Stories-Adapting
As Lynn’s multiple sclerosis has progressed over the years, we have gone through many different mobility assistive devices. Each has
I diligently worked to create a website to support caregivers for the past two years. Initially, I planned to have
For several months, we’ve seen groups proclaiming their rights for equal treatment under the law and by others. While I
Daily, the news carries reports of another state entering Phase One of returning to normal following the massive shutdown of
Caregivers never take a break because though they may not be physically present, mentally, they do not let go of
Since multiple sclerosis often strikes in early adulthood, many times, the family unit includes children who mature into adulthood, watching
Since I’ve retired, I’ve found myself on a mission to do something about the plight of caregivers. Why am I
One of the most important practices I have is checking my husband’s skin regularly for any signs of skin breakdown.
Did you know what to do, where to go, and what the medical terms being used even meant? Did you
I yell back, “Just a minute. Let me finish this sentence.” Then I try to recollect my thoughts and finish
The mysteries of MS always keep it interesting as I struggle to manage my husband’s medical care and assist him
Communication is a tricky process. When I make a statement, not only am I projecting what I think I intend
