About IIH UK
Over the course of 2016 IIH UK will continue to work to ensure that we become part of a collective voice of organisations that represent genetic and neurological conditions. This will enable further awareness and campaigning for improvement for the lives of patients and families affected by IIH. In addition, this will assist in IIH being better understood by the general public and by all professionals with whom IIH patients come into contact. IIH UK are working closely with Dr Alexandra Sinclair the UK's IIH expert and her team of clinicians in Birmingham. During 2015 we began the process of setting up a Priority Setting Partnership facilitated by the James Lind Alliance, where we will come together with clinicians and patients to prioritise and determine the Top Ten areas of IIH research that are deemed the most important and need further research.
IIH UK is members of the following organisations:
Visit Raremark's website here
IIH UK was the ‘brain child’ of Rachel Turner, an IIH sufferer and original owner of the IIH Support Forum. Back in 2004 Rachel and other support forum members realised that although there were other organisations that provided some information on Idiopathic Intracranial Hypertension there was no national organisation dedicated to the needs of sufferers in the UK. So why not set one up?
It took a while to get things moving but after much organisation IIH UK held their first AGM on 17th May 2008 and officially became a Voluntary Organisation.It was a step in the right direction. None were especially qualified to run a voluntary organisation and progress was slow. In 2009 Rachel made the difficult decision to stand down as chair of IIH UK and to close the support forum. The forum at that time was run solely by Rachel and was independent from IIH UK. She had dedicated years of her life to running the support forum and the setting up IIH UK and it was time for her to let go of the reins and get back to living life.
Of course IIH UK could not let the support forum close down, Rachel had dedicated so much of her life to it, hundreds of people relied on it and for many IIH sufferers it was the only place where they could come for support. IIH UK took over the day to day running of the Support forum and changed its name to the IIH International Support Forum. The IIH Support Forum has always been, and will always be for IIH sufferers worldwide. We opened our online store giving people the opportunity to buy IIH Awareness Merchandise. www.iihukshop.moonfruit.com
August 2011 saw IIH UK become registered with the Charities Commission fulfilling Rachel’s dream.
The enthusiastic Team of volunteers have enabled IIH UK to grow and we are busy providing information, promoting awareness and supporting sufferers and their families and friends.With this in mind, we created 11 UK regional support groups for members to meet up socially. The groups are growing weekly, the largest membership being in the South East with over 170 members. Some of the groups meet monthly and have enabled some firm friendships to develop.
With the help of our members and supporters, we are distributing IIH patient information leaflets and posters into hospitals, GP surgeries, opticians, anywhere that will have them, to enable more IIH sufferers to access the information and support we provide. We continue to support people via the support forum and hold our annual ‘Weekenders’ giving people the opportunity to meet other people suffering with IIH.
Dr Alexandra Sinclair is a Consultant Neurologist at Queen Elizabeth Hospital, University Hospital Birmingham NHS Foundation Trust and NIHR Clinician Scientist at the University of Birmingham. Working as a NIHR Clinician Scientist in Neurology with a role combining clinical and research work into IIH and the neuroendocrine aspects of headache, she runs specialist headache services at the Queen Elizabeth Hospital Birmingham and has a specific interest into headaches relating to changes in intracranial pressure. Dr Sinclair wants to evaluate the best ways to treat IIH, evaluate the causes of IIH and gain understanding of the long-term consequences of the condition on health and people’s lives.
So much is happening. We have come a long way since our formation in 2008 and we still have a long way to go. Membership of IIH UK has grown steadily year on year and we would like to take this opportunity to thank each and every one of our members and supporters, for without their belief that we could make this work, their fundraising efforts and infectious enthusiasm we wouldn’t be where we are today.
Imagine your head feels as though it's been crushed by a vice, a headache unlike anything you've ever felt before, where every part of your head hurts and the pressure is unbearable, and it's a pain no-one can see.
Imagine a world in permanent soft focus, where things come in twos, where things disappear momentarily, where you can't tell how deep a step is, where bright light is a pain you can't stand.
Imagine a world that sways around you, where you feel as though you're in the middle of a storm on a cross channel ferry, feeling dizzy and sick - yet you're standing still.
Imagine you're so totally exhausted that your body doesn't want to move and all you want to do is sleep, yet an incessant roaring in your ears keeps you awake.
Imagine feeling lost and fearful, confused in a place you used to know well.
Welcome to the world of IIH!
©Copyright 2003 – 2016 Rachel Turner IIH UK