#HydrocephalusWarriors 💙

There are only two ways to live your life. One is as though nothing is a miracle. The other is as though everything is a miracle. Albert Einstein

Wishing you all. Wherever you are on Planet Earth 🌍 A wonderful new week ❤️

When you feel a peaceful joy, that's when you are near truth. Rumi

Today is #WorldPrematurityAwarenessDay. 💜 Prematurity is the second leading cause of infant mortality in the U.S. Join us and @MarchofDimes to raise awareness—wear purple & show support! Learn how to get involved: https://t.co/TTo3q2wqs1 #NICUHeroes

For the fourth consecutive year, the U.S. earned a D+ for preterm birth. Nearly 380,000 babies were born preterm in 2024—1 in 10 births—placing the U.S. among the highest rates in developed nations. Read more: https://t.co/5dr0elg4NZ #MarchofDimesReportCard #MarchofDimes

Each year in the U.S., 1 in 10 babies is born too soon. Behind every number is a real family — a mom, a baby, a story of courage and hope. This Prematurity Awareness Month help us give every baby the best possible start. Donate today https://t.co/q3Fa9KbCCN

Parents of premature infants already face enormous stress in the NICU. When posthemorrhagic hydrocephalus is added, families need clear info & strong support. HA is here to help through guidance, connection & programs like RAISE. https://t.co/WmD0sEBxge

We’re excited to feature @bwepmd, pediatric neurosurgeon at @childrens & @UTSWMedCenter, as a #HACONNECT speaker. Sessions include: • Treating the Whole Person • Research in Action: Improving Patient Care • Partnering w/ Your Care Team https://t.co/2VwWFIeCJl

Watch HA Research Programs Manager Samantha Lanjewar interview Dr. Kenneth Iserson, a retired ER physician sharing his personal journey with Normal Pressure Hydrocephalus (NPH)—from unusual symptoms to delayed diagnosis and advocacy for earlier detection.

Today we celebrate 10 years of leadership from our President & CEO, Diana Gray! 🎉 Diana has been a steadfast steward of HA’s mission and we’re grateful for her vision, dedication, and ten years of transformative leadership  💙

Meet the newest member of HA — My Hydro Bear with a shunt!  🧸 This special companion helps kids understand hydrocephalus and feel supported every step of the way  💙  Check it out in the HA Store: https://t.co/NVAODK8MLj

To all caregivers in our community, thank you for the profound love you give every day 💙 Remember to refill your cup. Taking care of yourself helps you continue taking care of your loved one! Find support & encouragement here: https://t.co/Py59BY3qxA

Check out the latest Hydrocephalus Scoop on Capitol Hill for updates on healthcare, telehealth & the government shutdown. Then join us tonight for our grassroots advocacy meetup! https://t.co/diAsPooVIe Register here: https://t.co/24xONhVXlo

Congrats to our 2025 Hydrocephalus Association Scholarship Recipients! 🎉These remarkable young adults excel in school, volunteer, and give back—proving hydrocephalus doesn’t stand in the way of success. Learn more: https://t.co/dZHlo5dYNl

We’re kicking off #HACONNECT speaker announcements! 🎉 Dr. Bonnie Blazer-Yost from @IUIScience will be sharing: • The Hydrocephalus Research Center Meet & Greet + Lab Tours • Are We There Yet? Drug Development & Devices Check out other sessions: https://t.co/rirDeHMtO8

You may say I'm a dreamer, but I'm not the only one. I hope someday you'll join us. And the world will live as one. John Lennon

What's broken can be mended. What hurts can be healed. And no matter how dark it gets The sun is going to rise again.

Some days the bravest thing you will do is keep going ❤️

At the end of the day Give up your worries and give thanks for the journey. Ben Vereen

You may have heard the term pseudocyst, especially if you've had a VP or LP shunt. But what does it mean? Learn how these fluid collections form, what symptoms to watch for, and when to seek medical care. Read the full article: https://t.co/30eXESM4Ph