Hydrocephalus Association eNewsletter | NOVEMBER 2018

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FEATURED ARTICLES

Join the ONLY Hydrocephalus Patient Registry! Have you joined the Hydrocephalus Patient Registry?Whether you've had 1 brain surgery or 100, your experience matters! By sharing your experiences in the registry, you're helping accelerate hydrocephalus research! Read more                                       Support HA on Giving Tuesday! SAVE THE DATE!  Nov. 27 is Giving Tuesday, the global day of giving! Help us find a cure and improve the lives of those living with hydrocephalus by donating to HA on #GivingTuesday! Read more

Roadmap to A Cure is the Hydrocephalus Association's critical 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.  JOIN IN

UPCOMING EVENTS

11/13 Dallas/Fort Worth: Can't wait to Zoom with you! 11/14 FREE WEBINAR: Drug Development for the Management of Hydrocephalus 11/17 Baltimore and DC Area Mommy Meet Up  12/6 Columbia, SC Community Network Support Group Meeting

12/8 Missouri Community Network NPH-focused Meeting 12/11 Dallas/Fort Worth: Let's get Virtual! 12/13 FREE NPH Webinar 12/15 Maryland and DC Area NPH Meeting

OTHER STORIES view more stories

Upcoming Research Webinar: A Drug to Treat Hydrocephalus? Join us for our FREE Webinar on Nov 14th with Dr. Bonnie Blazer-Yost on the early-stage development of a new drug theraphy to treat hydrocephalus.  REGISTER New HA Board of Directors Chair  Please help us welcome TBS executive Brett Weitz as the new chair of our Board of Directors! Brett is a hydro dad and has been a member of the Hydrocephalus Association Board of Directors since 2016. READ MORE Add Your Voice to Our Library of Hydrocephalus Stories What have you learned from living with hydrocephalus? Share your journey and your insights by sending us your story today! Email ines@hydroassoc.org and you could be featured on our website!   READ MORE $3 Million Raised for Posthemorrhagic Hydrocephalus! Thanks to our generous benefactors, Craig and Vicki Brown, we held our annual Vision Dinner in NYC on November 2nd, celebrating the completion of our Posthemorrhagic Hydrocephalus Campaign, which raised $3M for critical research.  READ MORE Honor Your Preemie HydroHero on World Prematurity Day! Nov. 17 is World Prematurity Day, which highlights the health challenges premature babies face at birth and beyond. For us at HA, World Prematurity Day is a way to draw attention to Posthemorrhagic Hydrocephalus (PHH), one of the most insidious forms of hydrocephalus. This year, let’s use our collective voice to highlight our #PreemieHydroHeroes!  READ MORE Can a Drug Cure Hydrocephalus? Scientists are working on it! HA has invested nearly $8 million in pioneering science to improve the quality of life for people with hydrocephalus and to find a cure. Please support this vital work. YES, I'll GIVE JOIN US Our mission is to promote a cure for hydrocephalus and improve the lives of those affected by the condition. Copyright 2017 Hydrocephalus Association, All rights reserved. Unsubscribe