PRINTER'S NO. 1067 THE GENERAL ASSEMBLY OF PENNSYLVANIA HOUSE RESOLUTION No.137 Session of 2025 INTRODUCED BY MALAGARI, HILL-EVANS, FREEMAN, VENKAT, GIRAL, KHAN, HADDOCK, SANCHEZ, CONKLIN, D. WILLIAMS, GREEN AND CURRY, MARCH 19, 2025 REFERRED TO COMMITTEE ON HEALTH, MARCH 19, 2025 A RESOLUTION Recognizing May 17, 2025, as "World Neurofibromatosis Awareness Day" in Pennsylvania. WHEREAS, The Children's Tumor Foundation annually observes May 17 as "World Neurofibromatosis Awareness Day" to educate the public about this rare genetic condition; and WHEREAS, The global community recognizes the importance of raising awareness about neurofibromatosis, its impact on individuals and families and the need for continued research and support; and WHEREAS, Although more than 4 million people around the world are living with neurofibromatosis and 1 in every 2,000 births is diagnosed with neurofibromatosis, it is still relatively unknown to the public; and WHEREAS, Neurofibromatosis affects all populations equally, regardless of race, ethnicity or gender; and WHEREAS, Neurofibromatosis causes tumors to grow on nerves throughout the body and also can affect development of the 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 brain, cardiovascular system, bones and skin; and WHEREAS, The disorder can lead to blindness, deafness, bone abnormalities, disfigurement, learning disabilities, disabling pain and cancer; and WHEREAS, There are three different types of neurofibromatosis: neurofibromatosis type 1, neurofibromatosis type 2 and schwannomatosis; and WHEREAS, Signs of neurofibromatosis type 1 include light brown spots on the skin, known as café au lait spots, bumps known as Lisch nodules on the iris of the eye and freckles on the groin or armpits; and WHEREAS, Neurofibromatosis type 1 is one of the country's most common genetic disorders occurring in approximately 1 in 2,500 births; and WHEREAS, Neurofibromatosis type 2 is far less common, occurring in 1 in 60,000 people, and is typically characterized by tumors that grow on the nerves of the inner ear; and WHEREAS, Schwannomatosis is a rarer form of neurofibromatosis for which symptoms typically appear between ages 25 and 30; and WHEREAS, Schwannomatosis often forms on the spinal or cranial nerves and leads to symptoms like chronic pain or loss of muscle; and WHEREAS, Instances of neurofibromatosis occur due to mutations that either occur during conception or are passed down genetically through the parents; and WHEREAS, Family history, physical exams and genetic tests are currently used to diagnose neurofibromatosis in patients; and WHEREAS, While there is currently no cure available, there are multiple forms of treatment for patients dealing with neurofibromatosis; and 20250HR0137PN1067 - 2 - 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 WHEREAS, Mild instances of neurofibromatosis often do not require significant treatment outside of regular doctor visits and observation; and WHEREAS, More severe cases may require removal through radiation or surgery done by a nerve tumor specialist or a team of various surgeons; and WHEREAS, There are currently no medications that have been approved to treat neurofibromatosis, though researchers are investigating various methods and therapies; and WHEREAS, The Children's Tumor Foundation leads efforts to promote and financially sponsor world-class medical research aimed at finding effective treatments and, ultimately, a cure for neurofibromatosis; and WHEREAS, The Children's Tumor Foundation is connecting the unconnected, leading the way through innovative and inventive approaches to scientific advancement and improved patient care, revamping systems to accelerate the path from discovery to treatment; and WHEREAS, The Children's Tumor Foundation provides patient and family support through its information resources, youth programs and community activities; and WHEREAS, Much remains to be done in raising public awareness of neurofibromatosis to help promote early diagnosis, proper management and treatment, prevention of complications and support for research; therefore be it RESOLVED, That the House of Representatives recognize May 17, 2025, as "World Neurofibromatosis Awareness Day" in Pennsylvania. 20250HR0137PN1067 - 3 - 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28