the chicken or the egg

My recovery from Covid is making me very emotional. To be fair, people have always told me that I am overly sensitive. And I do cry a lot. Not over personal things or big things or real life things, but all of the little things that ultimately have nothing to do with me. That swell […]

Read More

MS Myth of the Week: Kiddos.

Myth: People with MS shouldn’t have children. I personally don’t want to have children at this point in my life and I am really, really good with that decision. There were several years in my 30s where I dreamed of kids and felt it was something I needed to experience. Now, in my 40s, single […]

Read More

new tricks.

My dad has never been a dog person and he is falling in love with mine. I am in my hometown, exploring the breathtaking marshes and soft, white sandy beaches. Meditating on bittersweet memories and mulling through ideas as I always do when I visit the home of my beloved and missed mother. I took […]

Read More

MS Myth of the Week: Exercise.

Myth: Exercise is bad for you if you have MS. The day I was diagnosed with Multiple Sclerosis my neurologist went over a huge list of things I should know about my disease. Thank goodness I had a friend with me to be my advocate, because in that moment about 9 out of 10 of […]

Read More

random acts Of Fear.

In my 20s I convinced myself I had drowned in a past life. We all have fears, yet some run deeper than others. Just like the mystery of MS, extra special phobias can seemingly come out of nowhere but feel like they are a part of our very core. Impenetrable and immovable, random but ever […]

Read More

MS Myth of the Week: The Chair.

I was recently ghosted because my date found out I have Multiple Sclerosis. This happens to be one of my top 5 MS fears and I will delve deeper into this topic as well as my personal experience in an upcoming post. But the triggering of this fear has motivated me to expand my writing […]

Read More

okay, hold the Phone.

The word “okay” is incredibly underrated. Whenever I get a call or an email from someone newly diagnosed, I feel so privileged they have chosen to speak with me. To connect, to vent, to cry, to express anger, or to simply ask a few of the hundred questions we all have at the very beginning. […]

Read More