Improve awareness into Congenital Hyperinsulinism and fund research
Improve awareness into Congenital Hyperinsulinism and fund research
Introduction
Hyperinsulinism (CHI)
Management of CHI
Background of the Children's Hyperinsulinism Fund
National Designated Centre
Children's Stories
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Other Sites of Interest
UK PHII Support Group
Improve awareness into Congenital Hyperinsulinism and fund research
UK PHHI Support Group

Patron:
Sir Terry Wogan OBE

Hi, my name is Julia Killengray and I am the mother of Ellie and Tate. They both have Congenital Hyperinsulinism (CHI) or you may know it as PHHI (Persistent Hyperinsulinaemic Hypoglycaemia of Infancy) or Nesidioblastosis. You can read their story in 'Children's Stories'. In 2000, I set up a support group for this condition and approximately every 1-2 years we have a meeting for parents to have the chance to meet and share experiences. We also meet the doctors and are able to ask them questions after their presentations which we find very helpful. I also endeavour to keep parents who have joined the group up to date with anything new that is going on with CHI.

Contact

Mrs Julia Killengray
17 Bridge End Lane
Great Notley
Essex
CM77 7GN
Tel: 01376 528569 time to ring: 10am - 4pm Mon - Fri
Email: juliakill@tiscali.co.uk

View Archive of Notes from UK CHI Support Group Meetings

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The Children's Hyperinsulinism Fund is a restricted fund to Great Ormond Street Hospital Children's Charity registration Number 235825