Lora Ruth Wogu (@loraruthw) 's Twitter Profile
Lora Ruth Wogu

@loraruthw

AHP|Patient Advocate|DEI in Quality Patient care|Global,Disability & Migrant Health Advocate |passion for Sickle Cell| Special needs mom|
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ID: 1274867810

linkhttps://sicklecellireland.ie calendar_today17-03-2013 12:34:13

1,1K Tweet

545 Followers

485 Following

European Sickle Cell Federation (@escfederation) 's Twitter Profile Photo

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 ASH Annual meeting 2023 is on! #ASH23. And it's a pool of knowledge, networking and clinical advancement for both Malignant & Non Malignant conditions!
European Sickle Cell Federation (@escfederation) 's Twitter Profile Photo

Our COO Lora Ruth Wogu is present at the #ASH23 Annual meeting. Europe is eager & ready to see advancements in Sickle Cell treatment options, disease management and improving involvement in Research and clinical trials.

Our COO <a href="/LoraRuthW/">Lora Ruth Wogu</a> is present at the #ASH23 Annual meeting. 
Europe is eager &amp; ready to see advancements in Sickle Cell  treatment options, disease management and improving  involvement in Research and clinical trials.
Rare Disease Clinical Trial Network, Ireland (@rare_trial) 's Twitter Profile Photo

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……

The patient voice is at the centre of everything we do, so expects loads of #PPI discussion at our upcoming conference! <a href="/avrilbdaly/">Avril Daly 💚</a> will talk about the patient perspective in clinical trials for #raredisease

REGISTER NOW: forms.gle/sozhmyvjQowL8N……
National Screening Service (@nsshse) 's Twitter Profile Photo

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

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
FutureNeuro Centre (@futureneuro_ie) 's Twitter Profile Photo

🌟 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

🌟 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 &amp; explore how you can get involved in some of these projects.

Register at forms.office.com/e/9QAh5pew9j
Health Research Charities Ireland - HRCI (@hrcireland) 's Twitter Profile Photo

📢 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

📢 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
Health Research Charities Ireland - HRCI (@hrcireland) 's Twitter Profile Photo

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…

HRCI members demand a Programme for Government which prioritises health outcomes. Investing in health research is vital for societal well-being, medical advances &amp; prosperity. Let's make this election a turning point for a fairer, healthier society! hrci.ie/hrci-manifesto…
Sickle Cell &Tha Irl (@sctireland) 's Twitter Profile Photo

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.

13 years of Advocacy, education &amp; awareness, patient &amp; parent support, improvement in health policy for #sicklecell &amp; much more! All without any government funding!! 
We are thankful for the support &amp; donations received over the years.
European Sickle Cell Federation (@escfederation) 's Twitter Profile Photo

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…

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…
Health Research Charities Ireland - HRCI (@hrcireland) 's Twitter Profile Photo

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

Dr <a href="/AvrilKennan/">Avril Kennan 🌍</a>, 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
European Sickle Cell Federation (@escfederation) 's Twitter Profile Photo

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!

This 19th June we remain committed to changing the myths &amp; 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!
PPI Ignite Network Ireland (@ppi_ignite_net) 's Twitter Profile Photo

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

Our Building Connections helped masters students supervisors &amp; communities to build partnership &amp; agree a research question of importance to the community
 
Arrived in Ireland in last 8 years? Tell your story to address this <a href="/mhaireland/">Migrant Health Alliance Ireland</a> question. <a href="/UoSIreland/">University of Sanctuary Ireland</a> <a href="/CURAMdevices/">CÚRAM</a> <a href="/TheUSI/">Union of Students in Ireland</a>
Department of Health (@roinnslainte) 's Twitter Profile Photo

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.

Improving women's healthcare and developing gender-specific interventions is a priority. Through the Women's Health Fund, we are supporting the <a href="/Irishheart_ie/">Irish Heart Foundation</a> Her Heart Matters campaign to highlight the risks and symptoms of heart disease and stroke experienced by women.
Department of Health (@roinnslainte) 's Twitter Profile Photo

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…

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…
Sickle Cell &Tha Irl (@sctireland) 's Twitter Profile Photo

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]

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: info@sicklecellireland.ie