huntingtonstudygroup huntingtonstudygroup

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Huntington Study Group  Network of 400 investigators and coordinators around the world, seeking treatments that make a difference for Huntington disease.

HSG and the HD community are lucky to count Tacie Fox and the Fox Family Foundation as friends. Learn more about Tacie and her family's foundation in the current issue of HD Insights. Link in bio. #rarediseaseday #huntingtonsdisease

The popular in-person health care professional training, CME4HD, is now available online -- for FREE! Earn CME/CNE credits and learn how to care for people impacted by Huntington disease. Spread the word! Details and info on incentive at link in bio. #huntingtonsdisease #cme #cne

For the first time, HSG offered exhibitor space at our annual meeting. It went very well, especially for HD Family Education Day. Thank you to all our exhibitors for providing such great information and opportunities to our attendees! #HSG2017 #huntingtonsdisease

We could post a photo every day for a year and still only get through the best of #HSG2017! Here's Anita Goh receiving a plaque from HSG Founder Ira Shoulson for winning the first Como Scholarship. Congratulations, Anita! #huntingtonsdisease

Thank you all for helping us seek treatments that make a difference, and special gratitude goes to our caregivers during Caregiving Month. #huntingtonsdisease #caregiversmonth #iamthedifference

#HSG2017 was a huge success! Save the date for #HSG2018 Unlocking HD Nov. 8-10, 2018, in Houston!

#HSG2017 is only a week away! If you haven't already, register TODAY!

Have you downloaded our event app yet for HSG 2017: Elevating HD Nov. 2-4, 2017, in Denver, CO? Go to the App Store or Google Play Store and search "HSG 2017." Get the most detailed information about our sessions there!

‪Are you at #MDSCongress2017? Stop by and say hello in Exhibit Hall C! ‬

What gives Dr. Ray Dorsey hope for HD? Seeking treatments that make a difference for HD. #hopeforHD #huntingtonsdisease #iamthedifference @hdyofeed

Happy Mother's Day to the strongest mothers in the world! #huntingtonsdisease #iamthedifference

"Ultimately, my hope is for a cure, but in the meantime, we want to make sure that people have a place they can go to get the help they need." Julia Iourinets, study coordinator at the University of Rochester's HDSA COE clinic. #hopeforHD #huntingtonsdisease #iamthedifference

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