Guest guest Posted January 10, 2009 Report Share Posted January 10, 2009 The second half of my post disappeared into cyberspace. There are 12 recliners in the treatment room and patients chat about why they are there and what has happened to them. Many were given only a year or so to live and are still around several years later. Some are just ok: some feel great. He treats all types of immune system disorders and some cancers. Many he treats have been through regular channels and told they are going to die or be permanently disabled and there is nothing left to do. My feeling is that the IV's work and the change depends on how sick one is. My labs were good going in (after 10 months on his recommended supplements) ALT--36 AST--47 Platelets--278 So I did not experience much change. I am on low dose naltrexone for my rheumatoid arthritis, but just started, so can't comment on that yet. Only one other Hep C person was there. He was a non-responder and has been there several times and is feeling good. My personal feeling is that if your numbers are low, you might want to try the supplements he suggests and see how it goes. If your numbers are high and you want to try alternative treatment or have been a non-responder, then the IV's might really help. ANY treatment is a personal choice. Again, I have had Hep c 43+ years, am 74, and this is my first treatment experience of any kind. The nurses tell me that some on transplant list heal sufficiently and do not require transplant and some go on to transplant. My other suggestions are--Whatever you decide--go to your doctor regularly--get your labs regularly--This disease is very sneaky and can change directions--DO NOT DRINK ALCOHOL--Watch your diet and eat well (I will post Dr Berkson diet) Exercise. There are new treatments coming up for Hep C that may not be as debilitating as those today. Do NOT panic because you have Hep C, especially if you are in the first stages. It is normally not an aggressive disease. Consider ALL options before doing ANY treatment and get all the info you can. Read the online book Choices on www.hepcchallenge.org. They have just published a new edition. If anyone wants to post me personally, feel free to do that. Cheers and health to all, SuziQ Quote Link to comment Share on other sites More sharing options...
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