🚨 NEW: Key deadlines for the GE on 4 July

⏲️ Register to vote: Tuesday 18 June at 23.59

⏲️ Applying for a Voter ID: Wednesday 26 June at 17:00

⏲️ Applying for a postal vote: Wednesday 19 June at 17.00

⏲️ Applying for a proxy vote: Wednesday 26 June at 17.00

Dear students, apply for a postal vote now if you haven’t done so already. Don’t leave it too late. Vote for whomever you like but please vote. It matters. gov.uk/how-to-vote/po…

🎓 We have an opportunity for a Professor to join our research centre Salford Human Movement and Rehabilitation Research at the University of Salford jobs.ac.uk/job/DHT127/pro… 🌟

📌 Applications by 30th June! Dr Gillian Rawlinson PhD Prof Rich_Jones Stephen Preece Professor Margaret Rowe University of Salford Dean Professor Vicky Halliwell (she/ her) Please RTW 🙏🏼

Sorry I’ve been quiet on the #AxialSpALife challenge. I’ve been unwell ( #dysautonomia / #EDS -related, not #axialSpA -related). I’ll catch up once I’m feeling well enough to 🤍

Crohn's and Colitis are invisible illnesses.They often cause symptoms that other people just won't see. Such as severe pain, diarrhoea, blood in your poo - or extreme tiredness.

Find out more: crohnsandcolitis.org.uk/get-involved/w…

#worldibdday #IBDmythbusting

'Identity is a place I always start with when I see people one-to-one, giving the time to find out how they saw themselves pre-diagnosis, and what's changed after diagnosis.'

- John Butler, Paediatric Psychologist in #rheumatology

#MentalHealthAwarenessWeek

Day 13 of the NASS #AxialSpA Life social media challenge: instagram.com/p/C6662fuoBNM/…

#AxialSpA #AnkylosingSpondylitis

Join ARMA on 3 June to celebrate our Act Now report on #MSKInequalities . Hear the key findings and how they can be put into practice. Discuss how you might be able to Act Now in your own practice, service or system.

Sign up
👇👇👇
us02web.zoom.us/webinar/regist…

Oops, I forgot to share yesterday’s post on here! Day 12 of #AxialSpALife is all about #axialSpA treatments: instagram.com/p/C64iSZcI8zF/…

We covered a lot of ground in our #YourSpAce online meetup on Thursday. We chatted about small changes that can make a big difference to life with #axialSpA . What would you add to our list? Share your tips in the comments

Who’s going to #EULAR 2024 ? I’m attending for the first time and really looking forward to catching up with friends and colleagues, meeting lots of new people, and attending some brilliant sessions. I’m also presenting on Saturday with some familiar faces! 🙌🏼 #EULAR

Just your disabled aunty reminding you that certain medications can make you more sun sensitive and likely to burn.

Drink plenty of water
Snack often
Reapply sun cream VERY OFTEN

The iO Census closes soon!
Are you a registered osteopath? Don't miss your opportunity to have your say by completing the iO Professional Census here > warpsurveys.com/ios2024
#StrongerTogether Inst of Osteopathy

The iO Roadshow, Southeast is underway, starting with a discussion on growth, recognition and accessability: the challenges and the opportunities. Inst of Osteopathy #ProudOsteopathy

Day 11 of #AxialSpALife , NASS social media challenge: not just back pain - share how #axialSpA affects other areas of your body

Meet Bethany.

She talks through her experience of developing #symptoms in her teens, not finding any answers and then being #diagnosed at such an early point in life, but overcoming that to live well with #axialSpA .

Read her story and more at bit.ly/3wZiXfg.

Day 10 of #AxialSpALife : What does a flare up look like for you?
My flares are quite unpredictable these days. Both in terms of what flares up and what triggers it. I’ve shared about the rib pain I experience, as it’s the most debilitating symptom I get: instagram.com/p/C6zMsBNIDV5/…

Belated day 9 of the @nass_exercise #AxialSpALife social media challenge - tell us about your support system. Late to the party because of yesterday’s brain fog and fatigue 🤦🏻‍♀️ But here’s a snapshot of my support system 💖 More info in the caption: instagram.com/reel/C6yeh4QIX…

On World Lupus Day, we continue to raise awareness of this condition, improve time to diagnosis, access to treatment, education and research #WorldLupusDay #lupus #SLE

If you have a diagnosis of endometriosis, or suspect you have endometriosis, we want to hear from you!

You can complete the questionnaire about pain management programmes here: lnkd.in/e9S8Di4k

Thank you!