POSITIVELY RARE
Erin Paterson shares her experience of being gene positive for the rare Huntington disease, and how she is on a mission to positively impact other
This Chronic Disease Awareness Day patient advocate Roxanne Murray strives to ensure no one is left unseen or unheard in the MS, chronic illness and disability community The Invisibility of MS: What You Don’t See Still Deserves Support As I approach my 19th year of living with Multiple Sclerosis, I’ve come to understand just how […]
Erin Paterson shares her experience of being gene positive for the rare Huntington disease, and how she is on a mission to positively impact other
Our Research Consultant Andrew Grant advocates for awareness of the physical and mental issues patients face while their condition remains undiagnosed Getting a diagnosis when
LDA Research is supporting CureLONP1.com Aria’s Miracle research fund and her parent’s conviction that hope lies within the global medical and scientific community Aria’s parents need to
Senior research manager, Rachel Barnes, discusses the methods LDA Research takes to prevent fraudulent respondents when recruiting for patient research providing a genuine and high
This month we profile Viviana Horwood, one of our research managers, who has worked with LDA Research for six and a half years and become
Senior research manager Rachel Barnes shares insights into how LDA Research recruits niche respondents and hard to reach patients worldwide for our clients Over the
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