Home Menu

Site Navigation



Caregivers Support A place for people who are a caregiver to another to find help and support.


advertisement
NeuroTalk Support Groups > > >

carers group

Reply
 
Thread Tools Display Modes
Old 08-14-2009, 08:10 AM #1
alisden alisden is offline
Junior Member
  
Join Date: Jan 2008
Posts: 35
15 yr Member
alisden alisden is offline
Junior Member
 
Join Date: Jan 2008
Posts: 35
15 yr Member
Default 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 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
tamiloo (08-16-2009)

advertisement
Old 08-16-2009, 03:45 AM #2
tamiloo's Avatar
tamiloo tamiloo is offline
Grand Magnate
  
Join Date: Oct 2006
Location: Northern Utah
Posts: 3,465
15 yr Member
tamiloo tamiloo is offline
Grand Magnate
tamiloo's Avatar
 
Join Date: Oct 2006
Location: Northern Utah
Posts: 3,465
15 yr Member
Default
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.

We caregivers have to stick together! Take care and I hope to hear from you soon!
__________________
My best friends live in my computer....
.
 Suffered with back problems since birth...7 back surgeries to date, the last one being on 5/13/2015. Fibromyalgia, PTSD, Chronic Pain

“Being my sweethearts full-time care partner, I have to remind myself, when some well-meaning friend or relative questions my methods or motives, that I know more than they do because I Live this life 24/7, and they only come for short visits.” Tamiloo

.
Gotta love my Olhipie! Dx'd RRMS 1986, SPMS 2004

.
Watch my Olhipie Skiing....

.
tamiloo is offline   Reply With QuoteReply With Quote
Reply

« Previous Thread | Next Thread »

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts
BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

Similar Threads
Thread Thread Starter Forum Replies Last Post
New to the group. TSB13 New Member Introductions 10 06-03-2010 01:30 PM
carers support groujp alisden Caregivers Support 0 08-12-2009 02:28 PM
Hello new to the group csinfo New Member Introductions 10 09-29-2008 01:29 AM
Appeal for carers' bonus to stay BobbyB ALS News & Research 1 03-11-2008 08:51 AM
Full-time carers for mum BobbyB ALS 0 12-06-2006 08:45 PM


All times are GMT -5. The time now is 02:10 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

All posts copyright their original authors.

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.

Always consult your doctor before trying anything you read here.

Home