Rolling Karaoke Party
Loud. Grassroots. Heart-first. Unapologetically alive.

Rolling
Karaoke Party

Rolling karaoke to raise awareness for Multiple Sclerosis.

We are a husband-and-wife rolling music mission built on real life, real heart, and the refusal to disappear quietly.

My wife has lived with MS since 1994. We deal with it in real life, every day. That is why this exists. We show up with a wheelchair, a huge boombox, a keytar, a wireless mic, and enough nerve to make a public scene for something that matters.

We are not here to beg. We are here to be seen, to bring joy, to make noise, and to raise money for the National MS Society because MS sucks and people living with it deserve more visibility, more support, and more life.

This is simple, humble, and real. We pull up, set up fast, play hard, make people smile, and keep moving.

Help Us Raise Money Read Our Story
Rolling Karaoke Party art featuring a singer, wheelchair energy, and loud colorful movement.
We show up. We park. We unload the chair, the boombox, the keytar, the mic, and the banner. We blast a few songs. We make people smile. We raise money for the National MS Society. Then we roll out and do it again.

What This Is

Rolling Karaoke Party is a grassroots public music project built to raise awareness and funds for the fight against Multiple Sclerosis. It is part street energy, part heart, part courage, and part pure stubborn joy.

We Live This

MS is not some abstract cause in our house. It is part of everyday life. That is what gives this project its honesty. We are not putting on borrowed emotion. We are taking our real life into public and turning it into motion.

We Keep It Real

We are filming on phones, hauling our own gear, and building this one pop-up at a time. No fake polish. No giant production. Just real people doing something bold because it matters.

We Raise Money With Heart

We want support, but not in a sad, needy way. We want people to feel what this is, love the spirit of it, and decide they want to help push it forward.

Our Story

We are a husband and wife doing this because life is short and hiding is overrated. My wife has MS. We deal with it. We live with it. And we are choosing to answer it with music, humor, visibility, stubborn love, and a little beautiful chaos.

We are tattooed, loud, passionate, and still here. We like the idea of rolling into parks, sidewalks, festivals, ponds, city spaces, and charity events with enough color and sound to make people stop and say, “What is this?” Then we give them the answer.

It is us. It is real. It is for MS awareness. And it is built to move.

What We Want People to Feel

“That is real. That is fun. That is brave. I want to help.”

Not pity. Not guilt. Just honest human connection, some laughter, some noise, and a clear reason to care.

How It Works

We roll into a public spot with the chair, the boombox, the keytar, the mic, and the banner.
We set up fast and hit people with a short, loud, unforgettable burst of music.
We keep the message simple: my wife has MS, we live this every day, and we are raising money because MS sucks.
We film it, share it, and keep building the mission one real-world appearance at a time.

The Gear and the Vibe

  • Wheelchair and high-visibility banner
  • Big boombox energy
  • Keytar and wireless microphone
  • Fast setup, raw footage, real reactions
  • Graffiti color, tattoo energy, rock-and-roll heart
  • Simple enough to repeat, strong enough to remember

Support the Mission

Every share, every follow, every conversation, and every donation helps us push MS awareness farther into the world.

This project is built from real life. Real people. Real effort. Real purpose.

GoFundMe: gofundme.com/u/rollingkaraokeparty
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Where This Can Go

It starts small and real. Local pop-ups. Public spaces. Short performances. Raw footage. Honest reactions.

Then it grows: more cities, more people, more awareness, more momentum, and more chances to turn music, courage, and public joy into support for people living with MS.