anise star
New member
hello, I am new here...
hi, my partner has CFS for a few years now. It started as fatig attacks for tow to three days in a month. gradually it became worse and now we are happy if there is a good day in a week or two. a year and a half ago he started a treatment with a belgian proffesor in the academic hospitol of Brussels. The doctor claimed he has reminesses of clamidia and this is the problem, or the initiator of the disease. He treated him with antibiotics for a year (a very heavy treatment, espacially for CFS patient). the antibiotics period ended in January, since then he is taking B12, E-vitamins and acetyl-cicteyin, almost for half a year now. but he is still sick. before all this agressive treatment we tried acupancture, tibatian medicens and of course healty dieet (which he still holds). we tried also a treatment with something called careten (not cratene) we are now thinking of going through a new natural treatment series with Dr. de Meier in the Netherlands (did someone heard about him or used his services?!) life is not easy for a CFS patient or to his/her partner, even if you don't have answers for me, it is nice to know there are people I/we can talk to about it. Are there also partners of patients around? hope to hear from you soon
hi, my partner has CFS for a few years now. It started as fatig attacks for tow to three days in a month. gradually it became worse and now we are happy if there is a good day in a week or two. a year and a half ago he started a treatment with a belgian proffesor in the academic hospitol of Brussels. The doctor claimed he has reminesses of clamidia and this is the problem, or the initiator of the disease. He treated him with antibiotics for a year (a very heavy treatment, espacially for CFS patient). the antibiotics period ended in January, since then he is taking B12, E-vitamins and acetyl-cicteyin, almost for half a year now. but he is still sick. before all this agressive treatment we tried acupancture, tibatian medicens and of course healty dieet (which he still holds). we tried also a treatment with something called careten (not cratene) we are now thinking of going through a new natural treatment series with Dr. de Meier in the Netherlands (did someone heard about him or used his services?!) life is not easy for a CFS patient or to his/her partner, even if you don't have answers for me, it is nice to know there are people I/we can talk to about it. Are there also partners of patients around? hope to hear from you soon