Reese starts summer school tomorrow. Our district offers a summer session for students with special needs to help keep them on target. I’m very thankful for it! Reese loves school and this is one way to ensure she that keeps that momentum up for the school year. It’s also a shortened school day with lots of fun planned into their academic day. Reese has really enjoyed it the past few years. There is usually just over a week in between the school year ending and summer session starting. I tend to go a little kooky during this time trying to pack a bunch of fun in for her. And this summer I was probably a bit more ridiculous than in the past, HA! And I’m not sure why. This is not her only free summer time. She actually gets about 4-5 weeks at the end of summer with no school. But you know me. I can’t help myself when it comes to my sweet little girl. I want Reese’s life to be magical and fun and full of wonderful experiences. Because let me tell you, in this mom’s eyes, there is absolutely nothing better in the world than seeing her happy.
Well, I hope you all have a day where you over do it!!!
Yesterday my oldest daughter, Sidney, came home for a few days. Sidney is a foodie just like me so when she is here on a quick trip it’s like a whirlwind of fun and eating!
Well, I hope you all have a day that is full of food and festivities!!!
Happy Mother’s Day everyone! Words can’t express how much I miss my mom. But in a way that comforts me. It means that I loved and still love that woman HUGE. Sometimes you get lucky enough to experience something in life and you get to just FEEL it. For me it’s the motherly love she filled my life with. I can still feel it. But to describe it, explain its’ influence over me and how I feel about loosing her, is not something I’m capable of. It’s just too big. But I try to express it in different ways like living genuinely, just the way she taught me. And in sharing her legacy of hope every single day and at every opportunity I get. It may be 24 years since her passing but her influence on me, my family and our little world will continue on forever. And that is certainly something to celebrate.
Well, I hope you all have a day where love leaves you at a loss for words!!!
Tomorrow Reese will be participating in her first Special Olympics Regional Games. She will be running the 25 and 50 and participating in the long jump. I am beside myself with excitement! This mama has one major feeling running through her body right now and it is the best!
Well, I hope you all have a day where you are proud!!!
Reese and I saw her pediatrician today. Although the appointment had nothing to do with her feeding issues, of course her doctor asked. And I’m glad she did because we brainstormed a little. AND I am excited to report that we have a new consultation scheduled! We have tried it all. Therapies, assessments, scans, (you name it) to figure out why Reese is still not chewing. It has presented as an issue for both her nutrition and her safety. Heck, one of the main reasons I went back to school was to make sure I was doing everything I could to keep her off a feeding tube! Although I’ve been successful with her nutritionally the choking risk remains. And it’s scary. So needless to say, I am THANKFUL for this new opportunity and GRATEFUL to still have more options to explore.
Well, I hope you all have a day where fresh eyes give you new hope!!!
Waking up feeling rested. Going for a nice walk. Holding deep yoga stretches. Decluttering … my home AND my mind. Eating strawberry salad. And playing Barbies with the cutest eight year old ever.
Well, I hope you all had a day where you got to do a few of your favorite things!!!
Today is World Down Syndrome Day! And we all know that I have someone very special in my life who has Down Syndrome. My beautiful 8 year old daughter Reese!
March 21st is a global day of awareness that has been officially observed by the United Nations since 2012. How cool is that?!?! This date was chosen to represent the triplication of the 21st chromosome (3/21) found in individuals with Down Syndrome. Today I celebrate Reese and the amazing community of people with whom we share our lives.
I was told when I was 15 weeks pregnant that Reese had Down Syndrome. I did not grieve or cry. I did the complete opposite. My heart was immediately filled with hope for the future. And not just for my future or hers. From the moment that I was told that she had Down Syndrome I knew that Reese was going to change the world for the better. It was like a blanket of understanding that I had never felt before. And I have witnessed her work her magic time and time again ever since. She has softened the hardest of hearts and changed the most ridged of minds. I am so proud of her! This little girl of mine is smart, silly, kind and caring. Her compassion for others runs deep. She is a bright light in this dark world. She has taught me SO SO SO much and has showed me what real strength and perseverance looks like. And best of all, she loves me HUGE! Reese is an incredible human being and I am humbled that God chose me to be her mommy. It is truly a blessing and an honor.
I love you my Reesey Roo. You are my hero!
Well, I hope you all have a day where you celebrate EXTRA!!!