Orla Hardiman
Biographic Data
| ID | 139303 |
|---|---|
| NAME | Orla Hardiman |
| GIVEN NAMES | Orla |
| FAMILY NAME | Hardiman |
| SIGNATURE | HARDIMAN O |
| AFFILIATIONS | Beaumont Hospital |
| ORCID | 0000-0003-2610-1291 |
| VERIFIED | Yes |
| TOTAL WORKS | 4 |
| TOTAL CITATIONS | 8 |
| WORKS AS AUTHOR | 4 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2001 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 2 |
A Social Network Analysis of Information Flow Between Specialists in a Multidisciplinary Motor Neurone Disease Clinic
Background: Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative condition that negatively effects multiple domains of functioning including movement, speech, swallow, cognition and behaviour. The clinical phenotype is variable, and 70% of patients die within 3 years of their first symptom 1,2 . While there are no effective disease modifying therapies, access to centralised multidisciplinary care improves outcomes, quality of life, and is c…
Acceptance and Decision Making in Amyotrophic Lateral Sclerosis From a Life-Course Perspective
Researchers have explored perceptions of health care services among people with amyotrophic lateral sclerosis (ALS), but little is known about how and why people with ALS engage with services. We undertook a grounded theory study to identify key psychosocial processes that underpin how and why people with ALS engage with health care services. We conducted in-depth interviews with 34 participants sampled from the Irish ALS population-based registe…
Exerting control and adapting to loss in amyotrophic lateral sclerosis
Assessing individual quality of life in amyotrophic lateral sclerosis
Exerting control and adapting to loss in amyotrophic lateral sclerosis
Acceptance and Decision Making in Amyotrophic Lateral Sclerosis From a Life-Course Perspective
Researchers have explored perceptions of health care services among people with amyotrophic lateral sclerosis (ALS), but little is known about how and why people with ALS engage with services. We undertook a grounded theory study to identify key psychosocial processes that underpin how and why people with ALS engage with health care services. We conducted in-depth interviews with 34 participants sampled from the Irish ALS population-based registe…
Assessing individual quality of life in amyotrophic lateral sclerosis
Acceptance and Decision Making in Amyotrophic Lateral Sclerosis From a Life-Course Perspective
Researchers have explored perceptions of health care services among people with amyotrophic lateral sclerosis (ALS), but little is known about how and why people with ALS engage with services. We undertook a grounded theory study to identify key psychosocial processes that underpin how and why people with ALS engage with health care services. We conducted in-depth interviews with 34 participants sampled from the Irish ALS population-based registe…
Exerting control and adapting to loss in amyotrophic lateral sclerosis
A Social Network Analysis of Information Flow Between Specialists in a Multidisciplinary Motor Neurone Disease Clinic
Background: Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative condition that negatively effects multiple domains of functioning including movement, speech, swallow, cognition and behaviour. The clinical phenotype is variable, and 70% of patients die within 3 years of their first symptom 1,2 . While there are no effective disease modifying therapies, access to centralised multidisciplinary care improves outcomes, quality of life, and is c…
Medicine (4 works) · Nursing (4 works) · Amyotrophic lateral sclerosis (3 works) · Amyotrophic Lateral Sclerosis Research (3 works) · Disease (3 works) · Psychology (3 works) · Sociology (3 works) · Gerontology (2 works) · Health care (2 works) · Neurogenetic and Muscular Disorders Research (2 works)