Originally posted by Suefromwakey
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Carer Support Groups
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Originally posted by denise View PostWhat usually takes place is we complain about lack of help and support. Sometimes we share tips . Mostly we just vent. Sometimes we just talk about anything but what we do. It's a difficult one because it can be depressing if someone is stressed you can come away feeling worse than you started. Basically I gave up. It didn't work for me.
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I've only attended two so hardly a good one to pass on anything.
My experience, on zoom only, was they already have built up rapports with each other and I felt like an outsider, I was sat on my office chair for a couple of hours in front of my lappy and my backside hurt so I wont be visiting again, having said that I'm not one for face to face either so I'm a lost cause,
I'll wing it
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What usually takes place is we complain about lack of help and support. Sometimes we share tips . Mostly we just vent. Sometimes we just talk about anything but what we do. It's a difficult one because it can be depressing if someone is stressed you can come away feeling worse than you started. Basically I gave up. It didn't work for me.
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Sorry unable to share any information as I don’t participate in any carer group. Good idea though
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Carer Support Groups
Hi everyone. My local branch is looking to set up a support group specifically for anyone caring for someone living with MND so I’m wondering if anyone runs or participates in such a group and would be willing to share either publicly or privately what sort of things take place. What works / doesn’t work for you.
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