Michigan Advocacy Update Lansing Days On Tuesday, March 21 and Wednesday, March 22, 2023, twenty-nine Michigan bleeding disorders advocates joined the Hemophilia Foundation of Michigan (HFM) for our legislative advocacy event, Lansing Days. Special thank you to our HTC representatives for joining us: Dave Rushlow, Kathi Sheldon, and Alice Cakebread! Together, our group of bleeding …
Open enrollment for the 2022 Marketplace health plans is open from November 1, 2021 through January 15, 2022 at www.healthcare.gov.
On Its Way to the Senate, House Bill 4353 Supports Patient Access to Critical Treatments by Banning Discriminatory Copay Accumulator Adjustment Program
House Bill 4353 Supports Patient Access to Critical Treatments by
Banning Discriminatory Copay Accumulator Adjustment Programs
House Bill 4353 Supports Patient Access to Critical Treatments by
Banning Discriminatory Copay Accumulator Adjustment Programs
The coalition that is fighting to protect patients from harmful insurance tactics.
As the 2019 legislative cycle begins, HFM will be monitoring the introduction of bills and assessing their possible impact on the bleeding disorders community
The bill also includes exemptions for disability caretakers, parents of children under six, pregnant women, people receiving disability benefits, and those who are medically frail, which includes patients diagnosed with hemophilia, VWD, and other factor deficiencies.
To educate and empower kids with bleeding disorders to live a life of freedom and independence.
1921 W. Michigan Avenue
Ypsilanti, MI 48197
Phone (734) 544-0015
Fax (734) 544-0095
