'I was nearly in tears': Father's relief as Pharmac proposes funding 'miracle drug' for toddlers

A family considering leaving New Zealand to access the life-changing medicine Trikafta for their toddler can now stay home ...
Stylist on MSN

Jesy Nelson meets health secretary, Wes Streeting, to campaign for rare muscle disease test for all babies

After her twin daughters were diagnosed with spinal muscular atrophy (SMA), Jesy Nelson is campaigning to get earlier routine ...
Healio

Topline results: Antibody therapy lowers inflammatory biomarkers in cystic fibrosis

In patients with cystic fibrosis, CMTX-101, an immune-enabling antibody therapy, lowered four inflammatory biomarkers and ...
Thorax

Antifibrotic therapy and lung cancer risk in patients with idiopathic pulmonary fibrosis: a large retrospective propensity-weighted cohort study

Background Antifibrotic (AF) therapy has been shown to potentially reduce the risk of lung cancer (LC) in patients with ...