All posts by: Heidi Wallis

About Heidi Wallis

“A Surprise Diagnosis” – Randi Sonnet was six and a half years old when we adopted her in the summer of 2016. She weighed only thirty pounds and was deemed […]

“New Year, New Boy?!” – Laura Hey everyone! I hope the new year is off to a great start! Levi has been in first grade this year, and absolutely LOVES […]

“Our Diagnosis Journey” – Shelly Some background to our story; I work in a well-baby nursery and Neonatal intensive care unit,  and most of my friends do as well… My […]

“Expectations” – Nathan Good day friends!  As I am traveling a bit with work right now, I have begun to think a few deep thoughts on what it is that […]

“Picturing the Future” – Beth During the winter break, we undertook the daunting task of organizing digital photos from the past fifteen years. We take a lot of pictures, so […]

“Back to Blogging” – Janet I love reading special needs blogs. They have lifted me up and carried me through some really tough years with my son. Ironically, it’s been […]

“Because” – Amy At the end of the year, I like to reflect back so I can look forward and plan for the new year. 2017 has been a challenging, […]

“The Magic of Christmas” – Laura There was a time I wondered if we would ever experience “normal” holidays with our cute Levi. We would, of course, go through the […]

“Got to Get You Into My Life” – Amy After learning about our son’s Creatine Transporter Deficiency (CTD) this past January, we started down the path to begin supplementing with […]

#SeasonofSmiles – Whitnie As we approach the holiday season, it is customary to reflect and give thanks for the blessings we have. It’s also the season of giving and a […]