Pennsylvania 2025-2026 Regular Session

Pennsylvania House Bill HR137 Latest Draft

Bill / Introduced Version

                             
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 
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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 - 
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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.
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