A Super-Hero Christmas

A Super-Hero Christmas

A year ago, I certainly wouldn’t have dreamed that Christmas 2024 would see me at the Cancer Institute, getting radiation therapy. For that matter, even when I was diagnosed back in April, I fully expected to be done with all treatment by now.

But…no. LOL.

The way the schedule worked out, and thanks to us scheduling a vacation for December 14-21 (since we couldn’t take one over the summer, we had to wait for another big break for our daughter), radiation got pushed back until “after the holidays,” they said. Turns out “after the holidays” means going up on Christmas Eve for a simulation and then starting on December 26th.

I met with my radiation oncologist a few weeks ago and we immediately liked him. He’s the head of the department, which is nice, and has a great sense of humor, which is even better. I jokingly asked him if this would give me super powers, and he didn’t miss a beat. He said, “Well, we can’t rule it out!”

So that’s my new line. I’m totally getting super powers for Christmas. 😉 And if that super power is Remaining Cancer Free, I will be thrilled.

I went up on December 9 to get a scan and make my mold–how they’ll ensure I’m in the exact same place each time. As already mentioned, I’ll have a simulation on Christmas Eve–I keep calling it the Test Run. 😉 But on the Second Day of Christmas, I’ll begin my first day of radiation. I will have 15 sessions total, skipping New Years Day and weekends, and will finish up on January 16.

My appointments are at 7 in the morning, which means early wake-ups for the 90 minute drive, but that’s okay. Xoe will be in until January 5, and I don’t want to miss time with her, so we’re not planning on staying up there or anything. I figure with those early morning appointments, I should be home before my night owl daughter even wakes up! 😉

They said that the most common side effects from this therapy are tiredness (not at the start, but by the end…it’s cumulative) and of course the skin at the sites could burn, so they recommend good lotion. A kind reader already sent me three tubes of medical-grade moisturizer formulated specifically for skin undergoing radiation, so I’m set!

So here we are. Today, I’m lounging on the beach in Marathon, one of the Florida Keys, where I was blessed to find a great deal on a condo through AirBnB. I’m enjoying the sun and the sand and the water and books. Everything for Christmas is set and ready at home. Gifts are bought and wrapped and waiting, the tree is up and decorated, and my mother-in-law is watering it and taking care of the cat. Today, I’m enjoying the trip that we called a celebration of being done with cancer, before we realized I wouldn’t be quite done with the treatments yet. That’s okay. Today, I’m celebrating anyway. We’ll get back home on the 23rd and jump right into Christmas…and that simulation.

And I’m so grateful. So grateful for this time with my family, for this year that took such an unexpected twist but which poured out so many blessings upon me. So grateful for the medical community that knows how to make me well again. So grateful for the Cancer Institute team who has had my back, laughed at my jokes, and rejoiced with me as we beat this thing.

So here we are. Not the circumstances I ever anticipated finding myself in for Christmas of 2024…but ready to enjoy my Super-Hero Christmas and take this last big step toward living cancer free for years to come.

Merry Christmas, everyone!

So Thankful

So Thankful

On this day of gratitude, I am overwhelmed. Overwhelmed with thankfulness. Overwhelmed with blessing. Overwhelmed with the faithfulness of our God.

Last Thanksgiving, I wouldn’t have dreamed that in the year to come, I’d go through cancer. I certainly wouldn’t have thought, had someone told me what was coming, that I’d come out of it feeling so humbled and blessed. Yet here we are. With a long road still ahead of me, but gratitude filling my heart as I look back on where I’ve been.

Thank you, Lord, for your faithfulness. Thank you for holding me so securely in the palm of your hand that I could not, for even a moment, doubt. I could feel no fear. I could experience only the smallest amount of sorrow. Thank you for bringing me through this, for obliterating the cancer cells from my body, for setting me on a path to full healing.

Thank you, family, for your endless support. For meals cooked and delivered, for the willingness to drive me to appointments, for gas money and check-ins, for loving me through every moment.

Thank you, friends, for your endless prayers. For a mailbox bursting with cards and “encourgement bombs.” For notes and emails that not only brightened my days with promises of those prayers, but which edified me as a writer and a person.

Thank you, strangers, whose names I didn’t recognize but who gave of yourselves, your hearts and your means, to support me in this time, proving that the family of God is bound by love that goes beyond all understanding.

Thank you, Church, for being the hands and feet of Jesus.

Tears are filling my eyes as I’m writing this, reflecting on the year it’s been. It’s a year I don’t want to repeat. A year of sickness and exhaustion and pain, when I focus on the physical. But a year of uncountable blessings too. A year that has left me in awe of this amazing community.

Thank you for being part of my life, part of my journey.

The Me I See

The Me I See

The image I see when I look in the mirror has only rarely matched the image I carry of myself in my mind. I imagine we’re all like that. There are those who see fat or skinny when the world disagrees with them. There are those see young or old, fit or flabby, pretty or ugly. We hear a lot about people who have a negative body image, despite everyone around them thinking of their looks in a very positive light.

I remember back in high school, when I was already dating David, who would become my husband, thinking very frankly about my looks. I knew well I wasn’t super-model material, that I was far from the prettiest girl in my school, even. But I also knew that I was the kind of everyday pretty that, when viewed through the eyes of love, would make someone say I was the most beautiful woman in the world. Something David has said to me countless times over the years. He tells me every day–multiple times a day–that I’m pretty, and he says it in a tone of love and adoration. Never has a day gone by that he didn’t affirm me in this way. My parents have always been so affirming as well.

Maybe that’s why I never lacked for confidence. I know my physical flaws–I have no delusions. And when someone (other than those who love me) are too effusive in their praise, I give them the side-eye. But the me I feel like as I’m going through my day has so little to do with the me I see when I look in the mirror. I feel like I’m exactly who I need to be (most of the time). I feel like the me other people see will reflect that. Is it true? No idea, LOL. But it’s how I’ve gone through life.

Then came cancer. When I responded to losing half my hair within 24 hours by shaving the rest off, the me I saw when I looked in the mirror definitely didn’t match my self-image. Five months later, I still don’t identify as that baldie. 😉 My hair is starting to grow back, and I laugh at how I now look like a balding man, with shiny spots still on top but a nice fringe around the back. My eyebrows and eyelashes have thinned, and I frequently have circles under my eyes (especially after surgery), so when I look in the mirror, I think “Wow, hello, cancer patient!”

But that’s not what I feel like when I’m not looking in the mirror. (Okay, there are days…LOL). I feel like…me. The same person who has always traveled through life with confidence and optimism, even when I probably shouldn’t, by rights. Yes, I get frustrated when the image doesn’t reflect that version of myself. I’m ready to look like me again, and I definitely don’t. But it’s easy to forget, as I’m going about my day. It’s easy to ignore.

Then came surgery. Bilateral mastectomy. Months before I even had the surgery, my physical therapist was writing a referral to get me in with a counselor who specializes in body image. I figured that would be smart, even though I didn’t have negative thoughts about it yet. I haven’t yet actually seen any mental health specialists, though, so these first weeks after surgery, it’s just been me and my family thinking it through.

Can I think myself to tears over the changes to my body? Yes. I did so one night. It was important to grapple with all that will never be the same, to realize that I no longer had the breasts that nursed my children. My husband and I had some long talks about what grieving a part of one’s body really is and looks like. And then…I felt like I had permission to just be me again. To be curious about these changes, and to be curious about how they’d continue to evolve as I go through the very lengthy reconstruction process.

David worried that I was just saying the right words, at one point. Words about how this body is not who I am, about how when I was struck with fear or worry in the weeks leading up to surgery, I’d make a concerted effort to pray. He was baffled at “how okay” I was. Was I just in denial? Was I not grieving properly? That would be when I took that night to cry and talk though it all.

In the first week post-surgery, I wasn’t allowed to take off the ace bandage they’d wrapped me in or take off the surgical compression bra, so I hadn’t seen myself. And I’ll admit it–I wasn’t exactly looking forward to that first full look. A few days afterward, my mom asked, “How did you feel when you first saw yourself?” her tone one of worry and love and sympathy.

I kinda laughed. “Well, I don’t exactly like the way it looks…but it’s interesting to see what they did and imagine how it’ll look as I go through the process. It looks funny, but it’s okay.” And I meant it. It’s not hideous. I look at the incisions that will become scars, and I see battle wounds that mean I’m still alive, that I’m reclaiming health.

It’s not the me I feel like, when I look in the mirror. But it rarely is. That’s okay. It’s the me I’ve earned. Just like those stretch marks on my hips tell the story of carrying a child, just like the scar on my ankle tells of rollerskating without socks as a child, just as the curve to my neck tells of too many hours hunched over my keyboard writing books. The bald head says that I’m fighting cancer (and winning!). And this new change just tells part of that ongoing story of claiming health and a future. I can’t hate the thing that will help me achieve that. I can think it looks funny, and I can certainly not love the painful process, but I made the decision with one goal in mind: never going through breast cancer again. I know this doesn’t guarantee it, but it makes it more likely. And so, I celebrate it.

The me I see in the mirror doesn’t match the me I see in mind…and yet, it does. Because the me I see in the mirror is a warrior, one who bears the marks of the battle but is still fighting. Can I pick out all my flaws, all the things I’m eager to see change, all the things I will mitigate with makeup and hats and wigs when I feel like altering that image for a while? Absolutely. But that doesn’t mean I don’t also see what lies beneath.

I am the most beautiful woman in the world to the man who loves me. I am a woman of strength and faith in the eyes of my family and friends. I am a mother who shows her children that we can fight and win whatever battles life throws at us.

I am a daughter of God, precious in His sight.

The me I see in the mirror matches none of my ideals of beauty. But the me I see in the mirror is beautiful. That reflection tells part of my story–and my reaction to it tells another part.

I daresay when you look in the mirror, you don’t see exactly what you wish you looked like either. But your reflection is part of your story. You have earned every curve, every dip, every scar, every freckle, every wrinkle, every line. You are exactly the you that God created in His image, and you are loved. You are beautiful. You are you.

The image that greets us in the mirror is part of us…but we are so much more than our image alone. We are His image. And that makes us all beyond compare.

Post-Op Update

Post-Op Update

Thank you all so much for praying for me as I went into surgery last Friday, and for continuing to pray for my recuperation! I appreciate it so much!

So last Friday, October 11, I had my double mastectomy. The “double” part was my choice, made because it decreases my chances of going through breast cancer again by 90%. I liked those numbers! Because of my size and the size of the tumor, a single mastectomy was necessary–a lumpectomy wouldn’t have left me with enough material for reshaping. I also needed to have all the lymph nodes in my right armpit removed, because they were still showing up as abnormal in the last MRI. Having the lymph nodes all removed puts me at a risk of lymphedema, swelling of the arm and hand, so I would definitely appreciate prayers that I can avoid that. I have exercises to do to help prevent it, and will be wearing compression sleeves to help with it as well.

The surgery went really well! Not that I got the update from the surgeon, LOL, but she reported to my family that everything was textbook or better. She was able to use a blue dye that tracks the drainage channels in my arm so that she could avoid them, which should help with that lymphedema concern. We all agree that we just love Dr. Bailey and always feel better about things after talking to her. She came in to see me before surgery and said, “I know you’re not looking forward to this, but look at it this way. After today, we know you’re cancer free. That makes today a great day.” And she is so right about that!

I only stayed one night in the hospital, which was fine by me. 😉 I did have a bit of swelling on my right side the morning after surgery, so they wrapped me up tight in an ace bandage and told me I wasn’t allowed to take it off until my follow-up appointment at the one-week mark. I absolutely understand that…but I’m looking forward to getting a break from it. I feel a bit like a mummy. 😉

As I’m sitting here several days post-surgery, I can report that I’m certainly nowhere near normal–my range of motion is hugely decreased, so there’s a lot I can’t do while incisions heal.  But the pain of the first day has faded into discomfort and aching, which is a big improvement. I’m able to sit at my desk and in fact find that it’s really comfortable to have my arms braced at that height. Convenient, since I just had digital galleys arrive for The Collector of Burned Books. Reading through it doesn’t tax me much but still makes me feel useful, so that’s nice. =)

My sister brought over a TON of food, and my mom and grandmother added to it, so we’re well stocked, for sure! Definitely a blessing, because I can’t even reach the microwave on my own, much less cook anything, LOL. Today I have an appointment with physical therapy, and tomorrow a follow-up with my surgeon at which I will hopefully get the drains removed and be cleared for things like showering. They expect to have pathology reports early next week, so I also have an oncology appointment on Monday to discuss treatment from here out. (UPDATE: Pathology reports came in, and I am CANCER FREE!! No cancer in any tissue or lymph nodes removed! Praise God!)

Again, thank you all so much for your support and encouragement and prayers! I don’t know where I’d be without it, but it means the world to me.

Inspiring

Inspiring

At one point over the summer, I found myself on a breast cancer forum on Reddit. It started as I looked for answers as to whether a side effect was common and what solutions others had found for it, but we all know how those can rabbit-trail, right? I ended up reading some threads that had me laughing, some that me blinking back tears, some that had me nodding along, and few that left me scratching my head.

One that has stuck with me was a rant–an understandable one, in one respect. The poster was saying how she hated to hear “you inspire me,” or “you’re such a warrior.” Her take, and the take of most of the people who commented in reply, was that she didn’t want to inspire anyone. This wasn’t a battle she’d chosen. She wasn’t a warrior, she was just a conscript in a battle that scientists and doctors were fighting, and she didn’t want to be there, so don’t call her a hero. I similarly heard from a few individuals along the way that they, too, hadn’t liked it when people said they were inspiring in a battle not of their own choosing.

I get that, in a way. But also…I don’t. Because here’s the thing.

We never get to pick which battles we’re tossed into in this world, not really. Much as “pick your battles” is an adage, it’s one with limited scope, right? Because it’s all about choosing not to make a battle of something when it’s all but useless. When it comes to health struggles, chronic illness, disease, behavioral health problems…no one chooses these battles. But that doesn’t mean we don’t have to fight them.

And most of all, it doesn’t mean we don’t get to choose HOW we fight them.

I know, I know, I’ve already talked quite a bit over the summer about choosing to approach our limitations with an attitude worthy of Christ, so I don’t want to just repeat myself. But at the same time, it bears repeating and dwelling on. And it bears it, in a way, because of its simplicity.

I’m still getting so many messages saying how inspiring my attitude is, and how it has proven an encouragement for other people going through their own struggles. And I hear, in the back of my mind, those people in the forums saying they don’t want to be that inspiration. And it makes me…sorrowful. Because why? Why wouldn’t you want to lend others strength simply by being there? Why wouldn’t you want to prove to them, by putting one foot in front of the other, that they can keep putting one foot in front of the other? What I love about that is that it doesn’t require giving up any of the measly strength I have to help someone else–it doesn’t weigh on me or hurt me at all. All that’s required is that we stand here, wherever God has put us, and say, “He’s got me. And because you can see He’s got me, you can know He’s got you too.”

I’ll be honest–optimism comes easily to me. It doesn’t, generally speaking, require effort. When my husband says, “I’m so proud of how you’re making the best of this,” the only possible response is, “What else am I supposed to do, make the worst of it? What would be the point of that?” But as my doctor pointed out, “You’d be surprised.” So often, we choose to dwell on the negatives instead of the positives. So often, we get worn down. So often, even what people intend as encouragement just grates on us, a reminder of what we’re going through and don’t want to be. Sometimes, it feels never-ending, and sometimes there really is no end in sight.

I get that in those times, the last thing we want to think about is the idea that God put us in this so that someone else could be inspired. That seems pretty awful, right? Why should we have to suffer just so someone else can see us and say, “Hey, I can get through it too”? But I would say that that isn’t the reason we suffer. But it can–and I daresay should–be a consequence of our suffering. It isn’t the reason, but it can be part of the meaning we take from it.

There are going to be days in all our lives when we don’t feel like smiling. When we’re miserable. When we just want it to stop. There are days when we struggle to remain positive, when tears come, and frustration and hurt and depression. It’s okay that we have those days. And when we’re in them, seeing someone else going through something with a smile might actually do us more harm than good, emotionally speaking. But when those days come, instead of thinking “I don’t want to inspire anyone in this battle,” I personally have found it to be a great help to just pause and think, “How is this inspiring?”

Seriously. On some of my worst days, when someone has commented or messaged to say how inspiring I’ve been, I have to ask how and why. I don’t feel inspiring. I don’t feel like I’m doing anything big or great. I’m not trying to project anything in particular or live up to anything for the sake of others. Those days, I am literally just plodding along, drained of energy and want-to. And then someone will say something like that, and I think of those people on the Reddit forum who would clench their teeth and bite back a sarcastic retort. And again I’m filled with that sorrow.

Because you know what I hear when someone says that? I hear, “God is capable of using my mess in ways I can’t imagine.” When I see someone blinking tears from their eyes for me, I see God binding His Church together in ways I could never do on my own. When someone reaches out to say they know they can keep fighting because I keep fighting, I marvel at how He is so strong, so capable of holding us in His hand, when we are at our weakest.

In my head, “positive” is just the default. I’m usually surprised when someone chooses a different perspective, LOL. I don’t think about it being anything unique, not until one of my doctors says something like, “And you’re still smiling and laughing. You don’t know what a difference that makes.”

I’m learning, though. I’m learning what a difference it makes–not just for me, but for everyone else. Because no, I didn’t choose this war or this battle, maybe I was drafted into it like everyone else. But that doesn’t mean it’s not my part to fight it valiantly and worthily. No, I didn’t choose this so I could inspire anybody–but that doesn’t mean God can’t and won’t use it to do just that. No, I don’t want to be going through this–but I am, and so I will walk through each day as a child of Light, not of darkness. And I will reflect that Light in whatever way I can. Through a smile, through a joke, through vulnerability.

Maybe none of us get to choose the fight…but we get to choose what we’re fighting for. And when we look beyond ourselves, when we embrace the inspiration we can be for others, just as we look to the inspirations those who came before us provided, it can change everything. We don’t need to set out to “be inspiring.” We simply have to open ourselves up to God and say, “Do with me, with this, whatever You will.” He’ll take care of the rest.

Chemo Is DONE!

Chemo Is DONE!

I am SO happy to report that on Monday, I received my LAST chemo infusion!

Cue the confetti!!!

I got to ring the bell, and afterward, we went to Cheddar’s Scratch Kitchen and celebrated with cheese fries and a giant slab of chocolate cake (over half of which we totally brought home, even with two of us eating on it. That slice was enormous!)

Of course, “finished” is a relative term when it comes to this sort of thing in a breast cancer journey, I’m learning. Depending on my surgery date, I may in fact need one more abbreviated round (only one chemo drug, and not the one that makes people sick) just to make sure everything stays shrunken before surgery. They have that on the calendar for Oct 7, but as of when I’m writing this, I don’t actually have my surgery date; it could be Oct 4, in which case this round would be cancelled.

So what’s coming next? Well, as I just mentioned, surgery is next up on the docket in early October. A lumpectomy is off the table for me due to the size of the tumor versus my size…it doesn’t leave me enough breast tissue. So mastectomy was a definite, and the choice I had to make was single or double. Due to my young age and the fact that I’ve already proven myself prone to breast cancer despite negative genetic testing, my chances of getting breast cancer in the other breast at some point in the future is quite high. If, however, I have it removed now, that chance drops by 90%. I am not interested in going through this again if I can help it, so I’ve opted for the double mastectomy, which is what they recommend for someone my age.

The next decision to be made then was what to do for reconstruction. The choices are between silicone and free tissue, which is when they basically give you a tummy tuck and use that tissue and skin to rebuild the breast. In some ways that’s the best option, but as my team put it, the chances of the skin being damaged in radiation is high, and if we’ve already used that skin from my stomach, there’s nothing to fix it with. If however, the skin is damaged and we’ve done silicone, we can still use that tummy/thigh skin to fix it. So they recommended starting with silicone and having the free tissue as a backup, which is what I was leaning toward as well and what I’ve decided on after much thought and prayer.

I still need to decide, then, where I want to do radiation, which will begin around 4 weeks post-surgery. I definitely did not want to do my chemo and main treatments in my hometown, but my oncologist on Monday said he wouldn’t hesitate to go to Cumberland for radiation–the treatments are standardized, and he knows and trusts the radiation oncologists there. He said he wouldn’t have recommended general oncology there–they don’t specialize, which means the same doctors are working with all kinds of cancer, and they have twice as many patients each as they do in Morgantown. As he put it, when you’re dealing with that many patients with that many cancers, there’s just no way to keep up with the details of each one. By focusing solely on breast cancer, my team in Morgantown can stay on top of all the developments in treatment, and they’ve found that making very small adjustments can make a big difference. As he explained it to me, radiation is very different. The plans are standardized, and they would come up with said plan in Morgantown and then Cumberland could just carry it out, and there’s little room for user error. And since it’s 5 days a week for a month, saving myself 3 hours of driving a day has definite benefits! I’ll continue to pray about it, for sure.

And even after radiation, I won’t be done. I will still have 11-14 more infusions of anti-HER2-protein meds, given every three weeks, back in Morgantown. Sometimes these can start during radiation, sometimes the radiation oncologist will advise waiting until radiation is complete. Sometimes they may involve the same chemo that I may get before surgery for 3 rounds or so, if they weren’t totally confident that all cancer had been obliterated by surgery, but if we see complete response beforehand, it won’t be necessary to tack that one on. Either way, I should be through the worst of the sickness here in the next few weeks, and the other side effects should start going away by surgery. Hair and nails should begin regrowing/repairing soon.

Have I mentioned the fingernail stuff? Before my 5th infusion, I began noticing my nail beds going wonky and pulling away from the nails, on some fingers more than others. I hadn’t been aware that this could happen to have looked up how to prevent it beforehand, but my oncologists, when I brought it up, did say that it’s pretty common and that I could lose some nails. They’re hanging on so far, and hopefully I won’t fully lose any at this point. I bought something called PolyBalm, which was developed in the UK–it’s a waxy/herbal product you apply directly to your nails twice a day. Their studies showed that of the people who used it the whole time during chemo, none experienced nail problems. The control group, however, did. Results are mixed when you start it after seeing issues, though plenty of patients had before and after shots showing it helped restore their nails. I got some, figuring it was worth a shot. I haven’t noticed them getting any worse since I started using it, so that’s a plus. And now I know what I’m going to send people when I hear they’ve been diagnosed with cancer!

I also met with PT on Infusion 5 day, and I’ve been doing exercises they gave me for leading-up-to-surgery. Because I have lymph node involvement and they will have to remove the nodes on my right side armpit, that means I’m at risk for lymphodema. The lymph nodes are the body’s drainage system, and removing them means fluids could stop draining properly in my arm. The exercises, and others I’ll be given for after surgery, are meant to help with that. I was also instructed to wear a ring on my right hand and pay attention to which notch my watch is buckled on–one of the first signs of lymphodema is swelling in the wrist and hand, and the ring and watch will help me know right away if that’s happening. If we catch it early, they can usually stop it without lasting effects; if you don’t catch it early, you can end up with mobility problems in your arm for the rest of your life. Not interested in that, thank you! So I will be paying close attention and doing my exercises religiously!

So as we can see here, chemo is done, but there is still quite a long road ahead of me; those anti-protein infusions will take up to 42 weeks to complete, which means I’ll have been in this whole process for more than a year before I’m officially “done.” Which in some ways is crazy to think about. When my sister had non-Hodgkins Lymphoma 8 years ago, it was serious. It was a dangerous cancer with incredibly intense chemo treatments–her infusions lasted a week each! She had to cart it around with her! But after her six rounds of super-chemo, she was done. No surgery, no radiation, no follow-up infusions. It’s funny to think that mine is the “easy” cancer by contrast, yet so much more involved and drawn out in the treatment process. Not that they can really even be compared, of course, but being most familiar with her treatment, I was quite surprised at how long mine would be.

But so, so happy to be finished this part of it! The rest shouldn’t make me sick, and I am SO ready to move out of the stage of constant nausea. Even though I haven’t had vomiting or diarrhea much since round 3, I have not had a single day since treatments began in May that I haven’t felt nauseous at some point in the day, even if it’s not all day. Three+ months of a rolling stomach is exhausting, and I am so ready to be out of this stage! I’m looking forward to celebrating the end of it with my writing retreat in Kansas City in September, and then going to my 20th reunion at our college Homecoming the last weekend in September. Those are two things that will be such fun before I move to surgery and recovery and then on to radiation! And of course, we have our December vacation to look forward to after surgery and radiation. Very excited for that!

My overall energy levels are already improving too, though these last few weeks my legs have felt so tight and tired whenever I walk. My labs on Monday showed my protein and iron levels were a little low, so maybe that has something to do with it. Clearly I need a nice steak. 😉 But at any rate, I’m already so much better than I was, and I am so looking forward to reclaiming health and getting my body back in shape! (Eating helps with the nausea, which means I’ve been gaining instead of losing weight, which is not what I wanted to happen! But I figured “Get through this first. Worry with that ten pounds later.”)

So here we are! DONE with the nastiest bits and ready to move on!! Thank you all SO MUCH for traveling this journey with me! Your constant influx of prayers and support have brought me countless smiles and made it so that I have never, for one minute, felt alone. I appreciate you all so much!