Jeff Craig
@drchromo.bsky.social
170 followers 170 following 61 posts
Nature-lover & teacher/researcher/learner. Epigenetics, twins, orchids, fungi, gardening, photography, neurodiversity. 🏳️‍🌈🏳️‍⚧️Ally. Guest on Wadawurrung Country.
Posts Media Videos Starter Packs
drchromo.bsky.social
ruthmchugh-dillon.bsky.social
The internet has been obsessed with identical twins Bridgette and Paula Powers, and the uncanny way they speak in sync. Jeff Craig @drchromo.bsky.social and Nancy Segal explain why twins might speak like this – and whether a secret "twin language" is a real thing theconversation.com/genes-enviro...
Genes, environment or a special bond? Why some twins talk and think in unison
Twins Bridgette and Paula Powers have gone viral for the way they speak in unison, using the same gestures and words.
theconversation.com
drchromo.bsky.social
I just wrote this with the Prof Nancy Segal, who has an encyclopaedic knowledge of twins. I hope you learn something. I did.

Genes, environment or a special bond? Why some twins talk and think in unison theconversation.com/genes-enviro...
Genes, environment or a special bond? Why some twins talk and think in unison
Twins Bridgette and Paula Powers have gone viral for the way they speak in unison, using the same gestures and words.
theconversation.com
drchromo.bsky.social
Happy Neurodiversity Celebration Week! Let’s celebrate the unique strengths and perspectives of neurodivergent individuals. Embracing diversity fosters creativity, inclusion and innovation. Learn, advocate, and listen—because different minds make a better world! #NeurodiversityWeek #InclusionMatters
drchromo.bsky.social
interesting point
drchromo.bsky.social
FOP (soft tissue turns to bone) – www.ifopa.org/support_groups
Alkaptonuria (black urine, joint issues) – akusociety.org
Kufs Disease (neurodegenerative) – bdsra.org
Stiff-Person Syndrome (muscle stiffness) – stiffperson.org/support-reso...
Online Support Groups
www.ifopa.org
drchromo.bsky.social
Today is Rare Disease Day

Rare diseases affect millions worldwide, often with limited treatment options. Rare Voices Australia (RVA) advocates for those living with rare diseases, connecting them to vital resources. Learn more: rarevoices.org.au
Five rare diseases and support groups:
Peak body for Australians with rare diseases including genetic disorders
An estimated two million Australians live with a rare disease. Approximately 80% of rare diseases are genetic disorders.
rarevoices.org.au
Reposted by Jeff Craig
odedrechavi.bsky.social
Almost 200 people signed up already - add your name soon before we have to stop registration for this once in a life time conference! docs.google.com/forms/d/1dm8...
drchromo.bsky.social
"Gender-affirming care is potentially life-saving, or at the very least life-affirming. It almost invariably leads to better social and emotional outcomes" Can a child legally take puberty blockers? What if their parents disagree? theconversation.com/can-a-child-...
Can a child legally take puberty blockers? What if their parents disagree?
Recent political attention might imply gender-affirming care is risky, controversial, perhaps even new. But Australian law views it as a legitimate medical treatment.
theconversation.com
Reposted by Jeff Craig
virusvoyeur.bsky.social
While the primary focus of this article is aimed at those in a relationship, I see benefits for colleagues, teachers, and friends. An opportunity to empathise with those living with ADHD and truly understand the struggles they encounter daily.
www.additudemag.com/slideshows/i...
"If You Love Me, Please Take This Seriously"
We don’t mean to hurt you. But we do — again and again. You feel like screaming, pulling out your hair, or lying in bed and crying, “When will she get it? Will this ever stop?” I don’t have all the an...
www.additudemag.com