{"id":148743,"date":"2025-08-15T20:42:14","date_gmt":"2025-08-15T20:42:14","guid":{"rendered":"https:\/\/www.europesays.com\/us\/148743\/"},"modified":"2025-08-15T20:42:14","modified_gmt":"2025-08-15T20:42:14","slug":"adam-andersons-sunshine-genetics-act-finds-a-friend-in-usf","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/us\/148743\/","title":{"rendered":"Adam Anderson\u2019s Sunshine Genetics Act finds a friend in USF"},"content":{"rendered":"<p class=\"p1\" style=\"text-align: justify;\">Rep. <strong>Adam Anderson<\/strong> is touring the state hyping the Sunshine Genetics Act at premier medical colleges and research institutions.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">On his third leg of the tour, Anderson is meeting with officials at the University of South Florida, which will be a Sunshine Genetics partner.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">Anderson ran a bill (<a href=\"https:\/\/www.flhouse.gov\/Sections\/Bills\/billsdetail.aspx?BillId=81532\" data-wpel-link=\"external\" target=\"_blank\" rel=\"external noopener noreferrer\"><strong>HB 907<\/strong><\/a>) this year, which Gov. <strong>Ron DeSantis<\/strong> signed in June, establishing the Sunshine Genetics Act. The Act greenlights pediatric rare disease research expansion and positions Florida as a national leader. It also established the Sunshine Genetics Pilot Program with $3 million in initial funding, laying the foundation for a new $100 billion genomic medicine industry in the state.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">USF is investing heavily in genomic medicine through both educational programs (MPH\/Ph.D., genetic counseling) and core research infrastructure, emphasizing interdisciplinary collaborations and public health impact. The USF College of Public Health hosts the first and only accredited genetic counseling graduate program in Florida. Anderson\u2019s Sunshine Genetics Act is expected to boost the university\u2019s research and partnership opportunities.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">The partnership was a natural fit in other ways too. USF established the Morsani College of Medicine in the late 1960s and has since grown into a leading institution, now nationally recognized for innovation in medical education, research and primary care. It is the top-ranked medical school in Florida and the only school in Florida to receive a Tier 1 medical school ranking by U.S. News &amp; World Report.<\/p>\n<p><a href=\"https:\/\/action.aarp.org\/secure\/pledge-fight-social-security-2\" target=\"_blank\" rel=\"noopener external noreferrer\" data-wpel-link=\"external\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-749058 size-full\" src=\"https:\/\/www.europesays.com\/us\/wp-content\/uploads\/2025\/08\/102269-023-AARP_FL_SocialSecurity90th-Awareness_728x90_r1-1.jpg\" alt=\"\" width=\"728\" height=\"90\"\/><\/a><\/p>\n<p class=\"p1\" style=\"text-align: justify;\">The Sunshine Genetics Act establishes a five-year genetic sequencing pilot program for newborns and creates the Sunshine Genetics Consortium, uniting Florida\u2019s top researchers, clinicians and biotech innovators.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">The law took effect July 1. The pilot program allows families to opt in to have their child\u2019s full genetic code sequenced for free, with the goal of identifying potentially serious, but treatable, conditions early. Early treatment can be life-saving, and can lead to better health outcomes, fewer hospital visits and higher quality of life.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">\u201cFor too many families, a rare disease diagnosis is a journey of heartbreak and uncertainty,\u201d said Anderson, whose son <b>Andrew<\/b> passed away from Tay-Sachs disease. \u201cThe Sunshine Genetics Act is a promise to those families \u2014 a promise of hope, early detection, and a future where no child\u2019s life is cut short by a rare disease. Florida is leading the way, and this historic investment will change lives for generations.\u201d<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">Tay-Sachs disease is an ultrarare fatal genetic disorder with only 16 cases annually nationwide. There are more than 7,000 known rare diseases that affect some 350 million people worldwide, according to Anderson\u2019s Office.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">USF is celebrating the partnership to enhance research and treatment.<\/p>\n<p><a href=\"https:\/\/katforcongress.com\/\" target=\"_blank\" rel=\"noopener external noreferrer\" data-wpel-link=\"external\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-748563 size-full\" src=\"https:\/\/www.europesays.com\/us\/wp-content\/uploads\/2025\/08\/KatCammack-DigitalAds-floridaPolitics-2025-728x90-1.jpg\" alt=\"\" width=\"728\" height=\"90\"\/><\/a><\/p>\n<p class=\"p1\" style=\"text-align: justify;\">\u201cThe University of South Florida is proud to be a partner in this important effort to develop solutions that will transform the lives of children and families,\u201d USF President <b>Rhea<\/b> <b>Law<\/b> said. \u201cThe Sunshine Genetics Act that Representative Anderson championed, and our state leaders have advanced, offers new opportunities to decode the mysteries of rare genetic disorders, bringing hope to thousands of families in Florida and beyond.\u201d<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">\u201cThanks to the Sunshine Genetics Act, Florida will be at the forefront of research and development of new tools to save babies\u2019 lives and improve their health,\u201d added Dr. <strong>Charles J.\u00a0Lockwood<\/strong>, executive vice president of USF Health and dean of the USF Health Morsani College of Medicine.<\/p>\n<p class=\"p1\" style=\"text-align: justify;\">\u201cUSF Health is honored to participate in the Sunshine Genetics Consortium, and we look forward to lending our considerable resources \u2014 from genetic counseling and education programs to our extensive research infrastructure \u2014 to collaborative efforts that will advance the science in an arena so important to the future of Florida.\u201d<\/p>\n<p class=\"p3\" style=\"text-align: justify;\">Since his son\u2019s death, Anderson and his family have been active in advancing research in rare diseases through the\u00a0<a href=\"http:\/\/www.curetay-sachs.org\/\" data-wpel-link=\"external\" target=\"_blank\" rel=\"external noopener noreferrer\"><b>Cure Tay Sachs Foundation<\/b><\/a>\u00a0and their\u00a0<a href=\"http:\/\/ajandersonfoundation.org\/\" data-wpel-link=\"external\" target=\"_blank\" rel=\"external noopener noreferrer\"><b>AJ Anderson Foundation<\/b><\/a>. Anderson previously worked with former House Speaker\u00a0<b>Chris Sprowls<\/b>\u00a0to create Tay Sachs Awareness Day in Florida on Aug. 10, Andrew\u2019s birthday.<\/p>\n<p class=\"p3\" style=\"text-align: justify;\">Last year, Anderson\u00a0<a href=\"https:\/\/floridapolitics.com\/archives\/665406-rare-disease-grant-program-to-push-the-boundaries-of-science-and-medicine-awaits-gov-desantis-signature\/\" data-wpel-link=\"internal\" target=\"_blank\" rel=\"noopener noreferrer\"><b>successfully ushered<\/b><\/a>\u00a0through a bill (<a href=\"https:\/\/www.flsenate.gov\/Session\/Bill\/2024\/1582\/?Tab=BillHistory\" data-wpel-link=\"external\" target=\"_blank\" rel=\"external noopener noreferrer\"><b>SB 1582<\/b><\/a>) that created a grant program to fund scientific and clinical research on rare diseases.<\/p>\n<p>&#13;<br \/>\n\t\t\t\t Post Views: 0&#13;\n\t\t\t<\/p>\n","protected":false},"excerpt":{"rendered":"Rep. Adam Anderson is touring the state hyping the Sunshine Genetics Act at premier medical colleges and research&hellip;\n","protected":false},"author":3,"featured_media":148744,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[26],"tags":[87622,87623,815,87624,14218,87625,14516,159,87626,67,132,87627,68],"class_list":{"0":"post-148743","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-genetics","8":"tag-adam-anderson","9":"tag-charles-j-lockwood","10":"tag-genetics","11":"tag-hb-907","12":"tag-rare-disease","13":"tag-rhea-law","14":"tag-ron-desantis","15":"tag-science","16":"tag-sunshine-genetics-act","17":"tag-united-states","18":"tag-unitedstates","19":"tag-university-of-south-florida","20":"tag-us"},"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@us\/115034727863661980","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/posts\/148743","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/comments?post=148743"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/posts\/148743\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/media\/148744"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/media?parent=148743"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/categories?post=148743"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/us\/wp-json\/wp\/v2\/tags?post=148743"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}