🟢 Who can parents turn to when they learn that their child has Extra X or Y chromosomes?
Why are so few people ever diagnosed, and health care provider awareness still low? How does AXYS fill the gaps for families and chromodiverse individuals?
What’s the golden standard today for care and research? How reliable is non-invasive prenatal screening?
Where can I meet other concerned people, families and experts? Is the neurodiversity call for “nothing about us without us” coming to chromodiversity?
To find out the answer to these and other urgent questions, listen to this highly informative conversation with Carol Meersheart, Executive Director of AXYS, the leading family association for X and Y chromosome variations based in the US.
For more information, check out the AXYS website featuring an abundance of useful resources and a hotline for one-on-one queries at genetic.org.
