1. Guest, the 'News in Brief' for the week beginning 14th June 2021 is here.
    Dismiss Notice
  2. Welcome! To read the Core Purpose and Values of our forum, click here.
    Dismiss Notice
  3. Contribute to feedback on the CDC Evidence Review, for more details click here
    Dismiss Notice

Civil Service blog - Personal Disability Stories - Kays story (ME sufferer)

Discussion in 'General ME/CFS News' started by Sly Saint, May 4, 2019.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

    Messages:
    6,141
    Likes Received:
    50,377
    Location:
    UK
    https://civilservice.blog.gov.uk/2019/05/03/personal-disability-stories-10-kays-story/
     
  2. chrisb

    chrisb Senior Member (Voting Rights)

    Messages:
    3,370
    Likes Received:
    23,325
    It is just a shame that the civil service does not seem to have such a concern for those not in its employ.
     
    Wonko likes this.
  3. NelliePledge

    NelliePledge Moderator Staff Member

    Messages:
    8,113
    Likes Received:
    47,995
    Location:
    UK West Midlands
    May not be immediately obvious but this isn’t a standard Civil Service example. She is a member of the armed forces not a civil servant. Civil servants get treated like employees in any large organisation depending on their immediate line managers it could be fair or it could be terrible. Occupational health advice is all on a private contact. Whereas health in the military is in house to an extent.

    In this individual case she clearly is accepting so far despite her relapse of the NHS approach or at least not willing or able to say anything different here. I didn’t pick out any mention of severe ME or of many having to give up work. I hope she is able to get back to work in the summer it will be interesting to hear how she is doing in 12 months time.

    This is in true civil service style representing the status quo. However I take a couple of positives out of it in the references to energy management and even a link direct to Jason paper. A mention of ME awareness which this is clearly timed for and at least it links to ME Association for more information.


    ETA. I should make it clear that if I had written this when I was doing the very gradual phased “return to work” my manager was flexible enough to allow I would have written a similar article. I had absorbed the AFME materials and believed it was achievable to return to working 85% of full time which was my contract at the time. I aimed for 40% of full time which I did achieve but only by continuing to go beyond my capacity and it was not sustainable.
     
    Last edited: May 6, 2019
    ladycatlover, Hutan, Amw66 and 4 others like this.

Share This Page