For patients and carers
This platform is not able to provide individual medical advice or support. If you are seeking help, please contact the ME Association helpline, your GP, or local support services. The resources page includes links to organisations that may be able to assist.
For clinicians and healthcare providers
If you are a healthcare professional seeking educational materials, clinical guidance, or information to support better care for ME patients, we welcome your enquiry. Please include your professional role and the specific resources or information you require.
For policymakers and institutions
Enquiries from government bodies, healthcare institutions, welfare agencies, and other public bodies are welcome. This platform can provide briefing materials, evidence summaries, and consultation on ME-related policy matters.
For journalists and media
Media enquiries are considered on a case-by-case basis. This platform prioritises accuracy and dignity in coverage of ME. Sensationalist or trivialising approaches will not be supported. Serious investigative enquiries are welcome.
For researchers
Researchers working on ME or related conditions may find the resources on this platform useful. Collaboration enquiries should include details of your institution, research focus, and how the work aligns with the principles of this platform.
Send a message
Messages are reviewed periodically. Response times may vary. This form does not create a professional relationship.
This platform exists to present truth, not to engage in debate about established facts. Correspondence that denies the biomedical nature of ME, promotes discredited treatments, or is otherwise contrary to the evidence will not receive a response.