I believe NHS ought to get its act to gather re: way it treats the muscuskeletal via independent physios & practitioners who are not the best medically qualified to Research & diagnose as have succumbed to remits & criteria ??!! Triaging is foolhardy surely? All this and with GPs who have allowed the funds to go to LAs maladministrating Social Services by questionable unfair assessments as in case of Alzheimers / MID . likewise the Mc Millan Nurses & the Charities such as those managing lipo lymphoedema , MS , Spina bifida , Arthritis discriminating against those who they consider can be discriminated against in fact those who could help them via Research yet Insurance companies regard as risky .
Otherwise why are a good proportion of those left in limbo made addicted to painkillers with no research & Patient orientated treatment .This is not acceptable .
Could CFS /fibro be a symptom, like utis , as why ,when investigating my case the family history genetics says it all . While admin[ Registrars in Hospitals] on remits to block are used as gateway with criteria this will always be ignored .I had troponin found & an A&E refused to do again having summoned back next day with GP not following up.
Ok there is self referral but just for their FINANCIAL benefit as can be seen in Minor Injuries run by Nurses refusing to assist the Chronic even when acute .
My problems relate to inflammation & plumbing sepsis relieved with antibiotics from a Prof of Urodynamics on a remit not able to refer or transfer or direct ? .CFS / fibro was confirmed when heart failure symptoms were ignored before cardiac arrest & the CFS trigger points are where there is weak heart pumping as spasmodic.this i have proved emanates from disability that it can't even educate its Drs about they told me THIS when it was found before the Cuts in 1980s & since always cutting in same places the easy targets the chronic the Vulnerable !
When NHS refuses to test & Refer to specialists how is it going to get to the nitty gritty when directed by non medical with other agendas .....
I think eventually stem cells will be the way forward as now the chronic are ignored to become acute too late when some help could have been accessed earlier.I wonder what statistics are ? I dread to think?
NB Below why didn't the realise the CFS/fibro patients could be the way forward?
Welcome to the PREVeNT RA study registration website
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My relative father pharmacist has been deceased a number of yrs attended St Georges Cardiac Tooting London W needed a new valve - suffered severely with putting joints out [ very sporty] Chelsea Football Teams Masseur .This was A BLOOD sample from me suspect my problems Microvascular - relating to breathing/heart pas Dr Coghlan Royal Free & Lipo-Lymphoedema St Georges diagnosed NOT Treated [ Prof Mortimer] .My late mother developed severe MID at same time as polymyalgia rheumatic affecting movement including speech & swallowing .At same time both attended Geriatric Dept Of Kingston Upon Thames Hospital Surrey NB There is a strong neurological component due to my spina bifida abnormal EEG relating to chronic utis acute 3 weekly & strength of testing microscopes as denying stable/unstable angina when had angioplsty to revive when MI 11 YEARS AGO classic heart failure symptons dysponea/PAH only revealing last year on Reveal device .i have spinal spasicity spasms not acknowleged fairly re directing to RNOH problem gettingsteroid injections renewed would like to try PRP or stem cells as prevention .MS Therapy could help? Why is the Alternative sector so much more effective?