Clinical Geneticist, Southampton, Rare Disease, PTEN, PHTS.
Joined October 2012
- Tweets262
- Following972
- Followers333
- Likes520
Katherine Lachlan retweeted
📣 We have an updated SWAN UK flyer! Perhaps you're a healthcare professional that could share some to help more families find SWAN UK sooner? Let us know here or by emailing [email protected].
#undiagnosed #SyndromeWithoutAName #UndiagnosedGeneticCondition #UCD2024
Katherine Lachlan retweeted
Why raise awareness? Shedding light on rare diseases is vital. Limited healthcare knowledge leads to delayed diagnoses, while expensive treatments pose financial burdens. Advocacy can drive better resources, research, and quality of life. 💙
#RareDiseaseDay #ShareYourColours
Thank you for the positive feedback. Great colleagues multi-disciplinary working towards diagnoses for more people, more quickly, improving healthcare for children with rare conditions
@DrJNurse
@CaS_Genomics
@SWAN_UK
@M4RareDiseases
@rarediseaseday
🦓
@UHSFT
Katherine Lachlan retweeted
Come and join our small but friendly and dynamic team! We are looking for a P/T information officer to help support our Unique families. More info 👇
If you didn't read the latest @PET_BioNews you won't know @unique_charity are recruiting a part-time Information Officer to cover maternity leave of a staff member. If you have an excellent understanding of #genetics/#genomics, this could be for you! See: progress.org.uk/jobs/part-ti…
Great news! Such an important initiative. Research relies on being able to contact people with rare conditions
🎉 Exciting News! 🎉 We're overjoyed to share that we've hit a milestone: 100 amazing individuals have joined our Patient Registry for PHTS! 🌟
If you haven't signed up yet, now's your chance! Be a part of this incredible journey by registering at buff.ly/40w0How 📋💙
Well I will give this a listen. Not everyday occurrence to get a mention in such company!
To hear some original #poetry about life with a #raregenetic condition written by parents as part of the #Eppigen project funded by @wellcometrust tune in to #westwiltsradio on Sun 25th at 3pm. @KLachlan @PhilandraC @SWAN_UK @CaS_Genomics @MichaelRosenYes @michaelsheen
Katherine Lachlan retweeted
We love this photo and hope you all had a great day, thank you for supporting our hospices. ♥
We did it!! Well done everyone!
justgiving.com/fundraising/L…
This Post is from an account that no longer exists. Learn more
Katherine Lachlan retweeted
PHTS can cause autism, developmental delays, and cancer predisposition. Families need care coordination and psychological support.
justgiving.com/fundraising/k…
If you haven’t sponsored me yet, could you spare just a few ££££?
And if you have, can you share this with anyone else who might sponsor me too?
Thank you again everyone for your kind words, sponsorship & support. I’ll be thinking about you on Sunday justgiving.com/fundraising/k…
PHTS can cause autism, developmental delays, and cancer predisposition. Families need care coordination and psychological support.
justgiving.com/fundraising/k…
5 days to go to half marathon! Thanks to all my supporters for believing in me and helping SMASH the fundraising goal #howhighcanwego
@PTENUKI #raredisease #PTEN #PHTS
#LLHM2023 #sundayrunday
justgiving.com/fundraising/k…
Only 9 days to go!
I'm fundraising for PTEN UK and Ireland Patient Group. Check out my @JustGiving page and please donate if you can. Thank you! #JustGiving justgiving.com/fundraising/k…
Based on the audience demographic tonight, it appears this is not of interest to 50% of the population
Katherine Lachlan retweeted
This #RareDiseaseDay we are keen to raise awareness about the conditions which can result from changes in the #PTEN gene.
Hear from our Medical Advisor Dr Katherine Lachlan talk about the conditions
#ptenawareness #PTEN #Cowdens #CareForRare #RareDiseaseDay2023 #RareDiseaseDay