Membership is open to national patient organisations which represent mitochondrial disease patients and their families.
Please join us and strengthen the international voice of mito patients around the world.
There is an annual membership fee which supports the work of IMP.
If you are interested in joining or have questions about the membership, please contact us.
Why become a member
IMP is the leading international body for mito patient advocacy groups. IMP facilitates connections with international networks within the medical world, researchers and industry.
Membership provides international validation of member organisations, can facilitate bilateral collaborations and adds weight to international funding consortium bids. It also provides an opportunity to be part of significant international projects such as Genomit and Simpathic, benefitting patients globally and locally.
IMP also offers the opportunity for global virtual and face-to-face forums where members can connect, communicate and collaborate.
We send out regular communications about international developments, and promotion of members' activities to a worldwide audience.
IMP is a critical source of best practice, experiences and ideas.
There are different ways we can help support you and connect you to the international mito community. To learn more about what members access by being part of IMP, see ‘support for patient organisations’.
If you are interested in joining or have questions about the membership, please contact us.