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X-WR-CALNAME:Virginia Bleeding Disorders Foundation
X-ORIGINAL-URL:https://vahemophilia.org
X-WR-CALDESC:Events for Virginia Bleeding Disorders Foundation
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DTSTART;VALUE=DATE:20220420
DTEND;VALUE=DATE:20220424
DTSTAMP:20260408T110035
CREATED:20220221T170007Z
LAST-MODIFIED:20220221T170007Z
UID:5947-1650412800-1650758399@vahemophilia.org
SUMMARY:Hemophilia Federation of America (HFA) Symposium
DESCRIPTION:This beloved family event has become known as a national “family reunion” for the bleeding disorders community\, allowing community members\, their families and caregivers to come together for camaraderie and education. HFA is excited to host their first in-person Symposium since 2019. They know everyone is not comfortable traveling just yet so some sessions\, such as the keynote presentations\, will have an online component. » Go here to learn more \nWhen: April 20-23\, 2022 \nWhere: San Antonio\, TX (with virtual options) \n» RSVP HERE
URL:https://vahemophilia.org/event-program/hemophilia-federation-of-america-hfa-symposium/
LOCATION:San Antonio Marriott Rivercenter\, 101 Bowie Street\, San Antonio\, Texas\, 78205
CATEGORIES:education
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220321T235900
DTEND;TZID=America/New_York:20220321T235900
DTSTAMP:20260408T110035
CREATED:20220221T170343Z
LAST-MODIFIED:20220315T171338Z
UID:5950-1647907140-1647907140@vahemophilia.org
SUMMARY:NHF Bleeding Disorders Conference Travel Grant - Application Due Date
DESCRIPTION:VHF is pleased to offer travel grants to attend national meetings. National meetings enable our community to come together and exchange information on a wide variety of topics\, from the basics of diagnosis to the most relevant developments in treatment and technology. If applying for travel assistance for a national meeting typical award amounts depend on the availability of travel scholarships offered by the national organization. See below to learn more and contact VHF at 804-740-8643 or info@vahemophilia.org if you have any questions.  \nNHF Bleeding Disorders Conference Scholarship: VHF Terry Lamb Enrichment Scholarship awards can be used to cover travel costs (airfare/mileage/train or bus ticket)\, hotel accommodations\, and meeting registration fees for the NHF Bleeding Disorders Conference. Not to exceed a total of $2\,000 per family. You will be responsible for all meals and other incidentals. Application Deadline Extended: 11:59 pm (EST)\, Monday\, March 21\, 2022 \n» APPLY HERE \n\nNHF’s BDC features educational sessions\, poster abstract presentations\, industry symposia\, networking and social events\, and exhibits. A lineup of dynamic speakers who provide essential information and insights on the evolving landscape in this exciting new era of treatment for hemophilia\, von Willebrand disease\, and rare bleeding disorders. To end the conference\, the NHF Awards Ceremony recognizes outstanding leaders of the bleeding disorders community whose achievements and contributions have helped transform treatment and care. » Go here to learn more \nWhen: August 25-27\, 2022 \nWhere: Houston\, TX (For those that cannot join NHF in Houston\, they will also be offering a virtual component.) \n» RSVP HERE
URL:https://vahemophilia.org/event-program/nhf-bleeding-disorders-conference-travel-grant-application-due-date/
LOCATION:Texas
CATEGORIES:education
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220313T160000
DTEND;TZID=America/New_York:20220313T170000
DTSTAMP:20260408T110035
CREATED:20220119T200206Z
LAST-MODIFIED:20220310T152627Z
UID:5907-1647187200-1647190800@vahemophilia.org
SUMMARY:Ages and Stages: Early Childhood
DESCRIPTION:RSVP HERE\n \nJoin VHF\, HTC staff and mentor families for a virtual program for new families! This program is designed to support families of infants and young children with hemophilia and other inherited bleeding disorders ages 0-10 with community connection and education. This program is free and open to VHF constituents. \nTopic: Ages and Stages: Early Childhood (Ages 0-10) \nThis virtual session will help parents better understand what they can expect behaviorally and emotionally throughout the early years of childhood. Child development\, temperament\, common mood and behavior problems and parenting strategies will be discussed. The session will include some bleeding disorder specific information\, for example\, when a child can start to self-infuse from a behavioral standpoint not a medical standpoint\, how (hemophilia) treatments progress with age\, and the prevalence of anxiety and other behavioral challenges among children with bleeding disorders.  \nPresenter: Juliana S. Bloom\, Ph.D.\, Pediatric Neuropsychologist at The Levin Center \n		\n			\n				\n			\n			\n		 \n		\n			Juliana S. Bloom\, Ph.D. is a licensed psychologist and pediatric neuropsychologist based in Orlando\, Florida. Dr. Bloom currently provides assessment\, therapy\, and consultation services. Dr. Bloom received her B.A. summa cum laude from Emory University and her Masters of Education and doctoral degrees from the University of Georgia. While at UGA\, she conducted clinical research on the neurobiological basis of dyslexia and ADHD. Dr. Bloom completed her internship and postdoctoral fellowship at the Children’s Hospital of Philadelphia\, where she worked with children and adolescents with complex medical and neurological illnesses\, including stroke\, epilepsy\, brain tumors\, cancer\, and traumatic brain injury\, among others. Dr. Bloom’s areas of clinical interest include dyslexia\, ADHD\, neuropsychological outcome and school re-entry following acquired brain injury and medical illness\, medical traumatic stress in patients and families\, and pediatric stroke. She is the author of seven peer reviewed journal articles\, five invited book chapters\, and more than 40 conference presentations. She is a member of the American Psychological Association and the International Neuropsychological Society. She loves spending her free time with her husband and two children.\n		\n			\n		 \nThis education program is presented in partnership with Hemophilia Federation of America (HFA). \nThank you to our New Family Education and Support Sponsors Genentech and Takeda. \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/new-family-education-and-support-ages-and-stages-early-childhood/
LOCATION:Zoom
CATEGORIES:community,education,New Families,virtual
ORGANIZER;CN="Heather Conner%2C VHF Interim Director":MAILTO:heather@vahemophilia.org
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220301T235900
DTEND;TZID=America/New_York:20220301T235900
DTSTAMP:20260408T110035
CREATED:20220221T165534Z
LAST-MODIFIED:20220221T165534Z
UID:5945-1646179140-1646179140@vahemophilia.org
SUMMARY:HFA Symposium Travel Grant - Application Due Date
DESCRIPTION:VHF is pleased to offer travel grants to attend national meetings. National meetings enable our community to come together and exchange information on a wide variety of topics\, from the basics of diagnosis to the most relevant developments in treatment and technology. If applying for travel assistance for a national meeting typical award amounts depend on the availability of travel scholarships offered by the national organization. See below to learn more and contact VHF at 804-740-8643 or info@vahemophilia.org if you have any questions.  \nMeeting: Hemophilia Federation of America (HFA) Symposium\nThis beloved family event has become known as a national “family reunion” for the bleeding disorders community\, allowing community members\, their families and caregivers to come together for camaraderie and education. HFA is excited to host their first in-person Symposium since 2019. They know everyone is not comfortable traveling just yet so some sessions\, such as the keynote presentations\, will have an online component. » Go here to learn more \nWhen: April 20-23\, 2022 \nWhere: San Antonio\, TX (with virtual options) \n» RSVP HERE \n\nHFA Symposium Scholarship: VHF Terry Lamb Enrichment Scholarship awards can be used to cover travel costs for the HFA Symposium. Typical award amounts are in the range of $250 – $500 per person (not to exceed $1\,000 per family). Application Deadline: 11:59 pm (EST)\, Tuesday\, March 1\, 2022 \nHFA offers a scholarship that will cover the cost of your hotel room stay (one (1) hotel room for up to four (4) nights). To apply\, you must first register for the HFA Symposium and then a link to the scholarship information will be found in your confirmation email. Scholarships are based on financial need and first-time attendees of Symposium will be given priority. Previous attendees of Symposium will be considered dependent upon space and availability. The HFA scholarship is on a first come\, first-serve basis so apply soon. For more information about the HFA Symposium scholarship go here.
URL:https://vahemophilia.org/event-program/hfa-symposium-travel-grant-application-due-date/
LOCATION:Texas
CATEGORIES:education
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20220127T190000
DTEND;TZID=America/New_York:20220127T200000
DTSTAMP:20260408T110035
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:20260408T110035
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:20260408T110035
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:20210819T190000
DTEND;TZID=America/New_York:20210819T200000
DTSTAMP:20260408T110035
CREATED:20210719T142246Z
LAST-MODIFIED:20210719T142246Z
UID:5576-1629399600-1629403200@vahemophilia.org
SUMMARY:Virtual Education Session - Lesson Plans: Navigating School with a Bleeding Disorder
DESCRIPTION:» RSVP Here \nTopic: Lesson Plans: Navigating School with a Bleeding Disorder \nLearn how students\, parents\, family members\, and school staff can work together to provide a positive learning environment for students with a bleeding disorder—from preschool through college. \nSpeaker: Jan Martin\, Nurse Educator\, Takeda \nThank you to our sponsor Takeda \n\nThis session is free and open to VHF constituents\, any constituent under the age of 12 will need adult supervision to participate. \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-lesson-plans-navigating-school-with-a-bleeding-disorder/
LOCATION:Zoom
CATEGORIES:education
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:20260408T110035
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:20201215T190000
DTEND;TZID=America/New_York:20201215T200000
DTSTAMP:20260408T110035
CREATED:20201001T141346Z
LAST-MODIFIED:20201001T141951Z
UID:4674-1608058800-1608062400@vahemophilia.org
SUMMARY:Virtual Education Session - Mindfulness as a Path to Resilience
DESCRIPTION:» RSVP HERE \nJoin us for a virtual education session for individuals with an inherited bleeding disorder. \nThe topic will be: Mindfulness as a Path to Resilience \nWhat is mindfulness and what are its benefits? How are stress and resilience related\, and why is resilience important? This presentation will offer patients a set of skills that they may use at home\, on their own. \nSpeaker: Jan Martin\, Nurse Educator\, Takeda \nThank you to our sponsor Takeda \n\nThis session is free and open to VHF constituents\, any constituent under the age of 12 will need adult supervision to participate. \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. \n 
URL:https://vahemophilia.org/event-program/4674/
LOCATION:Zoom
CATEGORIES:education
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:20260408T110035
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:20260408T110035
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