Hepatitis B :: Carrier And Now HbsAg Reactive (positive)
Jan 12, 2016
I am carrier of this virus (HbsAg) i just want to ask about the dosage if i am going to take this alinia.. how many tablets per day and how long should i take it... is it everyday? is it for 6 months before i go for another blood screening?
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I am a fresh graduate and I was looking for a job then found one, I was hired and before I could start they wanted to get my medical result first. They told me I won't be able to get the job anymore since my result in HBsAg was reactive. In the medical it says "3516.26 S/CO; The Cut-Off value reported for this assay cannot be correlated to an end-point titer; rechecked and verified." Is my Hep B chronic? And can I still get a job even though I am now a carrier of this disease? I am really depressed now it's like I've wasted 4 years of studying
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I got Hep B Vaccinated during birth as my mum has Hep B. It went extremely fine until recently I was required to undergo for Hep B blood test by a GP and my test results showed that HBsAg is reactive, and anti-HB is non reactive (Count < 3.1). Therefore my GP referred me to a hepatologist and he was surprised too as I did not share any needles, etc etc plus I got vaccinated during birth. He said it might be a false positive therefore he sent me for many blood tests including DNA sequencing as well as ultrasound scan and I can only find out the results 2 weeks later. I am extremely worried. Anyone encountered this before?
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Am hepatitis B positive. With negative e-antigen and virus dna load of 2369.
My wife is hbsag positive due to vaccination since 2009. We just have a baby boy.
My baby was given a shot of vaccination at birth.
Qs.
1.Is it safe for me to make unprotected sex with her, why she is still breastfeeding ?
2. Is my baby at risk ?
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I Know that she is highly contagious for that matter .. but can this be cured?
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I was tested positive for HSV2, but no symptoms
Also I would like to know the best way to prevent passing this HSV2 ...
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I had unprotected vaginal sex with a CSW almost 5 years ago. I tested for hepatitis B yesterday.
The test was
Australia antigen (HBsAg) Negative.
1)Am I safe from hepatitis B?
2)Do I need further testing??
3)If yes what test should I take? ?
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When we keep taking interferon and clear hbsag does it mean cure?
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A patient with chronic hepatitis B who had been taking drugs left and right and suddenly his hbsag quanti drops down from 5000ui/ml to 125ui/ml .if this patient takes peg , since it's a chronic virus can it clear the virus? if yes for how long ? 1 , 2 , 3 , months or years ?
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my father is 66 years old, it has been found out through blood test (ANTI HCV) his cutoff value is 1.00 and patient value is 12.51. which further reveals reactive hepatitis. what do you suggest for him?
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Two weeks ago i have sex with a crossdresser and after that i am scared about HIV infection. After 15 days of that exposure i opted for HIV Duo ultra test and test report showed this result- P24 Antigen:0.01; Antibody:0.03; i less than 0.25: non reactive for P24 antigen and antibody; i more than or equal to 0.25: reactive for P24 antigen and antibody.
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My sister in law, a very good doctor who has always given me sensible advice when I have asked, suggested I get my CRP checked. CRP is apparently a marker for inflammation in the body, although lupus and rheumatoid arthritis do not always trigger it.
I know I sound like a broken record, but I really think a lot of post-interferon syndrome can be explained by body-wide inflammation - chronic fatigue arises from an inflamed brain; psoriasis is inflamed skin; arthritis is inflamed joints; fibromyalgia is inflamed muscle tissue; vasculitis is inflamed blood vessels, etc.
Our immune systems were amped up by the drugs, and they never settled down again quite right. The drugs induce autoimmune disorders that can effect every system of our body.
If I eat bagels and cream cheese (I love bagels and cream cheese) for two or three days in a row, and throw in a pizza, all my inflammatory symptoms get worse, including depression and fatigue. My ankles swell. My psoriasis gets worse. My joints start aching worse. My fingers start trembling and twitching spastically. I had nothing like this before treatment.
So anyway, if anyone cares to follow this theory, it means eating a non-inflammatory diet - no pizza, no fast food, skip the sugar, read In Defense of Food. The more you want to live, the better you will eat. If anyone cares to follow this theory and is having their blood drawn anyway, be sure and get CRP checked. My sis-in-law says it's very inexpensive test. I'd love to hear of any correlation or thoughts on this subject.
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My new girlfriend, who I like very much, was very open with me about the fact that she had a blood transfusion as a baby for several surgeries she had to have, which left her HCV positive. She and I were about to move into the sexual part of our relationship, so we both got tested for STDs to show each other we had a clean bill of health. Well as it turns out, her bloodwork showed she was HCV positive again...this is after achieving SVR (not sure for how long she had achieved this yet). She told me and was very upset, so I obviously just gave her a hug and held her. No other way to respond she was so upset. I'm curious, does anyone on here have any experience with this? Possibility for false positives or possibility for her to need to seek additional treatment? I hope you can forgive any questions that may seem ignorant. I am mostly focused on her health, but naturally I'm also concerned about the implications for our future relationship (I understand it is very low risk to pass it to me through sex, but still, I'm human, and I'm just carefully looking at this situation). If anyone can shed some light on her situation, I'd love to hear it. She's a great woman and I'd like to get any info for her that could help.
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I ve been on viread for 3 months. The latest hbv dna is positive <20 ıu/ml. Before viread I was on lamivudine and hbv dna was generally again positive <20 ıu/ml. I think it was 3 times undetectable at different times. Alt Ast normal afp normal. Do you think dna will be und next time? If it comes positive again what. treatment or evaluation can you recommend ? I also started to take vit d3 daily 10 days ago.
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Found out through my OBGYN that i am Hep C positive. Shocking because I've never been a drug user, never had a transfusion, ext. Requested a retest which also came back positive, just to be sure. Then they did a RNA test and it came back with no viral load. Does this mean I cleared the virus on my own and won't ever need treatment? Should I do this test again? Also, since i'm pregnant and am wanting to breastfeed, I'm wondering if it is passable or not since I have no viral load? Will it be safe to breastfeed? I know it is not passable threw the actual milk, but am concerned with cracked/bleeding nipple or teething that could possibly cause me to bleed.
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I am 36 years old. My LFT levels are normal but HBV DNA Viral Load is 6200 IU/mL. HBe Antigen is negative and HBe antibody is positive. Can you please explain what all these mean and how likely is the sever damage to liver in this state? What do I need to do to reduce or finish the Viral load and how much time is it likely to take?
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I have read that in 99% of cases people who swab positive for hsv1 show positive for western blot. Does that mean wb is 99% accurate for hsv1 3 months after exposure ?
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Our 10 days old grandson was finally diagnosed with cystic fibrosis. I said finally, because it took doctors 6 days to determine the cause of baby's problems. They said that there is a possibility that one or both parents are illness carrier. Is that even possible? Can you be cystic fibrosis carrier and not know it through your entire life?
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So I have been sick with a mystery illness for the last year or so. I've seen every specialist, and the first thing they looked for was a malignancy, but there seems to be nothing. Then I saw a rheumatologist and she sent me for blood tests that came back with a positive ANA and positive anti ds-dna. From what I've read, positive anti-dsdna is VERY specific to Lupus. I never thought I had Lupus because my symptoms weren't specific to it, but after ruling almost everything else out, I'm thinking more and more that Lupus could be it. Because my symptoms weren't specific enough, my rheumatologist told me she wanted to see me again in 3 months to see if there were any progressions. I'm really becoming more certain that it has to be Lupus with these positive tests, and I'm worried that I won't be able to get a diagnosis for a long time to come.
Some of my symptoms include:
Extreme fatigue
Constant low grade fever
Neck discomfort
Headaches
Random pains in fingers and knees (not constant, every once in a while)
Chest pain when breathing deeply
A lot of memory problems
Thinning hair
Can barely work out or walk at the same speed as most people
What do you think I should do next in order to speed up finding a diagnosis? How do I make it clear to my rheumatologist that I feel like this is becoming more and more urgent?
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2 years ago it was ANA 1:80 and the anti-dsDNA was 10, now it's ANA 1:40 with anti-dsDNA 22. So which is worse ?
2 years ago they said it's borderline and if I don't have symptoms, let's wait, they didn't dx. me with lupus.
I had ( and still have ) unexplained hip pain ( comes and goes ), headaches and lightheadedness ( had them before, but usually around periods ), but 2 months ago they become very bothersome and almost constant. My vitamin D is 25 ( should be 30-70 ) and vitamin b12 is 244 ( should be 200-900 ) my dr.said is still kind a low
.
Are these lupus symptoms at all ?
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Do you think me and my husband should have some cystic fibrosis tests for I know I have this defective gene in my family history or precisely my mum has died from cystic fibrosis and I probably am a cystic fibrosis carrier. Anyway I am planning on getting pregnant and would like to hear would some cystic fibrosis tests help me with this decision for I won't like my kid have the same diagnose when it is born?
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