What's happening
This resolution urges Governor Cuomo to proclaim February 28, 2018, as Rare Disease Awareness Day in New York State.
Why it matters
Raises visibility of rare diseases. , which collectively affect over 30 million Americans, despite individual conditions often being overlooked due to their low prevalence.
Highlights the challenges faced by rare disease patients. including delayed diagnoses, limited treatment options, and higher medical costs—emphasizing the need for better support systems and awareness.
Connects research on rare diseases to broader medical advances. , underscoring that studying these conditions often leads to insights beneficial to more common diseases as well.
Recognizes the disproportionate impact on children and families. , as about half of those affected by rare diseases are children, calling attention to the urgent need for improved therapies, advocacy, and public understanding.
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Headline styles
Declare Rare Disease Day
Plain English, a few words. Used as the page title.
Sponsors
No co-sponsors yet.
History
- Referred to finance
Full text
1 pageUnderlined is new[Struck] is removedOfficial text on nysenate.gov ↗
Senate Resolution No. 3170 BY: Senator HANNON MEMORIALIZING Governor Andrew M. Cuomo to proclaim
February 28, 2018, as Rare Disease Awareness Day in the State of New York WHEREAS, It is the custom of this Legislative Body to recognize official days set aside to increase awareness of serious issues that affect the lives of citizens of New York State; and… Show allHide
February 28, 2018, as Rare Disease Awareness Day in the State of New York WHEREAS, It is the custom of this Legislative Body to recognize official days set aside to increase awareness of serious issues that affect the lives of citizens of New York State; and WHEREAS, Attendant to such concern, and in full accord with its long-standing traditions, it is the sense of this Legislative Body to memorialize Governor Andrew M. Cuomo to proclaim February 28, 2018, as Rare Disease Awareness Day in the State of New York, in conjunction with the observance of National Rare Disease Day; and WHEREAS, National Rare Disease Day is an observance to raise awareness of rare diseases and diseases of unmet need, few of which have cures or specific drugs to treat symptoms, and are often not diagnosed for many years; and WHEREAS, The first Rare Disease Day was held in 2008 on February 29th, a 'rare' date which happens only once every four years; ever since then, Rare Disease Day has taken place on the last day of February, a month known for having a 'rare' number of days; and WHEREAS, Rare Disease Day was established for the reason, according to the European Organization for Rare Diseases (EURORDIS), treatment for many rare diseases and diseases of unmet need is insufficient, as are the social networks to support individuals with rare diseases and diseases of unmet need and their families; and WHEREAS, One year later, in 2009, Rare Disease Day went global as the National Organization of Rare Disorders (NORD) mobilized 200 rare disease patient advocacy organizations in the United States in an effort to coordinate activities and better promote the day; and WHEREAS, 2018 marks the 10th Anniversary of Rare Disease Day; this year's theme is: "Research"; over the last few decades, clinical research has made remarkable strides in increasing funding and awareness of serious, rare conditions like bone cancer, multiple myeloma, and familial Alzheimer's, just to name a few out of the 7,000 known rare diseases; and WHEREAS, In 2013, in recognition of the needs of patients with rare diseases, Albany Medical Center and College established the Albany Medical Center's Rare Disease Forum which was the genesis of the New York State Rare Disease Alliance, whose purpose is to promote faster diagnosis of rare diseases, research into therapies and cures, and to foster wider public recognition of public health problems affecting 30 million Americans; and WHEREAS, There are nearly 7,000 diseases and conditions considered rare, each year affecting approximately 200,000 Americans; and WHEREAS, Of these 7,000 rare diseases, more than 80 percent are considered ultra-rare, affecting less than a few thousand Americans; and WHEREAS, While each of these diseases and disorders may affect a small number of people, rare diseases affect more than 30 million Americans; and WHEREAS, Since many rare diseases and diseases of unmet need are genetic, tragically, approximately half the people affected by rare diseases in the United States are children; and WHEREAS, Research on rare diseases, which are serious and often life-threatening, is vitally important due to it frequently adds significantly to the general understanding of more common diseases and conditions; and WHEREAS, People suffering from rare diseases typically experience difficulty in obtaining a timely, accurate diagnosis, finding physicians or treatment centers and experience limited treatment options, options generally considered more expensive than those for common diseases; and WHEREAS, It is imperative that there be greater public awareness of rare diseases and diseases of unmet need, and more must be done to increase activity at the local, state and national levels to support those afflicted as well as their families and caregivers; now, therefore, be it RESOLVED, That this Legislative Body pause in its deliberations to memorialize Governor Andrew M. Cuomo to proclaim February 28, 2018, as Rare Disease Day in the State of New York, in conjunction with the observance of National Rare Disease Day; and be it further RESOLVED, That copies of this Resolution, suitably engrossed, be transmitted to The Honorable Andrew M. Cuomo, Governor of the State of New York; the New York State Rare Disease Alliance; and NORD.
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