Register now for our upcoming webinar with Dr. Allison Lindauer, assistant professor and gerontological nurse practitioner at Oregon Health Science University on Wednesday, September 25th! ucsf.zoom.us/webinar/regist…
Watch our webinar for practical guidance on #CADASIL, covering genetic counseling, the testing process, and the implications of results. We discuss preparation, risks and benefits, insurance, family planning, and communication with family members.
youtu.be/AuDmDdn1Nw4
Please join us July 29 (5pm PST, 6pm MST, 7pm CST, 8pm EST) for a webinar on the controversies in #CADASIL led by University of San Francisco Principal Investigator, Michael Geschwind. Register using this link: ucsf.zoom.us/webinar/regist…
Join us for an upcoming #webinar, hosted by our central team on Wednesday June 26th, where some of our coordinators will discuss study updates and have a discussion with the #CADASIL community. Use this link to sign up: ucsf.zoom.us/webinar/regist…
Join us for an open discussion of resources for those affected by #CADASIL following CureCADASIL's morning session. Register for the United Leukodystrophy Foundation Family Conference ulf.org/news/conferenc… (Adult tickets: $50, Children: $30; cost covers entire ULF conference).
Please join the #CADASIL Consortium for our webinar, The Genetics of CADASIL, where University of Washington Principal Investigator, Dr. Suman Jayadev, will be discussing the varying factors implicated in the genetics of CADASIL. Thank you for registering!
ucsf.zoom.us/webinar/regist…
#CADASIL is heritable, but is not always passed on; the CADASIL consortium is recruiting familial controls in a national study to better understand this genetic disorder. See our link for more details: cadasil-consortium.org
Is your loved one living with #CADASIL? The CADASIL Consortium’s national study is currently looking for family members of persons with CADASIL as controls for our study. See more details at cadasil-consortium.org
We are actively enrolling family members of persons with #CADASIL as controls for our study.
Please see the link below for more information:
cadasil-consortium.org
Join us for an upcoming webinar with Dr. Stephen Salloway discussing the #CADASIL Consortium Study featuring a panel of participants on 10/17 5pm PT/7pm CT/8pm ET. Please use this link to register; ucsf.zoom.us/j/95589487353?…
If you missed Dr. Biller's #CADASIL webinar hosted by CureCADASIL, we are happy to provide a link to the recording for all those interested in viewing! Click here for more information; register.gotowebinar.com/recording/1679…
Up to 5 in 100,000 people in the United States are living with #CADASIL, but many live undiagnosed. The CADASIL consortium is seeking participants who have a family history of #CADASIL, but have not been tested for the disease themselves. See our website for more
details.
11K Followers 12K Followingthe website is for donations to CADASIL research
a cure is very close
please help Dr Fanny Elahi in any amount🇨🇦
we need to do this now
thanks🇲🇽
1K Followers 768 FollowingArtist/writer/music/dj. Run @Broken20_label & logicofthesignifier & No Roof Only Sky. Favourite Basic Channel is still Quadrant Dub. Usually in a huff. He/him.
4 Followers 156 FollowingMidwesterner living and working in Georgia. Photography and Fitness nut into cycling, hiking and traveling all around to experience art, culture, and people
183 Followers 216 FollowingWorking to increase awareness of #CADASIL, share resources and news, and secure funding for the advancement of therapies, treatments, and ultimately a cure.
208 Followers 584 FollowingShe/Her Certified Hospice and Palliative Nurse. HRB-TMRN PhD Scholar at the University of Limerick. All opinions are my own.
849 Followers 933 FollowingVascular Neurologist - Neurointensivist. The University of Oklahoma HSC 🧠 Soccer Fan ⚽️ Short Film producer 🎥 All you need 🇪🇨
457 Followers 91 FollowingcureCADASIL is a non-profit organization committed to curing #CADASIL and improving the quality of life for those affected by this genetic disease.
183 Followers 216 FollowingWorking to increase awareness of #CADASIL, share resources and news, and secure funding for the advancement of therapies, treatments, and ultimately a cure.
11 Followers 98 FollowingLa Papillon CADASIL Foundation, Inc. is a registered 501(c)(3) nonprofit organization that was founded by Renee Marie La Fleur, to help patients of CADASIL.
98K Followers 1K FollowingNeurology is the most widely read and highly cited peer-reviewed neurology journal. It is the medical journal for the American Academy of Neurology.
1K Followers 408 FollowingThe Department of Neurology at the University of Utah is committed to the conquest of neurological disease through patient care, research, and education.
165 Followers 97 FollowingCADASIL Support UK is a Registered Charity established in Nov 2017 . Our aim is to raise awareness & provide a network of support for patients, family & carers.
50K Followers 2K FollowingMaking health about people: When we ask how you’re doing, we actually want to know! Download our free app to join a community that gets it ✨
3K Followers 21 FollowingWorking toward treatments and a cure for Krabbe & Leukodystrophies, advocating for newborn screening and supporting those affected by these diseases.
21K Followers 2K FollowingNational campaign run by @GeneticAll_UK to improve the lives of those affected by rare conditions and all who support them.
#RareDisease.
42K Followers 3K Following29 February 2024 is Rare Disease Day. Raising awareness for patients, families and carers around the world that are affected by rare diseases. #RareDiseaseDay
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NIH...Turning Discovery Into Health®.
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6K Followers 1K FollowingThe Huntington’s Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease.
457 Followers 91 FollowingcureCADASIL is a non-profit organization committed to curing #CADASIL and improving the quality of life for those affected by this genetic disease.
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