Change is Inevitable. How We Respond is Not.I have PPMS. At last, after 15 years I have a proactive neurologist. I'm now doing hydrotherapy, physiotherapy, and learning more about...reactions4comments
Wondering About My Later Life DiagnosisI found out in my fifties I had MS. Doctors had confusing diagnoses for me and I am still learning about this...reactions10comments
I Love RollercoastersI have always loved rollercoasters. If there is a rollercoaster in an amusement park, I'm there! I grew up within walking distance...reactions4comments
I Have MS But It Doesn't Have ME!I have been diagnosed with Relapsing-Remitting Multiple Sclerosis since September 2020, and I can only describe my life as a roller coaster...reactions2comments
CuriosityI had my annual overhaul at rehab this past week. While I hate the idea of going, they have probably saved my...reactions4comments
Am I a fighter? I thought I was, but never imagined this kinda fight.Recently, my husband and I were discussing this. He said he thinks of different temperaments as one of three when faced with...reactions6comments
Understanding My Symptoms a Lil MoreI had an interesting read about our weird symptoms, as I learned the names of some of the ones I have been...reactions1comment
Where I Am NowI'd like to share with you guys, the goings-on over the last month of my life. What happened, the decisions I made...reactions1comment
My JourneyDisclaimer: The following story may be triggering to some as it mentions suicide attempts. If you or someone you know are currently...reactionscomments
My JourneyDisclaimer: Please be advised, this story mentions heavy drug and alcohol use and some violence. If you or a loved one is...reactions2comments
A Journey With 100 BeginningsWhere did my M.S. story start? I wish I could tell you. There was no moment when a doctor sat me down...reactions4comments
My Flare-Ups, Fighting BackThere has been a major progression I have noticed in my flare-ups. My first experience was as I said TM (transverse myelitis)...reactions3comments
My Daily RoutineI've introduced myself and explained who I am, what happened, and where I am now. As well as my latest circumstances and...reactions1comment
Looking Back on My First YearTODAY... is a HARD day for me. In so many ways I could easily fill an entire book with each challenge this...reactions3comments
MS HatredI was diagnosed with PPMS about 6 years ago. I was in a state of denial for at least a year. Finally...reactions10comments
Electric Chair Boo HissMy wife always counsels me to turn off my powerchair when not in use such as a visit to the bathroom, a...reactions3comments
A Lifetime Story with MSYes, we all have a story to tell or write. I’ve done both and I want to share my story. I lived...reactions8comments
The Invisible AbuserMS is a straight up abuser of the worst kind. An abuser you never even dated. Just showed up, knocked at the...reactions2comments
Anxiety Does Not Live in NowAnxiety is only in the future. I live with a chronic illness, with no cure, that only gets worse with time and...reactions8comments
Happy Birthday to MeAge 57 is a few days away. This wasn’t how it was supposed to be. I was supposed to be complaining about...reactions7comments
