Today, on #LongCovidAwarenessDay I spotted this pamphlet on a real life bulletin board, how retro! It say "Lockdown over? Not for me." as it highlights the continuing struggle of people with #LongCovid - like myself. Link is to a fundraiser for more medical research by www.stichtinglongcovid.nl

Beste @laurensdassen.voltnederland.org & @ineskostic.bsky.social, staan jullie morgen in debat weer op voor alle #PAIS & #LongCovid patiënten? Ik zit thuis met #Lyme & #MEcfs. Met meer geld voor onderzoek & behandeling kan ik hopelijk weer aan de slag als onderzoeker klimaat en circulaire economie 🙏

Clip from an NOS news report about the PAIS protest in The Hague. Wheelchairs symbolised those too ill to attend. Patients with post-infectious illnesses: long COVID, ME/CFS, Lyme, Q-fever and sepsis are calling for proper research and treatment.

Indrukwekkend #paisprotest vandaag voor al die mensen die #niethersteld zijn van bijvoorbeeld long covid, ME/CVS, Lyme, Q-Koorts en andere PAIS. Vandaag kregen de mensen die in stilte lijden een stem. Nu is het aan de politiek om daar naar te luisteren.

If you can, please consider donating to the Open Medicine Foundation this November. Your donation will be trippled 3️⃣✖️! OMF supports some of the most promising research to better understand and treat #MECFS & #LongCovid, which are making the lives of millions of patients deeply miserable. Thank you 🙏

Reassuring self-delusion: "participants in all wealth quintiles rated their personal carbon footprint far better than their perception of the carbon footprint of others would suggest. This was particularly striking among participants in the top 20% wealth group." www.nature.com/articles/s41...

📣 People with Long COVID face an increased risk of housing insecurity. Research shows this trend, which people with the disease have warned for years. Freelance reporter @jloeppky.com reports for @thesicktimes.bsky.social. thesicktimes.org/2025/06/17/l...

So, yeah... Being chronically ill isn't great, but it sure is expensive! After 10+ years of #Lyme and #MEcfs with years of #LongCovid on top, I realised I'm easily down (€) 200k in lost income and 50k in extra expenses. Could have bought a house, instead I buy supplements.

This is my 9th year advocating for #MyalgicEncephalomyelitis #MillionsMissing #MEAwarenessMonth. My health has only worsened since then (9 years ago I was able to work FT! Now I can't even work PT and am mainly housebound), but I'm hopeful because: (1/6)

New from Germany: Brainstem Reduction and Deformation in the 4th Ventricle Cerebellar Peduncles in Long COVID Patients: Insights into Neuroinflammatory Sequelae and “Broken Bridge Syndrome” www.medrxiv.org/content/10.1... #LongCovid #NeuroPASC 1/

Mood today. "I was still sick [...]. Feeling something like a cornered animal, I cast about in my mind for some way out of the maze, but could see none. Still my brain responded with a refusal to give in." From 'Lyme with a twist', by Lowell Miller. 📖

NEW: Cuts to Columbia University funding have shuttered a prominent research center into ME/CFS, a debilitating condition with no FDA-approved treatments. It's a gut punch to a community that for years has been frustrated by a lack of funding. Developing... www.statnews.com/2025/03/19/m...