Post on PR re this with some detail re lead researcher
http://forums.phoenixrising.me/index.php?threads/keele-university-seeks-cfs-patients-for-new-study-–-lead-researcher-carolyn-chew-graham.59378/
Was EC not the only speaker not to have their presentation on YouTube last year at CMRC? I could well be wrong as i was only dipping a toe into ME political waters then
I seem to remember Dr Rowe' s POTS lecture highlighting the huge gulf in paediatric knowledge. Up til then children did not...
Perhaps its the genetics - my daughter has genes that are different to " normal" for omega 3 and 6. If these are expressed then the ratio is well out of whack.
Really ironic- when we had bullying issues and tried to get gp and cahmns to share concerns with school ( who really were not interested in addressing root cause) this could not be done due to " confidentiality". So only when it suits ....
I don't think many of the figures would stand up to scrutiny - the 250,000 has been around for at least 10 years...
From forums, I would agree re the 25% being questionable
Perhaps a poll both here and on MEA website @Russell Fleming
Our issues here are that you will simply fail to be diagnosed...
I am on another online mum' s forum. Smaller but some have had similar opinions and experiences.
There are a few good stories, too where staff advise against doing too much too soon. It would seem to depend who you get ( no pun intended)
From parents' forum there does seem to be some correlation , particularly high functioning asbergers. Whether that is higher than general population, or within other chronic illnesses, i don' t know. Adolescent females seem particularly affected and female ASD does seem subtly different.
Rich...
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