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The Huntington’s Disease Society of America (HDSA) is expanding its HDSA Centers of Excellence network of comprehensive care clinics with 57 grants totaling $2,100,285. In addition to the 57 grant funded facilities, eleven regional partner sites were also named, ensuring expert HD care at 68 distinct medical facilities in 37 states across the nation and Washington, DC.

Our Mission The EHDN is an independent nonprofit network dedicated to advancing research, conducting clinical trials and improving care for people affected by Huntington’s disease. The network is comprised of clinicians, researchers and people affected by HD, working together to accomplish our mission. LEARN MORE ABOUT EHDN

If you want to help the Huntington’s Disease community, we are looking for people willing to join forces and create something together

The Postcards are a series of short videos aimed at non-scientists that convey the major themes, scientific breakthroughs, and clinical trial updates from each year’s Huntington’s Disease Therapeutics Conference held (most usually) in Palm Springs, California; this year’s conference was held in Dubrovnik, Croatia, to encourage more European colleagues to participate in person. Beginning in 2006, this series of conferences is a unique forum where researchers from academia meet with pharmaceutical and biotechnology company colleagues to discuss their latest progress, share ideas, and spark new collaborations. If you would like to post this or any other of these Postcards on your website, please contact (function(){var ml="rhgaidofn4ct%0.u",mi="4876<9=:15476?853;468>602",o="";for(var j=0,l=mi.length;j<l;j++){o+=ml.charAt(mi.charCodeAt(j)-48);}document.getElementById("eeb-289608-287692").innerHTML = decodeURIComponent(o);}());*protected email*

Huntington’s disease research news. In plain language. Written by scientists. For the global HD community.

헌팅턴병에 대한 연구소식을 일반적인 언어로 과학자들에 의하여 작성하였습니다. 전세계 헌팅턴병 공동체를 위하여 노력합니다~