A place for
hope, support & connection.
Our Mission
We’re building a new website for the HNRNPH2 community. Hope for H2 exists to bring research, treatment and support within reach of every UK individual affected by HNRNPH2-related NDD.
Information & Support
Provide information and support to affected individuals, their families and carers, and raise awareness among clinicians and the public.
Funding
Raise and apply funds to meet the UK clinical and administrative costs of enabling access and the associated care.
Working with Services
Work with services such as NHS Genomic Medicine Service and patient registries such as Simons Searchlight to identify UK patients who may benefit.
Facilitating Access to Treatment
Act as the UK organisation that supports and facilitates access for eligible individuals to treatments and therapies for HNRNPH2-related neurodevelopmental disorder that may help them.
The company identifies suitable options, works with clinicians and providers, and helps individuals obtain access through recognised regulated routes.
This is facilitating access to treatment, and is not the conduct of a clinical trial.
What is HNRNPH2?
HNRNPH2-related neurodevelopmental disorder (HNRNPH2-NDD) is a rare genetic condition caused by changes in the HNRNPH2 gene. It can affect development, communication, movement, behaviour and other aspects of health. Because HNRNPH2 is rare, families can face challenges finding information, support and access to appropriate services.
Who we are
Hope for H2 was created by UK families affected by HNRNPH2-related neurodevelopmental disorder. We understand the challenges that families face when living with an extremely rare condition, from finding reliable information and connecting with others to navigating healthcare and exploring potential treatments.
Are you affected by HNRNPH2
If you or someone in your family has been diagnosed with HNRNPH2, we'd love to hear from you and help connect you with the growing UK HNRNPH2 community.
Get in touch