Hep93 and Pink Grandma

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1Shelly1
Veteran Member


Date Joined Oct 2007
Total Posts : 502
   Posted 5/26/2009 11:30 AM (GMT -7)   
Hi Connie and Diane,
I Just wanted to say thak you for all your hard work on this forum. You two are such dedicated and wonderful human beings. Both of you have suffered and both have endured so much while coping with liver diseases and illnesses of your own or a loved one. Yet; you two have dedicated long hours, research time, love and committment to all of us here. So again I want to thank you. God Bless
 Shelly
 

“Life is not the way it's supposed to be. It's the way it is. The way you cope with it is what makes the difference."

 


bearhug
New Member


Date Joined Apr 2009
Total Posts : 12
   Posted 5/26/2009 11:37 AM (GMT -7)   
Very well put. Thank you both of you
"bearhug"


hep93
Elite Member


Date Joined Jul 2005
Total Posts : 12014
   Posted 5/26/2009 3:12 PM (GMT -7)   
Aww, Shelly and Bearhug, thank you.  Shelly, you have also added so much to this forum with your knowledge.  The educational threads you made for us are now stickied in the Hepatitis Resources section so we won't lose them!  Thanks so much for your contributions, as well.

hep93
Forum moderator - Hepatitis
 
"But that was yesterday, and I was a different person then."
Lewis Carroll, Alice in Wonderland


NanaKaki
New Member


Date Joined May 2009
Total Posts : 8
   Posted 5/26/2009 7:13 PM (GMT -7)   
I am new here and was delighted when I found this forum. I was diagnosed with Hep C last year after suffering for many years with vague symptoms that weren't diagnosed. I have fibromyalgia (diagnosed in 2004) chronic herniations in my spine, osteoarthritis in my spine, degenerative disc disease on top of the Hep C. I have the biggest problem with the fatigue. I get it from the fibro and the hep. I am in PM for the chronic back pain. There are days that I just do not have enough energy to even take a bath and comb my hair. With all of these problems I have a hard time trying to live a normal life. My quality time is minimum and I hate that. I just had a new grandson and I can't even hold him because of the pain in my back. It really is hard. I have tried everything. Physical therapy for 2 years and had to stop because the pain was just too much. I have now settled into a routine of just getting as much rest as I can and I do what I can do when I can do it. I used to worry about it but now I just accept the fact and if I have a good day I am so thankful. People don't understand the havoc this disease wreaks on your life. I am no longer able to work because of the fatigue and the pain and I am fighting with social security to get my benefits. It feels good just to talk about it to people who can understand how it is. Thanks for listening. NanaKaki

hep93
Elite Member


Date Joined Jul 2005
Total Posts : 12014
   Posted 5/26/2009 8:24 PM (GMT -7)   

Hi, Nanakaki.  To get the most responses, it would be best to start your own thread by clicking on New Topic.  You sound like you have a lot to deal with, so we don't want to see you "slip the the cracks."

Welcome to the forum.


hep93
Forum moderator - Hepatitis
 
"But that was yesterday, and I was a different person then."
Lewis Carroll, Alice in Wonderland


Pink Grandma
Veteran Member


Date Joined Nov 2006
Total Posts : 2445
   Posted 5/27/2009 10:02 PM (GMT -7)   
Hi Shelly and Bearhug redface That was so nice. Thank you.........thoughts and prayers.....
Pink Grandma
Forum moderator-Hepatitis

When the going gets tough....the tough get going! Don't always know where I going but I get there anyways.

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