Diagnostic odyssey

Medics4RareDiseases becomes a UK Registered Charity

Medics4RareDiseases registered as a UK charity who’s object is the relief of sickness and preservation of health of those suffering from rare diseases.

2 June 2019

The Diagnostic Odyssey – A Mother’s Experience

Jo Higgs congenital, daretothinkrare, disease, interview, patient CSID, Deficiency, diagnosis, Diagnostic odyssey, Diet, Enzyme, Enzyme deficiency, Gastroenterology, Mother, Nutrition, rare, rare disease, Rare reality, Sugar 2

The diagnostic odyssey is a term used to describe the long and arduous journey that many rare disease patients find themselves on in pursuit of a diagnosis. The charity, Rare Disease UK, estimate that a patient with a rare disease will wait an average of four years for a diagnosis and be given an average […]

Medics4RareDiseases becomes a UK Registered Charity

The Diagnostic Odyssey – A Mother’s Experience

Everything You Wanted to Know about Genomics but Were Afraid to Ask

The NF Conference

RAREsummit19

Pompe Preceptorship

The 33rd symposium: Cystic fibrosis in children and adults