5K for FOXP1 Syndrome Awareness
- Date Fri 15th August 2025 - Sun 17th August 2025
- Location Virtual Event
- Price $38.10
- Races 1 race
- Distances 5km
Event summary
Get ready for an inspiring and uplifting experience at the 4th Annual 5K for FOXP1 Syndrome Awareness, taking place from August 15th to August 17th, 2025, in the vibrant city of New York! This exciting event invites participants from all corners of the globe to come together to raise awareness and support critical research for FOXP1 Syndrome, a rare neurodevelopmental disorder. Whether you choose to run, walk, or roll, this inclusive event allows you to participate at your own pace, making it perfect for everyone—friends, family, and coworkers are all encouraged to join in the fun!
By taking part in this meaningful event, you’ll not only celebrate the achievements of those affected by FOXP1 Syndrome but also educate your community about this important cause. The funds raised will help empower families and individuals facing the challenges of this genetic disorder, fostering hope and promoting future research. Mark your calendars and get ready to make a difference while enjoying a fantastic weekend filled with camaraderie, support, and awareness!
By taking part in this meaningful event, you’ll not only celebrate the achievements of those affected by FOXP1 Syndrome but also educate your community about this important cause. The funds raised will help empower families and individuals facing the challenges of this genetic disorder, fostering hope and promoting future research. Mark your calendars and get ready to make a difference while enjoying a fantastic weekend filled with camaraderie, support, and awareness!
Organiser's Description
WERE BACK! JOIN US FOR THE 4TH ANNUAL 5K FOR FOXP1 SYNDROME AWARENESS
_HOSTED BY THE INTERNATIONAL FOXP1 FOUNDATION_
We're thrilled to launch the fourth annual 5K for FOXP1 Syndrome Awareness, bringing together participants from around the world to raise awareness and fund critical research into FOXP1 Syndrome.
WHAT IS FOXP1 SYNDROME?
FOXP1 Syndrome is a rare neurodevelopmental disorder caused by a mutation or change in the FOXP1 gene, located on chromosome 3. This gene plays a key role in the development and function of the nervous system and other body systems by regulating the activity of other genes. When FOXP1 doesnt function as it should, it can lead to a broad range of developmental challenges and medical needs.
ABOUT US
The International FOXP1 Foundation is a nonprofit organization. The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome, a rare genetic disorder characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment and behavior abnormalities, by sharing knowledge, inspiring hope, encouraging research, and raising awareness.
_Let us come together to raise awareness for our loved ones with FOXP1 Syndrome. This is a time for us to celebrate their successes and the joys that they bring to our lives, while also teaching our communities about FOXP1 Syndrome. _
THANK YOU FOR YOUR SUPPORT! WE CANNOT WAIT TO RUN/WALK/ROLL WITH YOU AND RAISE AWARENESS OF FOXP1 SYNDROME!
FEMALE SIGN HOW TO PARTICIPATE:
You can take part in this event from any locationwhether you run, walk, roll, or use a treadmill, go at your own pace!
Join the fun by signing up as an individual, starting a team, joining one, or simply by making a donation.
Everyone is welcome to get involvedinvite your friends, family, coworkers, and supporters to participate together!
_HOSTED BY THE INTERNATIONAL FOXP1 FOUNDATION_
We're thrilled to launch the fourth annual 5K for FOXP1 Syndrome Awareness, bringing together participants from around the world to raise awareness and fund critical research into FOXP1 Syndrome.
WHAT IS FOXP1 SYNDROME?
FOXP1 Syndrome is a rare neurodevelopmental disorder caused by a mutation or change in the FOXP1 gene, located on chromosome 3. This gene plays a key role in the development and function of the nervous system and other body systems by regulating the activity of other genes. When FOXP1 doesnt function as it should, it can lead to a broad range of developmental challenges and medical needs.
ABOUT US
The International FOXP1 Foundation is a nonprofit organization. The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome, a rare genetic disorder characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment and behavior abnormalities, by sharing knowledge, inspiring hope, encouraging research, and raising awareness.
_Let us come together to raise awareness for our loved ones with FOXP1 Syndrome. This is a time for us to celebrate their successes and the joys that they bring to our lives, while also teaching our communities about FOXP1 Syndrome. _
THANK YOU FOR YOUR SUPPORT! WE CANNOT WAIT TO RUN/WALK/ROLL WITH YOU AND RAISE AWARENESS OF FOXP1 SYNDROME!
FEMALE SIGN HOW TO PARTICIPATE:
You can take part in this event from any locationwhether you run, walk, roll, or use a treadmill, go at your own pace!
Join the fun by signing up as an individual, starting a team, joining one, or simply by making a donation.
Everyone is welcome to get involvedinvite your friends, family, coworkers, and supporters to participate together!
Races
-
5K for FOXP1 Syndrome Awareness
Incl. $3.10 Fee
$38.10
The 5K for FOXP1 Syndrome Awareness lets you run or walk from anywhere in the world. If you cant attend or host a local event, registering for the virtual race is a great way to show your support and help fund critical FOXP1 research.
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