Elevated #homocysteine levels: What inborn errors of metabolism might we be missing?
#rarediseaseday2023 onlinelibrary.wiley.com/doi/10.1002/aj…
Flying the UK HSP Support Group Hereditary Spastic Paraplegia flag with trustee Mike & Mitesh Patel at #RareDiseaseDay2023 Westminister Reception by Genetic Alliance UK
Highly appreciation to The Aga Khan Hospital-Dar es Salaam Branch in collaboration with HEALTH CLUSTER Lupus Warriors Tanzania Ali Kimara Rare Disease Foundation (AKRDF) for making this happen
#OxygenForAll #RareDiseaseDay2023 #SADCYouth
What better than #zebrafish to #showyourstripes on #rarediseaseday #rarediseaseday 2023. Reach out if you want to find more how we use #zebrafish #fly #organoids to model #leukodystrophy with LEUKOLABS
Dr. Jahnavi Aluri presenting our work on #TLR8GOF funded by Jeffrey Modell Foundation (JMF) at #RareDiseaseDay2023 MedGen_WashU Washington University Department of Pediatrics #primaryimmunodeficiency
I would like to take the opportunity to thank everyone who has been instrumental in #RareDiseases #education #research #Awareness over the last number of years University College Dublin UCD School of Nursing, Midwifery & Health Systems UCD Medicine #RareDiseaseDay2023
#RAINDROP #RAiN RAiN Rare Disease Clinical Trial Network, Ireland UCD Research
We are here in our nation’s capitol to be a voice for Elijah and so many others who live with #raredisease every day! Sarita Edwards Thank you for your inspirational message this morning! Let’s do this! 🙌🏻 EveryLife Foundation RDLA #RareDC23 #RareDiseaseDay2023
It's still Rare Disease Day in my house. How about you? #RareDiseaseDay 2023 #RareDiseaseDay #RareDiseases
Happy Rare Disease Day to my fellow zebras! 🦓🦓🦓 My rare disease is #MyastheniaGravis what's yours?! #NEISvoid #DisabilityTwitter #RareDiseaseDay #RareDiseaseDay 2023
As the end of #RareDiseaseDay2023 comes to an end, I am exhausted. I did not advocate as much as I should, I did not fundraise, I did not do much. Yet I am exhausted. The burden to do it all weighs me down and I just want to be a mom
Happy #RareDisease Day! Living with a rare genetic disease gives me a unique perspective while working within medical systems. It is important to advocate for patients and their families so everyone can receive equitable care. #RareDisease Day2023 #oipride
Erin Moriarty Wade myTomorrows Colin Hung Joe Babaian 🇺🇦 Stacy Hurt (she/her)🌻 Terri Ellsworth Chris Anselmo Beth Steckler (she/her) At around 8:30 tonight I will be wrestling this zebra trying to convince him that if he goes to sleep he won't miss anything and tomorrow is a whole new day. Sorry!
Boy is #RareDiseaseDay2023 being celebrated differently this yr
We’re closing out #RareDisease Day2023 from JMF HQ in NYC with a photo of the iconic Empire State Building lit up in the classic Rare Disease Day colors 💜💙💚 Thank you all for joining us in raising awareness for #RareDisease and #PrimaryImmunodeficiency today and every day 🌎✨
One day I will hear a talk delivered by my amazing colleague and friend Marcela Ferrada on Relapsing Polychondritis without crying. But that day is not today! 😭❤️ #Inspiring
#RareDiseaseDay2023
Fantastic to hear about colleagues’ research at National Horizons Centre on #RareDiseaseDay2023 and to learn about DYRK1A syndrome from Teddy’s parents, raising awareness of this condition. Thank you for organising Popplewell Research Group
So grateful to Deputy Chief Medical Officer Graham Ellis for visiting us with Genetic Alliance UK today and taking the time to hear about our work Graham Ellis Office for Rare Conditions Glasgow Glasgow Children's Hospital Charity University of Glasgow Child Health Royal Hospital for Children, Glasgow Jas Redfern Natalie Frankish #RareDiseaseDay2023
