About The Dementia Funders' Network
About The Dementia Funders' Network
Embedded Files
The Dementia Funders' Network is an independent private group of individuals and organisations who support dementia research around the world.
The initial aim is that the network will:
1) Provide a confidential forum for members to hear about, share and discuss possible research opportunities
2) Provide opportunities for funders to co-donate on research projects
3) Distribute news about key research progress and breakthroughs globally
4) Offer occasional educational talks on specific areas of dementia science or research
The network is specifically aimed at supporting and connecting those who are making significant philanthropic donations in the dementia space. While there are no fixed criteria for membership, we suggest that this might be those who have in the past, are currently, or intend to donate amounts in excess of $500,000 or the equivalent in other currencies.
There is no charge to join the network and no commitment to any level of involvement. The names of members will be confidential and only shared within the group.
The network will have not have any ties, commercial interests, allegiance or restriction to any specific research area, any specific country, or any specific research organisation or charity.
If you would like to join (or discuss joining) the network please email: members (at) dementiafundersnetwork.org
Our initial research focus areas will be:
Fundamental and pre-clinical
Mechanisms
Cell models
Animal models
Drug discovery
Drug development
Biologies
Genetic Therapy
Clinical
Diagnosis
Progression measures
Prognosis
Biomarkers/Imaging/Digital
Brain behaviour
Risk Factors
Delivery of prescription drugs
Repurposing existing drugs
Trials
Trial design
First in human
Early-phase
What we're doing now
What we're doing now
The network is being launched in Q4 2025.
Phase 1 (Q4 2025):
1) The initial phase will be to identify potential members. We will invite them to join the network, and consult with them, to hopefully verify that the four aims of the network (detailed above) are the right goals, and that they're aligned with their interests or needs.
2) We will identify sources of important dementia news, which we'll distil into a succinct summary that is digestible by members who are not clinicians or scientists. This will ultimately lead to a newsletter for members which will be distributed approximately monthly by email.
Phase 2 (Q1 2026):
1) Formal launch of the network. This will include the development of the website to include a secure and confidential forum.
2) We will investigate if we should partner in a non-exclusive and non-commercial way with any other relevant not-for-profit organisations in the dementia information space who might help us be more effective or whom we might help or support.
Phase 3 (Q2 2026):
1) Subject to levels of interest we will hold a number of trial educational video calls and assess the value of these to members.
Page updated
Google Sites
Report abuse