Jan Chisholm

Passionate about driving social change through collective effort.

[Muscular Dystrophy Australia @MDAust]

One of Australia’s most inclusive and accessible festivals returns at Birrarung Marr, Melbourne, on 25 March! 🥳🤩 #abilityfest #inclusion #musculardystrophy
https://t.co/qAfrYu6okb

[Jan Chisholm @janchisholm]

Come on airlines... take the challenge and invest in making the right to travel accessible. I'm waiting.

[Martyn Sibley @martynsibley]

Airlines are letting disabled people down! Please share

[Transport for All @TransportForAll]

What is commuting like for wheelchair users in London? 👩🏼‍🦽

Come along with @KatiePennick on her journey to Transport for All HQ.

[Muscular Dystrophy Australia @MDAust]

We're in the midst of Superhero Week fever and hope your fundraising events are going well. If you didn't get the chance to sign up. You can still donate at: https://t.co/4mBcN99QnK #shw2022💚

[Jan Chisholm @janchisholm]

So proud to be part of @MDAust team doing our bit to support @DuchenneDay

[World Duchenne Awareness Day 🎈 @DuchenneDay]

🎈𝗢𝗳𝗳𝗶𝗰𝗶𝗮𝗹 #𝗪𝗗𝗔𝗗𝟮𝟬𝟮𝟮 𝗩𝗶𝗱𝗲𝗼
Please share!
Duchenne Muscular Dystrophy is a genetic disease.
It leads to progressive muscle weakness.
There is no cure yet.
But the research is moving forward.
Better care has increased life expectancy.
https://t.co/AF2xluUKDJ

[Muscular Dystrophy Australia @MDAust]

Thank you @Hasbro for the fantastic giveaway prizes for Superhero Week. Petri the dinosaur went straight to work to learn all about muscular dystrophy and check who's been signing up and raising funds to be in the draw! 🤩💚 #SHW22

[Muscular Dystrophy Australia @MDAust]

National Superhero Week starts on September 5. Get your superhero capes and caps now! 100% of the proceeds in our store will go toward making MDA's mission possible - a step closer to finding a cure towards a world without MD! https://t.co/zDQ5Zsk25S #SHW22

[Lauren Sanders @LaurenSanders81]

From tomorrow, Australian adults with #SpinalMuscularAtrophy can now access nusinersen on the PBS! So excited to see this day but my heart breaks for the New Zealand SMA community who are still waiting.

[Pamela Appleton @PamAppletonNMC]

The new Fatigue Management resource for people with Neuromuscular Conditions is out now: https://t.co/a2iQTVj2gc
Thanks to @MDUK_News and the working group for making this project a reality!

[Jackie@MDUK(Scotland) @Jackie_MDUK]

The way you sit, lie, stand and move can influence your health and wellbeing. Find out more about 'Your Posture Matters' at the link below:

https://t.co/rTdltjX4yH

Get in touch to find out more about our postural care info sessions from @PAMIS_Scotland and @MDUK_News

[Jan Chisholm @janchisholm]

@simoninc Remember it well...

[VictorianMuscleNetwork @VicMuscleNet]

ATTENTION PhD/Masters/Hons students & Early/Mid-career researchers from Victoria & beyond!
Save the date for this year’s VICTORIAN MUSCLE NETWORK Annual Symposium
Keynote speakers: A/Prof Enzo Porrello @MCRI_for_kids
& Dr Sarah Lessard @JoslinDiabetes

More details to come...

[Jan Chisholm @janchisholm]

Always look forward to this week. Excited to see people already signing up to have fun, raise funds and support people living with MD

[Muscular Dystrophy Australia @MDAust]

Hey everyone, Superhero Week is back Sep 5-11 sign up now! https://t.co/xY9CZpHDG0

[Muscular Dystrophy Australia @MDAust]

We're looking for an Administration Coordinator to join our team! Apply on SEEK https://t.co/YAX6JViQiS
#administration #jobopportunity

[Muscular Dystrophy Australia @MDAust]

Run for Strength is back! Sunday 3rd April 2022. Participate IRL and join us at Princes Park, Melbourne, OR participate as a virtual challenge from anywhere! Sign up now! https://t.co/A5H65MleNz
#RFS22

[Muscular Dystrophy Australia @MDAust]

National Superhero Week is here! It's not too late to sign up and start fundraising today! If you can't join us this year, you can still make a positive impact by making a donation. Your donations go towards finding a cure for muscular dystrophy https://t.co/xwhtjfwFdN #shw21

[Muscular Dystrophy Australia @MDAust]

“I am raising money for Muscular Dystrophy Australia in honour of my dad who has Emery Dreifuss, a form of Muscular Dystophy. He is the best dad in the world. I hope all the money I raise goes to the scientists who can find a cure”
https://t.co/2GzAaunfpa #shw21

[Muscular Dystrophy UK @MDUK_News]

We’re delighted to tell you that the first boy with #Duchenne muscular dystrophy has been dosed as part of an international clinical trial sponsored by @GenethonFr to study a #GeneTherapy for the condition. Read more >> https://t.co/a5rcsKoISk

[Jan Chisholm @janchisholm]

@MDAust 5,000 skips and totally worth it (she says now). Feels fantastic to be part of such a worth effort and raise funds for people living with neuromuscular diseases.

[Muscular Dystrophy Australia @MDAust]

Double your impact! Your donation will work twice as hard thanks to THYSOL Australia. Thysol Australia has agreed to donate $2 for every $1 given to this appeal, up to a limit of $1,000. https://t.co/woXVeA6EjR #thysolaustralia #socialresponsibility #fundraising #MDA