivation and a little tug at the heart strings. However, it’s
very difficult to maintain a stance on something we know very little about. For
example, it’s easy for me to feel care and concern for your battle with heart
failure while you are there in the moment digging your way through the trenches,
but that care and concern rarely morphs into a passion as we move further away
from your event. A month or two later and I’m back to feeling something less than
advocacy for your struggle. My concern
for your experience over time is replaced by the urging demands of my own life.
This is why there is often loneliness in our plight after initial diagnosis. It’s
just a reality of doing life with other people. By design, we simply care a
whole lot about other people as they face the giant, but as the giant becomes
familiar and yesterday’s news, the giant takes a back seat for the rest of us
as we watch from the side lines. But give me a personal scare with pulmonary
fibrosis and I quickly become an expert in everything fibrosis and that
expertise will last for years to come.
I think God was brilliant in this design. We can’t all be
advocates for everything. The pool would be watered down. Unbelievable.
Un-motivating. If we all ganged up on raising awareness of absolutely everything,
we would put less than 1% of our efforts and wisdom into each issue. Instead, don’t
we become more relate-able, believable, trustworthy, impacting by advocating for
issues having been there ourselves? For example, I truly do not think you want
me to advocate for women on divorce. I simply know very little about it. I’ve never been divorced, no one in my family
had been divorced, I have very few friends that have been divorced. My knowledge
is third hand, from books, from movies, from conversations. So what merit do I
bring to the divorce table? In fact, instead of merit, if we all are going to
be honest here, I more likely bring a little bit of judgement to that table. I
am happy to support you, cry with you, pray for reconciliation with you, but I
seriously doubt I would have any impact as the advocacy-face of women going
through divorce, and because I haven’t been there myself, I risk coming to the table
full of preconceived ideas and judgement that simply doesn’t pan out. And as
someone looking for someone to advocate on my behalf for any topic I’m facing
do I not want someone who truly knows ( not from books but from experience) my stance?
I want to tell my deepest struggles to someone who has been there, someone who
gets it and brings no judgement to the table, someone who I believe truly knows
what I am fighting through and for. We are creatures of relationship, and we
naturally navigate toward what we know, and we also want to be known by other
people who have been there too. Our advocacy is a testament of our experiences.
And 24 hours, 6 months, 1 year from now,
we have no idea what we might find ourselves suddenly an advocate for.
Full transparency? I used to get really frustrated with the
Susan G. Komen platform. There, I said it, it’s out there on paper. If I had to
guess, breast cancer (BC) gets the most research, financial backing, commercial
propaganda, of anything else out there in the malignancy world (maybe even of
any disease state). Make something pink and sell it in October and it will be
bought. It wasn’t that I didn’t think BC was a worthy cause, it most certainly was,
but working in oncology and seeing all the malignancies not advocated for…well,
it frustrated me. Take pancreatic cancer
where the 5 year survival rate is a miserable 8%. Where is a month devoted to
it (it does exist but I bet most of us don’t know when it is)? Where are all the
football uniforms colored purple during pancreatic awareness month? I simply
wanted the attention/finances/research to be spread evenly across the causes. Breast cancer is worthy, but it totally
overshadows other killers out there. Then….I got my mastectomy news. I can’t
say my position on everything has changed, but it changed enough because now I
wasn’t an onlooker looking in from outside but rather a women staring statistics in the face. We simply care about what we have experienced,
and that can change at a moment’s notice. I now realize it isn’t the Susan G. Komen
Foundation that is at fault for the imbalance, she totally did her part to get
the news out there and sets the bar very high. It’s the under representation of
advocates for other areas of life. Liver
cancer awareness exists, but it’s not so in your face. Same with depression, Alzheimer’s,
Krabbe disease. ALS got a huge publicity projection with the recent Ice Bucket Challenges. It all came down to someone fighting the fight and then someone picking
up the reigns and being creative in their advocacy.
I need that creativity. I need that passion. I need to shout
out for the scars of mastectomy and so many other things in life. I need to be empowered to fight for what I
experience. I would have never even considered giving pulmonary fibrosis a
single funding dollar before last December. I would have given breast cancer
some funding because it’s so highly visible thanks to advocates that are hard core.
So I ask myself, what should I be advocating for that I am not? What is going
to happen in the next year of your life or my life that will suddenly change my
awareness? What has already happened in your life that you now need to be a
voice for? We won’t have the same passions. We aren’t designed to do so. We
should all be passionate about some things at baseline (injustice, persecution,
abuse, neglect, etc) and then we should individually become advocates for other things
because God allowed events in our lives to change us, or change someone around
us (malignancy, abuse, infertility, oh how the list goes on and on and on). In the
former we carry commonality (it’s a mandate of being a moral and ethical
humanity). The latter we sort of find ourselves in after we experience life
unfolding. We very simply need to be an advocate…for something. Otherwise, what’s
the point? Does it not instead become an experience and then an opportunity
lost? Do I not owe the next victim my
voice and experience? I certainly can’t save the world from everything, but I
certainly can use my individual experiences to do my best trying, in whatever
way I can no matter how big or how small. I’d say I get a failing grade on this
most days, but I’m hoping to one day be Most Improved.
Thank you, cleft lip, lymphoma, mastectomy, fibrosis, personal
failure, insecurity, and everything else that is still to be determined. I hope
to not let you down.
(As an update on my friend from my last post, her cancer has returned. Hers is not my story to tell, but I do ask that you pray for her as she navigates this again. We have been talking behind the scenes over the last 10 days and what a motivation her story is and will be to those she tells. God does great things, even in pain.)
To access previous blog posts - click HERE.
(As an update on my friend from my last post, her cancer has returned. Hers is not my story to tell, but I do ask that you pray for her as she navigates this again. We have been talking behind the scenes over the last 10 days and what a motivation her story is and will be to those she tells. God does great things, even in pain.)
To access previous blog posts - click HERE.
June 1, 2016 - The loss of We
Relapse. It’s a word that carries a lot of weight. Diagnosis
carries some punch, but the gut kick of relapse carries something altogether
different. It’s the knowledge that comes with Relapse that weighs it down. Been
there. Faced that. Grueling memories of what comes back around. The known is the shadow underneath the cheery day of normalcy. I have the badge of having kicked
diagnosis in the butt, but that shadow, it’s always there. In contrary, with
diagnosis, there is an unknown. It’s unchartered territories yet to be
traversed. You are limited to trying to recall the story of a friend’s
experience. “Wasn’t she nauseated all the time?” “Remember the time she threw
up at the mall?” “Didn’t she have to quit her job?” “How long did she get treatment?” Or you are
left to conjure up the lines out of a celebrity newscast. “Stage 3 liver
cancer”…”surgery scheduled for next week”…”she will fight the good fight
determined to overcome”…”so brave so strong”…”Hollywood rallies around her”. It’s
other people’s stories that give you a glimpse into what you may face with the same
diagnosis. But with Relapse, it’s a whole different ballgame.
You have walked the lines yourself before. You vividly
recall the gut wrenching heartbreak of hearing the devastating words heavily falling from his mouth, his lips moving in slow motion. And as the words tumbled off his lips they began to absorb every ounce of air around you making it harder and
harder to breath as he detailed this scan and that. Likewise, you can easily conjure up
the pains of toxicity like the back of your hand. You can feel the nauseating bile creep
up higher into your throat as your thoughts flow back to then. You are in
constant notice of the single strand of hair sitting on your shoulder as in
premonition of what could lie right around the corner without any warning
at all. You can pull into focus that moment when your spouse got the news and
the watery eyes that followed. You see, it’s all always there able to be pulled
back from the periphery into center view at any moment. You already know most of what
lies ahead. And therefore Relapse is weighted a little differently. It’s heavier.
It’s the sorrow and fear of “what if” that can come with knowledge. But if I were to be honest I need to dig a little deeper and ask myself what is that we are really afraid of?
I’ve never been plagued by the worries of a lymphoma
relapse. I don’t know if that was my naivety of “lightening never strikes
twice” (we totally know relapse is a daily occurrence in this now
cancer-stricken world) or my simple perspective of been invincible. You would
understand the absurdity of that statement had you truly known my track in life
thus far. But it’s still there, this cape of invincible carefully placed across
my shoulder and covering me with, well quite honestly, it covers me with
stupidity. Whatever we want to call it I simply lived in this world where
lymphoma would be a once in a lifetime moment never to be seen again. However,
as I matured out of my teenage years and started traversing the knowledgeable
days of adulthood and then accumulated the knowledge that comes with my career
path, the worry that began to skim its way across my pond of stupidity was
compiled not with fear of relapse, but fear of a secondary malignancy or unmanageable
toxicity. I guess this was why I was so decisive and so seamless in my decision
for mastectomy and so lacking in surprise at the development fibrosis. I simply expected…something…to come.
And I still do.
So while most sit mentally teetering on proverbial edge of
the Relapse “what if”, I rather thumb-my-nose in disregard to relapse as even
an option. My alternative “what if” is of second malignancy or life-reducing
toxicity, but let's face it. It floats in the very same pond as Relapse. They are joint in their
outlook. Dismal some might say. A constant undulating wave of “right around the
corner” pooling in the stomach of its owner, who is never quite at ease in the
peacefulness in which we try to sit. “Too good to be true”. “It’s only a matter
of time”. “I might be the one.” Once you successfully traverse diagnosis, you
never fully find yourself back into the peaceful mindset of the un-diagnosed.
“What is coming next?” is always there underneath. We constantly carry around
in our pockets the reality of statistics. The odds are always greater than
zero. 1% is not zero. That reality
changes your decision making. It blurs
the edges of your clarity. It makes even the smallest of odds a subtle player
in your everyday and can put a noticeable dent in your level of carefree. You
find yourself a little more guarded. A little less confident in tomorrow. A
nail biter when waiting for routine results. A single tinge of unexpected pain
can propel you to a comprehensive and immediate mental regurgitation of your
past experience. It’s there. “What if?”
I’ve recently been pondering what is it that drives that
apprehension of what if after a diagnosis? I don’t think it’s the inconvenience
(rearranging our schedules for appointments, avoiding this or that with our
lost immunity) that a diagnosis can bring that we loathe, nor do I think we
fear the pains of financial burden that will come. They most certainly come,
but they don’t hold us captive. Nor do we loathe the frustration of feeling our
absolute worst, weak, at risk, less than. That carries a ton of
merit, but neither is that the source of worry.
Let’s face it, we know all the nooks and crannies that come with the
diagnosis, and it’s not those that make us swell up with fear. These things
make diagnosis complicated, a nuisance, a hardship, and something most
certainly worthy of creating anger. But our fear is sprouted not of these worthy
sources, but rather I more recently find myself discerning that this underlying
root of fear is cultivated by the awareness of potential loss. The fear of not
winning this time and losing everything we hold precious is the source of our
fear and what keeps the “what ifs” of relapse or related complications in the
forefront of our minds…for the rest of time.
We are created to love and to be loved. It all comes down to
relationship. And in the diagnosis or the relapse we become acutely aware that
we have great risk in losing what we have so carefully cultivated. Our
children, our spouse, our family and friends. Not loss in that they will turn
away from us, but rather loss in that we could potentially leave them behind.
We are driven by our fear of outcome. There are other fears interwoven in the
strand of worry as supporting actors, each not to be stripped of their own
value, but at the core of the strand sits the knowledge that the next outcome
might not be “remission”. This time our luck may have run out. This time we may
get a different hand. This time…
I'm not afraid of relapse. I'm afraid of what relapse
can bring….loss. And honestly, I don’t think there is a single thing we can do
to circumvent that fear. It’s a normal response to a rational inherent risk. And
it is not something you fully understand until you have been there staring
diagnosis in the face, and then again, if you are selected, when you find
yourself on the other side now dodging relapse and the other sister follies.
But I am working diligently to instead focus on the comfort in what all of that
means. I simply value what we were intended to value: We. For in “we” lies our relationships with the
people around us, and we want to be around forever to relish in what all those
cumulative relationships bring us: joy, purpose, contentment, pursuit, love,
value, focus…and oh so many other things. We is the core of our everything.
As a friend of mine is facing potential relapse of breast
cancer this week and as so many of us as survivors sit in the shadows of a constant
awareness of “what if”, I wanted to mentally take a deep dive in to discern the heart of it all. Underneath it
all, I don’t fear relapse or related mishap (fibrosis, secondary malignancy
heart failure, or whatnot) in and of itself. I simply and very honestly down to the core of everything that I am fear
the loss of “We”. And it motivates everything I am and do from the day after diagnosis, and after remission, and now I'm finally realizing it's also in the prospects of "what if".
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Click www.tradinginthetatas.blogspot.com to access other posts.
May 23, 2016 - Ghost Boob
This week, we are back to mastectomy updates. At certain time points, I want to revisit the boob "status" so you have a concept of what to expect and when if you are in the middle of mastectomy. For this update, it’s been 9
months since surgery #6 and 3 years and 9 months since the mastectomy itself. Visually, Boob 1 and Boob 2.2 are pretty spot on. They do in fact mirror the former tenants, with
the exception of a few scars. All and all, we have
two boobs and therefore goal achieved. While visually, they pass inspection, there are other
aspects that remain a wee bit (or a lot of bit) wonky. I will start with sensation. We’ve touched on
this topic before, but I wanted to update you on the timing in case this
information is helpful to you in the future.
Let me introduce you to Ghost Boob. As a refresher, the breast is comprised of glandular tissue, ducts, fat
tissue, connective tissue, nerves, blood vessels and lymphatic vessels. Those
contents sit on top of the chest wall muscles. During the mastectomy procedure,
the entire contents of the breast (+/- the skin itself and the nipple) are
removed all the way down to the chest wall muscle. During reconstruction (as I
had; there are several ways to reconstruct a breast) a pocket is created within
the chest wall muscle and the implant is slipped into the pocket. This serves
as a holster per se for the weight of the implant to be supported. While the
implant is used to provide the breast structure, during reconstruction the
nerves, blood supply, adipose, and ducts are not returned to the breast. As a
result, women have a change in sensation, a sort of numbness due to the lack of
nerve endings, in the new breast. I’ve mentioned before what a strange feeling
this is to run your hand down your neck over the breast and onto the stomach. Feeling,
no feeling, feeling. It’s identical to what you (don’t) feel when you touch
your hand after it has fallen asleep. Ghost Boob! Overtime, some women regain
some (though usually not all) of the ability to feel pain or the sensation of
touch on the breast as nerve endings start to regrow in the area. So now, 3 years
and 9 months later, I can feel about half (the upper half) of my breasts. The
bottom half of the breasts are still Ghost Boobs. What I love about this is
when I go swimming I don’t have to worry about that awful moment of slinking
your chest down in to freezing cold water. I simply can’t feel it. What I
loathe about this, well, is that it is just plain weird. I’m not going to go
into great detail here, but there also is the impact on intimacy. You simply
need to know that if you are headed toward mastectomy. It is just something you
don’t realize going in. The good news is a year ago I truly could feel nothing,
so we have some progress as times goes on. It took about 3 years to
regain half of my feeling back.
Enter stage left - Frost Boob. The other wonky thing is also around the touch sensation.
Imagine you just ran 3 miles (or for some of us 0.0 miles). Your body temperature is soaring as you attempt
to dissipate heat. Touch your stomach and it feels very warm to the touch.
There may be a cool sensation on top of the warmth as you sweat out fluid,
leaving a clammy sensation overall. So
while your body is in temperature overload, if you touch your breast at the
same time, it is cool as a cucumber. Frost Boob. This is a result of having a
lessened blood supply to that area. Remember, the blood vessels were also
removed during the mastectomy. Blood flow is what brings warmth to an area. Limited
blood flow, cool to the touch. Over time, like nerves, blood vessels too start
to regrow, but the numbers are less. At 3 years 9 months Frost Boob still prevails.
It’s simply awkward, and quirky, and a good party trick??? Ok, no, but you get
the idea. It’s just something, like Ghost Boob, that you don’t know about going
in unless someone tells you. Now you know. This aspect of cold to the touch,
unlike ghost boob, has not improved over time as of yet.
Unrelated to sensation, enter stage right: Boob Brain. Early on in this ongoing process of
breast reconstruction, there wasn’t a single day (hour?) I didn’t think about the new
boobs. I simply always had these boobs on my brain. Part of the all-consuming thought process
was simply related to being in the middle of it. Day in and Day out. Early only your entire day is related to the boobs. Change the bandage, empty the drains, log the output, take your meds, keep your arms at your side, avoid looking at them, look at them, don't do this, do do that. It was 24 hours of boob brain! But as the weeks went on, the tasks became less, and then the thoughts would lessen too. But at any moment something would happen and Boob Brain would kick right back into gear. For me, every 6
months or so it was another surgery, so just when I would get out of the thought
process and back to normal life, I would find myself right back where I started again. Even on a “normal month” early on you still have at least a daily thought of these
boobs being what they are (or are not). Well now, with this being the first
time that I have gone 9 months without a surgery, it is awesome to see that
there are some days when they don’t even cross my mind at all. And to say that
is progress would be an understatement, it’s triumphant really! I truly didn't understand going in how 2 little sacks of gel could carry so much punch...or thought. But they do. And maybe I can soon say "they did". I am getting there, past this.
I guess the most recent months of having less boob on the brain is a
testament that life does in fact eventually return back to normal. You can't rush it. You just have to wait until it suddenly arrives. You will get to the point where
the breasts move out of your foreground and in to your background, only to be
thought of when you slip down into the freezing cold water…and feel nothing. Or at other random moments when anyone would be thinking about their breast (Changing clothes? Or trying on new bras? Or what not). There is a time point when the reconstructed breast no longer defines you. Instead of
defining you, it now merely designs you in that you are a changed being by its
presence. Not so much the breast itself, but the journey of getting there. You hear
stories of people who have a brush with death and how life simply looks different,
more precious, altered on the other side. Mastectomy, when prophylactic/chosen,
doesn’t necessarily carry the same weight as my brush with lymphoma did, but it
did change me in ways I might not have expected. While an implanted boob is most
certainly a boob, it carries a different weight. Both literally and
figuratively. More insight provoking. More impressionable. More focusing. I see life with
newly tweaked lenses which brings certain things into better focus with a better alignment
of perspective. While the feeling of touch, the sensation of cold, and even the thoughts of the breast may
transition over time, I hope my more finely focused perspective of mastectomy
remains with me always. I simply appreciate Post-Mastectomy Sally and all she
brings to my “after” life. I may be a little “off” at certain stages along the
way, but I certainly carry a new depth. And with that comes an advocacy I didn’t
carry before. Advocacy for empowering women with knowledge. Advocacy for loving
your body where it is. Advocacy for the spouses of mastectomy. Maybe even a
little advocacy for just doing life in general and doing it well with people in
tow – mastectomy or not. But when there is mastectomy, just know it isn’t the
end all, be all. But rather it is a starting point for what comes next in life.
There is an “after mastectomy”. Three years, 9
months. I’m getting there with Ghost Boob and Frost Boob as my side kicks.
Click www.tradinginthetatas.blogspot.com to access other posts.
Click www.tradinginthetatas.blogspot.com to access other posts.
May 17, 2016 - Horizontal stripes
I’m tired of these comparison games. I’m over women not
measuring up. I’m seriously over women making other women feel as though they
don’t measure up. It happens in the work place. It happens at home. It happens
in our minds. It happens in our words. And I for one am simply over it!
Who set the rule and standard that we have to make sure the
person next to us feels less? Who set the example that we have to use everything
in our arsenal to appear to be more? Certain people come to mind, trying to
make waves for other women co-breathing their air and carefully planting a jab
in the most vulnerable of soil to ensure the feeling of inadequacy grows. Often,
the attack sits unsaid to the intended target and instead flutters across the proverbial
acquaintance pool of whoever else happens to be in the room. I absolutely
detest this gossip mill that circulates the misfortune of being a target. Are
you a participator? Are you a propagator?....More importantly, am I?
I’d say at first response “I am
not.” But immediately, I feel that lie down in the pit of my stomach, and I can
do nothing less but accept my role in this perversion. While I desperately try
to find the good in any person that crosses my path and truly do want to foster
a safe environment lacking in judgement or gossip, I can at times fall prey to
the bad behavior that may plague my day. It’s so easy to get caught up in the
rip current of shaming. If she is a little less, and I make it known, doesn’t
this in turn make me a little more? Mercy! It is a lie of eternal consequence! There
are a hundred kind words said to me in a given year, yet it is that one unkind
rumor said out loud that forever comes back to mind 20 years later. One single sentence
can result in huge consequences. And one missed moment to provide kindness
instead of judgment can set the tone for that relationship for years to come. Nothing
hurts the heart more than making someone feel inadequate or indifferent and it
is a dangerous seed to plant. But if we want to falsely assume that we play no
role in the routine detriment and shaming of another person, I most certainly
am to blame for the shaming of myself where the ramifications are equally
eternal.
There’s rarely a week (day?) that goes by that I don’t find
myself in a liturgical play-out of inadequacy. I walk into a room of women and
immediately notice what I have or have not in comparison. I can count out loud
the number of potential “moments” I miss because I am too embarrassed to
partake. A hike with friends where I am afraid my performance won’t compete. A
cool dip in the pool where I am all too aware of this thigh or that. A dinner
skipped out on because of nothing to wear or a result of my pudginess being too pudgy that week. How many spectacular moments never came about
because we falsely believe the lie that we are less? Or better yet, what are we
instilling into the people around us (or our children!) when we make these
subtle statements of inadequacy. I distinctly remember a dinner invitation I
missed out on with a group of friends because I was standing in my closet
trying to make something work. Instead of throwing on the jeans and t-shirt and
letting reality be reality, I chose to miss the dinner. This was years ago, but
the impact remains. My thoughts of “not being enough” cultivated a lie and
resulted in missed laughter, missed fellowship, missed everything (they had the
absolute best time at dinner that night!). My choice spoke that my perceived appearance
mattered more than their time and friendship. And spoke the subtle words to
them that they need to have it all together in perfection too.
Are we teaching our children to choose the lies of
self-inadequacy over the joys of simply living life and all it brings? But you
say, Sally, my legs really are too skinny. To which I need to reply, too skinny
to have joy? Are the size of your legs more important than every single other
aspect of life? There are some things to which we can reply “God made me this
way” and therefore we need to embrace and get on with living life. Then there
are other things I need to say “Sally, I made myself made me this way”, and I either
need to take action to change, or embrace as being what it is and getting on
with enjoying life. But either way, there is a crucial and urgent moment for
conscious choice to choose which it will be. Will I perpetuate this self-deprecation,
or will I pick up my flubber, or skinny, or scars, or bra size and choose the
path of joy? The best example I can be to myself, my friends, and my daughter
(if I were to have one) would be to take everything I have and call it
precious. For that is exactly what it is: Precious, the bumps, bruises, lumps
and all. Every single day, our chosen spirit of being gracious and kind will
over shadow any perception of physical or emotional inadequacy. Alternately, we
choose to be remembered for our spirit of shaming of self or others.
Give yourself permission to not be perfect. Allow yourself
the occasional mistake. Embrace the less than and focus on the fact that we are
already enough. For we truly are that! Enough! Enough to be the daughter, wife,
mother, sister, coworker, friend, disciple, patient, introverted extrovert that
anyone else can be. Enough to throw on the pudgy dress in the closet and go to
the dinner! Enough to bring a kind word to the person next to you letting them
know they are enough as well. But it takes a purposeful approach to lose the
thoughts of being less. Remove ourselves from the unkind words of others.
Surround ourselves with women who not only get this, but live it. And if you
don’t have any of those. You start the trend! We have to go above and beyond to
actively praise the women around us. They aren’t perfect either, but there is
no reason on this planet that we can’t make them feel like that are. We have to
consciously drown out (and correct!) the negative words being said around us. We
have to lead the way by purposely speaking out loud the complimentary thoughts
that come to mind. We have to quit fertilizing our disastrous need to feel like
more by making her feel like less. And then we need to soak our minds in
reading the truth that we are enough. It takes a permanent reset! We may not be
able to change our self-perceived “less than”, but gosh darn it, we need to
take our dimply thighs to the beach and make some incredible memories! Show the
women around us that we value friendship and uplifting sisterhood over inadequacy
at every single turn. We need to stop losing out to our inadequacies and to quit
perpetuating the lies. Our role is two-fold: It is our choice to love others, and equally our choice to
love ourselves. And I need to start at ground zero. This week, I am putting on the dress with horizontal stripes. I'm starting with me.
To access previous blog posts - click HERE.
To access previous blog posts - click HERE.
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