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  1. JellyBabyKid

    Monitoring app - Visible - a platform "designed for any invisible illness that benefits from resting and pacing - including ME/CFS & Long Covid."

    Yes. Me. I score every morning immediately on waking and record symptoms every night. I recently added to which symptoms I track. I also message the team with any issues I find. I have not paid out for premium though, as I just bought a fitness tracker watch for less than twenty quid on amazon...
  2. JellyBabyKid

    UK Government ME/CFS Delivery Plan (includes Attitudes and Education Working Group and Living with ME Working Group) and consultation

    @Andy This is massively helpful, thank you very much! :thumbup: I was trying to get to a simple set of instructions, but currently very foggy brain wasn't cooperating:facepalm:
  3. JellyBabyKid

    UK Government ME/CFS Delivery Plan (includes Attitudes and Education Working Group and Living with ME Working Group) and consultation

    Thank you. Twitter is - understandably - getting a bit concerned about what all this means for the process. Especially that cannot access the consultation and the lack of publicity.
  4. JellyBabyKid

    UK Government ME/CFS Delivery Plan (includes Attitudes and Education Working Group and Living with ME Working Group) and consultation

    Seriously?! Surely this is something they do fairly regularly? Concerning that working group members are tweeting very publicly about not having had a copy either. All a bit fishy :emoji_fish: after what happened - and is still happening - with NICE
  5. JellyBabyKid

    Anomalies in the review process and interpretation of the evidence in the NICE guideline for (CFS & ME), 2023, White et al

    This makes me feel physically sick. What happened to going into medicine to help people? Or learning by 'standing on the shoulders of giants?' The hypocratic oath says "first, do no harm", right? I am thinking doctors should be forced to regularly re take their oath in the same way older...
  6. JellyBabyKid

    Pitching to Panorama: Efforts to commission a documentary on NICE guideline, bad science (PACE etc), and patient harm

    Can I ask which book? This has already been covered? Thanks! Gez Medinger and Danny Altman covered the ME situation really well in the Long Covid Handbook, which is a very good book. Gez is making a lot of short films on YouTube and talks to a lot of researchers. He might be a good person to...
  7. JellyBabyKid

    Long Covid in the media and social media 2023

    I wrote to complain about this week's incident. I didn't hear the previous one.
  8. JellyBabyKid

    UK: ME Association: Count ME In [survey]

    Done. They may regret asking, as I completed while fully PEM and more than a little grumpy "What improvements would you most like to see to the NHS that could improve your quality of life with regard to ME / CFS?" Not sure they were expecting an 8 point bulleted list...:whistle:
  9. JellyBabyKid

    UK Parliament: ME/CFS Announcements: Statement by Health Secretary Sajid Javid, 12 May 2022

    Followed your suggestion and also tagged in Frances Ryan so:emoji_fingers_crossed:
  10. JellyBabyKid

    Funding of ME/CFS research in the UK

    Thanks @ringding I refer back to post #31 on this thread, as I am part of the group working with with Alex Chalk
  11. JellyBabyKid

    Paul Garner on Long Covid and ME/CFS - BMJ articles and other media.

    I've just watched this segment on the BBC. Both were being presented as experts, but were discussing personal experience. Should this not have been made a lot clearer?! The plural of anecdote is not data
  12. JellyBabyKid

    UK - NHS England online tool and clinics for long Covid.

    An excellent explanation. Better than from some supposed experts...
  13. JellyBabyKid

    UK - NHS England online tool and clinics for long Covid.

    This is a really good, comprehensive letter. It really needs some good/big press coverage though
  14. JellyBabyKid

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    Update: I have had a lovely email from the New Scientist. They don't tend to report on project launches, preferring to report on results. They have made a note to keep an eye on this project.
  15. JellyBabyKid

    News about Long Covid including its relationship to ME/CFS 2020 to 2021

    Having a skim of this week's contents on the website : https://www.newscientist.com/issue/3292/ it's looking like my email didn't make any difference. Will double check when I download it tomorrow though.
  16. JellyBabyKid

    Waking up in the night and hearing a brain-generated sound

    I have had the sensation of my head feeling like it was actually exploding once while falling asleep. I have had tinnitus for about a year (different tone in each ear) i also get the extreme loud whine for a few seconds that then dissipates fairly regularly as well. I have that auditory...
  17. JellyBabyKid

    United Kingdom: North Bristol NHS Trust: ME/CFS clinic

    I think the idea is to teach people to be more "in the moment" and learn acceptance. It has been shown to be helpful in depression and pain management (Jon Kabat-Zinn has been credited for introducing it to the west and using it in this field, with good results) Personally i would feel...
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