@Linda_ANP Profile picture

Linda campbell

@Linda_ANP

Advanced Nurse Practitioner Down GP Federation. Chair & Educational Advisor Hope 4 ME & Fibro NI charity. Mum to son with Myalgic Encephalomyelitis for 14 years

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Linda campbell Reposted

“You can’t be clapped one minute, and declared disposable the next.” This week, RCN member Patricia Temple told the COVID-19 Inquiry how nursing staff with long COVID have been abandoned. We're calling on the UK government to classify long COVID as an occupational disease.…


Linda campbell Reposted

Other sources in the press have directly linked the death to a vascular event in #LongCovid but this remains to be officially confirmed, I think wwd.com/fashion-news/f…


Linda campbell Reposted

Charity begins at home. Today we started a monthly initiative at RSU Riga to empower our own colleagues, medical students with knowledge of post viral chronic diseases. It was an amazing evening. Full dose of Foods, drinks and science for one hour.

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Linda campbell Reposted

The Health Minister heard how multi-disciplinary teams are helping patients across the Causeway area. Minister Nesbitt met Causeway GP Federation and said MDTs in primary care settings are "one of the biggest success stories of recent years in transforming our health service."

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Very best wishes to you @taraand14 in your Pancreatic Cancer research endeavours! @hope4mefibroni

Meet Tara Anderson - @taraand14 She is one of four NIPANC supported PhD research students we are partnering with in collaboration with @QUBelfast Their work helps us get a better understanding of #PancreaticCancer Read more here: nipanc.org/post/phd-resea…



Well done to the ME advocates in Brazil 👏👍 @hope4mefibroni

Impressive advocacy in Brazil by Ivana Andrade and Mariana Ceratti meeting with Minister for Health Nisia Trindade on behalf of people with ME. The World ME Alliance will continue to support this important work! #MyalgicEncephalomyelitis #MECFS #pwME #EMSFC

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Many congratulations Louise! 🎉👏

Newry & District GP Federation would like to congratulate Advanced Nurse Practitioner, Louise Rush, on achieving her MSc in Advanced Nursing Practice. 🌟👩‍🎓🎓🥇 Louise is currently working in Summerhill Surgery and Mourne Family Surgery as an ANP. We wish Louise every success in…



Many congratulations Mairead! 💪👏

🌟Craigavon GP Federation would like to congratulate Advanced Nurse Practitioner, Mairead Watson on achieving her MSc in Advanced Nursing Practice . 🌟👩‍🎓🎓🥇 Mairead is currently working as an ANP in Brownlow Health Centre. We wish Mairead every success in her role as an ANP.🌟…



Many congratulations indeed ladies! 🎉👏

🌟Armagh Dungannon GP Federation would like to congratulate Advanced Nurse Practitioners, Joanne Maguire, Grainne Kelly and Amy Robinson on achieving their MSc in Advanced Nursing Practice. 🌟👩‍🎓🎓🥇 They are currently working as ANPs across practices in Armagh Dungannon…



Many congratulations indeed @rita_rdevlin29 a very well deserved honour!

Many congratulations @rita_rdevlin29 on your appointment of Honorary Professor of Practice. A wonderful acknowledgement of your work on behalf of Nursing in N.Ireland. @RCN_NI @holden_l



Linda campbell Reposted

This is proper consideration for patients & would certainly minimise #PEM for those with #ME & #LongCovid in all sorts of venues, including medical appointments 👇

This spinal CSF leak conference has cots set up for patients to lie down while listening to the talks! 👏 I wish all conferences did this.

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Great idea! Any knowledge of where to hire such a thing?

This spinal CSF leak conference has cots set up for patients to lie down while listening to the talks! 👏 I wish all conferences did this.

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Linda campbell Reposted

Stigma is common in #MECFS A Doctor called an ME charity worried they had ME because their practice had a policy to treat patients with ridicule and rejection. They were going to pretend to retire on grounds of depression because it has less stigma than ME. Nigel Speight 2017

Clip from James O'Brien on LBC: Hannah talks about her mum a retired doctor with #LongCovid and how her family of doctors, find it hard to believe because they see it in a similar category to ME.



Linda campbell Reposted

Suffering through years of diagnostic delay and misdiagnosis is not acceptable! Help us reduce diagnostic delays in #POTS and other forms of dysautonomia by making a contribution to support our clinician education programs at CureDys.org. #DysautonomiaAwarenessMonth

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Linda campbell Reposted

Found perfect pic for #MyalgicEncephalomyelitis #PEM Skull removed-sound too loud-light too bright-brain burning-extremities burning-nausea raging-pain soaring muscles/joints-bed floating on rough sea-temp paralysis with great desire to crawl out of own body & no relief just wait

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Linda campbell Reposted

🔎 Some parliamentary questions spotted today from @johnmcdonnellMP about research funding for #ME and #LongCovid. theyworkforyou.com/wrans/?id=2024…

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Linda campbell Reposted

UK Covid Inquiry 29 Oct Q: Is future planning & resourcing for LC care adequate? “I’m really concerned the clinical care & expertise has reduced, I’m concerned what it will look like a year from now. It’s (longcovid) not going away” @REvans_Breathe @covidinquiryuk


Many congratulations! 🎉 @maura_devlin

Massive congratulations to the one and only @maura_devlin ! An accolade that is so well deserved 👏congratulations from all the elective team 🥳@ni_gpecs @sinead1306 @EasternGp



Totally agree @bendymarsh

For those just learning about the history of the treatment of #MECFS #PwME please watch this excellent summary of how such deliberate neglect & minimising came to be dialogues-mecfs.co.uk/films/the-tang…



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