Maximum Milk Thistle Home Another Natural Wellness Solution

I truly believe that I would not be doing as well without Maximum Milk Thistle and could be in liver failure by now without it. Nancy  C.

I can’t say enough good things about  Maximum Milk Thistle. I have tried 3 different types of Milk Thistle. Although they did help some with my liver enzyme tests, I was ecstatic after taking your product for just 3 months.  Peggy M.

About after 1 year of being very sickly I began researching milk thistle...yours stood out as the purest and the most potent of all. I have  not missed a day of taking this herb and have been feeling just great. Robert H.

I started taking Maximum Milk Thistle about a year ago and within  two months my condition stabilized and has remained  so to this day. Richard G.

I am an R.N. I contracted Hep-C from a  patient and have been taking Maximum Milk Thistle for 4 years, as recommended by my gastroenterologist.  I believe this product is the best on the market. Clare G.

I have seen the benefits of MMT evidenced by improvement in lab tests and maintaining  an active lifestyle. Maximum Milk Thistle has been a valuable addition to staying healthy as a HEP C survivor." Michael D.

After a few months of taking Maximum Milk Thistle I went in for my quarterly blood work. Amazingly, my markers were all coming down, still not within normal ranges, but improving. After several years, all of  my markers are well within the normal ranges of people without liver disorders. Malcolm G.

My liver enzymes remain normal to a point or two above normal. I can attribute that in part if not all to Maximum Milk Thistle. Melvin E.

I have been taking MMT for 3 years and my reports are all absolutely normal! My liver enzymes have  not  increased  at all.  Craig T.

I feel that Maximum Milk Thistle was an important part of regenerating my liver. My Hepatologist called the regeneration  of my liver a miracle. I'd recommend MMT to anyone with Hep C undergoing  treatment. I'd also recommend MMT to anyone who has Hep C or just wants a healthy liver. Steven K.

I have been using Maximum Milk Thistle for over 1 year and my hepatic function blood panel  test have improved---along with the way I generally feel. Fred P.

I just had  my liver function test and they are the best ever. I have been  taking  MMT  for a month. Ruby B.

I feel great - no fatigue, no pain and stable enzymes. Dr. Timothy S.

I have just gotten my eight month blood  tests back and I am not free of the Hepatitis C virus, but  my AST and ALT levels are both in the 30's! I'm sure your product  is a good part of the reason. Thank you! Jim  O.

Last Tuesday, 2 months on Maximum Milk Thistle and 30 days on the diet, my blood tests came back the best ever in 3 years! Tracey K.

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Arzneimittelforschung 1992 Jul;42(7):964-8

Pharmacokinetics of silybin in bile following administration of silipide (Siliphos®) and silymarin in cholecystectomy patients.

Schandalik R, Gatti G, Perucca E

Surgical Department, Regional Hospital, Braunau am Inn, Austria.

See National Library of Medicine Citation

These data indicate that the bioavailability of silybin is much greater after administration of silipide (Siliphos®) than after administration of silymarin. This results in increased delivery of the compound to the liver, which represents the target organ for pharmacological action.

The biliary excretion of silybin, the main active component of silymarin, was evaluated by using a specific HPLC method in 9 cholecystectomy patients with T-tube drainage after intake of oral doses of silipide (Siliphos®) (Siliphos®) and of silymarin (120mg expressed as silybin equivalents)

After intake of silipide (Siliphos®), the concentration of silybin in bile reached a peak within 4 h and declined thereafter with a mean time of about 10 h. After administration of silymarin, biliary silybin concentrations were several-fold lower than those observed after intake of silipide (Siliphos®).

The bile collected after silymarin intake also contained considerable amounts of isosilybin (a silybin isomer) and very low levels of silydianin and silycristin. The amount of silybin recovered in bile in free and conjugated form within 48 h accounted for 11% of the dose after silipide (Siliphos®) and for 3% of the dose after silymarin. Plasma silybin concentrations, determined in 3 subjects, were several-fold lower than those in bile after intake of silipide (Siliphos®) and mostly undetectable after intake of silymarin.

 


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