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https://www.um.edu.mt/library/oar/handle/123456789/67245
Title: | Living with a rare disease |
Authors: | Axiak, Clayton John |
Keywords: | Rare diseases -- Diagnosis Hypogonadism -- Genetic aspects Fibroblast growth factors Polymerase chain reaction |
Issue Date: | 2019 |
Publisher: | University of Malta |
Citation: | Axiak, C. J. (2019). Living with a rare disease. THINK Magazine, 28, 13. |
Abstract: | Picture yourself waking up one morning with a severe, relentless itch that no clinician or diagnostic tool can understand. Your life would be thrown off kilter. Quality of life would suffer financially, psychologically, and socially as you try to look for a glimmer of light at the end of the tunnel. This is what life is like for most people living with a rare disease. Often barraged with terms like ‘unknown’ or ‘undiagnosed’, matters can get even more challenging when the condition becomes more elusive or develops life-threatening consequences. And all of this is exacerbated by inequities in treatment and high costs of the few existing drugs that are available. |
URI: | https://www.um.edu.mt/library/oar/handle/123456789/67245 |
ISSN: | 2306-0735 |
Appears in Collections: | Scholarly Works - FacSciBio Think Magazine, Issue 28 Think Magazine, Issue 28 |
Files in This Item:
File | Description | Size | Format | |
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Living_with_a_rare_disease.pdf | 526.44 kB | Adobe PDF | View/Open |
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