King Charles was cheating on Harrys mum when they got married. His uncle paid off a young woman £12m for a sex scandal to go away. He met up with Epstein ‘after’ he was found guilty of prostituting minors. The Queen publicly supported him. Harry moves to protect his wife….
STARTING SOON! Join the GBT-sponsored symposium ‘Shifting from an acute to a long‑term focus in SCD: early intervention and holistic care’ today at 13:00 CET, to discuss the importance of early intervention and comprehensive care in #sicklecell disease @GBT_news #ascatconference
Join us at the GBT-sponsored symposium ‘Shifting from an acute to a long‑term focus in SCD: early intervention and holistic care’ with Prof. Paul Telfer, Dr Ferras Alashkar and Dr Valentine Brousse, on Wednesday 26 January, 13:00–14:00 CET @GBT_news #ascatconference#sicklecell
I’ll never forget taking an iPad to the bedside of a young mother in intensive care. On the FaceTime call were her three young children, all shouting 'mummy, mummy, wake up, you’ve been asleep too long'.
At the same time, Downing Street held parties. It is unforgiveable.
Do you often feel you’re the only one struggling with depression? You’re not alone. The first step to #BreakingDepression is finding strength to start a conversation. Read below to learn more 👇#TimeToTalk
Do you have a loved one who lives with depression? If you need additional support you can find resources on the @EUFAMI website. Learn how to start one conversation about depression: https://t.co/DvUJaiy9wT #BreakingDepression#EndtheStigma
#PrimaryImmunodeficiency causes frequent infections that may be difficult to cure. Rieke explains some of the challenges of #LivingWithPI but how with the right support she's found her power again. Learn more at https://t.co/WjGReMNIqq #WorldPIWeek https://t.co/L7WQcYlkxo
Being diagnosed can be a turning point for people with #PrimaryImmunodeficiency and better awareness of the condition could help patients like Gary be diagnosed sooner. Hear more about what life is like #LivingWithPI here: https://t.co/5TzwX35bFP @WorldPIWeek#MyPIStory
COVID-19 has brought disruptions to all of us, but even more so for people living with #PrimaryImmunodeficiency. We're committed to helping people #LivingWithPI and their families by raising awareness and investing in research. Visit https://t.co/WjGReMNIqq to learn more!
We are excited to be supporting #WorldPIWeek again! This year @ipopi_info is focusing on the importance of protecting people #LivingWithPI and we are proud to be standing in solidarity with them. Visit https://t.co/WjGReMNIqq for more information! #MyPIstory
This #WorldPIWeek, our #PrimaryImmunodeficiency (PI) ambassadors have created moving artworks representing their individual journeys #LivingWithPI. To hear more stories from the ambassadors and to help us raise awareness watch https://t.co/WszSoIQnqq #MyPIStory
The #primaryimmunodeficiency community consists of patients, caregivers, researchers and healthcare professionals. They strive to spread awareness and support one another. Please share to show your support for them too! @WorldPIWeek#LivingWithPI
#Primaryimmunodeficiency affects everyone differently. #WorldPIWeek aims to raise awareness of PI and the importance of the right support for people #LivingWithPI. To learn more and see how you can help, visit https://t.co/rj6LSv9TqU @WorldPIWeek
For Ian, having his family around him to understand and support him was really important. Please share this video to raise awareness and support for people #LivingWithPI. #WorldPIWeek@WorldPIWeek https://t.co/iAI2ziNOBM
Moments of uncertainty like moving home, moving school or changing doctors can be a challenge for people with #primaryimmunodeficiency. Listen to Jennifer's story to find out more #LivingWithPI#WorldPIWeek
https://t.co/CE4azq7v5M
Bibian is lucky to have a really supportive group of friends, see her full story about #LivingWithPI here https://t.co/fNW9vHQpxO #WorldPIWeek@WorldPIWeek