Hydrocephalus Action Network

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RAISE YOUR VOICE!

The Hydrocephalus Action Network (HAN) is a grassroots network of volunteers “at the ready” who are willing to take action to help the Hydrocephalus Association advocate on behalf of all those affected by hydrocephalus. The best advocates are the patients, family members, medical caregivers, and others directly affected by the condition – WE NEED YOU!

By joining the Hydrocephalus Action Network, you are indicating your willingness to:

  • Familiarize yourself with issues.
  • Send letters, emails or make phone calls to Congress (or other government offices).
  • Willing to participate in District Days/Advocacy Days at the local, state or federal level.

Other activities/resources for members of the Hydrocephalus Action Network:

  • Special email list for updates on advocacy activities.
  • Special advocacy-focused portal on our web site.
  • Special webinar training.

Join us!

Become a Grassroots Advocate for Hydrocephalus today! Click here to join the Hydrocephalus Action Network.

Questions?

Please contact the Hydrocephalus Association by telephone at (888) 598-3789 or via email at advocacy@hydroassoc.org.

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