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.
Medics4RareDiseases registered as a UK charity who’s object is the relief of sickness and preservation of health of those suffering from rare diseases.
The tragic death of Elliot reminds us that knowing about rare diseases doesn’t just improve the patient journey but it can save lives in emergency situations. Find out more about Elliot and urea cycle disorders.
Our understanding about fibromuscular dysplasia is evolving. Find out more about this under-diagnosed and serious condition from Dr Tina Chrysochou, Consultant Nephrologist.
History, Examination, Investigation, Diagnosis…?
I must admit that, until recently, I hadn’t really given much thought to the issues surrounding rare diseases. When studying for exams, I dutifully learnt what I thought were all the steps in managing various conditions.
Dr Lucy McKay becomes the new (and first ever) Chief Executive Officer of Medics4RareDiseases.
Medics4RareDiseases are excited to announce the launch of their new research project: The M4RD Red Flags Survey. The purpose of the survey is to find out what different rare diseases have in common during the time before diagnosis, a period often called ‘the diagnostic odyssey’. We need all UK based patient groups to take part. Read more to find out how…
This week a brilliant campaign was launched to raise awareness of childhood dementia
VIDEO: Dan Jeffries, owner of two rare diseases and author of ‘Me, Myself & Eye’, interviewed M4RD Founder Lucy McKay. Watch the video to hear Dan’s interesting story of being diagnosed during an OSCE and to find out what M4RD is all about from the zebra’s mouth.
Another brilliant Rare Disease Day. This year we rebranded to Medics4RareDiseases!