Evidence map›Paper›PMID 40851522›Full record

ArticleNeurodegenerative disease management2026

You look at life through a different lens: a phenomenological study of living with amyotrophic lateral sclerosis.

Katherine Hope Morgan, Katherine Havranek, Chelsea Horn, Michelle Lanphere Lee, Sandra Thomas

Abstract read
In one paragraph

Article in Neurodegenerative disease management, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Katherine Hope MorganCollege of Nursing, University of Tennessee, Knoxville, TN, USA.
Katherine HavranekCollege of Nursing, University of Tennessee, Knoxville, TN, USA.
Chelsea HornCollege of Nursing, University of Tennessee, Knoxville, TN, USA.
Michelle Lanphere LeeClinical Nutrition, Department of Nutrition and Integrated Health Sciences, East Tennessee State University, Johnson City, TN, USA.
Sandra ThomasCollege of Nursing, University of Tennessee, Knoxville, TN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsAmyotrophic lateral sclerosis (ALS) is a motor neuron disease that progresses without periods of remission; few live more than five years beyond diagnosis. In this study we investigated the lived experiences of people diagnosed with ALS in the United States, in South Central Appalachia. PATIENTS &

methodsWe selected the philosophical and methodological approach of existential phenomenology of Merleau-Ponty to identify what was most important or figural to participants, within the contexts of Body, Other People, World, and Time.

resultsThrough phenomenological interviews with 10 people living with ALS, six themes and 17 subthemes were identified covering the process of diagnosis, loss and devastation, support from others, assistive devices, a new purpose, and a change in perspective.

conclusionsThese themes offer insight into life with an ALS diagnosis so that this unique patient population may be better understood from a physical, medical, emotional, and spiritual standpoint.

Indexed as

Amyotrophic Lateral SclerosisAdultAgedFemaleHumansMaleMiddle AgedQuality of LifeAmyotrophic lateral sclerosischronic illnessexistential phenomenologyillness perceptionnarrativesneuromuscular diseasepatient experience

Identifiers

PMID40851522
PMCPMC12826697

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.