Charity number: 1036419 / SC040452
@longcovidsupport.bsky.social
@longcovidkids.bsky.social
PoTS UK
Mast Cell Action
@longcovidsupport.bsky.social
@longcovidkids.bsky.social
PoTS UK
Mast Cell Action
The OIA also launched its first resource (a brief guide for parliamentarians) which is available on the OIA's website, along with a list of attendees 👇
www.overlappingillnessalliance.org.uk/parliamentar...
#OverlappingIllness #OIA #MECFS #MCAS #PoTS #PoTSUK#EhlersDanlos #EDS #LongCovid
The OIA also launched its first resource (a brief guide for parliamentarians) which is available on the OIA's website, along with a list of attendees 👇
www.overlappingillnessalliance.org.uk/parliamentar...
#OverlappingIllness #OIA #MECFS #MCAS #PoTS #PoTSUK#EhlersDanlos #EDS #LongCovid
Thank you to everyone who contacted their MP 🧡
Almost 80% of all MPs received constituent requests to attend - your voices truly made a difference
Attendees recognised how essential this joined-up, collaborative approach is for driving change & strengthening our collective voice 🗣️
#pwME
⬇️
Thank you to everyone who contacted their MP 🧡
Almost 80% of all MPs received constituent requests to attend - your voices truly made a difference
Attendees recognised how essential this joined-up, collaborative approach is for driving change & strengthening our collective voice 🗣️
#pwME
⬇️
Thank you to everyone who contacted their MP 🧡
Almost 80% of all MPs received constituent requests to attend - your voices truly made a difference
Attendees recognised how essential this joined-up, collaborative approach is for driving change & strengthening our collective voice 🗣️
#pwME
⬇️
Thank you to everyone who contacted their MP 🧡
Almost 80% of all MPs received constituent requests to attend - your voices truly made a difference
Attendees recognised how essential this joined-up, collaborative approach is for driving change & strengthening our collective voice 🗣️
#pwME
⬇️
#ChristmasChallenge #MECFS #pwME #MyalgicE #MyalgicEncephalomyelitis
#ChristmasChallenge #MECFS #pwME #MyalgicE #MyalgicEncephalomyelitis
👥 Reduce the isolation experienced by young people with ME through access to our Young People’s Community and Peer Support services.
👥 Reduce the isolation experienced by young people with ME through access to our Young People’s Community and Peer Support services.
🧡 Continue to be a ‘lifeline’ for people with ME of all ages, through our online information and resources, which have been accessed 3,500 times by the ME community in the past year.
🧡 Continue to be a ‘lifeline’ for people with ME of all ages, through our online information and resources, which have been accessed 3,500 times by the ME community in the past year.
The drop-in was well-attended and we truly appreciate the MPs who attended and showed their support for people living with ME/CFS, PoTS, EDS, MCAS and long Covid.
A more detailed update will be shared by OIA members later this week!
#MyalgicE
The drop-in was well-attended and we truly appreciate the MPs who attended and showed their support for people living with ME/CFS, PoTS, EDS, MCAS and long Covid.
A more detailed update will be shared by OIA members later this week!
#MyalgicE
www.actionforme.org.uk/big-give-2025/
www.actionforme.org.uk/big-give-2025/
By donating during the Big Give Christmas Challenge campaign, you will be helping us to improve lives and accelerate understanding for people of all ages affected by ME.
By donating during the Big Give Christmas Challenge campaign, you will be helping us to improve lives and accelerate understanding for people of all ages affected by ME.
It will also include recommendations that outline the steps that must be taken to improve the care and support available.
The report will be shared with all MPs and publicly, whilst also being used by the APPG to engage with the Government and create the change that is so urgently needed.
It will also include recommendations that outline the steps that must be taken to improve the care and support available.
The report will be shared with all MPs and publicly, whilst also being used by the APPG to engage with the Government and create the change that is so urgently needed.
As a reminder, the APPG will be discussing the evidence pack and live evidence provided by people with lived experience of severe ME at a previous meeting.
Members will then work to produce a formal report to highlight the immediate harms facing people with severe ME.
#MECFS #MyalgicE
⬇️
👉 Read the AI summary here: www.actionforme.org.uk/ai-summary-o...
👉 Read the AI summary here: www.actionforme.org.uk/ai-summary-o...