Family Registration Sponsorship

Initial Expression of Interest

Family Sponsorships Now Open for INDConf 2025
Join the Neurotransmitter Workshop in London

Thanks to the Chan Zuckerberg Initiative and Hrabrisa Charity Partnership we are pleased to be able to offer a limited number of sponsorship packages for families affected by rare neurotransmitter disorders to attend INDConf 2025, taking place 5–7 November 2025 at Goodenough College, London.

As part of the conference, families are invited to participate in a dedicated session:

Neurotransmitter Workshop for Patient & Public Engagement

Date: Friday, 7 November 2025
Location: Goodenough College, London

This interactive session will bring together families, clinicians, and researchers to explore:

• Diagnostic journeys
• Prognostic insights
• Therapeutic approaches
• Patient-driven priorities

Your voice matters. This session is designed to put families at the heart of the conversation.

What's Included in the Family Sponsorship Package

Each sponsorship includes support for up to 2 family members:

• ✅ Free registration for all 3 conference days (registration required)
• ✅ Accommodation and full board for 3 nights (meals included)
• ✅ Travel reimbursement of up to £275 GBP per person (max 2 individuals)

Accommodation will be arranged on your behalf. Travel costs will be reimbursed within 2 weeks after the event (families must book flights themselves).

What You Need to Know

• ⚠️ Attendance at conference sessions is mandatory for sponsored participants.
• Families can extend their stay in London at their own expense.
• Sponsorships are for families with a child diagnosed with a rare neurotransmitter disorder.
• Please indicate your child’s diagnosis when applying.
• The conference will be held in English. While no official translation is available, informal support will be provided as best we can.
• Visa support letters will be issued upon request for confirmed families.

How to Apply

To express interest, please submit a short letter of interest or motivation to:

📧  lisa.flint@ucl.ac.uk or 📧  office.hrabrisa@gmail.com

Applications are reviewed on a rolling basis. Space is limited.

Join us in London this November. Help shape the future of care and be part of an empowering international gathering dedicated to families living with neurotransmitter disorders.

We can't wait to welcome you!

This sponsorship is proudly supported by the Patient Organization for Rare Neurotransmitter Diseases – Lil’ Brave One (Hrabrisa) and has been made possible in part by grant 2024-347839 from the Chan Zuckerberg Initiative DAF, an advised fund of Silicon Valley Community Foundation.