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The Princess and The Prosthetic

Riding the Waves of Grief….

June 17, 2019 in Motherhood, Warrior Princess - 1 Comment

There is a unique kind of grief that comes along with being the mama of a child with special needs. For me, the grief has come in waves.  At the beginning, they were threatening to overtake me–constantly pulling me underwater while at other times softly ebbing and flowing–giving me the chance to get my head above water. 

I would be lying if I said I didn’t imagine how our life would be once Callie was born.  Big, grandiose, elaborate dreams.

And then life sidelined us.  Knocked us off the path that I had dreamed of and planned for us.  Onto this completely new path.  And the path it knocked us onto?  It turned out it was much harder, scarier, and we didn’t have a damn map for it.  No one we knew had walked the path before and we were alone on it.  Lost.

I grieved for small things.  I didn’t get to take maternity pictures with Callie because she was born so early.  After she was born if I saw a beautiful maternity photo session, it would send me into a tailspin of depression.  We didn’t get to send out a birth announcement or do newborn photos because Callie spent the first three months of her life in the NICU.  Getting birth announcements in the mail for the first few years would gut me.  The beautiful pictures marking another family’s joyous arrival of their healthy baby would rip me apart inside and I would have to quickly throw them in the trash to not have a physical reminder.  A reminder of what we didn’t get to have and what the first few months of Callie’s life was not……seeing other baby’s first steps, healthy baby milestone check ups, first soccer games, cheer camps, and learning to swim.  Even hearing about others normal daily lives would bring it on.  Seeing other kids running to their mamas.  Kids jumping into swiming pools.  All triggered waves of grief.  Grief for an experience we didn’t get to have like everyone else.

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It has taken me years to understand that it’s ok to grieve for what I thought would be……and isn’t.  I used to pair the grief with guilt.  How could I grieve for something when it’s Callie who has to deal with this stuff?  Could it have been my fault we are even dealing with this in the first place?  Why was I still upset years later?  Shouldn’t I have been able to move past it by now?  How can I be grief stricken when we have been so blessed?

The grief isn’t something that will end and I know that now.  I know that sometimes the tides will rush in to overtake me, slamming against me with incredible force.  Other times, they will lap at my feet and then recede quietly.  Sometimes I will go for months without thinking about it and other times we will simply have a bad day.  It could be an anniversary of a surgery, I will see something on social media, or we will just have a life experience that we have to deal with and boom.  The tide swells and grief is ignited.  I’m swept out to sea fighting to keep my head above water.  Now I understand that it doesn’t make me a bad mama or mean I love our little miracle any less.  It’s an emotion that I acknowledge……and then bounce back.

Because ultimately, that’s what life is about.  The bounce back.  When you are getting knocked down and drug out……it’s the times that you stand up that are important.  It’s the realization that this is now the path that you are on……and you have to own it.  You have to bloom in the garden that you’ve been planted in.  You can acknowledge the grief….but you can’t drown in it.  It’s the realization that its not the choices we’ve been given but how we react to them.  It’s the realization that I’m not invincible but we are resilient.  It’s the realization that we aren’t inspiring others because we have the perfect lives.  We are inspiring people with how we deal with our perfectly imperfect lives.  It’s the realization that all of these scars we are collecting are giving us a greater gift–the strength, courage, and tenacity to overcome them.  It’s the realization that comparison is the thief of joy and learning that our milestones and triumphs may be different than others–but none the less special.  It’s the realization that we were blessed with a little wildflower among a field of roses.  Some days it storms, and some days it shines.  This……. is how flowers grow.  And it’s time to BLOOM.

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Jaime

Hi everyone! Thanks so much for stopping by! My name is Jaime! Wife to my better half, James, who is my moon and all of my stars. We are parents to our little warrior princess, Callie Grace. We started this blog to share our journey as we navigate through our crazy beautiful life. Callie is a lower limb amputee and I am a Type One Diabetic. We are hoping to change the face of beauty one step at a time! We hope by sharing our story, you leave with a little bit more inspiration and hope! Thank you so much for stopping by and joining our tribe!

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    About Me

    About Me

    Jaime

    Hi Y'all! I’m Jaime, a proud working mama, author, girl boss and wifey to an ultra-adorable husband. I am a huge book nerd, I drink coffee like my life depends on it, and run on dry shampoo and Amazon Prime. Leopard print is my favorite color. I am a story teller at heart and this blog is a virtual scrapbook of our crazy beautiful life. I'm a Type One Diabetic and our little warrior princess Callie is a lower limb amputee. By sharing how we’ve chosen to flourish in the garden we’ve been planted in, we hope you can take some small nuggets of hope, inspiration, and laughter. We are so grateful that you’ve found us—welcome to the fam. We embrace our perfectly imperfect lives and don’t let the doctor’s appointments, spreadsheets, speaking engagements, 10th birthday parties to plan, housework or date nights overwhelm us. Those things are just the beautiful reminders of all the blessings in our lives. Read More

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