![]() ![]() Sponsored in part by Avidity Biosciences, MDF Scholarships are available for a few individuals living with DM and a caregiver who demonstrate financial need. There are two opportunities to request financial support to attend the conference in person this year. Information on virtual and recorded sessions coming soon. ![]() Late Registration accepted until September 1st.įor those unable to attend in-person, we welcome you to join us virtually! Please note that not all sessions will be recorded or made available to virtual attendees.We encourage all attendees to register early to take advantage of our discounted registration rates: Join us in Washington, DC, for our most anticipated event of the year!Ĭlick here to check out our 2022 MDF Annual Conference Highlight Video! REGISTRATION TYPES & FEESĬommunity Registration includes access to general sessions, community sessions, meals, and other activities.Ĭommunity members may attend Professional Track sessions, however priority access to these sessions will be given to those registered as Professionals.Ĭonference Registration does NOT include your hotel room. See the Hotel & Room Block section below for information about staying at the Renaissance Washington, DC Downtown Hotel and instructions on how to book a room at MDF’s discounted rate. This year's program includes educational sessions exploring research, drug development, symptom management, and other critical topics for DM families, plus opportunities for formal and informal networking, wellness, and fun. Conference sessions will begin on Friday, September 8th, and continue through Saturday, September 9th, 2023, at the Renaissance Washington, DC Downtown Hotel.įor those arriving early, we welcome you to join us for a Thursday evening Welcome Reception & Advocacy Awards Presentation, where we will recognize Senators Tim Kaine (D-VA) and Cynthia Lummis (R-WY) and their staff for their friendship and support of the myotonic dystrophy community. MDF invites you to attend the 2023 MDF Annual Conference - sometimes called the “DM family reunion” – kicking off with MDF Advocacy Day on Capitol Hill on Thursday, September 7th, where we will meet with Members of Congress and their staff to advocate for myotonic dystrophy research funding and awareness. ![]()
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