By Nick and Katie
Nick and Katie share their experience of H.I.E. and their beautiful daughter Alannis.
Family Stories
Stories from our families
We understand that H.I.E. can affect families in so many different ways. Our experiences may not always be the same, but having a sense of belonging, and reassurance that you aren’t on your own can be so important.
In this section you can read about other families who have been touched by H.I.E.
As always, if anything is a trigger, or you want a little support, please don’t hesitate to get in touch. We’re here for you.
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
