Click here for COVID-19 (coronavirus) advice for people living with psoriasis and psoriatic arthritis.
There are often opportunities to help raise awareness of psoriasis, contribute to projects and initiatives, and share your experiences.
Listed below are various opportunities that the Psoriasis Association, or other organisations, are looking for people to get involved with. If you are interested in getting involved in psoriasis research, please see our Research pages.
Share your experience of receiving the COVID-19 vaccination
The team behind the PsoProtectMe psoriasis and COVID-19 registry are interested to hear from people with psoriasis who have received the COVID-19 vaccination.
If you would like to share a quote or short written piece (250 words or less) about your experiences please do get in touch. In particular we would like to know why it was important for you to receive the COVID-19 vaccine. Submissions may be published on the Psoriasis Association and PsoProtect websites and/ or social media channels.
If you are interested in taking part please email email@example.com.
We would like to hear your experiences whether you have already taken the PsoProtectMe survey or not.
Join a project group to help shape dermatology services in Lancashire and South Cumbria - EXTERNAL OPPORTUNITY
NHS Clinical Commissioning Groups in Lancashire and South Cumbria (with the exception of West Lancashire), who buy health services on your behalf, are looking to procure new dermatology services and as part of the procurement, they would like to recruit some patient reps to help them shape how the services will look in the future.
The project group will meet online monthly for the next 12 months for around an hour. They will provide training and support to any patient reps so you don’t need to worry if you haven't done anything like this before. The patient reps will help design surveys, new patient materials, website content etc.
If you would like more information before committing to become a patient rep, please contact Bwdandeast.firstname.lastname@example.org.
Support the PsoProtectMe registry by sharing your experiences of psoriasis during the COVID-19 pandemic
The team behind the PsoProtectMe psoriasis and COVID-19 registry would be interested to hear more about how the pandemic has affected you in relation to your psoriasis.
Would you be happy to share a quote or a short written piece (250 words or less) about your experiences? Would you be happy for your experiences to be published (including on social media) in order to raise awareness of the PsoProtectMe initative?
If so, please contact email@example.com to register your interest in taking part.
We would be keen to hear your experiences whether you have already taken the PsoProtectMe survey or not.
Share your story with us
Are you inspired by other people's stories and interested in sharing your own experiences of psoriasis and/or psoriatic arthritis? Would you like your story to be featured on our website, and on our social media channels?
We are looking for...
- Your story of life with psoriasis or psoriatic arthritis (or both) in your own words
- Ideally 400 words or less (if you want to write more, that's fine too)
- A photo of yourself to accompany your story (you can provide as many photos as you like)
If you're interested in taking part and sharing your story, or you'd like more information about the project, please contact us at firstname.lastname@example.org
Take part in our new 'Active Lifestyles' Photoshoot (now due to take place in 2021)
The Psoriasis Association is currently looking for participants for our exciting new ‘Active Lifestyles’ photoshoot.
We are launching an exciting new project to refresh the look and feel of our website and promotional materials with a brand new set of vibrant images and photographs that focus on an active lifestyle.
It is hoped that the new images will show a more holistic approach to living with psoriasis, which shows the condition as one part of someone’s life, which does not have to stand in the way of them doing anything they want to do.
So, if there is a hobby or sport that you enjoy and would be interested in having your photo taken while participating in, then please do let us know. We are particularly interested in activities including swimming, cycling, dog walking, painting, rambling, reading, cooking, or chatting with friends.
The photoshoot will take place next year (2021) in venues around Northamptonshire using our head office as a base. The specific date has not yet been set due to current circumstances with COVID-19, however we are keen to get a feel for who might like to be involved.
For further details, or to register your interest, please contact Dominic Urmston via email at email@example.com.
We are always looking for volunteers who would like to help us with our work whether this is by becoming a media contact, reviewing our information or speaking at events or conferences. If you would like to be involved with any of the opportunities listed below please fill in this form and send it to firstname.lastname@example.org.
Whilst we try our best to match all of our volunteers with relevant opportunities, please keep in mind that due to the specific requirements of some requests we cannot guarantee you will be contacted.
Become a media contact
often receive requests from journalists at newspapers and magazines, or
production staff at TV companies looking for case studies. Sometimes we also
contact the media ourselves to raise awareness of Psoriasis Association events
and achievements. If you’d be willing to share your experiences of psoriasis or
psoriatic arthritis and raise awareness through the media, let us know.
Review our information
We're committed to producing high quality information about psoriasis and receiving feedback from people living with the condition is key to ensuring our information is accessible and easy to understand.
We regularly produce new information sheets and leaflets about psoriasis, psoriatic arthritis and their treatments and we are looking for people based in the UK who would like to feedback on our new and existing information.
Volunteer to be an event speaker
Occasionally we need people with psoriasis or psoriatic arthritis to share their experiences at an event such as a conference or lecture, support group or meeting. If you might be interested in any opportunities to tell an audience about your psoriasis let us know.
Join a consultation panel
Join a consultation panel if you’re happy to be contacted to offer your opinion or comment on anything from our own services and literature to taking part in industry or academic initiatives.
Distribute our posters or leaflets
If you’d like to take our literature into your local GP surgery or Dermatology clinic, do let us know and we can send you some information to distribute.
Join our Research Network
To receive emails with opportunities to take part in or to help shape psoriasis research sign up to our Research Network. Please note, these opportunities may come from third parties e.g. academic researchers as well as from the Psoriasis Association.