Hydroassoc.org Website Review

KnowledgeHydrocephalusLa HidrocefaliaNormal Pressure HydrocephalusPhysician DirectoryPublicationsResource LibraryCommunityCommunity Network - HydrocephalusCONNECT Peer SupportContact UsParentsTe*ns and Young Ad*ltsAd*lts and CaregiversNPH and CaregiversOur Hydrocephalus StoriesResearchPursuing a CureConferences and WorkshopsResearch ProgramsPatient StudiesHAPPIER - Patient RegistryAbout Us - Who We AreBoard of Directors - Medical Advisory BoardMeet the StaffNewsroomGet InvolvedDonateWALK ScheduleDo It Yourself Fundraising - AdvocateEducation DaysConferenceEvents - VolunteerOur Blog Roadmap to A Cure is the Hydrocephalus As*ociation's crucial initiative to accelerate critical research, expand patient support and education, and raise unprecedented public awareness about hydrocephalus. Join us on our journey to raise $20M by 2020. MORE INFO Hydrocephalus Patient Registry Join the first ever Hydrocephalus Patient Registry and help accelerate Win a #NOMOREBS t-shirt! Make a recurring monthly gift of $25 or more to help us bring attention to the lack of treatment options for the one million Americans living with hydrocephalus--and win a #NOMOREBS t-shirt to No More Brain Surgeries Join our awareness campaign and help us bring attention to the lack of Dealing with your child’s hydrocephalus diagnosis can be overwhelming. It’s common to have countless questions that range from learning more about what hydrocephalus is to what one can expect a child’s experience to be across the life spectrum. If you’re a te*n or young ad*lt affected by hydrocephalus, we want you to know that you are not alone. Browse our te*n and young ad*lt pages to learn about resources to help you. This is YOUR place for information and empowerment. A hydrocephalus diagnosis is overwhelming, whether you’re a recently diagnosed ad*lt, someone who’s been living with the condition for many years, or a friend or family member. Here you will find information enabling you to have more control of your life.