Stories

I never thought of myself as being that creative of an artist but this is one thing I did take the time to learn and it reigns in the depression...

You might be scratching your head about now wondering what the heck I mean. Not sure about you but vision is one of the top symptoms I deal with. For...

Hello to whoever read this. My writing in English is not perfect. I saw this wed site and I have been reading the stories, and I decided to write something...

I know you cannot even imagine why someone with MS would fall. It is just hard to believe with such bad balance, dragging numb feet, weak legs, vision issues, dizziness...

I was diagnosed when I was around fifty plus. I was on Copaxone for ten years. It was quickly apparent to me that my MS specialist and the MS "nurse"...

Life was just another day of work and fun in the sun before MS or was it? Oh boy, I know that statement has risen a few eyebrows. Yes, life...

Hi to all, I am about 16 years into living with undiagnosed MS…I think. And my PCP thinks. Other Drs think so when they look at my medical history and...

Hello. I am a newbie. I was diagnosed in April. I really didn’t know what was wrong with me. I knew I was taking care of my grandmother who died...

How did you deal with your first signs of what you now know was MS? Just another day of getting older is how I handled it day after day for...

Throw it all in the air Throw it all at a wall The various symptoms Come raining down Umbrella Umbrella You are too small Umbrella Umbrella Will you break the...

You have MS, but you look so healthy! Yep, I know you have heard this before and I know the thought going through your mind. As an MS warrior, like...

This is a story of how I received a diagnosis, fighting for yourself, questioning yourself, and ultimately growing as a person. All throughout this journey that I am still on...

The best description I can give to people of what living life with MS is like would be to imagine if Satan were your conjoined twin. The alarm clock goes...

Like you, I have asked myself this very question time and time again. I have volunteered my medical data to research projects hoping to ease others' journey. Joined Facebook groups...

I’m an optimistic person, I always have been. People wonder how someone who has PPMS and is bedridden be optimistic? After all, it’s incurable. I am also a person who...

My father passed away on September 22, 2020. It was really hard. My sister is a remarkable lady. Sitting at my kitchen table we are a mess. After arrangements were...

Before we get the MS diagnosis, we know something is wrong with our bodies but don’t have the answers so we face confusion and fear of the unknown. Then we...

Upon this last year I've noticed my memory started getting worse.Not trying to cut people off,but if I don't say when it comes to me its gone and may or...

I was diagnosed with MS Relapsing in 2015. I didnt know what was going on my feet where stiff and red im a nurse so I assumed that I had...

I’ve had Multiple Sclerosis for more than forty years, and I can tell you that I see a real difference between the twenty two years I spent without using a...