Evidence map›Paper›PMID 41166164›Full record

ArticleJournal of neuromuscular diseases2026

Disease modifying therapies for children with spinal muscular atrophy - parents' experiences of hopes, grief and need for rehabilitation for their child.

Charlotte Handberg, Pia Zinck Drivsholm, Ulla Werlauff, Sanne Okkels Birk Lorenzen, Annette Mahoney

Abstract read
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Article in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

Charlotte HandbergNational Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.ORCID 0000-0002-1378-2449
Pia Zinck DrivsholmNational Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.ORCID 0009-0009-5109-9147
Ulla WerlauffNational Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.ORCID 0000-0002-5294-2046
Sanne Okkels Birk LorenzenNational Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.ORCID 0009-0006-7194-6831
Annette MahoneyNational Rehabilitation Center for Neuromuscular Diseases, Aarhus, Denmark.ORCID 0000-0002-8567-9686

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate how parents of children with SMA who are treated with disease modifying therapies cope with hopes and worries related to disease progression, and to investigate their needs for counseling and rehabilitation initiatives.

methodsThe design of this study was qualitative using the Interpretive Description methodology and Joyce Travelbee's theory of interpersonal aspects. The method was semi-structured interviews conducted in Denmark at the homes of the parents or through the online platform Teams between February 29 and May 3, 2024.

findingsSeventy-five parents representing 41 children were invited. Twenty-six parents of 20 children participated in the study. Twenty-four parents were interviewed at home and two were interviewed online. The key element of the parents' narratives was the reality of the diagnosis: the trajectory toward the diagnosis, getting the diagnosis, and the hope related to the effect af disease modifying therapies. At the same time, they experienced grief related to the uncertainty of the disease progression while hoping for normalcy in the future: a 'normal' child and a 'normal' life. Finally, they struggled with balancing professional counseling to maintain hope.

conclusionsThe families need coordinated, multidisciplinary care and information on disease modifying therapies, including what they can actively do to increase the effectiveness of the treatment. Counseling should include facilitated peer-support and acknowledge differences in children in terms of development, how they respond to the disease modifying therapy, and its long-term effects. Health professionals must tailor their support to the families' needs and sustain their hopes for the future.

Indexed as

GriefHopeMuscular Atrophy, SpinalParentsAdaptation, PsychologicalAdolescentAdultChildChild, PreschoolCounselingDenmarkDisease ProgressionFemaleHumansMaleQualitative Researchdisease modifying drugsdisease modifying therapyhopenewborn screeningparentsrehabilitationspinal muscular atrophy

Identifiers

PMID41166164
PMCPMC13438409

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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.