In response to the #ACHDNC dissolution, ACMG is organizing a new advisory framework for #newbornscreening, starting with a virtual stakeholder roundtable this summer. Outreach to key groups begins soon. More to come. https://t.co/NBMFrN8QBj #MedicalGenetics#RUSP#PublicHealth
Today, the U.S. #Senate passed legislation that, if signed into law, would impose dramatic and harmful barriers to #Medicaid, threatening access to quality, affordable health care for the #RareDisease patients who need it most. The fight isn’t over, and we urgently need your help! TAKE ACTION TODAY and urge your Representatives in the House to reject the Senate-passed bill!
1. Call the Capitol Switchboard at (202) 224-3121 and request to be connected with your Representative’s office. We prepared this quick script to help guide your conversation: https://t.co/AHfFnv3Vc5
2. Send this action alert urging your Representative to stand with the rare disease community and protect Medicaid: https://t.co/G16NnDISVC
With #IndependenceDay near, exercise your voice! Use ACMG’s interactive State Policy Map to track genetics bills by state or topic. View bill details, sponsors & status - and advocate for responsible #genetics policy: https://t.co/3zZwQhrMiX
🚨BREAKING NEWS🚨Champions reintroduce the Improving Seniors’ Timely Access to Care Act! The bill already has support from over 140 organizations, 47 senators, and 73 representatives. #FixPriorAuth
Wonderful session at #ACMGMtg25 on how to implement N of 1 antisense oligonucleotide therapies – eligibility, design, institutional support, costs, & FDA regulations. #PrecisionMedicine#GeneticTherapy
Unless Congress intervenes, clinical laboratories will face Medicare cuts, stifling investment in next-generation diagnostics. Congress must pass a long-term solution to #StopLabCuts: https://t.co/qbFCXzCotE.
Day of Caring - always the highlight of the conference! ACMG Foundation provides customized bikes to local kids. This year’s partner is Down Syndrome Association of Los Angeles @DownSyndromeLA#ACMGMtg25#WorldDownSyndromeDay
Session on Navigating the Current Landscape in Prenatal Genetics- interesting discussion on how an Alabama abortion law continues to impact IVF services #ACMGMtg25
Opening Reception tonight! Stop by the ACMG booth (#423) in the LACC West Exhibit Hall A beginning at 5:00 PM! Take a selfie in front of our #MedicalGeneticsAwareness wall, learn about ACMG programs, member benefits & discounts. Eat, drink, be merry! #ACMGMtg25
#ACMGMtg25 plenary session - Dr. Wayne Grody has the audience laughing with stories about consulting on movies/shows incorporating genetics in their story lines. #genetics#Hollywood
#ACMGMtg25 is officially in full swing as ACMG President @SusanKlugman gets us started with the Presidential Plenary - Genetics in the Media – Entertainment, Public Education, Controversies and Ethical Dilemmas
“Rare Disease Advisory Councils – State Advocacy for the Rare Disease Community” will begin at 1:30 in LACC, Rm 408 B at #ACMGMtg25. Learn about Rare Disease Advisory Councils in NH, MN & UT. #ELSI#publichealth#advocacy.
Hey, it's #MedicalGeneticsAwareness Week (March 18-21)! Celebrate by sharing your joy about working in the medical genetics field in a short video (30-45 secs) posted to social media during this week. Visit https://t.co/CCjBqpQcpd for details.