Nurse Practitioner Natasha Weems Talks Dravet Syndrome, Epilepsy, and Caregiving with Jenece Bond and Neurologist Dr. Holder episode artwork

EPISODE · Feb 6, 2025 · 12 MIN

Nurse Practitioner Natasha Weems Talks Dravet Syndrome, Epilepsy, and Caregiving with Jenece Bond and Neurologist Dr. Holder

from Unboxed and Fearless Podcast with Dr. Natasha Weems, DNP-BC · host Dr. Natasha Weems

In this episode of Unboxed & Fearless with Dr. Natasha Weems, DNP-BC, we bring attention to Dravet Syndrome, epilepsy awareness, and the vital role of caregivers. During Tay’s Play Day, Neurologist Dr. Holder highlighted that over 600 genes are linked to epilepsy, emphasizing the importance of specialized treatment and expert care. Jenece Bond, founder of the Taylen Lauren Horton Foundation, shared her mission to support caregivers and families navigating Dravet Syndrome and special needs challenges. A special acknowledgment to event coordinator Ebony Edwards, whose dedication made this impactful event possible. Caregivers play an essential role in supporting their loved ones, often sacrificing their own needs to provide care. Their resilience and dedication deserve recognition, and community support can make a significant difference in their journey. Listen to the full conversation and be part of the movement advocating for awareness, better resources, and stronger community support. Listen and Subscribe: Deezer: Listen Here Spotify: Listen Here Apple Podcasts: Listen Here Pandora: Listen Here iHeartRadio: Listen Here Amazon Music: Listen Here Order My Book, The Unbreakable Woman: 📕 Amazon Resources for Caregivers: For those caring for loved ones with Dravet Syndrome, epilepsy, or special needs, the following organizations offer support, guidance, and resources: • Inland Regional Center – Provides services and support for individuals with developmental disabilities in Southern California. Website: inlandrc.org • Easter Seals – Offers disability and caregiving resources, therapy, and support for individuals and families. Website: easterseals.com • Taylen Lauren Horton Foundation – Advocacy and support for families navigating Dravet Syndrome and epilepsy. Website: taylenlaurenhortonfoundation.org • The Epilepsy Foundation – Comprehensive resources, advocacy, and research for those affected by epilepsy. Website: epilepsy.com Caregiver Resources:Email: [email protected] Website: www.thepearlhealthfoundation.com Advocacy and awareness are critical in ensuring better care and resources for those affected. Support caregivers, educate communities, and take action toward meaningful change. Follow Dr. Natasha Weems: Instagram: @drnatasha_ Podcast: @unboxedandfearlesspodcast Website: drnatashathenp.com #UnboxedAndFearless #DrNatashaWeems #DravetSyndrome #EpilepsyAwareness #CaregiverSupport #Neurology #MentalHealthMatters #SpecialNeedsFamilies #PodcastLife #AdvocateForYourself #Philanthropy #InlandRegionalCenter #EasterSeals #TaylenLaurenHortonFoundation #EpilepsyFoundation #Empowerment #MakingAnImpact

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Nurse Practitioner Natasha Weems Talks Dravet Syndrome, Epilepsy, and Caregiving with Jenece Bond and Neurologist Dr. Holder

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This episode was published on February 6, 2025.

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