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Blog Archive

  • Speak Up for ME and Fibromyalgia

    Speak Up for ME and Fibromyalgia

    25% of people with ME/CFS are severely ill, leaving them housebound or bedbound.Funded by a Healthwatch Sheffield #SpeakUp Grant, Sheffield ME and Fibromyalgia Group are conducting a survey and focus groups to help improve access to health and social care support for people living with the conditions.

    FULL ARTICLE
  • Jingle and Mingle with Sheffield ME Group

    Jingle and Mingle with Sheffield ME Group

    Sheffield ME and Fibromyalgia Group is hosting a Jingle & Mingle online Christmas festival from the 14th to 18th of December, designed for people with ME/CFS, Fibromyalgia and/or long Covid symptoms.The group describes it as a great opportunity for people with chronic illnesses to feel less isolated in the Christmas period and to socialise with others who understand their condition.

    FULL ARTICLE
  • Get Together at the Octoberfest

    Get Together at the Octoberfest

    Sheffield ME Group are hosting a series of online activities from the 5th to the 23rd of October designed for people affected by ME/Chronic Fatigue, Fibromyalgia and/or long Covid symptoms. It’s their very first Octoberfest. Their October calendar has daily events including , mindfulness, nutrition, playreading, singing and writing workshops and a murder mystery! Get together and share good moments with people who understand your condition.

    FULL ARTICLE
  • Job Opportunities at Sheffield ME And Fibromyalgia Group

    The Sheffield ME and Fibromyalgia Group is advertising three new vacancies. Please note that the deadline for applications for the Activities Co-ordinator post is Monday October 15th and the deadline for the Information Officer and Benefits Advisers posts is October 22nd.

    FULL ARTICLE
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Disability Sheffield is a forward-thinking, energetic organisation doing a lot of positive work in Sheffield. I have no doubt they will continue to do so for a long time to come.
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Ruth

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When I moved to Sheffield nearly five years ago it was my "go to" organisation. I expect it to stay that way. All the staff and volunteers seem to pull out little gems of effort that disabled people like me couldn't do without. Professionally and personally - I love em :)
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