Posts - Encephalitis Society | HealthUnlocked

Encephalitis Society

606 members • 440 posts

All posts for March 2020

Best experience of being part of the encephalitis society community?

Has anyone got a best experience/s, interaction or memory? For me it was attending my first event with my wife. Meeting other members and staff Having a...

Has anyone got a best experience/s, interaction or memory? For me it was attendi...

•4 years ago

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 survivors that really helped me. Has anyone else found...

When I joined the Encephalitis Society in 2019 it was the personal accounts of m...

•4 years ago

Mind and seek podcast

With Every one spending more time at home one idea is to listen to the "Mind and seek" podcast. It is a young couples experiances of Encephalitis, they touch...

With Every one spending more time at home one idea is to listen to the "Mind and...

•4 years ago

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Attending any support groups or meetings?

Other than this community and health unlocked platform, does anyone attend any support groups, charity organisations or meeting? I recently found a great group...

Other than this community and health unlocked platform, does anyone attend any s...

•4 years ago

Has reading others stories helped reduce isolation or increase understanding?

It took me many to start the process of understanding Encephalitis and my journey. But reading encephalitis society members stories made such a huge difference...

It took me many to start the process of understanding Encephalitis and my journe...

•4 years ago

Thoughts and ideas since starting this trial

After 3 days I have started to communicate with other users/members and communities which, I think might be relavent or useful for my understanding of...

After 3 days I have started to communicate with other users/members and communit...

•4 years ago

Changing relationship with parents

My parents have been with me through this 17 year journey every step of the way. Over the years they have struggled to change their role from care giver back...

My parents have been with me through this 17 year journey every step of the way....

•4 years ago

I am New Here

My hope by being part of the community is to learn more about encephalitis and ABI by listening to others, posting questions and supporting others. I have been...

My hope by being part of the community is to learn more about encephalitis and A...

•4 years ago

Hello to everyone!

Hello to everyone. I’m new to this but I’m really hoping that being part of this community will help our struggle with Encephalitis. It will be a year next...

Hello to everyone. I’m new to this but I’m really hoping that being part of this...

Ilovecornwall4ever

•4 years ago

When were you/your loved one diagnosed with encephalitis?

Hello everyone! To get the ball rolling, lets have a question. When were you/your loved one diagnosed with encephalitis? What was the trigger for diagnosis?...

Hello everyone! To get the ball rolling, lets have a question. When were you/yo...

EncephInternational

Partner•4 years ago

Community Guidelines

Welcome to the Encephalitis Society Community for support of encephalitis! We’re very glad you have chosen to be a part of our community. The Encephalitis...

Welcome to the Encephalitis Society Community for support of encephalitis! We’r...

EncephInternational

Partner•4 years ago

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