This is a very important issue.spouses, girlfriends or boyfriends would  
appreciate having someone to talk to. I know when I went to meeting at  
independent living center in Kansas City. I remember there were several persons 
 
working at the independent living center that had able-bodied partners. We 
have  a spinal cord Association that I'm sure would have someone in your same  
position. I have not been able to go to any other meeting.

I watched the  video about sexuality that was on Friday. You can go to the 
website and watch  although I don't think it really dealt with spousal 
caregiver issues. It is  through the national spinal cord injury Association.
Something you would need  to talk to another person in your same situation 
and level of injury.
The  University hospital might also have someone to talk to in their spinal 
cord  unit. I would hope that they give more guidance than they did when I 
was injured  in 1974 . I can imagine the strain that are injuries, put on 
our  significant others and just are caregivers and families. The 
responsibility is  enormous. I have two brothers and sisters but there's only 
one 
brother that will  make himself available to help me when he can. The video 
talk 
about having more  services regarding sexuality in California. The presenter 
was from New  York..
Dana

if you have a wife or husband in California are you able  to get caregivers 
from the state.


There's a  caregiver forum at _www.sciwire.com_ (http://www.sciwire.com/)  
Reeve Foundation and United Spinal have services for  caregivers/families

On Feb 22, 2013, at 11:05 AM, Dave Krehbiel wrote:



 
I  was injured at the beach about five years ago, just before my 50th 
birthday. I  am now a C4/C5 quad who is now living at home with the combination 
of  insurance, Medicare, Medicaid, and care by my family.

My  accident was a life changing experience for me and for my family, 
especially  for my wife.

She  has tried to find someone to talk to about her issues, but there are 
precious  few people who understand what it is like to be a quadriplegic or 
to care for  a quadriplegic. For example, since I have control of my shoulder 
muscles and  biceps, people see my arms moving and don't understand the 
severity of my  injury.

Are  there any family caregivers (preferably spouses) out there who would 
be  available to have a chat by phone with my wife?

Thanks,

Dave  Krehbiel
(301)  924-4530






=
 
 
In a message dated 2/23/2013 11:55:50 A.M. Central Standard Time,  
[email protected] writes:

There's a caregiver forum at _www.sciwire.com_ (http://www.sciwire.com/)   
Reeve Foundation and United Spinal have services for  caregivers/families

On Feb 22, 2013, at 11:05 AM, Dave Krehbiel wrote:



 
I  was injured at the beach about five years ago, just before my 50th 
birthday.  I am now a C4/C5 quad who is now living at home with the combination 
of  insurance, Medicare, Medicaid, and care by my family.
 
My  accident was a life changing experience for me and for my family, 
especially  for my wife.
 
She  has tried to find someone to talk to about her issues, but there are  
precious few people who understand what it is like to be a quadriplegic or  
to care for a quadriplegic. For example, since I have control of my shoulder 
 muscles and biceps, people see my arms moving and don't understand the  
severity of my injury.
 
Are  there any family caregivers (preferably spouses) out there who would 
be  available to have a chat by phone with my wife?
 
Thanks,
 
Dave  Krehbiel
(301)  924-4530






=

Reply via email to