Hairy Cell Leukemia Foundation @HCLFoundation
Official Twitter profile for the Hairy Cell Leukemia Foundation, a nonprofit dedicated to patient education and research in HCL. https://t.co/jOwrcRSFER hairycellleukemia.org New York, NY, USA Joined July 2021-
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This #BloodCancerAwarenessMonth, join us in advocating for greater awareness of HCL. Together, we can continue saving lives and improving patients' quality of life through critical research and evidence-based patient education. 👉 hairycellleukemia.org/support-patien…
We are thrilled to partner again with Blood Cancer United (formerly LLS) on HCL2030. Together, we will support new studies in HCL and HCLv and advance our goal of improving treatment and quality of life for patients. hairycellleukemia.org/hcl2030-release
Pelle’s story shows why personalized care matters: before starting HCL treatment, doctors treated his pneumonia first—making therapy safer. Read his and other inspiring journeys: hairycellleukemia.org/stories #VoicesOfStrength #HCLF40YearsAnniversary #HairyCellLeukemia
☝️ You can still join our Women’s Group Roundtable tomorrow, September 18th, from 3:30 to 4:30 PM eastern time. Open to all women impacted by HCL everywhere! Register, there's still time! hairycellleukemia.org/calendar/2025/…
📬 Stay in the loop—sign up for the HCLF e-newsletter! ✅ Be the first to know about upcoming events, research updates, stories from patients, and important news related to Hairy Cell Leukemia. 🟢 Join our mailing list today: lp.constantcontactpages.com/sl/zXgaTYb/lin…
🟢 Bill’s journey shows treatment can be manageable—and his practical outlook offers hope to others starting theirs. Read his story plus more in our 40th Anniversary Voices of Strength Campaign: hairycellleukemia.org/stories
🟢 With the support of patients and families, the Hairy Cell Leukemia Foundation invested $1.4M+ in 2024 to drive breakthroughs toward safer, more effective HCL therapies. Meet the world-class researchers leading the way in our Annual Report: hairycellleukemia.org/2024report
🟢 TOMORROW There's still time to join us for the HCL Community Roundtable on September 11th at 4:00 PM Eastern. This is an excellent opportunity to connect with fellow members *virtually* over coffee ☕ ! Sign up: hairycellleukemia.org/calendar/2025/…
🟢 Register for our next Women's Roundtable! Join us next week on Thursday, Sept 18 from 3:30–4:30 PM ET for a supportive virtual gathering of women with Hairy Cell Leukemia. 💬 Share experiences 🤝 Connect with peers 💚 Build community Register here 👉 hairycellleukemia.org/calendar/2025/…
🟢 We’re proud to share the Hairy Cell Leukemia Foundation’s 2024 Annual Report, a comprehensive reflection of what we’ve achieved together this past year! Thank you for being an essential part of our journey. ▶️ Dive into the full report here: hairycellleukemia.org/2024report
🟢 Únase a la Mesa Redonda para la Comunidad Hispana y Latina sobre la Tricoleucemia/ Leucemia de Celulas Peludas. El Sábado, 6 de Septiembre Hora: 11:00 a. m. - 12:00 PM (hora del Este de Los Estados Unidos ) via Zoom Inscribirse: hairycellleukemia.org/calendar/2025/…
Jerry's journey is a powerful reminder that we can find strength, even when facing the tough challenges of recovering from hairy cell leukemia. Read Jerry's story and share your own: hairycellleukemia.org/stories #VoicesOfStrength #HairyCellLeukemia #40YearsStrong
You’re Not Alone. Join us on September 11 from 4–5 pm ET for an HCL Community Roundtable—a welcoming, judgment-free space for anyone impacted by Hairy Cell Leukemia (HCL) or HCL variant. Register now and be part of the conversation >> hairycellleukemia.org/calendar/2025/…
🟢 Register for our next HCL Women's Group Roundtable! Join us on September 18th from 3:30–4:30 PM ET for a Zoom-based roundtable. This meeting is for all women living with HCL. 💚 Listen, share, and be part of the conversation. 👉 Register here: hairycellleukemia.org/calendar/2025/…
💚 Support the Hairy Cell Leukemia Foundation! Your contribution funds research, education, and patient support — bringing hope where it is needed most. Together, we can overcome every challenge. 👉 Donate today: form-renderer-app.donorperfect.io/give/hclf_dona…
💚 Tania’s story highlights that living with HCL goes beyond challenges — it's also about personal growth and resilience. Read her full journey: hairycellleukemia.org/stories Got a story to share? hairycellleukemia.org/share-your-sto… #HCLF40YearsAnniversary #HairyCellLeukemia #40YearsStrong
💚 Join our no-judgment Community Roundtable on Sept 11, 4–5pm ET (1PT/3CT)! Peer support, real talk, and connection—open to all patients, families & caregivers. Register here 👉 hairycellleukemia.org/calendar/2025/…
🟢 Melanoma is a serious yet preventable skin cancer! Hairy Cell Leukemia patients may have an increased risk for melanoma. Prevention and early detection are vital. Know your skin. Protect it. 🔗 cancer.osu.edu/blog/tips-for-…
🟢 Sábado 6 de Septiembre. Únase a la Mesa Redonda para la Comunidad Hispana y Latina sobre la Tricoleucemia/ Leucemia de Celulas Peludas el Sábado, 6 de Septiembre. Hora: 11:00 a. m. - 12:00 PM (hora del Este de Los Estados Unidos) via Zoom. Inscribirse: hairycellleukemia.org/calendar/2025/…
David’s journey reminds us that while HCL can shape our path, it doesn’t define who we are. Read David’s story and explore other journeys: hairycellleukemia.org/stories Have a story to share? hairycellleukemia.org/share-your-sto… #HCLF40YearsAnniversary #HairyCellLeukemia #40YearsStrong
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