A recent story from CBS 17 Raleigh, North Carolina, highlights the journey of Dr. Kim Stephens and her family’s experience living with Hunter syndrome (MPS II). The article also features ongoing research efforts at the UNC School of Medicine focused on developing new treatment approaches for rare genetic disorders.
In the story, Dr. Stephens shares how her son’s diagnosis with Hunter syndrome shaped her commitment to advancing awareness, research, and care for families affected by Mucopolysaccharidoses (MPS). Hunter syndrome is a rare genetic condition that can lead to progressive physical and neurological symptoms and often requires specialized, multidisciplinary care.
The article also highlights the work of Dr. Joseph Muenzer, who has spent decades leading clinical research focused on MPS disorders. Through clinical trials and collaborative research efforts, Dr. Muenzer and colleagues continue to investigate new therapeutic approaches aimed at improving outcomes for individuals living with Hunter syndrome and related conditions.
Stories like this help raise awareness of the challenges families face when navigating rare diseases and underscore the importance of continued research, clinical care, and patient advocacy.
The Muenzer MPS Research & Treatment Center remains committed to advancing care, education, and research for individuals and families affected by MPS.
Read the full article:
https://www.cbs17.com/news/local-news/orange-county-news/as-rare-genetic-disorder-causes-her-son-to-regress-carrboro-mom-teams-up-with-unc-doctor-studying-new-treatment/