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BEGIN:VEVENT
DTSTART;TZID=America/New_York:20230124T190000
DTEND;TZID=America/New_York:20230124T200000
DTSTAMP:20260407T093901
CREATED:20221104T200135Z
LAST-MODIFIED:20221107T183700Z
UID:6178-1674586800-1674590400@vahemophilia.org
SUMMARY:VIRTUAL - VHF & HACA Advocacy Education Meeting
DESCRIPTION:RSVP HERE\n  \nJoin VHF & Hemophilia Association of the Capital Area (HACA) for a virtual advocacy education program that will focus on the 2023 Virginia General Assembly. Join in and hear details from advocacy consultant\, Becky Bowers-Lanier\, about proposed legislation of interest to the bleeding disorders community\, its partners and other stakeholders. \nYou will also learn more about the VHF/HACA legislative updates that will occur weekly via zoom during the 2023 General Assembly session and how you might be able to get more involved »Go here to learn more. \nThis session is free and open to anyone interested in learning more about advocacy and how it relates to the Virginia inherited bleeding disorders community. \n\n»RSVP HERE once you RSVP you will receive the zoom link separately via email from heather@vahemophilia.org.  \n\nAs we gather virtually to discuss\, share and learn\, we ask that all Virginia Hemophilia Foundation (VHF) virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. »Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/vhf-haca-virtual-advocacy-education-meeting-2/
LOCATION:Zoom
CATEGORIES:advocacy,community,education,virtual
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20230117
DTEND;VALUE=DATE:20230222
DTSTAMP:20260407T093901
CREATED:20221104T203759Z
LAST-MODIFIED:20221108T145525Z
UID:6180-1673913600-1677023999@vahemophilia.org
SUMMARY:VIRTUAL - Virginia General Assembly Weekly Check In
DESCRIPTION:RSVP HERE\n  \nJoin VHF & Hemophilia Association of the Capital Area (HACA) for a quick weekly General Assembly check-in. We will gather to get an overview of the past week’s events in the Virginia General Assembly and get insight from our advocacy consultant\, Becky Bowers-Lanier\, on what to look for\, trends and any actions that will need to be taken about proposed legislation of interest to the bleeding disorders community. \nPlease note that these are informal weekly check-ins and if you register you are not required to attend all dates listed – feel free to join us for one session or for all! \nWEEKLY CHECK IN DATES: \nTues.\, Jan 17\, 2023  4:30 PM\nTues.\, Jan 31\, 2023  4:30 PM\nTues.\, Feb 7\, 2023    4:30 PM\nTues.\, Feb 14\, 2023  4:30 PM\nTues.\, Feb 21\, 2023  4:30 PM \n» RSVP HERE Once you RSVP you will receive a zoom link separately via email from heather@vahemophilia.org – you will use the same link each week. \n\nAs we gather virtually to discuss\, share and learn\, we ask that all VHF virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/virtual-virginia-general-assembly-weekly-check-in/
LOCATION:Zoom
CATEGORIES:advocacy,community,education,virtual
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20221109T160000
DTEND;TZID=UTC:20221109T180000
DTSTAMP:20260407T093901
CREATED:20220901T143421Z
LAST-MODIFIED:20221104T201150Z
UID:6118-1668009600-1668016800@vahemophilia.org
SUMMARY:VIRTUAL - VHF/HACA Advocacy Stakeholder and Education Meeting
DESCRIPTION:RSVP HERE\nJoin constituents\, advocacy committee members\, and community stakeholders from throughout Virginia for an education meeting that will cover a wide range of advocacy topics relevant to the bleeding disorders community! \nMEETING AGENDA \nState Update AND What Can We Expect in 2023 General Assembly Becky Bowers-Lanier\, VHF/HACA Advocacy Consultant and Heidi Dix\, Senior Vice President of Policy\, Virginia Association of Health Plans \nVirginia Bleeding Disorder Program (VBDP) Update Lauren Dunn\, Health Insurance Consultant\, VA Bleeding Disorders Program \nFederal Update Miriam Goldstein\, J.D\, Director of Policy at Hemophilia Federation of America (HFA)\, Nathan Schaefer\, MSW\, VP of Public Policy at National Hemophilia Foundation (NHF)\, and Matt Delaney\, Government Relations Specialist at National Hemophilia Foundation (NHF) \n» RSVP HERE Once you RSVP you will receive the zoom link separately via email from heather@vahemophilia.org.  \n\nThank you to our sponsors: Genentech\, National Hemophilia Foundation (NHF)\, Pfizer\, PhrMA\, Takeda and We Work For Health \n\nAs we gather virtually to discuss\, share and learn\, we ask that all Virginia Hemophilia Foundation (VHF) virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/vhf-haca-virtual-advocacy-stakeholder-and-education-meeting-3/
LOCATION:Zoom
CATEGORIES:advocacy,community,education,virtual
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20221020T120000
DTEND;TZID=UTC:20221020T130000
DTSTAMP:20260407T093901
CREATED:20220901T150459Z
LAST-MODIFIED:20221013T180017Z
UID:6120-1666267200-1666270800@vahemophilia.org
SUMMARY:Virtual - Advocacy Education “Testifying and Serving on Boards and Commissions”
DESCRIPTION:RSVP HERE\nJoin constituents\, advocacy committee members\, and community stakeholders from throughout Virginia for a virtual advocacy education meeting that covers topics relevant to the bleeding disorders community! \nTopic –  \n“Testifying and Serving on Boards and Commissions” \nJoin us to learn about developing and providing testimony in legislative and regulatory meetings\, as well as applying and serving on local and state-based boards and commissions. \nSpeakers –  \nBrenda Bordelon\, Executive Director\, Hemophilia Association of the Capital Area (HACA) \nBecky Bowers-Lanier\, VHF/HACA Advocacy Consultant \n\n» RSVP HERE \nYou will receive the zoom link separately via email from heather@vahemophilia.org. \n\nThank you to our sponsors: National Hemophilia Foundation (NHF)\, PhRMA and Takeda
URL:https://vahemophilia.org/event-program/virtual-advocacy-education-testifying-and-serving-on-boards-and-commissions/
LOCATION:Zoom
CATEGORIES:advocacy,community,education,virtual
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=UTC:20221016T080000
DTEND;TZID=UTC:20221016T103000
DTSTAMP:20260407T093901
CREATED:20220623T210633Z
LAST-MODIFIED:20221012T204603Z
UID:6065-1665907200-1665916200@vahemophilia.org
SUMMARY:Unite For Bleeding Disorders at Great Wolf Lodge
DESCRIPTION:JOIN YOUR VIRGINIA BLEEDING DISORDERS COMMUNITY AND UNITE FOR BLEEDING DISORDERS!\n \nREGISTER TODAY to help us raise $35\,000! Every dollar raised for Unite For Bleeding Disorders stays 100% local to VHF and goes toward supporting our many educational events\, advocacy efforts\, and community programs. \nNEW THIS YEAR – “Walk Your Way” After registering yourself and/or your team you can then decide when and where you want to walk! Choose your neighborhood\, favorite park\, the beach\, the options are endless! Send VHF photos of your walk and then\, plan to gather yourself and your friends and family to celebrate with us on Sunday\, October 16th at Great Wolf Lodge in Williamsburg\, VA – if you are unable to coordinate a walk for your team or join us for the celebration you can still register as a virtual walker and fundraise or donate! \nEvent Schedule: \n8:00 am – 9:00 am Registration\, Breakfast Buffet\, Entertainment & Activities\, Visit with Sponsors\n9:00 am – 10:00 am Entertainment & Activities\, Visit with Sponsors\n10:00 am – 10:30 am Unite Walk Program\, Pinwheel Ceremony\, and Prize Announcements \nRegistered individuals who make a $25 minimum donation will receive a 2022 Unite for Bleeding Disorders T-shirt AND be on the look-out for fundraising incentives and exciting prizes leading up to the walk! » Go here to register your team or donate to the walk! \nYOUR FUNDRAISING MAKES AN IMPACT – CONSIDER THESE AMOUNTS WHEN SETTING YOUR INDIVIDUAL OR TEAM FUNDRAISING GOALS \nWhen you register and fundraise for VHF you help us to educate\, advocate\, build community\, and empower those impacted by an inherited bleeding disorder so join us in helping make a real impact so that our community members can lead long\, productive\, and healthy lives. For more information contact Kelly Waters at 804-740-8643 or info@vahemophilia.org. \n$2\,000 funds a Lyman Fisher Scholarship\, allowing a student with a bleeding disorder or from a family impacted by a bleeding disorder to pursue higher education.\n$1\,000 supports a Travel Scholarship\, enabling a patient or family member to attend a national education and/or a federal advocacy meeting.\n$500 helps to send a child or teen to Camp Youngblood where they gain an increased sense of independence in managing their bleeding disorder.\n$250 provides a patient and/or their family emergency financial assistance.\n$100 supports a patient and/or their family’s attendance to VHF’s Annual Education Meeting and/or state Advocacy Training.\n$50 pays for a lifesaving Medic Alert Tag.\n$25 pays for direct patient support (in partnership with HTCs) by providing resources such as new family welcome kits and ensuring gas cards are available for transportation to medical appointments. \n» Go here to register your team or donate to the walk! \n\nThank you to our generous sponsors!\nLOCAL SPONSORS \nGold Level: CSL Behring\, Genentech and Octapharma \nSilver Level: BioMatrix and Medexus \nBronze Level: DrugCo Health \nNATIONAL SPONSORS \nPresenting Partners: Hemophilia Alliance and Takeda \nNational Community Partners: Biomarin and Sanofi \nNational Partners: Ascella Health\, Bayer\, and Hema Biologics \n\nCheck out some awesome photos from past VHF Unite Walks!\n  \n→ 2018\n→ 2019\n→ 2020\n→ 2021
URL:https://vahemophilia.org/event-program/unite-for-bleeding-disorders/
LOCATION:Great Wolf Lodge\, 549 E Rochambeau Dr.\, Williamsburg\, VA\, 23188
CATEGORIES:advocacy,community,education
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220625T090000
DTEND;TZID=America/New_York:20220625T160000
DTSTAMP:20260407T093901
CREATED:20220404T193252Z
LAST-MODIFIED:20220617T160253Z
UID:5979-1656147600-1656172800@vahemophilia.org
SUMMARY:Annual Meeting - Community Member Registration
DESCRIPTION:RSVP HERE\n  \nVHF’s Annual Meeting brings together the inherited bleeding disorder community to share information on a wide variety of topics and it is a great opportunity for networking and support for individuals and families. \n» Go here to view the meeting agenda \nAnnual Meeting Highlights and Sessions Include: Understanding all sides – Keys to effective grassroots advocacy on the state and federal level\, Looking from the Outside in: Musculoskeletal Ultrasound\, Strategies for Managing Child\, Adolescent\, and Caregiver Mental Health\, Aging as a Person with a Bleeding Disorder and more; Lyman Fisher Scholarship recognition; VHF chapter updates; and on-site children and teen programming with Camp Holiday Trails. \nSaturday\, June 25th | 10:00 am: Annual Meeting will begin (light refreshments starting at 9:00 am and meeting will conclude by 4:00 pm) \n\nYou Do Not Want To Miss our Community Event – Richmond Flying Squirrels Baseball Game on Sunday\, June 26th! » Go here to learn more and register *Community event is optional and is not a part of the annual meeting. \nOvernight accommodations at Virginia Crossings Hotel & Conference Center are available on Saturday\, June 25th. Educational programs\, scheduled meals\, community events\, and overnight accommodations are provided at no cost for constituents that live in the VHF coverage area. There is a $25 registration fee per household (after you register you will receive a link to pay your fee.) \nIf you are a constituent that lives outside of the VHF coverage area and you are interested in registering for this meeting\, please email heather@vahemophilia.org for more information. \n\nThank you to our sponsors –  \nPremier Sponsors\nPfizer and Takeda \nPlatinum Sponsors\nAccredo\, Bayer\, CSL Behring\, Genentech\, HemaBiologics\, Octapharma\, Sanofi\, and Spark Therapeutics \nCorporate Sponsors\nBioMarin\, BioMatrix\, Children’s Hospital of The King’s Daughter’s (CHKD) and the University of Virginia’s (UVA) 340B Factor Program\, CVS Specialty Pharmacy\, DrugCo Health\, NovoNordisk\, and Optum \nFriends – National Hemophilia Foundation (NHF)
URL:https://vahemophilia.org/event-program/annual-meeting-community-member-registration-2/
LOCATION:Virginia Crossings Hotel\, Tapestry Collection by Hilton\, 1000 Virginia Center Pkwy\, Glen Allen\, VA\, 23059\, United States
CATEGORIES:advocacy,community,education
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220127T190000
DTEND;TZID=America/New_York:20220127T200000
DTSTAMP:20260407T093901
CREATED:20211116T204521Z
LAST-MODIFIED:20211208T235725Z
UID:5861-1643310000-1643313600@vahemophilia.org
SUMMARY:Virtual Education Session - Keeping and Maintaining Health Insurance During Uncertain Times
DESCRIPTION:» RSVP HERE\n\nTopic: Keeping and Maintaining Health Insurance During Uncertain Times \nGet your insurance questions answered and learn more about:\nPrior authorizations – commercial plans and documentation required for initial authorization/reauthorizations.\nMedicare eligibility and Medigap enrollment.\nAdditional protections under the Build Back Better infrastructure bill. \nSpeaker: Lynne M. Szott\, RN\, RMC\, CCM\, Senior Manager\, Reimbursement & Access\, CSL Behring\n \nThank you to our sponsor CSL Behring \n\nThis session is free and open to VHF constituents. \nAs we gather virtually to discuss\, share and learn\, we ask that all VHF virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/virtual-education-session-keeping-and-maintaining-health-insurance-during-uncertain-times/
LOCATION:Zoom
CATEGORIES:advocacy,education,virtual chat
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220117T190000
DTEND;TZID=America/New_York:20220117T200000
DTSTAMP:20260407T093901
CREATED:20211116T193321Z
LAST-MODIFIED:20220125T142452Z
UID:5859-1642446000-1642449600@vahemophilia.org
SUMMARY:VHF & HACA Virtual Advocacy Education Meeting
DESCRIPTION:» RSVP HERE\n\nJoin VHF & HACA for a virtual advocacy education program on Martin Luther King Jr. Day\, our traditional date for our annual advocacy day. This program will focus on the 2022 General Assembly. Join in and hear details from advocacy consultant\, Becky Bowers-Lanier\, about proposed legislation of interest to the bleeding disorders community\, its partners and other stakeholders. You will also learn more about the VHF/HACA legislative updates that will occur weekly via zoom during the 2022 General Assembly session and how you might be able to get more involved. \nThis session is free and open to anyone interested in learning more about advocacy and how it relates to the Virginia inherited bleeding disorders community. \n\nThank you to our sponsors: Genentech\, National Hemophilia Foundation (NHF)\, Pfizer\, and Takeda. \n» Please go here to view our Virtual Sponsor Program This program is one way our generous sponsors can virtually connect with the community by providing links to their electronic resources\, brochures\, websites\, social media sites and more! \n\nAs we gather virtually to discuss\, share and learn\, we ask that all VHF virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/vhf-haca-virtual-advocacy-education-meeting/
LOCATION:Zoom
CATEGORIES:advocacy,education,virtual chat
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20210928T190000
DTEND;TZID=America/New_York:20210928T200000
DTSTAMP:20260407T093901
CREATED:20210818T191146Z
LAST-MODIFIED:20210920T194433Z
UID:5619-1632855600-1632859200@vahemophilia.org
SUMMARY:VHF/HACA Advocacy Chat - Getting into Committee
DESCRIPTION:» RSVP HERE \nEver wonder how a bill winds its way from a proposed bill\, through both houses of the General Assembly to enacted legislation? Committees are the answer — and where much of the debate about any bill take place. Join us to learn more about the process as we hear from State Senator Ghazala F. Hashmi and Delegate Roxann Robinson – key committee members that work on issues that affect our community. \nThank you to our sponsors: National Hemophilia Foundation (NHF) and Takeda \nRead this article for more information on how to join a virtual meeting on the zoom platform using a desktop computer\, mobile device/tablet\, from a landline or a mobile phone. If you need assistance or have any barriers that are keeping you from participating in virtual programs please call 804-740-8643 or email info@vahemophilia.org.  \n\n\nAs we gather virtually to discuss\, share and learn\, we ask that all Virginia Hemophilia Foundation (VHF) virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/vhf-haca-advocacy-chat-getting-into-committee/
LOCATION:Zoom
CATEGORIES:advocacy,education,virtual chat
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20210527T190000
DTEND;TZID=America/New_York:20210527T200000
DTSTAMP:20260407T093901
CREATED:20210420T164415Z
LAST-MODIFIED:20210519T192805Z
UID:5186-1622142000-1622145600@vahemophilia.org
SUMMARY:Advocacy Chat with Delegate Kathleen Murphy
DESCRIPTION:» RSVP HERE \nJoin us as we chat with Delegate Kathleen Murphy (34th District\, Virginia House of Delegates) to learn more about the passage of HB 1995 that created the Rare Disease Advisory Council and its proposed scope of work. Hear more about Del. Murphy’s interest and advocacy for creating the Council AND for her general impressions on the virtual nature of the General Assembly meetings. \nThank you to our advocacy chat sponsors National Hemophilia Foundation (NHF) and Takeda \nRead this article for more information on how to join a virtual meeting on the zoom platform using a desktop computer\, mobile device/tablet\, from a landline or a mobile phone. If you need assistance or have any barriers that are keeping you from participating in virtual programs please call 804-740-8643 or email info@vahemophilia.org.  \n  \n\n\nAs we gather virtually to discuss\, share and learn\, we ask that all Virginia Hemophilia Foundation (VHF) virtual program participants be thoughtful in their interactions and follow video meeting etiquette and rules of engagement. Disruptions to a session may lead to the removal and/or disabling of the participant’s video and microphone for part of or for the entire session. Thank you for helping VHF ensure a safe\, productive\, and welcoming environment for all meeting participants and staff. Go here to read video meeting etiquette and rules of engagement.
URL:https://vahemophilia.org/event-program/advocacy-chat-with-delegate-kathleen-murphy/
LOCATION:Zoom
CATEGORIES:advocacy,education,virtual chat
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20201114T160000
DTEND;TZID=America/New_York:20201114T180000
DTSTAMP:20260407T093901
CREATED:20200930T195502Z
LAST-MODIFIED:20201111T180321Z
UID:4661-1605369600-1605376800@vahemophilia.org
SUMMARY:VHF/HACA Virtual Advocacy Stakeholder and Education Meeting
DESCRIPTION:» RSVP HERE \n\nJoin HACA/VHF constituents\, advocacy committee members\, and community stakeholders from throughout Virginia for an education meeting that will cover a wide range of advocacy topics relevant to the bleeding disorders community! \nSaturday\, November 14\, 2020 | 4 PM to 6 PM \nAgenda – \n\nWelcome/Introductions\nHealth Policy in the Intersection of Policy and Politics – Del. Dawn Adams (D\, 68th)\nVirginia Bleeding Disorder Program (VBDP) Update – Jan Kuhn RN\, MPH\, Coordinator of VBDP\nState Update AND What Can We Expect in 2021 General Assembly – Becky Bowers-Lanier\, VHF/HACA Advocacy Consultant\nFederal Update – Miriam Goldstein\, J.D\, Director of Policy at Hemophilia Federation of America (HFA)/Nathan Schaefer\, Vice President of Public Policy at National Hemophilia Foundation (NHF)\nWrap-Up\n\nThank you to our advocacy sponsors: Bayer\, CSL Behring\, CVS Caremark\, Genentech\, National Hemophilia Foundation (NHF)\, PhRMA\, Pfizer\, Sanofi Genzyme\, and Takeda \nWe could not provide these important events without the help of our generous sponsors – please go here to view our Virtual Sponsor Program. This program is one way our generous sponsors can virtually connect with the community by providing links to their electronic resources\, brochures\, websites\, social media sites and more!
URL:https://vahemophilia.org/event-program/vhf-haca-virtual-advocacy-stakeholder-and-education-meeting/
LOCATION:Zoom
CATEGORIES:advocacy,education
ATTACH;FMTTYPE=image/jpeg:https://vahemophilia.org/wp-content/uploads/2020/09/49070330053_1e501533f5_o.jpg
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20200512T190000
DTEND;TZID=America/New_York:20200512T200000
DTSTAMP:20260407T093901
CREATED:20200424T174936Z
LAST-MODIFIED:20200424T182132Z
UID:4099-1589310000-1589313600@vahemophilia.org
SUMMARY:HACA/VHF Advocacy Committee Virtual Chat
DESCRIPTION:Join the HACA/VHF advocacy committee for a virtual chat! \nAdvocacy Amid Upheaval: Making it Work \nJoin Miriam Goldstein\, HFA Director of Policy\, and Becky Bowers-Lanier\, advocacy consultant for HACA and VHF\, for a webinar devoted to advocacy in our newly configured COVID world. Join us as we share what we’ve learned since mid-March and how we can maintain our voice when we cannot physically be present. We’ll talk about strategies and answer your questions. \n All virtual chats will be recorded if you are unable to join us live online. When you register you will receive instructions on how to join in\, either by video conference or by phone call. Please join us! \n\n» Go Here to Register
URL:https://vahemophilia.org/event-program/haca-vhf-advocacy-committee-virtual-chat/
LOCATION:Online
CATEGORIES:advocacy,education,virtual chat
ORGANIZER;CN="Kelly Waters%2C VHF Executive Director":MAILTO:info@vahemophilia.org
END:VEVENT
END:VCALENDAR