Duchenne Foundation

Focusing on Improving the quality and length of life for those living with Duchenne across Australia, through, research, education, support, care and advocacy.

[Duchenne Foundation @DMDfoundation]

Good to see the WA community supporting @SaveOurSons - like the #SaveOurSons Twitter page to stay up to date! #like https://t.co/YacT3sIvUZ

[Save Our Sons Duchenne Foundation @SaveOurSons]

Thank you Calista Primary School for your donation and Duchenne awareness campaign! #studentsuccess #SaveOurSons

[Duchenne Foundation @DMDfoundation]

Like the @SaveOurSons Twitter page to stay up to date and before this page closes on 18 October 2016 #SaveOurSons https://t.co/EnIyVJ5K2w

[Save Our Sons Duchenne Foundation @SaveOurSons]

Save Our Sons is now the national peak body for Duchenne and we welcome Klair and Kristina to the team! #SaveOurSons

[Duchenne Foundation @DMDfoundation]

Exciting announcement via the @SaveOurSons Facebook page at 11am today! https://t.co/8uOiJdbG1d

[Duchenne Foundation @DMDfoundation]

We are excited to announce that the WA Gala To Save Our Sons co host is Johnny Ruffo. Johnny is well know for... https://t.co/IKw0NhSthm

[Duchenne Foundation @DMDfoundation]

Meet Save Our Sons Ambassador and one of our hosts for the WA Gala ! Lynne McGranger. Lynne is an... https://t.co/qfvLktZYQz

[Duchenne Foundation @DMDfoundation]

TICKETS ARE NOW AVAILABLE FOR PURCHASE!
Click on the link below or on the "Book Now" button in our cover image.... https://t.co/LDT4N63xsb

[Duchenne Foundation @DMDfoundation]

Tickets to the Gala to Save Our Sons will be on sale very soon. Watch this space for the Trybooking link to buy... https://t.co/j0Rs15vKLJ

[Duchenne Foundation @DMDfoundation]

NDIS Newsletter https://t.co/yOslfKAze1 https://t.co/zQgqNa8NPx

[Duchenne Foundation @DMDfoundation]

I have a family wanting to make contact with other families in Australia who have a young child (3-6 years) with... https://t.co/p0GTGqBgnh

[Duchenne Foundation @DMDfoundation]

WA parents you might be interested in participating in this survey about school aged children https://t.co/WSAPH81gi8

[Duchenne Foundation @DMDfoundation]

https://t.co/ubRzdytpot

[Duchenne Foundation @DMDfoundation]

https://t.co/vLnUgbf4EY

[Duchenne Foundation @DMDfoundation]

Day 12 of #Duchenne Awareness month is the Duchenne Foundation from Australia. (Please Share)

Duchenne... https://t.co/TJMiTGmZPe

[Duchenne Foundation @DMDfoundation]

2 years ago we were counting down to Gala Blue Ball 2014 . This year it's August 20....got some surprises... https://t.co/6SaqgFxtxj

[Duchenne Foundation @DMDfoundation]

Keep an eye out for #buildingforthefuture2016 https://t.co/5DwMjLHXbz

[Duchenne Foundation @DMDfoundation]

We are pleased to announce that a live stream of next week's conference will be available!

Next week the... https://t.co/hmTwxlSSlO

[Duchenne Foundation @DMDfoundation]

Santhera have published further results from their phase 3 trial of Raxone for Duchenne which show that this... https://t.co/WLOYhzB3Dx

[Duchenne Foundation @DMDfoundation]

As we look through our news feed, things intrigue us and we want to watch videos of cats, other people's family... https://t.co/v6inWQKE9M

[Duchenne Foundation @DMDfoundation]

@fith122 results were very variable and side effects. FDA refused approval in Jan and Europe said that they prob wouldn't approve

[Duchenne Foundation @DMDfoundation]

Disappointing news - Biomarin have decided to not take it's exon skipping drugs for Duchenne, including... https://t.co/cWTNh7Asco