Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2024

Open Access 01-12-2024 | Ameloblastoma | Letter to the Editor

Embracing the unknown: investigating medical communication around uncertainty and the implications on patient and family well-being

Author: Leisha Devisetti

Published in: Orphanet Journal of Rare Diseases | Issue 1/2024

Login to get access

Abstract

Rare diseases present immense challenges to physicians, patients, and the healthcare system at large due to a scarcity of research and knowledge in the field. This contributes to uncertainty surrounding rare diseases, which can hinder the management of these chronic conditions. An analysis of my family’s experience battling my mother’s ameloblastic carcinoma highlights the difficulties in communicating the uncertainty around rare diseases and their damaging effects on our family’s well-being. Here, we will recognize the importance of acknowledging uncertainty during diagnoses and advocating for enhanced detection strategies. The goal of this article is to emphasize that effective medical communication around rare diseases, accessibility to accurate information, proper services, and a shift toward a culture that prioritizes patient well-being are critical for improving health outcomes for rare disease patients.
Literature
1.
go back to reference Commissioner Oofthe. (2018,March9).Orphan Drug Act Excerpts.U.S.FoodandDrugAdministration.https://www.fda.gov/industry/designating-orphan-product-drugs-and-biological-products/orphan-drug-act-relevant-excerpts. Commissioner Oofthe. (2018,March9).Orphan Drug Act Excerpts.U.S.FoodandDrugAdministration.https://​www.​fda.​gov/​industry/​designating-orphan-product-drugs-and-biological-products/​orphan-drug-act-relevant-excerpts.​
2.
go back to reference U.S. Department of Health and Human Services. (2023,February28).Rare diseases.NationalInstitutesofHealth.https://www.nih.gov/about-nih/what-we-do/nih-turning-discovery-into-health/rare-diseases#:~:text=Advances%20in%20diagnosis%20of%20rare,about%20500%20have%20approved%20treatments. U.S. Department of Health and Human Services. (2023,February28).Rare diseases.NationalInstitutesofHealth.https://​www.​nih.​gov/​about-nih/​what-we-do/​nih-turning-discovery-into-health/​rare-diseases#:~:text=Advances%20in%20diagnosis%20of%20rare,about%20500%20have%20approved%20treatments.
6.
go back to reference Ameloblastoma - symptoms, causes, treatment: Nord.NationalOrganizationforRareDisorders.(2023,January12).https://rarediseases.org/rare-diseases/ameloblastoma/. Ameloblastoma - symptoms, causes, treatment: Nord.NationalOrganizationforRareDisorders.(2023,January12).https://​rarediseases.​org/​rare-diseases/​ameloblastoma/​.​
12.
13.
go back to reference Ashtari S, Taylor AD. (2022).The internet knows more than my physician: qualitative interview study of people with rare diseases and how they use online support groups.Journal of Medical Internet Research,24(8).https://doi.org/10.2196/39172. Ashtari S, Taylor AD. (2022).The internet knows more than my physician: qualitative interview study of people with rare diseases and how they use online support groups.Journal of Medical Internet Research,24(8).https://​doi.​org/​10.​2196/​39172.​
18.
go back to reference Mund M, Uhlenbusch N, Rillig F, Weiler-Normann C, Herget T, Kubisch C, Löwe B, Schramm C. (2023).Psychological distress of adult patients consulting a center for rare and undiagnosed diseases: a cross-sectional study.Orphanet Journal of Rare Diseases,18(1).https://doi.org/10.1186/s13023-023-02669-7. Mund M, Uhlenbusch N, Rillig F, Weiler-Normann C, Herget T, Kubisch C, Löwe B, Schramm C. (2023).Psychological distress of adult patients consulting a center for rare and undiagnosed diseases: a cross-sectional study.Orphanet Journal of Rare Diseases,18(1).https://​doi.​org/​10.​1186/​s13023-023-02669-7.​
Metadata
Title
Embracing the unknown: investigating medical communication around uncertainty and the implications on patient and family well-being
Author
Leisha Devisetti
Publication date
01-12-2024
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2024
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-024-03050-y

Other articles of this Issue 1/2024

Orphanet Journal of Rare Diseases 1/2024 Go to the issue