delia hollingworth
@dee_laah
delayed teenager! Living with Lynch Syndrome and trying to raise awareness of a rare disease that's not really that rare just unknown by to many!
ID:201002005
10-10-2010 20:52:02
5,1K Tweets
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Thanks to Julian G Barwell Vaila Morrison jo balfour
and Helen Bufton for a great session yesterday on:
- Cambridge Rare Disease Network (CamRARE) patient passport
- Lynch Syndrome UK patient passport and co-produced Lynch Syndrome patient app ๐ฑ
Watch here: youtube.com/watch?v=W3qVPYโฆ
Less than 4 weeks to go until #BSGLIVE24 kicks off in Birmingham on 17th - 20th June! ๐คฉ Check out the full agenda online and plan your schedule for this year's 4-day conference. If you haven't already, register today to join us next month! ๐ live.bsg.org.uk/register/
Very excited to represent The University of Edinburgh and The Centre for Reproductive Health today in the SULSA Post Doctoral Prize. The competition is stiff, against some incredible scientists, which show cases the health of research in Scotland. Wish me luck
InSiGHT have organised a free online meeting specifically for patients with hereditary colorectal cancer, Lynch syndrome or polyposis on June 18th at 6pm (Irish time) as part of their scientific conference in Barcelona in June this year. Register here ๐ register.gotowebinar.com/register/67309โฆ
Privilege to collaborate with this amazing ladies! Well done to Lauramonje ๐ for her new position!
Our presentations at Oncology Professional Care conference today went very well! Thank you to everyone I presented with and everyone who came to see us. I've never spoken at an in-person conference before... 1/2 #OCP24 Bowel Research UK Lauramonje ๐
Check out our new article in collab. with Tom van Wezel's group.
>Evidence linking germline NPAT mutations with colorectal cancer predisposition
>NPAT deficiency might lead to high chromosomal instability in tumors
IDIBELL, LUMC Leiden
European Journal of Human Genetics
rdcu.be/dIMv7
๐จ EHTG-N Nursing Group & Conference ๐จ
We're excited to announce the new EHTG-N nursing group and the upcoming EHTG 2024 Conference! EHTGtweets
I am honoured to have been elected to the EHTG board as the first nurse representative. Our dedicated organising committee,
Do you have Lynch Syndrome or a Rare Condition?
Join us this Wednesday at 12pm to find out about:
- Cambridge Rare Disease Network (CamRARE) patient passport
- Lynch Syndrome UK patient passport
- LS patient app developed at Leicester's Hospitals
Register your FREE place: events.eahsn.org/GenomicsBITEInโฆ
๐จ Next session!
2๏ธโฃ 'Patient Stories' โ Hear firsthand accounts from patients from LynchSyndrome_Polyposis@StMarks's 'Polyposis and Lynch enrichment team'. They'll share their journeys, with live visual minutes by an artist! St Mark's Hospital Foundation Kevin Monahan Victoria Cuthill MSc RN ๐ Claire Taylor
Excited to announce I'll be presenting at the Oncology Professional Care conference Oncology Professional Care with Sam Sam Alexandra Rose:
๐ ExCeL: This Wednesday, 22nd May
Join us for our two sessions:
1๏ธโฃ 'Why and How of PPI'
2๏ธโฃ 'Patient Stories' โ With visual minutes!
#PPI #CancerAwareness
Weโre hoping to enrich the evidence for testing all with our Bowel Cancer UK funded project sequencing germline of all GI cancer patients before treatment using ultra rapid Oxford Nanopore adaptive sequencing of 187 genes associated with hereditary cancer
bowelcanceruk.org.uk/research/our-rโฆ
Group project complete โ
at #IBTN2024
Congrats T-CELLS team!!! ๐ Noemie Tremblay Tamanna Islam Jordan Pumphrey (she/her) sarah chehayeb ะถะธัััะบ Dr. Nicole Alberts , Meike, and Susan
Just done my bit for science by having my blood taken for WGS for Our Future Health - also found out alarmingly my triglycerides are 4.15 so Iโll have to start laying off the cheese! Curse middle age!
