Hi, my name is Paul. Back in the mid to late 90’s I started getting flu like symptoms, severe fatigue, stomach problems, colds, you name it. I was at the doctor’s office three to four times a month. I was going to the doctors with every sickness possible. My wife thought I was a hypochondriac. Finally I started reading about every symptom I had and was sure I had Aids and was dying, so I asked for an Aids and Hepatitis test. I was given all the tests and sure enough I was positive for Hep C. After all the tests came back, he said I was OK’d for Ribavirin- Interferon treatment, but he would have to put me on a waiting list. Within two weeks the Doc called and said a slot had opened up for me to receive treatments. After reading all the side effects and months it would take to complete the process with my family, we were sure of one thing. If I didn’t die of the virus, I surely was going to die of the treatment. We decided to wait until possibly some other type of treatment was approved. I discussed this with my Doctor and he said he understood, and I should come back in six months to a year to re-evaluate the situation. After a year went by I went back to try to talk to him and possibly try the treatment. He then told me the treatment was not working for my particular type of Hep C – Type 1A. He then said he was sorry and was sure they were working on a vaccine to prevent Hep C. There was not a cure to help us.
All along I’m getting more and more fatigued and sick. Then in 2003 I moved to Riverside County and was assigned to a new Medical Group. Thank God for the health benefits I receive on my job. A new doctor now. Lots more office visits, more ultrasounds, biopsy, blood work, nuclear medicine x-rays and the final prognosis is I have Hep C, type 1A. High iron loads and a viral load of 25 million. There was nothing the medical group or insurance could so, so would not authorize more treatment or specialists I was sent a form letter with my right to appeal the decision. My Mom and I then went to the Doctors office for an understanding of the letter in which they said they were sorry and there was nothing they could do except put me on permanent disability. Then came the tears from my Mom, and I reassured her that everything was going to be all right. This meant my relationship with God was good and he would accept me in heaven.
My mother would not take this ending, so after weeks of research and calls, we ended up at a Wellness Center who specialized in Integrative Medicine; meaning they are Medical Doctors who treat you first with natural supplements and nutrition. They can also prescribe drugs if all else fails. We met with an MD (also scientist) and after hearing my symptoms and background he said my immune system was the problem. He and several other doctors were doing clinical trials a few years back with a product called Leukomeal, treating Hep C and other life threatening illnesses, but he said there had been greater results with Hep C patients. He said if we could locate the Leucomeal I would be much better off and have a happier long life. In his opinion, it worked faster and better than any treatment he had seen. He then proceeded to make several calls, trying to track down the doctor who was using the product. After getting the information he needed, he handed us the name and number of the MD at another wellness center who practices modern medicine with integrated medicine.
After getting an appointment at this new wellness center December of 2004, the doctor spent 45 minutes asking me questions, then showed us several studies she had done with patients who have Hep C (names withheld, of course). She then sent me home with a low carbohydrate diet, no sugar, vitamins, and glutamine for the lump feeling I had in my right side. Most important, a vial of Leukomeal. After getting a GGTP test the next day I began using Leukomeal two times a day. My energy level went up and my GGTP lowered from 128 to 67 in 10 days, down to 42 when tested 14 days later, then an amazing reading of 18 on my next testing 4 months later. It’s now over two years and the GGTP and all liver panel tests remain low. I feel great. I still see my wellness doctor once a year and only have to take the Leukomeal once a day for maintenance. I now work 6 days a week, have a very good attitude about life, visit church regularly, own two houses, an RV and can plan ahead for the future with my wife and two sons.
Life is good, and I would like to share my good fortune with others who have not been exposed to this great product Leukomeal.
P.S. I now have plenty of sick and vacation time to spend with my family and the energy to enjoy it, thanks to the wellness center and my mom for leading me to Leukomeal.
