Where can I find out more about ERNs?
You can find out more about ERNs on the European Commission website
This website is available in multiple different languages.
You can also find out more by watching this video and by reading this flyer. These are available in all European languages and can be accessed via this link under 'Related information': https://ec.europa.eu/health/ern_en
How can I stay updated on ERN CRANIO activities?
How do I become a patient representative for ERN CRANIO?
If you are interested in being a patient representative for ERN CRANIO you can express your interest to Olivia Spivack (Project manager): firstname.lastname@example.org
She can then explore this further with you. If you want to find out more about patient involvement you can also email Olivia.
How can my or my family member's clinical care be supported by ERN CRANIO?
If you are a patient or a family member of a patient with a rare and/or complex craniofacial anomaly or ENT disorder, ERN CRANIO may be able to support you clinically. Patients cannot refer themselves directly to receive the support of an ERN. However, with a patient's consent and in accordance with the rules of their national health system, a patient’s information can be referred to the relevant ERN member in their country by their local healthcare provider. Their local health care provider can then access expert advice from the network, if this is needed.
If you are interested in accessing support from ERN CRANIO, we encourage you to speak to your local healthcare provider. You can let them know about ERN CRANIO, a multidisciplinary network of highly specialised healthcare professionals from across Europe who may be able to provide expert advice specific to your rare disease or condition.
These are available in all European languages and can be accessed via this link under 'Related information': https://ec.europa.eu/health/ern_en