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An Update from our CEO

A message to our members and supporters

Matt & Becky - A pituitary love story!

Is this the first pituitary romance?

#EveryDayCounts Campaign

We urgently need your help

Emma's Story

A positive story to brighten your day

A personal message from our Head of Patient Services, Pat McBride (pituitary patient)

Some common sense in the madness

Online Shop - Reduced Service

A limited service is available

Two New Publications

Two new free publications available now

Coronavirus Update

The latest coronavirus update from Public Health England

Rare Disease Film Festival

Rare Disease UK held a special screening of Rare Disease short films

Pauline's Blog: An insight into our Nurse Helpline

Pauline's quarterly blog on the calls she receives on our Endocrine Nurse Helpline