my feedback

[flyinsky]

hi everybody
here is my feedback from i know that i have heb till now
my biliburine prothrombine all in normal range


  05/06/2011(pregnant)
alt                   12
ast                   09
hbsag              2700ui
adnhbv            2500ui
hbeag and ab not done            
fibroscan          0.16kps
ultra sound       normal

     //11/2011(pregnant)
alt                   09
ast                  04
hbsag            3000ui
adnhbv          <20ui
ultrasound     normal
fibroscan        0.24kp
hbe not done

     03/2012'  (after delivery baby in january 2012)
alt                 16
ast                 12
adn undetectable  <12ui
ultrasound        normal
hbeag        ----
hbeab        ++99%inhibition
hbsag             3500ui
pre c mutant

    12/2012
nearly same results with march2012

     7/2013   (pregnant)
alat        26
asat       19
hbv adn    2600ui
hbsag       3700ui
ultrasound    normal
fibroscan      2.5kp
hbe ag -
hbeab+

january(feeling pains in arms and every where lUck of vit d  17ui
4/03/2014)
alat      166ul
asat       87
adn        44million

24/4/2014
alat   123
asat    65

7/4/2014
alat  111
asat 60

  22/4/2014
alat     169
asat    97

  10/05/2014
alat209
asat 102
adn   54 million

29/5/2014
fibroscan 6.1
  
7/06/2014
alat   156
asat    83

21/6/2014
alat     80
asat     49
fibroscan   7.4

05/07/2014
asat    49
alat     80

26/07/2014
asat    50
alat     78
adn     119 million
fibroscan  4.2

29/10/2014
asat   48
alat    70  waiting for check for 18/11(maybe fibroscan or biopsy)
viral load  80million
thans i  advance  about your opinions





    

  

[flyinsky]

Stef anf others waiting for your answer
By the way vit d is in normal range i did test and i take my amples regularly

[flyinsky]

Hi every body
It a long time i didnt post
My news
I was prégnant in which all was cirrect may dna was 200in september alat asat in normal range.... I jave delivred baby on december... And now here my résults
Alat 50
Asat45.
Dna50ui
Ggt15
And the rest is normal
Please help me to interprett my results....... Dna is lowering but alat is little high....... Sti

[Airquake]

My dna fluctuates as well. My blood test is normal including ast and alt. I do the test every quarter and so far I observed that starting october 2015 my dna was at 40, 150, 240, 90 and now is at 50ui. I'm not on anit-viral meds. Per my doc it is normal.

[flyinsky]

Hope so.thanks

[flyinsky]

Hi everyone
Here is my update
All blood test within normal rage
Alat16asat21
Viral load 314ui so rise from 199to this
Rise is it significant?and also I have a doubt maybe because I have stopped honey and blackseeds?

[StephenCastlecrag]

Rise is not significant (to be significant, must be 10-fold increase, that is to over 3,000 iu/ml). So it is most likely to be fluctuation, as Airquake commented.

[flyinsky]

Thanks a lot

[Cabin3]

Flyinthesky:  I've been following your information.  I'm sorry but unclear.  Are you chronic HBV and were you ever on any antivirals to lower your numbers?  This is impressive results.  Are your European decent or Asian?  
Also did you experience symptoms like orange or dark urine during your flare?  I'm trying to see at what point should I be concerned as well.  I have high viral load and high ALT 384.  No ultrasound. And pregnant.  I too would like to have my body fight this on its own but would not want to also wait too long until it's irreversible.  Please provide info.  Also how old are you?

[StephenCastlecrag]

Don't use angle brackets (LT, GT) - any text in between LT and GT is deleted by Medhelp. This problem is known to Medhelp.

[Aduiski]

i see, thx for the info Stephen

[flyinsky]

Hi every body
I did this morning m'y transaminases test and results are good.
Alat 14
ASAT 16
So I think till now is good my full panel is on November hope my DNA will be end

[flyinsky]

Yes but m'y Doc refusésto put me on any ttreatment since m'y conditions are not bad and tell me that m'ybody react maybe better than antivirals and maybe get same results......

[Aduiski]

That message was directed to Stephen specifically not to you.

As your ALT is <19, your DNA <2000 and your Fibroscan 19), and Fibroscan once per year.  Once either A) Fibroscan goes > 6, OR B) ALT>19 with DNA >2000 on two measurements 3+ months apart I would initiate the treatment.

[Aduiski]

my text was cut. it was supposed to be:

As your ALT is <19, your DNA <2000 and your Fibroscan 19) and Fibroscan once per year.  

Once either A) Fibroscan goes > 6, OR B) ALT>=19 with DNA >2000 on two measurements 3+ months apart I would initiate the treatment.

[Aduiski]

hmmm...my text keeps being cut for no apparent reason...so please disregard the above 2 messages

[flyinsky]

M'y fibroscan Is never 19 now it Is 5.4

[Aduiski]

I wrote fibroscan >= 6 but text got cut and so it appeared like 19

[flyinsky]

hhhhok

[flyinsky]

My last test of hbsag was arround 3000but this few years go.i dont know now.i hope my body will be able to clear.thanks lot for your comment and hope thèse treatment Will bé availible sooner

[Aduiski]

now it is probably (but not surely) lower then that...it usually tends to slowly decrease with time

[StephenCastlecrag]

Your numbers are looking very good now. HBVDNA  less than 2,000 iu/ml and ALT is normal. So what will happen in the near future? A lot of research indicate that if your HBsAg is below 100 iu/ml then the chance of s-seroconversion is high within the next few years. At the least, you will need a steady decline of HBsAG. Others suggest HBcrAg (core related antigen) may be a better or just as good predictor - but the test for HBcrAg is not widely available. I think we can only monitor regularly and see what will happen. Hopefully, new drug candidates such as ABX203 (a therapeutic vaccine now available in Cuba) may help; ARC521 should be able to reduce HBsAg, but it is only in Phase1 at the moment. Other potentials, such as capsid inhibitors from Novira should also help. Experimental treatments with existing PegIFN and oral antivirals together with better selection and stopping rules may help a certain % of patients.

[Aduiski]

I believe the time has now come when it would be better to get on tenofovir/entecavir earlier rather then later. Being 10 years on tenofovir/entecavir seems to be safe, and within 10 years other treatment options would arrive. Until then, 5-10 years of tenofovir/entecavir would allow for  reduction of HBsAg for about 1 log or to about 1/10 of the initial value (for hbeag positive even more). Someone starting with HBsAg of 2000 IU/ml for example, would within 5-10 years of treatment come down to about 200 IU/ml, a level which would offer him/her a realistic chance of cure.

[flyinsky]

Sorry for appearance measures
In brief now alat 17
ASAT 20
Viral load  199ui

[flyinsky]

Hi everyone
My tests were done
I have a check every 6monthes but blood tests of transaminases each 3monthe
here are m'y new result
February2015          november  February 2016.  May2016
Alat 69.                18                      25.                 17
ASAT high.           12.                    16.                  20
viral load.            199000ui.                                 190ui
And all other good test are in normal range especially before I suffered from low level of platelets now they are in normal range 210000
Fibroscan 5.4
Ultrasound   no abnormalities
Thank you all In advance for your opinions

[flyinsky]

Hi everyone
Today I did asat alat to see if they are in normal range
Here are result
alat 18
ASAT 12 this 3monthes ago
Today
Alat 25.  Normal range <33
ASAT 16.
It is in normal range but afraid of augmentation
Thanks in advanced

[flyinsky]

Thanks i Willtake a look over forums and see from where here in France peole buy it.

[flyinsky]

Yes sure
I ask m'y family doc to prescribe me daily vit d doses.he told me that vit d alone in pharmacy there is not but including with other vitamins(multiple vitamins drugs like juvamin defenced or with calcium)and I can't take it Daly.so he just ask me to take ample each 3monthes and drink milk with vit d.eat 3or 4times fish a week.and in summer I should be exposed lot to sun.i ask him about products on net.he told me that he don't trust them.
I think docs here in France are not giving a great importance to vit d but for me I am sure that pains are due to this luck.next month I will do a check and see my level.

[twinboys1girl4me]

Can you buy vitamin D over the counter, like at a grocery store?  If not, online should be easy.  Many people take vitamin D daily and when I started my viral load went lower than its ever been (off treatment).

[stef2011]

yes all good results, pain is probably just low vit d or high norm range pth

[flyinsky]

Hi every body
Finally I get my result[sorry in French
Protein c reactive.      3mg/l.          normal   <5
Facteur rhumatoide.    7ui/ml.        normal.  <14
Facteur rhumatoide igm.  1ui/ml.     normal< 14
Anti corp anti nuclear.      negatif
Cryoglobulenomie.          absence
Could someone interpret(if I understand well no system illness?)
Thanks in advance

[flyinsky]

Ok thanks lot.
Hope results will be ok most of them I did it last year when I had pains. And i was negative for it only low vit d.
I will post my result .thanks again

[stef2011]

http://www.vitamindwiki.com/Rheumatoid+Arthritis

check here.

there is no cure for Rheumatoid+Arthritis but only immune suppressing drugs and steroids which you can t use otherwise hbv would flare up free.the usual proposal is antivirals plus immune suppressing drugs, they get double the money from you without curing anything
its way better checking if vit d can repair your abnormal immune system in case you have Rheumatoid Arthritis

[flyinsky]

Yes tomorrow I will do what she asks me and she told me if abnormalities in result immediately should seen rumato.for vit d I will see my general doc in month
So is my doc do the right things?

[stef2011]

it is best to optimise vit d and pth too, we cant think of being healthy if vit d is not optimal because immune system doesn t work properly plus bone problems are common on hbv carriers due to the low vit d and the vdr receptor mulfunction

it makes sense to check both what yoour doc prescribed but also making vitd25oh and pth optimal

[flyinsky]

Hi  members
I have my check today wich didn't convinced me and have an other fear to have an other desease
My doc not interested lot inbhbsag quantity.
She told me that she want again to see my alat in 3monthes then a complete panel including us and fibroscan in 6monthes
For my arm pains she gives me an other blood test here are
Fan
Creative proteins
Latex
cryoglobulinémie
In French
.so and yesterday I have kyste on my hand for this she asks me to do that.
And she told me that the pains i suffer from are mot due to vitamins d defiance.but a probleme with hbv wich may affect articulations or other desease
What do you think?

[flyinsky]

Ok I will ask her to prescribed it if she refuse I will do it by my own money.

[stef2011]

do you think black seeds play a role  concerning my result?

it didnt work for me but it makes no harm so it is good to try.for vit d do not wait for doc start at least 5000iu of d3 daily, low vit d is also a concern for the baby because low vit d in the mother can make many health problems for babies during life so check also the baby and keep best levels for him/her too

hbsag is key to understand immune system/virus balance and if it ever reaches 1000-1500iu/ml that is good for peg try

[stef2011]

starting nucs during this immune/virus re-balance is not good, nucs might stop immune system re-balance.i think they re useful only if we have bad liver damage if you can still monitor to see when hbsag/hbvdna stop the decline is best

[flyinsky]

Thanks for comment
So just monitoring right now.i did in April biopsyf0a1.
For hbsag my doc not a lot interested in just in case of treatment.
For vit d I have already a problem with it I will discuss with my doc about .
I wanted to use interferon but with present result I don't think she will prescribed it to me.do you think black seeds play a role  concerning my result?