To help raise awareness of rare disease dyskeratosis congenita, Julian’s mom Mayra has kindly shared his journey through 4 stem cell transplants this Rare Disease Day. At the age of 3, our son was diagnosed with a rare genetic disorder called, dyskeratosis congenita. We were really fortunate our search led us to the Jimmy Fund […]
In this blog we examine what short telomeres are and what short telomere syndromes can mean for certain individuals. What are telomeres for? Our chromosomes need to be protected to prevent damage, or them fusing with other chromosomes. Telomeres are the protective structures found on the end of chromosomes. They are made up of thousands […]
To mark Telomere Biology Disorder Month (TBD Month) this November, Brian is kindly sharing his journey of being diagnosed with dyskeratosis congenita, liver failure and undergoing a liver transplant. My journey with dyskeratosis congenita (DC) started in September 2016 when I was first diagnosed. I had become pretty sick in a short period of time, […]
This Telomere Biology Disorder Awareness Month (TBD Month) we have a guest blog from Colleen, Team Telomere President & Chair of Legacy. Colleen is kindly sharing her families’ story from unexpected diagnosis, to health care journeys, to the strength she has found in the Team Telomere community. If you would’ve told me 15 years ago […]
The results are in from our annual customer telomere testing satisfaction survey, here we take a look… Hearing from our customers is very important to us. We want to ensure that ordering a telomere test from us is as easy and straightforward as possible, as well as meeting the highest expectations in terms of turn […]
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 […]
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 […]
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 […]
RepeatDx offers both 2- and 6-panel tests, here we outline some of the advantages of ordering the 6-panel telomere test. What telomere length tests are available? There are a range of telomere length tests available, however, the clinical laboratory at RepeatDx conducts specialist Flow FISH telomere testing (fluorescence in situ hybridization with flow cytometry). This […]
Over the past 30 years we have learned a lot about telomeres, including what they are and where they are found. In this blog we will discuss why exactly we need telomeres and the important processes that they have a role in. What are telomeres made of? Telomeres are repetitive DNA sequences found at the […]