Latest posts from the chronic-illness indie web — page 9

  1. 241.

    Hitting the Target? ME/CFS and long COVID T-cell Researchers on Uncovering the Precise Drivers of the Illnesses

  2. 242.

    This Is What Lockdown Looks Like for Me — And It Never Ends

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    Activity & Pacing Diary: a printable 4-week, hour-by-hour tracker for ME/CFS pacing

  1. 243.

    Carers Week 2026: Yvette’s Story

  2. 244.

    The Truth According to Wired (and Alan Levinovitz)

  3. 245.

    The ME Association joins other organisations to sign an open letter to the Royal College of Psychiatrists

  4. 246.

    Carers Week 2026: Dave’s Story

  5. 247.

    All About Me: Living With Myalgic Encephalomyelitis (ME/CFS)

  6. 248.

    ME/CFS Scottish Parliament | NHS debate | June 2026

  7. 249.

    WeakNotes 2026-06-05

  8. 250.

    The Elephant in the Room: the NIH, Long COVID, ME/CFS, POTS and Post-infectious Illnesses

  9. 251.

    BBC Radio Gloucester | ME/CFS Research Funding - Part 1

  10. 252.

    Living With De Quervain’s Syndrome: My Experience, Symptoms and Treatment

  11. 253.

    ME Awareness Week: ME/CFS Friendship Group organise an information stand at Gloucestershire Hospitals NHS Foundation Trust

  12. 254.

    BBC Radio Gloucester | ME/CFS Research Funding

  13. 255.

    Major Study Finds Autoimmune long COVID Subset

  14. 256.

    ME Association provides information for BBC Morning Live interview with Dr Ranj on ME/CFS

  15. 257.

    BBC Morning Live Explains ME/CFS After Viewer Feedback

  16. 258.

    Eight-year-old Chester school boy takes on 50 mile bike ride for ME/CFS in honour of his mum

  17. 259.

    London To See Darren Criss: A Journey I Will Never Forget

  18. 260.

    BBC Morning Live covers ME/CFS – ME Association Response

  19. 261.

    Gordon family issue an update on Karen health and emails from NHS ESHT solicitors

  20. 262.

    Interview with Chris Ponting about “Sequence ME & Long Covid”

  21. 263.

    Announcing Fanfiction.lol: A Manifesto on Human Creativity and AO3

  22. 264.

    WeakNotes 2026-05-30

  23. 265.

    I Was No Longer Living, I Was Existing

  24. 266.

    Homelab For the Beginner: You Can Self-host Your Own Server on $50 Hardware

  25. 267.

    Geoff’s Hyperadrenergic POTS Saga and a Blood Vessel Subset Shows Up

  26. 268.

    Actionable Steps to Build Shame Resilience

  27. 269.

    My Exchange with an FND Physical Therapy Specialist

  28. 270.

    Oxford ME/CFS Research: Highlights and Final Report (2019–2026)