carers group
 

hi there i currently care for my husband with a brain injury and also my disabled son.My husband attends headway brain injury association in the uk two days a week and i am currently trying to set up a carers group there for families i wondered if anyone had any ideas on activities that i could offer people as well as the well earned cup of tea or coffee and time out that we all need .Im open to any suggestions thanks ali :)

Alisden, you have a busy life. My husband has SPMS. I also have my 86 year old Mom living with us…and of course my own challenges.

I attend my hubby’s MS support group…I’m the only caregiver. It is interesting to hear others experience with MS.

I really think it is a great idea to start a group…it would be respite, which is something that is hard to come by when you are a fulltime caregiver.

Run some ideas past me and maybe I could help in any way I can. :hug:

We caregivers have to stick together! Take care and I hope to hear from you soon!
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