A few important things we live by…

Compassion

 

It takes far too long for many genetic diseases to be diagnosed! Therefore, innovative genomic techniques must be employed cutting through the odyssey.1,2

Commitment

 

More than 50% of all rare diseases affect children. 30% of whom will not see their fifth birthday. We’re committed in providing a better healthcare to the community.3,4

Collaboration

 

There are nearly 7,000 rare diseases with only a few hundred available therapies! The need remains immense to invest in collaboration within research and diagnostics.5

 

References

  1. ISEBOX Ltd/Shire. Rare disease impact report: insights from patients and the medical community 2013.
  2. Muir E. Reality – an insight into the patient and family experience of rare disease. London: Rare Disease UK for Genetic Alliance UK; 2016.
  3. Rare-disease (2022) Murdoch Children’s Research Institute. Flagship-Research. Available at: https://www.mcri.edu.au/
  4. England-rare-diseases-action-plan-2022 (2022) GOV.UK. UK Government. Available at: http://www.gov.uk/
  5. The “Right to Health” in Rare Diseases (2018) NGO Committee for Rare Diseases. Available at: ngocommitteerarediseases.com.
  6. GeneOriginS Genetic Service Menu; Download Brochure
  7. Gene Discovery & Research Collaboration; Download Brochure