💬 “What’s that badge?” “It’s for Severe M.E. - a condition that leaves thousands bedbound.” Start the conversation. Wear the badge. Support the cause. Buy now - bit.ly/4paVqPe #BedForSevereME #PJsAndProtocol #MEAwarenessHour

Slowly doing the behind the scenes BED for Severe M.E. stuff from the comfort of my sofa. You don't have to wait until 29th October to get involved! Check it out - www.mefoggydog.org/bed-for-seve... #pwME #MEcfs #BedForSevereME

After months of campaigning, ME Foggy Dog & @voiceswales.bsky.social are closing our petition for a dedicated Minister for Disabled People. 💔 8,909 supporters stood with us. The fight ends here but our advocacy continues. Thank you. 💙 mefoggydog.org/2025/09/16/p... #Disability #PwME

I've read the NHS 10 year plan multiple times but completely missed this! 'They' want to abolish local Healthwatch. Sharing this to reach more people (hint hint) I don't have the bandwidth to campaign on this but maybe YOU do? (again hint hint) localdemocracyandhealth.com/2025/09/14/d... #pwME

It's coming...... 29th October! All info - www.mefoggydog.org/bed-for-seve... #pwME #SevereME

Seen on backpacks, lapels, laptops, and lanyards - the BED badge is more than a pin. It’s a statement. Buy here - bit.ly/4paVqPe Support @SmileForMEUK & @MEcfsBiobank this 29th Oct. #BedForSevereME #PwME #SevereME

Time for change 🩵 #pwME #MyalgicE Shop - www.mefoggydog.org/shop/

No treatment. No cure. No NHS protocol. But YOU can help. Buy a BED for Severe M.E. badge and support those living in silence. Let’s raise our voices for those who can’t. Buy here - bit.ly/4paVqPe #SevereME #BedForSevereME #PwME

Let’s make Severe M.E. visible. On 29th Oct, wear your ‘BED for Severe M.E.’ badge with pride. Every badge sold supports @SmileForMEUK and @MEcfsbiobank. Start a conversation. Buy here bit.ly/4paVqPe Spark change. #BedForSevereME #SevereME #PJsAndProtocol #pwME

We've been on TV, radio, and built a social media mini-empire, but we want to do more! Got an idea to help us spread the Foggy love and fight for the M.E. community? Get in touch! Let's make some noise together. 📣 #SocialEnterprise #GetInvolved 👉 www.mefoggydog.org/2025/08/20/f...

Every hero needs a sidekick... or in Foggy's case, a P.A.! Sally, who has lived with M.E. since 2007, is the human powerhouse behind our pup. Her incredible work even won her an 'Influencer' award! 🏆 #MEawareness #InvisibleDisability #PwME

Meet Foggy, the (soft toy) dog on a mission! With every paw-step since 2014, he has raised awareness for M.E. across the globe. We're a social enterprise giving 50% of our surplus to Cure ME for vital biomedical research. 🐾 #SocEnt #Health #TeamFoggy

🌫️ Living with M.E. isn’t just exhausting, it’s misunderstood. At ME Foggy Dog, we’re changing that. One blog at a time. 💬 From raw personal stories to sharp advocacy insights, these blogs shine a light on the realities of Myalgic Encephalomyelitis and the fight .. 1/2 #PwME #Advocacy

Who are ME Foggy Dog? Check out mefoggydog.org - everything you need to know can be found in one place! Blogs, a game, info - perfect! #pwME

Merging the #Disability Minister role with Social Security guarantees insufficient focus on the real issues. We won't stop demanding a dedicated Minister with the power to make change. This campaign isn't going away. Please sign and share: chng.it/vZfxTDjPGJ #Carers #UK #MEcfs

Disability rights need a full-time champion, not a part-time role diluted by other duties. We're still fighting for a dedicated Minister for Disabled People with real authority. Keep the pressure on, add your name now! chng.it/vZfxTDjPGJ #Disability #MEcfs

The current Minister for Disability has a clear conflict of interest, serving the DWP's agenda. We demand a dedicated Minister for Disabled People, a true advocate with cross-government power. We are not backing down. Sign the petition: chng.it/vZfxTDjPGJ #pwME #MEcfs #Carers #Disability

Sent formal complaint in Feb re: ME/CFS treatment harms. Govt ignored 9K+ voices. Escalated to Ombudsman in April, they can’t act unless Govt replies (how convenient 🙄). Still no response. Chasing again next week. #PatientSafety #MEcfs #NHS www.mefoggydog.org/2025/02/26/s...

Repost of our blog written in June 2025 - www.mefoggydog.org/2025/06/09/h... Context matters. This is not offensive language when in an M.E context. #pwME #Disability

A combined Social Security & Disability role fails us. We're petitioning for a dedicated Minister for Disabled People with real power across government. Let them know we're not giving up. Sign now! chng.it/vZfxTDjPGJ #pwME #Disability

He may have retired his travel paws, but Foggy's mission to raise M.E. awareness is just getting started. Let's make his next chapter even more incredible! #MEcfs #pwME

Foggy the Dog's globetrotting adventures are on hold, but his mission isn't! We're looking for creative minds to help shape his next chapter in raising M.E. awareness. Join us and let's keep the momentum going! #FoggyTheDog #PwME #SocEnt #VCSE www.mefoggydog.org/2025/08/20/f...

I had an interesting afternoon yesterday.... Ordered a new desk for Foggy HQ (sad times- NOSTALGIA- but necessary) and had a ☎️ chat with my knee specialist physio re my MRI results. I wasn't expecting anything to show up, but..... I have a 'loose object' inside my knee 😱. #pwME 1/2

*Foggy* We're off to the post office this morning! We've sold 6 #BEDforSevereME badges in the past week!! If you'd like your badge to be in the post TODAY, buy it by 10am ☺️ www.mefoggydog.org/product/bed-... #pwME #MEcfs

Imagine having an invisible debilitating illness, having no idea what caused it and having no prognosis. Welcome to the world of Myalgic Encephalomyelitis. Blast from the past! (c 2014) #pwME

Foggy's no longer a Globetrotting Adventurer, but his heart is still with the M.E. community! We're planning our next big adventure. Stay tuned! #pwME #MEcfs

On Oct 29th, we’re all about the #BEDforSevereME! 💖 For 25% of M.E patients, life happens mostly from bed. Let's champion better care & recognition for #SevereME, when even chewing can be a challenge. #pwME www.mefoggydog.org/bed-for-seve...

Want to spark a vital conversation? Our BED for Severe M.E. badges are doing just that - spotted everywhere from meetings to backpacks! Wear yours to make Severe M.E. visible & support Smile for ME & Cure ME. Get your badge & get talking! #BEDforSevereME www.mefoggydog.org/bed-for-seve...

For #SevereMEDay (Aug 8), we are remembering the lives of those lost with Severe M.E. We invite family and friends to honour their loved one by adding a memory to our 'In Loving Memory Board'. You can contribute here: www.kudoboard.com/boards/uGGhC... #MyalgicEncephalomyelitis

This #SevereMEDay, we hold space to remember the precious lives lost to this devastating illness. Their stories, told by those who loved them, matter deeply. Lost a loved one to M.E.? Please consider adding a tribute to our In Loving Memory Board. ➡️ www.kudoboard.com/boards/uGGhC... #pwME

On #SevereMEDay, my heart goes out to the millions trapped in darkened rooms, living with the devastating reality of this disease. To witness the raw, unfiltered truth, I urge you to watch the videos by Anil van der Zee - www.youtube.com/@anilaboutme Sending so much love and strength to 1/

That's it, I'm logging off. Back in a couple of weeks. Want to know more about M.E., ME Foggy Dog, or any of our campaigns? Go to mefoggydog.org 🛥️ 🛟 ⚓ #pwME #MEcfs

Watching Mad Men (again). Series 1 ep 2. Don Draper to Betty - 'Drs must love that they now have an answer for 'I don't know what's wrong'. Betty had been told she should see a psychiatrist as Drs couldn't find anything physically wrong. 🙄 Too familiar for #PwME

As #SevereMEDay approaches (August 8th), we want to honour those we have lost to #SevereME. We gently invite family and friends to share a memory, photo, or tribute on our 'In Loving Memory Board'. A space to remember them, through your eyes. ➡️ [https://www.kudoboard.com/boards/uGGhCBOt] #pwME

Because I am on holiday on 8/8, I'll schedule a post to mark the occasion this year (I'll be enjoying a 2 week digital detox 🥳). Severe M.E is always on my radar and I'm sending love to all affected by the severe end of our spectrum (#pwME and families). 1 day to go 🛥🛟⚓️

This Oct 29th, let's get into #BEDforSevereME! 🛌 It's more than just a bed; it's a sanctuary for those living with severe Myalgic Encephalomyelitis. Understand their unique needs & the daily battle they face. #SevereME #pwME www.mefoggydog.org/bed-for-seve...

*Foggy* 'Just'...... 😆🐶 #pwME www.bbc.co.uk/news/article...

Home. 'Neuro-exhausted'. That's the tweet. #pwME

Metal free and crumpled 🤷‍♀️🤭 MRI here I come. #pwME

Want to spark a vital conversation? Our BED for Severe M.E. badges are doing just that - spotted everywhere from meetings to backpacks! Wear yours to make Severe M.E. visible & support Smile for ME & Cure ME. Get your badge & get talking! #BEDforSevereME www.mefoggydog.org/bed-for-seve...

How are you doing M.Eeps? I'm just having a love-in with my camera-shy furbaby. Outside, nice and quiet 😊 #pwME

A selection of disability focused designs available in my Redbubble shop. I rarely see bedridden people represented in iconography and illustration around disability. www.redbubble.com/i/t-shirt/Va... #Disability #DisabledArtists #illustration #TeeDesign

The pre-holiday 'wind down' continues today 😊 Slow and gentle tiptapping on my laptop is in my future today. #pwME

Everyone watching #ITAENG who is a #pwME will know why I need us to win (or lose) in the next 30 mins. Penalties hurt my M.E (heartrate). Football is bad for my health!

🕰️ 9 months. That’s how long charities, orgs, and disabled people educated MPs on the reality of benefits. We did our job. MPs listened. And then… www.mefoggydog.org/2025/07/20/l... #pwME #WelfareCuts #TakingThePIP

This Oct 29th, let's take a moment for those who can't not be in bed. It's #BEDforSevereME awareness day! Severe ME is debilitating, with symptoms like paralysis & blackouts. No cure, no NHS protocol... YET! Your support matters. ❤️ #SevereME #MEcfs www.mefoggydog.org/bed-for-seve...

MPs who did their job and voted against the bill? Punished. Now it’s being steamrolled through the House of Lords as a Money Bill. No scrutiny. No debate. If it’s the right move, why avoid scrutiny? www.mefoggydog.org/2025/07/20/l... #DemocracyMatters #Disability #pwME

Let’s bust some myths: ❌ PIP fraud rate? Just 0.2%. ❌ “Economic inactivity”? Most disabled people pay taxes, or did before illness/#disability. ✅ Benefits aren’t wasted. They fuel the economy. But you wouldn’t know it from the headlines. www.mefoggydog.org/2025/07/20/l... #pwME

MPs who stood with disabled people? ❌ Silenced. ❌ Lost the whip. ⚠️ Labour said they “went against the team.” But what kind of team ignores disability rights? www.mefoggydog.org/2025/07/20/l...

Labour’s handling of the welfare reform bill proves one thing: they have a disability problem. No consultation. No accountability. Just cuts, spin, and silencing. 🧵Blog here 👇 www.mefoggydog.org/2025/07/20/l... #DisabilityRights #Labour #WelfareReform #pwME