Four years of Ezzy: Year 1

January 10, 2015Advocacy, Special Needs Child

Since I am on a photo kick, it seems like the right time to do a post with photos of Ezzy over the years in honor of her fourth birthday. We will start with her first year. The day Esmé was born is kind of a big blur. She arrived around 7 am–weighing 6 pounds … Read More

The best thing ever

January 8, 2015Special Needs Child 4 Comments

I’ve been digging through my old photos over the last few days, deleting and archiving in an effort to speed up my aging and overworked computer. Last night I got to a set of photos taken while I was in between 19 and 20 weeks pregnant with Esmé. We were on vacation in New Brunswick, … Read More

You’re in my spot

January 7, 2015Advocacy, Special Needs Child

I wish I didn’t have to say this, but here goes: Those parking spots, the ones designated as reserved parking, you know the ones, with the little stick-figure in a wheelchair? They aren’t there for just anyone’s convenient parking while they just “pop in” somewhere. And the spots alongside those spots, the ones with all … Read More

The Cute Syndrome Blog’s best of 2014

December 31, 2014Advocacy, Special Needs Child

In scouring all of the posts this year I am struck by what a big year it has been for Esmé. 2014 has been filled with a lot of firsts, moves toward Esmé’s independence, and a general coming to terms with our world. Here is my list of the most popular blog posts (based on … Read More

Under the Christmas Tree

December 26, 2014Special Needs Child

These days I have been feeling like an exposed nerve. Crying easily, being incredibly moved by the smallest kindnesses, wincing in pain at remarks that might have just slid off my back a month ago. I have also been reading a lot lately, primarily memoirs about families with children who have special needs. I cannot … Read More

Things Change

December 22, 2014Special Needs Child

A change that I had been avoiding thinking about for weeks now is finally upon us. And I am still a little bit in denial, to tell you the truth. Wednesday was Esmé’s last session with her speech therapist, Diana. Oh, crap. Now I am crying. You see, Diana has been one of the most … Read More

Laughter

December 22, 2014Special Needs Child

There is nothing, I mean absolutely nothing in this world that makes me happier than hearing Esmé laugh. Esmé smiled early on–by only a few weeks old she was making vaguely judging smiles in our direction. By two months she would produce smiles that just took over her entire face, with these smiles would come … Read More

Christmas.

December 19, 2014Special Needs Child

With Christmas and the New Year approaching I think many of us start to take stock of our lives–what we’ve accomplished, where we’ve fallen short and hope to improve, what we have to be grateful for… For me these holidays are also inextricably linked to Esmé’s birthday, which comes relatively soon after the holidays. So … Read More

Good News

December 15, 2014Special Needs Child

After awhile you get pretty used to expecting doctors to tell you the kind of news you’d prefer not to hear…not necessarily horrible stuff, but discouraging stuff. It has become a sort of an expectation of interacting with doctors that the news about Esmé will not be “great.” We do hear a lot of “good … Read More

Kisses

December 12, 2014Special Needs Child

Last weekend Esmé and her Papa had a few days all to themselves–while I traveled across the country for the American Epilepsy Society conference in Seattle. The week previous, when my husband was gone for several days, Ez asked for “Nay Nay” (her version of Papa since she cannot produce a “p” sound) repeatedly. So … Read More