Category: Family Life

Benefits of Practicing Daily Gratitude

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My 2018 gratitude journal. I started last year with these goals and added an entry every day.

We’re already a month into the new year. Hard to believe how fast time flew by this month. Resolutions were made and broken within the first few weeks of the year. One poll suggested that 80% of the people who set a resolution failed by February. Yikes!

Don’t despair if the resolution didn’t work out for you. We always go for the brass ring and create the lofty resolutions that are hard to achieve. It’s the consistent, daily efforts that turn into the big wins over time. The small practices benefit you more in the long run.

Gratitude is one of those practices that’s been part of my daily routine for years now. I’m not talking about daydreams with rainbows and unicorns, although I love both of those things. It’s the daily thought about what you are grateful for. And I get it that some days just really suck. I had a few of those days in January. Continue reading →

Kids, Bikes and Adaptive Play

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Riding a bike is like a right of passage for a young child. It’s the moment when the training wheels come off and they take off with that little wobble. I saw a father help his girl take that first ride in a field behind our house the other day. She was smiling and beaming with excitement. She fell once and then got back on long enough to ride away.

For moms like me, watching that moment is inspiring and also bitter sweet. It’s hard for me to imagine our girl taking off on her own two-wheeled bike.

She has balance and coordination challenges along with other conditions and intellectual disability. She tries very hard to ride her bike and she really just wants to join in play with others. Continue reading →

Planning a Petting Zoo Birthday Party for Special Needs Kids

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Birthday party invitations are few and far between when you have child with disabilities. My daughter who is part of the SPED program at school has been invited to two birthday parties in the last 8 years. My son who is able-bodied and has a group of buddies he hangs with will get invited to birthday parties throughout the year.

Before we moved out of state from our hometown, it didn’t matter if the party invites came in for her because we had big birthday parties with grandparents, family and cousins. Living in Arizona, we don’t have that network so her parties became dinners with cake and a couple of my son’s friends. Continue reading →

Horse Therapy for Kids with Disabilities

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Horse Therapy for KidsI love horses. I do. I rode for years with a friend when I was growing up. She was a natural trainer when we were kids and has a successful training business today.

When my husband and I relocated to Arizona, I remember telling him one of my goals was to get back in the saddle. I missed it and was determined to start riding again.

Our new town has an equestrian culture and I stumbled across a horseback riding class for special needs kids. I put my riding aspirations on hold and enrolled our daughter who has disabilities. I was nervous the first session, but it was amazing to see her light up. Continue reading →

Sensory Processing Issues and The Morning Routine

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Sensory Processing DisorderSequence, lace and bows make little girl clothes cute and adorable. For the little girls with sensory processing issues, cute and adorable becomes a nightmare. It’s scratchy. It burns. It irritates.

Sensory processing issues was a new term we learned when our daughter’s conditions were finally diagnosed. Her conditions include a lengthy list with sensory processing issues plus developmental delays and intellectual disability.

Sensory processing refers to the way the brain receives messages from the senses and turns them into the appropriate motor and behavioral responses. Continue reading →

30 Days of Teal for Ovarian Cancer Awareness

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What's the Story Behind Be Positive Mom?September is National Ovarian Cancer Awareness Month and September 1 marks the start to 30 days of teal. The month will include gatherings, celebrations and fundraisers across the nation. It’s a reminder to educate ourselves and be diligent with our health. Ovarian Cancer whispers during the early stages so it’s important to listen to the subtle signs.

My sister was diagnosed when she was in her early thirties. She fought the battle for over two years and passed away when she was just thirty-four. Ovarian Cancer Awareness Month marks the a time to educate others and is a reminder the anniversary of her passing is October 4. It’s the season of remembrance and gratitude for the short time we had together. She always said if her story could help another woman detect this disease earlier than she found hers, then her fight was worth it. Continue reading →

5 Ways Stay-at-Home Dads Are Changing the World

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Stay-home Dads RockWhen we lived in Silicon Valley, we did what a lot of what Silicon Valley parents do. We had the double income, two mortgages and two car payments. We also had two kids with two childcare bills. The American Dream, right?

We struggled. We were miserable and knew it wasn’t for us anymore. It was hard to let go because we were both born and raised in San Jose, before the term “Silicon Valley” became so popular. We wanted something different from the norm and California was too expensive to raise our kids on our terms. It took us a few years to decide to relocate. We relocated to Arizona before we had kids and then moved back to the Bay Area. After we had kids, we realized we couldn’t make it work there and the costs were a constant struggle. Continue reading →

What Intellectual Disability Means to Me

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Baby GirlI couldn’t stop staring at two words on my computer screen: Intellectual Disability. After 5 years of doctor appointments, tests and more tests, we had several conditions finally diagnosed for our daughter.

Our journey included two neurologists, two geneticists, pediatricians and development delay specialists that spanned two states. It’d been a long road to diagnosis and after talking with other special needs parents, I learned that’s kind of the norm. It can take several years to diagnose a child who has disabilities. It’s like a puzzle and every appointment or phone call provides a piece of hope you’ll find an answer or in our case answers. Continue reading →