Celebrate HOPE Wherever You Are and Raise Awareness for IH
Welcome to the First Annual IHope Day!
IH can be a challenging disease. With constant head pain, dizziness, nausea, ringing in your ears, vision problems, and balance issues plaguing IH'ers daily it's hard sometimes not to fall into depression and give up the fight.
This day is to celebrate the HOPE that there will be a cure discovered and an effective medical treatment found that will help IH'ers not only get through the day but look forward to pain free days and months and years ahead.
We will celebrate the HOPE that IH'ers and their caregivers and support teams show every day as we fight this disease and don't let it get the best of us.
Join us by wearing blue and green (the IH colors) on June 25th! And when someone asks you why you're wearing such a fantastic color combination, tell them about IH and our need for a cure. Share our website and the IH Research Foundation website, where they can find out about this rare disease. Encourage them to pass it on.
Want to join the Facebook IHope Day revolution? Click HERE! We'd love to see your pics and hear your stories of HOPE. Who knows, maybe you'll be on our blog afterward!
IHope Day -- A day of HOPE for Those Affected by Intracranial Hypertension
Please sign our online petition to have IHope Day recognized nationally and globally as an official annual awareness day for Intracranial Hypertension. CLICK HERE to go to the petition site.