My day had started like any other, I was up at 5 packing lunches and backpacks, while trying to gulp down some coffee. I had an appointment at the office later, so I spent a few minutes standing in front of my closet perplexed and sighing. I looked in the mirror, briefly noting the major damage 40 plus years and nightly interrupted sleep can bring. Finally, by 7 am, we were all dressed and ready, so we hit the road to drop Zoe’s big sister O, at her school first.
Later, it was just Zoe and I in the car. The sun was streaming through the car windows, the radio was on and I was trying to make Zoe laugh.. we were singing to the music and making small talk about her day.
I am used to the starts and stops in our frequent conversation. Zoe, almost 10 now, is a thinker- yet she slowly forms her thoughts, chooses her words and processes it into speech. There are pauses as she searches for the word she wants, and fatigue can slow the pace, slur the word . Remembering all the years she could barely even communicate, I wait patiently and am still grateful each time she begins to speak.
Her thoughts come in word pieces and listening carefully, I fit the puzzle together ..
“ Mom, when I grow up and become a Mom, would this be a good car for me to drive and how do you learn to be a Mom anyway?” There it is, her question. And suddenly it’s as if the clouds have pushed the sun away, and my daily “ cup half full" approach to life has been smashed to hell. Zoe can't see my face, and I am glad. I don't want her to know the raw pain that is causing me to to hold my breath .
My girl is growing up, and thoughts of the future, are naturally close ,more menacing than when she was 3 or 5, and although she is an awesome kid doing amazingly well- she still has a progressive metabolic disease. She still has generalized epilepsy, kidney disease and although she grows more steady with the growing size of her body- she uses a wheelchair and a walker to discover and experience her world.
What I couldn’t say to Zoe is that with her vulnerabilities I can’t imagine her “ being a mom”- that her physical impairments alone ,will prevent her from ever driving a car. I refuse to even contemplate the complex medical conversations we have had about Zoe’s life expectancy, we just don’t go there.
Yet this reality is what sometimes separates me from other Mom’s. Tragedies that take kids too soon are always unexpected. As busy Mom’s we just forget that we are all fragile. We sometmes forget that the messy room, the lapse in homework , the bad grade -aren’t the important things about mothering.
In the last few months, my local community of special needs families have lost two girls, and this loss hits close to home. These girls were very close to Zoe’s age, with some similar issues. These families were fighting, and winning. Their kids survived surgeries, hospitalizations, and the everyday challenges that often come with raising a special needs kid. These parents were managing their kids health, their kids were stable, even improving with therapies. Their parents were seeking refuge in that stability that meant success-until the day their kids weren’t stable. Until one day their physical vulnerabilities were cause for taking their child’s life, and they were just gone.
I am guilty of doing it too sometimes. Getting caught up in the day to day. Zoe is doing well, we are managing , we are “winning” and then an illness comes along, a medical test, or a conversation like this one Zoe and I shared - and reality comes crashing through, grounding me again to what is really important.
And it’s this reality , that I wish every mom knew. It sounds harsh, I know.. - but it’s a secret that special needs moms have learned along the way. It’s something that I think all Mom's should know, or just think about sometime. That all that other stuff- just really doesn’t matter.
Let your KIDS be that sunshine that lights your soul and commit to really love your kids, love like they are the MOST important , love with the heartbreaking pain that comes with it. LOVE your kids, as if they were dying.

I will have to consider addressing this on my site. Hadn't thought about how this would affect divorceing parents.
Posted by: Eddie Holland | May 17, 2012 at 09:41 PM
I just happened to Google "special needs mom" today as I was having one of those moments where I just needed to identify with another mother in my world. Excellent post! Those 'stable' moments are infrequent in my household of twins with different special needs. I wonder, on a daily basis, what it might feel like just to 'breathe' and relax. Living in constant high alert / no sleep / too much to do - well, as we all know it's exhausting. In my 'special need' circle, not many of the kids have the ongoing medical issues of my daughter. They do not identify with the possibility of losing their child - we're on 40+ procedures... I live my life day to day; Evaluate each day at the end of the day and prepare for the next day. Again, excellent post!
Posted by: Mom of Twins in VA | February 19, 2012 at 11:18 AM
What a lovely and heartfelt post. Every parent would be better for reading it.
Posted by: Lisa | February 18, 2012 at 05:26 AM
This is a theme that is important for all parents- of special needs children or not. Thank you so much for sharing you sweet daughter with us.
Posted by: Mary Lauren @My3LittleBirds | February 17, 2012 at 11:49 AM
Junkman's Daughter in Atlanta kicked a family of a medically fragile 3 year old child out of their store because they cannot walk and the child was too heavy for the parents to carry.
The following took place over the weekend.
"We went to a store called junkman's daughter today. They said my son was not allowed in the store because he could not get up and walk, no strollers allowed. The people shopping that heard left because they were upset he was not allowed in. I wish i could get them to change their mind. I used to really like the store. I explained to the manager, I can't carry him because he is almost 3. I told them his wheel chair is big and bulky so we try to use his stroller as much as we can. He can not even sit up on his own. We have a handicapped pass also but they didn't care"
http://www.change.org/petitions/junkmans-daughter-please-allow-special-needs-kids-to-use-medical-strollers-in-your-stores
Posted by: special needs mom | February 13, 2012 at 10:09 AM
This was such a beautiful post. I became curious after reading it about how you answered her question. Do you project her, conversationally, into a future where anything is possible?
Posted by: Rachel | February 13, 2012 at 03:06 AM
Hello. My name is Allison Carmen and I just posted a comment about your post on blogstar. thank you for your courage and strength to share what is in your heart so all of us can open our hearts more to life and to our children. There is a book that you might find interesting to read. It is call The Tibetan Book of Living and Dying by Sogyal Rinpoche. It makes us see that our relationship with death and uncertainty dictates how we live. It helps us see and hold the precious moment we are in.
Posted by: Allison Carmen | February 12, 2012 at 09:40 AM