Virtual. Global. Community of Younger-Onset Dementia

About Us

Lorenzo's House is a virtual, global organization that empowers sons, daughters, children and families affected by younger-onset dementia (YOD).

“Healing begins with us and stigma ends with us. Not just a condition for older adults, younger-onset won't wait - and neither will we.”

- Daughter of YOD

raising awareness

Understanding...
younger-onset dementia (YOD)
What is younger-onset dementia (YOD)?
Younger-onset dementia (YOD) is defined as a condition where someone shows symptoms of brain change before age 65.

There are hundreds of types of younger-onset dementias, including Alzheimer’s Disease, Frontotemporal Degeneration, Lewy Body Dementia, Vascular Dementia and many other neurological conditions.
Why 'younger' vs 'early'-onset dementia?
The term "early-onset dementia" is often misunderstood as referring to the early stage of dementia, rather than the age at which symptoms begin.
How many people are affected by younger-onset dementia (YOD)?
• Approximately 7.8M people worldwide are living with younger-onset dementia (YOD) (Nature, 2025).

• If we multiply 7.8M by a family of 4, more than 31 million family members are affected by younger-onset dementia.

• 200% uptick in YOD cases in the US (Blue Cross Blue Shield, 2020).
What are the unique challenges of YOD?
YOD affects people in their 30s, 40s, 50s and early 60s… often while they are working, raising families or becoming financially stable.

Resources designed for families affected by YOD are sparse.

Families living with younger-onset dementia (YOD) are unseen, misunderstood, under-resourced and under-researched.

Younger people are more likely to experience other symptoms first (such as personality change, language difficulties or movement problems) rather than just memory loss, which can delay diagnosis.

the inspiration of Lorenzo's House

Founding Story

Our sons were 9 and 13 when brain change showed up in our home. Three years later, my husband, Lorenzo, was diagnosed with younger-onset Alzheimer’s. The culture in our home changed as we took on a complicated new identity; younger, with younger kids, with dementia. I call it a diagnosis of the family because of its far-reaching impact. As my husband bravely faced this condition, so did our sons, as they were witness to a complex, unforgiving, terminal brain condition in their Dad, while navigating changes in their mom. I was changing too, and like so many spouses, I soon became primary care-partner, sole breadwinner and solo parent.

Quickly, I recognized the massive support gap for families like ours. Younger families with dementia are unseen, misunderstood and under-resourced. We are undiagnosed, misdiagnosed and under-researched. There are millions of us worldwide, yet the resources designed for us are sparse to none. I was determined to make meaning of things and to bridge this support gap. I envisioned a place where we could find others with our similar story…a virtual, innovative, brave place where sons, daughters, children and families of YOD could belong, build community and find light. I imagined Lorenzo’s House.

In 2021, after a 25+ year career as an educational entrepreneur, and co-founder & president of a network of public schools in Chicago, I took a leap of faith and founded Lorenzo's House out of our son’s bedroom. With the metaphor of light guiding our family journey, our tagline ‘We Bring Light’ permeates our mindset and language at Lorenzo’s House. We are shifting the narrative for younger families…from isolation to connection, stigma to strength and dark to light. Together, we heal in community, advocate for dementia justice and educate for a YOD informed society. With a focus on developing leadership in our sons, daughters and children of younger-onset, we are changing the way the world thinks, experiences and responds to dementia. - Diana, Founding Executive Director, Lorenzo's House

bringing light since 2021...

Impact Over The Years

2021 Impact Report

OUR YEAR AROUND THE SUN
21 young people at SUMMIT, 18 US States, 12 partners,
125 donors
Received $1M anonymous donation
View Impact 2021 Report  >

2022 Impact Report

We Bring Light
200+ families connected & empowered, 32 US states & 3 countries,
43 young people at SUMMIT, 60 MATCH connections,
40+ partnerships & collaborations, 176 donors
Launched our CLUBS-virtual spaces to share common stories, exchange insights and find community
View Impact 2022 Report  >

2023 Impact Report

BUILDING COMMUNITY CURING ISOLATION DRIVING DEMENTIA JUSTICE
1000+ families connected & empowered, 46 US states & 5 countries, 89 young people at SUMMIT, 40+ partnerships & collaborations,
188 donors
Created our youth-designed EmpowermentPLUS Model to dismantle dementia stigma.
View Impact 2023 Report  >

2024 Impact Report

WHAT HAPPENS WHEN FAMILIES IMPACTED BY YOUNGER-ONSET DEMENTIA FIND EACH OTHER?
WE ARE EMPOWERED.
2200 + family members connected & empowered, 48 US States &
15 countries, 203 young people at SUMMIT, 400 MATCH connections, 50+ partnerships & collaborations, 350 donors
Spread our mission as keynote at Alzheimer’s Disease International Conference in Krakow, Poland; Alzheimer’s Association Conference, Wisconsin, United States; ALTER Summit in Georgia, United States; and more!
View Impact 2024 Report  >

2025 Impact Report Coming soon.....

our people

Our Team

Diana Shulla Cose
Founding Executive Director
Stephanie Fitzgerald
Growth & Impact Lead
Bree Ruge-Ginley, CDP
Chief of Staff
Patti LaFleur
Programs Lead
Grania McKittrick
Global Outreach Lead
Swetha Karunakaran
Project & Comms Coordinator, NEXTGEN
Jessica Eggert
Youth Programs Lead
part-time
Tessa Garcia McEwen
Programs Support & Grief Specialist (LCSW)
part-time
Nicole Will
Development & Strategic
Partnerships Lead
part-time
Chelsea Mowery
Programs Support
part-time
Justin Cose
Technology Support
part-time
Shanelle Snowdon
NEXTGEN Liaison ‘Wisconsin’
part-time
Lenny Marsh
MMC Educator
& Musician
part-time
Lucas Cose
Social Media Support
part-time
Dan Healey
Social Worker &
Program Support (LCSW)
part-time
Glennese Ray
Chicago Community Partnership Liaison
part-time

our leadership

Board of Directors

Diana Shulla Cose
Rhonda Hopps
Jonny Imerman
Carine Kanimba
Leslie Knight
Bill Lowe
Tessa Garcia McEwen
Kitty Rothschild
Alisha Stickney
Arne Duncan
Honorary 
Board Chair

George Vrandenberg
Honorary 
Board Chair
Marc Wortmann
In loving memory of Marc

There are some who bring a light so bright to the world that even after they are gone it remains.

our advisors

Innovation, Medical, Science Advisors

Dr. Neelum Aggarwal, MD, FAMWA

Neurological Sciences, RUSH Alzheimer’s Center

Dianne Campbell

Founder & Former ED, The Village Chicago

Walt Dawson, DPhil

Co-Director, Oregon Center Behavioral Health & Aging

Dr. Fayron Epps, PhD, RN

Founder, ALTER, Emory University

Susan Frick 

Director of “Without Warning” Program

Judy Holstein, MS, LPC, RDT

Board Secretary, Institute for Therapy Through Arts

Carl Honoré

Author, speaker, broadcaster, longevity expert. Pioneer of the Slow Movement

Berna Huebner

Co-Director, I Remember Better When I Paint

Dr. Robert Luby, MD

The Institute for Functional Medicine

Lori La Bey

Founder and CEO, Alzheimer’s Speaks

Angela Lunde, M.A

Outreach & Education Lead, Mayo Clinic

Dr. James Mastrianni, MD, PhD

Director, The Memory Center at UChicago Medicine; Professor of Neurology

Darby Morhardt, MSW, LSW

Outreach Director, Mesulam Center, Northwestern Medicine and research professor

Daniel C. Potts, MD, FAAN

Neurologist, U.S. Department of Veterans Affairs

Adria Thompson MA, CCC-SLP

Founder, Be Light Care, influencer

David Troxel

Founder, Best Friends, Memory Care Model

Dr. Raj C. Shah, MD

Neurological Sciences, RUSH Alzheimer’s Center

Carrie Shaw

CEO & Founder, Embodied Labs, Daughter of YOD

Wendy Weidner

Former Research & Policy Head, ADI 

our community leads

Lead Volunteers &
Club Facilitators

Stephanie Adler
Haley Boyle
Kimberly Cruelle
Dan Hoffman
Eirwen Kamphorst
Joe Kruger
Jessie Piltch-Loeb
Victoria Slater
Alisha Stickney
SJ Townsend
Melissa Tucker
Neve Wilson

Collaborate &
partner with us

From sharing resources for younger families, learning about our virtual, global support model or sharing research.

Together we shine brighter!