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Thank you Beaches so much.
I feel calmer now and not afraid to go through the treatment. I do not have anyone else to ask about all these things as my doctor told me if I will buy treatment on-line she will not look after me. In this case I can come back after I will finish my meds and only then she will do tests if everything have cleared. Feels very scary to do it without any support from my doctor.
I am very gratefull for any advice I can get.
Thank you Dr Freeman for your quick response.
My GP was always telling me that I was exposed at some point in my life, but my body have cleared it so that is why I have antibodies.
I am not sure have he done any other tests, but he told me that this is nothing to worry about.
Now I’m thinking, should I try to get tested for this once again?
If I had exposure and now virus is cleared, what is the chance for it to come back? I have read that someone is offering to get vaccinated for hepB before treatment to prevent from reacuring.
What if is is not cleared does that mean that I am not going to be able to have a treatmen now or in the future?
Hello I am pretty new to this forum. Just yesterday I have registered to Redemtion trial 2 and still waiting for appointment with monkmeds. Doctors in London do not want to help me in my journey to get better so with a help of fixhepc I am trying to figure out eveything myself. Coud anyone please help me to figure out what theese test results means as I am completely lost. I knew long time ago that I have Hep B antibodies and a year ago I have find out that I have Hep C as well. I really want to get treated, but I am scared that Hep B reactivate it self. On my blood result sheet says:
HB surface antigen qualitetive (HBsAG)- Dublicate request
HBe antigen quatative (HBeAG) – antigen not detected
HB e antibody qualitative (anti HBe) – antibody detected.
Could somebody please help me to understand what does that mean? And how big is the chance for Hep B to be activated. And how big is the risk of using those meds?Hello rightsaidfred,
The GP clinic I am registered to is more like walk in clinic. They have a few doctors and whenever I need to see GP it is never the same person. They have referred me to do all my tests and treatment in the hospital.
As every time I have to see a different GP it would be so uncomfortable to tell my story to each one of them. I think I should find another clinic and be looked after by one person.Hi everyone!
Does anyone have any experience with a Whipps Cross University hospital?
Hi everyone,
I was diagnosed just a few months ago. I was reading everyones stories and this forum helped me alot. It gives me a hope. I have HepC 3. I live in London. I was offered a half a year of peg interferon +ribabirin treatment by NHS. I have a very active job, I spend all day on my feet. I am so scared that I will not be able to have a treatment or I will have to leave my job. I would love to buy Sof+Dac on line but I am afraid to tell my doctor about that as someone mentioned that he might refuse to treat me. Please help me. I do not know should I ask my doctor about it. Does anyone have any advice Please.
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