Community is about support. Natural disasters are currently creating challenges to care, access, and overall health for many affected by rare and inheritable bleeding disorders. If you are amongst those currently seeking help, please connect with the National Bleeding Disorders Foundation, the Hemophilia Federation of America and/or Hope for Hemophilia for guidance and support. You are not alone. #hemophilia #bleedingdisorders #rarediseases #chronicdiseases #community #healthcare #publichealth #naturaldisasters #disasterrelief
BloodStream Media
Media Production
Los Angeles, CA 545 followers
Bringing education and inspiration to those living with rare and chronic diseases. 🩸
About us
BloodStream Media is a rare and chronic disease podcast network bringing education, inspiration, and community-building to the fastest growing media format in the world. BloodStream podcasts are produced by Believe Limited’s team of award-winning writers, best-in-class producers, and empathetic advocates. Subscribe to BloodStream Media podcasts on Apple Podcasts, Spotify, Downstream, Stitcher, Overcast or your preferred podcast player, and engage with BloodStream Media on Twitter, Facebook and Instagram, where we regularly post content from and about our shows.
- Website
-
www.bloodstreammedia.com
External link for BloodStream Media
- Industry
- Media Production
- Company size
- 11-50 employees
- Headquarters
- Los Angeles, CA
Updates
-
Alternative Funding Programs are a nightmare new insurance tactic that has experts concerned. We’ve got Zack Duffy and Roland Lamy from Hemophilia Alliance to break it down and tell you what to look out for. Plus, the Hemophilia Federation of America's Project ECHO and the latest Gene Therapy segment, all about Myths and Misconceptions (like we have any of those. Spoiler alert: WE DO)! Listen, Rate, Review, and Subscribe where you get your podcasts! https://lnkd.in/eQKP4F9f Presenting Sponsor: #Takeda, visit bleedingdisorders.com to learn more. It’s a Whole New World brought to you by CSL #hemophilia #vwd #bleedingdisorders #raredisease #chronicdisease #haemophilia #hemofilia #sicklecell #podcast #digitalhealth #genetherapy #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare
-
Breaking taboos and guessing how many menstrual products fit in a bag - it’s time for this month’s FLOW (straight talk about extreme periods)! In this live episode from the Hemophilia Foundation of Michigan’s Conference for Women and Teens, hosts Jessica Richmond and Sarah Watson, LPC, CST, Sex Educator, Speaker create an open dialogue about menstruation, aiming to normalize the conversation and encourage self-advocacy. The episode passionately encourages advocacy, community support, and broader education on menstrual health. Available now: https://lnkd.in/gREHM97T Presenting Sponsor: #Takeda, visit bleedingdisorders.com to learn more.
-
No joke, Alternative Funding Programs are the new dangerous insurance tactic that has experts concerned. We’ve got Zack Duffy and Roland Lamy from Hemophilia Alliance to break it down and tell you what to look out for only on tomorrow's BloodStream. Listen, Rate, Review, and Subscribe where you get your podcasts! https://lnkd.in/eQKP4F9f Presenting Sponsor: #Takeda, visit bleedingdisorders.com to learn more. It’s a Whole New World brought to you by CSL #hemophilia #vwd #bleedingdisorders #raredisease #chronicdisease #haemophilia #hemofilia #sicklecell #podcast #digitalhealth #genetherapy #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare
-
Dr. Julia Xu discusses their role in both clinical and research settings, focusing on young adults transitioning from pediatric to adult sickle cell programs. She emphasizes the challenges these patients face as their disease changes and the importance of educating them about new treatment options. Listen, rate, review, and subscribe: https://lnkd.in/dsk6QgEP Cheat Codes is a podcast for the sickle cell community that brings listeners a series of segments and interviews packed with critical education that patients and families need to know, as well as updates and clarifications from the social media "buzz" around sickle cell. Hosted by Ahmar U. Zaidi, MD (Dr. Z) & Michael Callaghan, MD (Dr. C). Cheat Codes is sponsored by Agios Pharmaceuticals Visit Agios.com to learn more. This podcast is not intended as medical advice. Please consult your healthcare team with any treatment related questions. #RedBloodCellDisorder #HereditaryDisease
-
En 2014, Merlina llegó de Venezuela y se estableció en Dallas, TX, junto a su familia. En el 2019 su hija Rosanna fue diagnosticada con SYNGAP1 a la temprana edad de 4 años, tras haber sido erróneamente diagnosticada con retraso global del desarrollo e hipomielinización. Merlina comparte con nosotros su proceso de aceptación de este diagnóstico, cómo la motivó a profundizar su comprensión de esta enfermedad y cómo se ha convertido en una líder en la comunidad hispana de SYNGAP1. Escucha y suscríbete!🎧 https://lnkd.in/gHWyMisv Deborah Requesens | Victoria Arteaga #másqueraras #español #spanish #salud #enfermagem #desarrollodefármacos #hemofilia #podcast
-
📢 Big news! Jessica Richmond and Sarah Watson, LPC, CST, Sex Educator, Speaker will be co-hosting a live recording of The FLOW Podcast at this weekend’s National Conference with Women and Teens with Hemophilia with the Hemophilia Foundation of Michigan! 🎉 They're bringing challenges, giveaways, and so much more this weekend, so register today! https://lnkd.in/gWPyKziB #LiveRecording #FLOWingTogether #HowsYourFlow #BleedingDisorders #WomenWithHemophilia #HemophiliaCommunity #GirlsBleedToo
-
Guest host Michael Bishop shares his experience on the latest I'm Fine segment. Available now on BloodStream! Listen, Rate, Review, and Subscribe where you get your podcasts! https://lnkd.in/eQKP4F9f Presenting Sponsor: #Takeda, visit bleedingdisorders.com to learn more. I’m Fine is presented by Sanofi #hemophilia #vwd #bleedingdisorders #raredisease #chronicdisease #haemophilia #hemofilia #sicklecell #podcast #digitalhealth #genetherapy #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare #bloodstreammedia #hemophiliacommunity #hemophiliaA #hemophiliaB #healthcare
-
Voices For Policy Change is headed to the Chapter Leadership Seminar! 🎉 Can’t wait to see you at CLS! Join us for impactful sessions and networking opportunities. National Bleeding Disorders Foundation #VoicesForPolicyChange #bleedingdisorders #policychange #NBDF #patientadvocacy #health