Hemo Alliance Newsletters

Washington Update, September 2023

Advocacy Update

What’s happening in Congress?
by Artemis Policy Group, Hemophilia Alliance Advocacy Consultants

Congress returned to Washington after Labor Day with a jam-packed schedule for fall. Top of mind for everyone is the September 30th deadline to fund the federal government by passing all 12 appropriations bills for fiscal year (FY) 2024. If lawmakers do not act in time, Congress could pass what is known as a continuing resolution (CR), which would fund the government at current FY 2023 levels until next year’s funding bills are passed, or we could see a government shutdown.

For the bleeding disorders community, the appropriations bills include funding for the U.S. Department of Health and Human Services (HHS) Health Resources and Services Administration (HRSA) HTC Grant program, the Centers for Disease Control and Prevention’s HTC and Hemophilia Education grant programs, as well as for the National Institutes of Health and biomedical research funding.

In addition to the funding bills, the House is moving forward on a package of bills introduced as HR 5378 which includes the reauthorization of a number of federal programs also set to expire on September 30th, including community health center funding and the National Health Service Corps, as well as many of the bills related to the practices of pharmacy benefit managers (PBMs) and Medicare and Medicaid transparency. While some provisions of the bill have bi-partisan support others do not, so it is unclear if the bill will move in its current form. A planned vote on the package was tabled, so the path forward and timing are up in the air as of this writing.

While 340B reform ideas continue to be floated to Congress, we are yet to see any bills introduced. We are watching the group of Senators who sought input on their Request for Information on contract pharmacy issues, since they may start working on a bill. We continue to monitor the situation to make sure that any proposed policies don’t harm HTCs. The Alliance Advocacy Committee is also working to evaluate various policy options that could address HTC challenges. More to come on those!

Also in this Issue…

Notes from Joe
· New Hemophilia Alliance President & CEO Search Update
· Partners Physician Academy – Second Annual Meeting held in Carmel Indiana on September 18, 2023

Payer Update
· In Good Times and in Trying Times

Notes from the Community
· Alliance Sponsors Reception for National Youth Leadership Institute (NYLI)

Alliance Update
· Did You Know…
· 2024 Meeting Schedules

Team Alliance Contact Information

We work for you! Please don’t hesitate to contact any of us with any questions or concerns:

Name Email Phone
Jeff Blake jeff@hemoalliance.org 317-657-5913
Jennifer Borrillo, MSW, LCSW, MBA borrillo@hemoalliance.org 504-376-5282
Heidi Lane, PT, DPT, PCS heidi@hemoalliance.org 435-659-1230
Jeff Amond amond@hemoalliance.org 608-206-3132
Jennifer Anders jennifer@hemoalliance.org 954-218-8509
Angela Blue, MBA angela@hemoalliance.org 651-308-3902
Karen Bowe-Hause karen@hemoalliance.org 717-571-0266
Zack Duffy zack@hemoalliance.org 503-804-2581
Michael B. Glomb MGlomb@ftlf.com 202-466-8960
Johanna Gray, MPA jgray@artemispolicygroup.com 703-304-8111
Kiet Huynh kiet@hemoalliance.org 917-362-1382
Elizabeth Karan elizabeth@karanlegalgroup.com 612-202-3240
Kollet Koulianos, MBA kollet@hemoalliance.org 309-397-8431
Roland P. Lamy, Jr. roland@hemoalliance.org 603-491-0853
Dr. George L. Oestreich, Pharm.D., MPA george@gloetal.com 573-230-7075
Theresa Parker theresa@hemoalliance.org 727-688-2568
Mark Plencner mark@hemoalliance.org 701-318-2910
Ellen Riker eriker@artemispolicygroup.com 202-257-6670