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These are just a few of my favorites lately- I hope you enjoy!
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It's summer. In Georgia. So it's HOT. And one thing I'm learning about these long, hot days is that being inside in the cool AC with a fan whirring in the background and nature showing off outside my window gives me both energy and rest simultaneously. Yes, the kids are out of school. Yes, there are lots of "mom, I'm bored" whines followed almost immediately by "mom, I'm hungry." But there is something about summer that makes us all kids again, isn't there? We stay up later than we should. We eat popcorn for dinner if we want to eat popcorn for dinner. We "don't have any homework" and most of us "don't have practice" and a messy house is expected with kids out of school. Pools call our names and floating counts as exercise. Ice cream outings beckon us to sidewalks in small towns. A live band on a starlit night with a warm breeze gives me enough wattage to survive this Georgia heat and sink into my sheets at night both tired and invigorated. We talk to our neighbors more. The same ones we see all year walking their dogs. But it's summer. And summer gives us permission to interact even in this lonely digital world. Movies are cast on campers and garage doors. Glow sticks compete with fireflies and fireworks happen a few times each summer- all over the world. Smores become dessert and even church seems more fun in the summer. God must be showing off a little more with these summer rules and nature's beauty on display. Books are suddenly important to moms and sometimes even dads. And not books for the kids, books for US. We suddenly want to read... by the pool, at the lake, on the beach. Clothing is thinner and shorter so even laundry is less cruel and mundane. Work is necessary for most of us, but even WORK in the summer is better. Frankly we are all in a better mood. So I ask you to sit for a minute or two and consider all the things you LOVE about summer. There is so much going on in the world this June of 2022, that I chose to focus on any summer, all summers, just summer for my reflection post. Life has been heavy, but I need light. We head to the beach in a few weeks and my children's' excitement is like a drug. They giggle and ramble on about all the things we will do and how fun it will be. And I join in! Because I was 10 years old one time, without a bank account or work deadline or relationship issue to worry about. I was 10 years old. Out of school. Staying up late. And catching fireflies after I rode my bike and jumped in the pool with my friends. Allow yourself to be 10 years old today. The world needs that right now. Godspeed. After writing School Colors as I processed the Uvalde tragedy, I kept feeling and seeing the word BRAVE creep into my mind and body. As with any tragedy, loss, or wonkiness we endure, I think people turn to comedy for some type of comfort or relief. Pandemic comedians, where you at? (yes I used improper grammar and I liked it)... Anywho, I've had a lot of ICKY after this most recent school shooting, and I have found myself SCROLLING more than usual- I guess as a form of searching for both relief and answers. 😞 Upon scrolling, I saw a meme of the 80's mustachioed dad tossing his bewildered 7 year old into the pool as his form of "swim lessons." Ha ha- so funny- so true (established 1976 right here), keep scrolling. Still smiling as my right thumb hovered over my phone, I felt a small nudge. Brave. Kids. Brave kids. Kids who are brave. Parents who allow kids to BE BRAVE. Now I'm NOT thinking or talking about Uvalde, but I'm thinking and talking about the kids I see and know. The ones in my house. The ones in my neighborhood. The ones on my son's team. The ones in my son's acting group. The ones in their classes. My cousins' kids. My friends' kids. MY KIDS. Last night I watched my youngest son do something SO BRAVE. It took so much courage to do what he did. After his brave act, I asked him how he felt. He had mixed emotions (because his efforts were great but not PERFECT) and he was exhausted. I explained to him that what I loved the most about his endeavor was the COURAGE he displayed to even attempt his feat. Good, bad, perfect, terrible, wonderful, awful, whatever... he DID IT! And he did not give up. And he did not waiver. He believed in himself and he followed through without the 2022 SAFETY NET of PARENTS and SOCIETY. But friends, are we the NET we think we are for these children? Are we catching them when they fall or are we blocking the ladder to get to the scary top? Are we so worried about their potential failure (and heaven forbid it being captured on social media) that we are keeping them from even DREAMING or BELIEVING or TRYING to reach for the stars? Are we modeling GOING FOR IT and TRYING NEW THINGS or are we waiting on the sidelines watching reels of strangers going for it? Did we "see it on TikTok" or did we actually try it ourselves? Are we letting them FAIL or are we making sure they SUCCEED at all costs? Are we celebrating the lessons learned or only the medals won? So I challenge you, Moms and Dads, Aunts and Uncles, Grannies and Nannies and Pappaws... talk to the children in your life about COURAGE and BRAVERY. Discuss success and failure at the supper table. On the way to the "brave feat" last night, that same son asked me if some celebrity was a millionaire. My response: "I'm sure he is, but that doesn't mean he's happy. Ask that celebrity what matters to him, what he stands for, who he has helped in his life - that's a better question." Give your dear ones a little wiggle room to make mistakes. Let them have an original thought and better yet, AN OPINION. Encourage them when they are frustrated, but please do not fix it all for them. Allow them to clean up their own messes. If I have learned anything in the past few weeks, it is that my children and the children in this world are BRAVE SOULS, braver than we will ever imagine. Let us unlock their courage and model resiliency after "failure." Put your phone down. Talk to the kids in your life. Ask them what courage means to them. SHOW THEM how to be brave. Godspeed. AUTHOR'S NOTE: I am still not okay after what happened in Uvalde, Texas. I am okay with not being okay. This post is not meant to belittle those events in any way. I'm watching my children as they move through this. I'm learning from them how to be brave. School colors like black and gold Varsity cheerleaders Marching bands with trombones Or school colors like yellow and black Lines of school buses Bring excited August students back School colors like green and white Chalkboard and chalk Now Chromebooks and a mic School colors like Crayola in a pack All the colors of the rainbow Glue sticks, play-doh, and papers stacked School colors like pink and purple Little girls' hair bows and backpacks On their devices playing IXL & now Wordle School colors like navy and grey Quarterbacks and point guards Breaking records, making their way School colors like off-white and beige Tile floors and cement walls Janitors mopping, cafeteria workers wave School colors like baby blue and white Pep rallies and pom poms It's homecoming tonight! School colors like silver and black TURN THE LIGHT OFF!!!! BE QUIET!!!! HE'S GOT A GUN!!!! DON'T LOOK BACK!!!! DON'T MOVE- JUST BREATHE NO NOISE - WE NEED TO STAY QUIET, SO QUIET COUNT 1, 2, 3 DON'T CRY, IT'S OKAY YOU WANT YOUR MOMMY SWEETIE JUST STAY VERY STILL, SO VERY STILL I AM NOT SURE IF HE WILL COME TO OUR ROOM POW POW POW SCREAM SCREAM SCREAM NOW NOW NOW IT'S SO FAST, SO VERY FAST IT'S SO LOUD, SO VERY LOUD yet so quiet and so lonely am I frightened or just zoning out or am I in? is it over? did we win? no we lost and school colors are red for blood shed and white for those who died and black for the marks on our souls don't look back School Colors, School Colors I don't trust you anymore. I am hiding behind a bookshelf with America's children on the floor. Honors Day comes every May and with it comes some pain Pain for those who watch from afar Pain for those who were never the star and sometimes, a feeling unnamed This feeling of reeling from dealing with life and school and kids and daily strife There's work and marriage and laundry and dishes and unfulfilled goals, broken promises, forgotten wishes And all of a sudden we are all 16 again full of both awkwardness & confidence with our acne and our hormones watching the principal hold the microphone And we wait for our names to be called 1 2 3 and the teacher didn't call it they didn't pick me Pick me or my kid? What's going on in my head? Am I rejected for their rejection? Is this about me instead? Oh Honors Day, dread Honors Day I love you when you call my name I hate you when forget about me Wasn't I good enough? Don't you see? The joke is on us friends for life is its own Honors Day Your boss, your friend group they always pick who they want to stay We want to belong we want to matter to feel seen and heard But what I have just realized What I have finally learned Is that I throw my own Honors Day EVERY DAY for myself for my kids, for my spouse WE are the trophy, WE are the shelf I won plenty of ribbons and plaques and awards But they're somewhere in a box And now my family is my sword to keep fighting this fight we call life every day so when your lovely looks up to you disappointed from Honors Day just tell them, no SHOW them, about the true trophies in life Like kindness and empathy and perseverance. Hold that baby tight. Look right in their eyes and tell them YOU are their shelf. And no matter how good someone measures them to be, they are HELD. Don't push your sweet lovelies to climb to the top. Let them be who they will be. Let them stop if they need to stop. Honors Day comes every May and with it comes some pain just let it go on and do its thing. Don't let it determine the gain. Brought to you by a trophy-winning, plaque-possessing, still-trying-to-figure-it-out 16 year old stuck in a midlife body. Honors Day is just another day. Your sweet babies are the TROPHY. Please be a kind and loving SHELF. Godspeed. Southland in the Springtime- that's a song by the Indigo Girls in case you didn't know- check it out 🎶
Now I challenge you. Think of what you love about spring. Sit outside. Write it down or note it in your head. And give thanks. On our first day and our last day, we are all the same. Godspeed. If you have a pet of any kind, you know the joy that pets bring into our lives. While they do come with a certain level of commitment and work, they offer benefits that far outweigh what they require of us. Now that I am six years into my primary chronic illness, sarcoidosis, I feel like I can discuss pet therapy with conviction. Prior to becoming "sick," I always had a pet - from childhood on. It wasn't really until I became ill, however, that I realized what my dogs had done for my mental health. My physical health has also improved thanks to being a pet-owner. Here are 10 ways owning a pet can help you with your chronic illness:
Charlie the Dachshund is always there for me. He will wait on me wherever I go and follow me no matter what. He needs my help to get his food, water, and to let him outside. It feels good to be needed by someone or something that doesn't really expect much in return, ESPECIALLY with a chronic illness. I can be sick, tired, or both in front of him and not feel self-conscious. I can tell him all my thoughts and fears, and he won't judge me. I can even moan out loud in pain or cry at my medical misfortune and he doesn't flinch. Instead, he meets me with loving kindness and is a steady force of calm in my daily life. Friends, Family, and Coworkers can all form extremely close bonds. Statistics show that we spend more hours at work with coworkers than with our own family members. If we are lucky, we find certain individuals that vibe with us. We may share common interests or common talents. We may have a similar sense of humor or taste in music. It's kismet and it's beautiful when that happens. But years pass. Life marches on and with that comes love, loss, and change. Some of us grow and some of us remain stagnant. Some minds open and some minds close. I'm sure you have felt it. You're having lunch with someone from one of those 3 groups (family, friend, or coworker), and you run out of things to say. Your common interests and similar values seem further apart. In the worst cases, this person sitting across from you is your spouse or partner. Perhaps you are the one who is growing or perhaps you are the one stuck in your ways. Invariably, one of you is going to be growing in a different direction than the other person. Just because you grow in different directions doesn't mean you have to grow apart. It can mean that, however, if you are not careful. Having worked in healthcare for decades, I have learned how important it is to meet people where they are. If you love someone, you can meet them where they are without expecting or pushing them to change. My oldest, bestest friend once commented "it takes all kinds." It wasn't a grand statement or momentous event when those words tumbled out of her mouth. I must have said something judgy, and she course-corrected me. How lovely would it be if we embraced each day and each relationship with that same framework? I cannot recall the moment in which she said those words, but I have never forgotten them. IT TAKES ALL KINDS. How boring and monotonous would life be if we were all the same? As polarized as our country has been of late, imagine us all agreeing on everything? Where would the passion lie? What would spark change? What would we learn? So today, as I begin another day of onboarding for my new day job,
I sit with a smile on my face and love in my heart. I have learned the most from those that challenged me. I have grown the most being surrounded by those that questioned me. I have loved the most by offering compassion and empathy to those that may not even like me. The next time you catch yourself thinking "we are just too different. I've changed (or she's / he's changed)." Pause. Take a deep breath. Silently name all the reasons you loved them initially and why you still care for them today. Who are you to say you are too different? What can you learn from them? What can they teach you about yourself? It takes all kinds. Godspeed. 💜💚💜 Have you ever been picked last for a team or a project? Have you ever been sitting at the END of a table and no one really acknowledged your presence during the lively, laugh-out-loud dinner that everyone else seemed to be having? Have you ever been cut off during a conversation when someone "cooler or prettier or funnier or more magnetic" stepped into the mix? What if you vote a certain way but you're surrounded by others who vote differently? You want them to love you for you, but are you having to hide part of yourself in order to belong? What if you have a different opinion but keep it to yourself in fear of others' reactions? What if you don't even feel like you belong in your own home? Isn't home supposed to be your safe space?
So, again, I think we have all experienced this feeling. Disconnected. Cast out. Overlooked. Unwanted. Unnecessary. Unimportant. Small. Invisible. Rejected. Source: Brene Brown's Atlas of the Heart Since we all know we can't control the thoughts or actions of others, let's focus on what WE can do the next time we feel this way. Here are 10 ways you can (and I do these myself) try to reach the feeling of BELONGING again:
Now let us review. Somebody somewhere made you feel left out, unwanted, or overlooked. You start to list all the reasons you are just that: unwanted and overlooked. Then you REMEMBER these tips to get back to belonging and you pull at least one of them out. Consider it a secret weapon. Use it. Allow yourself to feel both ways - both the ickiness of unbelonging and the comfort of true connection once you have found your way back. Teach someone else you love how to do this the next time they call you searching for validation. And hey. Just so you know, I would pick you. Godspeed. How are you? Good, how are you? Fine, today was busy. Yeah, me too. Ready for some downtime. Did you go by the drugstore? I did (even though he could have). Did you run the dishwasher? I did (even though she could have). What's going on this weekend? A Saturday-Sunday tournament and I really need to get some of my charts done. (He didn't ask if I wanted to do anything as a couple. I guess he doesn't care). (She is always working- she never even mentioned anything I might want or need). Okay- sounds good. Sound familiar? We both have needs, but we are not making them known. We both have resentment, but we speak like polite coworkers. The conversations are transactional and not RELATIONAL. We are co-parenting and room-mating - but where is the love? Unfortunately, as the years passed and the kids got older, we seemed to have fewer transactional conversations. Homework wasn't AS MUCH of a chore. Snacks were often handled by the kids independently. Routines were established and roles were pretty defined (though unspoken) in the home. In ways, this meant less bickering and smoother mornings and evenings, but were we connected? OR were we just 2 lonely adults passing in the hallway - each longing for a real connection but not knowing where to start? We have both been married before, so we both know the pain of divorce. We vowed to make this marriage work, but was it working? Was it tolerable or was it phenomenal? I have been going to THE BEST counselor on the planet for about 18 months now, and I asked her for a few suggestions. Regardless of each person's love language, she made clear that time and non-sexual touch are both very necessary for meaningful connection. Since I work days and my husband works nights, we don't have a TON of time together - and very rarely is it without children. We both commute so that takes away even more of our precious time. The kids are busy year-round it seems, so where was I supposed to carve out both TIME and TOUCH? I decided that we needed ONE HOUR per day to talk, sit close to each other, and just be together. I named it the POWER HOUR and I told the kids this was Mom and Dad's time together and it should not be interrupted unless there is an emergency. They heard "screen time" and were all for it. I decided kids' screen time is worth the investment in our marriage. I claimed 7-8 pm to be our ONE HOUR per day to sit on the couch together - touching!- to watch TV, chat, whatever. I am not gonna lie, 9 times out of 10 my feet and legs are in his lap and he's using my massage gun on my calves while I scratch his non-massage-gun-holding arm and hand. He likes scratches, I like massages. The point is, though, that we are touching and there is no pressure surrounding the touch. All adults everywhere know what I mean by that. He has to leave for work by 8 pm, so once he leaves I call the kids back into the living room and we finish out our family time before bed. If he's off that night then we may continue past 8 pm. The rules are simple: he needs to be showered and ready for work by 7 not 8 so I can have that hour with him. I need to ignore work and personal messages during that precious hour so that I can give him my undivided attention. Sometimes there is a late practice or rehearsal and our POWER HOUR is skipped or delayed, but it is a daily priority now. We both look forward to that time together, and the kids are still alive. It is so much easier to hash out a BIG issue when you are sitting next to your spouse touching them instead of over the phone or (worse) text. If you are both relaxed and physically touching each other, it is harder to become defensive or to go into attack mode. A quick squeeze of the arm or hand can reassure your partner that you are, in fact, on the same team. Close eye contact can remind your spouse that you love them and that you each have the same end goals. You may read this and be thanking the heavens that you've never felt disconnected from your spouse. Having worked with married patients for years, I would venture to guess you'd be in the minority. I know most of us have felt like our marriages have become mundane or on auto-pilot at various times. It doesn't necessarily take a marriage retreat or some crazy new "trick" to get your marriage back on track. For us, it just took a shared couch, one hour per day, and our hands. It took putting the phone down. It took managing our time to preserve that one hour per day. It took biting our tongues when we wanted to be snappy and waiting until we were together to have that hard conversation.
My life isn't perfect nor is my marriage. My house isn't perfect. My kids are not perfect. I am far from perfect. But, I am trying. He is trying. We are trying. Effort is attractive and kindness matters. Godspeed. Just like a plant first emerges from the soil, I feel that burst of energy after my labor and my toil I have prepared this new beginning that was written in the stars. Will I miss my sweet darlings? Will they always be in my heart? Of course they will for that is who God made me to be. A person who loves and stays committed to thee. ❤️ But I am so very excited to plant new seeds. To bear new crop, to have more reach. Will I miss my old garden and all my farming friends? Of course, but this is just a new plot of land. Some bare acres await me and all my ideas. How exciting to lead, to lift others, to calm fears. The doubters might think "yeah she is in for a treat." But the treat is in the soil, the gardeners, and the seeds. 🌱 I am not the treat. I am simply the sun, ☀️ the rain, and one of the tools to help the garden run. I am not all of that of course. I am no fool to this game. But to be on the team and be invited to play! 🥳 Is the best feeling in the world to be appreciated, to feel heard. The anticipation explodes inside me. No longer a noun, I can be a verb! Some tears will be shed over the last garden I built. I will see you all again. This flower just had to leave before she wilt. 🌸
The following post is one mom's experience with autism. One family's experience. This author and I both understand that autism exists on a spectrum and this is just one example of the spectrum. What do I want you to know about autism? Since I am neuro-typical, I can only give you a mother’s perspective. So, last night, I asked my 15-year-old with autism what they want people to understand about autism. After a moment’s thought, they had two things to tell others. First, in their typical blunt manner, C said, “Autism is a spectrum, it doesn’t always look like a little 6-year-old boy who can’t control himself.” I thought this was a great point. Our autism story isn’t typical. My kid, born in a female body, wasn’t diagnosed until last year, when they were 14. (For the purposes of this post, I’m using gender neutral pronouns and the letter C for their name.) They’ve struggled with a number of things for years: reading was hard, paying attention in school was a disaster, building and maintaining relationships with “normal” peers was super challenging. The autism diagnosis was a sigh of relief for all of us. Finally, we had a name that encompassed a wide variety of things: social skills that were getting harder to manage in middle school, sensory issues that seemed to becoming more intense, and a hyper-fixation on a growing, rotating range of topics. Autism was not a negative diagnosis for us. It was an answer and in it, I found hope. It took years for me to start thinking about autism for my kid. To me, autism looked like one of two things: it was either the young boy whose autism made them unpredictable, a person with special needs, or it was the savant, again a boy, who could tell you everything you needed to know about his particular fascination. In fact, it was C who came to me and said, “Mom, I think I have autism.” In the next breath and typical fashion, “I’ve been doing some research.” My sweet kid, from the moment they were born, was never typical. They were happy and silly and the third born. They could be laughing one minute and asleep on your lap the next. C was cuddly and tender one moment, but at the next moment, trying some stunt that would make a mom’s heart stutter with nerves. They could listen to me read to them for long hours or play a silly made up game all afternoon, but could never concentrate long enough to finish math problems. We got an ADHD diagnosis when C was quite young. (That’s another thing C would want you to know: often Autism is misdiagnosed in females as ADHD because Autism presents differently in girls and practitioners don’t think females have autism.) And in that moment, an ADHD diagnosis was a tool—it gave our family a framework for understanding that our kid’s brain worked differently. We could accommodate their learning and home life to best suit their needs. C is smart, funny, talented, creative, and silly. Their diagnosis forced me, as a mom, to reframe the negative lens through which this is seen. I wasn’t going to let them think their ADHD was an affliction. Instead, ADHD was their superpower—they saw the world differently than I did. It’s just that the world isn’t really made for kids whose brains aren’t like everyone else’s. Everything fell apart in Middle School. Well, Middle school and a pandemic and online learning and adolescence. It was the perfect storm of horrible-ness. It has been a rocky couple of years for my kid (and me) as we’ve discovered the autism diagnosis and struggled mightily with mental health. (One more thing C would say, because they think of things at random times unrelated to anything else, is that because autism is diagnosed so late in girls, most girls with autism struggle with depression, anxiety and a sense of “who am I?” and “why can’t I be like everyone else?” An earlier diagnosis could help relieve some of that angst.) This is the first time I’ve ever put this story down in words. It feels rather momentous to do so. Yet, when I tell people in my orbit that C has autism, some are surprised, but for most, who know us, it just rolls off their back. “Huh,” they say and move on to something else. Because for them, as well as us, it’s just a way to define the way my kid is, the way they move and think and interact with the world. And someday, this culture will understand what a gift a brain like that is. I am convinced that someday C is going to change the world. Oh, and C wants everyone to know something else about autism: “Mom, make sure you say that moms who have kids with autism aren’t superheroes. They’re just moms. Like you.” C makes me laugh so hard I can’t breathe. They will share their saved memes with me for 30 minutes just to get some parental attention and then later lock themselves in their room and not want to talk to anyone. They challenge the way I think and expand my view of what success looks like in the world and teach me a gazillion things I never thought I would have to know. While I wish the world was an easier place for my sweet one, I would never, in a million years, change this part of who they are. And that is what I want you to know about autism. Sammy Beuker is a wife, mom, Youth Worker, friend, and writer who lives in Grand Rapids, Michigan. When she isn’t managing her complicated family life, she works with teenagers at her local church. You can find her and her newsletter at sammybeuker.com where you can follow along on her journey to publication or on IG @sammyanne_b where she posts about her life, writing, books, food, family, faith and her golden retriever, Monty. Thank you Sammy (and C!!!) for sharing your words with my readers. Thank you for having the courage to tell your story. This touched me! ❤️ -Amy at Taylored Intent If you are a mother, you know the feeling. You're at work instead of field day. You're at one child's band performance while the other child has an academic bowl meet. You missed that baseball practice out of sheer exhaustion and that's the one where he hit it over the fence. "Mom, can you pick me up car rider? Can you check me out early like all my friends? When are you going to be off work again? Mom, why are you on your laptop so much? Mom, are you listening?" Some of those innocent but real questions can cut me like a knife, leaving me gutted and riddled with GUILT. Mom Guilt. It's a thing. And I think we should talk about it. AND we certainly do not help ourselves as a gender or a community. Not only do our KIDS make us feel guilty, our fellow moms can inadvertently or purposefully trigger shame and guilt at any given moment. Pam made homemade Christmas cookies for the entire class while we can barely pack lunches each day. Trisha made Halloween goodie bags with a punny handmade tag using her Cricut. Allison sewed personalized pencil pouches for the entire third grade while we are struggling to sign each kid's agenda every night. Then there's social media. Be sure to only buy non-GMO Organic foods. Is your car seat in the top 3 for safety? How often is your child brushing their teeth? Gluten is the devil. ADHD is real - oh wait, no it's not - you're just a lazy parent. Discipline your kids. Don't discipline them, let them find their own way. All babies should cry it out. Babies who cry it out have attachment issues and end up in therapy before age 30. Limit that screen time. Make sure they play outside, but you must watch them outside AND still get all your paid-work done and maintain a spotless house with home-cooked meals. Cloth diapers. Breastfeeding. Well, if you work then store-bought baby food might be okay- but only if you work now. And don't forget to recycle. Make it stop. When my boys were 2, 4, and 12, I walked into my CEO's office and said "I quit. Other women are raising my children and I quit." I didn't have another job lined up. Fortunately, I had some savings, but that was mainly because I was working SO HARD and barely had my head above water that I never had time to shop or vacation (ie spend money). I was justifying myself to a man (my CEO) whose wife did not work and I "knew" he was coming home to beautifully home-cooked meals, a clean house, freshly washed and ironed clothes, and a wife who probably still had energy for sex instead of one who was collapsing into bed every night. OR SO I THOUGHT. He kindly and calmly asked me to take a deep breath, sit down, and reconsider. What about part time or PRN (the medical term for as needed)? Did I want to lose my 6-7 years of tenure with the company? Did I always want to stay home or did I just need a break? Did I still enjoy being a nurse practitioner? The truth was, I did not know the answers to his questions. I had ZERO plans, which goes against my basic core (search "plan" on this blog and you'll quickly see I plan everything). I had not asked myself if I enjoyed my work because I barely knew what day it was. I felt pulled in every direction by every person in my life and I was dreaming of ways to "get off the treadmill." My husband's lawn business was booming, and I was quickly running out of bandwidth to help him with that as well as my other demands at home and work. I felt like I was choking, but I wasn't sure WHAT was choking me the most. I just knew in my SOUL that I had to make a change. I prayed about it. I took a few days to write it all out - not my feelings - I had not found a therapist yet. 👀 Who had time for therapy? BUT, I did somehow remember some of my high school and college skills for decision making and scribbled down ALL the reasons that quitting my job would make me happier overnight. In the end, I heeded my younger-than-me CEO's advice and worked PRN the first year and part-time the second year before returning full-time when my youngest started pre-K. Since I am not independently wealthy, I did eventually have to bring home some more bacon. So, then what happened? Was my life immediately better once I was home more? Did the MOM GUILT end over night? Was I making beautifully home-cooked meals, providing freshly washed and ironed clothes, maintaining a perfectly clean house, and bursting with energy for sex every night since I no longer "worked" every day? Turns out, the joke was on me. Not really a joke though my friends. It's the truth. My 4 year old was in Pre-K, but my 2 year old was suddenly out of daycare. My 12 year old was in honors classes in middle school and I found myself juggling potty training, phonics, and puberty. 3 P's that should never go together. 😜 I was waking almost as early as I had been when I commuted to my demanding NP job. I was feeding kids, washing clothes, and picking up toys all day it seemed. I was helping with homework instead of paying my babysitter to do that. I was making brownies for the PTO instead of money for retirement. I was just as tired, but it was more of a physical tired than a mental exhaustion. I was able to go to the gym regularly, and THAT was amazing. Our gym had childcare, so I would tell the boys if they wanted a "nice mommy and not a mean mommy" then we would be going to the gym, thank you very much. I DID have more downtime. I laughed regularly. For the first time in YEARS. I WAS able to take and pickup my kids from school. I had never before and never since had that luxury. The pure joy of seeing my boys' faces when I picked them up each day was worth the frequent melt-downs when I had to wake the 2 year old to go pick up the 4 year old. (How do we do these things and no one discusses it?) I learned lyrics to Disney movies instead of new treatment guidelines for diabetes. I never took the kids to school in my pajamas, but I suddenly realized why so many women did. I dropped ALL judgment of other mothers, because I was IN THE TRENCHES. I missed adult conversation. I missed feeling important- there - I said it. I lost my temper, and I raised my voice on occasion. Sadly... and this really does make me sad... I simply had not been around my babies enough HOURS of the day to really, really lose my patience with them. Not until I was home. Cutting coupons. Cutting Play-doh with tiny plastic scissors. And realizing that THIS was the real work. THIS was the important work. And so I sit here tonight with tears in my eyes.
One launched and doing well. One in middle school with puberty and insecurity competing for his time. One who still lets me hug him in front of his friends. And I don't know much more than I did 8 years ago when I walked in my boss's office overwhelmed and undone. I'm still in awe of and in love with those 3 beautiful minds and faces that call me Mom. But guilt? Will I wallow in guilt when I reflect over my presence in their lives? Maybe on a bad day. Maybe for a minute or two when I have a "mom fail." BUT I BEG OF YOU. OF ALL OF US. TO MAKE IT STOP. WE ARE WARRIORS IN OUR OWN RIGHT. WE KISS THE BOO-BOOS AND SCARE AWAY THE MONSTERS. WE QUIZ THE SIGHT WORDS AND TIE THE LACES. WE FEED THEM SOMETHING SEVERAL TIMES A DAY, AND WE ENSURE THEY ARE CLOTHED. WE ARE DOING THE BEST WE CAN. WE ARE FLAWED BUT PHENOMENAL. WE ARE IMPERFECT BUT IRREPLACEABLE. WE ARE MOTHERS. LET US UNITE AND HOLD SPACE FOR ONE ANOTHER. Godspeed. There is nothing worse than having a fight or flight response. It can last for hours once the adrenaline and cortisol dump into the bloodstream. It is bad enough when you have that response and you know what caused it, but imagine having that response without knowing what caused it. That can feel defeating and depleting. Since I have had too many panic attacks to count over the years, I have started to identify ways and places I feel safe. If I am able to get to one of these places, I can sometimes head off a panic attack or restore a calm mood. I hope you can start to identify your safe places and safe activities. For ME, my top 7 are:
I created a Power Hour with my husband 1-2 years ago. This hour from 7-8 pm is sacred and did not happen until at least 10 years into my marriage. There were lots of reasons we were not connecting regularly, but one of them was some strained family dynamics. I created this time and location so that we could start to connect regularly and so that other family members would respect that time we both needed so desperately. Naming what you need is so important. Deciding what will happen and when it will happen is paramount for consistency and expectations in a relationship. As I have said many times, I am not a licensed therapist.
When I found my AMAZING current therapist, one of the very first things she guided me to ask myself regularly was "do I feel safe?". I barely had time to stretch for 5 minutes a day, so how was I going to remember to ask myself if I feel safe? What in the world was she talking about? I soon realized that the simple, brief, piercing question "do I feel safe?" would become a huge turning point for healing in my life. Do I feel safe in this friendship? Do I feel safe in this marriage? Do I feel safe at work? Do I feel safe with just me, myself, and I? And if I don't feel safe, can I ask those that love me for what I need? Are there some strategies we could implement that would help me to feel safe? Do I need to close spend more time with those people and in those places that help me feel safe? Will that help me navigate the unavoidable situations where I do not feel safe? And most importantly, if I start to feel unsafe (which can sometimes lead to a panic attack), HOW can I get back to safety both mentally and physically? She freed up my LIFE when she explained that I don't have to "fix" whatever is making me feel unsafe. I just have to learn how to regulate my own body and get back to a place of calm and centeredness. Wow. Mic Drop. I don't have to fix it! I can't fix it! This is one of those posts I encourage you to read a few times and perhaps grab a pen and paper. Jot down the places and people who make you feel icky. Write down the people and places that make you feel GOOD. And try to stop focusing on fixing the first list. You can't fix it. Focus on spending more time in and around the second list. And find your seven ways and places to feel safe. Godspeed. In 2016, at the age of 40, I received a sarcoidosis diagnosis that rocked my entire world. My kids were 4, 6, and 14 at the time. I was at the pinnacle of my NP career, and I was coming off a 2 year "break" from full-time work. From 2014-2016 I was working 2 or 3 days a week and was able to spend more time with my family. I was also able to go to the gym regularly and prepare healthy meals. I felt like my health was also better than it had been in the past 7 years. My sarcoidosis symptoms started abruptly in September and were very noticeable. I would walk to my car that was parked on a hill after work and be extremely short of breath (think huffing and puffing as if I had just sprinted 100 yards). I would go to the gym and feel completely wiped out after 20 minutes of my workout when normally my full hour workout left me energized and not depleted. I would walk out of an exam room and forget the name of a medication or stop mid-sentence when trying to give my nurse a verbal order. I also felt very dizzy and lightheaded and was not sure what was causing all of my symptoms. I decided to go see my colleagues in cardiology once I realized my blood pressure was dropping. My blood pressure was dropping as low as 80s/50s. I was also having numbness and tingling in both arms and hands and my hands were turning blue. I thought there had to be some type of blockage or blood flow issue. Ultrasound evaluation of my carotid arteries and upper extremities were normal. EKG, basic labs, and chest x-ray were normal. My echocardiogram (heart ultrasound) was the first test that came back abnormal. It showed an elevated pressure reading between my heart and lungs (pulmonary hypertension). My providers were not really sure what would be causing that because I was "so healthy." I plugged along from early September to late September before seeking a second opinion. My symptoms were progressing and persistent, and I knew something was not right with my body. My fatigue was worsening to the point I would count down the hours until I could get into bed. My shortness of breath was limiting my daily activities and I was beginning to cough every time I ate or talked for more than a few minutes. I also had an episode while driving where the left side of my face went numb and my breathing became very shallow and irregular. That sent me straight to my second opinion! That second provider ordered a chest CT and a brain MRI which were performed on a Thursday morning. That following Monday in early October, I was at work for a 12-hour day. I received a phone call mid-morning from a nurse in my second opinion provider's office. The nurse said "you have brain lesions and you need to see a neurologist to rule out MS (multiple sclerosis). You also have enlarged lymph nodes throughout your chest and you need to see an oncologist to rule out lymphoma." As you can imagine, I was in shock and called my manager to tell her I needed to leave for the day and to go speak to my husband and my parents. Did I mention my youngest child was 4 years old? Fast forward to a bronchoscopy mid-October with lymph node and lung needle biopsy as well as a trip to a neurologist which resulted in EEG and extensive lab testing. My neurologist ordered more MRIs and tried to ease my fears of MS (though he could not totally rule MS out). My pulmonologist was unable to get a conclusive diagnosis from the bronchoscopy and recommended a mediastinoscopy which would involve drilling through my sternum (breastbone) to remove lymph node tissue for biopsy. I told him that I felt a large lymph node above my left clavicle and we opted to have that node excised for pathology instead of the mediastinoscopy. That left supraclavicular node excision was done the last week in November under general anesthesia at the hospital since it was so close to my carotid artery and jugular vein. That node biopsy was negative for lymphoma and positive for non-caseating granulomas (the definitive diagnosis for sarcoidosis). I was started on 60 mg of Prednisone per day that would be tapered over 6-12 months and referred to a rheumatologist.
After starting high dose Prednisone in December of 2016, I was placed on weekly Methotrexate injections which (who knew at the time?) would last another 4 years. The only reason I stopped Methotrexate is because I later developed psoriasis (for that story, click here). I was finally able to wean off prednisone late May 2017 though the side effects lingered at least another 6 months. I plan to write an entire post on surviving long-term prednisone, but I will leave it at that for now. 2017 seemed somewhat stable throughout the end of that year, but the next 3-4 years had their own hiccups. Over those next 3-4 years I found out that the sarcoidosis was affecting my esophagus. 3 EGDs in 6 months and tons of other GI testing led to the conclusion that my esophagus has no peristalsis ("squeeze'). The only thing helping my food reach my stomach is gravity. This makes eating challenging, especially talking while eating (cough, choke). I also found out I had sarcoidosis spleen lesions, ocular involvement, and another fun lung condition called bronchiectasis. For the esophageal involvement, I take 2 pills per day for life. For the bronchiectasis, I take one pill twice a day for life. See how I organize my meds here. I have also been tested and monitored for small fiber neuropathy. The MS surveillance continues. My neuropathy is currently of unknown etiology, but my neurologist does think sarcoid plays a role. I was also sent to endocrinology at one point to check for adrenal insufficiency after steroids since my blood sugar and blood pressure still bottom out at times. Another hiccup involved an overnight hospital stay and a kidney biopsy (ouch by the way) after I noticed my urine was foamy like dishwashing liquid (that is abnormal and a sign of protein in your urine- tell your provider if you ever see this). I'm on another daily pill to help protect my kidneys for that confirmed renal sarcoidosis. Every year I see a rheumatologist, general cardiologist, pulmonary hypertension cardiologist, pulmonologist, gastroenterologist, neurologist, ophthalmologist, dermatologist, nephrologist, and my PCP and Gyn. I now see a counselor regularly to help me process all that I juggle. I have mandatory quarterly labs, an annual heart ultrasound, CT's and MRI's every year, breathing tests every year, and whatever else comes up. Gone are the days of a routine wellness visit or not meeting my deductible. Gone are the days of only taking a multivitamin. I sleep with oxygen mainly for the pulmonary hypertension, and I'm okay with that. It was my little secret until now. Right now, my sarcoidosis seems fairly well-controlled with Humira. When I met my rheumatologist in 2016, he told me he hoped he could get me into remission within 2 years. That was 5 and a half years ago. I haven't given up hope and I will continue to fight this fight as long as I can.💜 Below, I have included two great visual aids to raise awareness for our family and friends. The mental health effects of sarcoidosis are widespread and often overlooked by our clinicians. Sometimes just "being there" is all we need from our loved ones. 💜
I hope this post has raised your awareness of sarcoidosis whether you are a patient, loved one, or healthcare professional. As I told a friend after she learned of my chronic illness, "My entire life changed after being diagnosed with sarcoidosis, but I didn't stop living." I hope this offers hope to anyone who is newly diagnosed or any sarcoidosis patient struggling right now. I see you. 💜 My husband owned a small lawn business for 13 years. While it definitely had it perks, he has since returned to working for a large corporation. Boy do I wish someone had told me all the things THEN that I know NOW about owning a small business- especially one in which services are sold versus products. Labor services at that. There was a steep learning curve for this NP, but it definitely added to my life experience and business savvy.
This post does not align with most of my content, BUT with mowers buzzing outside my window as spring marches on, it prompted me to reflect on those years in the lawn industry. I do not regret those years at all. They afforded me the opportunity to work part-time for 2 years when my boys were little. I was very proud of the services we provided, and I was extremely proud of my husband's efforts as a business owner and entrepreneur.
At the end of the day. At the end of my life. When I'm old and gray. When I'm free from strife. I will smile every time I remember your face. And no one can take that from us. Godspeed.
One of the most common questions I am asked during a wellness visit (routine physical) is "when should I get a colonoscopy?" . I was not asked this question as often 10 years ago or even 5 years ago, but there has finally been an increased awareness among the general population with colorectal cancer. As a former med/surg nurse, I took care of countless patients after their colonoscopy or even their colon resection for colon cancer. I helped care for their fresh colostomy site and stumbled to find the "right" words to give them comfort. I have one patient etched in my heart who lost his battle to CRC (colorectal cancer) at age 27. I was only 23 or 24 myself at that time. His young wife and 2 year old son stayed with him as much as they could. He had a suprapubic catheter (one that came out of his abdomen directly from his bladder to drain his urine) because the cancer had eaten through his entire pelvic cavity. I cried on my way home every time I took care of him. But I wanted to take care of him. I wanted him to see someone close to his age. Someone that didn't pity him like a child "poor dear" and all the other patronizing words I heard some of our senior nurses mumble. He and I would talk about TV shows and popular songs, whatever we could that would help him feel a little more "normal." This post isn't about him, it's about all of my patients. That said, I couldn't write this post without mentioning him because his life mattered and my time with him touched me forever. I could not write this post without telling you about another dear friend who lost his 6-year battle with CRC in 2020 at the age of 44. Out of love for his family, I will leave his story at that but HE MATTERED and MATTERS and cancer statistics are NOT just numbers my friends! They are mothers, fathers, sisters, brothers, sons, daughters, friends, employees, bosses, lovers, neighbors, coworkers, and beyond. The next time you see a cancer statistic on the news, I hope you pause and remember reading this post. So the question remains: When should I get a colonoscopy? In the words of my beloved GI colleague, "45 is the new 50!". The earlier CRC is found, the better the 5-year survival rate. We can easily remove a 5mm or smaller polyp in the colon and prevent it from ever becoming a malignant tumor. Yes there are some other screening tests on the market that have their place and time, BUT nothing beats a visual inspection by a well-trained eye looking for colon cancer. Direct visualization - there is nothing better!
The prep is not always "a gallon of nasty stuff" anymore either. There are a variety of prep techniques, so please don't let a colonoscopy prep prevent you from possibly saving your own life. You are NOT awake during the procedure. I have had one and I can tell you with certainty that I do not remember any of it AND I had zero soreness after the procedure. It was honestly a much-needed fantastic nap and a day off work. I urge you to see your PCP for a colonoscopy referral from a GI specialist if you are 45 years old or older and have never had one. If you have certain risk factors or family history, you should have a colonoscopy before age 45. Your PCP should be able to guide you. Any bright red rectal bleeding or alternating constipation and diarrhea needs to be worked up by your medical team. Please do not hesitate to seek care for those issues! I hope this answers your questions about colonoscopy screening. If polyps are found on your colonoscopy, your GI provider may want to repeat your scope in 2 years, 3 years, or 5 years depending on they type of polyp (per pathology diagnosis). If your colonoscopy is clear and there is no family history of CRC (or other extenuating risk factors), you will probably receive a 10-year pass. Most insurance companies pay very well for colonoscopy screening, BUT most insurances have a certain deductible each year that enrollees must meet, so do not be surprised when the procedure is not 100% free like your mammogram or pap smear was. Do not let cost stop you, though! It is well worth your insurance deductible. You can always call ahead to find out what your out-of-pocket expense will be, and most healthcare facilities offer payment arrangements. Please comment below if you have any other specific questions. There she is, bright red hair Big blue eyes, skin so fair All those freckles, my oh my Surely, she can never hide “Hey girl, hey”, the boys looked on Look at her with that black dress on But she’s not the same as the other girls She speaks her mind, she says big words You’re just a friend, Aim, it’s no big deal I can’t look at you as more, that’s just how I feel You’re one of the guys Aim, don’t get so mad Now why on Earth would that make you sad? Does she like me? Does she think I’m cute?!? All the boys would ask me about my friends in suit Will she date me? Can I make her mine? All the guys looked past me. I never crossed their mind. Should I play dumb? Should I change my ways? Am I that unattractive? Am I just that plain? I could dye my hair. I could bat my eyes. I could try to say less. I could minimize Myself for them. I would do it, I would. If I act helpless or scared, will that make me good Enough to touch and think about at night? Because I can change, I can dim my light Think small, do less, don’t let the boys see That you are the QUEEN, Her Majesty Just play it cool, don’t reveal your Ace Giggle at their jokes, soften up your face All the boys like a damsel in distress Stop keeping it clean, try to create a mess They can rush in and "fix" and make things nice Let them be the best; don’t forget they’re always right Change is hard, you know – it’s okay to cry I don’t cry though boys – I’m just one of the guys If I’m being honest, I’m more like you than them I’m an Alpha with a D cup bra, where does that fit in? Yeah, I said it, I can say it, I’m tired of playing along This is my little poem, this is my Fight Song I am done with placating; I am done being small This is me, Smart and Driven, this is me, Curves and Gall I will no longer apologize for my strength I will face you head-on, I do not hesitate There she is, bright red hair Big blue eyes, skin so fair photo credit: www.gretchenrubin.com Gretchen Rubin is an author, podcaster, mom, wife, lifelong learner whom began her career as a lawyer. I have read 4 of her books and saw her at a live event in Atlanta in 2019. I listen to her podcast when I can, and I love her curiosity about life, community, relationships, and self. Gretchen developed a framework from which she thinks people are motivated and then named the 4 tendencies based upon said motivations. Gretchen's 4 Tendencies are:
More about each of the 4 Tendencies:
I asked my parents, spouse, and oldest child to take the quiz so that I can better understand what motivates them. Knowing the tendency of someone you love has made a difference in my life. If that person is not easily motivated by external forces, then I may realize that my actions may not affect their efforts whatsoever. If the ARE motivated by external sources, I take that into consideration before asking them to do something. Jan 30, 2021- Feb 3, 2021 Red, painful eyes start with painful vision and light sensitivity (UVEITIS). Feb 3, 2020-Feb 8, 2020 Tiny dots of a rash begin on my neck- they don't itch, burn, or hurt at this point. I call my dermatologist to schedule a biopsy, assuming this must be related to my sarcoidosis. Feb 3-March 8, 2021 Rash kept getting bigger and more painful. Not responding to topical Rx creams. Went for 2nd biopsy on March 8th, the day I started my 30-day medical leave. Focused on walking, sleeping, hydrating, and eating clean. Also journaling and resting. March 8-April 8, 2021 Off work. Tried the AIP Diet. No gluten, no dairy, no sugar. Derm and Rheum also put heads together to double my Methotrexate dose. The diet was difficult but my joints and skin "felt" better even though my skin still needed lots of help! April 8- August 8, 2021 Back at work. Still working covid. Boys off for the summer during some of that time. Started Humira in May 2021 and stopped Methotrexate. Skin would wax and wane, but I would say it eventually cleared by early to mid-August. Joints feel much better on Humira. Energy level too. September 2021 Had my 2nd episode of uveitis. That responded quickly to Prednisone eye drops. Skin pretty clear, but under more stress with some work and family stuff. Delta variant of covid is ravaging my patient population and friends. Evidence of proteinuria again so will follow-up with my nephrologist (that's more sarc-related, less psoriasis-related). Still on Humira. Echo and PFT's slightly worse than last year, but lung & spleen CT's show that the Humira is controlling my sarcoidosis. March 2022 I have had at least 2 more episodes of uveitis since the last update. Skin stays mostly clear with the occasional flare in the anterior portion (front) of my neck. I wrote this piece for all of my fellow Psoriasis Warriors who are walking this painful, lonely road. It is SO HARD. One can think they are not a vain person, but when your LARGEST ORGAN (your skin) is literally on fire with inflammation, it's hard to "hide" from vanity, comparison, self-loathing, and frustration. If you love someone with psoriasis, please share this with them and with others who love them. I hope it brings someone comfort to know they are not alone and that there are those people who will love us no matter what. Monthly meal planning has taken me YEARS to develop. One thing to note is that there are 3 adults rotating the cooking in my family. My parents live 2 doors down from us and we decided many years ago that it was easier to feed 7 than 2 (for them) and that mom didn't mind cooking for 7 twice a week if it meant she and dad would be fed by us several nights per week. Some weeks that looks different. Since my husband and I both commute about an hour each way to our jobs, and he works night shift, my mom may have to cook 3 times some weeks. Kids' sports and school activities can also affect our cooking rotation. Let's look at monthly meal planning with a few good tips or rules to get you started:
Now let's look at each question in more detail:
Pro tip: track what you are currently eating for a week or two as you are mentally preparing yourself to begin this process. Just like "getting on a budget" - it is extremely helpful to see what you are currently eating as a family. If you are eating out 5 out of 7 nights, it is unfair to expect you will start cooking 5 out of 7 nights immediately. That is a recipe for disaster! Pun intended! Maybe try cooking 3 nights at first. START SMALL! Good luck and just remember: it doesn't have to be fancy, it just has to be planned. Photo Credit: Annie Spratt I was eager and he was young I was ready but he was numb I was happy and he was still I was hopeful but he was nil We had some laughs We had some smiles I read to him at night Does he remember those times? Then I had his brothers and he backed away or did I hedge him out? who could truly say? Come to me sweet boy not you, I mean him I mean all 3 of you silly I mean all of 3 of them It's different they all say he's not your blood Is it different? Aren't they all different? It's clouded. It's mud. I'm stuck and he's stuck. He looks and I look. We smile and they smile. I ache and he aches. We give and we take and sometimes it all breaks. His daddy can't get it. How could he? It's pointless. But I have to get it. And do it. And "go on, sis" Keep going. Keep numbing. I didn't know it. He didn't know it. We didn't know it but we did it and here we are and we are in it. So I look at him, a product as much of me as his dad. And I don't know what to do with it. I have these other 2 on my tab. The deductions, subtractions, additions?, conditions? It's all hard and whoever says that it isn't just ISN'T telling the truth dear. See I try to be real. He's "not mine" but I'm his and we're each other's and how does that feel? Would I change it? Some days I would. In a heartbeat. Not a second thought. But does he need me and do I need him and are we better because we came together when we were both broken and wounded and bleeding and cold Now we're mending and warmer and dare I say, a little old. Was it easy? It's been the hardest thing I've ever done. It can push 2 lovers apart quicker than any weapon, any gun, any bullet to the heart that's how some moments felt I have wept, I have wailed, I have screamed, I have knelt But one day his daddy may find out what it took to hold it ALL together and to remain unshook in the quake of dysfunction and abandonment and grief of a sweet little boy looking helplessly at me. She didn't stay, sweet baby, and I'm so sorry. I can't explain it. But I'm here and I'm not leaving, and I promise - I wouldn't change it. To every little boy or every little girl who had a mama or a daddy step up outside of the DNA lines. This is to you dear ones and to the strong adults who have rearranged their hearts and lives for you. We wouldn't change it. |