This forum is for hepatitis patients, family members, loved ones, friends or anyone with an interest in hepatitis, to have open social conversations about any topic they choose, with the exception of religion and politics. Please note that our standard “Rules for Posting in Public Areas”, which are found in our
Terms of Use , also apply in this community.
If you are newly diagnosed with Hepatitis or you have questions or information to share about current treatments, research studies, clinical trials, or other medical issues pertaining to Hepatitis, please post it in one of our Hepatitis Communities (
Hep A ,
Hep B ,
Hep C or
Hep-autoimmune ).
What have you been diagnosed with - what genotype, what grade, what stage?
If you have hep-c i know you have to be careful of what pain meds you take. some don't agree with the liver.
and, yes, there is treatment.
good luck.
wyntre
THANKS KEITH
THANKS KEITH
At best, colloidal silver is ineffective; and *can* be toxic. Here is a counterpoint to the proponents of the product. From Quackwatch:
http://www.quackwatch.org/01QuackeryRelatedTopics/PhonyAds/silverad.html
Colloidal silver is a suspension of submicroscopic metallic silver particles in a colloidal base. Long-term use of silver preparations can lead to argyria, a condition in which silver salts deposit in the skin, eyes, and internal organs, and the skin turns ashen-gray. Many cases of argyria occurred during the pre-antibiotic era when silver was a common ingredient in nosedrops. When the cause became apparent, doctors stopped recommending their use, and reputable manufacturers stopped producing them. The official drug guidebooks (United States Pharmacopeia and National Formulary) have not listed colloidal silver products since 1975.
The picture of the couple in the article with the black eyes is enough to scare me off. My uneducated advice is to stay away from that cr@p. Make sure that you have your doctors blessings prior to taking any medswhether prescription, OTC, or supplements.
Take care
Bill
I APPRECIATE YOUR ADVICE AND WILL SPEAK TO MY DR ON THE 6TH OF JULY. I WILL FIND OUT MORE WHERE I AM WITH MY TESTING THEN. ILL SHARE WITH EVERYONE AND HOPEFULLY ILL GET SOME GOOD ADVICE. EVERYONE SEEMS PRETTY GROUNDED ON THIS SIGHT AND SUPPORTIVE OF EACH OTHER. THAT'S GREAT. AGAIN THANKS
KEITH
http://janis7hepc.com/
Click on just diagnosed in the blue box. Spend a few hours reading through this site, as well as Medhelp to better familiarize yourself with this disease. Then make a list of questions for your doctor appointment; youll be much better informed and able to ask some pertinent questions from your busy doctor. Continue to ask questions as needed in here- theres usually someone here that will be happy to help you.
Take care,
Bill