Join the all-new week-long ME Pyjama Party and Raise Awareness for Myalgic Encephalomyelitis and Myalgic Encephalomyelitis week!

Each year, during ME Awareness Week in May and on Severe ME Day in August, we wear our pyjamas to shine a light on Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS).

🩵 It’s a simple but powerful way to show solidarity with those living with ME/CFS.

And the best part? Joining in is as easy as putting on your PJs!

How to Join the ME Pyjama Party

1️⃣  Put on your pyjamas – Whether you’re at home, work, or out and about, get comfy in your favourite PJs!

2️⃣ Take a picture – Snap a photo of yourself, your family, your colleagues, or even your pet in pyjamas!

3️⃣ . Post on social media – Share your PJ pics on your favourite platforms and tag us using the hashtag #MEPJParty

📢 Follow and tag us on social media:

📌 Facebook – ME Pyjama Party
📌 Twitter/X – @mepyjamaparty
📌 Instagram – @mepjparty

Why Your Support Matters

💙 Every post, every picture, and every hashtag helps raise awareness. ME/CFS is often misunderstood, and many people struggle without adequate support or funding for research.

🛏️ By wearing your PJs, you’re making a statement – You’re showing the world that ME/CFS deserves recognition, better healthcare, and more funding.

🙌 Together, we can make a difference.

Thank you for being part of this meaningful movement! I can’t wait to see all of your wonderful PJ pics.

Warm regards,
Alisha 💙

📢 Use these hashtags to spread the word:
#MEPJParty #SevereMEDay #MECFS #MyalgicEncephalomyelitis #InvisibleIllness #ChronicIllnessAwareness

More Blog Posts

Disabled people make up over 16 million in the UK, yet only a handful are represented in Parliament. This post explores the barriers disabled candidates face—like inaccessible campaigning, ableism, and lack of funding—and why increasing disabled representation is urgent for real political change.
The sight of the bustling crowds heading towards that beautiful fortress of a football stadium fills me with immense pride as a Scouser. The Scouse girls, as always, looked absolutely stunning, but their allure seemed to reach ethereal levels for the Taylor Swift concert.
Anfield is one of the most iconic stadiums in the world, but how accessible is it for disabled supporters? As a lifelong LFC fan, I recently attended an event at Anfield in a wheelchair—here’s everything you need to know about their accessibility services, ticketing, and top tips for an inclusive experience! Read the full guide to make the most of your visit and ensure a smooth experience at this legendary stadium. ⚽💙 #AccessibleAnfield #YNWA #DisabilityInSport
Living with ME/CFS means every bit of energy counts. In this post, I’m sharing the Amazon finds that help me manage daily symptoms, conserve spoons, and stay as independent as possible—from smart tech to mobility aids and comfort tools that truly make life a little easier. Let me know if you’d like a more playful, SEO-rich, or community-style version too! 💛
This blog shares my lived experience with ME/CFS flares—from symptoms like pain and cognitive fog to tools, medications, and routines that help me cope.
Struggling to access a dentist due to chronic illness or disability? Learn how domiciliary dental care changed everything for me in Liverpool.