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If you have ongoing, recurrent or long-term symptoms after COVID-19, can you help our Long COVID study by describing various symptoms? Share your experience of post-exercise malaise, brain fog, fatigue... in words, drawings, however you want.
Thank you!
https://www.voice-global.org/public/challenges/defining-long-covid-symptoms/

1/3 Something for the weekend👓📖☀️

Genetic architectures of proximal and distal colorectal cancer are partly distinct

Recent @Gut_BMJ 📰co-authored by our PI @DrAmandaJCross @ImperialSandC @ImperialMed @imperialcollege

https://gut.bmj.com/content/70/7/1325

#colorectalcancer
#bowelcancer

Published today.

NBOCA short report on Early Onset Colorectal Cancer (EOCRC) - bowel cancer diagnosed in patients aged under 50.

👇👇
https://www.nboca.org.uk/reports/short-report-1-2021/

@cam_colorectal @ACPGBI @ACPGBI_PLG @BCI_UK @BowelResearch @asgbi @Mikebraun1Braun @HQIP @SarahHQIP @RCSnews

UK National Screening Committee #UKNSC Consultation on the permanent discontinuation of Bowelscope in the English Bowel Screening Programme https://bit.ly/3x0xzpy
Read our earlier commentary 👉 https://twitter.com/CSPRG_Imperial/status/1350182599092793344?s=20
Find out about UKFSST results🔍📖

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Public involvement

We believe that public and patient involvement (PPI) in the design and conduct of trials and studies improves the quality of the research that we undertake. The value of the patient perspective and experience is integral to any research activity that affects patients. PPI gives the patients and members of the public the opportunity to have their say in the way our studies are conducted and help suggest important changes to benefit future and on-going research.

There are lots of ways you can get involved in our research, including joining one of our trial steering groups as a patient representative, joining in discussions on new research ideas, helping design study questionnaires and reviewing patient information sheets.

We are interested in hearing from you, whether you are a patient affected by bowel cancer, or are caring for someone with bowel cancer. If you have any suggestions or comments, or want to be a patient representative for our research please contact us.

For researchers

Data used in CSPRG research was collected subject to the informed consent of the participants and / or under section 251 support. Access to the individual level anonymised data will only be granted in line with the relevant informed consent form or section 251 support, subject to approval by the appropriate research ethics committee, Health Research Authority (HRA) and HRA Confidentiality Advisory Group (HRA-CAG) as required, under a formal data sharing agreement.

To discuss a request for data please contact the CSPRG by completing the contact form with the following information: the proposed study objectives, the data you require and timelines for completion of the research.