Hard to believe we were all in DC this weekend meeting other parents and patients fighting and advocating for hydrocephalus. Blessed to have met so many fighters. Thankful to God for those speaking up and our PHF familia!!
Washington - August 22 & PHF
Washington is over 3 months away! Right around the corner to advocate for hydrocephalus Advocacy.......to help Hawke and all the people fighting this condition. Advancement is sparse, no cure and current treatment options are less than promising. Keep this trip and cause in prayer! In the meantime children and people will suffer when the weather changes due to Hydrocephalus, endure many brain surgeries sometimes one after another, suffer brain damage, terrible quality-of-life for many just to name a few.
www.hydrocephaluskids.org
Jason@hydrocephaluskids.org
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