🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

The ASH Annual meeting 2023 is on! #ASH23. And it's a pool of knowledge, networking and clinical advancement for both Malignant & Non Malignant conditions!

The patient voice is at the centre of everything we do, so expects loads of #PPI discussion at our upcoming conference! Avril Daly 💚 will talk about the patient perspective in clinical trials for #raredisease REGISTER NOW: forms.gle/sozhmyvjQowL8N……

We've launched a new online survey to get your ideas for a national action plan to eliminate #cervicalcancer in Ireland. We can make cervical cancer rare and you can help make it happen. Take the survey now: tinyurl.com/cce-survey-mak… #TogetherTowardsElimination #HPVAwarenessDay

🌟 Passionate about shaping neurological research? Join us on April 13 from 11-1pm in RCSI! Meet our researchers and clinicians, dive into our cutting edge of neurological research & explore how you can get involved in some of these projects. Register at forms.office.com/e/9QAh5pew9j

📢 Save the date! The next Irish Health Research Forum is taking place on May 16th at the Ashling Hotel, Dublin. The event theme is 'Empower, Innovate, Transform: Driving the Future of Health Research'. Join our mailing list for early registration access. hrci.ie

Super excited to see this!! Thank you Diane for choosing #Sicklecell. There is nearly no research on Sickle Cell Disease in Ireland. This means alot to us!! Thank you!!! European Sickle Cell Federation ERN EuroBloodNet Sickle Cell &Tha Irl Migrant Health Alliance Ireland PPI Ignite Network Ireland

HRCI members demand a Programme for Government which prioritises health outcomes. Investing in health research is vital for societal well-being, medical advances & prosperity. Let's make this election a turning point for a fairer, healthier society! hrci.ie/hrci-manifesto…

13 years of Advocacy, education & awareness, patient & parent support, improvement in health policy for #sicklecell & much more! All without any government funding!! We are thankful for the support & donations received over the years.

🎙️ New Episode Alert: Exploring Public Involvement in Health Research! Dive into the transformative world of PPI with us. 👂👉bit.ly/CCS_63 Lora Ruth Wogu Jon Salsberg PPI Ignite UL University Of Limerick Sickle Cell &Tha Irl HealthResearchBoard ICPHR PPI Ignite Network Ireland Health Research Institute #HealthResearch #PPI

🤝 Lora Ruth Wogu shares how engaging migrant communities enhances research and healthcare outcomes. #DiversityInHealth #PatientAdvocacy 🎙️👉bit.ly/CCS_63 Lora Ruth Wogu Jon Salsberg PPI Ignite UL University Of Limerick Sickle Cell &Tha Irl HealthResearchBoard ICPHR PPI Ignite Network Ireland PPI Ignite Network Ireland PPI Ignite Network @ University of Galway

FINALLY! Some great news as the struggle to keep Voxelotor in the UK 🇬🇧 is ovee. Now, the rest of Europe waits! theguardian.com/society/articl…

Dr Avril Kennan 🌍, CEO of HRCI, opens the event by reflecting on 10 years of the Irish Health Research Forum, its impact and the many recommendations to improve health research in Ireland which have come from previous events #HealthResearchMatters

This 19th June we remain committed to changing the myths & perceptions surrounding the racial structure of #Sicklecelldisease genetic prevalence! Sickle Cell is NOT a black people's disease! Join us by sharing this message widely. Together we are Stronger!

Our Building Connections helped masters students supervisors & communities to build partnership & agree a research question of importance to the community Arrived in Ireland in last 8 years? Tell your story to address this Migrant Health Alliance Ireland question. University of Sanctuary Ireland CÚRAM Union of Students in Ireland

My hero. She held a benefit for children with #sicklecell in Las Vegas and I’ve been he fan every since. God bless you in your journey to be well 🙏🏽💪🏾🙏🏽

Improving women's healthcare and developing gender-specific interventions is a priority. Through the Women's Health Fund, we are supporting the Irish Heart Foundation Her Heart Matters campaign to highlight the risks and symptoms of heart disease and stroke experienced by women.

The Minister for Health Stephen Donnelly has announced a call for expressions of interest for membership of the National Screening Advisory Committee (NSAC). gov.ie/en/press-relea…

September is here! And the focus is on raising awareness of the importance of; blood donation, newborn screening, advancement in treatment options for Sickle Cell Disease. Join us to donate, fundraise or organize a blood drive. Contact us via; Email: [email protected]

Lora Ruth Wogu Migrant Health Alliance Ireland bring talks about the importance of build connections between all relevant community organisations interested in bringing Migrant voices to the health research table. HealthResearchBoard

Thank you @linkedin for inviting, partnering, & supporting Sickle Cell& Stanford Blood Center.ie for a talk on Sickle Cell Disease, the Importance of blood donation, the need for more blood donors . Thanks to Axelle & the Black Inclusion Group for the blood drive at IBTS offices in Dublin