{"id":250863,"date":"2025-04-14T12:34:25","date_gmt":"2025-04-14T11:34:25","guid":{"rendered":"https:\/\/ftww.org.uk\/?p=250863"},"modified":"2025-04-26T06:48:16","modified_gmt":"2025-04-26T05:48:16","slug":"me-voices-wales-have-your-say","status":"publish","type":"post","link":"https:\/\/ftww.org.uk\/cy\/2025\/04\/14\/me-voices-wales-have-your-say\/","title":{"rendered":"ME Voices Wales \u2013 have your say!"},"content":{"rendered":"

\"IllustrationHow can people with ME in Wales have a louder voice?
\n<\/strong>
\nWho do we want to listen to us?
\n<\/strong>
\nWhat changes do we want to see take place?
\n<\/strong>
\nHow can we find out about things that affect us?<\/strong><\/p>\n

ME Voices Wales is an exciting new project to bring people together so we can listen to each other and work out ways we can communicate about things that are important to us.<\/p>\n

Individuals and groups have been supporting each other and raising awareness of ME\/CFS in Wales for decades. Now that there is more acknowledgement of the condition and people say they actually want to hear from us, WAMES<\/a><\/strong> and FTWW are inviting people with ME throughout Wales to join us and help us make a louder noise.<\/p>\n

Numbers matter<\/strong><\/p>\n

Often WAMES is asked by services or politicians \u2018how many members do you have\u2019 & \u2018where do they live\u2019? The more members, the greater a reason for paying attention. WAMES is not a membership organisation, though from the beginning we have collected experiences and opinions to shape our advocacy work.<\/p>\n

We think there could be over 65,700 people with ME in Wales, since so many developed ME following COVID, but how many want to be heard?<\/p>\n

The more people that sign up, the bigger the impact we can make!<\/p>\n

Whose voices do we want to hear?<\/strong><\/p>\n

Since Oct 2021 the description of ME in the NICE guideline<\/strong><\/a> is one we recognise. Anyone living in Wales with ME or suspected ME, as described by NICE, or who lives with, or cares for someone with ME, is invited to join us.<\/p>\n

The NICE guideline definition (even though it is not perfect!) gives us a recognisable and acceptable identity.<\/p>\n

What will the project do?<\/strong><\/p>\n

First we need to listen to each other so we can understand what we want to talk about.<\/p>\n

We are therefore planning an initial on-line event \/ series of events to discuss, listen and for you to have your say. We are also considering using other virtual events, local get togethers, short questionnaires, snail mail and polls to gather information.<\/p>\n

Then we need to present our voices in a way that our target audience (NHS, politicians\u2026) will hear so we might produce reports, statistical diagrams, infographics, videos etc. Whatever is needed.<\/p>\n

How can you get involved?<\/strong><\/p>\n

Sign up to be kept in touch with the project as it develops<\/p>\n