Category Archives: A Couple Takes on MS

Life with MS: MS4MS brings diamonds in the rough

Sam Greenberg had a vision of diamonds and a match made in heaven.

Sam Greenberg brings MS4MS to Comerica Park August 10, 2019.

And we saw firsthand in Detroit that baseball has a welcomed place in the efforts to enhance and improve the lives of people and families living with Multiple Sclerosis.

Sam is the founder and CEO of Mission Stadiums for Multiple Sclerosis (MS4MS), a non-profit organization committed to hosting events nationwide to increase MS awareness and raise money to support research at top MS research centers.

It was on Dec. 13, 2018, that Sam first reached out to us on Instagram to let us know how much we inspired him and invited us to share our story on the MS4MS blog. It turns out we were equally as moved by his story.

He was a senior at Southern Connecticut State University in 2011 when he led off with the MS4MS idea, inspired by his grandmother who lived with MS most of her life before she passed away in 1986.

In his quest to host events at more professional baseball stadiums, Sam set his sights this year on Comerica Park, home of our beloved Detroit Tigers. Of course we would love to participate!

We, and nearly 60 other MS warriors from Michigan, got way more than we ever could have imagined. Check out the highlights of our experiences and see:

• Why MS4MS is such an important organization for the MS community

• The ways you can get involved in supporting MS4MS

• And how these words from the movie Field of Dreams (as said by James Earl Jones’ character Terrence Mann) still ring true today, “The one constant through all the years, Ray, has been baseball. America has rolled by like an army of steamrollers. It has been erased like a blackboard, rebuilt and erased again. But baseball has marked the time.” 

With Detroit Tigers pitcher Nick Ramirez, who made it possible for some of us MS warriors to make it on the field for Tigers batting practice before the MS4MS game against the Kansas City Royals.

Catch our Facebook Live interview with Sam

On the field with Sam following Tigers batting practice.
Because who doesn’t cheer for Miguel Cabrera?
Jennifer now knows why getting on the field for pregame batting practice was such an honor and big deal 😊
Perfect night for baseball and the first MS4MS event at Comerica Park.

Listen to our A Couple Takes on MS episode about MS4MS

OMG! Dan really does have MS!

We often say that together we show how Multiple Sclerosis affects everyone differently. While it’s easy to see that MS impacts Jennifer’s ability to walk (hint: she sits in it every day and it’s the key to her independence), most times you never could tell Dan is living with this chronic progressive disease of the…Continue Reading

MS advocacy on my own… or was I?

It’s not like I haven’t ever advocated at the State Capitol in Lansing, Michigan, before, but this year I was nervous. This was the first time I went without Dan, my advocacy partner in crime. He unfortunately couldn’t get away from work to attend this year’s 12th Annual Older Michiganians Day. Sure, I had my…Continue Reading

Winter is coming: MS preparations for when it’s here

Talk to people about their Multiple Sclerosis symptoms, and many are quick to come forward with sensitivity to the heat. Jennifer and I get it. We also are weakened most times the temperature tops 80.3 degrees, give or take a few depending on weather wildcards like direct sunshine and hovering humidity. Summer heatwaves are so…Continue Reading

Sharing knowledge for the newly diagnosed with MS

Jennifer and I spend a lot of time on our blog writing about the things we are doing despite and in spite of our Multiple Sclerosis. Our hope is that by showing what still is possible, these stories will help other people to move beyond their MS or whichever challenges they’re facing. These are the…Continue Reading

Taking MS back to school

Catching the “Back to School” spirit, Jennifer and I remember the excitement that came with each new year. Things like new clothes. An unopened box of 64 Crayola crayons, with the color sharpener in back. Promising yourself that this is the year you’re going to stay on top of your homework, get a good night…Continue Reading

#ProgressiveMSDay

Dan and I knew something epic was brewing when a big white moving-van-type truck pulled up to our house around 7:45 a.m. A man got out of the truck and walked toward our house. Dan greeted him at the garage door. “Are the home owner?” he asked Dan, who confirmed his role with a quick…Continue Reading

Get inspired to overcome MS-related frustrations

Getting upset seems like it happens several times each day when you’re living with Multiple Sclerosis. Common occurrences include dropping your phone because your numb hands can’t feel it. Missing a social event because you know the freshly fallen snow will compromise your balance. Getting to the bathroom two seconds too late. Frustrations happen. So…Continue Reading

Our online radio show: A Couple Takes on MS

What an opportunity Dan and I have been given. Not only are we living with Multiple Sclerosis — that’s how we found each other — but MS & Me Radio Network has found us and wants other people to hear more of our stories. And what’s really cool is the network wants to hear from…Continue Reading