Virginia Bleeding Disorders Foundation

CHARLOTTESVILLE-Educational Dinner "Adversity, Strength, and Resilience"
2025-08-07 18:30 - 20:00 (America/New_York) | Burtons Grill & Bar – The Shops at Stonefield, 2010 Bond St., Charlottesville, VA, 22901, United States
RSVP HERE!
Join us for an evening of education, connection, and support! This educational dinner program is for VHF constituents (and their immediate family and/or household members.) Dinner will be provided and there is no fee to attend.
Location: Burtons Grill & Bar – The Shops at Stonefield, 2010 Bond St. Charlottesville, VA 22901
Program Topic: Adversity, Strength, and Resilience
Coping with a chronic condition, communicating with the health care team and others, financial considerations of health care through life stages, and the importance of staying physically active with appropriate activities are all addressed in this overview. This discussion includes modules on communication with your health care team, staying physically active, managing your care, treatment support, and an insurance review.
Speaker: Linda L. Pollhammer, Patient Affairs Liaison, Pfizer Rare Disease
Please note: Space may be limited, if this event fills up priority will be given to individuals and families living in the Charlottesville area.
Thank you to our sponsor, Pfizer, for supporting this program.

RICHMOND - Community Event at TopGolf
2025-08-03 11:00 - 14:00 | Topgolf Richmond, 2308 Westwood Ave, Richmond, Virginia, 23230
RSVP IS NOW CLOSED – email heather@vahemophilia.org to be placed on the waiting list!
Get Active with YOUR Bleeding Disorders Community at Topgolf Richmond!
Join the Virginia Hemophilia Foundation (VHF) on Sunday, August 3rd for a fun and educational community event focused on health, fitness, and connection. This unique outing offers opportunities to learn more about managing your bleeding disorder, build relationships within the community, and enjoy the game of golf—no experience required!
🎯 What to Expect:

A supportive and engaging environment
Community building and family fun
Lunch and two hours of golf, provided at no cost

Educational Topic: Choosing the Right Footwear for Back-to-School, Sports, and Everyday Activity
Footwear plays a key role in injury prevention and joint health, especially for those with bleeding disorders. This talk will offer practical tips on choosing the right shoes for all ages and activity levels—from everyday use to back-to-school and sports.
Presenter: Allyson D’Esopo, DPT, PT at VCU-HTC
This event is free to attend and open to individuals diagnosed with an inherited bleeding disorder and their immediate family or household members who reside within the VHF coverage area.
VHF community events are held throughout the year to provide social and educational experiences for individuals and families. These gatherings are an excellent way to increase knowledge, find support, and enjoy time together.
We can’t wait to see you there!
Thank you to our current sponsor(s): CSL Behring, CVS, Genentech, NovoNordisk, Pfizer, Sanofi, and Superior Biologics
Colburn-Keenan Foundation – “Bay Fees”

CHARLOTTESVILLE - Camp Youngblood at Camp Holiday Trails
2025-07-13 - 2025-07-18 | Camp Holiday Trails, 400 Holiday Trails Lane, Charlottesville, VA, 22903
REGISTRATION IS CLOSED
The Virginia Hemophilia Foundation (VHF), the Hemophilia Association of the Capital Area (HACA), and Camp Holiday Trails (CHT) are teaming up again for Camp Youngblood (CYB) in 2025.
Camp Youngblood is a week-long overnight camp at CHT for children ages 7-17 with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the VHF or HACA coverage area. Kids enjoy a week of fun and learning with others that are faced with similar challenges and life experiences. Go here to learn more about the 2025 CYB admission guidelines.
Dates: Sunday, July 13 – Friday, July 18, 2025
Location: Camp Holiday Trails, 400 Holiday Trails Ln, Charlottesville, VA 22903
Open Enrollment Application: The CYB application process is open enrollment and not first come first served. This will allow VHF, HACA, and CHT the chance to review applications and manage the roster according to the application/admission guidelines. *Must adhere to all application deadlines to be considered*
Who is Eligible: Camp Youngblood at CHT is for children ages 7-17 with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the VHF or HACA coverage area.
Cost: $25 registration fee (per child)
How to Apply:

Pre-screening: Fill out a short survey to see if your child is eligible. This is required for all applicants, even returning campers. You’ll receive notice of eligibility within one week from either VHF or HACA.
Application: If eligible, you’ll receive a link to the official Camp Youngblood application which is managed by Camp Holiday Trails.

Application Deadlines:

Registration closed Wednesday, April 23, 2025
All paperwork & medical assessment due: Friday, June 6, 2025
Welcome email sent to confirmed campers: Friday, June 13, 2025

Thank you to our Camp Youngblood sponsors: Bayer, CSL Behring, CVS, Genentech, Novo Nordisk, Pfizer, Sanofi, Takeda, UVA-HTC, and VCU-HTC
Thank you to the Colburn-Keenan Foundation for sponsoring our Thursday and Friday Summer Camp Experience Program and helping us provide gas cards to attendees!

VIRGINIA BEACH - Community Event at TopGolf
2025-06-08 11:00 - 14:00 | Topgolf Virginia Beach, 5444 Greenwich Road, Virginia Beach, VA, 23462, United States
THIS EVENT IS NOW FULL. Please email heather@vahemophilia.org to be placed on the waitlist.
Get Active with YOUR Bleeding Disorders Community at Topgolf Virginia Beach!
Join the Virginia Hemophilia Foundation (VHF) on Sunday, June 8th for a fun and educational community event focused on health, fitness, and connection. This unique outing offers opportunities to learn more about managing your bleeding disorder, build relationships within the community, and enjoy the game of golf—no experience required!
🎯 What to Expect:

Learn more about Comprehensive Care for bleeding disorders – what it is and meet some of the folks that make up the CHKD-HTC team.
A supportive and engaging environment
Educational content tailored to individuals with bleeding disorders
Community building and family fun
Lunch and two hours of golf, provided at no cost

This event is free to attend and open to individuals diagnosed with an inherited bleeding disorder and their immediate family or household members who reside within the VHF coverage area.
VHF community events are held throughout the year to provide social and educational experiences for individuals and families. These gatherings are an excellent way to increase knowledge, find support, and enjoy time together.
We can’t wait to see you there!
Thank you to our current sponsor(s): CSL Behring, Genentech, Novo Nordisk, Optum, Sanofi, and Superior Biologics
Colburn-Keenan Foundation – “Bay Fees”

CHARLOTTESVILLE - VHF Family Camp at Camp Holiday Trails
2025-05-16 - 2025-05-18 | Camp Holiday Trails, 400 Holiday Trails Lane, Charlottesville, VA, 22903
A spot is open – if you are interested please email heather@vahemophilia.org
Date: Friday, May 16 – Sunday, May 18, 2025
Location: Camp Holiday Trails, 400 Holiday Trails Ln, Charlottesville, VA 22903
Experience an unforgettable weekend at Camp Holiday Trails (CHT) with the Virginia Hemophilia Foundation (VHF)! Connect with other families affected by bleeding disorders while enjoying education, community, and classic camp fun. This special program is designed for families with at least one child living at home who is between the ages of 5 – 17.
At Family Camp, participants will enjoy a supportive environment where they can connect with others who understand the challenges of living with a bleeding disorder. Families will have the opportunity to attend educational sessions, learn about self-advocacy and resilience, and engage in fun outdoor activities that promote confidence, teamwork, and friendship.
Who Can Attend: Family Camp is open to families impacted by an inherited bleeding disorder and is designed for families with at least one child living at home who is between the ages of 5 – 17. This program is for VHF constituents (and their immediate family and/or household members only) and is not open to individuals employed or compensated by Industry. Go here to read more about family camp guidelines.
Important Dates:
Friday, April 11, 2025 – Registration closes
Monday, April 14, 2025 – Registration fee link and confirmation email will be sent out
Wednesday, April 16, 2025 – Registration fee due, $50 per family
This program is a perfect opportunity for families to relax, learn, and grow together. Don’t miss out on this incredible experience! For questions, email info@vahemophilia.org or call 804-740-8643.
Thank you to our current sponsors: Colburn Keenan Foundation, Inc., CSL Behring, Genentech, and Takeda

APPLICATION DUE: VHF Lyman Fisher Scholarship
2025-05-01 | VA
VHF Lyman Fisher Scholarship Application Procedure & Guidelines
APPLICATION PROCEDURE
Application Deadline: Thursday, May 1, 2025, at 5:00 pm
Applications must be completed using our online application form or email the pdf version to info@vahemophilia.org.
Go here to apply via JotForm
Go here to download PDF version of application
All letters of recommendation are to be sent electronically to info@vahemophilia.org. Applications and/or supporting documents received after 5:00 PM on Thursday, May 1st will not be considered. It is up to the applicant to follow up and make sure these items are received by the deadline. Incomplete applications will not be considered.
Please read and follow the application and instructions very carefully to receive full consideration for a VHF Lyman Fisher Scholarship. If you don’t know the answer, please type N/A. DO NOT leave any section blank.
Scholarship applicants will be notified of the committee’s findings by June 1st and winners will be recognized at VHF’s Medical Symposium September 13, 2025.
ELIGIBILITY
Individuals living with an inherited bleeding disorder, their sibling or their parents who live in the territorial jurisdiction of VHF, which includes the Commonwealth of Virginia, with the exception of the following: The cities of Alexandria, Fairfax, Falls Church, Herndon, Manassas, and Vienna and the counties of Arlington, Fairfax, Fauquier, Loudon, Prince William and Stafford.
SCHOLARSHIPS
In 2025, VHF will offer up to $12,000 in scholarships. The award amount will vary based on the number of applicants that are selected and the scholarship rubric that the VHF scholarship committee uses to evaluate academic performance, participation in school, community, and VHF activities, a personal essay detailing educational and future career goals, and recommendation letters. The scholarships may be used at any accredited college, university, or vocational/technical school in the United States and are to be applied toward a student’s educational expenses. VHF is not obligated to award scholarships in a given year.
A student who receives an award one year may reapply in later years but winning a scholarship in one year does not necessarily mean that the student will win in a later year. Also, a student who applies in one year and does not receive an award is eligible to apply the following year for the scholarship.
Scholarship applicants must have participated in VHF activities.
PAYMENT OF SCHOLARSHIP FUNDS
Scholarship payments are not distributed directly to an individual, but are made via scholarship checks, payable to the schools. VHF staff will work with the award recipient(s) to process the scholarship funds.
RESPONSIBILITIES OF RECIPIENTS
Scholarship recipients must enroll as a college student in the fall of the year in which the scholarships are awarded and continue in school for the entire academic year without interruption, barring illness, emergency, or military service. If a scholarship recipient leaves school during the scholarship period, VHF may ask for reimbursement of scholarship funds.
Scholarship recipients are responsible for making certain that their scholarship checks are delivered to their colleges. Recipients must provide VHF with information on where to send the check, as well as other pertinent information such as student identification number.
The recipient is responsible for determining the impact of the scholarship or grant on their annual tax returns. For more information, talk to a tax return preparer or go here.
QUESTIONS
If you have questions about this scholarship (application process, whether the program and/or activity that you are requesting assistance with fits within the guidelines, how much funding is available, etc.) please reach out to Kelly Waters at 804-740-8643 or kelly@vahemophilia.org.

Scholarship Background
The Virginia Hemophilia Foundation (VHF) Lyman Fisher Scholarship was established to honor Dr. Lyman Fisher, a teacher, researcher, and clinician in hemostasis. For many years, he directed the adult hemophilia program for Virginia. He will be remembered for his steadfast commitment to his patients and students, his respect for those who served under him, his community service and his affection for his family.

RICHMOND - New Family Support and Education
2025-04-26 10:00 - 12:00 | Richmond Metro Zoo, 8300 Beaver Bridge Rd.,, Moseley, VA, 23120, United States
Registration is closed, email heather@vahemophilia.org if you have any questions.
Join VHF for a special program designed to support families of infants and young children diagnosed with inherited bleeding disorders. This event offers an opportunity to connect with the bleeding disorders community and gain valuable education and resources.
Topic: Beyond Bubble Baths: Real Self-Care for Caregivers
Caring for others, especially in the midst of chronic illness—can feel all-consuming, leaving little room for our own well-being. This session goes beyond surface-level self-care and explores deeper, more sustainable ways to restore ourselves while continuing to show up for those we love. Through reflection, discussion, and practical strategies, we’ll explore how to integrate real self-care into our lives in ways that actually stick.
Presenter: Sarahbeth Spasojevich, NCC, MA, MBA, MEd
Sarahbeth Spasojevich is a mental health clinician at Connected Resilience and a mother of three – including Jack, a fourth-generation hemophiliac. As an active member of the Virginia Hemophilia Foundation community, she deeply understands the emotional and practical challenges of caregiving in the rare disease space.
What to Expect:

A private meeting space for our group
Continental breakfast provided for all attendees
Time for Q&A
Networking opportunities with other parents and families
Time to enjoy the Richmond Zoo and see Poppy – America’s pygmy hippo princess!

Who Can Attend: This program is tailored for families affected by inherited bleeding disorders with children ages 10 and under who reside in the VHF coverage area and is not open to individuals employed or compensated by Industry.
We look forward to providing you with a supportive and welcoming environment to learn, share, and connect!
Thank you to our current sponsors: CSL Behring, Genentech, Takeda and VCU-HTC

APPLICATION DUE: Camp Youngblood at Camp Holiday Trails
2025-04-23 | VA
Application Closed Wednesday, April 23, 2025
The Virginia Hemophilia Foundation (VHF), the Hemophilia Association of the Capital Area (HACA), and Camp Holiday Trails (CHT) are excited to partner once again for Camp Youngblood (CYB) — a week-long overnight camp designed just for kids in our inherited bleeding disorders community!

About Camp Youngblood
📅 Dates: Sunday, July 13 – Friday, July 18, 2025📍 Location: Camp Holiday Trails, 400 Holiday Trails Ln, Charlottesville, VA 22903
Camp Youngblood is open to children ages 7–17 who:

Have an inherited bleeding disorder
Are siblings of a child with an inherited bleeding disorder
Are children of members of the inherited bleeding disorder community

All campers must reside within the VHF or HACA coverage areas.
Kids will enjoy a week of fun, connection, and growth—surrounded by peers who understand their challenges and experiences. Learn more about the 2025 Camp Youngblood admission guidelines.

How to Apply
Step 1: Pre-Screening SurveyAll applicants, including returning campers, must complete a short pre-screening survey. This helps determine eligibility.
You will be notified of your eligibility within one week by VHF or HACA.
Step 2: Camp ApplicationIf eligible, you’ll receive a link to the official Camp Youngblood application, managed by Camp Holiday Trails.
Cost: $25 registration fee per child

Important Deadlines
Application Closed Wednesday, April 23, 2025All Paperwork & Medical Assessments Due: Friday, June 6, 2025Welcome Emails Sent to Confirmed Campers: Friday, June 13, 2025

Camp Youngblood operates on open enrollment—not first come, first served. Applications are reviewed carefully based on the admission guidelines, so please ensure all deadlines are met to be considered.

Thank You to Our 2025 Sponsors
Novo Nordisk, Pfizer, Takeda, and VCU-HTC

WILLIAMSBURG - World Hemophilia Day 2025 "One Family" Program
2025-04-17 18:30 - 20:00 | Thai Tara Sushi, 240 Mclaws Circle Unit 117, Williamsburg, VA, 23185, United States
THIS EVENT IS NOW FULL – Please email heather@vahemophilia.org to be put on the wait list. Thanks!
You’re invited to a World Hemophilia Day Event!
Sanofi’s 2025 One Family program will focus on the innate ties that bind the bleeding disorders community. This family friendly event will explore shared experiences, how to forge deeper relationships, and how the power of connection uplifts everyone.
Who: This VHF Educational Dinner is tailored for individuals and families of all ages affected by inherited bleeding disorders who are VHF constituents and their family and/or household members.
What: An interactive and educational event, where you will receive helpful information that will foster a sense of connection within the global hemophilia community in recognition of World Hemophilia Day 2025! There will be activities such as beaded bracelet making, instant camera selfie stations, DIY photo frames, and photo prop crafts. After the education session there will be plenty of time for discussion, catching up, and enjoying time with your family and friends! Dinner will be provided and there is no fee to attend.
Where: Thai Tara Sushi 240 Mclaws Circle Unit 117, Williamsburg, VA 23185 – Serving Thai food, Japanese Hibachi, Sushi, and more!

When: Thursday, April 17th – World Hemophilia Day!
Thank you to our sponsor Sanofi.

APPLICATION DUE: VHF Travel Grant for NBDF Bleeding Disorders Conference
2025-04-04 | VA
VHF Travel Grants to National Meetings: The Virginia Hemophilia Foundation (VHF) is pleased to offer Travel Grants to attend national meetings as part of the Terry Lamb Enrichment Scholarship. National meetings enable our community to come together and exchange information on treatment and technology. Click here to learn more about the Terry Lamb Enrichment Scholarship program.
National Bleeding Disorders Foundation (NBDF) Bleeding Disorders Conference (BDC) features educational sessions, 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. Go here to learn more about NBDF BDC.
Meeting Dates: August 21 – 23, 2025
Meeting Location: Aurora-Denver, CO
VHF travel grant deadline:5:00 pm, Friday, April 4, 2025
Go here to apply online via JotForm.
Go here to download the PDF version of the application.

RICHMOND - VHF 50th Anniversary Celebration! A Golden Milestone: Honoring Our Past, Building Our Future
2025-03-16 10:30 - 13:30 | Lewis Ginter Botanical Garden, 1800 Lakeside Ave., Richmond, Virginia, 23228
RSVP HERE!
A Golden Milestone: Honoring Our Past, Building Our Future. Celebrate 50 Years of the Virginia Hemophilia Foundation (VHF) at the beautiful Lewis Ginter Botanical Gardens! On March 16, 2025, everyone is welcome to join us for this special celebration as we come together to honor 50 years of support, connection, and progress within our bleeding disorders community. Set against the backdrop of Lewis Ginter’s 50 acres of year-round beauty with themed gardens like the Rose Garden and Cherry Tree Walk, a children’s area, and the iconic domed Conservatory, this celebration offers a perfect space for reflection, connection, and inspiration.
March is Bleeding Disorders Awareness Month, a time to raise awareness, promote education, and celebrate the achievements of our community. Join YOUR VHF family for a special 50th Anniversary Celebration at Lewis Ginter Botanical Garden, where we will come together to connect, reflect, and create lasting memories while enjoying great food and the chance to explore exhibit booths from our industry partners. Capture the moment with a caricature artist and photo booth and you do not want to miss our inspiring program, where we will honor 50 years of support, advocacy, and connection, recognizing the impact of those who created and shaped our mission.
At 1:00 PM, take part in a group walk through the gardens for the first look at the new VHF Sitting Wall. Overlooking the gardens and water, this peaceful space will feature an engraved memorial plaque, serving as a tribute to those we have lost, a celebration of the contributions of so many, and a lasting symbol of our community’s strength and unity. Wear your favorite VHF T-shirt/sweatshirt or shop our exclusive 50th Anniversary merchandise—$1 from every sale supports the creation of VHF’s Sitting Wall learn more here. After the event, guests are welcome to continue exploring the gardens. We look forward to celebrating this milestone with you!
Program Schedule:
10:30 AM – 11:15 AM: Guest Arrival, Refreshments, Photo Booth, Caricature Artist, and Exhibit Tables
11:15 AM – 11:25 AM: Welcome & Opening Remarks
11:25 AM – 11:35 AM: Greetings and Recognition Ceremony led by Dawn Rotellini, NBDF COO
11:35 AM – 11:40 AM: Moment of Silence led by Don Smith, VHF Board Member
11:40 AM – 12:00 PM: “Honoring Our Past” – Reflections from past leaders and contributors
12:00 PM – 12:10 PM: “Celebrating Our Present” – Keynote by Phil Gattone, NBDF CEO
12:10 PM – 12:25 PM: “Building Our Future” – Closing Remarks
12:25 PM – 1:00 PM: Networking, Refreshments, Entertainment, Exhibit Tables, Walk to Sitting Wall
The event is free to attend, and casual dress is encouraged, but we kindly ask that you register in advance here. If you have any questions contact Kelly Waters at info@vahemophilia.org or 804-740-8643.
Thank you to our current sponsor(s): Accredo, Bayer, DrugCo Health, Genentech, Novo Nordisk, Optum, Pfizer, Takeda, and UVA Hemophilia Treatment Center
VHF Behavior Guidelines: VHF is committed to offering programs that are safe and inclusive for all members of the inherited bleeding disorders community. All participants—including attendees, exhibitors, vendors, staff, volunteers, and other stakeholders—are expected to adhere to the VHF Event Behavior Guidelines.

SPONSORS AND PRESENTERS - Registration for Annual Meeting
2025-03-15 08:30 - 16:00 | Hilton Richmond Hotel & Spa/Short Pump, 12042 W Broad St, Richmond, VA 23233, Richmond, VA, 23233, United States
Register Here
We appreciate your interest and support of our 2025 Annual Meeting, contact Kelly Waters at kelly@vahemophilia.org or 804-740-8643 for more information about sponsorship. Closer to the date of the event we will send a detailed email to all registered industry supporters and presenters. This email will include the agenda, booth set up times, what to bring, how many people to expect, etc.
Overnight accommodations at Hilton Richmond Hotel & Spa/Short Pump are available on the nights of Friday, March 14th and Saturday, March 15. Scroll down for more information.

Saturday, March 15th (Tentative Timeline)
7:00 am – 8:00 am Exhibit set-up (for those that plan to arrive on Friday, March14th there may be time to set-up your exhibit that evening)
8:30 am – 9:30 am Breakfast and visit exhibits
9:30 am – 4:00 pm Education presentations, visit exhibits, lunch and snack breaks, and more!
4:00 pm Meeting wrap-up

PLEASE NOTE: We will not make hotel reservations for speakers, Industry Agents OR Industry Agents who are Consumers. However, we do have a courtesy room block at Hilton Richmond Hotel & Spa/Short Pump for Friday, March 14 and Saturday, March 15 and they will extend the group rate of $179 (does not include taxes and fees). There are a limited number of rooms and they will be first come first served and please be advised that the cut-off date for the room block will be on Thursday, February 20th, 2025.
Go here to book your room online (the link is pre-set for 2 nights please edit your stay if you are only staying for 1) Booking Link: VHF Annual Meeting
If you run into any issues, please do not hesitate to reach out to the reservation coordinator Jaynec Dickens, jaynec.dickens@hilton.com, 804-592-2247.

For Industry Agents who are Consumers and a VHF Constituent: If your family members plan to attend the annual meeting go here to register them. As a reminder we still ask that you register yourself as an industry representative and make your own hotel reservation.
VHF makes every effort to ensure that members of the bleeding disorders community are able to make a clear distinction between its own activities and those of Industry. Further, it is essential that we create beneficial and pressure – free experiences for our community members, and to protect participants in VHF events and programs. Accordingly, VHF has developed a set of standards. Go here to read Standards for Industry, Associated Organizations, and their Agents. In addition, VHF is committed to offering programs that are safe and inclusive for all members of the inherited bleeding disorders community. All participants—including attendees, exhibitors, vendors, staff, volunteers, and other stakeholders—are expected to adhere to the VHF Event Behavior Guidelines.
Thank you for your continued support!
Register Here

COMMUNITY MEMBERS - Registration for Annual Meeting
2025-03-14 - 2025-03-16 | Hilton Richmond Hotel & Spa/Short Pump, 12042 W Broad St, Richmond, VA 23233, Richmond, VA, 23233, United States
RSVP HERE!
RSVP Deadline: Thursday, February 20, 2025
VHF’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.
What to expect: The event kicks off Friday evening with an educational dinner and time to catch up with friends and family. Saturday begins with breakfast and an opportunity to explore exhibits hosted by our generous industry sponsors, showcasing the latest treatments and therapies. The day continues with engaging educational sessions, updates from VHF, and on-site childcare for ages 0-17 provided by A Helping Hand.
March is Bleeding Disorders Awareness Month: A time to raise awareness, promote education, and honor the dedication and achievements of the bleeding disorders community. Join YOUR VHF community to celebrate this meaningful month at our Annual Meeting and again on Sunday, March 16, 2025, for our milestone 50th Anniversary Celebration at Lewis Ginter Botanical Garden. Together, we’ll learn, connect, and create lasting memories in a festive and supportive setting. Don’t forget to check out our exclusive 50th Anniversary merchandise—$1 from every sale supports the creation of VHF’s Sitting Wall, a serene memorial to honor our community, which will be unveiled at the celebration. Learn more here.
Overnight Accommodations: We are pleased to offer overnight accommodations at the Hilton Richmond Hotel & Spa/Short Pump for Friday, March 14, and Saturday, March 15.
Registration Fee: There is a $25 registration fee per household and payment instructions will be sent via email after registration closes. This event includes educational programs, meals, community activities, and overnight accommodations for constituents living within the VHF coverage area.
Tentative Schedule:
Friday, March 14
7:00 PM: Educational Dinner
Saturday, March 15
8:30 AM – 9:30 AM: Breakfast and Exhibit Visits
9:30 AM – 4:00 PM: Educational Presentations, Exhibit Visits, Lunch, Snack Breaks, and More
4:00 PM: Meeting Wrap-Up
6:00 PM: Educational Dinner
Sunday, March 16
10:30 AM – 1:00 PM: Celebrate VHF’s 50th Anniversary at the Lewis Ginter Botanical Garden in Richmond *50th Anniversary Celebration event is optional and is not a part of the annual meeting.
We can’t wait to see you there for this memorable weekend filled with education, connection, and celebration!
Thank you to our current Annual Meeting sponsors: Accredo, Bayer, BioMatrix, Cottrill’s Pharmacy, CSL Behring, DrugCo Health, Genentech, Hemabiologics, Novo Nordisk, Octapharma, Pfizer, Sanofi, Soleo Health, Superior Biologics, Takeda, UVA-HTC, and VCU-HTC
RSVP HERE!

MONTPELIER - Women’s Retreat Weekend
2025-02-15 - 2025-02-16 | Shalom House Retreat Center, 15340 Robert Terrell Rd., Montpelier, VA, 23192, United States
RSVP HERE!
RSVP Deadline: Monday, February 3, 2025
Join us for a rejuvenating weekend retreat designed to bring together women affected by and connected to inherited bleeding disorders. This special weekend is an opportunity to learn, grow, and build lasting connections within a supportive community. Download Agenda Here.
Retreat Location: This inspiring weekend will be held at the Shalom Retreat Center, a peaceful and welcoming venue that offers the perfect setting for reflection, learning, and connection. Nestled in a serene environment, the Shalom Retreat Center provides comfortable accommodations, beautiful surroundings, and a calm atmosphere that encourages personal growth and community bonding.
Please Note: The VHF Women’s Retreat is designed for VHF constituents age 21 and up with inherited bleeding disorders and/or adults whose lives are impacted by an inherited bleeding disorder (i.e. caregivers, spouses, carriers, immediate family members – some restrictions do apply) and is not open to individuals employed or compensated by Industry.
Registration Fee: This fee helps cover the retreat costs, including access to educational programs, scheduled meals, and overnight accommodations. Saturday night accommodations will be provided at the Shalom Retreat House. Due to a limited number of rooms, we encourage attendees to consider sharing a room if possible. Thank you for your understanding and cooperation in helping us make this retreat accessible for everyone!
Payment: After submitting your RSVP, you will receive a confirmation email from heather@vahemophilia.org with a link to submit the registration fee.
Deadline: Registration will close on Monday, February 3, 2025 and the registration fee must be paid by Friday, February 7, 2025.
Don’t miss this unique opportunity to connect with others who truly understand. We look forward to seeing you there!
Thank you to our current sponsor(s): CSL Behring, Genentech, and Takeda

Richmond Days
2025-01-27 09:00 - 10:30 | General Assembly Building, 201 North 9th St., Richmond, 23219, United States
REGISTER HERE
RSVP Deadline: Thursday, January 16, 2025
Monday, January 27, 2025: Join VHF and the Hemophilia Association of the Capital Area (HACA) for an opportunity to advocate for policies that improve access to care, support, and resources for those living with bleeding disorders. Your voice can directly impact legislation that affects the lives of individuals with bleeding disorders by meeting with your state legislators. Open to all community members.
What to Expect: We will reserve space in the General Assembly building from 9:00 am to 10:30 am and aim to schedule two in-person legislative visits for each participant—one with your State Senate office and one with your State Delegate office. You may be joined by other advocates during these meetings and have opportunities to participate in additional legislative visits.
Sunday, January 26, 2025: There will be an optional education dinner and hotel rooms available for VHF/HACA community members at Hampton Inn & Suites Richmond – Downtown 700 East Main Street – Suite A, Richmond, Virginia, 23219.
We hope you’ll join us on Tuesday, January 21, 2025, at 6:00 pm for our Virtual Advocacy Education Training where we’ll cover tips for your visits and share our 2025 legislative priorities, RSVP here.
Thank you to our current sponsor(s): CSL Behring, Genentech, National Bleeding Disorders Foundation (NBDF), Takeda, and VCU-HTC

VIRTUAL – 2025 Advocacy Education Training
2025-01-21 19:00 - 20:00 | Zoom
REGISTER HERE

Join VHF and the Hemophilia Association of the Capital Area (HACA) for a virtual advocacy education training program that will focus on the 2025 Virginia General Assembly. Join in and hear details about proposed legislation and state policy issues that focus on access to quality healthcare.This training will be in preparation for Richmond Days but you do not have to be registered for Richmond Days to participate. Open to all community members.
This session is free and open to anyone interested in learning more about advocacy and how it relates to the Virginia inherited bleeding disorders community.
» Go here to download the 2025 VHF Advocacy Calendar
Thank you to our current sponsor(s): Takeda

As 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.

VIRTUAL – VHF/HACA Camp Youngblood Information Session
2025-01-16 19:00 - 20:00 | Zoom
RSVP HERE!
Are you thinking about sending your child to Camp Youngblood at Camp Holiday Trails (CHT) for the first time in 2025, have questions, or would you just like a refresher on the camp experience? Join the Hemophilia Association of the Capital Area (HACA), CHT, and VHF for a virtual information session via Zoom on Thursday, January 16, at 7:00 pm to learn more about Camp Youngblood – even if you aren’t quite ready to send your kids this year.
What to expect: Staff from CHT will talk more about camp activities and facilities; longtime Camp Youngblood parents will share their experiences with sending their kids to camp, and staff from VHF and HACA will be available to answer any additional questions. This virtual session will be a great opportunity to learn more and get all your questions answered in real time!
Camp Youngblood is a week-long overnight camp at Camp Holiday Trails (CHT) for children ages 7-17 with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the VHF or HACA coverage area.
» Go here to learn more about the Camp Youngblood registration process
» REGISTER HERE Once you RSVP you will receive the zoom link separately via email from heather@vahemophilia.org.

As 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.

VIRTUAL – Virginia General Assembly Weekly Check In
2025-02-04 - 2025-02-18 | Zoom
REGISTER HERE
Join VHF & the Hemophilia Association of the Capital Area (HACA) for an informal, virtual 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. These check-ins are open to all community members.
Once you register you will receive a zoom link separately via email from heather@vahemophilia.org – you will use the same link each week.
Please 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!
WEEKLY CHECK IN DATES:
Tues., Feb 4, 2025 12:00 – 12:30 PM
Tues., Feb 11, 2025 12:00 – 12:30 PM
Tues., Feb 18, 2025 12:00 – 12:30 PM
Go here to download 2025 VHF HACA Advocacy Calendar
Thank you to our current sponsor(s): National Bleeding Disorders Foundation (NBDF) and Takeda

As 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.

RICHMOND - Winter Gathering - Tacky Lights Bus Tour
2024-12-07 16:00 - 20:00 | VA
REGISTRATION IS FULL – email heather@vahemophilia.org if you would like to be placed on the waiting list.
VHF invites you to our Annual Winter Gathering – come celebrate the winter season with your bleeding disorders community! We will start the afternoon with holiday refreshements and time to gather with friends and then we will hop on a motor coach for a Tacky Lights Bus Tour of Richmond. A fun tradition that is fun for all ages and a great way to get into the holiday spirit. Please come whether you are young or just young at heart…
We will meet for holiday refreshments at 4:00 pm in the community room at the Publix Supermarket located in John Rolfe Commons 2250 John Rolfe Pkwy, Henrico, VA 23233 and will board the bus from there.
This event is limited to constituents that live within the VHF coverage area and their immediate family and/or household members. There is no fee to attend and space is limited.
Please note that this will be the only Winter Gathering of the season.
Thank you to our sponsors: CSL Behring and Takeda

VIRTUAL – VHF/HACA Advocacy Stakeholder and Education Meeting
2024-11-07 16:00 - 18:00 | Zoom
Join community stakeholders within the bleeding disorders community for a virtual education meeting. Stay informed with the latest state and federal advocacy news, connect with fellow Virginians, and collaborate on improving the lives of those affected by bleeding disorders. Share experiences, gain knowledge, and build a stronger community. Go here to download a copy of our 2025 Advocacy Calendar.
MEETING AGENDA
Welcome and Introductions
Advocacy From the Perspective of a Legislative Assistant
Luke Sweeney, Chief of Staff to Delegate Betsy B. Carr
Virginia Bleeding Disorders Program Update (VBDP)
Lauren Dunn, MSW, Health Insurance Consultant, Virginia Bleeding Disorders Program AND Erika J. Martin, MT (ASCP) Program Manager, Virginia Bleeding Disorders Program
What Can We Expect in the 2025 General Assembly
Becky Bowers-Lanier, VHF/HACA Advocacy Consultant
Federal Update
Matt Delaney, Government Relations Manager at National Bleeding Disorder Foundation (NBDF)
Once you RSVP you will receive the zoom link separately via email from heather@vahemophilia.org.
Thank you to our sponsors: Genentech, NBDF, Pfizer, PhRMA, VCU-HTC, and Takeda

As 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.

RICHMOND - Adult Retreat Weekend
2024-11-01 - 2024-11-03 | Hyatt House Richmond / Short Pump, 11800 W Broad St #1098, Henrico, VA, 23233, United States
*Registration is now closed, email heather@vahemophilia.org to be placed on the wait list.
Hyatt House Richmond/Short Pump11800 West Broad Street Suite 1098, Henrico, VA 23233 (located in Short Pump Town Center)
VHF’s Adult Retreat is a weekend designed for education, relaxation, support, and friendship. This fall retreat is the perfect opportunity for you to learn, unwind and connect with others who share your experience. Registration will close Thursday, October 10th.
Enjoy an (optional) Friday night educational dinner “Cognitive Conversations: Think, Feel, Act” and movie screening of On The Shoulders Of Giants, then on Saturday GutMonkey facilitator Joe Torrey, will present their leading Edge Program which will tackle topics like building communities, teamwork, getting clued in on current topics in bleeding disorders, and shared decision making. Joe will have you laughing and making new connections in the community. There will be an (optional) Saturday night educational dinner “Fueling Your Future with Smart Choices” where you will learn healthy eating habits to fuel your body and improve your emotional well-being and we will end the weekend with an educational breakfast “Better Together: Integrating Mind, Body, and Joint Health in Bleeding Disorders.” Go here to see the agenda.

Presenter: Joe Torrey believes good learning begins with intentional design and a playful approach. With a degree in Outdoor Education and years of professional experience in team building, summer camp, and environmental education programs, Joe crafts and implements experiences to facilitate positive change in communities, teams, and mindsets. At GutMonkey, Joe uses creative design and digital content to empower folks to share their stories.

PLEASE NOTE:

The VHF Adult Retreat is designed for VHF constituents age 21 and up with inherited bleeding disorders and/or to adults whose lives are impacted by an inherited bleeding disorder (i.e. caregivers, spouses, carriers, immediate family members – some restrictions do apply) and is not open to individuals employed or compensated by Industry.
Educational program, scheduled meals, and Friday and Saturday night overnight accommodations are provided at no cost for constituents that live in the VHF coverage area. There is a $25 registration fee to attend (a link to pay will be sent out after registration closes on October 11th.)

Thank you to our current sponsors: BioMarin, CSL Behring, Genentech, Hoos at Home, and Takeda

WINCHESTER – Educational Dinner
2024-10-23 18:30 - 20:00 | IJ Canns American Grille, 3111 Valley Ave, Winchester, VA, 22601, United States
Unfortunately, this educational dinner has been canceled. Please contact info@vahemophilia.org for more information.
Join us Wednesday, October 23rd at 6:30 pm for an educational program for VHF constituents (and their immediate family and/or household members.) Dinner will be provided and there is no fee to attend.
Location: IJ Canns American Grille
The topic will be: Gene Therapy for Hemophilia
Presentation on the advances in gene therapy research for hemophilia.Join us for a session which dives into gene therapy for hemophilia, how it works, and the goals of gene therapy.
Speaker: Betsy Koval, Patient Resource Navigator, CSL Behring

Betsy Koval is a Patient Resource Navigator with CSL Behring and will be working with patients who are interested in gene therapy. She has over 15 years of experience in the bleeding disorders community. Betsy has industry experience as a senior clinical educator and in training within learning and development. Prior to that she was the lead pediatric and adolescent transition nurse coordinator at the Hemophilia of Georgia Center for Bleeding and Clotting Disorders at Emory University and Children’s Healthcare of Atlanta. She has presented posters and spoken at regional and national conferences on bleeding disorders and transition of care. She was a certified clinical research coordinator for a multispecialty clinic which supported research for cardiovascular, diabetic, pulmonary, dermatologic and other conditions as well as having worked in critical care and solid organ transplantation in the ICU at Emory University Hospital. Empowering patients, families and providers with knowledge for improving health is Betsy’s favorite part of her role and she is honored to work within the bleeding disorders community.

Space is sometimes limited and if so, priority will be given to those members that live within the Shenandoah region.
Thank you to our sponsor CSL Behring.

CHESAPEAKE – Educational Dinner
2024-10-17 18:30 - 20:00 | Cutlass Grille, 725 Eden Way N, Ste 700, Chesapeake, VA, 23320
Join us for an educational program for VHF constituents (and their immediate family and/or household members only.) Dinner will be provided and there is no fee to attend.
Location: Cutlass Grille Restaurant 25 Eden Way N #700, Chesapeake, VA 23320
The topic will be: Shared Decision Making
Shared decision making is a partnership between people with hemophilia and their care teams that may help them better manage their condition. This interactive session covers how to take an active role as part of your treatment team, discuss therapy considerations, and find quality sources of information.
Speaker: Linda L. Pollhammer, Patient Affairs Liaison, Pfizer Rare Disease

Space is sometimes limited and if so, priority will be given to those members that live within the Hampton Roads region.
Thank you to our sponsor Pfizer.

CHARLOTTESVILLE - Educational Dinner
2024-10-09 18:00 - 20:30 | Crozet Pizza, 5794 Three Notch'd Rd., Crozet, VA, 22932
Join us for an educational program for VHF constituents (and their immediate family and/or household members only.) Dinner will be provided and there is no fee to attend. PLEASE NOTE: The physical well-being and exercise component of this program has been canceled.
Educational Dinner
Time: 6:00 pm
Location: Crozet Pizza 5794 Three Notch’d Rd, Crozet, VA 22932
The topic will be: The Joint Movement: Come Together: The Intersection Between Joint Health, Hemophilia and Joint Pain
An interactive workshop focused on the importance of joint health for those living with hemophilia.
Speaker: Nick Cady, Community Relations & Education Manager, Sanofi
The educational dinner is for VHF constituents of all ages (and their immediate family and/or household members) and there is no fee to attend.

In-Person Events: Covid-19 Safety Guidance: For all in-person events VHF will follow CDC guidance for COVID-19 safety and prevention. This policy can be found here and will continue to be updated as CDC guidance changes. Please read and contact VHF with any questions or concerns at 804-740-8643 or info@vahemophilia.org.

WILLIAMSBURG - Medical Symposium at Great Wolf Lodge
2024-09-28 08:30 - 16:00 | Great Wolf Lodge, 549 E Rochambeau Dr., Williamsburg, VA, 23188
REGISTRATION IS CLOSED.
The VHF Medical Symposium will provide consumers with the opportunity to learn more about new and current treatment options, access to care issues and other medical/health related topics. This program will be held at the conference center at the Great Wolf Lodge (GWL) in Williamsburg. Overnight accommodations are available at Great Wolf Lodge and entrance to the water park is included in your stay (all registrants must attend the Medical Symposium meeting for access to the water park and overnight accommodations.)
What To Expect From The Weekend:
(Optional) Friday, September 27th, 7:30 pm –
* We will kick off the weekend with a family friendly movie night! Enjoy refreshments and view Redefining Impossible, a 40-minute documentary following five elite athletes living with hemophilia – as they share their stories of being told that they couldn’t play because of their condition and still persevering to redefine what’s possible for people living with hemophilia. There will be time for Q&A with the film’s Executive Producer, Rob Bradford from Believe Limited.
* If you plan to stay overnight on Friday, you will be able to access the water park any time after opening on that day and you can check in to your room at 4:00 pm (all Friday activities are optional.)
Saturday, September 28th, 8:30 am –
* The day will start with breakfast and time for you to visit with industry sponsors to learn about the latest treatments and therapies.
* This year’s keynote presentation “Candid Conversations” is a moderated panel discussion that will provide you with a “bird’s eye view” into the real-world experience of both consumers and providers, the path to shared decision-making, and how innovative therapies are changing the landscape of the bleeding disorders community and afternoon breakout sessions will give you a small group experience with diagnosis specific content.
* On-site childcare and children/teen programming with Camp Holiday Trails will be provided.
* You do not want to miss the Science Fair Roadshow, brought to you by Believe Limited, this inspiring, larger-than-life, community-facing exhibit presents teens, adults, and families alike with the opportunity to learn about the science behind bleeding disorders by combining the interactivity of a true “science center” exhibit with the visual style of the classic science fairs we all grew up with.
* Overnight stay for Saturday night is also available so that you and your family can enjoy time with your community and access to the waterpark that evening.
Sunday, September 29th –
* There are no scheduled meals or activities.
Important Information:
* Registrants’ place/number on the RSVP list will be determined by our Program Registration Guidelines.
* This event is open to ALL AGES (not just for families with household members under 18.) To book overnight accommodation for you and/or your family, at least one member of your group must be age 21+.
* Overnight accommodation and scheduled meals will be provided at no cost to VHF constituents. There is a $25 registration fee to attend (a link to pay will be sent out after registration closes on August 16th.)
* All registrants must attend the Medical Symposium meeting for access to the water park and overnight accommodation.
* Overnight stay on Fri. & Sat. and time at the waterpark are optional, you are welcome to attend the meeting only.
* To Be Eligible for a Spot You Must Meet ALL the Following Eligibility Criteria: Have an inherited bleeding disorder, have a spouse with an inherited bleeding disorder, or be the parent/caregiver of a child with an inherited bleeding disorder; Live in the VHF coverage area (go here to learn more) and/or location of primary bleeding disorder treatment i.e. Hemophilia Treatment Center (HTC), hematologist, etc. is in the VHF coverage area.
Thank you to our current sponsors!
STAR: BioMarin, CSL Behring, Novo Nordisk, Sanofi, and Takeda
PREMIER: Genentech
CORPORATE: Accredo, Bayer, BioMatrix, Cottrill’s Pharmacy, CVS Health, DrugCo Health SP, Hoos at Home, Kedrion, Pfizer, Soleo Health, and Superior Biologics.

RICHMOND - Community Event Kickers Soccer Game
2024-08-10 18:30 - 21:00 | City Stadium, 3201 Maplewood Ave., Richmond, VA, 23221, United States
REGISTRATION IS CLOSED. To be added to the waitlist email heather@vahemophilia.org
VHF community events are social and educational gatherings that occur throughout the year. These events bring together the Virginia inherited bleeding disorders community and are an excellent opportunity for networking, support, increasing knowledge, and for fun for all ages. These programs are designed for VHF constituents (and their immediate family and/or household members only) tickets to the match will be provided and there is no fee to attend.
What to Expect: Community building with new and old friends, education, and plenty of time to enjoy the Richmond Kickers match.
Thank you to our sponsors – CSL Behring, Genentech, Sanofi, and Takeda

ROANOKE - Community Event Salem Red Soxs Game
2024-07-27 17:30 - 20:30 | Carilion Clinc Field at the Salem Memorial Ballpark, 1004 Texas Street, Salem, Virginia, 24153
VHF community events are social and educational gatherings that occur throughout the year. These events bring together the Virginia inherited bleeding disorders community and are an excellent opportunity for networking, support, increasing knowledge, and for fun for all ages. These programs are designed for VHF constituents (and their immediate family and/or household members only) dinner and tickets to the game will be provided and there is no fee to attend.
What to Expect: A private, picnic style dinner on The Patio (reserved for our group throughout the game) with an amazing field view, just feet off of the right field foul line, education, networking with new and old friends, and plenty of time to enjoy the Red Sox game.
Carilion Clinc Field at the Salem Memorial Ballpark is one of the larger ballparks in the Carolina League and has a gorgeous view of the Blue Ridge Mountains in the distance over the right field wall. This makes Salem Memorial Ballpark one of the best views in Minor League Baseball and giving you a ballgame with a view!
Thank you to our sponsors – CSL Behring, Genentech, Sanofi, and Takeda

CHARLOTTESVILLE - Camp Youngblood at Camp Holiday Trails
2024-07-14 - 2024-07-19 | Camp Holiday Trails, 400 Holiday Trails Lane, Charlottesville, VA, 22903
The Virginia Hemophilia Foundation (VHF), the Hemophilia Association of the Capital Area (HACA), and Camp Holiday Trails (CHT) are teaming up again for Camp Youngblood (CYB) in 2024!
Camp Youngblood is a week-long overnight camp at CHT for children ages 7-17 with inherited bleeding disorders, their siblings, and children of members of the inherited bleeding disorder community that reside within the VHF or HACA coverage area. Kids enjoy a week of fun and learning with others that are faced with similar challenges and life experiences. Go here to learn more about the admission guidelines.
Dates: Sunday, July 14 – Friday, July 19, 2024
NEW THIS YEAR: Friday, July 19, will be “CYB Family Friday.” Camper families are invited to join in on all the fun starting at 9 a.m. Lunch will be provided by CHT, and everyone will depart at 2 p.m. During this time, there will be a mini “family day camp” that will allow campers and their families a glimpse of Camp Magic together! VHF/HACA are looking into providing an overnight stay at a hotel close to CHT on that Thursday, July 18; in the pre-screening survey, please let us know if this would be of interest to you and we will be in touch with more details.
Location: Camp Holiday Trails, 400 Holiday Trails Ln, Charlottesville, VA 22903
Open Enrollment Application: The Camp Youngblood application process is open enrollment and not first come first served. This will allow VHF, HACA, and CHT the chance to review applications and manage the roster according to the application/admission guidelines. *Must adhere to all application deadlines to be considered*
» Go here to learn more about the admission guidelines.
» Go here to learn more about the pre-screening process and to apply

Thank you to our Camp Youngblood sponsors: Bayer, CSL Behring, CVS, Genentech, Grifols, Novo Nordisk, Sanofi, Takeda, and VCU-HTC
Thank you to our Camp Youngblood Family Education sponsors: CSL Behring, Genentech, Novo Nordisk, and Takeda

HAMPTON – Community Event at Sandy Bottom Nature Park
2024-06-29 10:00 - 12:00 | Sandy Bottom Nature Park, 1255 Big Bethel Road, Hampton, VA, 23669
VHF community events are social and educational gatherings that occur throughout the year. These events bring together the Virginia inherited bleeding disorders community and are an excellent opportunity for networking, support, increasing knowledge, and for fun for all ages. These programs are designed for VHF constituents (and their immediate family and/or household members only) lunch will be provided and there is no fee to attend.
What to Expect: A picnic style lunch, a playground for the kids, games, education, networking with new and old friends, and plenty of time to enjoy the park (we have reserved the lakeside pavillion shelter). We are also excited to have Tim G., a CSL Behring Gettin’ in the Game Athlete, join us for an informal presenation on how to stay active at every stage of life and then he will lead the group on a trail hike.
Sandy Bottom Nature Park Hampton’s premier park is a 456-acre environmental education and wildlife management facility. Born from borrow pits and garbage dumps, the park is truly a success story of reclamation of our natural resources. From the 10,000 square foot nature center overlooking Sandy Bottom Lake to the elusive creatures that inhabit the wetland marshes, there is something for everyone at Sandy Bottom Nature Park.
Thank you to our sponsors – CSL Behring, Genentech, Sanofi, and Takeda

Gettin' in the Game Junior National Championship (JNC) - Application Deadline
2024-06-23 | VA
VHF Nominee Application Deadline: 5:00 pm EST, Sunday, June 23, 2024
Gettin’ In The Game Junior National Championship (JNC)
Date: September 20 – 22, 2024
Location: Henderson, Nevada
Who is eligible: Children between 7–18 years of age with a bleeding disorder (nominees must be accompanied by a caregiver 25 years of age or older at the event. Due to state and federal laws, CSL is unable to permit healthcare professionals to attend.) Special consideration will be given to first time attendees, but all children who have attended in the past are welcome to apply again!
Cost: Free. CSL Behring will sponsor two chapter nominees and one accompanying caregiver for each nominee to participate in the program. This sponsorship will include the coordination and cost of airfare, ground transportation in Henderson, Nevada, and hotel arrangements (attendees will be responsible for transportation to/from their hometown airport). This event is limited to the nominee and one caregiver only. CSL is unable to accommodate additional family members at any JNC related events.
Program Description: Developed by CSL Behring, the Gettin’ in the Game Junior National Championship (JNC) was the first and is currently the only national sports competition designed specifically for the bleeding disorders community. The JNC features accomplished Gettin’ in the Game Athletes who themselves have been diagnosed with a bleeding disorder. Go here to learn more.
VHF (along with other chapters across the nation) have been given the opportunity to nominate up to two participants, girls and boys, each selected for either baseball, basketball, golf, or swimming. Go here to read about Matthew Lee, one of the 2023 VHF nominees, who was the national winner in swimming at the 2023 Gettin’ in the Game Junior National Championship (JNC)!
During the JNC program nominees will have the opportunity to:

Choose from FOUR sports – baseball, basketball, golf, and swimming.
Learn about the importance of physical fitness in managing a bleeding disorder and receive instructions on proper techniques and good form.
Show off their abilities in a national competition with fellow nominees from around the country.
Connect and build relationships with fellow members of the bleeding disorders community.

VHF Nominee Application Process:

Fill out the brief application form below.
The child applying will need to answer one essay question and provide a heartfelt answer to the question “Why do you love the sport you chose and/or why would you like to attend the JNC?” (Length should be age appropriate and around 1-2 paragraphs.)
Essays must be original and written solely by the child applying (please, no parental help writing the essay!)
Submit the application and essay by the deadline, 5:00 pm EST, Sunday, June 23, 2024.

For an idea of the program expectations go here to read the 2024 JNC nominee information packet.
If you have any questions please contact Kelly at info@vahemophilia.org or 804-740-8643.
