[Irish Times] ‘There is a treatment and she’s not getting it’: Calls for HSE to fund drug for rare disease

Emily Felix (28) and her family were ‘killed’ by the news that a drug to treat Friedreich’s ataxia may not be considered for reimbursement by the HSE.

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Campaign for Friedreich's Ataxia Treatment Access Continues — Read the Latest

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Minister for Health announces introduction of screening for Severe Combined Immunodeficiency and Spinal Muscular Atrophy