Hepatitis B Support Group
Hepatitis B virus infection may either be acute (self-limited) or chronic (long-standing). Persons with self-limited infection clear the infection spontaneously within weeks to months. There are currently several treatments for chronic hepatitis B that can increase a person's chance of clearing the infection.
Guys I know you may be struggling and thinking negative things and feel like you want to commiserate but its doesnt have to be this way there are cures we that are being with held from us. Think if even 1% of us unite and circulate a petition then we can make a change or even show. Think do you want this thing to run your life as it has done to so many already? Or do you want to look back and know you were part of the generation the changed things. LET USE THE INFORMATION AGE TO OUR ADVANTAGE :D
You know I was thinking about the scientist in Germany Proffessor Ulrike Protzer who has eradicated this virus in her tests by immune boosting instead of viral suppression.
When I spoke with her she out right refused to help me nor give me any info accept maybe one day it may be in clinics in about 10 years if at all. (the impression i'm under is big Pharma's interests are being looked after not man kinds)
These people have no conciseness whatsoever and if we sit back and do nothing we'll get more of the same "treatments" we will be enslaved to for the rest of your life. Don't we deserve a cure? It means we need to do things different to get something required. I promise you this it won't be easy but for hummanities sake then isn't it worth trying?
I was thinking if there are 400million of us suffering this disease then why don't we start a petition for the university to volunteer this information for all suffers to make our own informed decision regardless of Pharma regulation. bypass it as its corrupt to the core and totally untrustrable which is evident
I was thinking what would be needed would be to recruit out of 400million suffers following roles
#Lawyers
#I.T/social media marketers
#Journalists
#Even anyone in politics who may suffer from this.
#MOST I IMPORTANTLY ANYONE WHO REALLY WANTS A CURE AND WILL SETTLE FOR NOTHING LESS
The petition would need to force the university to disclose the detailed research to the public by the end of 2014. Who wants to wait 10years? Surely the right thing needs to happen even if it costs some jobs in the pharma industry
Anyone who wants the professors contact details let me know you are welcome to she is a immunologist.
Anyone who wants to do this we need numbers. Please think about copy and paste this in other forums and see if we can combine our energy and free the 400 million.
Contact me if your interested lets try to turn the tide
THINK ABOUT IT PLEASE
You know I was thinking about the scientist in Germany Proffessor Ulrike Protzer who has eradicated this virus in her tests by immune boosting instead of viral suppression.
When I spoke with her she out right refused to help me nor give me any info accept maybe one day it may be in clinics in about 10 years if at all. (the impression i'm under is big Pharma's interests are being looked after not man kinds)
These people have no conciseness whatsoever and if we sit back and do nothing we'll get more of the same "treatments" we will be enslaved to for the rest of your life. Don't we deserve a cure? It means we need to do things different to get something required. I promise you this it won't be easy but for hummanities sake then isn't it worth trying?
I was thinking if there are 400million of us suffering this disease then why don't we start a petition for the university to volunteer this information for all suffers to make our own informed decision regardless of Pharma regulation. bypass it as its corrupt to the core and totally untrustrable which is evident
I was thinking what would be needed would be to recruit out of 400million suffers following roles
#Lawyers
#I.T/social media marketers
#Journalists
#Even anyone in politics who may suffer from this.
#MOST I IMPORTANTLY ANYONE WHO REALLY WANTS A CURE AND WILL SETTLE FOR NOTHING LESS
The petition would need to force the university to disclose the detailed research to the public by the end of 2014. Who wants to wait 10years? Surely the right thing needs to happen even if it costs some jobs in the pharma industry
Anyone who wants the professors contact details let me know you are welcome to she is a immunologist.
Anyone who wants to do this we need numbers. Please think about copy and paste this in other forums and see if we can combine our energy and free the 400 million.
Contact me if your interested lets try to turn the tide
THINK ABOUT IT PLEASE
I'm sure there will be some people here and there signing but it would have to get a response world wide to get anywhere in my opinion...
I mean if a petition was created and every carrier could post in every forum they are in it would build momentum.
What do you think?
So you wouldn't have to tell the public of your condition at all plus if down the road the petition gains momentum you may be "freed" of your condition. How does that sound?
https://www.facebook.com/hepbfoundation
To start with this is the birth of the idea
1
So we need someone whos already public with their condition to be the face of it.
2Face book link is a good idea however I think the HBF may have a vested interest in or work closely with BIG PHARMA. So I think asking them for advice is not the way to go. However it would be a good spot to regularly post the petition because alot of suffer's look at that site.
3. We need someone with enough I.T knowledge to start the online petition
4.Is there anyone here who is public about their condition?
pls share us the result of your doctor visit next week. thanks
When it comes to someone who's in the public meaning someone who's open about their condition like you Necko. As you know for the majority of the rest of us feel alot of stigma.
Someone who's willing to front the online petition. Necko would you be interested in that?
Someone willing to go public would be good as well but if not
I've checked on wiki google I'm struggling to find a celeb who's open about it.
Lexi did you find any?
The communications so far with Hep B foundation have not really been fruitful if I'm honest.