2015 // Our Year in Review

I always find these last two weeks of the year to be a great time of reflection before jumping forward into the new year.  In 2014, I went from pregnant in January, to giving birth to Parker in April and navigating everything that comes with that first year of motherhood.  You don’t get that time back and it is so special, but I have to say that it was nice to start 2015 out with a 9 month old who was sleeping through the night on occasion and with a pretty trustworthy routine already in place.  I had established (through much trial …

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Take the Stress out of the Holidays

Last December, Parker was an 8 month old babe on the move and I decided to approach the holiday season exactly like I had in years past.  I hand addressed and mailed over 150 holiday cards.  We hosted a big family Christmas party complete with our favorite Santa Claus and I also threw a holiday party for our TEC team here.  By the end of it all I was beyond drained! Never again.  Instead, this year I had a Tasker from TaskRabbit come over last weekend and take care of the bulk of my to-do list for me.  It meant that everything got done, …

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DIY // Deconstructed Garland

A few weeks ago we were shooting at a studio downtown and decided to go for a little lunch break walk to Poppy + Rose.  After enjoying one of the best burgers of my life there, we strolled through the flower district I did my best to withstand the temptation, but ultimately I caved, took the last of the cash in my wallet (a whopping $8!), and bought what I could.  (Turns out I used up all of my willpower on the chocolate croissant that was sitting on the counter at lunch.)  I left the flower mart with armfuls of greenery and one small …

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Trykes for Tykes with GoFundMe!

Here on the blog I talk sometimes about the challenges of motherhood– working, the best childcare situations, sleeping issues.  None of those compare, though, to the challenges that can accompany having a child with special needs.  My nephew TJ (pictured above!) was diagnosed as a baby with Angelman Syndrome and over the last six years I have watched as my sister constantly advocates for his best care, his best treatments, and his best therapies; all the while trying to provide him with the same joys and experiences that we all …

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