Support for parents, families & friends of those who have experienced an H.I.E. event
(Hypoxic-Ischaemic Encephalopathy)
Welcome to Peeps
We pride ourselves on the support we can offer those who have been touched by H.I.E. We also aim to raise awareness of H.I.E. – some of the things we do include:
- Provide information (translations are available)
- Peer Support
- Counselling and therapy
- Funding for equipment.
- Events to connect families.
Register with Peeps
For those who may be looking for information, or want to join our community, please fill out this form - we are here for anyone touched by H.I.E., whether families, friends, or those who support in a work capacity.
I acknowledge that by submitting this form I allow Peeps to use this information to process my referral in line with our website Privacy Policy .
Meet The Team
Stacey Attaway
Trustee
Aishat
Leah
Events Coordinator
Jess
Income & Engagement Officer
Sarah Land
Co-Founder & Charity Manager
Jen Cawthorne
Chair of Trustees
Hannah Adams
Dr Ela Chakkarapani
Erika Lucas
Trustee
Jenny Clough
Trustee
Peeps on Twitter
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@CHillemand can provide advice to Peeps families about making a compensation claim for their child (and themselves) as well as getting or challenging an EHCP. This os a free service for Peeps families so please contact her if you have questions.
A reminder @CMooreSolicitor, Partner has been holding free virtual legal clinics for @PeepsHie every Thursday this month. There is one more session available tomorrow (30 January 2025). To enquire with Charlotte contact her on charlotte.moore@clmedilaw.co.uk or 07388 949953.
Can you help improve data on avoidable brain injury around the time of birth? Maternity/obstetric/neonatal/paediatric colleagues please complete/retweet this survey https://ths.im/4iLI7kY
@MidwivesRCM @RCObsGyn @BAPM_Official @RCPCHtweets @NeonatalSociety @ScotNeoNurses @NNAUK1
