Kingdom Focus is what first comes to mind. Those of us who are married and have someone in our life with special needs for whom we have responsibility (often 24/7 and 365!) know that without focus, we are doomed. AND for those of us who are believers in Jesus, we add to that His Kingdom focus and our part in it.
For us, we have 5 top ways to work on our marriage and keep it strong. There are more, of course, but let’s not get overloaded!
A few years ago, I made a change in the way I interact with my children. It’s a small practice, but it has profoundly helped our family understand and grasp the truth that God loves and delights in us. Every single day, I tell my kids, “I love being your mom.” This intentional habit has transformed not just my relationship with my children but also how I relate to God.
As the New Year begins, we are often bombarded with messages encouraging us to aim high, make big resolutions, and do more. But as parents—especially those navigating disability—this approach can feel overwhelming. Instead of striving for lofty goals, what if we embraced the sacredness of small steps and new beginnings? What if we allowed ourselves the grace to parent differently—in a way that meets the unique needs of our families and honors the season we’re in? For many families like mine, Sunday mornings don’t look like they “should.” We are navigating multiple invisible disabilities—diagnoses like autism, ADHD, anxiety, and more—and we’ve had to embrace flexibility, creativity, and sometimes just letting things go when things feel too hard
When God redeemed my worst Christmas ever by using it for good, it came as a big surprise. Most likely because 1982 was the year of my worst Christmas ever, and the using it for good part didn’t come along until December of 2024. 42 years is a long time, which explains my surprise.
Seasons help us to realize we’re not alone. We might still feel alone but we can see things differently and then change our thinking, and even our responses. We know everyone goes through “stuff” but sometimes we need to recognize it just happens to be our turn. The harder part is that we still have someone we are caring for full time, 24/7 added to the new hard stuff!
The six caregiving advocacy tips I’m learning all over again come with compliments from my mom. She’s experienced some health challenges over the past few months, so my siblings and I are advocating on her behalf. During my years as caregiver for my young son with chronic medical needs, my husband and I gradually discovered six caregiving advocacy tips that work in any caregiving situation.
All life is God-given and is to be celebrated. There was a time long ago that I lost sight of this perspective. God patiently waited for me to look past the words of a diagnosis to see my daughter for who she was created to be. On this World Down Syndrome Day, I appreciate all the time I have spent raising my child with Down syndrome.
I am no stranger to struggles as someone raising a child with special and medical needs. It is easy for me to downplay the degree to which I am mentally struggling. But I now see that when I claim to be fine when reality suggests otherwise, that’s an unhealthy denial. Here are four signs that my struggles are not “fine,” and some things that have been helpful for me, when I acknowledge these symptoms.
