Elliana’s Army Presents ‘Light The Night For Darcie’
Elliana’ s Army is a compassionate community united to honour the legacy of Elliana Rose Campbell, who passed away at just 10 months old from Junctional Epidermolysis Bullosa (EB). What started as a social media group has turned into a non-profit. We are dedicated to raising awareness and funds to combat this devastating genetic skin condition. Through fundraising initiatives, merchandise sales, and memorial events, we support existing organisations such as EB Research Partnership, DEBRA UK, debra of America, and others, providing resources for affected families and advancing research toward a cure. This is our promise, our passion, and our purpose: Mission: End EB.
Through a powerful night of light, remembrance, and hope, the event raises critical funds for EB research and family support for DEBRA UK. We’re inviting compassionate brands to partner with us in this growing movement that spans across continents and touches thousands. Sponsors will gain visibility, emotional connection with a loyal and cause-driven community, and a chance to create genuine impact.
Target Audience
Approximately 140 attendees, from the community of Suffolk and surrounding areas, who are actively engaged in charitable initiatives. Many are affluent professionals, business owners, and local leaders who value giving back and supporting meaningful causes. Sponsors can expect an audience that is financially capable, socially connected, and deeply committed to community engagement, providing excellent visibility for supporting brands.
EA outreach appeals to: Families, healthcare advocates, rare disease supporters, 25–50 age range, parents, educators, socially conscious individuals.
ABC1 demographic, community-driven and active on social media. UK and US-based participation.
Key Dates and Timings
6pm- 10pm, Friday 7th November, 2025, Seckford Hall, Woodbridge, Suffolk, IP13 6NU
Specific Opportunity Details
Light the Night for Darcie; Partnership Opportunities
Light the Night for Darcie is more than a gala, it is an annual premier fundraising event created to raise awareness and support for Epidermolysis Bullosa (EB). This elegant evening unites sponsors, community members, and advocates to drive critical funding for research, family assistance, and public education.
*Hosted at the prestigious Seckford Hall in Woodbridge, Suffolk, the event features:
*Fine dining in an elegant Tudor setting
*Dancing and live entertainment
*A silent auction with curated items
*A candlelight vigil honouring those who have lost their battle with EB
Proceeds benefit DEBRA UK, the National Charity supporting individuals and families affected by EB. Your sponsorship not only helps fund groundbreaking research but also ensures families receive the care and resources they need as we work toward a cure.
Why Partner with Light the Night for Darcie?
Brand Exposure & Recognition
Prominent logo placement, social media shout-outs, and event signage, creating meaningful visibility before, during, and after the gala.
Emotional Connection & Cause Led Storytelling
Sponsoring builds emotional resonance through Darcie’s journey and the wider EB community, aligning your brand with compassion and hope.
Community Engagement
An opportunity to connect with a compassionate and engaged audience, potential customers and collaborators.
Support with Tangible Impact
Every pound raised goes directly to DEBRA UK,(Registered Charity Number, 1167938) funding vital research, patient services, and advocacy for EB families.
Inclusive, Multi Format Engagement
Your impact extends beyond the gala. At-home supporters engage through the purchase of candles and ornaments, potential for broadening reach and reinforcing your brand’s involvement. We have 5,925 followers 149.2K Likes on Tik Tok and growing outreach on Social Media.
The Value of Your Support
As a sponsor, you are not only funding an unforgettable evening, you are bringing vital support to Darcie and countless others living with EB. You are helping families today while investing in a future free from this devastating disease.
With its annual format, Light the Night for Darcie offers an enduring platform for visibility, community impact, and brand alignment with a powerful cause.
Features and Benefits
Branding on event materials as below, signage and digital promotion. Elliana’s Army platform is extensive. We can offer; Logo on official event materials, keepsakes, and thank-you mailers.
Promotion via email, Facebook and TikTok
Sponsor spotlight in post-event video tribute
Opportunity to be featured in video/storytelling content
Emotional alignment with a rare cause creating long-lasting brand loyalty
Recognition in press releases, marketing campaigns and event programs.
Sign with logo/QR code on Cake Table
Photographer will wear a badge with your logo
Sign with logo/QR code on DJ Booth
Swag Bags- Add your products and swag to our VIP bags
Bar- Logo featured on cocktail napkins, sign on the bar
Photo Booth- Logo featured on all photo strips from Photo Booth
Lighting- Your name in lights on the dance floor
Decor- Logo featured on candles for vigil, and on signs throughout
Catering- Logo featured on dinner menu, food table, and all guest tables
All sponsorship contributions directly support EB research, family support services and public awareness initiatives. Sponsors are publicly recognised for their vital role in making this event possible.
Other Partners
EB Research Partnership
DEBRA UK (collaborative awareness)
Investment
We are looking for between £500- £5000
Cash preferred, but product or promotional support (e.g., printing, candles, lighting, video services) also welcomed.
Sponsorship required for:
Cake £250
Photography £300
Music £400
Swag Bags £450
Bar £750
Photo booth £800
Lighting £1000
Decor £2000
Catering £5000
Other Info
We think it is important that you are introduced to Darcie Game, daughter of Alice and Ben Game, who was born on December 4, 2024, with a rare and devastating genetic condition known as Junctional Epidermolysis Bullosa (JEB). This disorder causes fragile skin that blisters and tears from even the gentlest touch or movement and also affects internal areas like the digestive tract and oesophagus. Despite these unimaginable challenges, Darcie greets most days with her signature smile. Her strength, resilience, and joy touch everyone she meets and serve as a powerful reminder of the courage found in even the smallest warriors. Babies born with severe forms of JEB often do not survive past their second birthday. Darcie’s story underscores the urgent need for better treatments and ultimately, a cure for all those affected by Epidermolysis Bullosa.
This is a unique opportunity to support a growing movement around an under-represented but critical cause. The event stands out for its emotional power, storytelling, and family-centred design. Our sponsor family becomes part of a global fight for awareness, hope, and healing.