Happy New Year greetings from Down Under!
We are from Australia and wish to use our limited savings to have our son treated in the US. He is currently under the care of a GP 'with interest in CFS'. This doctor has been treating 4500 patients since 1985, so it is very hard for him to be actively involved in caring for each individual patient. My son's condition has deteriorated rapidly and all this good doctor said was, "hang in there, there is hope".
I heard about Dr Chia from the Invest in ME Conference. Would appreciate comments from his patients. He does not seem to have a dedicated, informative website.
Any idea on the cost of investigations/ treatment/ consultation as an international patient of Dr Sharp? What is the length of stay we should be looking at on the first appointment?
Also, has anyone tried traditional Chinese medicine? Has it a role in the treatment of ME/CFS?
Cheers,
Zuriel
Aussie Newbie
We are from Australia and wish to use our limited savings to have our son treated in the US. He is currently under the care of a GP 'with interest in CFS'. This doctor has been treating 4500 patients since 1985, so it is very hard for him to be actively involved in caring for each individual patient. My son's condition has deteriorated rapidly and all this good doctor said was, "hang in there, there is hope".
I heard about Dr Chia from the Invest in ME Conference. Would appreciate comments from his patients. He does not seem to have a dedicated, informative website.
Any idea on the cost of investigations/ treatment/ consultation as an international patient of Dr Sharp? What is the length of stay we should be looking at on the first appointment?
Also, has anyone tried traditional Chinese medicine? Has it a role in the treatment of ME/CFS?
Cheers,
Zuriel
Aussie Newbie