Services provided:
The Degos Disease Support Network is a contact group, a support group and an information hub for those affected by Degos disease.
Medical professionals who are seeking help will find information, links to medical sites and to ongoing research.
As Degos disease is an extremely rare disease, the Support Network welcome input from those affected by it. They also welcome donations to help with the running of the Support Network and to assist the research into the disease.
Opening hours:
Can be contacted seven days a week, twenty four hours a day.
Address
Website: http://www.degosdisease.com/
Email: judith@degosdisease.com
