The weekend was spent on the couch. Man oh man talk about fatigue!
I just don't even have the energy to even post today.
I'm sorry....maybe tomorrow will be better.
Have a nice Monday everyone
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Life and times of Dealing with a Dragon named Hep C
I found that Hep C has a nick name.
The Sleeping Dragon.
It's fitting.... Strange thing is that I've always loved Dragons.
I guess I never could have imagined that I'd have one of my own.
About Me
- Laurie
- I'm a 42 year old Mother of 5. 3 of my own and 2 of my Husbands. My 3 are 13, 17 and 21. His are 22 and 26. We have 3 boys and 2 girls. In my life I've had 17 surgeries, a tatoo and a blood transfussion. So your guess is as good as mine as to where I contracted Hep C. I do not believe it was from the tat. The gentleman that did the art was very careful with sterile tools. But who knows. I was diagnosed with Hep C on March 22, 2007. Geno type 1b with a viral load of almost 5 million. And now I turn the corner and yet a new path lay ahead of me...... A new Journey begins
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7 comments:
Yes, Laurie, the fatigue definitely seemed much greater this weekend and today, headache and nausea has been added for me :-(
~sharon
Laurie, Don't ever worry about it if you are just to tired to post. I am like that often. Rest when you can is my motto.
Had my 24 wk visit fri. still don't have all the results but the platlets have dropped slightly so they are keeping me at 1/2 shot.I was told that if your virus "decides" to become immunne to the drugs it will usually start around week 24. I also found out that the pharmaystical(sppelling sucks these days!)companys level to be undetecable is <15 and that Kaiser's level is 613 or so. Big difference to my brain. So sounds like the next few weeks or month will tell me more. So here is the double edge sword...on the one hane I am glad to be at 1/2 shot...not as sick and all but then the other side says whoa...if this dragon is going to become immune lets up that drug. Time will tell. When I get my test I'll let you know.
We have quite the group going here Laurie you have done a good thing!
Today you feel like shit...tommorrow could be good so hold on to that thought for now
Hugs Rosie
Some days it was all I could do to get the mail and walk the dog. No one will ever understand what fatigue ease if they haven't txed. I'm with you every day of your strugle.
ease should read "is"
Sharon,
I feel your pain!!
((Hugs))
Laurie
Rosie,
The little bastard would dare rear it's ugly little head now!
Possitive thoughts....tx is working!
<15 or 613.....that's a real big difference! Wonder why?
Yes, please let us know. My fingers are so crossed for you!! It'll be good news I'm sure!
Today will get better....it has to!
((Hugs))
Laurie
Oh Terry.....this reminds me of all those times that you had it ruff. You're right, until you do this tx you just can't comprehend what it feels like.
To be honest, I don't think that I want anyone to fully comprehend it. I don't think I would wish this on even people that I don't like!
Thank you for your support...I don't know what I would do without you and Iris. You inspire me to complete this.
((Hugs))
Laurie
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