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RE: Ladonna/everyone

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I don't have a strong will to live....there's been too many things happen just recently and along with this disability...things are getting too much for me.......were you able to take the medications? I'm really scared because I truely believe I got this from blood transfusions in the late 70's and if so.....how much damage has already occured? My doctor will be calling a specialist for an appt when the offices opens on Wed....I pray I don't have to wait forever for that appt.

Someone said something about the viral load count.....all I know is my primary doctor did several blood tests and the last one she sent to the Mayo clinic....she called and said they all verified Hep c and that it was chronic and incurable and she said when you have the symptoms I have, that you've usually already had the hep c for 20 years or more. Now would one of the tests she did have been for the viral load count? Why did she send the one to the Mayo clinic? I'm going by her office Wed just to get copies of all this blood work.....

I appreciate any help you guys can offer.....judy

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JUDY REMEMBER THAT YOU ARE A STRONG PERSON. AND DONT THINK THE WORSE. WAIT

AND SEE WHAT THE SPECILISTS HAS TO SAY. AND REMEMBER WE ARE ALL IN THIS WAR

TOGETHER. BARB HERE.

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The will to live is important. Keep the faith and remember to get on line and talk about how you feel. It is scary and there is a lot of uncertainty in life with Hep C. Please don't make a death wish but a wish to live. I think the most problem come from late stages of Hep C. Try not to worry and find out first what is your viral load is and what stage you are in. Most of all start learn about the disease. Everyone is pretty depressed when they first hear the news that they have Hep C. We need to stick together give each other support. One of the things is to start to change your life, eating foods that are good for you, resting more and drink lots of water. God Bless and Happy new year

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