Sophie Rees

@sophierees.bsky.social

Research Fellow at University of Bristol. Researches vulval disorders and women's health. Also qualitative research in randomised controlled trials at Bristol Trials Centre.

I was a researcher on AFRI-c, conducting the process evaluation (paper here: lnkd.in/deFSQCeT). It was a large cluster randomised controlled trial that took three years to complete. Using air filters in care homes did not reduce respiratory infections in residents.

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lnkd.in

Centre for Academic Primary Care (CAPC), Bristol@capcbristol.bsky.social · 2mo ago

Portable HEPA filters made no difference to rates of respiratory and other infections in older people’s care homes, finds new @nihr.bsky.social funded research published in @jamainternalmed.com. Care homes should continue with standard infection control, including vaccines. 👉 tinyurl.com/bdhe42bn

The LS Guide is here! Please take a look to learn more about LS, and share with others. This is an under-recognised, but not uncommon, condition which can have a huge impact especially if not diagnosed and treated properly. Lots of information and advice for patients and health professionals alike!

LS Guide@lsguide.bsky.social · 2y ago

The Lichen Sclerosus Guide is now LIVE! Empowering everyone with vulval lichen sclerosus (LS) to learn about the condition, access the right treatment and live more comfortably. If you’ve got vulval LS, or you’re supporting someone who has, we’ve created this guide to help you.

The Lichen Sclerosus Guide is now LIVE! Empowering everyone with vulval lichen sclerosus (LS) to learn about the condition, access the right treatment and live more comfortably. If you’ve got vulval LS, or you’re supporting someone who has, we’ve created this guide to help you.

SNEAK PEEK! We are so excited to launch in just 2 days' time on 17th January, World LS Awareness Day. LS Guide will be a brand new resource about vulval lichen sclerosus, providing information to empower everyone to learn about the condition, access the right treatment, and live more comfortably.

Our paper about the lived experience of shingles is out. We found that for some people, linking it with 'low mood' or poor mental health was stigmatising, and resulted in shame and self-blame. Generally people don't know how debilitating shingles can be until they experience it.

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