From my wall on Facebook:
Action for M.E. wants all children living with M.E./CFS to get the support they need in school. We need to make sure we are focusing on the issues that matter most to families affected.
So please complete our five-minute feedback form and tell us what it's really like managing your condition in school. Whether you a parent of a child living with M.E./CFS or currently in school yourself, we'd be happy to hear from you. Complete this here: https://tinyurl.com/ybnkx74w.
Your responses will be completely anonymous, and the details you share will be used to help us understand how we can better support children living with M.E./CFS through their school education. The results of the survey will also be used to help shape our campaigns and support the work of the Medical Conditions at School Alliance.
The deadline for completion is Monday 18th February.
ALSO! The disability benefits consortium are asking for one final push on their #UCandme survey. If you are a disabled person who has applied for Universal Credit please take the disability benefits consortium's survey. They want to hear your experiences, good or bad so they can lobby for change -https://disabilitybenefitsconsortium.wordpress.com/univers…/
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