Everyone had questions about bus schedules, school forms and cafeteria lunches. Everyone tried to keep one eye on their children while maintaining appropriate eye contact with the teachers providing answers. Everyone forgot half the questions they wanted to ask as well as each other’s names seconds after every awkward handshake.

And since I had to bring my two year old twins along for the ride, I was probably the worst of the overwhelmed, overstimulated bunch. But there was one conversation that didn’t end with the tug of a small hand or the sudden realization that a child was no longer visible.

I met one woman who tugged at my heart with her obvious loneliness and her own perceived invisibility. Her need for connection and understanding was palpable. And I recognized all of this in her pleasant smile and bright small talk because I have felt all of the same things myself.

I too have a special needs child.

All parents of children with special needs have felt alone and confused. And we all need to find others. People just like us, who know what it’s like to watch other children effortlessly join playground games and amaze grownups with their precocious conversation. We’ve all been on the other side of that social fence, blending in like chameleons. Hoping that no one notices our own child’s challenges and questions them. Or worse – makes uninformed excuses for them.

I listened to this woman’s story about how friends she’s had since childhood now avoid her. They have typical children and no tolerance for her son’s “bad” behavior. They either don’t want to put up with it, or possibly they just feel uncomfortable around her. But the outcome is the same. She is alone. She doesn’t fit in with them anymore.

I gave her my phone number and told her to call me any time. Maybe we could have a play date since her son and my twins are very close in age. My twins are what I’ve learned to call “typical,” but I have no fear of exposing them to a child who isn’t. They live with one already. And I know how much that little boy, like his mother will need friends who understand.

Oliver is four years old and has been in Fairfax County’s special preschool program since he was two. Looking back, I realize how incredibly lucky we were to find out about his delays so early on.

He was our first baby, so we had no means of comparison. Sure, we have plenty of friends with children the same age, but when they’re so little, those differences can easily be explained away. You can say that all babies develop at different rates (true) and that their very unique personalities would encourage different areas of strength (also true). But without that personal experience of watching another child grow and learn, you just don’t have that instinct that tells you “something isn’t right this time.”

Some mothers claim that even without older children, they just knew. But I looked at my big (and I mean HUGE), healthy 18 month old and thought he was fine. In fact, I thought he was better than just fine. I thought he was beautiful, wonderful…miraculous. And he was…he is. But he does have significant speech and social delays.

He did then too. But he was so young. And so much could be explained away. AND he had just become a big brother to newborn twins.

What child wouldn’t withdraw, act out and even regress a little? So what if he didn’t quite fit in with the others? His whole world had been turned upside down. Of course it affected him. It all seemed pretty normal to me. But months later I had to admit that he just wasn’t catching up. He wasn’t like my friends’ “normal” toddlers.

With some prompting from concerned relatives, we took him to a private child psychologist who established that he was in fact very delayed and would benefit from early intervention as soon as possible.

Then we got smart and started talking to people. We discovered that there were county funded programs for special needs children (although we weren’t actually using that term yet…not yet…) And we contacted Child Find.

We learned that we never needed to pay for that first round of testing since our tax dollars afforded us free services. But of course this is the lot of special needs parents – to continually learn what we didn’t have to do, what we should have done, what we could have given our child, but just didn’t know…

But we quickly learn to move on from that and not beat ourselves up. Or at least we try.

It’s hard to accept this inability to identify your child’s need. Your baby cries and you feed him, change him or hold him. He gets sick and you take him to the doctor. He grows and you buy him new clothes. Your job is to meet these needs. Any and all needs. It is your new reason for being. The most important job you’ll ever have.

And then, one day you find that you failed.

But these new needs allow no room for self flagellation. There is too much to learn and do. And to waste time on guilt seems pretty selfish.

So does the new source of anxiety for a special needs parent: the fact that you no longer fit in either.

Special needs don’t start and end with the child. They are part of the family as a whole. You become a group of misfits. A band of intrepid explorers, thrust into uncharted territory without a map or a compass. All families are different, as are the journeys they take together – so no one gets a guide. Survival hinges on everyone doing their part. Loyalty to the team is imperative. There are no solo missions.

Unfortunately, the leaders rarely volunteer for the post. It’s the lottery ticket that no one really wanted or expected. And not one of us could claim to be instantly skillful team captains. Basically – it all really sucks, and our initial reaction is to avoid ever leaving the ship.

Suddenly the voice mail from a friend wanting to set up a play date doesn’t make you smile and run to check your calendar. It makes you begin the endless cycle of “what if” worrying: “What if he doesn’t want to be there and cries? What if he plays rough and hurts the other child? What if he refuses to listen to me and I have to go through the motions of yet another ineffectual time out, just to look like I’m TRYING to be a good parent?” And the deepest, darkest of worries – the one we so rarely speak aloud: “What if he embarrasses me?”

It’s so tempting to go for the isolation option. To stick with your own kind.

But all of that changes when you meet other special needs families. It’s so comforting to be with the other misfits. They get it. They don’t look uncomfortable when your son is rolling around on the ground. Or kicking up dust clouds without any regard for the people next to him. Or pushing other children to get their attention. They don’t assume that his age or size would make him more mature. They don’t assume anything. They just smile and nod. There’s no need for words. They just know. We all know.

And that is what special preschool has become for me. A safe haven. An oasis in a desolate landscape. A private island where no one gets voted off. Acceptance is mandatory. In fact, it’s second nature.

The children get the special services they so desperately need, but they also become part of a community. They meet children with the same challenges, with worse delays, with higher functionality and with very limited scope for improvement. They are all misfits. All broken to one degree or another. But all deserving of love and appreciation.

They are safe on their island, and they are loved. Their needs are recognized and prioritized, and their triumphs – no matter how small – are celebrated.

The parents spend no more time in the special preschool classroom than do parents of children in private preschools. But our hearts are there every second of the day. And not just in the expected way that parents claim to leave a piece of themselves behind at drop off. For those of us with special needs kids, those classrooms aren’t just a place for learning – they are a place for hope.

And oh – but isn’t that the most beautiful, terrible, spirit lifting, soul crushing, incandescent word that a parent can say, feel, pray….”hope.”

Because that’s what it boils down to in the end. We sit on that island with our polka dots and square wheels and inability to fly and our…what exactly was wrong with that doll again? I never did understand that one… But we all sit there together. And we hope.

Together.

Which is the opposite of alone.

But it doesn’t end there. It can’t. Because hope isn’t enough. You can’t live on an island.

It’s nice to have a port in a storm, but we all live in the real world where (to really beat a metaphor to death) it isn’t always smooth sailing. People are unkind. They are busy and cranky, and they would rather gossip than research. The real world isn’t perfect and neither are the people in it.

Which brings up an interesting point: no one is perfect.

No child is perfect. No parent is perfect. No family is perfect.

We’re all flawed. We’ve all felt like outsiders at one time time or another. We’ve all felt lonely – even invisible. So in a way, we’re all misfits. Atypical.

And what defines typical anyway? I think it’s simply a majority rule. But a majority based on sweeping generalizations.

Which is fair. Because who has time for case by case living?

But I would ask one thing of the more typical misfits out there. Please try to make time for compassion.

Don’t assume that a child is “bad” based on their behavior. Don’t assume that their parents aren’t trying. Don’t assume anything.

You never know when you might be on that side of that fence. And when you are, you’ll appreciate a little empathy. Not sympathy – never sympathy – but an acknowledgement that things are usually more complicated than they appear. Something that everyone knows from personal experience.

Your polka dots may not match my square wheels. In fact, you probably look like that totally normal doll (I think she may have had a psychological problem?) But we’re all misfits in our own way. And you should make a little time to recognize this.

Because it takes one to know one.