Twenty14 Foundation

One Team.
One Fight.

No family should face ALS alone.

ALS changes lives. It affects families, relationships, routines and futures. We believe in showing up, standing together, and making sure families know they aren't alone.

Scott Taylor with his family at a volleyball game
Scott with his family

Our story

Why Twenty14?

Twenty14 is a foundation born from friendship, built on loyalty, and driven by the determination to make a difference for families navigating ALS.

Meet Scott

Scott Taylor is a devoted husband to Stephanie and dad to Keira, Maddox, and Logan. Family is everything to Scott, and their home is full of laughter, game nights, creativity, and a love for playing games together. Scott is even a board game inventor!

Scott is a nationally recognized Kubb player and a member of the Kubb Reapers.

  • 2026 U.S. National Kubb Champions with the Kubb Reapers
  • 2025 Kubb All-American First Team
  • 2025 Kubb Team of the Year, the Kubb Reapers
  • 9th of 172 teams at the World Kubb Championship in Sweden, a lifelong dream
The Kubb Reapers raising the trophy at the 2026 U.S. National Kubb Championship
The Kubb Reapers celebrate winning the 2026 U.S. National Kubb Championship.

But what makes Scott special goes far beyond Kubb. He's funny, creative, competitive, fiercely loyal, and someone who makes people feel welcome. He's a teacher and mentor who has made a lasting difference in the lives of at-risk youth, showing up for his students in ways that extend far beyond the classroom. He's the kind of person who builds friendships, brings people together, gives big hugs, and makes life more fun for everyone around him.

At his core, Scott is a fighter, a family man, a friend, and someone who has spent his life making a difference in the lives of others.

In March 2026, Scott was diagnosed with ALS, and life changed for Scott, Stephanie and the kids.

Inspired by Scott and the friendships formed through the Kubb Reapers, his friends created Twenty14 to show up for Scott and his family, and for every family facing the same fight. One way we do that is by helping ease the financial challenges families face while navigating ALS.

20Scott's former Kubb number
14Scott's current Kubb number

And his favorite color? Bright neon yellow. You'll see it in our star, and you'll see a lot of it at our Yellow Tie Event.

Scott's story is why Twenty14 began. Its purpose reaches every family facing ALS.

Our mission

Inspired by courage and driven by compassion, the Twenty14 Foundation supports families navigating ALS and works to create lasting change through awareness, resources, and expanded support for communities in need.

What we do

Showing up matters.

Sometimes the greatest gift is knowing someone is standing beside you. Our work rests on three pillars.

Family Support

  • Helping families with the unexpected financial burdens of ALS
  • Supporting practical needs and home accessibility
  • Connecting families with resources that make everyday life more manageable

ALS Awareness

  • Sharing stories and lived experiences
  • Increasing understanding of ALS
  • Starting conversations that bring attention to the disease and the families it affects

Community Impact

  • Bringing people together to make a difference
  • Creating opportunities to give back
  • Extending support to communities and families in need

Get involved

Everyone has something to give.

Your generosity, time and support can change what the journey looks like for a family.

Donate

Give online with PayPal, on Venmo at @Twenty14, or by mailing a check.

Host a fundraiser

Organize a night, tournament or drive in your community.

Donate goods or services

Raffle prizes, auction items, food, venues and skills.

Volunteer

Help run events or lend a hand to a family.

Come to an event

Play, cheer, bid and bring friends.

Share our mission

Follow us and pass Twenty14's story along.

Events & fundraising

Come out and stand with us.

Fundraising nights, Kubb events, raffles, auctions and community get-togethers.

Early 2027Q1
Upcoming · Date coming soon

One Team. One Fight. The Yellow Tie Event

A kubb community rally for Scott Taylor and his family. This is a casual night: come as you are, no dressing up required. Add a splash of yellow, Scott's favorite color, if you like. Eau Claire area · Date, venue and tickets coming soon

Sponsor
Jul 202724
Upcoming

Twenty14 Kubb Scrambler

Saturday, July 24, 2027 · Location and registration details coming soon

Details
May 20262
Past event

Wisconsin State Kubb Championship

With the Kubb Reapers. Thank you to everyone who came out.

Watch

ALS resources & support

You are not alone.

An ALS diagnosis affects the entire family. We've compiled these resources to help people living with ALS, their families and caregivers find medical care, community support, equipment, financial guidance and practical help. Please contact each organization to confirm current programs, eligibility, schedules and contact information.

Newly diagnosed? Where to start

  1. Connect with a neurologist or multidisciplinary ALS clinic.
  2. Contact the ALS Association Wisconsin team for care navigation and local services.
  3. Ask about equipment, communication tools, insurance and benefits before urgent needs arise.
  4. Find an ALS support group for yourself and your family or caregiver.
  5. Review disability benefits, health coverage and caregiver support options.

Wisconsin ALS resources

Specialized ALS clinics in Wisconsin

Ask about multidisciplinary ALS care, referrals, insurance and appointment availability.

Froedtert & Medical College of Wisconsin

9200 W. Wisconsin Avenue
Milwaukee, WI 53226

froedtert.com →

UW Health University Hospital

600 Highland Avenue
Madison, WI 53792

uwhealth.org →

Gundersen Health System

1900 South Avenue
La Crosse, WI 54601

gundersenhealth.org →

Milwaukee VA Medical Center

5000 W. National Avenue
Milwaukee, WI 53295

va.gov/milwaukee-health-care →

To find and verify ALS clinics and current certifications, see the ALS Association's clinic directory.

More support

ALS support groups6
Milwaukee Area ALS Support Group

For people living with ALS, families, friends and caregivers. Previously listed as the second Wednesday of each month, 1:00–2:30 p.m. Central, in person and virtual. Confirm details before attending.

Contact previously listed: Lisa Marie Idzikowski, 414-305-0389

Milwaukee Area Caregiver Support Group

For caregivers of people living with ALS. Previously listed as the third Wednesday of each month, 5:00–7:00 p.m. Central, in person. Confirm details before attending.

Contact previously listed: Robin Stanczyk, 262-402-8148

ALS Association Support Groups / Nationwide Connect

Online and local support groups, including groups for caregivers and other specific communities. Check the current calendar for virtual meetings and eligibility.

Les Turner ALS Foundation: Online Support Groups

Professionally facilitated support for people with ALS, caregivers, young adults and people experiencing grief. Confirm current groups and registration.

Wisconsin Family Caregiver Support

Local caregiver support groups and programs through Wisconsin caregiver resources and county Aging and Disability Resource Centers (ADRCs).

More Wisconsin groups

For other regional groups, contact the ALS Association Wisconsin care team.

National ALS organizations6
The ALS Association

ALS education, research, advocacy, care services, support groups and treatment-center information.

Team Gleason

Assistive technology, communication support, equipment and programs focused on quality of life for people living with ALS.

I AM ALS

Peer community, navigation resources, advocacy and opportunities to take part in research initiatives.

Muscular Dystrophy Association (MDA)

Neuromuscular disease care centers, education, research and resources for people living with ALS.

Les Turner ALS Foundation

ALS education, support services, online groups and research resources.

Your ALS Guide

Practical information on living with ALS, caregiving, mobility, communication and planning.

Caregiver & family support2
Wisconsin DHS: Caregiver Programs

Family caregiver support, respite care and connections to local assistance.

Wisconsin Aging and Disability Resource Centers (ADRCs)

Local help with benefits counseling, long-term care options and caregiver resources.

Equipment, accessibility & communication2
ALS Association Wisconsin

Ask about equipment loans, mobility needs, communication resources and referrals.

Team Gleason

Assistive communication technology, equipment support and other quality-of-life programs.

Financial assistance & benefits5
ALS Association Wisconsin

Care coordinators can help families find local programs and assistance options.

Social Security Administration

Disability benefits, eligibility and how to apply.

Medicare

Health coverage and eligibility.

Wisconsin Medicaid / ForwardHealth

Wisconsin health coverage and benefits programs.

Wisconsin ADRCs

Benefits counseling and guidance on long-term care programs.

Veterans living with ALS2
U.S. Department of Veterans Affairs (VA)

Eligible veterans living with ALS may qualify for VA healthcare, disability compensation, equipment and more. Contact the VA to review eligibility.

Milwaukee VA Medical Center

5000 W. National Avenue, Milwaukee, WI 53295

ALS research & clinical trials2
ClinicalTrials.gov

Search for ALS studies and clinical trials, and discuss taking part with your ALS care team.

ALS Association: Research

Research updates and educational information.

These listings are for informational purposes only and do not constitute medical, legal or financial advice. Organizations, meeting times, contacts, eligibility requirements and services may change. Contact providers directly for current details. Inclusion does not imply endorsement or affiliation with the Twenty14 Foundation. Last updated November 2026.

Financial transparency

Know where your gift goes.

We want every donor to feel confident about how their money is used.

Status
501(c)(3) nonprofit
EIN
42-2013553
Annual report
Coming after our first year