Have YOUR say on future of Psoriatic Arthritis research Take the @BritPACT priority setting partnership survey help identify the top 10 unanswered questions you want research to address: https://t.co/8Ht9RQEgsy https://t.co/CJSsxZkrXR @BritishPainSoc @FlippinPain @loulouscorpio

We just submitted our paper for peer-review which analyzed 134 "popular" Homeopathic products sold in the Indian market funded from our own pockets (we spent quite a bit on this one). This is our penultimate self-funded pro-public health project before we wind down self-funded

📢 Keynote Speaker Announcement – ‘Psoriasis Update: What you need to know’ Conference With an unmatched level of expertise, Professor Darren Ashcroft, Foundation Chair in Pharmacoepidemiology at The University of Manchester, will discuss psoriasis epidemiology in the UK. (1/2)

There are over 16 million Disabled people in the UK! We deserve to have our say at the ballot box! If you haven't already registered to vote and apply for voter ID do it NOW. Don’t leave it until the last minute. #generalelection https://t.co/2XWBDQRBKC

The #GeneralElection has been called. We remind ALL parties that Disabled voices must NOT be ignored. Share & read the The Disabled People's Manifesto. Nothing about us without us! Ask your local MP to support! Manifesto | DPO Forum Manifesto ( https://t.co/P6E086Xjdb)

Disabled people demand the next Government tackle disablist policy making, oppression and injustice, to create a society where everyone has equal life chances and is valued and treated equally! #GeneralElection Read our: Manifesto | DPO Forum Manifesto ( https://t.co/P6E086Xjdb)

Don't ever stop sharing this video. The Tories have ruined this country. RUINED it. All the while lining the pockets of themselves and their mates. #generalelection #JulyToryWipeOut #ToriesLiedPeopleDied

The dedicated Pain Toolkit workshop myself and @grainne_daniels are delivering is really going to well #SelfmgtLIVING-Works

Join our study! 📚 Help us create a user-friendly guide for navigating diet and psoriasis info. Use the guide, give feedback, and shape its improvement. Your input matters! Email @poppyhawkin at p.hawkins@herts.ac.uk for more info or visit our website https://t.co/2NsAkyJ25I

#craniosacral therapy is very similar to cranial #osteopathy. Both are based on the idea of manipulating "cranial rhythms", which is complete nonsense. Here is yet another paper that found no evidence of effectiveness, this time for headaches:

Today was the second Pain Toolkit Conversation and it was on meaningful movement, but we covered so much more. What an amazing group: @paintoolkit2 @RestoringVenus @Jerry_DurhamPT @Virginia_McI @adiemusfree and Dr. David Flusk. The next conversation has already been scheduled.

🧵 In almost every country, men die by suicide at much higher rates than women We must prioritise male suicide research NEW international collaboration led by @susie_research We identified 22 research priorities for Male Suicide Risk & Recovery 🔗 https://t.co/X0vm8HTOOl 1/4

Your donations are crucial, to ensure that we continue our research and are able to support people living with #psoriasis and #PsoriaticArthritis every day. Every donation we get makes a difference. You can donate on our website https://t.co/xcbbh5sMF7

Have you taken the @myskinstudy survey yet? mySkin has been created by the doctors and scientists of St John’s Institute of Dermatology at Guy’s Hospital, King’s College London and aims to understand how and why psoriasis changes over time. Find out more https://t.co/V6ShC02Q3f

Hello, please dont consume mercury. It will kill you. Also please dont handle mercury with your bare hands. It is one of the most toxic substances known to humankind. Also, mercury is not medicinal. It is poison. Conman Guru speaking good English in Gibberish here is

Great little animation about pain @paintoolkit2 thanks for sharing 🙏 listened to a great podcast with @fionatalkington @PainCast_

Calling all Pain Support groups! 📣 We’d love to create a map of groups that we can share with the people who need it most. If you add your group to ADoddle below and include ‘Pain Support’ in the project name, we’ll be able to find you 🥰 https://t.co/SLzdPYsqpE

Looking for advice to help with managing scalp #psoriasis? Check out our tips sheet which includes info for caring for your scalp, applying treatments, & visiting the hairdresser too.💇 Get your copy: https://t.co/Uc8k3GT2D5

Take part in @myskinstudy! mySkin has been created by the doctors and scientists of St John’s Institute of Dermatology at Guy’s Hospital, King’s College London and aims to understand how and why psoriasis changes over time. Find out more on their website https://t.co/V6ShC02Q3f

@Channel4News As someone diagnosed and living with cognitive decline, removing the ticket office would also impact my reliance on asking for help and support and having a ticket. It's already challenging enough to navigate the world and stay focused.

"If they shut down the ticket offices all over the country, it'd be horrendous." As big rail companies try to get rid of ticket offices, Ruber Reuter speaks to people with disabilities to find out how the move could affect their daily travel.