The Childhood Arthritis & Rheumatology Research Alliance–or CARRA–conducts collaborative research to prevent, treat and cure pediatric rheumatic diseases.
Fibrocell is honored to support this CARRA event:
The Scleroderma Foundation is the national organization for people with scleroderma and their families and friends. Their mission is to provide support, education, and research to improve treatment and ultimately find the cause of and cure for scleroderma and related diseases.
Fibrocell is honored to support this event of the Scleroderma Foundation:
The Scleroderma Research Foundation (SRF) is America’s largest nonprofit investor in scleroderma research. Patients and their loved ones find hope in the fact the SRF is dedicated exclusively to funding medical research that will help them live longer, fuller lives.
NORD provides a unified voice for people battling rare diseases – those courageous individuals, and the parents and other caregivers seeking to help them, so that they won’t have to fight that battle alone.
Global Genes™ is one of the leading rare disease patient advocacy organizations in the world. Their mission is to build awareness, educate the global community, and provide critical connections and resources that equip advocates to become activists for their disease.