by idfa | Feb 11, 2022 | News
2022 Rare Disease Day What is Rare Disease Day? Rare Disease Day is the globally-coordinated movement on rare diseases, working towards equity in social opportunity, healthcare, and access to diagnosis and therapies for people living with a rare disease. Since its...
by idfa | Feb 3, 2022 | News
Managing your child’s return to the classroom This information has been provided by IDFA member, teacher and mum of two, Bianca. You can read more about Bianca’s story here. Bianca is one of our friendly family support group moderators. If you are...
by idfa | Feb 1, 2022 | News
Managing your child’s fatigue and over-stimulation when they return to school This information has been provided by IDFA member, teacher and mum of two, Bianca, to offer you and your child some tips on managing fatigue and overstimulation as they return to...
by idfa | Feb 1, 2022 | News
Back to School Tips for Parents and Carers of PID/SID Children This information has been provided by an IDFA member to offer you and your child some tips and tools for a smooth transition back to school this year. This IDFA member has significant experience in...
by idfa | Jan 24, 2022 | News
Help IDFA Advocate for Access to Rapid Antigen Tests for Immunodeficient Patients and Carers We understand that many of you are feeling anxious, stressed, frustrated and/or concerned given the current COVID-19 developments and the risk that this exposes to your...
