DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
Check out resources at the top of the home page for further info.
Connie
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
Thanks again
flopsie
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
Hello,
My alt was 54 and ast was normal when I started the meds. My viral load was 8 million. I have 7 more shots and was told a month ago that my alt is now 24 and ast normal and my viral load is undetected. I'm genotype 2B .
On the sick part I've not been throwing up but I do have my mood swings....
lol Hopefully not for long.....I had a crying spell last night because I'm overwhelmed with everything going on in my life.....My hair is really thinning, but if this cures me its worth it....
You'll do fine I work full time and have a lot going on at home, but by staying busy it goes quick.
any questions please ask...
hugs eileen
ps I lost 24 lbs
Everyone take care,
flopsie
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
Ye gads! That doesn't sound right! Well, hang in there, and keep posting!
Connie
flops
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
Yes I have Hep C and last Thursday the doctor told me he wanted me to start on these meds. However, I have to wait until they find out what type I have, he says it depends onn the type as to the lenght of TX. I heard several people talking about numbers up in the million and I was concerned because my liver enzymes were only in the higher 300's. I posted on here and learned what they are referring to is the viral load. So I called the doctor yesterday to find out what mine was and they told me they would find out when my genotype came back and that would take about 10 days as they send it to California.
I knew I had Hep for a long time, just was never advised to seek TX for it as I was not sick and my Liver panel did not show damage as it does now. Sorry so many questions, but this is a big learning process for me!
Hugs
flopsie
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
if ya viral load comes back very low,thats a GOOD thing,,,the higher the viral load the more hep has to be fought off,,,and the more thats attacking your liver,,,my husband has hep b,and his is at 110 million,,,,,after 6 mths of interferon treatment,,his dr says taking the combo doesnt help at all with hep b so he gets 6 more months of interferon. was a big disappointment but hep c has a much better chance of being cured and/or controlled then hep b does,,,so definately do as your dr says and take the treatment,,,hubby is not quite as sick from treatment as at the beginning,but its taking a toll on him mentally and on his blood work,,,his platelet count is extremely low and hes worn out,,but has other health issues now with his heart so its hard to tell whats causing what symptoms,,good luck and please come back :)
trish
trish
flopsie
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
The bad part is that the treatments took away the Hep C and HIS LIVER with it. He is currently in the V.A. Hospital having his liver drained because it no longer functions. He refuses to look at what is going on. (And I can't blame him).
What I need is a diet plan for him when he gets home next week.
I remember lots of fresh fruit and veges, NO sodium.
Can anyone give me a hand on this????
Thanks!! sassybratt
I hate to hear that about your brother, I am so sorry. I also hate to hear that about the therapy. I had my first injection on July 6 and am taking Ribavarin 400 mg 2 times a day. I am drained. I have no energy for anything. Some days it is all I can do just to get up and go to the bathroo,m. My White blood count last week was 3.1, normal is 4.0 to 10., so right now I am still good. Have had to take nausea meds just aabout every day and sleep medicine also.
Medicine that will make you well makes yo so very sick
DON'T WALK BEHIND ME......I MAY NOT LEAD
JUST WALK BESIDE ME AND BE MY FRIEND
ALBERT CAMUS
Today is the first day of the rest of your life. Rejoice and be glad in it...
hello to each and every one, I have had a liver transplant 6 years ago due to having hepC Is there any happy
searchers, still trying to come to terms with the Drugs and their side effects, that I need to take to stop rejection problems ? help! please! best wishes joa
Let us know exactly how you think we might help you!
Connie