Guest blog: Team Telomere launches new TBD Diagnosis and Management Guidelines

Team Telomere launch new clinical guidelines

The second edition Telomere Biology Disorders: Diagnosis and Management Guidelines have been officially published. This is a comprehensive reference manual for patients, physicians, and researchers. These updated guidelines are the result of a multi-disciplinary international collaboration between clinicians and scientists united by the goal of improving the lives of people with Telomere Biology Disorders and […]

Guest blog: The CPFF are honouring those touched by pulmonary fibrosis during Awareness Month

Guest blog from CPFF for PF Awareness Month

This guest blog, from Sharon Lee, Executive Director at CPFF, is to mark Pulmonary Fibrosis Awareness Month this September. Find out what the organization is doing to raise awareness and how you can show your support. Throughout the month of September, the Canadian Pulmonary Fibrosis Foundation (CPFF) is sharing the stories of those living with […]

Guest blog: A Patient’s Guide to Participating in Pulmonary Fibrosis Awareness Month

Pulmonary Fibrosis Awareness Month presented by RepeatDx

Ahead of Pulmonary Fibrosis Awareness Month, which is marked every September, Laura Devitt, Director, Programs at Pulmonary Fibrosis Foundation kindly shared the below information about getting involved. Every September, those who have been impacted by pulmonary fibrosis (PF) unite for Pulmonary Fibrosis Awareness Month (PFAM). Melissa King, a PFF Ambassador from New York, has participated in […]

Why do telomeres shorten?

Why do telomeres shorten

Telomeres play an important role in protecting our chromosomes, but as we age, they decrease in length. In this blog we explore how and why telomeres shorten. Telomere structure Human telomeres are made up of thousands of repeats of the same DNA sequence (TTAGGG), bound by a special set of proteins called shelterin. They are […]

Guest blog: Heather shares her experience with IPF for PF Awareness Month

Heather shares her experience with IPF for PF Awareness Month

This Pulmonary Fibrosis Awareness Month we have a guest blog from Heather, who is kindly sharing her experience with IPF to help raise awareness. IPF diagnosis I was diagnosed with Idiopathic Pulmonary Fibrosis (IPF) in February, 2013. I was 43 years old. My father and grandfather both passed from IPF so I knew there was […]

Guest blog: Canadian Pulmonary Fibrosis Foundation launches Hope Breathes Here

Canadian Pulmonary Fibrosis Foundation Hope Breathes Here Awareness Month

This guest blog from the Canadian Pulmonary Fibrosis Foundation marks Pulmonary Fibrosis Awareness Month and explains the events and activities they have coordinated for September. Register now for fun and informative activities during Pulmonary Fibrosis Awareness Month Despite the pandemic, Pulmonary Fibrosis Awareness Month this September may be the best ever from the Canadian Pulmonary […]

Guest blog: PFF presents Pulmonary Fibrosis Awareness Month 2020

Pulmonary Fibrosis Awareness Month

In support of the Pulmonary Fibrosis Awareness Month we are pleased to share a guest blog from the Pulmonary Fibrosis Foundation explaining the theme for this year’s campaign, and how to get involved.  September marks Pulmonary Fibrosis Awareness Month (PFAM), presented by the Pulmonary Fibrosis Foundation (PFF). This annual awareness campaign spreads the word about pulmonary fibrosis […]

3 reasons it may be helpful to order a telomere test for idiopathic pulmonary fibrosis

Reasons telomere testing may be useful for idiopathic pulmonary fibrosis

There is a growing body of clinical research investigating idiopathic pulmonary fibrosis and telomere biology – here we explore some reasons why ordering a telomere length test may provide useful insight when diagnosing or treating someone with idiopathic pulmonary fibrosis.   What is idiopathic pulmonary fibrosis? Idiopathic pulmonary fibrosis (PF) is a complex disorder characterized […]