We care givers need our own space. This situation prohibits emotional release. And that's what we have to do. It's like you don't only have to deal with your own spouse's disabilities, you have an army of disabled people reading your every thought. I read "our" site as far back as it went. And I said: omg I met the Stepford wives. I'm doing it again, i'm laying myself out there: this is not working. This site sucks for the other half. The other side of the equation. give me feed back, please
Privacy
Started by
*onion*
, Mar 10 2006 04:12 AM
3 replies to this topic
#2
Posted 10 March 2006 - 08:16 PM
No, No, No......Sorry Onion but I disagree.
Ok, you have disabled people reading your thoughts on here as well as other spouses\caregivers but I have found nothing but support.
Also I think that its good for disabled people to know what its like on our side, as its good for us to know what its like for them. This is a hell of a situation that none of us would ever wish to be in,
but its here and we need to get on with it the best we can. If you have issues that you want to talk about - but dont want the whole world to comment on why dont you try sending a personal message to someone, and talk that way. (drop me a line whenever you like!)
A lot of us are isolated and dont know anyone else who can relate to what we are going through and this site is an excellent way to find that understanding. (and have a few laughs!)
This spouses and carers forum is our space, and I know that some of the disabled people who use this site dont post in here because they respect that. However I personally dont mind if they wish to add their comments and opinions. It all helps see each others perspective on things, and I like hearing from everyone....anyway.... thats just my opinion.
Ok, you have disabled people reading your thoughts on here as well as other spouses\caregivers but I have found nothing but support.
A lot of us are isolated and dont know anyone else who can relate to what we are going through and this site is an excellent way to find that understanding. (and have a few laughs!)
This spouses and carers forum is our space, and I know that some of the disabled people who use this site dont post in here because they respect that. However I personally dont mind if they wish to add their comments and opinions. It all helps see each others perspective on things, and I like hearing from everyone....anyway.... thats just my opinion.
#3
Posted 12 March 2006 - 04:08 AM
You know I have had some nice people here give me advice and help me with things I didn't understand. I really do feel thankful for them and you. well I better get some sleep cause hubby wakes up in the night and that means I do to, see what he needs and then Ican't get back to sleep. That means I would be grumpy so early to bed and God help us get the good nights sleep we need.
Hang in there, Katie.
#4
Posted 29 March 2006 - 03:28 PM
Onion
I disagree too. I read the general site as well as the caregivers. If it were not for the help on this side of the board my former Partner & I would have floundered.
I dont mind people venting their thughts - I do too from time to time. However, I appreciate all the advice I get be it from caregivers or the general site.
Sometimes I crossover to the other parts of this board just to see what is happening there.
My parents are now my "support" since my partner left and although a fully independent para, I still need some support when things go belly up and, indeed, my parents do too. They read this site too and often find folks out there feeling as they do.
Kick - scream - do whatever but let it out - who cares who reads it. I dont. On other sites not connected with SCI injuries, I have had some good humdingers with folks.
As my old Scots Granny said "Dont let your erse touch the glaur" in other words "keep you bum up off the ground." Hang in there.
I disagree too. I read the general site as well as the caregivers. If it were not for the help on this side of the board my former Partner & I would have floundered.
I dont mind people venting their thughts - I do too from time to time. However, I appreciate all the advice I get be it from caregivers or the general site.
Sometimes I crossover to the other parts of this board just to see what is happening there.
My parents are now my "support" since my partner left and although a fully independent para, I still need some support when things go belly up and, indeed, my parents do too. They read this site too and often find folks out there feeling as they do.
Kick - scream - do whatever but let it out - who cares who reads it. I dont. On other sites not connected with SCI injuries, I have had some good humdingers with folks.
As my old Scots Granny said "Dont let your erse touch the glaur" in other words "keep you bum up off the ground." Hang in there.
ALWAYS REMEMBER - The darkest hour is only 60 minutes long and what won't kill you will make you stronger.
cauda equina lesion resulting in lack of ability to walk. Spinal cord undamaged and intact. NOW ABLE TO HOBBLE AROUND ON 2 STICKS AFTER LOADS OF PHYSIO.
cauda equina lesion resulting in lack of ability to walk. Spinal cord undamaged and intact. NOW ABLE TO HOBBLE AROUND ON 2 STICKS AFTER LOADS OF PHYSIO.
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