Solidarity can sometimes feel in short supply for people living with ME and Long Covid, but recently we’ve seen hopeful signs - both in the wider disability community and specifically in support of those affected by these conditions.
Thank you so much, not only for what you do, but for connecting us all and communicating with us. I think other ME charities do wonderful things in the background but we don’t know about it a lot of the time and we need to know people are fighting for us and that we aren’t invisible or forgotten. Please keep doing what you’re doing, it’s great!
Blimey Alice's words were so moving and what a wonderful way to think about things; being so stuck but yet still connected albeit just by the finest of threads! Incredible 💔
I'm really impressed with you how you've managed to unify the dozens of ME and Long Covid charities.
The United To End MND Campaign succeeded in getting £50 million for research for MND (Motor Neurone Disease) from Government (https://www.mndassociation.org/get-involved/campaigning/take-action/united-to-end-mnd#:~:text=The%20United%20to%20End%20MND%20campaign%20began%20in%202019%20with,in%20years%20rather%20than%20decade.)
I hope we can do similar
A hopeful message and wonderful words of heart and spirit despite such suffering from Alice.
Wonderful hopeful words💙❤💙❤💙
Thank you so much, not only for what you do, but for connecting us all and communicating with us. I think other ME charities do wonderful things in the background but we don’t know about it a lot of the time and we need to know people are fighting for us and that we aren’t invisible or forgotten. Please keep doing what you’re doing, it’s great!
Thanks for this. Also a deep heartfelt thank you to Alice for her lovely and moving poem. It brought tears for me, as a carer.
🙏💙🫂
Blimey Alice's words were so moving and what a wonderful way to think about things; being so stuck but yet still connected albeit just by the finest of threads! Incredible 💔