Grief, what should have been and what never will be.

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Grief, we typically equate it to the loss of a person. Grief that is the loss of what was or should be is like a wave you see coming but can’t avoid. It knocks you down with one fell swoop, dragging you out to sea, you are left fighting your way back to shore, yet finding nothing looks quite as you thought it did once get there. I know that grief all too well, it’s the wave that is called your child’s diagnosis.

We, parents of children who live with disabilities or medical complexities, are often sent out to sea in one quick fell swoop, our head’s bobbing, gasping for air. We find the will to swim, often alone, until the rescue boat that is other medically complex parents pulls you aboard, landing on an opposite shore.

You see grief in medically complex parenting comes in waves, you learn to brace for impact, there are times you are pulled out to sea and there are times your feet dig so far in the sand that nothing can bring you down. But it’s the waves of childhood milestones that hit the hardest.

Middle School. I knew it would hit hard, nonetheless I wasn’t quite prepared. It’s THAT wave, the one that came in gently but it knocked me down, I was sent out to sea once again. This time head bobbing, smiling though screaming, too far out for anyone to hear the cries for help. As I’ve listened to other parents whose children have also entered new stages I’m reminded of the nevers, the most likely nots and the harsh reality of epilepsy.

You are battling your way through the nuances of adolescent parenting. I’m grieving not getting to experience those normalcies.

You are worried that the ice cream shop moved making the walk there not as safe, I’m wishing that my kid could just walk there at all with friends.

You are letting go, allowing your kid to go out to lunch sans parents. I’m wishing I didn’t have to be there all the time, giving my kid freedom and independence.

You snuck away for a quick dinner out with your spouse, your kid is now at the age they can be alone for a few hours. My kid will NEVER get to be alone.

Friday night football games, middle school dances, clubs or organized activities sans Mom…the list of nevers and most likely nots goes on and on.

Every new phase of life I’m faced with a new different wave of grief. I’m reminded that my child who lives with a disability doesn’t get “normal”, therefore as a parent neither do I and sometimes I feel robbed. Robbed because I know “normal”, I lived it, but she likely never will. Robbed because “normal” parenting to me includes administering daily medications, tracking seizures, scheduling appointments with a lengthy list of doctors and specialists, making sure an IEP is being followed and trying to find camps and activities that don’t shy away the minute they hear the word epilepsy.

As the waves of grief roll in, I am reminded, I swam to shore before. The grief though, it’s not left out there, it comes back with you, it stays with you, it lives in you. You learn that normal is subjective and though others aren’t navigating the same treacherous waters as you are, they are navigating. Those parents on the boat that picked you up along the way, those are the ones who will hear your silent screams, they too know the same grief of what should have been and what never will be.

*Disclaimer – Grief, is incredibly personal. I do not know the grief that comes with a loss of a child that so many in my epilepsy community do. I do however admire and keep them in my heart.

Secondly, this is not to say adolescent parenting isn’t HARD, I am watching those around me battle through. Often when I share these types of posts they are met with “the grass is always greener”, I can assure you the grass on this side isn’t the place you would rather be.*

Seasons of Change

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Seasons change. Every four months we anticipate the renewal of spring, the warmth of summer, the crispness of fall and the cold, cozy days of winter. The shifts come and we embrace them.

Yet, when the seasons of our lives shift, it’s often met with anxiety and trepidation. In one short week a shift will happen in our home. From little girl in elementary school to tween in middle school. There is much anxiety around this shift. The soon-to-be middle schooler has no desire to leave the bubble of elementary school, does not want new teachers or therapists and is beyond nervous to meet new kids. Yet, I don’t see a little girl anymore, she’s taller, more independent and often times full of sass. The Mom of said soon-to-be middle schooler is anticipating a lot of time spent educating a new group of educators on what epilepsy, cerebral palsy and disability looks like for my child. Yet, this isn’t my first rodeo, I am comfortable in my skin as an advocate.

The season of my own life, or should I say decade, changed a mere two months prior to the pandemic. I met 40 with fear and quite honestly regret. The decade prior brought motherhood that threw me for a loop. I became a mother, a caregiver, an expert on my child’s medical and educational needs, an advocate, and threw myself into volunteering for everything possible related to Reagan, mainly so she could participate with her peers. All things I’m incredibly proud of, yet none of those things were solely for me. While I would never go back and change putting my medically complex child’s needs first, I would have advocated better for myself, asked for more help and found a way to not lose focus on my own hopes and dreams.

I’ve shifted my mindset recently. I’ve made the conscious choice that not every decision will be made solely for Reagan but also with my own interests and sanity in mind. All while knowing I’ll never be the “put your own oxygen mask first Mom” and accepting it none the less.

We are both a bit in denial, trying to get a grasp on the changes ahead. I hope to walk hand in hand with my tween (while she’ll still hold my hand) into this next season with grace and understanding that all the seasons before prepared us for this one. Seasons of change are inevitable, true shifts happen when we embrace them.

*To all the early-to-mid-to-late-fourties’ Mamas going through the tween and teen years with your kids, while reclaiming and owning your own life’s path and purpose, I see you and walk with you into this season. Also, who thought this was a good idea?! #allthehormones*

Self Care and the Caregiver

April 16, 2021April 16, 2021 ~ erinmonast ~ Leave a comment

Self care it’s the hot topic these days. I’m constantly hearing things like take time for yourself, put your own oxygen mask on first or you need to be the best version of yourself for your child. Moms, we are the last ones to put ourselves first, I saw this first hand growing up with a single Mom, raising three girls. Add a child or children living with complex medical and educational needs, your title soon expands from Mom to nurse, teacher, advocate and caregiver and your own needs fall even further down the list.

As a trained yoga instructor, I know the importance of self care, in fact yoga helped me cope with Reagan’s diagnosis early on. It’s the application of self care that is a true challenge.

When I started this post in January of 2020, Reagan was in a place of stability for the very first time. A place where we were not at the pediatricians office every other week. A place where the school nurse wasn’t calling me multiple times a week. A place where medications weren’t being changed every few months. A place where we didn’t live in a constant state of panic. While much of that holds true still, we aren’t in that same space of seizure freedom. The pandemic added the stress of virtual schooling, loss of services and keeping Reagan healthy.

Leading up to 2020 we pushed, we added on, we doubled up. We did all the stuff. It paid off, Reagan benefited in ways I couldn’t even dream of. In doing all this, I realized the person who fell behind was me.

My two to three days of yoga slowly started to phase out making way for more therapies, appointments and even cheerleading. The once a week yoga class I taught was replaced by swim lessons, since every other night was already booked. My weight fluctuated as I let pizza and chicken cheesesteaks sneak back in because I was too tired to make healthy meals after hours of Keto prep. My hair speckled with grays and lines have creased my forehead. My body and mind are fatigued, the emotion that lies behind all the “stuff” is draining and all consuming.

You see self care is easier said than done, especially when there are complexities to your life that take precedent.

I didn’t take the best care of myself , I didn’t do all the things I wanted to do before I turned 40, I didn’t do anything for me. And I was more than okay with it because Reagan was thriving (and even with break through seizures, still is). I was okay until I wasn’t.

In the past six months I’ve found myself in the emergency room twice and at more doctors appointments than I can count. The general diagnosis was this….”you have stress and anxiety and need to dedicate time to yourself”. Now, there are a few really fun (sense the sarcasm) underlying female things going on as well (hello perimenopause at 41), some that require every six month checkups but at the core was stress and anxiety. I think any “special needs”, medically complex parent can relate.

This isn’t “oh a pandemic happened”, this has been going on for years and it finally came to a head. Looking back I never asked for help, I just kept plowing through. Travis and I haven’t been away just the two of us for even an over night in well over three years, maybe more and I can count the amount of date nights on one hand. I didn’t ask for help out of fear. Fear of not being there for Reagan. Fear someone else wouldn’t be able to handle all the stuff. Fear a seizure would happen and I wouldn’t be there. Fear a seizure would happen and whomever was with her would experience the same trauma I did after witnessing her first seizure.

I also didn’t ask for help because I didn’t realize I needed it. Sometimes help comes in the form of letting go of what doesn’t serve you. I’ve let go of a job that caused undue stress, I’m learning to say no, I’m learning to see things as they are and not as they should be. I’m learning that self care doesn’t just happen on Sundays in the form of a bubble bath and face mask. Self care is doing the things that make you, feel more like you.

This post isn’t for pity, it is a cautionary tale for those living in this world. In the midst of doctors appointments, specialists, new diagnosis’s, therapies, IEP meetings, etc., make space for yourself, for your spouse, for the person you were before this crazy ride.

This post sat dormant for well over year, a year that I lost, don’t lose the year, don’t lose yourself.

Just Breathe

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I remember the day so vividly, not the date or the year, just the day. I hadn’t been practicing yoga that long and wasn’t really into all the quotes and mediation stuff, I was simply trying to take back a bit of myself after the first few years of motherhood. The teacher started the class by saying, “Our minds don’t let go of trauma until our bodies do, take a deep breath and let it all go”. It was in that moment that I realized I had been carrying the trauma from Reagan’s early and scary birth with me. I had been carrying the guilt of her diagnoses, because she lost oxygen during some point of my pregnancy. I had been silently grieving motherhood knowing it would never be what I had envisioned. I never viewed this as trauma, until that moment and knew it was time to let them go.

For the first few years of Reagan’s life I swore off any type of physical activity, I felt guilty that my body was so easily able to do things and hers was not. If she couldn’t do these these things than I shouldn’t either. As she started to walk around two years of age, I slowly gave myself permission to get back out there. I started practicing more and the opportunity came about to attend a 200 hour teacher training with my sister (who was already teaching and running a studio). I thought sure, but I will never ever teach a class, this will just be a great opportunity to learn more. I spent a few months diving into poses, breathing techniques and learning about myself and fellow teacher trainers.

Over the years I have had to step away from my practice, first when I had a surgery that was necessary but solidified our family would remain just the three of us. And a year later another surgery which proved to be my saving grace, sparing me from something much more serious. During one of the surgeries I remember asking if I could have a moment to breathe, you know those really deep calming belly breaths?! I vaguely remember the anesthesiologist saying he felt calm just watching me. I found my way back to my mat eventually after recoveries that were most likely easier due to my yoga practice.

Most recently, last year I stepped away from my practice because Reagan needed me more. With age, her academic and physical demands are greater leading to more therapies and doctors appointments. And when she started the ketogenic diet, there was absolutely no room for error. Though a challenge for me personally it was the right decision, as Reagan thrived and made the most gains she has in years. This year with all the craziness of the pandemic, I have finally found myself back on my mat a lot more, often times with a partner in tow.

The physical practice of yoga lead me to a mental practice of learning when to let go, to breathe through discomfort and the importance of finding one thing that you can turn to. And while I swore I would never teach a single class, I did, and not just one, more than I can count (though I did take a break from teaching at the same I stepped away from my practice last year). The most beautiful part of my practice has been sharing it with Reagan. All those years I worried about what she wouldn’t be able to do, I never thought about what she could. Through Reagan I have learned that truly yoga is for every body. There is beauty in the ability to find stillness, grounding and peace.