Have you seen this advert on TV or social media?
Autistic people are more likely to get overwhelmed and experience sensory overload in loud, bright, busy places. They can't change the way they respond to overwhelm, but you can #ChangeYourReactions
To all our lovely SWAN Mum's - Happy International Women's Day.
You do an amazing job every day at looking after your family and you should celebrate. It is not always easy being a SWAN mum so today is the day to be proud of what you and your children are achieving. #SWANaus
Thank you @RealSamHumphrey for raising awareness of #RareDiseases and #SWANaus. We have already gained new members who found out about us from watching your interview.
Great to see one of our lovely SWAN families raising awareness of Rare Diseases. Thank you Rachel and Trent for sharing Hamish's story. https://t.co/MfdWElxQ6h #RareDisease#SWANaus#rarediseaseday2020
Meet mum, Kris, and her son, Will, who is living with a rare genetic condition known as SCN2A, who are raising awareness of the need for improved access to genetic services, funding and treatments for rare disease families
@GeneticAll_AU#ColourYourHairForRare#reframerare
#RareDiseasesday2020 with @GaRDN_WA to raise awareness about sickle cell disease in Australia. We also took time to learn about other rare diseases affecting other Australians. #SCD is considered a rare disease in Australia. @RareVoices Great to meet Hon Matt Swinbourn.
It's the evening in Australia and #RareDiseaseDay is almost over! Check out Yagan Square in Perth lit up in Rare Disease Day colours! @RareVoices Light up organised by Andrew Bannister.
Today on #rarediseaseday2020 I grateful for all the health care professionals, researchers and families for all that you do to make our lives and experiences better 👏
Rare Disease Day is here! The main objective of today is to raise awareness among the general public & decision-makers about #rarediseases & their impact on people's lives. Tag us in any photos you have today & we'll re-tweet them.
"When Kane Blackman's son started experiencing severe symptoms of an unknown condition, he was told his child was delayed and would eventually catch up." A brief recap of last week's National Strategic Action Plan for Rare Diseases launch event: https://t.co/6WzOArWslz
What an absolute pleasure it was for @SusanWhiteAuth1 and myself to be guests on @too_peas. Kate and Mandy, thank you for being such warm and funny hosts and having us on the show so we can raise awarness of @swanaus and support more families. https://t.co/CS0ZRrshsz #RareDisease
Not all genetic conditions are inherited in the same way, but how exactly does inheritance work? Find out more in our NEW short online course! https://t.co/MkKSiX69w4 #genomics#genetics#STEMeducation
Can't believe a week has gone by without me sharing these delightful photos of our SWAN Siblings enjoying a SWAN Sibs bowling session. The kids had a ball! #SWANsibs#PeerSupport#SWANaus
I am excited to be attending the @agbt 20th anniversary meeting this week. I look forward to engaging with genomics researchers and others about the new discoveries and cutting-edge breakthroughs in genome biology and technology. I will be sharing photos and updates, stay tuned!
Great article @GallacherLyndon @SusanWhiteAuth1#NatalieTan. #SWANaus children certainly benefit from an early diagnosis which is why we need free and equitable access for all #SWANaus children @GregHuntMP. It is an emotional rollercoaster when you don't have a diagnosis.
SWAN members, please don’t forget our Informal Virtual Chat session on Monday night. There is still time to register https://t.co/fPuGx5vkcc This is your opportunity to chat with SWAN members all around Australia. #PeerSupport#SWANaus#RareDisease