My Brain: My Story: My Family Event 1... - Encephalitis Inte...

Encephalitis International

644 members456 posts

My Brain: My Story: My Family Event 12th October 2024

EncephInternational profile image
1 Reply

We would love you to join us in Newcastle, England or virtually at My Brain : My Story : My Family this October 12th (10am to 6pm)

This hybrid event is for anyone who wants to listen to the experiences of people who have been directly or indirectly affected by encephalitis. There will be opportunities to ask questions of the speakers and join us afterwards for a drinks reception (in person attendees) or the virtual support gathering.

At this years event we will be having a session in the morning which will be aimed at encephalitis in children. The afternoon session will be aimed at encephalitis in adulthood.

You are welcome to attend one or both sessions.

Children and young people are welcome to attend and we will provide activities throughout the day (the activities are suitable for ages 4+ and are available to in person attendees only). Please note we are not able to provide one to one specialist care.

Confirmed Children’s workshops

Big Science UK – a fantastic opportunity for children to participate in hands on science experiments which may include slime, sherbert making, film canister rockets as well as Big Science demonstrations.

____________________________________________________________________________________________________________

Confirmed Speakers:

Encephalitis in children and young people

Diane Adebayo (UK) – Person Affected and Team Encephalitis Volunteer

Kellie Murphy (Ireland) – Parent of child affected

Encephalitis in adults

Hannah Rowlands (UK) – Person Affected and Team Encephalitis Volunteer

Jim Cooper (US) – Person Affected.

Chris Moore (UK) – Person Affected.

Eduarda Moreira (Brazil) – Person Affected.

------------------------------------------------------------------------------------------------------------------------

Programme

10am – Arrivals

10.30am-12.00pm Parents/young person ‘lived’ experience speakers. Children/young people workshop activities

12.00pm Lunch

1pm-5pm – Adult ‘lived’ experience speakers. Children/young people workshop activities.

5pm – Drinks reception (in person attendees) / On line after event support gathering (virtual attendees)

6.00pm – Close

____________________________________________________________________________________________________________

Ticket Information

The cost to attend in person is £5.00 per adult (25+)

Tickets for Children/Young people (25 & under free of charge)

If you are joining virtually tickets are free of charge.

____________________________________________________________________________________________________________

The Venue

Northumbria Students Union: 2 Sandyford Road Domain Newcastle upon Tyne NE1 8SB

Venue is accessible by public transport.

There are a limited number of car parking spaces available. To reserve a space please register for a car park ticket if required.

Lunch and refreshments will be provided.

Book your place here:

encephalitis.info/event/my-...

Written by
EncephInternational profile image
EncephInternational
Partner
To view profiles and participate in discussions please or .
1 Reply
Paula-38 profile image
Paula-38

I have booked my virtual ticket and the break out room, as soon as it was first advertised on Twitter, I quote tweeted a while ago just after it advertised. Have a look. I have saved the date.

Not what you're looking for?

You may also like...

Hi my journey is a little different.......

Hi All, Apologies, that this will read a little different from so many of your posts. My journey...

My Brain and Me video and Your stories

When I joined the Encephalitis Society in 2019 it was the personal accounts of members, carers and...

A comeback is possible

Happy New Year all! Firstly, I want to say sorry in advance to anyone reading this who is having...

Pushing limits again!

Hello fellow e-peeps! As December has once again gotten here too fast, so has the holiday season!...

NO END IN SIGHT

Last month, I was officially diagnosed with seronegative autoimmune brainstem encephalitis, which...