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 IIH Social Inclusion Campaign

IIH Social Inclusion
©2016. I Have IIH Foundation. All Rights Reserved. Design by BimboIIH Social Inclusion ©2016. I Have IIH Foundation. All Rights Reserved. Design by Bimbo

People who have IIH aren't viewed as being ill because their condition is an invisible one. You can't see a headache, or any of their other symptoms and because IIH is rare, people are not as familiar with it as they are other well known conditions. The person who has IIH often find themselves isolated, misunderstood and feeling totally alone. 

Join us in our campaign by raising awareness for Idiopathic Intracranial Hypertension and visibility for the unrecognised people living with this disease. If you have IIH we'd love to add you to our gallery and give you the recognition and visibility you deserve. Together we can stand up and say "IIH is invisible but I am not!" Send us your photo with your name, age and where you're from.

We'd like to thank Design by Bimbo for our artwork and our friends with IIH in America for helping us with our campaign by sending in their photo's. 


Opinions are made to be changed - or how is truth to be got at? Lord Byron

Add our banners to your social media and join us in promoting social inclusion for people living with IIH. Just click on the links to download them.The more people who join us the greater the impact. You don't even have to be from the UK.

Use #IIHSocialInclusion #StandproudforIIH


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We are the TRUE faces of IIH

We have a rare disease you cannot see.
We could be YOU!

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