The Sun, the Moon, and the Trap of Comparison

It has become incredibly easy to look at someone else’s life and quietly decide that you are somehow behind. Behind in success, behind in happiness, behind in parenting, behind in health, behind in just about everything. The internet has given us a front row seat to everyone’s highlight reel. We see the vacations, the perfectly decorated homes, the thriving businesses, the glowing smiles in family photos. What we don’t see are the quiet, messy, complicated parts of life that everyone carries behind the scenes. And yet, if we’re not careful, we start measuring our ordinary Tuesday afternoons against someone else’s carefully curated moments.

I came across a quote recently that stopped me long enough to really think about it: “Don’t compare your life to others. There’s no comparison between the sun and the moon. They shine when it’s their time.” It’s such a simple image, but the more I thought about it, the more it made sense. The sun and the moon were never meant to compete with each other. The sun doesn’t look at the moon lighting up the night sky and think it’s somehow falling behind. It doesn’t rush the horizon trying to prove it can shine brighter. And the moon doesn’t apologize for not lighting up the middle of the day. They simply show up when it’s their time.

Life has seasons that feel like bright sunshine. Things move forward easily. Plans fall into place. You feel productive, hopeful, and confident that everything is working the way it should. But life also has seasons that feel more like moonlight. Those are the quieter seasons. The slower ones. Sometimes they’re the seasons where you’re healing from something, learning something hard, facing uncertainty, or just trying to make it through the day without letting worry take over. Those seasons can feel uncomfortable, especially when everyone else seems to be standing in the sunlight.

But the truth is, the moon is just as necessary as the sun. The world needs both. We tend to celebrate the bright seasons in people’s lives — the accomplishments, the milestones, the moments when everything seems to be going right. What we rarely see are the quieter seasons where people are rebuilding, recovering, grieving, growing, or simply learning how to keep moving forward. Some of the most important growth in life happens in those darker skies. When things slow down enough for us to listen to ourselves. When life forces us to reevaluate what actually matters. When we learn patience, resilience, and grace in ways that sunny days never quite teach us.

Comparison assumes that everyone is living on the same timeline, but that has never really been true. Some people are standing in their sunrise years. Others are in the bright middle of the day when everything seems clear and certain. And some of us are walking through a quieter stretch where the light looks different. None of those seasons mean someone else is ahead. They simply mean it is their time to shine in a different way.

The sun and the moon never rush each other. They never compete for the same sky. They simply take their turn lighting it up. Maybe life works a little like that too. Maybe your season right now looks different from someone else’s, and maybe that’s exactly how it’s supposed to be. It doesn’t mean you’re behind or that you’ve somehow missed the moment when everything was supposed to happen. It might simply mean that right now you’re walking in the softer light of the moon, and there is still something beautiful about that kind of glow.

Eventually the sky shifts again. It always does. The sun rises, the moon returns, and both continue doing exactly what they were meant to do — shining when it’s their time.

Blessings y’all – Amy

Learning to Live With the Weather

For a long time I thought depression and anxiety were problems to solve. Something broken in me that I needed to fix or snap back together.

Like a puzzle with the right pieces hidden somewhere. If I just worked hard enough, prayed enough, exercised enough, organized enough, went through enough counseling, or “thought positively” enough, eventually I would arrive at the finish line where they no longer existed.

But that’s not really how it works.

Depression and anxiety aren’t always dragons to be slain. They’re more like weather patterns that move through your life. Sometimes the skies are clear and bright and everything feels easy. And sometimes the clouds roll in without warning and the air gets heavy and dark.

For a long time I kept trying to conquer the storm.

I thought if I could just be stronger, or more disciplined, or somehow “fix” myself, the clouds would disappear for good. When they didn’t, I felt like I was failing some invisible test everyone else seemed to be passing.

But somewhere along the way I realized something important.

This isn’t something I conquer. It’s something I learn to live with.

Some days the sky is blue and the sun is warm and I move through life easily. I laugh, I create, I plan, I feel hopeful. Those days remind me that the storm isn’t permanent. But other days the clouds roll in again. Anxiety hums quietly in the background of everything. Depression makes even small things feel heavy. Getting through the day can feel like walking through deep water. Dealing with other humans, especially at work, can feel insurmountable.

And those are the days when I have to remind myself that storms are not personal failures.

They are just weather.

I’ve learned that living with depression and anxiety isn’t about eliminating the storms. It’s about learning how to ride them out without believing they will last forever.

Some days that means doing the smallest things and counting them as victories.

Getting out of bed.

Taking a walk.

Answering one email.

Not yelling at someone who probably deserves it and more importantly not taking it out on someone who definitely doesn’t deserve it.

Small things that other people might not even notice can feel like climbing mountains on the hard days.

And that’s okay.

One of the greatest gifts through these storms has been having someone who loves me through it. Someone who doesn’t expect me to always be sunny and easy and carefree. Someone who understands that sometimes the weather in my mind changes without warning.

Someone who stays anyway. Tim is amazing that way.

There is a quiet kind of grace in being loved through your storms. Not fixed. Not judged. Not told to simply “snap out of it.” Just loved — patiently and steadily — while the clouds pass through.

That kind of love doesn’t erase depression or anxiety.

But it makes the storms easier to weather.

Over time I’ve stopped measuring my life by how often the clouds appear. Instead, I’m learning to measure it by how I move through them. By the resilience that grows quietly inside the hard seasons. By the compassion I’ve learned for myself and for others who are fighting battles no one else can see. I’ve also learned it’s ok to cry and feel the things I feel – no one else has to understand the storm raging inside me.

The truth is, many people are walking through storms we know nothing about. Depression and anxiety are invisible companions for millions of people. Some days they whisper. Some days they roar. But they do not define the whole landscape of a life.

They are just part of the weather.

And like all weather, they change.

The sun returns eventually.

The air clears.

The world feels lighter again.

Living with depression and anxiety has taught me something I might never have learned otherwise: strength isn’t always loud or heroic.

Sometimes strength is simply surviving.

Staying in the middle of the storm.

Staying in the middle of the uncertainty.

Staying long enough to see the sky clear again.

And if you’re someone who walks through these storms too, I hope you know this:

You are not broken.

You are not weak.

You are simply learning how to live with the weather.

And that is a kind of courage the world doesn’t talk about nearly enough. And isn’t nearly patient enough with.

Blessings y’all – Amy

Today Is Mom’s Birthday

Today is my grandma’s birthday. We called her Mom.

My mother was 17 when she had me and we lived with my grandparents in my early years. I grew up hearing her be called Mom and it stuck. Somehow, that name fit her perfectly.

Birthdays after someone is gone are strange things. They don’t announce themselves loudly, but they sit with you all day. They show up in quiet moments—when you’re folding laundry, when you smell something familiar, when your hands are busy and your mind wanders back to her without asking permission.

Some of my deepest comforts came from Mom. Sewing, for one. My love of sewing—of fabric, and texture, and making something useful and beautiful with my hands—came straight from her. When I sew now, it feels like a conversation that never really ended. Every stitch carries a little bit of her patience, her practicality, her quiet creativity. It still feels like being close to her, even all these years later.

Then there’s the food. I miss her slumghetti—that wonderfully imperfect, comforting dish that somehow tasted like home no matter how simple it was. No one else makes it quite the same, and maybe that’s the point. It wasn’t just about the meal; it was about the care behind it, the way she made it for me as many times as I asked as an act of love.

Some of the moments I miss most are the smallest ones. When I was little and didn’t want to nap, she’d let me hold her ring finger while she told me to “rest my eyes.” I can still feel it—how safe that felt, how the world quieted down just enough. That tiny gesture held so much comfort. It was her way of saying, I’m here. You’re okay.

Mom had that rare gift of making you feel steady just by being present. Not the dramatic kind of safe—the quiet kind. The kind where the edges of the world soften. Where you don’t have to explain yourself. Where being loved is as natural as breathing.

I think about the lessons she taught without ever formally teaching them. How love looks like showing up. How strength can be gentle. How kindness doesn’t have to be loud to be powerful. How family is built on consistency, not perfection.

There are days I wish I could tell her who I’ve become since she left. About the life I’m building. About the ways her influence still shows up—in my hands, in my kitchen, in the way I care for the people I love. I think she’d smile at that.

Sometimes I catch myself doing something and think, That’s Mom. A habit. A phrase. A moment of patience I didn’t know I had. And when that happens, the ache softens, because it reminds me she’s still here—stitched into who I am.

Today, on her birthday, I miss her deeply. I miss her hands, her food, her quiet reassurances. But I’m also grateful. Grateful for a love so strong that it still shows up in the smallest moments of my life.

Happy Birthday, Mom.

I still hold your hand—just in different ways now.

Blessings Y’all – Amy

PawPaw’s Birthday

Today is my Pawpaw’s birthday.

Almost twelve years have passed since we lost him, and that number still surprises me. You’d think time would sand the edges down more than it has. It does soften some things—the sharpest ache, the shock of realizing he’s gone—but it never erases him. Not really. Not the way someone like Pawpaw could ever disappear.

There are days when I don’t think about him much at all, and then there are days like today when he feels right there. In the pauses. In the memories that show up uninvited. In the garden when the sun warms my face and it feels like one of his hugs. In the way I still catch myself wishing I could tell him something small and ordinary, just to hear what he’d say.

What I miss most isn’t one single moment or story. It’s the steadiness of him. The feeling that no matter what was going on in the world, Pawpaw was solid and safe and exactly who he’d always been. He didn’t need to be loud to be influential. He didn’t need to say much to say enough. Just being Pawpaw was more than sufficient.

Grief this far out looks different than it used to. It’s quieter. It doesn’t knock the wind out of me the way it once did. But it’s persistent in a gentle way, like a low hum that never fully goes silent. I miss him when something good happens. I miss him when life feels heavy. I miss him when my roses bloom and remind me of him. I miss him when I laugh at something and think, he would’ve loved that.

Birthdays have a way of doing that—of reopening doors you didn’t realize were still unlocked. Today isn’t sad exactly, but it’s tender. It’s a reminder that love doesn’t expire just because someone does. Almost twelve years later, Pawpaw is still part of who I am, still woven into my life in ways time can’t undo.

Happy birthday, Pawpaw. You are still missed. Still loved. Always remembered.

Blessings y’all – Amy

What’s Changed in 19 Years…

Today would have been my 19th wedding anniversary with Fred.

That sentence still lands with weight.

Not because I am stuck there. Not because I want to go back. But because love leaves fingerprints on time, and some dates never become neutral again.

Nineteen years ago, I married a man who shaped me. We built a life in the way couples do—messy, hopeful, unfinished. We grew up together. We learned who we were by learning how to be married. And when he died, that chapter didn’t close neatly. It ended mid-sentence.

Grief doesn’t respect calendars, but anniversaries have a way of knocking anyway.

What anchors me on days like today is gratitude.

Because the love we shared didn’t disappear with him. It lives on in the children he shared with me, in the family we built together, in the relationships and roots that still surround my life. I am profoundly grateful for that legacy. For the laughter that still sounds like him. For the people who carry pieces of him forward without even realizing it. For the fact I can still see his smile in our children’s. He didn’t just leave me memories—he left me a family.

And here’s the part that still feels strange to say out loud: I am deeply, fully, undeniably in love with Tim.

Not instead of loving my Fred.

Not in competition with that love.

Just… also.

For a long time, I thought love worked like a single chair—you vacate it, or you sit in it. One at a time. I didn’t understand that love is more like a house. Rooms get added. Some doors stay closed most days, but they’re still there.

Today is one of those days when an old door creaks open.

I can miss the man I lost and still laugh with the man I married.

I can honor a marriage that ended in death and still be fiercely committed to the one I’m in now.

I can feel the ache of “what would have been” without wishing away what is.

Loving my Tim does not erase my past. And remembering my Fred does not diminish my present.

That’s the juxtaposition people don’t talk about enough—the quiet coexistence.

Tim didn’t replace Fred. He met me after loss reshaped me. He loves a woman who knows how fragile life is, how precious ordinary days are, how deeply commitment can root itself in the bones. He loves me with patience on days like today, when the calendar carries more emotional weight than usual. And that love is not smaller because it came later. If anything, it is more intentional.

Grief taught me that love is not scarce. It expands. It stretches. It surprises you.

So today, I hold both truths.

I remember the man I married nineteen years ago, with gratitude—for our life, for our children, for the family he left behind that still carries me forward.

And I choose the man I wake up next to now, with joy, loyalty, and a full heart.

Both can be true.

Both are true.

And that doesn’t make love complicated.

It makes it real.

Blessings y’all – Amy

Choosing Intentional in the Middle of Chaos

I know we’re halfway through January and I’m just now trying to form coherent thoughts about everything that’s hit my world over the last few weeks—but bear with me.

My word for 2026 is intentional.

I intend (no pun intended) to keep that word front and center as a reminder that life only happens to me if I let it. If I hand over control of my emotions and thoughts to the things that scare me, then I’m the one who pays the biggest price. And since my emotions and thoughts have been in a pretty steady free fall since before Christmas, I clearly need that reminder.

Someone once said—at least Fred repeated it often—that when life stops changing, you get about the business of dying. I know that. Even with as much growth as I’ve had in therapy, change still rocks my world. Nothing triggers my depression and anxiety faster than everything around me shifting for reasons I didn’t choose and can’t control.

Right now, I’m standing in the middle of massive change and chaos at work and last week Lilah was diagnosed with a soft tissue sarcoma. Either one of those alone would be enough to shake me. Both together have left me struggling to function… or even want to get out of bed.

Professionally, after almost 15 years in this place, I know I’ll be fine. Eventually.

Right now? I’d rather not be around anyone. I’m not fit company, and my patience is nonexistent.

My brain feels like someone dumped a bucket of ping-pong balls inside my head and then said, “Function as you normally would.”

Sometimes in life, you just get tired of operating at 200% when everyone around you struggles to hit 75% or to care as much as you do. But slacking off isn’t how I’m wired—no matter how bad I’m struggling. That’s the thing that keeps me being overlooked. Amy will always rise to the occasion no matter what.

And that’s exhausting.

Re: Lilah.

She is my baby. The other half of my heart.

We’ve lost so much in the last year—dog-wise—to cancer. Our vet firmly believes the surgery scheduled for the 23rd will put this monster to bed, but the fear is still there. We’ve already said goodbye to Paris and Hope because cancer and tumors won.

Does anyone really blame me for being just a little resistant to the idea that everything will be rosy?

I’m not sure any of this even makes sense, but the urge to get it out of my head and into written words was stronger than my need for polish. I’m carrying so many emotions right now.

Anger is at the top of the list. I’m tired of giving everything I have and being overlooked like paint on a wall.

Worry is right there with the anger.

Fear and anxiety have joined the line.

Tim would tell you depression is here too—and I know he’s right.

But circling back to my word.

Intentional.

I’m going to be intentional about how much I give.

Intentional about what I carry.

Intentional about where my energy goes.

Intentional about protecting the parts of me that are worn thin but still standing.

I don’t have answers. I don’t have clarity. I don’t even have peace right now.

But I do have intention—and for now, that’s enough to keep me trying to move forward.

Blessings y’all – Amy

When Did We Stop Listening?

I almost never watch the news. Honestly, I can’t stand it.

But this week, during an hour-long nail appointment, the television was on. In that short time, I heard stories of a shooting at an ICE facility in Dallas, a semi-truck being pursued by police in Anaheim, and a stabbing at a school on the East Coast. And of course, you’d have to be living under a rock not to have heard about the Charlie Kirk shooting.

It struck me how much heaviness, violence, and grief can fill just sixty minutes of airtime. For me, that’s exactly why I usually avoid tuning in. Still, the stories linger, and they’ve left me chewing on something deeper: when did we stop listening?

Over the last twenty plus years, we’ve gotten very good at talking. With social media, 24-hour news, and endless platforms, everyone has a microphone, and everyone wants to be heard. But somewhere along the way, listening seems to have fallen out of practice.

When did we stop breaking bread with friends and neighbors and really trying to put ourselves in someone else’s shoes? Right, left, polka dot, or rainbow—it doesn’t matter the label. When did our brains stop stretching to see the world from another vantage point? When did the sound of our individual voices grow louder than the sound of voices bonded together—as Americans, as human beings, as family by blood or by choice?

Lately, I’ve struggled most with understanding the tragedy around Charlie Kirk. The things I’ve learned about him since his death make me wish I’d paid more attention before. But more than that, I keep coming back to his widow. Watching her carry herself with such strength in public, knowing the depth of pain and grief she must be enduring, moves me deeply. I imagine how all she must want is to pull the covers over her head and wish it all away.

And I find myself asking: when did the world become a place where taking another person’s life was seen as an acceptable way of dealing with conflict? When did celebrating the loss of someone’s husband and father become okay?

Maybe it’s age. Maybe it’s the season of life I’m in. But I feel like I see things through different glasses now. I long for a time when I could keep my babies close and not have to trust this cruel world to spare them. These days, my heart aches as I wonder where all of this is headed.

I don’t have tidy answers. But I do know this: the more cruelty I see, the more convinced I become that compassion is the only way forward. Listening doesn’t mean agreeing. It doesn’t mean silencing your own beliefs. It means making space, honoring another perspective, and remembering that life is fragile, sacred, and shared.

Maybe the first step is simple. Notice how much we talk. Notice how little we listen. And choose, in small ways, to listen again.

Because the sound of voices joined together—not in anger, not in argument, but in genuine listening—is still one of the most powerful sounds in the world.

Blessings Y’all. Pray for each other and our country.

Amy

At The Intersection of Joy & Grief

I made a decision about a month or so ago that I was slowly going to come off the anti-depressants I’ve been on since PawPaw died. That we maxed out after Fred died and had to change completely during COVID because they weren’t working. I’ve reached a chapter in my life where I have such a strong support system and I’ve done so much work in counseling I felt like it was time.

But it’s that time of year again. The month or so I spend holding my breath each day as I open TimeHop and each time I talk to my kids. The memories of him that are in my oldest daughter’s smile, in my son’s laugh, or in my youngest daughter’s tender heart. The anniversary of Fred’s passing is today and, as this new season of my life progresses, the time of year I am so besieged with emotions I can barely sort them.

Guilt is constant because I have found joy again. I wouldn’t ever want the kids to think I’ve forgotten the life we had with their dad. Yet I made a promise to Fred that I wouldn’t be sad too long and that I would marry again. Grief because no matter what I still miss him. Confusion over missing him when I have a man in my life now that loves me to a depth that is indescribable. Sadness because he’s missing out on momentous occasions in my children’s lives. Our first grandchild will make an appearance in September and I know his presence will be missed even more than it already is.

I know that it’s been long enough since he’s been gone that most days I choose joy. I choose to thank God each morning when I do my prayers for the life I have now and the blessings he’s given me. On days like today I feel like I’m standing at an intersection of joy and grief and while I know I need to choose joy more today than any other day the sadness of grief is so deep it’s hard not to give in to it.

Trying to focus on joy I think back to that last “perfect” Lanford Saturday we shared with Fred. It was May 20, 2017 and Fred had been home from the hospital for about a month. It was one of those days where none of us could sit still and were so joyous from having gotten Fred through rehab and home that we just wanted to be out in the world. It was still spring and the weather was gorgeous. We spend the day doing some of our most favorite things. We went to Grapevine and had wine and snacks on Main Street. It was Main Street days in downtown Grapevine and we wandered around different booths for quite a while. The kids each got to have a cast made of their hand holding their dads. Something we didn’t know how very soon would be an irreplaceable treasure from the day. We finished in Grapevine around 3 pm and by 6 pm were back out headed to go see live music at The Truck Yard. With Tigre in tow.

Those are the days I look back on and remember how very much he lived during his time on earth. Those are the days I hope bring a smile to each of my kids when they are sad. And that is the Fred I remember with a heavy heart on the days I am sad. He was a good man. He gave me my family and for that I will forever be grateful.

If you have a favorite Fred memory I’d love to hear it today.

Blessings – Amy

A Little News and a Lot of Anxiety

Twenty plus years ago I was told I had Hashimoto’s. All I remember a the time was being told it was an autoimmune disorder and that I needed to make sure we kept my thyroid levels in balance. Given that I’ve been on thyroid medicine since about four months after Em was born didn’t seem life altering.

What I didn’t know over the ensuing twenty years of fighting to keep my thyroid levels stable through insurance insisting on generic thyroid medicine my body didn’t respond to (and being told I was crazy because I thought that), ups and downs in my levels due to weight gain and loss, hair loss, dry skin, and just general life was that that diagnosis meant my body was attacking itself and slowly killing off my thyroid.

In December of 2022 my company changed insurance companies. What ensued was the gluten free thyroid medicine I had finally gotten stable on for almost five years no longer being an approved medicine. Being shoved onto generic thyroid hormone that sent my body into a cycle of weight gain, hair loss, and general yuck. When Tim and I got married he did the research and we figured out how to go back to the right medicine albeit it of pocket. Though that was fall of 2023 we’ve fought all this time to get my thyroid to stabilize. Finally in February after another off kilter set of labs my GYN said “you have to see an endocrinologist”. Back story there – I hate endocrinologists. Between the fact that they are insanely smart humans usually who don’t know how to relate to you and listen to you when you talk and the one that prescribed Fred medicine and didn’t follow up on him thus leading to his kidney failure I’ve got no patience for them. My GP and GYN have managed my thyroid for years.

I procrastinated until end of February and finally got a referral sent to Tim’s endocrinologist. The ONE I actually like cause he listens to Tim and isn’t a condescending human. We expected it to be months before I could get in and after ten days without a phone call was surprised to finally get one Monday – with an opening the next day. Still calling that a God thing.

Dr. Burney walked in, sat down, and said tell me what’s up with your thyroid. IMMEDIATELY went to food…doctors don’t do that…and explained that Hashi’s patients can’t eat gluten. It inflames the gut and limits the absorption of the medicine. Do you know how many other docs had dismissed my saying I noticed a difference when I didn’t eat gluten even though I was negative for Celiac???

First change he made was saying from here on out it’s a strict gluten free diet. Also an unprocessed chemical free (whole foods) as much as possible. Hashi’s patients bodies attack foreign stuff and get inflamed and that prevents absorption of the medicine. Next up is continuing with getting some more of the weight off. The goal is to get me to ONE pill a day of the thyroid medicine so that if I’m going to pay for it out of pocket it’s not three boxes every six weeks to the tune of $185.

Then he took a look at my thyroid. It’s dead and gone. Shriveled up and fibrotic. The out of control Hashi’s has done its thing and I’ll be on the hormone therapy the rest of my life. As it has sunk it that how I feel will be a direct correlation to how I take care of myself for the rest of my life the more overwhelmed I’ve felt. Those close to me can tell you – the one thing I am worst at is taking care of me. And there is something different between choosing gluten free and being told it’s not an option anymore. As much as we travel it makes it a challenge.

I’m still exhausted, still have very little energy, and that’s as much mental exhaustion as it is physical. I have so much I want to do and right now nothing is cooperating. I am trying to lean into the amazing support that my hubby and kids are being but it’s hard. I am also angry. The ONE thyroid medicine most effective for Hashi’s patients most insurance companies don’t like and thus won’t pay for. To me that’s like saying you won’t pay for insulin for a diabetic. How dare you? Who made them God? It’s maddening.

If anyone with Hashi’s is reading this – your diet is as important as the medicine. You have more control than just the medicine. Take control and keep your thyroid functioning as long as you can.

Blessings y’all – Amy

Medical Madness

I grew up in the medical system. For those that don’t know this about me I was born with a birth defect that meant I had my first corrective surgery at 3 months old and my 50th right before my 18th birthday. There have been a few others since then but the bulk were in my childhood. I’ve depended on doctors and medicine my entire life. Honestly never was taught to question them or their orders.

As I have grown older and run into periods where I suffered consequences of some of those orders I’ve begun to wonder if the doctor is always right. For example when I received the COVID vaccine and subsequently suffered through 3 months of full body hives that the doctors swore couldn’t possibly be a side effect of the vaccine I was itchy, angry, and pretty sure the medical community was full of morons.

I find myself sort of here again. My middle child and his wife question EVERYTHING. As I ask questions and find myself dissatisfied with the side effects of multiple rounds of antibiotics and steroids I grow increasingly more curious about their perspective on things. And how to balance that with conditions I have like Hashimoto’s and hypothyroidism. And dysfunctional ears and sinuses that periodically, like now, just flat refuse to cooperate.

I left on vacation with an ear infection. My second in a month. Though I completed a full ten day round of antibiotics while on my trip I came back with a double middle ear infection, RSV, and a sinus infection. Was put on a different round of antibiotics when I got home, given a steroid shot, and oral steroids. The antibiotics have upset my gut. The oral steroids keep me up at night and make me angry at everything and everyone. I’m sleep deprived and cranky. By now I should be getting better but woke up with the room spinning. Like WTF.

Where is that line that we trust doctors or we say nope this isn’t working and I have to try something else? How does someone like me with all kinds of complications wean myself off of depending on doctors? One of the things pressing on my mind is the shingles vaccine. I’m not quite at the age for it yet but I had HORRIBLE chicken pox as a kid and I’m a prime candidate for shingles. But after the reaction I had to the last vaccine I let someone put in me why on earth would I sign up for another? But I know from seeing people around me go through shingles that those can be excruciating too. Which is worse?

And even if I did figure any of it out and think I have a plan then the damn insurance company would weigh in and say NOPE you can’t have that drug. Perfect example is my thyroid medicine. I was stable on one drug for over five years. But my insurance changed and they wouldn’t cover it. My body doesn’t respond to the one they do cover and even though we switched me back to the good one by paying out of pocket for it it’s now two years later and we still haven’t gotten my thyroid back under control from having been off it for 9 months. Why the hell does insurance get to dictate what we take if patient and doctor have determined that one medically won’t work?

It’s all madness. Just fiscally driven madness where money is most important and we are secondary. There’s my brain dump for the day. 😉

Blessings y’all. – A