
LGD Alliance Europe
@lgda_eu
The LGD Alliance Europe is dedicated to patient support, advocacy and research to find treatments and cures for lymphangiomatosis and Gorham's disease.
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http://www.lgda.eu 01-03-2016 10:09:53
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Come, ask questions, and share your experiences! Join us for our DISH monthly support group on Saturday, May 14 at 10:00 am ET. Open to our global CLA community of both patients and parents. facebook.com/events/s/dish-… LGD Alliance Europe #rarediseases #supportgroups



Worldwide LGD Awareness Day in on May 26. Join us in sharing our CLA story. Share your stories using #lgdawareness. lgdalliance.org/legacies-2/jan… #LGDAwareness LGD Alliance Europe #rarediseases



Share your experiences finding medical care for vascular anomalies in a study being conducted by Bryan Sisk and Anna Kerr Must be over 18 years of age or older. Open to US and non-US participants. kerrcommlab.wixsite.com/vacomsurvey LGD Alliance Europe #rarediseases #WUSTL


Special Topic Support Group May 28 at 11:00 am Eastern Time Sponsored by the Young Adults and Millennial Support Groups. This special support session is dedicated to family planning and reproductive health. Register Today! us06web.zoom.us/meeting/regist… LGD Alliance Europe #rarediseases



Share your experiences finding medical care for vascular anomalies in a study being conducted by Bryan Sisk, MD and Anna Kerr, PhD. Must be over 18 years of age or older. Open to US and non-US participants. Questions – Contact (link kerrcommlab.wixsite.com/vacomsurvey) LGD Alliance Europe



The Orphan Disease Center’s MDBR Young Investigator grant is a $25,000 award that supports early career researchers pursuing research ideas related to lymphatic anomalies. orphandiseasecenter.submittable.com/submit/223019/… #MDBR2022 #UPENN #research #rarediseases LGD Alliance Europe


EXTRA! EXTRA! READ ALL ABOUT IT! May 26 is Awareness Day and LAUNCH DAY for special initiatives that honor our origins and patient community! LGD Alliance Europe



Bikers Wanted! Plan on attending UPenn’s 2022 Million Dollar Bike Ride on June 11th. Don’t forget to register at milliondollarbikeride.org/registration/#… Can’t attend in person, there is a virtual spin class on June 6th at 7:00 pm. LGD Alliance Europe #MBDR2022


Dr. Michael Dellinger to present "New Diagnostic Tools and Treatment for Central Lymphatic Abnormalities". A webinar series on complex lymphatic anomalies. Watch the recorded webinar. (link to youtube.com/watch?v=1ZCx8U…) LGD Alliance Europe #rarediseases #czinitiative #RareAsOne #CZIscience

Join Taylor and Liz, moderators for LGDA’s support groups, on their @NotSoRarePodcast as they share their experiences. ·podcasts.apple.com/us/podcast/not… · open.spotify.com/episode/5kgWoF…... LGD Alliance Europe @NotSoRarePodcast



DISH A friendly reminder! Our monthly The DISH (Drop in and Share) support group will meet on Saturday, August 13 at 10:00 am Eastern Time! Join here: us06web.zoom.us/j/94210215213?… LGD Alliance Europe
