Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 Hi Agent! Your kidding, aren't you? You are obviously not suffering from CFS.... BW Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 I want to share with you my latest cure. It is a self made protocol and I am not a doctor so that should help. It consists of doing 3 hours of plastering a day, or as much as you can manage to start. Plastering is one of the most physical jobs one can do especially in France where the plaster goes off even quicker. My thesis is that we have let the buggers disturb our normal rhythm. Kids run about all day, and never seem to tire, yet we sit on our computers waiting for the cure, when really what we all need to be doing is sweating the beasts out and waking up our immune systems. No better way to make the body more alkaline than to oxygenate it through physical work. One should not stop until one has sweated enough that everyone knows. After that you get plastered with 3 glasses of good quality red wine. Th next day starts with 6 oysters and what ever else you fancy. To start do one day on, one off, and after a week, every day you do a min of 3 hours. To relax in the evening it is essential that you do 20-30 minutes of deep relaxing stretching and breathing. This is most essential for the colon and sleep. Agent Bleu On 12 May 2005, at 05:28, Ken wrote: > Folks, > We seem to have run out of steam!!! > > To get the fires going again may I suggest that people posts > descriptions of what they feel may be the physiological cause of > CFIDS/ME. Things from Secondary Adrenal Insufficiency to specific > infections etc. > > Start the email with CAUSE:?????????? > > Once we get a ton of causes posted, we can walk thru them and discuss > them, and how they could or should be tested for, or treated.... > > Are there any new protocols out there? Is it time to revisit protocols > from 10 years ago and critically review them? > > > > > > > > This list is intended for patients to share personal experiences with > each other, not to give medical advice. If you are interested in any > treatment discussed here, please consult your doctor. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 my main disease was reactive arthritis which came with its own bout of CFS, that is almost gone but I still have a few issues left. B vits are working great. > Hi Agent! > > Your kidding, aren't you? > > You are obviously not suffering from CFS.... > > BW > > > > > > This list is intended for patients to share personal experiences with > each other, not to give medical advice. If you are interested in any > treatment discussed here, please consult your doctor. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 Bleu: With all due respect, if you can physically exert yourself and drink alcohol, then you don't have the same illness I do. Your idea of a cure would kill me. I used to walk several miles a day, when I got ill there were no computers to sit in front of. Helen > > > Folks, > > We seem to have run out of steam!!! > > > > To get the fires going again may I suggest that people posts > > descriptions of what they feel may be the physiological cause of > > CFIDS/ME. Things from Secondary Adrenal Insufficiency to specific > > infections etc. > > > > Start the email with CAUSE:?????????? > > > > Once we get a ton of causes posted, we can walk thru them and discuss > > them, and how they could or should be tested for, or treated.... > > > > Are there any new protocols out there? Is it time to revisit protocols > > from 10 years ago and critically review them? > > > > > > > > > > > > > > > > This list is intended for patients to share personal experiences with > > each other, not to give medical advice. If you are interested in any > > treatment discussed here, please consult your doctor. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 Yes there are two things that make my condition a 1000 times worse. One is alcohol and the other is physical exercise. When I was first ill I tried to go out for a walk each day and each time it made me exhausted. Stupidly I kept pushing myself though and ended up in a wheelchair. Re: The Plastering Cure > Bleu: > > With all due respect, if you can physically exert yourself and drink > alcohol, then you don't have the same illness I do. Your idea of a > cure would kill me. I used to walk several miles a day, when I got > ill there were no computers to sit in front of. > > Helen > > > >> >> > Folks, >> > We seem to have run out of steam!!! >> > >> > To get the fires going again may I suggest that people posts >> > descriptions of what they feel may be the physiological cause of >> > CFIDS/ME. Things from Secondary Adrenal Insufficiency to specific >> > infections etc. >> > >> > Start the email with CAUSE:?????????? >> > >> > Once we get a ton of causes posted, we can walk thru them and > discuss >> > them, and how they could or should be tested for, or treated.... >> > >> > Are there any new protocols out there? Is it time to revisit > protocols >> > from 10 years ago and critically review them? >> > >> > >> > >> > >> > >> > >> > >> > This list is intended for patients to share personal experiences > with >> > each other, not to give medical advice. If you are interested in > any >> > treatment discussed here, please consult your doctor. >> > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2005 Report Share Posted May 12, 2005 as i said > Bleu: > > With all due respect, if you can physically exert yourself and drink > alcohol, then you don't have the same illness I do. Your idea of a > cure would kill me. I used to walk several miles a day, when I got > ill there were no computers to sit in front of. > > Helen > > > >> >>> Folks, >>> We seem to have run out of steam!!! >>> >>> To get the fires going again may I suggest that people posts >>> descriptions of what they feel may be the physiological cause of >>> CFIDS/ME. Things from Secondary Adrenal Insufficiency to specific >>> infections etc. >>> >>> Start the email with CAUSE:?????????? >>> >>> Once we get a ton of causes posted, we can walk thru them and > discuss >>> them, and how they could or should be tested for, or treated.... >>> >>> Are there any new protocols out there? Is it time to revisit > protocols >>> from 10 years ago and critically review them? >>> >>> >>> >>> >>> >>> >>> >>> This list is intended for patients to share personal experiences > with >>> each other, not to give medical advice. If you are interested in > any >>> treatment discussed here, please consult your doctor. >>> Quote Link to comment Share on other sites More sharing options...
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