Latest Blogs
Caregivers are Special People
If you have a caregiver, be sure to thank them and tell them – often… Read More
Me and My “Happy Pill”
If only someone had told me early on that depression was a symptom of MS,… Read More
Living the American Dream with MS
It has been assumed that MS uncommon in the Hispanic/Latino population, but that is not… Read More
Vote Down MS
Our generation can be the generation that ends MS. Please join me and use your… Read More
Learning to Like My Cane
Whether you use a wheelchair, cane, walker, crutches, steerable knee scooter, motorized wheelchair, hoveround or… Read More
The Tale of the Concerned Wife and Resistant Husband
Today I realize that I’m not confined to a wheelchair. I’m enabled by my wheelchair.
Sex, Intimacy & MS
Intimacy with a neurological disease can make things interesting, to say the least.
(Not) The Sound Of Music
The truth is, I am claustrophobic. But really, is there anyone who enjoys having their… Read More
Advocating for My Father, Myself, and My Children’s Future
I want my children to grow up in a world where the phrase “you have… Read More
Thriving in the Face of Adversity
Life is going to challenge you at some point. When this happens you have a… Read More
Impacting MS Patients in Puerto Rico
There are only about 113 neurologists that care for about 3.3 million people in Puerto… Read More
Accessibility Claps and Slaps
I often find myself doing accessibility assessments. These may range from big, obvious things to… Read More
3 Ways My Tired Is Different from Your Tired
The one thing I find the most annoying though is how other people see fatigue…. Read More
6 Things You Need to Know About MS and the COVID-19 Vaccines
The National MS Society convened a group of MS experts to develop guidance so that… Read More
Tongue-Tied: 4 Things to Say
Since people don’t generally have a firm grasp of the disease, the comments we receive… Read More