Re: Was CFS or Heaptitis C DiscussedatLDNConference?

[Guest guest]

You could always call one of my doctor friends Neil Ahner at 561-630-3696 and ask about his friend who is an expert on mycoplasmal bacterium's. NAC is wonderful cleanser for anything lung related and olive leaf extract helps those mycoplasmal creatures die. There are things I think would help you but I don't want to take up others time. You can e-mail me if you like.Olive leaf extract is a natural antibiotic and you cantake it everyday to get rid of the yeast those antibiotics caused. Take care, Kathy

Re: [low dose naltrexone] Was CFS or Heaptitis C DiscussedatLDNConference?

No, I don't really think I have 3 diseases but CFS is very similar toMS. Also there is a Lyme MS. I do have punctate lesions but only onelarger one that is inactive. I just had MRI and will be seeing a neuroin August for the comparison with previous. Sheremata based diagnoseson clinical before looking at MRI. By he way Lyme has some type oflesions also. I am not certain is they are all located in differentareas of the brain. I had ocular ataxia, some graphestenia problems onone side, parapheresis, balance and gait problems. I took someantibiotics for about 6 months and my symptoms gradually subsided. Idid have something strange in my lungs that they thought could be mildfibrosis that disappeared when I took antibiotics. I was takingantibiotics for intra cellular mycoplasma pneumonia. Sheremata wanted to start me on a beta but I declined. My brain was sobad before the antibiotics I had difficulty completing a sentence. Ithas gradually improved but not back to normal. I just heard about LDN so am checking out your site. There has alsobeen implications of bacteria such as chlamydia pneumonia in MS thatwould respond to antibiotics.CFS also effects the immune system, Klimas in Miami is also an expert inthat field. Most people don't take CFS seriously and her first papershe referred to it as a form of AIDS, of course it is an acquired immunedysfunction syndrome, but people with CFS had a hissy.Of course most CFIDS people refer to it as myalgic encephalomyelitis.