ME Foggy Dog

I've developed a love for homemade Hummus.

The olive oil / chickpeas help with perimenopause stuff too.

Win - win! (Part of the losing weight stuff).

No - I am not doing weight-loss jabs (in case you were wondering!). I'm sensitive to too many chemicals/medications- too risky for me personally

Donate to Support BED for Severe M.E. | ME Foggy Dog Each organisation is doing vital work to support those affected by Severe M.E., and we want to help them go even further.

*Foggy* The JustGiving pages for
CureME/MEcfs biobank and
@smileformeuk.bsky.social
are live on the #BEDforSevereME webpages now!!!! Whoop!!!

Check it out! mefoggydog.org/bed-for-seve...

29th October here we come!!

#pwME #MEcfs #SevereME

We are thrilled that #BedForSevereME is coming soon (29th Oct!), but we need YOU! Help us raise funds for @SmileForMEUK and Cure ME/ @mecfsbiobank . Share, donate, spread the word. Let’s make this huge! 💙 #pwME #SevereME #PJsAndProtocol

Whole video - youtube.com/live/L-YCeTq...

I don't doubt it. Reform are getting backs up by saying the quiet part out loud. Factions of other parties will be saying this behind closed doors.

*Foggy* Stinky!!!

The upper part of my body is smothered in Deep Heat.

I smell like a rugby player....without the exertion.

Pain in my shoulder blade, neck, shoulder, upper arm still hasn't eased.

Heat pads and meds haven't worked so far.

#pwME

YouTube video by M.E Foggy Dog Myalgic Encephalomyelitis International Consensus Criteria

International Consensus Criteria within our campaigning and social entrepreneurship. #pwME #MEcfs #Health #ChronicIllness

⚠️ Warning - movement in video may not be suitable for some #pwME with visual disturbance.

youtu.be/RKuCjV37dQw?...

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How is Myalgic Encephalomyelitis (M.E) diagnosed?

There is no test but there are numerous diagnostic criterion available (some better/more scientifically rigorous/reliable than others) for clinicians to use to give a clinical diagnosis.

ME Foggy Dog prefers to use the M.E.

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💬 “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

BED for Severe M.E. | ME Foggy Dog 8th August 2024 will mark the first annual BED for Severe M.E. Campaign! 25% of people living with Myalgic Encephalomyelitis are severely affected. Those living with Severe M.E are either bedbound and...

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

Petition Closed: The Campaign for a Dedicated Minister for Disabled People Ends, Here’s Why | ME Foggy Dog ME Foggy Dog and Voices Adfocad have made the difficult decision to close our petition calling for the creation of a dedicated Minister for Disabled People.

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

Don’t Silence the Patient Voice: Why Abolishing Healthwatch is a Mistake Abolishing local Healthwatch is NOT a foregone conclusion – now is the time for MPs and national and local allies to defend independent public voice in health and care The NHS 10 year plan fl…

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

From Passport to (Increased) Purpose: What's Next for Foggy? | ME Foggy Dog Foggy has been a globetrotting adventurer with a purpose, raising funds and awareness for M.E, for over a decade. It's time to plan his next chapter.

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

Blog | ME Foggy Dog For over a decade, Foggy the Dog has been more than just a cuddly companion; he’s been a globetrotting force for good. With purpose, he’s zipped across the Atlantic, lounged by a pool in Mexico and in...

for #disability justice. Whether you're navigating chronic illness yourself or want to be a better ally, there's something here for you.

🔗 Dive into the archive, challenge your perspective, and join a community that refuses to be invisible. 👉 mefoggydog.org/blog
#MEcfs 2

🌫️ 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 ..

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#PwME #Advocacy

ME Foggy Dog - Adventures of a soft toy, raising money for M.E. Research Foggy is a soft toy dog on an adventurous quest to raise awareness and fund for M.E. research. Foggy's favourite human has M.E./C.F.S.

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

Thanks for sharing!

We Can Make an Impact. Create a Dedicated Minister for Disabled People Role

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

We Can Make an Impact. Create a Dedicated Minister for Disabled People Role

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

We Can Make an Impact. Create a Dedicated Minister for Disabled People Role

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

Shake It UP - Formal Complaint re Negligence in Patient Safety | ME Foggy Dog Shake It Up demands the creation of a reporting system to report adverse events from non-pharmaceutical 'treatments'. This formal complaint is the next step.

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...

'House-or-bedbound': Accurate Lived Experience, Not Offensive Language | ME Foggy Dog As we navigate the complex realities of energy-limiting conditions like M.E, we can sometimes find ourselves at the crossroads of language and lived experience

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

We Can Make an Impact. Create a Dedicated Minister for Disabled People Role

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