M.E, Myself and I

Award winning drama web series based on the experiences of real life M.E sufferers, which hopes to shine a spotlight on the issues sufferers face.

[M.E, Myself and I @MEdramaseries]

M.E, Myself and I - Episode 6 (The final episode). Watch now: https://t.co/kzs6x8Ajt6 #pwME #MECFS #MEawareness #MyalgicEncephalomyelitis #MyalgicE #LongCovid #Hiddendisability #invisibleillness

[#MEAction Scotland @meactionscot]

Take action for World ME Day 2024!

Call on the United Kingdom to become a #GlobalVoiceForME

https://t.co/KNgHGlg54q

#TeachMETreatME #MillionsMissing

[Hope 4 ME & Fibro NI @hope4mefibroni]

🌍 Today, on World M.E. Day, we stand in solidarity with the millions worldwide affected by Myalgic Encephalomyelitis (M.E.). 🌍

Join us in spreading awareness, breaking stigmas and fostering hope for a future where M.E. no longer limits lives💙

#WorldMEDay #MEAwareness

[M.E, Myself and I @MEdramaseries]

So thank you for covering M.E and promising to return to the topic at a later date. I will say however please mention that even though it’s more common in females, males do get M.E too. I was 12 when I was diagnosed and as a teenage boy I felt like I was some anomaly.

[M.E, Myself and I @MEdramaseries]

@thismorning thank you for covering M.E today on your show. I tried for years to get through to you as I always felt M.E needs more spotlight on it from shows like yourself. I even wrote and directed a film about my experiences in the hope to help shine a light.

[Out for a Film Media @outforafilm]

Add some Movie Magic into your Hen or Stag party, fulfil you or your loved ones Birthday dreams or even a unique way to celebrate your wedding? Well look no further! We can’t wait to create something for your special occasion! #birthdayparty #northwaleswedding #northwales

[M.E, Myself and I @MEdramaseries]

If like me you are in need of a laugh lately. The final outtakes: https://t.co/OJiR7Zv5hN #MyalgicE #film

[M.E, Myself and I @MEdramaseries]

@VancityReynolds @RMcElhenney I always am really bad at this stuff. But any chance you could share our North Walian community made film highlighting the illness M.E. Today is #MEAwarenessDay

[M.E, Myself and I @MEdramaseries]

Today is #MEAwarenessDay. I was diagnosed with M.E when I was 11. I spent over a decade of my life house bound. In 2016 I started writing a drama about some of my experiences. This is the complete series. I hope it helps people. https://t.co/04MRJpBg2J #MECFS #spoonie

[M.E, Myself and I @MEdramaseries]

Today is #MEAwarenessDay. I was diagnosed with M.E when I was 11. I spent over a decade of my life house bound. In 2016 I started writing a drama about some of my experiences. This is the complete series. I hope it helps people. https://t.co/04MRJpBg2J #MECFS #spoonie

[ME Association @MEAssociation]

Today is International ME/CFS Awareness Day!

ME/CFS is a complex multisystem disease with a wide range of disabling symptoms.

Factsheet: What you need to know about ME/CFS is available to download for free via the link below:

https://t.co/SPiui0f6OS

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #MEAwareness #MEAwarenessDay #MEAwarenessWeek #MEAW2023

[M.E, Myself and I @MEdramaseries]

Today is #MEAwarenessDay. I was diagnosed with M.E when I was 11. I spent over a decade of my life house bound. In 2016 I started writing a drama about some of my experiences. This is the complete series. I hope it helps people. https://t.co/04MRJpBg2J #MECFS #spoonie

[Action for ME @actionforme]

For this #WorldMEDay, we want to highlight the devastating impact of post-exertional malaise (PEM) on people with severe and very #SevereME.

[ME Association @MEAssociation]

Booklet: Diagnosing #MECFS – The Importance of an Early & Accurate Diagnosis.

If you are currently going through the #diagnosis process, this comprehensive booklet has everything you need to know.

https://t.co/Zx3JfCUIIS

#pwME #MyalgicE #MEAwarenessWeek #MEAW2023

[ME Association @MEAssociation]

Leaflet: Explaining ME/CFS to Other People

If you are struggling to explain ME/CFS to others, please find our free leaflet available as a direct download here:

https://t.co/pu89mSxARj

#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #MEAwareness #MEAwarenessWeek #MEAW2023

[M.E, Myself and I @MEdramaseries]

M.E, Myself and I - Episode 6 (The final episode). Watch now: https://t.co/kzs6x8Ajt6 #pwME #MECFS #MEawareness #MyalgicEncephalomyelitis #MyalgicE #LongCovid #Hiddendisability #invisibleillness

[M.E, Myself and I @MEdramaseries]

@treeshadefrance Thank you so much. Congratulations to you as well. Using creativity to talk about M.E is such an important and vital way to raise awareness.

[M.E, Myself and I @MEdramaseries]

#MEawarenesshour Check out the 6th and final episode of our show. The first drama series focusing on #MECFS. Watch and share. This has been a 7 year endeavour. https://t.co/kzs6x8Ajt6

[M.E, Myself and I @MEdramaseries]

Don’t forget to check out all the wonderful work done by charities and organisations such as: @MEAssociation @MEActNet @tymestrust @actionforme @IrishMECFSAssoc and sooooo many more. Feel free to tag other organisations and individuals who deserve the recognition. #MEawareness

[M.E, Myself and I @MEdramaseries]

M.E, Myself and I - Episode 6 (The final episode). Watch now: https://t.co/kzs6x8Ajt6 #pwME #MECFS #MEawareness #MyalgicEncephalomyelitis #MyalgicE #LongCovid #Hiddendisability #invisibleillness

[M.E, Myself and I @MEdramaseries]

M.E, Myself and I - The Series finale. April 12th! #MyalgicEncephalomyelitis #MEAwareness #CFS #cfsme #longcovid

[M.E, Myself and I @MEdramaseries]

@MEAssociation @RydalPenrhos @TheWestonMale @ITVWales @BBCWales @BBCWalesToday @rjournal @northwaleslive @NWPioneer