Researchers at the University of Aberdeen who are part of the Advanced Pain Discovery Platform [APDP] (apdp.community/ and the PAINSTORM consortium painstorm.co.uk) want to understand what it is like for you to live with Neuropathic Pain (Nerve pain).
Would you be willing to take part in a telephone interview and/or two focus groups that last around one hour each? More information can be found here: abdn.ac.uk/iahs/academic/pr...
If you are willing to help with this research and/or would like more information, please email PAINSTORM@abdn.ac.uk for more information. Participants will be compensated for their time.
Thank you!
Do you live with Neuropathic Pain? Would you be willing to help us explore what it’s like living with Neuropathic Pain? You can find out more about the research at abdn.ac.uk/iahs/academic/pr... or phone Dr Katie Allan on 01224 437426 for more information. Participants will be compensated for their time.
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I reckon I can get you some volunteers from the CPSP group in our " Stroke Improvement Group". There's a lot of "what the daily challenge is like" there already
(The Stroke Improvement Group are a loose affiliation of people who believe that stroke care (all ABI care, all chronic care!!) will be significantly improved when institutions learn how to Listen & HEAR us and embrace digital community)
Hi, I have lived with nerve pain in my lower legs and feet for almost 10 years, from Peripheral Neuropathy. I have been diagnosed by Professor Sir Pir Mohamed, Consultant in Parmacogenetics Liverpool Royal, with PN due to the antibiotic Ciprofloxacin. This antibiotic has caused me other injuries, if you are interested, I can tell you about those further down the line.
Hi Defenders. Sorry to hear about the pain you are experiencing. If you are interested in taking part in our research, please email me at painstorm@abdn.ac.uk. Thanks
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