Stories

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...

Had ìt before i was 35. Diagnosed; in my late 50's;  Secondary Progressive.  Survived.   3x pneumonia,  covid, streptococcus.  MRSA  im in a powered chair. and  my Guy  is still by...

Let’s talk sex Or, the don’t ask, don’t tell symptom. Ok, now that I have your attention. I wanted to talk about one of the more rare symptoms of MS...

My wife was diagnosed with M years ago. It took a long time of suffering before the diagnosis. She has moved from RRMS to SPMS. She is in pain 100%...

Hi.  My name is Dorcas.  I was diagnosed with MS in 2003.  With all the aches, pains and aggravating symptoms,  I am still standing. I didn't ask for this one...

August 2010. It was a Saturday. I was sick with what I thought was a 24 hour bug. Both ends going continually and a massive headache. Sunday felt like ‘the...

On Thursday, August 26, 2004, I woke up with a slight pain above my right eyelid along with blurriness in my right eye and a headache. I called our family...

Howdy y’all! To be honest, I don’t know where I fit in these conversations anymore. Let me tell ya what happened. Back in 2009, using two canes, I drug myself...

Life has changed but I am only looking towards my future. When I was diagnosed in 2004 at the age of 27 I was working full time had two young...

Dear family and friends, First of all, MS is NOT contagious. Sadly, some people still think that it is. I am trying my best to remain strong and independent, but...