How to use this board

Test out the forum before you post!

Testing

Postby Terry » Sun Jun 19, 2005 12:26 pm

This is a great site. I hope I can get the hang. Am I there yet? :roll:
Terry
 
Posts: 4
Joined: Sat Jun 18, 2005 12:07 pm
Location: Vermont

Wow, finally a place

Postby nolifewife » Mon Jul 04, 2005 11:34 pm

:cry: finally a place to put all the feelings that come with being in the caregiver/breadwinner role. Thank you.
nolifewife
 
Posts: 1
Joined: Mon Jul 04, 2005 11:05 pm
Location: Maryland USA

Postby Guest » Tue Jul 05, 2005 12:16 am

Yup, you're both "here" ---both got it to work.
Welcome to "the club no one wants to qualify for"...
post away....
Guest
 

Re: How to use this board

Postby Pat Roebke » Fri Jul 08, 2005 3:13 am

Erin wrote:Hello Wellspouse.org member!

This is a place to test out how to post before you enter the main realm of Wellspouse discussion.

Try out replying to this message, using emoticons, your signature, quoting other people's messages, etc.

This software is pretty easy to use and I'm sure you'll get the hang of it quickly! If you are having problems or have questions, pm me. (Click on my username and then hit the 'pm' button to send me a personal message.)

You can also post a question in the 'questions and suggestions' forum, since if you're having a problems, it's very likely that someone else is having the same problem!
Pat Roebke
 
Posts: 2
Joined: Fri Jul 08, 2005 3:04 am

New Member From New Jersey

Postby Daisy » Fri Jul 15, 2005 8:43 pm

Hello Everyone,
Caregiver for my husband and parents for last 3 to 4 years.
I have found this site very helpful. It is great to know there are others out there.
Daisy
 
Posts: 148
Joined: Fri Jul 15, 2005 8:28 pm
Location: New Jersey

Postby msrpark » Thu Jul 28, 2005 6:53 pm

New member just testing. Will get bold when I have more time. Am currently dealing with whether or not it is time for me to put spouse in nursing home. Pretty difficult.....
Spouse has had Parkinson's for many years, 1 adult child
msrpark
 
Posts: 3
Joined: Wed Jul 27, 2005 4:31 pm

just joined

Postby buffchick » Wed Aug 03, 2005 11:58 pm

Hey, Erin,

Thanks for getting me up and running. I'm not very computer capable.
I am 40. My husband is a 48 y/o C-4 quad injured at age 20. We have no children of our own, but are legal guardians of a 4 y/o since Aug/04. We are the caregivers for my 89 y/o grandma with lung cancer since Dec/04.
First marriage for both of us.
buffchick
 
Posts: 12
Joined: Sat Jul 30, 2005 9:52 pm
Location: California

Postby Erin » Thu Aug 04, 2005 10:29 am

No problem at all! Anytime!
- Erin
My best friend and IS has had Chronic Fatigue Syndrome since July 1999
User avatar
Erin
 
Posts: 947
Joined: Sat Oct 25, 2003 9:35 pm
Location: Ottawa, Canada

Did I do it this time?

Postby dd » Fri Sep 16, 2005 12:29 am

Did I do it this time? Me :oops:
dd
 
Posts: 7
Joined: Fri Sep 09, 2005 2:05 am

First time post

Postby LucyinNC » Sun Oct 02, 2005 2:01 pm

Hello all,

It's such a treat to find a site where I can see everyone freely talking about those things that are front and center on my mind but rarely make it out of my mouth. You know, those things you think every day but are afraid if you voiced them out loud everyone would think "What has she got to complain about? Her husband is the one with the Parkinson's. " Actually I have wonderful friends but after awhile we all worry about wearing out our friends' store of empathy.

Thanks for being there.
Husband with Parkinson's now 54, diagnosed 5 years ago. Son 15 and two labrador retrievers that help keep me going.
LucyinNC
 
Posts: 4
Joined: Sun Oct 02, 2005 1:52 pm
Location: Chapel Hill, NC

Postby Richard » Mon Oct 03, 2005 8:43 am

Lucy:

Welcome to the club no one wants to join. Your feelings are normal, of not being understood by friends, however kind, who don't have to live with the "elephant in the living room" that chronic illness/disability can be. It can be very isolating and depressing for the caregiving "well" spouse, and while there is very little or no official support available, and often little or no support from the family, the WSA can be a great help as a source of peer support.
Richard, WSA Pres. 05-09. Mantra: WIT - Whatever It Takes! FWS1:died 2004-IS scleroderma,cancer. FWS2: Divorced 2010-IS mild stroke'07,anxiety. Married July 2012 to a wonderful woman. BLOG: http://www.carepages.com/blogs/lifeofwellspouse/posts
User avatar
Richard
Site Admin
 
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Joined: Fri Oct 31, 2003 5:23 pm
Location: Norfolk VA (From Arlington, VA and Fredericton, NB, Canada)

Postby Elle » Mon Oct 17, 2005 11:10 pm

I must say this again, as I am new, but have posted already. This place is like a home away from home. I am glad there is someplace for someone in these types of situations to come and just 'vent' with no repercussions of any type. Being the caregiver is a job that should be up for sainthood.

Anyone who is just 'lurking', please, do not be afraid. Welcome and come get your hugs.

Elle
59 Y/O hubby is undiagnosed but in lots of pain.
Elle
 
Posts: 8
Joined: Sun Oct 16, 2005 12:09 pm
Location: NW Ohio

Postby coss41 » Sun Nov 13, 2005 8:20 pm

[color=bl :arrow: :arrow: :?: :?: :twisted: :D :shock: ue][/color] :roll:
i,m a newbe,, really pray this site works? testing the cool cool waaateeerrr.god bless
coss41
 
Posts: 34
Joined: Sun Nov 13, 2005 8:05 pm

Postby camille » Wed Dec 14, 2005 1:03 am

new and testing :(
IS is 47 and suffers from intractable pain (Trigeminal Neuralgia) causing electrical shock pain on right side of face. Married 25y, been living with illness for 20. We have two boys 15/11
camille
 
Posts: 9
Joined: Wed Dec 14, 2005 12:55 am
Location: las vegas, Nv

Newbie Testing

Postby Oneday » Tue Dec 20, 2005 2:25 pm

:) I am new to this site. What a blessing! None of my peers are on the journey - I am not alone.
Oneday
 
Posts: 3
Joined: Tue Dec 20, 2005 1:55 pm

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