On Father’s Day, and on every milestone or holiday, I have only one wish, one hope. I hope that my husband will be restored to his former self. Before Multiple Sclerosis reared its ugly head. I love him as he is now, however I know that it what he longs for, and we all long […]
Many caregivers know that prescription medications are a double-edged sword. In many cases, they are necessary to improve, or sustain, life – or quality of life. But prescriptions are expensive. And when you’re on a multitude of medications, it adds up. I’m not talking about the $4 generic antibiotics you pick up at the drug […]
Almost a year ago to the day, our lives were forever changed when a relapse of my husband’s Multiple Sclerosis (MS) snuck up on us over the course of a few months. We struggled to understand why everyday tasks seemed more difficult for him and why an uncharacteristic fatigue had washed over him and wouldn’t […]
I like to think that when I’m not in the middle of a panic-inducing week (or month, or year) I’m a fun person to hang out with. I have been blessed with friends, coworkers, neighbors, and family members who want to hang out with us. We enjoy a good time and good food – who […]