This forum is for questions about medical issues and research aspects of
Hepatitis C such as, questions about being newly diagnosed, questions about current treatments, information and participation in discussions about research studies and clinical trials related to Hepatitis. If you would like to communicate with other people who have been touched by Hepatitis, please visit our new
Hepatitis Social/Living with Hepatitis forum
i doubt it is gall stones or kidney stones as these sx tend to be sharpe pains.
stop drinking if you do, get some bloods done could be inflamation (inflammation), or could be something else un related, try to be calm,
jessie
my aches got heaps worse when i started tx and my LFTs have gone down even more since tx so the better my LFTs get the worse my liver aches.
my LFTs have always been ok...so stop thinkin u r dying,it could just b part of havin hepc...doesnt mean our liver is on its way out necessarily.
thats just what iv experienced,we r all different.
good luck.
i also found ut this way, can i ask what condition your liver is in? as i have not had biopsy nd i am wondering what damage may have been done,
feel freeto say sod off
thanks
Jessie
So, for as much as they say your liver doesn't hurt, I believe it does whether it's by referred pain or whatever.
By the way, the pain doesn't necessarily mean anything as far as how good or bad your liver is.
There is also a part of the intestine that tucks up next to the liver that can feel pain, and the GI is directly linked to the nervous system, so if you are stressed, anxious, etc. that may contribute.
This is my theory based on my limited knowledge, but it goes something like that.
That area of the intestine is also where gas gets trapped, but you are correct that if you are feeling it more in your back, it could be kidney infection. One thing you can do is make a fist and tap on the area on you back, if it is sensitive that is one sign, or you could go to the doctor, who would do the same thing.and other things.
Meakea
thanks for your reply too, cant believe what you went through before finding out you had hep c !, again can i ask you what condition your liver is in~? iam looking for comparisons to help myself and others,
thank you
Jessie
i do not think you have gall stones because it is usually a sharpe pain, but please get some bloods done to put your mind at rest, did you achieve SVR ?
have you had tx?
this sounds like symptoms of hep c, you know the condition of your liver (last year) and so it sounds like you are NOTt about to die, but please get some TEST to put your self at rest .
Jessie
In the interem I've completed TX and so far I'm undetectable. It's been about 2-1/2 months since EOT and I'm still getting URQ pains from time-to-time. Maybe it wasn't HCV related at all. Maybe I am imagining it. In any case I'm still here.
54 years and only s1/g1 thats amazing you say you had treatment did you clear? i hope so!! after all your ordeals,
chuckles
glad you are und still,
thanks for your input,
Jessie
I would check and see if perhaps there is another cause.
I have symptoms that no doctor was relating to hep c neither before nor after dx.
It is a mixed blessing because if I did not have them I would not have been
able to find out I was infected.
I keep hearing how the liver does not feel any pain but the capsule around it
can built up fluid , stretch ect...
I have abdominal pain , burning,stabbing,soarness,aching you name it.
Left side , right side , middle ,sides and back. It comes and goes in different
intensities and different areas mostly starts in the afternoon.
I had an ultrasound in March another one end of Aug showing everything
perfectly normal. I had 6 doctors palpatate my liver and all said it was not enlarged.
I did FibroSure and FibroScan both F2 , ALT 61,VL 100K IU/ml.
Nothing in me labs or tests is extreme only my symptoms are extreme.
Before I had all the tests done I just had the diagnosis with the symptoms.
It was sheer horror because it made me feel like I was in much worse shape than
I am.
Anyway until this day no one has an explanation for my symptoms. All I know for
sure is that they are chronic and the only chronic illness I have is hep C
so it must be what some call hep c sx although nobody can tell me exactly
what this is.