Breastfeeding :: Hepatitis C Positive With Viral Load
Jul 17, 2015
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 been on Viread for three years and my viral load never goes undetectable. The viral load went down in the past two years. However, it has been up and down in the range of 100 to 300 IU in the past year. It seems that it will never go down to undetectable. The test for mutation failed three times because of very low viral load. Am I non-responder to Viread? Should I switch to another treatment? Should I be concerned?
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Is the presence of anti-HbeAg an indication for low levels of viral DNA? Does it have any significance in the prognosis of chronic hepatitis b?
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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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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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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 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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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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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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About 3 months ago (Nov 1). I woke up one morning and did not feel dizzy but definitely off. Groggy, lightheaded, wonky I guess you could say. I can describe it like how it would look if you were standing at the top of a tall building. Things just looked foggy to me. It scared the hell out of me. I waited about 2 weeks because I thought I was just tired. It wasn't going away so I went to the emergency room and the first thing he did was check my ear and told me it was red and inflamed which is causing me to feel wonky. He said it was a mild Vestibular Neuritis. He said it's just viral and it will go away on it's own. Well, I have gone to my family doctor about 5 times since then JUST to have her check in my ear. It's now February and she still sees that it is red and inflamed. She said she doesn't want to just throw antibiotics at it because it DEFINITELY is NOT an infections and that it is viral. She said she also does not want to prescribe dizzy meds because if the room is not spinning then she doesn't want me to take them. I feel like I'd rather feel dizzy than feel this!!! How long does this "viral" crap last???? I have not felt ANY improvement since it started. Unless I am just used to feeling this way so it doesn't seem as scary anymore?? The only way I can describe it is that I am the most tired I have EVER been in my life. (gone for TONS of bloodwork and I am totally fine everywhere). SO just super tired and I have MASSIVE sensitivity to certain lights. I work under one at work and maintenance had to come in and dim the light for me. It's so frustrating because people look at me and automatically know that something is wrong with me because they see I am trying to focus on their faces. It's been like 4 months and I can't even deal with this anymore. My doctor seems as if she is fed up with me which I hate because I obviously wouldn't be going there if there weren't a problem. Last time I went she said the ear was still red and that she was going to send me to an ENT specialist. I have been waiting SO long for this appointment and it is finally on March 3. I just have the strongest feeling they are going to send me away AGAIN saying I need an MRI and then I have to wait even LONGER. My husband and I want to try and have a baby and we have totally put our lives on hold because I don't want to be pregnant and not being able to go for these tests that you can't go to when pregnant. I just want answers. I'm so upset. I know it's not vertigo because things aren't spinning. It's so hard to describe I'm just so tired and have a foggy head and sometimes that same ear aches and even that side of my head aches too. And forget being under certain lights. Does anybody know what I am talking about?? Please help me. I'm so nervous about going to this END as well because I don't want them finding anything super serious. I am so scared from all of this and I just wish I could get some answers. Will the ENT confirm that it is in fact VN? My doctor hasn't confirmed that. She just keeps saying "it's red and it's viral." I am so fed up and so sick and tired of feeling tired and foggy and wonky.
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Long story short I went to urgent care about 5 months ago because I was feeling lightheaded and disoriented. The NP told me I had an inner ear infection and gave me meds.
About 4 days later my symptoms had not improved and I went to the ER. They ran tons of tests and all were clear, then told me they also thought it an ear infection. I was diagnosed with a middle ear infection and sinusitis, told to stop my old meds and take some new ones.
I took a full round of antibiotics to clear the infection and after the bottle was empty i noticed no improvement, and may have felt worse.
I made an appointment for balance testing and an MRI with my ENT. The MRI come back squeaky clean. The balance test revealed that I had sustained "low frequency nerve damage in both ears". I now realize he probably meant vestibular nerve damage.
It's been close to 6 months now, I do feel much better than when this started but I still have constant brain fog and a feeling of imbalance. I also seem to feel worse when I go to stores or busy places. (oddly enough this excludes the gym, it's the one place I feel normal some times, I believe due to the fact working out releases endorphins, i'm not sure). I took an auditory test and they said everything seemed normal which is why I think it is neuritis and not labyrinths, as labs usually also causes hearing damage?
What do you guys think, sound like vestibular neuritis?
P.S. I'm doing some at home vestibular exercises, I meet with my ENT on the 22nd and am going to get him to refer me to VRT. At the moment the hardest thing to deal with is the brain fog, and anxiety it causes. I was thinking about asking to be put on Zoloft as my mother takes this and says it does wonders for her. I'm just nervous that it could make my brain fog worse, or slow down compensation. Do you think either of these could happen?
P.P.S. if you have a success story in dealing with this or know someone who has I would love to hear it. I'm beginning to feel that my life will always be like this and it's <seriously depressing> to be honest.
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After 3 long months and what seems like an endless struggle to get diagnosed, I have been diagnosed with an imbalance between my inner ears due to a viral infection, leading to a diagnosis of vestibular neuritis. The doctor said my migraines could also possibly be presenting themselves atypically and aggravating the situation.
I am doing vestibular rehabilitation exercises and taking steps to unclog my sinuses.
This is the longest ailment I've had and quite frankly I'm fed up, I know rehabilition will take a while, however does anyone know how long this thing can last??? It's ruining my concentration at work and puts me off social situations (I can't drink, it makes me wake up the next day feeling extra dizzy)
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I been diagnosed with vestibular neuritis I am dizzy taking valtrex and Valium can anyone give me some imput on this I had my first vertigo spell on sat.
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I live near Sydney , Australia, 49 years old, normally very fit and healthy. 8 weeks ago I was bitten by a large adult tick on right shoulder while hiking. It was on me for about 24hrs before I noticed, killed and removed it. A week after bite, chronic dull headaches started, sinus pain focussed on left side with whitish foamy post nasal drip, neck like a pepper grinder when I turn it, jaw joints clicking and stiff, darkened hollows around eyes, extreme unnatural fatigue. Have been to 3 separate GP doctors and local hospital ED several times and they were at a loss except to give me painkillers and antibiotics. Given 4 blood tests and all returned completely normal with no markers for inflammation, serology negative for infections. Had sinus x-ray: normal. Had brain MRI: normal Have taken so far in sequence, Doxycycline 100, then Amoxicillin Forte with Clavulanic Acid, now on Cephalexin and Metronidazole in combination with grape seed extract. None have made much difference except to lessen the headaches and I suppose rule out bacterial infections, so what I have is probably viral. Taking loads of vit C, garlic, horseradish, etc and resting in bed but nothing is helping. This going on for 6 weeks now, very debilitating.
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I have seasonal allergies, although, this may not be that case, because this year I have not had allergies.
I have had a BAD sore throat, and it really tends to hurt when I swallow. I've taken cough drops, honey, salt water rinses, tylenol and ibuprofen, and even gargled my prescription Lidocaine for numbing, and none of its working. I can't post a picture because I don't know how right now, but my throat is red, but no pus spots, no swollen tonsils, or anything else seems wrong. My sore throat has been accompanied by a fever that comes and goes, and a headache that lasts and day and goes, then comes back, and goes again. Is there anything I can take for what is going on, and can you tell me what I might have?
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I was diagnosed with post viral fatigue this year following a bad virus. Before that I was pretty healthy, I walked to work everyday and was at the gym a few times a week. Now, although I have recovered a lot from when it first hit, I still struggle day to day. Something as small as walking up the stairs knocks me ill, and a few hours out can leave me aching for days. Even cooking a meal isn't usually an option.
I'm getting frustrated because although I can accept that nights out and shopping centres are out of the question (I'm in my mid twenties, so what I usually did), I'm still working full time, even though this means that most of my time off is spent resting (in pain) to try and keep myself fit for work. I can't quit my job because we need the money but I'm not coping very well. My employer is usually good but because there is technically nothing wrong with me (my doctor thinks it will pass, and its not classed as a disability) they won't make any allowances or accommodations, which means that its not unusual for me to work very late nights or six days a week. My performance is suffering and I worry about dismissal. I want to work part time to give myself more rest (and be better at my job) but I won't be able to pay the bills, and my family don't think this is an option for us.
I've tried going back to the doctors but although she has run blood tests etc, I kind of get the feeling that she doesn't see why I'm bothering her, as she just tells me that recovery can take several months, and it's not quite been six.
It just leaves me frustrated because I feel so guilty about being ill. Although they tell me to rest and recover, it seems to be as long as I can manage pretty much as I did before. I know I put too much pressure on myself, but I feel as though I'm doing something wrong by needing help now, even though I've worked my whole life.
Does anyone else feel this way?
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I have had a viral chest infection for 10 weeks, have just gone back to work part time after 6 weeks off sick. My cough went weeks ago but I still feel unwell (which varies day to day) with lung pain (worse when I lie down, walk, bend etc) and ringing in the ears.
I am worried about how long it is taking to get better, the Doctor gave me nothing apart from painkillers and said it is just a nasty bug. I am also worried whether going back to work was the right thing, do you think it will make it worse?
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