W
elcome to the I Have IIH Foundation Patient Insights Network (PIN). By participating in this registry, you will enable researchers and clinicians to identify and understand the definitive symptoms of IIH, advance research into medications and alternative treatments, and help enhance the lives of people with this condition.
The more information gathered for research into IIH, the better the chances of finding more effective and less invasive treatment methods. You can make a difference by joining the registry and sharing your voice.
Each day, people are affected by idiopathic intracranial hypertension (IIH), riddled with debilitating symptoms and chronic headaches. Affecting anyone of any age, gender, body type and ethnic group, IIH primarily starts with an unbearable headache, neck stiffness, balance and memory problems, among other symptoms.
Our mission is to support, advocate and raise awareness for patients with IIH. We can only do this with your help. Join the registry today and become a partner in these efforts.
W
elcome to the I Have IIH Foundation Patient Insights Network (PIN). By participating in this registry, you will enable researchers and clinicians to identify and understand the definitive symptoms of IIH, advance research into medications and alternative treatments, and help enhance the lives of people with this condition.
The more information gathered for research into IIH, the better the chances of finding more effective and less invasive treatment methods. You can make a difference by joining the registry and sharing your voice.
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