Open doors for families with Lowe syndrome: sponsor Walk & Roll 2026
Last year, 15 families raised more than $68,000 in our first Walk & Roll campaign. This year, we’re aiming higher, and we’re inviting businesses to walk, roll, and open doors with us as sponsors of the 2nd Annual Walk & Roll for Lowe Syndrome, November 24 through December 2, 2026.
Lowe syndrome is a rare disease, and pharmaceutical companies rarely prioritize rare diseases. No one is coming to solve this for us. The Lowe Syndrome Association (LSA) is building the path ourselves, and our sponsors are how we move faster.
Choose the impact you want to make
Every level unlocks something specific for families:
- Presenting Sponsor, $10,000: Drives medical research toward targeted therapies and breakthroughs.
- Diamond Sponsor, $5,000: Directly funds clinical research grants and scientific data collection.
- Platinum Sponsor, $1,000: Accelerates rare disease awareness and national advocacy.
- Gold Sponsor, $750: Expands family access to information, toolkits, and care guidance.
- Silver Sponsor, $500: Fosters family support networks, educational webinars, and peer connections.
- Friend, $250: Provides vital online educational resources to newly diagnosed families.
That last one matters. When a parent gets a diagnosis at 2 a.m., those resources are often the first thing they find.
What your company gets
Your team is recognized as the partner it is, with logo placement on our Walk & Roll page and campaign materials, features in the LSA Quarterly Newsletter, and dedicated social media spotlights. Higher levels add co-branded banners, custom thank-you videos from our leadership and board, and for our Presenting Sponsor, an exclusive email to LSA’s donor network. The full packet has every detail.
Why this is a can’t-miss moment
Sponsoring Walk & Roll puts Lowe syndrome in front of employees, customers, and neighbors who have never heard of it. Some will become donors and advocates. More awareness leads to more funding, and more funding leads to better treatments. That is how a rare disease stops being invisible.
Behind every logo on our page is a team that chose to show up for a family they may never meet. Our families remember that.
Three ways to act today
- Pick your level. Choose the impact that fits your team.
- Send your commitment. Complete the Sponsorship Commitment Form and email it to lsa-admin@lowesyndrome.org, or make your sponsorship gift online. It takes just a few minutes.
- Introduce us to your employer. Families, this one is yours. Forward this post to your workplace, a local business, or a friend who owns one. Your story is the most persuasive pitch we have.
Become a Walk & Roll sponsor and open doors for every family living with Lowe syndrome.
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