Maurita Andrews lives in Washington state with her husband and their two sons. Diagnosed with pulmonary arterial hypertension in 2019, Andrews has dedicated her time to raising PH awareness. She felt called to share her story with members of Congress during PHA’s Hill Day in 2025 and encourages others to share their PH stories, too.  

“I am a speech language pathologist and am used to advocating for vulnerable populations,” Andrews says. “I also have a son with cerebral palsy who is primarily nonverbal. “As his mother, I always want what is best for him and will advocate relentlessly for what he needs to be successful. I hoped sharing my story would help raise awareness and get the support our community and other vulnerable communities need.”

Andrew’s 14-year-old son, Nolan, traveled with her to Washington, D.C., last year to support her.  

“He was amazing and even shared his own perspective of having his mom and our entire family impacted by PAH,” Andrews says. “I am still so proud of him for using his voice to advocate for those who need help. I hope that these lessons follow him into adulthood, and he can continue to make a difference for vulnerable populations.”  

Andrew’s advocacy efforts didn’t stop after her trip to D.C. When she returned home, she reached out to her representative in Eastern Washington and his health care liaison to continue advocating for accessible health care and oxygen for the PH community.  

“It is important for our elected officials to hear from their constituents about the issues that are impacting us, and it can be very empowering to share your story,” Andrews says. “I remain hopeful for changes in government that support our community and everyone with a rare disease.”