An Update from our CEO
14/04/2020
A message to our members and supporters
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A personal message from our Head of Patient Services, Pat McBride (pituitary patient)
19/03/2020
Some common sense in the madness
Rare Disease Film Festival
24/02/2020
Rare Disease UK held a special screening of Rare Disease short films
Pauline's Blog: An insight into our Nurse Helpline
23/02/2020
Pauline's quarterly blog on the calls she receives on our Endocrine Nurse Helpline
