Lloyd Wright contracted Hepatitis C in 1979 from blood transfusions. A liver biopsy in 1994 revealed Chronic Hepatitis C. The medical establishment advised him to get his papers in order and expect to live another 3 to 5 years, and hope that something would come along to help. Lloyd has been Hepatitis C Free for [...]

Lloyd Wright the “guy who was cured from Hep C” and the author of Triumph Over Hepatitis C the book that describes the alternative medicine approach he used to heal himself and achieve being “hep C free”. Hepatitis C is the most prevalent liver disease in the world. The World Health Organization considers Hepatitis C [...]

From: Carla Sent: Saturday, November 14, 2009 2:26 AMTo: Lloyd WrightCc: Subject: TLM Dear Mr. Lloyd, I am writing you because I recently heard about your alternative TLM medicine (http://tinyurl.com/6n6yy) . My Dad needs a liver and kidney transplant ASAP, but not after he undergoes Hepa C treatment for 3 months. Doctors say his liver will fail in 6 months to 1 year so we need to act quickly. We've already started his first Peg-Intron shot yesterday. But today we got to speak to Mrs.Quiazon who told us this story of how her husband had liver cirrhosis but couldn't get a transplant because of a weak heart and didn't want an Interferon Treatment for fear of damaging the liver even more.. so she instead opted for your TLM (http://tinyurl.com/6n6yy) ... and it worked wonders for her husband! While the doctor told them he only had 2-3 months to live.. it's been 3 years and he's still alive.. Thus, we find it very inspiring and promising.. So now my family is seriously considering this option. But can you let me know please what the implications are given that my dad has end stage kidney failure apart from his liver cirrhosis. He's been undergoing Dialysis for almost 3 years now, but we only found out about the liver problem about 3 months ago. Is TLM the right alternative medicine for him given his condition? What are the implications? Any side effects? If you're able to answer these questions right away, we might place an order already as early as tomorrow.. Thanks so much,CARLA From: Lloyd WrightSent: Tuesday, November 17, 2009 8:46 AMTo: 'Carla Subject: RE: TLM Hello Carla, TLM (http://tinyurl.com/6n6yy) is good for his liver and his general health. What concerns me is that interferon does cause heart attacks and it does cause kidney failure, remember Natlie Cole? I am aware that the liver transplant people demand this but it is wrong. There are no negative side effects from TLM (http://tinyurl.com/6n6yy) .

Hi. I received my paperwork and was pleased to see that not only had my viral load dropped from 3.2 million to 1.1 million but my AST went from 35 to 25 and ALT from 45 to 33. I have since ordered the blueberry (https://www.hepatitiscfree.com/appieshop/index.cgi?mhhepatiSTORE:CKIE:pr...) and have been taking it as well. Thanks again, Mary

Hi Lloyd, I'm freaking out a litle bit right now. I just got my latest viral load back and it is back up to 8 mil from a low of 2 mil a year ago. My liver counts are slightly elevated again also, but only in the high 40's I don't have the paper work in front of me yet as they failed to send them off to me. I've been noticing slight irritation in the liver area, front and back. I can't believe this, I was sure I would be real low on the viral count this time. I strarted at 19 mil 3 years ago and dropping ever since. Now it is spiked again. My Doctor wants me to see a G.I. I've already been that route and don't really feel like revisiting it. I am type 1a so even if I was crazy enough to give inerferon a try it wouldn't work for me!! No I'm not going that route!!! I have been slacking off on the teas so I thought that probally had to do with the elevated liver counts but now that the viral load is back up I'm very concerned!!!!! Could coffe be effecting the viral load, I drink about 2 cup a day. I know i'm all over the place with this e-mail I just don't know what I have been doing wrong! Help Please. Carol Besides what I have checked off for supplements I also have been taking Laktoferrin (https://www.hepatitiscfree.com/appieshop/index.cgi?mhhepatiSTORE:CKIE:pr...) for about 2 months. So I thought for sure my liver counts would finally be below 30's, NOT! Hello Carol, I understand how this affects you completely. HCV is an independent entity. It is not always something you may do wrong, the viral load can rise because the virus has a desire to live. When it drops as much as yours has, there will be times when it rises again and the higher it was the more it is liable to rise. That is what I see. Doctors are not close enough to patients to observe these things the same way I do. This is not a big deal, other than on your mind.

From: Danny Sent: Monday, October 26, 2009 4:00 PMTo: Lloyd WrightSubject: Re: Hep C Heamocramatosis Dear Lloyd, Thanks for your help. I am getting Phlebotomy done I want to share some interesting result with you.. I was diagnosed with Hematochromatosis Hep c on 7th of this month. started Phebotomy My First Phlebotomy was on 12th. Blood bank where I go has small lab too I ask them to do LFT when they draw my blood for Phlebotomy. As Blood bank tech is my customer he does favor to me to do this test. My liver enzyme on 12th ALT 178 AST 130 At my second Phlebotomy on 19th ALT 172 AST 125. On 19th I talk to you first time order level 5 Program (http://tinyurl.com/5n5dy) ask your staff to send to me next day delivery, I received on 21st started on 22nd. I am still waiting for my Aloe Juice (http://tinyurl.com/luook) still not started any of tea. Today is 5th day of my Program got 3rd Phlebotomy done. ALT 80 AST 115. 4 days in to Program My ALT dropped 50% I am really excited. I am tolerating your Program OK Except have some loose BM approximate 5 to 6 a day lots of gas can you suggest something? My Genotype Viral load results are with my hepatologist but he has refused to give it to me. I have ask my Primary care Physician to request my medical record to her. Hopefully she will get it. I have appointment with her next week once I will get it I will forward that to you. Thanks for all your help I really apprecite it Danny From: Lloyd Wright Sent: Tuesday, October 27, 2009 8:39 AMTo: 'Danny Subject: RE: Hep C Heamocramatosis Hi Danny, I am thrilled that every is working out well! Often people with hep c have high amounts of yeast in the small intestine which will cause gas and loose bowels when doing my programs.

From: Donna Sent: Monday, October 12, 2009 10:42 AMTo: lloydSubject: Is there any concrete proof how dangerous the pegintron is and the lasting side effects? Hello Lloyd, I have an email from you years back [2005-2006] advising me of side effects from the interferon. You were right; I wish I had not taken the treatment because it did not work. Six months past the treatment my hep C returned and I am not very functional in life. I was calling out of my job two – three days a week because my knees hurt so much to walk, and that was a part of my job. I began the pegintron in summer of 2007 and had the last dose on J an. 4th 2008. I was assured by doctors that I was curable. With the insistence from doctors staff and my husband, I went with the treatment. Also, I was having so much pain which I know is caused by Hep. C, even though the medical staff will not concede it is so. I just wanted my life back and believed I would be cured. Now I battle to get out of bed. I can’t think clearly. I forget things all the time and my 24, and 18 year old let me know about it because it is things which are important in their lives. My knees stay swollen and I do not walk very well anymore. My GP once prescribed an anti-steroid, anti-inflammatory hoping that would work but that did not. I have to take something to help me sleep because of the pain. If I don’t, I am in so much pain and turn throughout the night because I can not find comfort to rest. My eye sight is so bad I use a magnifying glass to read letters, newspapers, etc. I am unable to work anymore and now fighting for disability. They denied me saying my condition is controlled with medication. I need information of the dangers and side effects from the pegintron to take for my disability hearing. I was so outraged when they told me; my illness is controlled with medication. I can not look for the information very long myself due to the constant headache I am battling.