Polyposis Registry Information Evening 16/09/2021

17:00–19:00, 16th September 2021

Information Evening for patients with a diagnosis of a polyposis syndrome and their families

About this event

How we are delivering services in the COVID era and beyond. Listen to what’s new in clinical management and research. Hear from the chair of the polyposis support group and get involved. Plenty of opportunity to ask questions in the Consultant Q&A session and to meet the team.

1. Welcome: Cheryl Grainger polyposis patient support group
2. Service delivery in the covid era and beyond: Vicky Cuthill
3. What’s new in clinical management and research: Dr Andrew Latchford
4. Polyposis patient support group: Cheryl Grainger
5. Consultant Q&A Panel: Professor Sue Clark, Dr Andrew Latchford, Dr Kevin Monahan, Vicky Cuthill and the polyposis registry team

1 Welcome – Vicky Cuthill and Cheryl Grainger

2 Service delivery in the COVID era and beyond – Vicky Cuthill

3 What’s new and what’s on the horizon in polyposis syndromes – Andrew Latchford

4 Polyposis Patient – Cheryl Grainger

5 Questions and Answers – Panel