WHY WE’RE HERE

Our son was diagnosed with ATR-X (alpha thalassemia intellectual disability x-linked syndrome) in June 2016. My husband and I received the diagnosis via a phone call from our geneticist while sitting in a grocery store parking lot in our car. That phone call changed our lives but we’d known from the moment our son was born (and had to be immediately resuscitated) that something wasn’t right. It’s been incredibly hard to find information which is why we started this website. We want to make the journey easier for everyone else diagnosed after us. It’s not a life we ever imagined. We hope this website helps you understand how to live with ATR-X too.

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Connect

If you have a family member who has been diagnosed with ATR-X, I highly suggest joining the closed Facebook group, ATR-X. You must be approved and will be added once the admins confirm you have a connection with ATR-X.

If you live in the US, there is also an ATR-X American Families Facebook group that facilitates a yearly meetup and other geo-specific conversations. I suggest joining both, but most conversations around the syndrome take place in the main ATR-X group.

You can also email me at allaboutatrx@gmail.com

STAYING STRONG

This syndrome is TOUGH. When you’re first diagnosed, get help. Build your community and army of support. It took 11 long months from the day we were diagnosed for me not to cry daily and be able to speak about it without being overwhelmed by emotion. But. Somehow you come to the realization that while this is still completely heartbreaking and awful and not the life you had planned, it’s the life you have so you might as well make the best of it. As Sheryl Sandberg would say, there is no option B. It forces you to get to the most basic understanding of being a parent and that is to raise a child who feels loved and happy and safe. And nothing else. Nothing else matters. So you do your best. And maybe have an extra glass of wine at night. Because you deserve it.

And this poem helps (no offense to the Dutch):

Welcome To Holland

(c)1987 by Emily Perl Kingsley. All rights reserved

I am often asked to describe the experience of raising a child with a disability – to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It’s like this……

When you’re going to have a baby, it’s like planning a fabulous vacation trip – to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It’s all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, “Welcome to Holland.”

“Holland?!?” you say. “What do you mean Holland?? I signed up for Italy! I’m supposed to be in Italy. All my life I’ve dreamed of going to Italy.”

But there’s been a change in the flight plan. They’ve landed in Holland and there you must stay.

The important thing is that they haven’t taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It’s just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It’s just a different place. It’s slower-paced than Italy, less flashy than Italy. But after you’ve been there for a while and you catch your breath, you look around…. and you begin to notice that Holland has windmills….and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy… and they’re all bragging about what a wonderful time they had there. And for the rest of your life, you will say “Yes, that’s where I was supposed to go. That’s what I had planned.”

And the pain of that will never, ever, ever, ever go away… because the loss of that dream is a very very significant loss.

But… if you spend your life mourning the fact that you didn’t get to Italy, you may never be free to enjoy the very special, the very lovely things … about Holland.