01/01/2022How Chronic Illness Affected My Education – This blogger has some thoughts on extending her CF school experience to deal with the impact COVID has had on education.

01/03/2022 = Being Diagnosed With ADHD Made Life With CF Easier – Another reminder that CF does not exempt you from other disorders.

01/04/2022Top 10 Cystic Fibrosis Stories of 2021 – The annual practice of looking back for the biggest stories of the past year.

01/06/2022Cystic Fibrosis Foundation ResearchCon 2022 Prioritization Survey – Here’s an opportunity to influence the agenda for CFF’s ResearchCon. [NOTE: Survey expired 01/12/2022]

01/07/2022Iron Buildup May Lead to Death of CF Airway Cells, Study Suggests – This article is fairly dense but it points to another chemical balance issue associated with CF.

01/08/2022How I Learned to Let Go as a Parent of a Child With CF – “Letting go” is a very difficult transition. Like everything else, CF complicates that transition.

01/10/2022Using the Cystic Fibrosis Program for Individualized Therapy (CFIT) to enable therapy discovery for those people with rare CF-causing mutations – Cystic Fibrosis Canada supports a program designed specifically to look for therapies that address rare CF mutations.

01/11/2022CFF’s Rapid Fire Deals Prove There is Still a Market for New CF Drugs – Gunnar Esiason’s view of the Cystic Fibrosis Foundation’s investment strategy is a good companion view to the news from Canada that was shared here yesterday.

01/12/2022 “My hope for the future is to watch Katy live a long and healthy life”: Stacey reacts to the Kaftrio news – Many new futures are envisioned as the use of Trikafta (Kaftrio in Europe) spreads around the world. This article also includes the pledge in the UK to continue to seek treatments for those not helped by the current CFTR modulators.

01/13/2022Educating Others About CF to Protect Our Daughter – Maintaining a healthy environment requires cooperation from the family and friends in your close circle. Those lessons are even more important in the current circumstances.

01/14/2022Living With an Invisible Illness – This discussion of the mental health aspects of an “invisible disease” is somewhat of a companion piece the blog we shared yesterday. That is, we need to educate our family and friends about the mental, as well as physical, aspects of CF.

01/17/2022Looking after your mental health and wellbeing in difficult times – Once you recognize the importance of mental health, you need strategies to deal with it. This article from Cystic Fibrosis Trust offers some suggestions. NOTE: Resource references are specific to the UK, but you can substitute CFF’s Compass program.