EDS ECHO Event Series: Allergy and Immunology Complications
December 4-5, 2021
We are delighted to be hosting a dedicated event for allergy and immunology complications in the Ehlers-Danlos syndromes and hypermobility spectrum disorder. Join us as leading experts present the latest research, management, and scientific information.
We will be offering live translations during this event in English (original language), French, German, Spanish, and Italian.
December 4, 2021, will be Healthcare Professionals Day. CME/CEU/CE Credits will be available (pending approval), and available to claim for sessions that are viewed LIVE.
The healthcare professional’s day will take place from 08:45 AM – 4.45 PM Eastern Time.
December 5, 2021, will be Community Day.
This day is for members of the EDS and HSD community, their families, and caregivers. The community day will take place from 08:45 AM – 4:45 PM Eastern Time.
(Please use the converter world time buddy to find the correct times in your location)
The agenda will be announced soon.
The conference will take place online via Zoom Webinar. If you have questions please email email@example.com.
Registrations for our EDS ECHO Event Series: Allergy and Immunology Complications are now open!
Please follow the community or healthcare professionals sign up buttons below to sign up to our EDS ECHO Event Series: Allergy and Immunology Complications event.
WE ARE DELIGHTED TO BE OFFERING LIVE TRANSLATIONS DURING THIS EVENT INTO THE FOLLOWING LANGUAGES:
English (Original Language), French, German, Spanish, and Italian.
Making our conferences and resources more accessible worldwide is a long-term goal that we have to continue spreading awareness, and we hope to be able to offer an even larger range of translation services at future conferences.
Lipedema is a chronic medical condition characterized by asymmetric buildup of adipose tissue (fat) in the legs and arms that occurs almost exclusively in women. It is a common but underrecognized disorder. Lipedema may cause pain, swelling, and easy bruising and be accompanied by an unusual texture within the fat that can feel like rice, peas, or walnuts beneath the surface of the skin.
At the Lipedema Foundation, we support collaborative research that addresses the basic biology, genetics, and epidemiology of lipedema with a mission to define, diagnose and develop treatments.
Please visit our website lipedema.org to learn more about the Lipedema Foundation.
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