To provide people with Hereditary Haemorrhagic Telangiectasia (HHT), also know as Osler-Weber-Rendu Disease and their families with information about the condition.
- Put people with HHT in touch with one another
- Keep people with HHT informed of developments in research and treatment of this condition.
No charge for membership, though all donations are welcome.
Monday – Friday, 9.00am – 5.00pm.
Although this organisation serves mainly the UK, it does have some international contact.
39 Sunny Croft