My relative and his wife both have ME / CFS and after a lengthy interaction with the local council they have finally been awarded a budget to get a Personal Assistant. We are so pleased with this and extremely grateful as it will vastly improve their quality of life (which is almost non-existent at the moment!). As they are unable to do so, I am helping to find a carer and will be taking care of the employment side of things.
My question goes to people caring for someone with severe ME / CFS and also for those with ME who receive care:
What should I include in the 'job description' and what should I be telling the carer before they start?
I have found some great information on the 25% ME Group website, but I would really appreciate any help and advice coming from personal experience.
Thank you so much in advance!
My question goes to people caring for someone with severe ME / CFS and also for those with ME who receive care:
What should I include in the 'job description' and what should I be telling the carer before they start?
I have found some great information on the 25% ME Group website, but I would really appreciate any help and advice coming from personal experience.
Thank you so much in advance!