Kay and I had the pleasure of joining our first-ever LMNOP class at GiGi’s Playhouse since its opening, alongside our friends! LMNOP, short for Language Music N’ Our Peeps, is a dynamic program designed to facilitate parent-child learning through basic sign language and other communication methods, all set to the backdrop of music and…
This weekend marked a significant milestone for Kay as she participated in her very first t-ball game! The weather couldn’t have been more perfect, and I’m immensely grateful for organizations like Miracle League that offer Kay the chance to engage in enjoyable activities alongside her peers. The sheer delight on Kay’s face upon arriving…
Kay, my boyfriend, and I decided to dedicate a day to pure enjoyment and bonding! It had been a while since Kay had visited Wally Wombats, so I thought it was time to let her revel in the fun. Wally Wombats holds a special place in both our hearts as it’s a haven where Kay…
March hasn’t been too kind to our T-Ball plans! Despite having one event and two games scheduled this month, all of them had to be postponed because of the weather. But I’m keeping my fingers crossed that April will bring us better luck and we can finally kick off the T-Ball season! Last Sunday…
Kay’s recent visit to her ENT for her routine 6-month check in was reassuring. Given the smaller ear canals often associated with Down Syndrome, individuals like Kay are more prone to ear infections, along with enlarged tonsils and adenoids. At just a year old, Kay underwent surgery to address her enlarged tonsils and adenoids, which…
Sunday marked the 3rd annual GiGi’s Playhouse GiGi Fit Acceptance Challenge, a vibrant event featuring a 5k Fun Run, a 1-mile inspirational walk, and a Kids Dash for Down Syndrome. Each year, I eagerly anticipate this wonderful occasion. It’s a chance to wear playful attire like tutus and whimsical socks, along with shirts bearing…
Saturday was supposed to be Kay’s debut T-Ball game, an event eagerly anticipated by both of us. However, Mother Nature had different plans, leading the league to call off the game due to inclement weather. While disappointed by the cancellation, I agreed that it was better for the kids not to endure unpleasant conditions on…
Last Friday, Kay’s school organized a family engagement event for the Pre-K students. Since Kay doesn’t usually have classes on Fridays, these special activities are a treat for her from time to time. The focus of last week’s gathering was a hands-on pizza-making session! Pizza happens to be Kay’s absolute favorite food, and she…
On Thursday, March 21st, we celebrated World Down Syndrome Day! Each year, I find myself deeply thankful for the opportunity to honor this remarkable day because of Kay. It’s a time when we rally our loved ones to sport silly or mismatched socks, symbolizing chromosomes, in celebration. The significance of socks in representing chromosomes…
Kay’s weekly therapy sessions have transitioned from Friday afternoons to Tuesday afternoons, a change I believe will greatly benefit us. By tackling therapy early in the week and maintaining the same schedule, it feels like a seamless transition. Witnessing Kay’s growing independence has been a remarkable experience. As she confidently walks hand in hand…
