The Abby Grace Foundation is making news! Read some of the articles AGF has been mentioned in or that applies to Sanfilippo Syndrome.
Running for research at the Trooper Footchase 5K
3/30/2015
Genzyme, Voyager Launch Up-to-$845M Gene Therapy Collaboration
2/11/2015
Why 2014 has been a ‘breakthrough year’ for gene therapy
12/30/2014
2015: Year of Gene Therapy for the Treatment of Children with Rare Diseases – Sanfilippo Syndrome
12/29/2014
Abeona Therapeutics Raises Foundation-led $3.6M to Develop Therapies for Children Suffering from Rare Sanfilippo Diseases
12/1/2014
Giving Thanks In The Face Of Trials
11/26/2014
Cherry pushing to raise awareness of rare disease
11/22/2014
Surviving the Rare Disease Roller Coaster
11/20/2014
Charity run focuses on community outreach
10/15/2014
Looking for Answers: Rare Diseases and Gene Therapy Research
10/6/2014
Event held for little girl battling rare disorder
9/20/2014
Dallas NC Family Fight for a Cure
9/19/2014
School supports fundraiser to help student
9/19/2014
Carnival For A Cure
9/9/2014
Abby: Heading To The Fourth Grade, Hoping For Many More
8/17/2014
Help NC Trooper FootChase 5K Choose A Charity
8/11/2014
Family battles rare disorder
7/21/2014
Abeona Therapeutics Receives U.S. Orphan Drug Designations for treatment of Sanfilippo Syndromes A and B
5/12/2014
Sanfilippo Syndrome: FDA Orphan Designations For Gene Therapy
5/1/2014