Researcher looking for someone of African or Afri... - LUPUS UK

LUPUS UK

32,248 members28,606 posts

Researcher looking for someone of African or African Caribbean ancestry who has lupus to join PhD study

Chanpreet_Walia profile image
Chanpreet_WaliaLUPUS UK
5 Replies

PhD researcher, Suzanne van Even is looking for someone of African or African Caribbean ancestry who has lupus to join her PhD supervisory team as a patient research partner. For more information please contact: Suzanne van Even, Suzanne.Vaneven@uwe.ac.uk or 07873 618919.

"I am looking for someone of African or African Caribbean ancestry who has lupus to join my PhD supervisory team as a patient research partner. You don’t need to have any research or academic experience, the expertise you bring to the team would be your experience of living with lupus. We really need the input of someone who has experience of living with an autoimmune rheumatic disease to help shape this project.

You don’t need to have any research or academic experience, the expertise you bring to the team would be your experience of living with lupus. We really need the input of someone who has experience of living with an autoimmune rheumatic disease to help shape this project.

I am doing this research to find out how people with African and African Caribbean ancestry cope with having an autoimmune rheumatic disease. I am particularly interested in finding out how they cope with anxiety and depression which are often associated with having a chronic illness such as lupus.

The aim of the project is to get a better understanding of what the specific support needs are of people with African and African Caribbean ancestry, if they have any unmet support needs and how these can best be met.

The project is at its early stages and it would be fantastic to have your views as to how to shape it going forward with your guidance, lived experience and suggestions.

There aren’t any formal requirements for this role, but you would need to have African or African Caribbean ancestry, be aged 18+, live in the UK and be happy to meet using online platforms (for example Microsoft Teams, Skype or ZOOM)."

Contact Suzanne van Even, Suzanne.Vaneven@uwe.ac.uk or 07873 618919.

Written by
Chanpreet_Walia profile image
Chanpreet_Walia
LUPUS UK
To view profiles and participate in discussions please or .
Read more about...
5 Replies
djsema profile image
djsema

Good evening, I can help if you need me.

Chanpreet_Walia profile image
Chanpreet_WaliaLUPUS UK in reply todjsema

Hi, thank you for expressing your interest in this research. Please contact Suzanne van Even at Suzanne.Vaneven@uwe.ac.uk or on 07873 618919.

Kuntxd profile image
Kuntxd

Hello I’m interested, is this paid or voluntary?

Chanpreet_Walia profile image
Chanpreet_WaliaLUPUS UK in reply toKuntxd

Hi, thank you for expressing your interest in this research, I believe this research is voluntary.

I-am-AKA profile image
I-am-AKA

Hello, I'm interested in being part of your research & have sent you an email

Not what you're looking for?

You may also like...

"A Year Since Lockdown" Online Survey - NOW CLOSED

***THIS SURVEY IS NOW CLOSED*** Thank you so much to everyone who took the time to complete it...
Paul_Howard profile image
Partner

RAIRDA Survey - Please spare a few minutes to complete it

Hi everyone, The Rare Autoimmune Rheumatic Diseases Alliance (RAIRDA) has just launched a new...
Paul_Howard profile image
Partner

The Rare Autoimmune Rheumatic Diseases Patient Survey

If you have a rare autoimmune rheumatic disease such as lupus, scleroderma or vasculitis, please...
Paul_Howard profile image
Partner

Press Release: People with rare autoimmune rheumatic diseases at increased risk of death during COVID-19 pandemic.

The National Disease Registration Service at Public Health England and the British Society for...
Paul_Howard profile image
Partner

RAIRDA launches survey for patients in Wales

Hi everyone, The Rare AutoImmune Rheumatic Disease Alliance (RAIRDA) has launched a survey for...
Paul_Howard profile image
Partner