In addition to cherry blossoms, spring brings the budget season to Washington, DC. Through March, April and May, members of Congress and their staff are considering funding levels for a variety of medical research programs, including those essential to hydrocephalus patients. They’ll be less likely to reduce or eliminate funding for programs that directly and profoundly benefit their constituent communities – and that’s where you come in!
Join this webinar to gain a not-so-boring understanding of the budget process. You’ll come away with the five essential things every citizen should know about government funding as well as tips on how YOU can make a difference. If you support ongoing investments in efforts to find alternative treatments and cures for hydrocephalus, you’ll want to tune in.
Join the Hydrocephalus Action Network (HAN) for our upcoming Advocacy webinar on Tuesday, March 29 at 3:00 PM EDT. Register today!
This webinar is ideal for anyone touched by hydrocephalus who wants to work through political channels to advocate for appropriate funding levels for hydrocephalus research. If you are not yet a member of our Hydrocephalus Action Network, learn more and join today!
We are pleased to offer advocacy webinars to help you stay informed and current on the latest legislation and political action surrounding hydrocephalus. These interactive, webinars are completely complimentary.
Please contact the Hydrocephalus Association by telephone (888) 598-3789 or via e-mail at firstname.lastname@example.org.